| ID: 130067553 | ATAC-STARR-seq lymphoblastoid silent region 13796 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41699476..41699575) | | |
| ID: 130067552 | ATAC-STARR-seq lymphoblastoid active region 19128 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41696883..41697262) | | |
| ID: 130067551 | ATAC-STARR-seq lymphoblastoid active region 19127 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41696793..41696872) | | |
| ID: 130067550 | ATAC-STARR-seq lymphoblastoid active region 19126 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41688787..41688966) | | |
| ID: 130067549 | ATAC-STARR-seq lymphoblastoid active region 19125 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41688067..41688236) | | |
| ID: 130067548 | ATAC-STARR-seq lymphoblastoid active region 19124 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41619129..41619188) | | |
| ID: 130067547 | ATAC-STARR-seq lymphoblastoid active region 19123 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41619049..41619118) | | |
| ID: 129664866 | ReSE screen-validated silencer GRCh37_chr22:42084352-42084551 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41688348..41688547) | | |
| ID: 127896409 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:42026409-42027062 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41630405..41631058) | | |
| ID: 127896408 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:42016465-42017066 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41620461..41621063) | | |
| ID: 107985567 | protein LLP homolog [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41675202..41677160, complement) | | |
| ID: 106479777 | RNA, U6 small nuclear 476, pseudogene [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41679711..41679817) | | |
| ID: 106479553 | RNA, U6atac small nuclear 22, pseudogene [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41722043..41722131, complement) | | |
| ID: 150365 | meiotic double-stranded break formation protein 1 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41699503..41799454) | HYDM3, SPATA38 | 608797 |
| ID: 79640 | chromosome 22 open reading frame 46, pseudogene [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41688937..41698136) | C22orf46 | |
| ID: 27351 | desumoylating isopeptidase 1 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41598028..41621043, complement) | D15Wsu75e, DESI2, DJ347H13.4, DeSI-1, FAM152B, POST, PPPDE2 | 614637 |
| ID: 23606 | high mobility group nucleosomal binding domain 2 pseudogene10 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41709025..41709585, complement) | HMG17L2, HMGN2L10, bK216E10 | |
| ID: 4809 | small nuclear ribonucleoprotein 13 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41673933..41690480, complement) | 15.5K, FA-1, FA1, NHP2L1, NHPX, OTK27, SNRNP15-5, SPAG12, SSFA1 | 601304 |
| ID: 2547 | X-ray repair cross complementing 6 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41621295..41664041) | CTC75, CTCBF, G22P1, KU70, ML8, TLAA | 152690 |