ID: 130056212 | ATAC-STARR-seq lymphoblastoid active region 8828 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (81256749..81256828) | | |
ID: 130056211 | ATAC-STARR-seq lymphoblastoid active region 8827 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (81235373..81235532) | | |
ID: 130056210 | ATAC-STARR-seq lymphoblastoid silent region 5986 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (81220824..81221123) | | |
ID: 130056209 | ATAC-STARR-seq lymphoblastoid silent region 5985 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (81220744..81220793) | | |
ID: 130056208 | ATAC-STARR-seq lymphoblastoid silent region 5984 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (81220094..81220213) | | |
ID: 130056207 | ATAC-STARR-seq lymphoblastoid active region 8824 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (81170411..81170780) | | |
ID: 130056206 | ATAC-STARR-seq lymphoblastoid active region 8823 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (81170131..81170190) | | |
ID: 129663471 | ReSE screen-validated silencer GRCh37_chr14:81507651-81507772 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (81041307..81041428) | | |
ID: 108251794 | GTF2A1 intron CAGE-defined high expression enhancer [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (81219169..81219753) | | |
ID: 105370594 | uncharacterized LOC105370594 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (81168772..81171835) | | |
ID: 101928504 | GTF2A1 antisense RNA 1 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (81221218..81223380) | | |
ID: 101928462 | uncharacterized LOC101928462 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (81014066..81170406, complement) | | |
ID: 677845 | small nucleolar RNA, H/ACA box 79 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (81202695..81202834, complement) | ACA65A, SNORA79 | |
ID: 326607 | NMNAT1 pseudogene 1 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (81032474..81032979) | NMNATP | |
ID: 319122 | uracil-DNA glycosylase pseudogene 3 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (81258328..81260234, complement) | | |
ID: 246720 | dynein light chain LC8-type 1 pseudogene 1 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (81246010..81246671, complement) | DNCL1P1 | |
ID: 7253 | thyroid stimulating hormone receptor [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (80955621..81146306) | CHNG1, LGR3, hTSHR-I | 603372 |
ID: 2957 | general transcription factor IIA subunit 1 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (81175452..81221390, complement) | TF2A1, TFIIA, TFIIA-42, TFIIAL | 600520 |