ID: 130000042 | ATAC-STARR-seq lymphoblastoid silent region 19030 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (23682610..23683119) | | |
ID: 130000041 | ATAC-STARR-seq lymphoblastoid silent region 19029 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (23682520..23682569) | | |
ID: 127458958 | H3K4me1 hESC enhancer GRCh37_chr8:23641595-23642178 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (23784082..23784665) | | |
ID: 127458957 | H3K4me1 hESC enhancer GRCh37_chr8:23566930-23567494 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (23709417..23709981) | | |
ID: 127458956 | H3K4me1 hESC enhancer GRCh37_chr8:23561989-23562888 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (23704476..23705375) | | |
ID: 127458955 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:23507883-23508510 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (23650370..23650997) | | |
ID: 126860327 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr8:23655625-23656824 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (23798112..23799311) | | |
ID: 124900262 | uncharacterized LOC124900262 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (23806229..23806377, complement) | | |
ID: 113788271 | BRD4-independent group 4 enhancer GRCh37_chr8:23618596-23619795 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (23761083..23762282) | | |
ID: 107986930 | uncharacterized LOC107986930 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (23663078..23802942) | | |
ID: 101929258 | uncharacterized LOC101929258 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (23712864..23726943, complement) | | |
ID: 646721 | SINHCAF pseudogene 3 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (23634875..23635649, complement) | FAM60DP | |
ID: 137814 | NK2 homeobox 6 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (23701740..23706756, complement) | CSX2, CTHM, NKX2F, NKX4-2 | 611770 |
ID: 4824 | NK3 homeobox 1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (23678693..23682938, complement) | BAPX2, NKX3, NKX3.1, NKX3A | 602041 |