| ID: 129999836 | ATAC-STARR-seq lymphoblastoid silent region 18906 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (9151413..9151662) | | |
| ID: 129999835 | ATAC-STARR-seq lymphoblastoid active region 26981 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (9151053..9151292) | | |
| ID: 127458615 | H3K4me1 hESC enhancer GRCh37_chr8:9176987-9177486 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (9319477..9319976) | | |
| ID: 127458614 | H3K4me1 hESC enhancer GRCh37_chr8:9176485-9176986 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (9318975..9319476) | | |
| ID: 127458613 | H3K27ac hESC enhancer GRCh37_chr8:9134231-9134732 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (9276721..9277222) | | |
| ID: 127458612 | OCT4-NANOG hESC enhancer GRCh37_chr8:9127271-9127799 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (9269761..9270289) | | |
| ID: 127458611 | NANOG-H3K27ac hESC enhancer GRCh37_chr8:9120655-9121382 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (9263145..9263872) | | |
| ID: 127458610 | H3K27ac hESC enhancer GRCh37_chr8:9114015-9114515 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (9256505..9257005) | | |
| ID: 127458609 | H3K4me1 hESC enhancer GRCh37_chr8:9106826-9107326 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (9249316..9249816) | | |
| ID: 127458608 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:9041503-9042488 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (9183993..9184978) | | |
| ID: 127458607 | NANOG-H3K27ac hESC enhancer GRCh37_chr8:9040517-9041502 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (9183007..9183992) | | |
| ID: 127458606 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:9007568-9008516 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (9150058..9151006) | | |
| ID: 127458605 | H3K4me1 hESC enhancer GRCh37_chr8:8997999-8998498 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (9140489..9140988) | | |
| ID: 126860299 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr8:9046079-9047278 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (9187937..9189768) | | |
| ID: 124901883 | uncharacterized LOC124901883 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (9303997..9307412) | | |
| ID: 124901882 | uncharacterized LOC124901882 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (9141419..9145510) | | |
| ID: 124049162 | Sharpr-MPRA regulatory region 719 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (9263873..9264653) | | |
| ID: 107986914 | ubiquitin-conjugating enzyme E2 variant 1-like [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (9232904..9233575) | | |
| ID: 106481543 | RNA, U6 small nuclear 1151, pseudogene [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (9287472..9287578, complement) | | |
| ID: 102724880 | PPP1R3B divergent transcript [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (9151725..9169597) | AC02278.4 | |