| ID: 130067539 | ATAC-STARR-seq lymphoblastoid active region 19113 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41382701..41382780) | | |
| ID: 130067538 | ATAC-STARR-seq lymphoblastoid silent region 13785 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41367384..41367443) | | |
| ID: 130067537 | ATAC-STARR-seq lymphoblastoid silent region 13783 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41301212..41301551) | | |
| ID: 127896392 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:41760009-41760569 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41364005..41364565) | | |
| ID: 127896391 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:41756523-41757045 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41360519..41361041) | | |
| ID: 127896390 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:41756000-41756522 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41359996..41360518) | | |
| ID: 127896389 | H3K27ac hESC enhancer GRCh37_chr22:41720150-41720650 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41324146..41324646) | | |
| ID: 127896388 | H3K4me1 hESC enhancer GRCh37_chr22:41704863-41705362 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41308859..41309358) | | |
| ID: 127896387 | H3K4me1 hESC enhancer GRCh37_chr22:41704361-41704862 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41308357..41308858) | | |
| ID: 127896386 | H3K27ac hESC enhancer GRCh37_chr22:41697637-41698138 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41301633..41302134) | | |
| ID: 125446243 | Sharpr-MPRA regulatory region 10804 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41296805..41297099) | | |
| ID: 121627945 | Sharpr-MPRA regulatory region 9842 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41381161..41382490) | | |
| ID: 106481337 | RNA, U6 small nuclear 495, pseudogene [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41377177..41377283, complement) | | |
| ID: 105373042 | uncharacterized LOC105373042 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41370648..41381911, complement) | | |
| ID: 100996598 | uncharacterized LOC100996598 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41369082..41370396) | | |
| ID: 23264 | zinc finger CCCH-type containing 7B [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41301525..41360147) | ROXAN1, RoXaN | 618206 |
| ID: 7008 | TEF transcription factor, PAR bZIP family member [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41367455..41399326) | | 188595 |
| ID: 5905 | Ran GTPase activating protein 1 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41244779..41302369, complement) | Fug1, RANGAP, SD | 602362 |