ID: 130067335 | ATAC-STARR-seq lymphoblastoid active region 18938 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36529037..36529436) | | |
ID: 130067334 | ATAC-STARR-seq lymphoblastoid active region 18937 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36528677..36528726) | | |
ID: 130067333 | ATAC-STARR-seq lymphoblastoid active region 18936 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36511344..36511423) | | |
ID: 130067332 | ATAC-STARR-seq lymphoblastoid silent region 13670 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36506787..36507286) | | |
ID: 127896054 | H3K4me1 hESC enhancer GRCh37_chr22:37080862-37081403 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36684817..36685358) | | |
ID: 127896053 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:37006222-37006886 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36610175..36610839) | | |
ID: 127896052 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:37005558-37006221 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36609511..36610174) | | |
ID: 127896051 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:37004893-37005557 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36608846..36609510) | | |
ID: 127896050 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:36966399-36966990 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36570352..36570943) | | |
ID: 127896049 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:36959107-36959622 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36563060..36563575) | | |
ID: 127896048 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:36878117-36879063 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36482070..36483016) | | |
ID: 127896047 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:36865950-36866786 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36469903..36470739) | | |
ID: 125446228 | Sharpr-MPRA regulatory region 13009 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36544402..36544696) | | |
ID: 105373020 | uncharacterized LOC105373020 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36496025..36497999) | | |
ID: 100500719 | HPS1, biogenesis of lysosomal organelles complex 3 subunit 1 pseudogene [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36536609..36537756, complement) | | |
ID: 80020 | FAD dependent oxidoreductase domain containing 2 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36487190..36507040, complement) | ERFAD | 613777 |
ID: 25828 | thioredoxin 2 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36467046..36481640, complement) | COXPD29, MT-TRX, MTRX, TRX2, TXN | 609063 |
ID: 10369 | calcium voltage-gated channel auxiliary subunit gamma 2 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36560857..36703752, complement) | MRD10 | 602911 |
ID: 8664 | eukaryotic translation initiation factor 3 subunit D [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (36510855..36529166, complement) | EIF3S7, eIF3-p66, eIF3-zeta | 603915 |