| ID: 130065977 | ATAC-STARR-seq lymphoblastoid active region 17956 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (45972605..45972824) | | |
| ID: 130065976 | ATAC-STARR-seq lymphoblastoid silent region 12968 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (45971715..45971834) | | |
| ID: 130065975 | ATAC-STARR-seq lymphoblastoid active region 17955 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (45933584..45933733) | | |
| ID: 129664627 | ReSE screen-validated silencer GRCh37_chr20:44531171-44531366 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (45902532..45902727) | | |
| ID: 127893443 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:44603922-44604458 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (45975283..45975819) | | |
| ID: 127893442 | H3K4me1 hESC enhancer GRCh37_chr20:44567720-44568234 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (45939081..45939595) | | |
| ID: 127893441 | H3K4me1 hESC enhancer GRCh37_chr20:44567204-44567719 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (45938565..45939080) | | |
| ID: 127893440 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:44563324-44564014 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (45934685..45935375) | | |
| ID: 127893439 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:44562632-44563323 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (45933993..45934684) | | |
| ID: 127893438 | H3K4me1 hESC enhancer GRCh37_chr20:44561248-44561940 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (45932609..45933301) | | |
| ID: 126863038 | MED14-independent group 3 enhancer GRCh37_chr20:44572602-44573801 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (45943963..45945162) | | |
| ID: 125387278 | Sharpr-MPRA regulatory region 14031 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (45924570..45924864) | | |
| ID: 121853008 | Sharpr-MPRA regulatory region 10402 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (45927310..45927604) | | |
| ID: 107985388 | pre-mRNA-splicing factor cwc22-like [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (45933494..45935071, complement) | | |
| ID: 170514 | ferritin light chain pseudogene 1 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (45975117..45976268, complement) | FTLP, bA465L10.3 | |
| ID: 63935 | phosphorylated CTD interacting factor 1 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (45934683..45948020) | C20orf67, CAPAM, MT-A70, PPP1R121, hCAPAM, hPCIF1 | 618626 |
| ID: 63925 | zinc finger protein 335 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (45948660..45972203, complement) | MCPH10, NIF-1, NIF1, NIF2 | 610827 |
| ID: 5476 | cathepsin A [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (45891335..45898820) | GLB2, GSL, NGBE, PPCA, PPGB | 613111 |
| ID: 5360 | phospholipid transfer protein [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (45898620..45912155, complement) | BPIFE, HDLCQ9 | 172425 |