ID: 130065324 | ATAC-STARR-seq lymphoblastoid silent region 12617 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (3239280..3239439) | | |
ID: 130065323 | ATAC-STARR-seq lymphoblastoid silent region 12616 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (3239000..3239179) | | |
ID: 130065322 | ATAC-STARR-seq lymphoblastoid silent region 12615 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (3218602..3218871) | | |
ID: 130065321 | ATAC-STARR-seq lymphoblastoid active region 17476 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (3204374..3204593) | | |
ID: 130065320 | ATAC-STARR-seq lymphoblastoid silent region 12614 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (3173433..3173772) | | |
ID: 129664552 | ReSE screen-validated silencer GRCh37_chr20:3163335-3163502 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (3182689..3182856) | | |
ID: 127892474 | H3K4me1 hESC enhancer GRCh37_chr20:3276431-3276932 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (3295785..3296285) | | |
ID: 127892473 | H3K4me1 hESC enhancer GRCh37_chr20:3230929-3231429 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (3250283..3250783) | | |
ID: 127892472 | H3K4me1 hESC enhancer GRCh37_chr20:3229525-3230269 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (3248879..3249623) | | |
ID: 127892471 | H3K4me1 hESC enhancer GRCh37_chr20:3228779-3229524 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (3248133..3248878) | | |
ID: 127892470 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:3210499-3211281 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (3229853..3230635) | | |
ID: 127892469 | H3K27ac hESC enhancer GRCh37_chr20:3189739-3190387 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (3209093..3209741) | | |
ID: 127892468 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:3183418-3184016 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (3202772..3203370) | | |
ID: 107985414 | uncharacterized LOC107985414 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (3173690..3179063) | | |
ID: 106480015 | RNA, U6 small nuclear 1019, pseudogene [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (3360036..3360142) | | |
ID: 101618237 | ubiquitin conjugating enzyme E2 F (putative) pseudogene [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (3295496..3296373, complement) | | |
ID: 83959 | solute carrier family 4 member 11 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (3227417..3239559, complement) | BTR1, CDPD1, CHED, CHED2, NABC1, dJ794I6.2 | 610206 |
ID: 65992 | DDRGK domain containing 1 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (3190350..3204682, complement) | C20orf116, SEMDSH, UFBP1, dJ1187M17.3 | 616177 |
ID: 25943 | dynein axonemal assembly factor 9 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (3249306..3407669, complement) | C20orf194 | 614146 |
ID: 3704 | inosine triphosphatase [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (3204065..3227449) | C20orf37, DEE35, HLC14-06-P, ITPase, My049, NTPase, dJ794I6.3 | 147520 |