Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:110339129-110339473 | Common:1; Rare:103 | ||||
chr1:110407632-110407787 | Common:2; Rare:71 | ||||
chr1:111140083-111140258 | Common:1; Rare:56 | ||||
chr1:112396003-112396257 | Common:1; Rare:79 | ||||
chr1:112619132-112619190 | Rare:23 | ||||
chr1:112619710-112619863 | Common:1; Rare:57 | ||||
chr1:112956169-112956467 | Common:5; Rare:129; Clinvar:9; Clinvar (benign):3 | ||||
chr1:113905039-113905402 | Common:5; Rare:100 | ||||
chr1:117060037-117060359 | Common:7; Rare:86 | ||||
chr1:117929591-117929800 | Common:1; Rare:57 | ||||
chr1:119140647-119140761 | Rare:33 | ||||
chr1:145823937-145824265 | Rare:117 | ||||
chr1:145918693-145919042 | Common:2; Rare:73 | ||||
chr1:145927431-145927667 | Common:1; Rare:69; Clinvar (pathogenic):1 | ||||
chr1:145958007-145958223 | Rare:52 |