Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:100266113-100266294 | Common:2; Rare:65 | ||||
chr1:101025754-101025894 | Rare:42 | ||||
chr1:101236583-101237037 | Common:5; Rare:89 | ||||
chr1:103525911-103526018 | Rare:26 | ||||
chr1:108200154-108200438 | Common:9; Rare:86 | ||||
chr1:109090682-109090860 | Common:2; Rare:41 | ||||
chr1:109548562-109548703 | Common:3; Rare:51 | ||||
chr1:110339153-110339476 | Common:1; Rare:101 | ||||
chr1:110407603-110407802 | Common:2; Rare:89 | ||||
chr1:111140046-111140263 | Common:1; Rare:77 | ||||
chr1:112619738-112619842 | Common:1; Rare:40 | ||||
chr1:113929512-113929662 | Common:1; Rare:40 | ||||
chr1:114716713-114717071 | Common:4; Rare:131; Clinvar:5; Clinvar (benign):1 | ||||
chr1:117929622-117929802 | Common:2; Rare:46 | ||||
chr1:119140632-119140671 | Rare:21 |