Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:92298934-92299094 | Common:1; Rare:80; Clinvar:2; Clinvar (benign):1 | ||||
chr1:92831863-92832113 | Common:1; Rare:114; Clinvar:6; Clinvar (benign):5 | ||||
chr1:93079060-93079422 | Common:4; Rare:138 | ||||
chr1:93180061-93180103 | Rare:15 | ||||
chr1:93180141-93180214 | Rare:27 | ||||
chr1:93180242-93180758 | Common:2; Rare:207 | ||||
chr1:93345797-93345946 | Common:3; Rare:56 | ||||
chr1:93448002-93448234 | Common:2; Rare:77 | ||||
chr1:93879144-93879299 | Common:2; Rare:54 | ||||
chr1:94418291-94418470 | Common:2; Rare:70 | ||||
chr1:94541806-94541991 | Rare:47 | ||||
chr1:94820212-94820375 | Common:2; Rare:44 | ||||
chr1:94903132-94903445 | Common:1; Rare:63 | ||||
chr1:94926944-94927473 | Common:4; Rare:166 | ||||
chr1:95233955-95234236 | Common:5; Rare:85 |