Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:89994981-89995214 | Common:2; Rare:87 | ||||
chr1:91886012-91886340 | Rare:133 | ||||
chr1:92298908-92299090 | Common:1; Rare:87; Clinvar:2; Clinvar (benign):2 | ||||
chr1:92832000-92832133 | Rare:80; Clinvar:7; Clinvar (benign):7 | ||||
chr1:92961411-92961581 | Rare:64 | ||||
chr1:93079102-93079303 | Common:2; Rare:85 | ||||
chr1:93179855-93179961 | Common:1; Rare:26 | ||||
chr1:93180051-93180357 | Rare:101 | ||||
chr1:93180362-93180744 | Common:2; Rare:166 | ||||
chr1:93345766-93345953 | Common:4; Rare:74 | ||||
chr1:93847213-93847273 | Common:1; Rare:14 | ||||
chr1:93879097-93879274 | Common:1; Rare:68 | ||||
chr1:94237529-94237744 | Rare:84 | ||||
chr1:94541606-94542000 | Common:1; Rare:114 | ||||
chr1:94820264-94820382 | Common:2; Rare:33 |