Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:24291615-24291663 | Rare:16 | ||||
chr14:24298958-24299305 | Rare:105 | ||||
chr14:24299633-24299850 | Common:4; Rare:55 | ||||
chr14:24309980-24310164 | Common:1; Rare:38 | ||||
chr14:24313212-24313398 | Rare:37 | ||||
chr14:24314844-24314885 | Rare:5 | ||||
chr14:24429855-24429980 | Rare:30 | ||||
chr14:24442658-24443046 | Common:5; Rare:122 | ||||
chr14:30622235-30622410 | Common:1; Rare:90 | ||||
chr14:31025419-31025653 | Common:2; Rare:55 | ||||
chr14:31207419-31207849 | Common:2; Rare:140 | ||||
chr14:31208120-31208212 | Common:1; Rare:22 | ||||
chr14:31420486-31420654 | Common:4; Rare:72 | ||||
chr14:31561081-31561506 | Common:5; Rare:116; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr14:32076244-32076330 | Rare:25 |