Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:14953996-14954195 | Rare:70 | ||||
chr10:15097270-15097378 | Common:2; Rare:57 | ||||
chr10:15860455-15860583 | Rare:36 | ||||
chr10:16817345-16817744 | Common:4; Rare:144 | ||||
chr10:17228987-17229026 | Common:1; Rare:9 | ||||
chr10:17229108-17229369 | Common:2; Rare:52 | ||||
chr10:17643871-17644303 | Common:2; Rare:133 | ||||
chr10:18261246-18261264 | Rare:4 | ||||
chr10:18340572-18340728 | Common:3; Rare:34; Clinvar (benign):2 | ||||
chr10:18651549-18651748 | Common:1; Rare:85 | ||||
chr10:18659231-18659635 | Common:2; Rare:140 | ||||
chr10:19815673-19815762 | Rare:24 | ||||
chr10:19816117-19816478 | Common:5; Rare:74 | ||||
chr10:21497255-21497381 | Rare:24 | ||||
chr10:21524525-21524676 | Rare:27 |