Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:17230555-17230710 | Rare:67; Clinvar:1 | ||||
chr10:17617172-17617640 | Common:6; Rare:162; Clinvar:1 | ||||
chr10:17643871-17644315 | Common:2; Rare:138 | ||||
chr10:18140441-18140899 | Common:4; Rare:155; Clinvar:5; Clinvar (benign):9 | ||||
chr10:18140908-18141165 | Common:2; Rare:59 | ||||
chr10:18141570-18141713 | Common:2; Rare:27 | ||||
chr10:18340572-18340830 | Common:3; Rare:55; Clinvar:1; Clinvar (benign):2 | ||||
chr10:18651553-18651778 | Common:1; Rare:92 | ||||
chr10:18659226-18659585 | Common:2; Rare:116 | ||||
chr10:19816123-19816612 | Common:6; Rare:113 | ||||
chr10:20897541-20897721 | Rare:32 | ||||
chr10:21497247-21497410 | Common:1; Rare:34 | ||||
chr10:21524581-21524712 | Rare:22 | ||||
chr10:22316288-22316478 | Common:1; Rare:81 | ||||
chr10:22325520-22325671 | Rare:67 |