Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:102714271-102714627 | Common:2; Rare:119 | ||||
chr10:102776078-102776228 | Common:1; Rare:23 | ||||
chr10:103193248-103193354 | Common:5; Rare:36; Clinvar (benign):1 | ||||
chr10:103396411-103396702 | Rare:104 | ||||
chr10:103451235-103451331 | Rare:27 | ||||
chr10:103452262-103452453 | Rare:56 | ||||
chr10:103917750-103917822 | Rare:16 | ||||
chr10:103918118-103918517 | Common:5; Rare:107 | ||||
chr10:104254546-104254955 | Common:4; Rare:88 | ||||
chr10:104268980-104269182 | Common:2; Rare:44 | ||||
chr10:104338377-104338522 | Rare:40 | ||||
chr10:109923423-109923686 | Common:2; Rare:103 | ||||
chr10:110005877-110006094 | Common:4; Rare:60 | ||||
chr10:110007862-110008120 | Common:1; Rare:61 | ||||
chr10:110008162-110008268 | Common:1; Rare:50 |