Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:102394315-102394587 | Common:1; Rare:74 | ||||
chr10:102395581-102395731 | Common:1; Rare:43 | ||||
chr10:102420959-102421150 | Rare:74 | ||||
chr10:102644967-102645136 | Rare:38 | ||||
chr10:102714271-102714637 | Common:2; Rare:122 | ||||
chr10:102776078-102776195 | Common:1; Rare:16 | ||||
chr10:103193243-103193512 | Common:5; Rare:80; Clinvar (benign):1 | ||||
chr10:103396395-103396719 | Rare:113 | ||||
chr10:103452241-103452453 | Rare:64 | ||||
chr10:103918110-103918645 | Common:5; Rare:137 | ||||
chr10:103967018-103967057 | Common:1; Rare:3 | ||||
chr10:104032940-104033065 | Rare:37; Clinvar:3 | ||||
chr10:104121760-104122171 | Common:3; Rare:137 | ||||
chr10:104268902-104269208 | Common:3; Rare:74 | ||||
chr10:104338388-104338528 | Rare:39 |