Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:104338322-104338549 | Rare:58 | ||||
chr10:110007716-110008009 | Rare:83 | ||||
chr10:110008162-110008281 | Common:1; Rare:56 | ||||
chr10:110872257-110872574 | Rare:106 | ||||
chr10:110919289-110919632 | Common:7; Rare:89 | ||||
chr10:112446892-112447346 | Common:3; Rare:116 | ||||
chr10:112950048-112950266 | Common:2; Rare:41 | ||||
chr10:113854392-113854658 | Rare:56 | ||||
chr10:117542261-117542390 | Rare:32 | ||||
chr10:119080742-119081149 | Common:1; Rare:134 | ||||
chr10:119651638-119651846 | Common:1; Rare:73; Clinvar:8; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
chr10:119892544-119892765 | Common:3; Rare:83 | ||||
chr10:120851085-120851411 | Common:8; Rare:98 | ||||
chr10:122019147-122019465 | Rare:62 | ||||
chr10:122290896-122291127 | Common:4; Rare:50 |