Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:102394337-102394582 | Common:1; Rare:65 | ||||
chr10:102395581-102395793 | Common:1; Rare:53 | ||||
chr10:102420797-102420843 | Rare:11 | ||||
chr10:102432546-102432681 | Rare:35 | ||||
chr10:102714271-102714659 | Common:2; Rare:127 | ||||
chr10:102776078-102776279 | Common:1; Rare:34 | ||||
chr10:103193240-103193603 | Common:5; Rare:91; Clinvar (benign):1 | ||||
chr10:103396411-103396724 | Rare:109 | ||||
chr10:103918120-103918523 | Common:5; Rare:110 | ||||
chr10:104121878-104122174 | Common:2; Rare:95 | ||||
chr10:104268912-104269212 | Common:4; Rare:73 | ||||
chr10:109923423-109923619 | Common:1; Rare:67 | ||||
chr10:110007690-110008028 | Rare:98 | ||||
chr10:110008156-110008281 | Common:1; Rare:58 | ||||
chr10:110567391-110567745 | Common:2; Rare:89; Clinvar:1; Clinvar (benign):5 |