Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:69539135-69539287 | Common:3; Rare:31 | ||||
chr10:70019436-70019594 | Common:2; Rare:27 | ||||
chr10:70335937-70336043 | Rare:23 | ||||
chr10:70862156-70862520 | Common:4; Rare:102 | ||||
chr10:70923859-70924017 | Common:2; Rare:32 | ||||
chr10:71377441-71377595 | Common:4; Rare:36 | ||||
chr10:71511936-71512128 | Common:2; Rare:35 | ||||
chr10:71725301-71725371 | Rare:22; Clinvar (benign):1 | ||||
chr10:71817422-71817768 | Common:2; Rare:87; Clinvar:1; Clinvar (benign):1 | ||||
chr10:71831837-71832055 | Common:5; Rare:54; Clinvar (benign):3 | ||||
chr10:71970426-71970588 | Rare:46 | ||||
chr10:71999412-71999433 | Rare:2 | ||||
chr10:72326626-72326788 | Rare:43 | ||||
chr10:72847914-72848101 | Rare:32 | ||||
chr10:73246918-73246961 | Rare:15 |