Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:97498694-97499063 | Common:2; Rare:108 | ||||
chr10:98268180-98268440 | Common:3; Rare:67 | ||||
chr10:99659247-99659554 | Common:1; Rare:77 | ||||
chr10:99732070-99732331 | Rare:97; Clinvar:4; Clinvar (benign):1 | ||||
chr10:100185926-100186135 | Rare:78 | ||||
chr10:100229553-100229640 | Rare:27 | ||||
chr10:100286605-100286750 | Common:5; Rare:82 | ||||
chr10:100912751-100912993 | Common:1; Rare:76 | ||||
chr10:100987273-100987577 | Common:1; Rare:114; Clinvar:1; Clinvar (benign):1 | ||||
chr10:101588211-101588329 | Rare:48 | ||||
chr10:101818361-101818778 | Common:1; Rare:111 | ||||
chr10:102714275-102714627 | Common:2; Rare:118 | ||||
chr10:103396419-103396702 | Rare:102 | ||||
chr10:110005784-110006084 | Common:4; Rare:74 | ||||
chr10:110007698-110008016 | Rare:92 |