Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:102645153-102645189 | Rare:7 | ||||
chr10:102645191-102645248 | Rare:26 | ||||
chr10:102714275-102714667 | Common:2; Rare:128 | ||||
chr10:103193245-103193328 | Common:4; Rare:27; Clinvar (benign):1 | ||||
chr10:103396426-103396733 | Rare:106 | ||||
chr10:104122053-104122171 | Common:2; Rare:53 | ||||
chr10:104268893-104269254 | Common:4; Rare:92 | ||||
chr10:104338436-104338528 | Rare:24 | ||||
chr10:110076749-110077075 | Common:1; Rare:52 | ||||
chr10:110567412-110567740 | Common:2; Rare:79; Clinvar:1; Clinvar (benign):4 | ||||
chr10:110871665-110872014 | Rare:117 | ||||
chr10:110884262-110884412 | Rare:19 | ||||
chr10:110919128-110919647 | Common:8; Rare:135; Clinvar:1 | ||||
chr10:112183733-112183851 | Common:3; Rare:45 | ||||
chr10:112446881-112447285 | Common:3; Rare:100 |