Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:111938646-111939046 | Common:6; Rare:132 | ||||
chr11:116424930-116425240 | Common:3; Rare:56 | ||||
chr11:116427670-116428608 | Common:11; Rare:260 | ||||
chr11:116808250-116808670 | Common:2; Rare:78 | ||||
chr11:116808860-116809230 | Common:1; Rare:63 | ||||
chr11:116826800-116827190 | Common:4; Rare:111 | ||||
chr11:116832229-116832629 | Common:3; Rare:96 | ||||
chr11:117096329-117096533 | Common:1; Rare:39 | ||||
chr11:118195080-118195500 | Common:6; Rare:109 | ||||
chr11:118435361-118435660 | Rare:128 | ||||
chr11:118791699-118791836 | Rare:41 | ||||
chr11:118912395-118912587 | Rare:96 | ||||
chr11:118918390-118918590 | Common:1; Rare:50 | ||||
chr11:118921260-118921660 | Common:9; Rare:163 | ||||
chr11:119027086-119027236 | Rare:50; Clinvar (benign):4 |