Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:44238855-44238915 | Rare:8 | ||||
chr11:44804325-44804540 | Rare:43 | ||||
chr11:44928803-44929132 | Common:2; Rare:64 | ||||
chr11:45658730-45658792 | Common:1; Rare:19 | ||||
chr11:45910205-45910526 | Rare:86; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr11:45972407-45972536 | Common:1; Rare:12 | ||||
chr11:46382290-46382746 | Common:1; Rare:146 | ||||
chr11:46383274-46383448 | Common:1; Rare:40 | ||||
chr11:46578932-46579039 | Common:2; Rare:6 | ||||
chr11:46656430-46656442 | Rare:1 | ||||
chr11:46680249-46680518 | Common:2; Rare:67 | ||||
chr11:46688236-46688533 | Common:2; Rare:54 | ||||
chr11:46759007-46759276 | Common:1; Rare:61 | ||||
chr11:46772655-46772718 | Rare:6 | ||||
chr11:46807856-46808143 | Common:1; Rare:45 |