Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:506732-507005 | Common:3; Rare:93 | ||||
chr11:560732-561021 | Common:5; Rare:130 | ||||
chr11:576412-576559 | Rare:60 | ||||
chr11:615946-616073 | Common:1; Rare:40 | ||||
chr11:695647-695833 | Rare:50 | ||||
chr11:747335-747514 | Rare:76; Clinvar:2; Clinvar (benign):1 | ||||
chr11:777458-777638 | Common:1; Rare:81 | ||||
chr11:790045-790163 | Common:1; Rare:28 | ||||
chr11:798204-798446 | Common:2; Rare:83 | ||||
chr11:809516-809665 | Common:2; Rare:41 | ||||
chr11:832819-833018 | Common:7; Rare:66 | ||||
chr11:842476-842978 | Common:8; Rare:207 | ||||
chr11:2992239-2992516 | Common:2; Rare:108 | ||||
chr11:3057365-3057553 | Rare:68 | ||||
chr11:3379082-3379309 | Common:3; Rare:59 |