Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:130912807-130912913 | Rare:28 | ||||
chr7:130913112-130913474 | Rare:62 | ||||
chr7:131106390-131106543 | Rare:28 | ||||
chr7:131108088-131108327 | Rare:43 | ||||
chr7:134432377-134432587 | Rare:67 | ||||
chr7:143836684-143837012 | Common:1; Rare:11 | ||||
chr7:148987246-148987494 | Common:8; Rare:83 | ||||
chr7:151233268-151233503 | Common:1; Rare:47 | ||||
chr8:26641023-26641151 | Common:2; Rare:36 | ||||
chr8:48407845-48408002 | Rare:32 | ||||
chr8:56559473-56559624 | Common:1; Rare:27 | ||||
chr8:66113902-66113984 | Common:4; Rare:22 | ||||
chr8:132321516-132321750 | Rare:37 | ||||
chr8:143932011-143932189 | Common:2; Rare:103; Clinvar:6; Clinvar (benign):5 | ||||
chr8:145002839-145002941 | Common:1; Rare:27 |