Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:123644788-123645030 | Common:8; Rare:26 | ||||
chr8:123653599-123653977 | Rare:65 | ||||
chr8:124271579-124271745 | Common:1; Rare:26 | ||||
chr8:141417689-141418001 | Common:3; Rare:105 | ||||
chr8:144508242-144508263 | Rare:4 | ||||
chr8:145002827-145003038 | Common:2; Rare:74 | ||||
chr9:4804756-4804876 | Rare:41 | ||||
chr9:5630041-5630278 | Common:2; Rare:68 | ||||
chr9:15469296-15469395 | Rare:31 | ||||
chr9:19123563-19123779 | Common:1; Rare:71 | ||||
chr9:35067896-35068362 | Common:2; Rare:89; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
chr9:35520584-35520660 | Rare:10 | ||||
chr9:35604048-35604427 | Common:2; Rare:96 | ||||
chr9:35723951-35724227 | Rare:68 | ||||
chr9:40991952-40992421 | Common:7; Rare:32 |