Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:44229748-44229977 | Rare:49 | ||||
chr6:44387447-44387761 | Common:4; Rare:84 | ||||
chr6:45377855-45378189 | Common:2; Rare:114 | ||||
chr6:46921817-46922056 | Common:3; Rare:62 | ||||
chr6:46922069-46922085 | Rare:5 | ||||
chr6:47477664-47478017 | Common:2; Rare:93; Clinvar:3; Clinvar (benign):3 | ||||
chr6:47478067-47478246 | Common:2; Rare:67; Clinvar:2; Clinvar (benign):3 | ||||
chr6:49463174-49463431 | Common:1; Rare:75; Clinvar:1; Clinvar (benign):1 | ||||
chr6:52420122-52420378 | Common:3; Rare:106; Clinvar:1; Clinvar (benign):2 | ||||
chr6:52671054-52671190 | Rare:37 | ||||
chr6:52995260-52995813 | Common:4; Rare:228 | ||||
chr6:53065352-53065598 | Common:1; Rare:78 | ||||
chr6:53348853-53349211 | Common:2; Rare:148 | ||||
chr6:56542720-56543014 | Common:2; Rare:53 | ||||
chr6:57222274-57222383 | Rare:41 |