Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:128856512-128856921 | Rare:131; Clinvar:18; Clinvar (benign):8 | ||||
chr7:130912208-130912369 | Common:1; Rare:27 | ||||
chr7:130941429-130941735 | Common:1; Rare:46 | ||||
chr7:130944976-130945103 | Common:1; Rare:14 | ||||
chr7:131052424-131052467 | Common:1; Rare:8 | ||||
chr7:131106852-131106864 | Rare:1 | ||||
chr7:131107021-131107257 | Common:1; Rare:41 | ||||
chr7:131107713-131107939 | Common:1; Rare:36 | ||||
chr7:131107947-131108232 | Common:1; Rare:49 | ||||
chr7:143836668-143836903 | Common:1; Rare:11 | ||||
chr7:148987246-148987493 | Common:8; Rare:83 | ||||
chr7:152436515-152436898 | Rare:131 | ||||
chr7:158863114-158863419 | Common:4; Rare:84 | ||||
chr8:2057445-2057685 | Common:4; Rare:100 | ||||
chr8:6516434-6516558 | Common:4; Rare:35 |