Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:139109327-139109495 | Common:1; Rare:50 | ||||
chr7:139133675-139133798 | Rare:28 | ||||
chr7:139341234-139341380 | Rare:34 | ||||
chr7:139359692-139359977 | Common:3; Rare:114 | ||||
chr7:140398453-140398591 | Common:1; Rare:44 | ||||
chr7:140479350-140479595 | Rare:77 | ||||
chr7:141551297-141551423 | Rare:41; Clinvar:4; Clinvar (benign):2 | ||||
chr7:141737960-141738455 | Common:5; Rare:147 | ||||
chr7:142749296-142749536 | Rare:67; Clinvar:5; Clinvar (benign):1 | ||||
chr7:142749653-142749907 | Common:3; Rare:37 | ||||
chr7:142749934-142750109 | Rare:31 | ||||
chr7:142750213-142750475 | Common:5; Rare:55; Clinvar (benign):1 | ||||
chr7:142760083-142760445 | Common:1; Rare:36 | ||||
chr7:142770725-142771022 | Common:11; Rare:52 | ||||
chr7:142771258-142771302 | Rare:5 |