Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:7771090-7771488 | Common:5; Rare:141 | ||||
chr1:7771515-7771632 | Rare:25 | ||||
chr1:7771633-7771692 | Rare:12 | ||||
chr1:7783860-7784028 | Common:2; Rare:45 | ||||
chr1:7784059-7784420 | Common:5; Rare:147 | ||||
chr1:7954072-7954398 | Common:5; Rare:99 | ||||
chr1:7961167-7961301 | Common:1; Rare:39 | ||||
chr1:7961332-7961806 | Common:4; Rare:157; Clinvar:3; Clinvar (benign):3 | ||||
chr1:7961879-7962028 | Common:1; Rare:43 | ||||
chr1:7962111-7962196 | Common:1; Rare:27 | ||||
chr1:8026132-8026545 | Common:3; Rare:179 | ||||
chr1:8026584-8026752 | Rare:36 | ||||
chr1:8318042-8318150 | Rare:35 | ||||
chr1:8423344-8423399 | Rare:14 | ||||
chr1:8423667-8423702 | Rare:12 |