Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:7940747-7941147 | Rare:146 | ||||
chr1:7953775-7954450 | Common:13; Rare:654 | ||||
chr1:7961311-7962023 | Common:30; Rare:947; Clinvar:15; Clinvar (benign):20; Clinvar (pathogenic):1 | ||||
chr1:7962010-7962410 | Common:5; Rare:127 | ||||
chr1:8026190-8026612 | Common:8; Rare:404 | ||||
chr1:8422485-8423147 | Rare:338 | ||||
chr1:8423553-8424080 | Common:7; Rare:500 | ||||
chr1:8424171-8424647 | Common:3; Rare:252 | ||||
chr1:8424596-8424996 | Common:3; Rare:97 | ||||
chr1:8525120-8525440 | Common:2; Rare:56 | ||||
chr1:8525873-8526380 | Common:7; Rare:210 | ||||
chr1:8590837-8591111 | Common:2; Rare:54 | ||||
chr1:8702802-8703204 | Common:1; Rare:142 | ||||
chr1:8703280-8703890 | Common:5; Rare:391 | ||||
chr1:8817560-8818400 | Common:23; Rare:847 |