Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:7784057-7784412 | Common:5; Rare:144 | ||||
chr1:7954188-7954290 | Rare:24 | ||||
chr1:7961455-7961758 | Common:4; Rare:106; Clinvar:2; Clinvar (benign):3 | ||||
chr1:8026310-8026493 | Common:2; Rare:77 | ||||
chr1:8318015-8318140 | Rare:40 | ||||
chr1:8423665-8423899 | Common:1; Rare:102 | ||||
chr1:8424091-8424364 | Common:2; Rare:71 | ||||
chr1:8525891-8526019 | Rare:25 | ||||
chr1:8878637-8878880 | Rare:133 | ||||
chr1:9239505-9239827 | Common:2; Rare:76 | ||||
chr1:9239830-9239897 | Common:1; Rare:14 | ||||
chr1:9943280-9943488 | Common:2; Rare:53 | ||||
chr1:9997126-9997251 | Common:2; Rare:40 | ||||
chr1:10032763-10032965 | Rare:53 | ||||
chr1:10398727-10399108 | Common:2; Rare:135 |