Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:6393332-6393532 | Common:2; Rare:71 | ||||
chr1:6485893-6486113 | Common:1; Rare:46 | ||||
chr1:6490465-6490639 | Common:1; Rare:34 | ||||
chr1:6497321-6497652 | Common:2; Rare:100 | ||||
chr1:6579781-6580069 | Common:5; Rare:96 | ||||
chr1:6613726-6613824 | Rare:52 | ||||
chr1:6701760-6702016 | Rare:80 | ||||
chr1:6785441-6785571 | Common:2; Rare:46 | ||||
chr1:7771116-7771378 | Common:4; Rare:109 | ||||
chr1:7961415-7961803 | Common:4; Rare:134; Clinvar:3; Clinvar (benign):3 | ||||
chr1:8015671-8015842 | Common:2; Rare:25 | ||||
chr1:8026158-8026503 | Common:3; Rare:155 | ||||
chr1:8318015-8318166 | Rare:48 | ||||
chr1:8423240-8423491 | Rare:66 | ||||
chr1:8423695-8423988 | Common:2; Rare:120 |