Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:6261066-6261189 | Common:3; Rare:44 | ||||
chr1:6385763-6386065 | Common:2; Rare:71 | ||||
chr1:6393343-6393605 | Common:4; Rare:97 | ||||
chr1:6393755-6393956 | Common:1; Rare:67 | ||||
chr1:6419873-6420017 | Common:1; Rare:45 | ||||
chr1:6420180-6420430 | Rare:36 | ||||
chr1:6424655-6424804 | Common:1; Rare:48 | ||||
chr1:6440383-6440685 | Common:11; Rare:92; Clinvar (benign):3 | ||||
chr1:6447798-6448116 | Common:3; Rare:66 | ||||
chr1:6497414-6497656 | Common:2; Rare:69 | ||||
chr1:6554477-6554671 | Common:4; Rare:68 | ||||
chr1:6579784-6580075 | Common:5; Rare:99 | ||||
chr1:6602832-6603132 | Common:4; Rare:115 | ||||
chr1:6603498-6603674 | Common:1; Rare:37 | ||||
chr1:6613448-6613867 | Common:2; Rare:158 |