Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:633655-634016 | Common:7; Rare:117 | ||||
chr1:778601-778819 | Common:3; Rare:93 | ||||
chr1:827504-827702 | Common:1; Rare:81 | ||||
chr1:9687488-9687604 | Common:1; Rare:31 | ||||
chr1:12619964-12620177 | Common:1; Rare:32 | ||||
chr1:15834900-15835134 | Common:1; Rare:104 | ||||
chr1:15835804-15836095 | Common:6; Rare:135 | ||||
chr1:16217419-16217668 | Rare:40 | ||||
chr1:16499217-16499383 | Rare:78 | ||||
chr1:16644637-16644789 | Common:1; Rare:2 | ||||
chr1:16895622-16895794 | Common:2; Rare:32 | ||||
chr1:16913997-16914121 | Common:4; Rare:25 | ||||
chr1:21827892-21828044 | Common:2; Rare:49; Clinvar:1; Clinvar (benign):1 | ||||
chr1:21857166-21857324 | Common:1; Rare:43; Clinvar:2 | ||||
chr1:25875506-25875780 | Rare:73 |