Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:778608-778812 | Common:3; Rare:87 | ||||
chr1:827503-827706 | Common:1; Rare:83 | ||||
chr1:9182107-9182229 | Rare:32 | ||||
chr1:9687517-9687655 | Common:1; Rare:36 | ||||
chr1:11731824-11731947 | Common:4; Rare:32 | ||||
chr1:12619027-12619282 | Rare:52 | ||||
chr1:15834913-15835169 | Common:1; Rare:109 | ||||
chr1:16514277-16514574 | Common:3; Rare:97 | ||||
chr1:16644646-16644805 | Common:1; Rare:3 | ||||
chr1:16895690-16896001 | Common:4; Rare:62 | ||||
chr1:16913864-16914100 | Common:8; Rare:47 | ||||
chr1:20654294-20654633 | Common:4; Rare:106; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:21261930-21262083 | Common:2; Rare:31 | ||||
chr1:22025449-22025518 | Common:4; Rare:24 | ||||
chr1:25875503-25875776 | Rare:72 |