Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23558486-23558630 | Common:1; Rare:50 | ||||
chr1:23558722-23558863 | Common:1; Rare:48 | ||||
chr1:23559222-23559292 | Rare:30 | ||||
chr1:23559390-23559713 | Common:2; Rare:136 | ||||
chr1:23691606-23691925 | Common:6; Rare:110; Clinvar:2; Clinvar (benign):3 | ||||
chr1:23742931-23743076 | Rare:36 | ||||
chr1:23743121-23743696 | Common:2; Rare:165 | ||||
chr1:23743716-23744033 | Rare:87 | ||||
chr1:23744037-23744169 | Rare:29 | ||||
chr1:23777945-23778037 | Rare:17 | ||||
chr1:23778204-23778533 | Common:9; Rare:147 | ||||
chr1:23778603-23778667 | Rare:12 | ||||
chr1:23778773-23778802 | Rare:4 | ||||
chr1:23791018-23791266 | Rare:73 | ||||
chr1:23791637-23792002 | Rare:52 |