Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:629888-629980 | Common:1; Rare:32 | ||||
chr1:630316-630450 | Common:2; Rare:38 | ||||
chr1:630610-630749 | Common:3; Rare:14 | ||||
chr1:633825-633886 | Common:2; Rare:16 | ||||
chr1:633985-634072 | Rare:43 | ||||
chr1:634228-634323 | Rare:20 | ||||
chr1:634422-634602 | Common:1; Rare:28 | ||||
chr1:778581-778896 | Common:5; Rare:119 | ||||
chr1:826767-826818 | Rare:15 | ||||
chr1:827228-827310 | Common:1; Rare:17 | ||||
chr1:827499-827763 | Common:2; Rare:92 | ||||
chr1:904627-904819 | Common:3; Rare:67 | ||||
chr1:996311-996390 | Common:1; Rare:7 | ||||
chr1:1021236-1021398 | Rare:39 | ||||
chr1:1043452-1043653 | Common:3; Rare:87; Clinvar:3; Clinvar (benign):3 |