Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:156068050-156068459 | Common:1; Rare:108 | ||||
chr1:156114544-156114826 | Rare:65; Clinvar:4; Clinvar (benign):1 | ||||
chr1:156193817-156194172 | Common:3; Rare:88 | ||||
chr1:156212838-156213070 | Common:1; Rare:68 | ||||
chr1:156241959-156242189 | Common:3; Rare:61 | ||||
chr1:156282728-156283027 | Common:3; Rare:82 | ||||
chr1:156284041-156284344 | Common:1; Rare:56 | ||||
chr1:156338152-156338570 | Common:2; Rare:152 | ||||
chr1:156500768-156501148 | Common:1; Rare:140 | ||||
chr1:156591678-156591849 | Common:4; Rare:91 | ||||
chr1:156593110-156593540 | Common:3; Rare:101 | ||||
chr1:156601407-156601495 | Common:1; Rare:39 | ||||
chr1:156641997-156642169 | Rare:45 | ||||
chr1:156728383-156728491 | Common:1; Rare:23 | ||||
chr1:156729079-156729155 | Rare:32 |