Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:156500697-156501141 | Common:3; Rare:161 | ||||
chr1:156501146-156501244 | Rare:28 | ||||
chr1:156572478-156572683 | Common:2; Rare:73 | ||||
chr1:156591192-156591464 | Common:1; Rare:43 | ||||
chr1:156591600-156591906 | Common:6; Rare:129 | ||||
chr1:156591957-156592081 | Rare:38; Clinvar (pathogenic):1 | ||||
chr1:156601198-156601243 | Rare:6 | ||||
chr1:156601258-156601619 | Common:2; Rare:102 | ||||
chr1:156601667-156601762 | Common:1; Rare:23 | ||||
chr1:156677327-156677499 | Rare:38 | ||||
chr1:156705478-156705720 | Common:2; Rare:47 | ||||
chr1:156706060-156706236 | Common:1; Rare:30 | ||||
chr1:156728372-156728600 | Common:2; Rare:63 | ||||
chr1:156728665-156729017 | Rare:92 | ||||
chr1:156729025-156729182 | Common:1; Rare:51 |