| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:86704451-86704918 | Common:2; Rare:175 | ||||
| chr1:86914339-86914766 | Common:1; Rare:132 | ||||
| chr1:87328296-87328449 | Common:2; Rare:38 | ||||
| chr1:87329086-87329270 | Common:1; Rare:50 | ||||
| chr1:87331582-87331797 | Rare:67 | ||||
| chr1:88684064-88684573 | Common:4; Rare:134 | ||||
| chr1:88891484-88891708 | Common:1; Rare:99 | ||||
| chr1:88992600-88992978 | Common:3; Rare:98 | ||||
| chr1:89065198-89065440 | Common:1; Rare:35 | ||||
| chr1:89632917-89633192 | Common:1; Rare:77 | ||||
| chr1:89995015-89995170 | Common:2; Rare:66 | ||||
| chr1:91021943-91022152 | Rare:57 | ||||
| chr1:91500802-91501153 | Common:2; Rare:109 | ||||
| chr1:92029890-92030046 | Rare:44 | ||||
| chr1:92298944-92299070 | Common:1; Rare:59; Clinvar:1; Clinvar (benign):1 |