| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:225841003-225841121 | Common:2; Rare:21 | ||||
| chr1:225842118-225842400 | Rare:76 | ||||
| chr1:225981352-225981622 | Common:1; Rare:52 | ||||
| chr1:226083480-226083590 | Common:1; Rare:37 | ||||
| chr1:226404965-226405146 | Common:1; Rare:34 | ||||
| chr1:227638357-227638473 | Rare:16 | ||||
| chr1:228464621-228464826 | Rare:52 | ||||
| chr1:229174296-229174571 | Common:4; Rare:52 | ||||
| chr1:229178763-229179061 | Common:11; Rare:55 | ||||
| chr1:229253352-229253393 | Common:1; Rare:12 | ||||
| chr1:229486596-229486896 | Rare:51 | ||||
| chr1:230121971-230122102 | Rare:18 | ||||
| chr1:230426307-230426629 | Common:3; Rare:123 | ||||
| chr1:230607295-230607441 | Common:1; Rare:21 | ||||
| chr1:231422265-231422430 | Common:4; Rare:77; Clinvar:4; Clinvar (benign):4 |