| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:168481245-168481730 | Common:2; Rare:121 | ||||
| chr2:168856752-168857038 | Common:2; Rare:61 | ||||
| chr2:168964160-168964750 | Common:5; Rare:144; Clinvar:9; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr2:169329797-169329978 | Common:2; Rare:40 | ||||
| chr2:169364452-169364766 | Rare:84 | ||||
| chr2:169562646-169562840 | Rare:23 | ||||
| chr2:169695779-169696018 | Common:1; Rare:48 | ||||
| chr2:169715389-169715536 | Rare:22 | ||||
| chr2:170126110-170126460 | Rare:104 | ||||
| chr2:170238753-170239170 | Common:2; Rare:132 | ||||
| chr2:170321541-170321941 | Common:3; Rare:93 | ||||
| chr2:170530170-170530520 | Common:2; Rare:78 | ||||
| chr2:170679614-170680314 | Common:2; Rare:223 | ||||
| chr2:170714420-170714850 | Common:1; Rare:176 | ||||
| chr2:170770230-170770484 | Common:1; Rare:49 |