| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:70086486-70086520 | Rare:22 | ||||
| chr2:71226400-71226473 | Rare:21 | ||||
| chr2:71416730-71417058 | Common:2; Rare:66 | ||||
| chr2:74120096-74120367 | Common:1; Rare:90 | ||||
| chr2:74120562-74120608 | Common:1; Rare:12 | ||||
| chr2:74165340-74165402 | Rare:13 | ||||
| chr2:74370464-74370820 | Common:1; Rare:87; Clinvar:3; Clinvar (benign):3 | ||||
| chr2:74459790-74459941 | Rare:52 | ||||
| chr2:74872026-74872354 | Common:3; Rare:65 | ||||
| chr2:85542692-85542960 | Common:1; Rare:82; Clinvar (benign):6 | ||||
| chr2:85543483-85543780 | Rare:51; Clinvar (benign):1 | ||||
| chr2:85660156-85660236 | Rare:13 | ||||
| chr2:85660894-85661692 | Common:2; Rare:154; Clinvar:2 | ||||
| chr2:85661787-85662162 | Common:1; Rare:99 | ||||
| chr2:85662351-85662439 | Common:1; Rare:13 |