| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:70225111-70225216 | Rare:33 | ||||
| chr2:70258076-70258258 | Common:1; Rare:72 | ||||
| chr2:70293676-70293821 | Common:2; Rare:47 | ||||
| chr2:70900377-70900609 | Common:5; Rare:72 | ||||
| chr2:71068539-71068685 | Rare:62 | ||||
| chr2:71073524-71073684 | Common:1; Rare:63 | ||||
| chr2:71130221-71130741 | Common:7; Rare:157; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:73071298-73071377 | Rare:27 | ||||
| chr2:73112867-73113151 | Common:4; Rare:78 | ||||
| chr2:73926718-73926939 | Common:2; Rare:115; Clinvar:7; Clinvar (benign):3 | ||||
| chr2:74147821-74148100 | Common:2; Rare:81; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:74421645-74421781 | Rare:42 | ||||
| chr2:74465343-74465459 | Common:1; Rare:31; Clinvar:1 | ||||
| chr2:74482949-74483120 | Common:1; Rare:68 | ||||
| chr2:74503307-74503475 | Rare:43 |