| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:69387190-69387373 | Rare:47; Clinvar:2 | ||||
| chr2:69643622-69643817 | Rare:68 | ||||
| chr2:69829508-69829735 | Common:1; Rare:93 | ||||
| chr2:70087373-70087768 | Common:2; Rare:152 | ||||
| chr2:70258007-70258158 | Common:1; Rare:52 | ||||
| chr2:70293645-70293942 | Common:3; Rare:92 | ||||
| chr2:71068551-71068699 | Rare:60 | ||||
| chr2:71130225-71130662 | Common:6; Rare:122; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:71453840-71453893 | Rare:9 | ||||
| chr2:73071701-73071861 | Common:2; Rare:60 | ||||
| chr2:73737286-73737505 | Common:3; Rare:70 | ||||
| chr2:73828804-73829028 | Common:1; Rare:52 | ||||
| chr2:74147849-74148045 | Common:2; Rare:57; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:74421582-74421759 | Rare:62 | ||||
| chr2:74458116-74458419 | Common:1; Rare:88 |