| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:68467179-68467642 | Common:6; Rare:346 | ||||
| chr2:68643320-68643680 | Common:12; Rare:169 | ||||
| chr2:69013218-69013452 | Rare:91 | ||||
| chr2:69386840-69387100 | Common:1; Rare:75; Clinvar (benign):1 | ||||
| chr2:69387113-69387588 | Common:4; Rare:309; Clinvar:6 | ||||
| chr2:69436850-69437143 | Common:2; Rare:113 | ||||
| chr2:69437061-69437279 | Rare:59 | ||||
| chr2:69437322-69437670 | Common:3; Rare:365; Clinvar:14; Clinvar (benign):11 | ||||
| chr2:69643040-69643503 | Common:4; Rare:124 | ||||
| chr2:69643570-69643921 | Rare:295 | ||||
| chr2:69644400-69644503 | Common:1; Rare:16 | ||||
| chr2:69741361-69741730 | Common:1; Rare:109 | ||||
| chr2:69741697-69742270 | Common:6; Rare:219 | ||||
| chr2:69829428-69829784 | Common:3; Rare:310 | ||||
| chr2:69893873-69894033 | Rare:106 |