| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:61471245-61471342 | Common:1; Rare:30 | ||||
| chr2:61888405-61888727 | Common:1; Rare:146 | ||||
| chr2:63588639-63589040 | Common:1; Rare:127; Clinvar (benign):1 | ||||
| chr2:63840822-63841133 | Common:1; Rare:85 | ||||
| chr2:65227590-65227949 | Rare:96 | ||||
| chr2:66434969-66435347 | Common:2; Rare:92 | ||||
| chr2:66439166-66439327 | Common:1; Rare:33 | ||||
| chr2:68157454-68157962 | Common:2; Rare:262 | ||||
| chr2:68467277-68467606 | Common:1; Rare:83 | ||||
| chr2:70087313-70087995 | Common:2; Rare:233 | ||||
| chr2:71130220-71130371 | Common:2; Rare:56; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:71130437-71130677 | Common:3; Rare:61 | ||||
| chr2:73071693-73071833 | Common:2; Rare:59 | ||||
| chr2:73828801-73829023 | Common:1; Rare:51 | ||||
| chr2:74147821-74148140 | Common:2; Rare:85; Clinvar:2; Clinvar (benign):2 |