| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:65227591-65227885 | Rare:85 | ||||
| chr2:66434802-66435130 | Common:1; Rare:81 | ||||
| chr2:67397245-67397358 | Rare:30 | ||||
| chr2:68157456-68157985 | Common:3; Rare:273 | ||||
| chr2:68252468-68252850 | Common:3; Rare:123 | ||||
| chr2:68319384-68319588 | Common:1; Rare:70 | ||||
| chr2:68319904-68320228 | Rare:79 | ||||
| chr2:68467267-68467685 | Common:1; Rare:111 | ||||
| chr2:68774740-68774954 | Rare:39 | ||||
| chr2:69387065-69387373 | Common:1; Rare:87; Clinvar:3 | ||||
| chr2:69437404-69437552 | Rare:71; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:69437590-69437669 | Rare:42; Clinvar:3 | ||||
| chr2:69643598-69643855 | Rare:92 | ||||
| chr2:69829517-69829781 | Common:1; Rare:97 | ||||
| chr2:70086938-70087270 | Common:1; Rare:142 |