| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:150763458-150763610 | Rare:38 | ||||
| chr3:152268439-152269217 | Common:3; Rare:260; Clinvar (benign):1 | ||||
| chr3:152269226-152269342 | Rare:36 | ||||
| chr3:152269509-152269772 | Common:2; Rare:75 | ||||
| chr3:152298667-152299077 | Common:1; Rare:71 | ||||
| chr3:152834700-152835221 | Common:7; Rare:144 | ||||
| chr3:153161911-153162240 | Rare:99 | ||||
| chr3:154121264-154121457 | Common:3; Rare:83 | ||||
| chr3:155854355-155854748 | Rare:108 | ||||
| chr3:155870323-155870752 | Common:2; Rare:120 | ||||
| chr3:156555059-156555318 | Common:1; Rare:108 | ||||
| chr3:156674343-156674653 | Common:4; Rare:92 | ||||
| chr3:156826251-156826379 | Common:1; Rare:45 | ||||
| chr3:157159831-157160360 | Common:1; Rare:204 | ||||
| chr3:158644505-158644671 | Common:5; Rare:63; Clinvar (benign):6 |