| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:40309477-40309808 | Common:9; Rare:112 | ||||
| chr3:40524821-40524916 | Common:1; Rare:22 | ||||
| chr3:42581909-42582106 | Common:2; Rare:64 | ||||
| chr3:42600418-42600491 | Common:1; Rare:23 | ||||
| chr3:42600545-42600749 | Rare:85 | ||||
| chr3:42685369-42685562 | Rare:39 | ||||
| chr3:42702646-42702722 | Rare:24 | ||||
| chr3:42804417-42804657 | Common:2; Rare:71 | ||||
| chr3:42936337-42936402 | Common:1; Rare:23 | ||||
| chr3:43621907-43622316 | Common:2; Rare:120; Clinvar:7; Clinvar (benign):1 | ||||
| chr3:43690839-43690993 | Common:3; Rare:86; Clinvar:7; Clinvar (benign):2 | ||||
| chr3:44338651-44338797 | Common:3; Rare:55 | ||||
| chr3:44477646-44477694 | Rare:11 | ||||
| chr3:44761584-44761835 | Common:3; Rare:92 | ||||
| chr3:44861811-44861928 | Common:2; Rare:56 |