| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:48301325-48301500 | Common:1; Rare:54 | ||||
| chr3:48429970-48430210 | Common:1; Rare:58 | ||||
| chr3:48440011-48440316 | Common:2; Rare:116 | ||||
| chr3:48446632-48446743 | Rare:40 | ||||
| chr3:48473458-48473579 | Common:1; Rare:27 | ||||
| chr3:48504084-48504323 | Common:2; Rare:73 | ||||
| chr3:48556841-48557175 | Common:1; Rare:63 | ||||
| chr3:48685817-48685994 | Common:1; Rare:62 | ||||
| chr3:48847648-48847944 | Common:1; Rare:77 | ||||
| chr3:48918702-48918930 | Common:2; Rare:119 | ||||
| chr3:49007198-49007432 | Common:2; Rare:92 | ||||
| chr3:49021502-49021712 | Rare:53; Clinvar:1 | ||||
| chr3:49029346-49029564 | Common:2; Rare:157 | ||||
| chr3:49104616-49104934 | Common:1; Rare:127; Clinvar:3; Clinvar (benign):7 | ||||
| chr3:49166289-49166437 | Common:1; Rare:38 |