| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:36877103-36877144 | Rare:16 | ||||
| chr5:37371053-37371382 | Common:2; Rare:79 | ||||
| chr5:37379085-37379364 | Common:3; Rare:68 | ||||
| chr5:38557246-38557281 | Rare:6 | ||||
| chr5:38845746-38846053 | Common:2; Rare:80 | ||||
| chr5:39074346-39074474 | Common:1; Rare:56 | ||||
| chr5:39364389-39364743 | Common:2; Rare:80; Clinvar (benign):1 | ||||
| chr5:39425130-39425308 | Common:1; Rare:45 | ||||
| chr5:40798089-40798394 | Common:1; Rare:112 | ||||
| chr5:40835173-40835321 | Common:2; Rare:60 | ||||
| chr5:41000106-41000253 | Common:3; Rare:33 | ||||
| chr5:41213393-41213637 | Rare:38 | ||||
| chr5:41510571-41510814 | Common:1; Rare:57 | ||||
| chr5:42825856-42825999 | Rare:27 | ||||
| chr5:43121420-43121655 | Common:1; Rare:88 |