| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:37379080-37379380 | Common:3; Rare:80 | ||||
| chr5:39074327-39074495 | Common:1; Rare:80 | ||||
| chr5:40755832-40756039 | Rare:53 | ||||
| chr5:40798144-40798353 | Common:1; Rare:81 | ||||
| chr5:40835173-40835406 | Common:2; Rare:91 | ||||
| chr5:41510549-41510672 | Rare:35 | ||||
| chr5:41510726-41510814 | Common:1; Rare:15 | ||||
| chr5:41870336-41870670 | Common:2; Rare:104; Clinvar:4; Clinvar (benign):2 | ||||
| chr5:41903999-41904396 | Common:2; Rare:126 | ||||
| chr5:41925103-41925391 | Common:2; Rare:102 | ||||
| chr5:43064958-43065143 | Common:1; Rare:50 | ||||
| chr5:43067438-43067520 | Rare:13 | ||||
| chr5:43121404-43121655 | Common:1; Rare:96 | ||||
| chr5:43192016-43192276 | Common:2; Rare:70 | ||||
| chr5:43313150-43313542 | Common:4; Rare:95 |