| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:186191508-186191870 | Common:6; Rare:117; Clinvar:3; Clinvar (benign):5 | ||||
| chr4:186723759-186723903 | Common:4; Rare:59 | ||||
| chr4:189940588-189941000 | Common:15; Rare:137 | ||||
| chr5:218108-218369 | Common:4; Rare:108; Clinvar:7; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr5:443095-443275 | Common:9; Rare:81 | ||||
| chr5:693289-693586 | Common:6; Rare:88 | ||||
| chr5:892541-892855 | Common:5; Rare:90 | ||||
| chr5:1344883-1345206 | Common:2; Rare:104 | ||||
| chr5:1799791-1799988 | Common:4; Rare:92 | ||||
| chr5:1801295-1801460 | Common:4; Rare:82; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:5422375-5422712 | Common:2; Rare:115 | ||||
| chr5:6378498-6378706 | Rare:83 | ||||
| chr5:6633289-6633429 | Common:2; Rare:47; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:7869000-7869204 | Common:2; Rare:103; Clinvar (benign):1 | ||||
| chr5:9546000-9546333 | Common:8; Rare:83 |