| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:185656955-185657280 | Common:1; Rare:57 | ||||
| chr4:185657299-185657482 | Common:2; Rare:52 | ||||
| chr4:186723753-186723897 | Common:4; Rare:61 | ||||
| chr4:186726526-186726646 | Rare:30 | ||||
| chr4:189940588-189941046 | Common:18; Rare:159 | ||||
| chr5:218104-218396 | Common:4; Rare:121; Clinvar:11; Clinvar (benign):9; Clinvar (pathogenic):2 | ||||
| chr5:443084-443272 | Common:10; Rare:85 | ||||
| chr5:612203-612358 | Rare:61 | ||||
| chr5:892541-892947 | Common:5; Rare:125 | ||||
| chr5:1799791-1799993 | Common:4; Rare:94 | ||||
| chr5:1801287-1801523 | Common:4; Rare:124; Clinvar:3; Clinvar (benign):3 | ||||
| chr5:5422334-5422665 | Common:2; Rare:103 | ||||
| chr5:6632934-6633691 | Common:11; Rare:235; Clinvar:10; Clinvar (benign):6 | ||||
| chr5:7868991-7869204 | Common:2; Rare:109; Clinvar (benign):1 | ||||
| chr5:9546069-9546390 | Common:7; Rare:75 |