| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:184649406-184649797 | Common:4; Rare:126 | ||||
| chr4:185396572-185396851 | Rare:90 | ||||
| chr4:185425864-185426305 | Common:4; Rare:143 | ||||
| chr4:185535352-185535640 | Common:2; Rare:105; Clinvar:1; Clinvar (benign):9 | ||||
| chr4:185589063-185589348 | Common:1; Rare:47 | ||||
| chr4:185932981-185933153 | Rare:33 | ||||
| chr4:189940649-189941012 | Common:14; Rare:136 | ||||
| chr5:218114-218392 | Common:3; Rare:117; Clinvar:11; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr5:443084-443266 | Common:9; Rare:82 | ||||
| chr5:612211-612351 | Rare:55 | ||||
| chr5:892528-892596 | Rare:13 | ||||
| chr5:892726-892967 | Common:3; Rare:93 | ||||
| chr5:1799791-1799996 | Common:4; Rare:97 | ||||
| chr5:1801300-1801447 | Common:4; Rare:71; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:6378143-6378238 | Common:1; Rare:17 |