| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:123036176-123036920 | Common:9; Rare:423 | ||||
| chr5:123422474-123422874 | Common:1; Rare:91 | ||||
| chr5:123423097-123423851 | Common:8; Rare:1040 | ||||
| chr5:123511820-123512357 | Common:10; Rare:675 | ||||
| chr5:123512340-123512520 | Rare:56 | ||||
| chr5:124644157-124644559 | Common:3; Rare:335 | ||||
| chr5:124746660-124747170 | Common:5; Rare:101 | ||||
| chr5:126422870-126423170 | Common:5; Rare:113 | ||||
| chr5:126423190-126423560 | Rare:148 | ||||
| chr5:126423510-126423956 | Common:6; Rare:328 | ||||
| chr5:126600620-126601060 | Common:7; Rare:317 | ||||
| chr5:126601180-126601600 | Common:3; Rare:334 | ||||
| chr5:126775983-126777251 | Common:34; Rare:1427; Clinvar:39; Clinvar (benign):45 | ||||
| chr5:126777323-126777723 | Rare:164; Clinvar (benign):1 | ||||
| chr5:126777705-126777833 | Common:1; Rare:38; Clinvar (benign):1 |