| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:16465723-16465939 | Common:1; Rare:48 | ||||
| chr5:31532037-31532352 | Common:3; Rare:88 | ||||
| chr5:33440679-33441058 | Common:6; Rare:104 | ||||
| chr5:34915529-34915737 | Common:1; Rare:43 | ||||
| chr5:36151885-36152168 | Rare:87 | ||||
| chr5:36876650-36876859 | Common:1; Rare:63; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:39074383-39074559 | Common:1; Rare:78 | ||||
| chr5:40798152-40798367 | Common:1; Rare:82 | ||||
| chr5:40835181-40835386 | Common:2; Rare:82 | ||||
| chr5:41925190-41925296 | Common:1; Rare:44 | ||||
| chr5:43064939-43065141 | Common:1; Rare:51 | ||||
| chr5:43067139-43067162 | Rare:3 | ||||
| chr5:43067422-43067532 | Rare:17 | ||||
| chr5:43121365-43121660 | Common:1; Rare:112 | ||||
| chr5:43483831-43483947 | Common:1; Rare:43 |