| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:135352950-135353148 | Rare:46 | ||||
| chr5:138573766-138574030 | Common:1; Rare:89 | ||||
| chr5:140651721-140651934 | Rare:44 | ||||
| chr5:140711168-140711275 | Common:1; Rare:27 | ||||
| chr5:146059727-146060008 | Common:1; Rare:73 | ||||
| chr5:148072144-148072465 | Common:2; Rare:74 | ||||
| chr5:148094003-148094239 | Common:1; Rare:41 | ||||
| chr5:148309818-148310127 | Common:3; Rare:43 | ||||
| chr5:148315510-148315738 | Common:1; Rare:82 | ||||
| chr5:148826373-148826654 | Common:3; Rare:71 | ||||
| chr5:148914218-148914250 | Rare:5 | ||||
| chr5:148917376-148917522 | Common:3; Rare:29 | ||||
| chr5:148970396-148970478 | Common:1; Rare:12 | ||||
| chr5:150056286-150056452 | Rare:34; Clinvar (pathogenic):1 | ||||
| chr5:150402561-150402708 | Rare:42 |