| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:138542925-138543512 | Common:3; Rare:174 | ||||
| chr5:138753255-138753499 | Common:2; Rare:85 | ||||
| chr5:138875337-138875452 | Rare:23; Clinvar (benign):1 | ||||
| chr5:139198277-139198519 | Rare:78; Clinvar (benign):1 | ||||
| chr5:139561104-139561398 | Common:1; Rare:117 | ||||
| chr5:139561734-139561803 | Rare:28 | ||||
| chr5:140303065-140303165 | Common:1; Rare:29 | ||||
| chr5:140564284-140564462 | Common:1; Rare:53 | ||||
| chr5:140564676-140564837 | Rare:48 | ||||
| chr5:140647579-140647911 | Common:5; Rare:134; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:140691309-140691625 | Common:1; Rare:110; Clinvar:8; Clinvar (benign):1 | ||||
| chr5:141320750-141320920 | Common:1; Rare:57 | ||||
| chr5:141476227-141476279 | Rare:16 | ||||
| chr5:141682191-141682407 | Common:2; Rare:59 | ||||
| chr5:141923741-141923889 | Common:1; Rare:34 |