| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:137880335-137880731 | Common:2; Rare:67 | ||||
| chr5:138033062-138033169 | Common:1; Rare:36 | ||||
| chr5:138178615-138178717 | Rare:26 | ||||
| chr5:138543110-138543571 | Common:2; Rare:153 | ||||
| chr5:138753255-138753507 | Common:2; Rare:87 | ||||
| chr5:139395088-139395216 | Rare:29 | ||||
| chr5:139561100-139561408 | Common:1; Rare:122 | ||||
| chr5:139561728-139561810 | Rare:31 | ||||
| chr5:140043240-140043318 | Rare:24 | ||||
| chr5:140107549-140107843 | Rare:102 | ||||
| chr5:140175048-140175283 | Common:2; Rare:57 | ||||
| chr5:140346601-140346889 | Common:1; Rare:74 | ||||
| chr5:140564280-140564470 | Common:2; Rare:55 | ||||
| chr5:140564528-140564846 | Rare:82 | ||||
| chr5:140647497-140647924 | Common:5; Rare:175; Clinvar:4; Clinvar (benign):5 |