| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:65750922-65751080 | Common:2; Rare:60 | ||||
| chr7:66493536-66493742 | Common:4; Rare:87 | ||||
| chr7:67302409-67302670 | Common:5; Rare:81 | ||||
| chr7:73005879-73006140 | Rare:23 | ||||
| chr7:74890532-74890812 | Common:2; Rare:89 | ||||
| chr7:94409365-94409608 | Rare:65; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr7:100335879-100336141 | Common:1; Rare:83 | ||||
| chr7:130541203-130541218 | |||||
| chr7:137721725-137721970 | Rare:36 | ||||
| chr7:148987246-148987527 | Common:8; Rare:90 | ||||
| chr8:9903396-9903528 | Rare:29 | ||||
| chr8:9904284-9904533 | Common:1; Rare:69 | ||||
| chr8:9906646-9906967 | Common:1; Rare:113 | ||||
| chr8:11347483-11347649 | Common:1; Rare:91 | ||||
| chr8:37829803-37829888 | Common:1; Rare:24 |