| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:99919128-99919363 | Rare:73 | ||||
| chr7:99919490-99919657 | Rare:55 | ||||
| chr7:100081686-100081898 | Common:1; Rare:65 | ||||
| chr7:100082564-100082631 | Rare:13 | ||||
| chr7:100088886-100089017 | Common:1; Rare:46 | ||||
| chr7:100100679-100100852 | Common:1; Rare:69 | ||||
| chr7:100101336-100101711 | Common:1; Rare:144; Clinvar (benign):1 | ||||
| chr7:100119320-100119717 | Rare:115 | ||||
| chr7:100127140-100127266 | Common:1; Rare:32 | ||||
| chr7:100148716-100149047 | Common:1; Rare:145 | ||||
| chr7:100158688-100158802 | Rare:30 | ||||
| chr7:100373263-100373535 | Rare:47 | ||||
| chr7:100428246-100428959 | Common:7; Rare:225 | ||||
| chr7:100429135-100429451 | Common:4; Rare:144 | ||||
| chr7:100435994-100436215 | Common:1; Rare:75 |