| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:74964028-74964618 | Common:4; Rare:135 | ||||
| chr7:75073738-75073924 | Common:2; Rare:65 | ||||
| chr7:75486216-75486382 | Common:1; Rare:67 | ||||
| chr7:75738914-75739144 | Common:2; Rare:62 | ||||
| chr7:75878805-75879083 | Common:12; Rare:100 | ||||
| chr7:75914880-75915194 | Common:4; Rare:113; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:75967585-75967856 | Common:5; Rare:60 | ||||
| chr7:75994590-75994806 | Common:4; Rare:115 | ||||
| chr7:76047917-76048157 | Common:1; Rare:81 | ||||
| chr7:76235230-76235500 | Common:2; Rare:76 | ||||
| chr7:76273100-76273570 | Common:2; Rare:82 | ||||
| chr7:76282400-76283061 | Common:4; Rare:226 | ||||
| chr7:76302467-76302677 | Common:2; Rare:63; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:76303460-76303830 | Common:2; Rare:158; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:76358952-76359132 | Rare:70 |