| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:73308720-73308897 | Rare:72 | ||||
| chr7:73557076-73557373 | Common:1; Rare:104 | ||||
| chr7:73557453-73557812 | Common:2; Rare:119 | ||||
| chr7:73683383-73683659 | Common:4; Rare:129 | ||||
| chr7:73738723-73739017 | Common:1; Rare:100 | ||||
| chr7:74174056-74174412 | Common:1; Rare:167 | ||||
| chr7:74209842-74210032 | Rare:49 | ||||
| chr7:74254288-74254531 | Rare:113 | ||||
| chr7:74289257-74289437 | Common:3; Rare:64 | ||||
| chr7:75073466-75073547 | Rare:27 | ||||
| chr7:75882248-75882545 | Common:2; Rare:64 | ||||
| chr7:75914933-75915169 | Common:2; Rare:77; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:75994497-75994773 | Common:4; Rare:137 | ||||
| chr7:76047744-76048223 | Common:4; Rare:142 | ||||
| chr7:76302482-76303075 | Common:3; Rare:243; Clinvar:17; Clinvar (benign):13; Clinvar (pathogenic):5 |