| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:66996555-66996872 | Common:2; Rare:74 | ||||
| chr7:71131468-71131721 | Common:5; Rare:87 | ||||
| chr7:72412338-72412607 | Common:2; Rare:66 | ||||
| chr7:73327957-73328208 | Rare:80 | ||||
| chr7:73557585-73557780 | Common:2; Rare:72 | ||||
| chr7:73683265-73683659 | Common:6; Rare:173 | ||||
| chr7:73738721-73739028 | Common:1; Rare:102 | ||||
| chr7:73769661-73769867 | Rare:57 | ||||
| chr7:73842496-73842686 | Common:6; Rare:28 | ||||
| chr7:74254385-74254528 | Rare:66 | ||||
| chr7:74657478-74657730 | Common:2; Rare:76 | ||||
| chr7:75914876-75915173 | Common:4; Rare:100; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:75994512-75994772 | Common:4; Rare:132 | ||||
| chr7:76047943-76048194 | Common:2; Rare:86 | ||||
| chr7:76302844-76303075 | Rare:98; Clinvar:11; Clinvar (benign):4; Clinvar (pathogenic):3 |