| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:66682005-66682210 | Common:6; Rare:99 | ||||
| chr7:66996564-66996872 | Common:2; Rare:69 | ||||
| chr7:73683396-73683628 | Common:3; Rare:98 | ||||
| chr7:73719625-73719798 | Common:3; Rare:54 | ||||
| chr7:73738786-73739033 | Common:1; Rare:74 | ||||
| chr7:73842514-73842714 | Common:5; Rare:28 | ||||
| chr7:74028007-74028171 | Common:1; Rare:48; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:74174157-74174429 | Common:1; Rare:140 | ||||
| chr7:74254319-74254559 | Rare:113 | ||||
| chr7:75486250-75486489 | Common:2; Rare:86 | ||||
| chr7:75878824-75879094 | Common:12; Rare:96 | ||||
| chr7:75914957-75915164 | Common:1; Rare:67; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:76047932-76048176 | Common:1; Rare:82 | ||||
| chr7:76303472-76303827 | Common:2; Rare:154; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:76627248-76627408 | Common:6; Rare:47 |