| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:140697089-140697258 | Rare:50 | ||||
| chr7:141551291-141551432 | Rare:43; Clinvar:4; Clinvar (benign):2 | ||||
| chr7:141738027-141738401 | Common:4; Rare:110 | ||||
| chr7:143380955-143381391 | Common:1; Rare:143 | ||||
| chr7:149147121-149147476 | Common:5; Rare:70 | ||||
| chr7:149262091-149262236 | Common:1; Rare:52 | ||||
| chr7:149873763-149874051 | Common:3; Rare:116 | ||||
| chr7:150405897-150406147 | Common:1; Rare:47 | ||||
| chr7:150800309-150800822 | Common:7; Rare:130 | ||||
| chr7:150801144-150801372 | Common:4; Rare:48 | ||||
| chr7:151249223-151249350 | Common:1; Rare:26 | ||||
| chr7:155644394-155644708 | Common:2; Rare:104 | ||||
| chr7:156640537-156640685 | Common:3; Rare:77 | ||||
| chr8:1755620-1755776 | Common:3; Rare:52 | ||||
| chr8:6406536-6406668 | Common:3; Rare:74; Clinvar:2; Clinvar (benign):1 |