| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:6272475-6272759 | Common:1; Rare:121 | ||||
| chr7:6374262-6374533 | Common:3; Rare:103 | ||||
| chr7:6401953-6402296 | Common:4; Rare:88 | ||||
| chr7:6447888-6448087 | Common:2; Rare:77 | ||||
| chr7:6484061-6484247 | Common:1; Rare:100 | ||||
| chr7:6577356-6577625 | Common:3; Rare:84 | ||||
| chr7:6706919-6707098 | Rare:76 | ||||
| chr7:7566666-7567109 | Common:6; Rare:156 | ||||
| chr7:8262102-8262317 | Rare:94 | ||||
| chr7:8262553-8262631 | Rare:17 | ||||
| chr7:14902722-14902784 | Rare:20 | ||||
| chr7:16645598-16646165 | Common:2; Rare:194 | ||||
| chr7:17940439-17940569 | Common:1; Rare:64 | ||||
| chr7:19116670-19117115 | Common:3; Rare:165; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr7:19117357-19118046 | Common:4; Rare:214 |