| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:4686331-4686508 | Rare:41; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:5112874-5113168 | Common:1; Rare:113 | ||||
| chr20:5119929-5120168 | Common:1; Rare:78 | ||||
| chr20:5126541-5126814 | Common:3; Rare:78 | ||||
| chr20:5610867-5611154 | Common:2; Rare:98 | ||||
| chr20:5950391-5950695 | Common:8; Rare:92 | ||||
| chr20:10673942-10674127 | Common:2; Rare:69; Clinvar:3; Clinvar (benign):3 | ||||
| chr20:13784878-13785080 | Common:2; Rare:90; Clinvar (benign):3 | ||||
| chr20:14337561-14337612 | Rare:12 | ||||
| chr20:16573293-16573543 | Common:1; Rare:71 | ||||
| chr20:16729861-16730064 | Rare:62 | ||||
| chr20:17558418-17558563 | Common:1; Rare:22 | ||||
| chr20:17569094-17569192 | Rare:20 | ||||
| chr20:17569218-17569244 | Rare:5 | ||||
| chr20:17569966-17570202 | Common:3; Rare:103 |