| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:69186582-69186793 | Common:1; Rare:31 | ||||
| chr16:69186982-69187175 | Rare:69 | ||||
| chr16:69187675-69187815 | Rare:33 | ||||
| chr16:69188022-69188088 | Rare:13 | ||||
| chr16:69311027-69311428 | Common:1; Rare:112 | ||||
| chr16:69330064-69330192 | Common:3; Rare:75 | ||||
| chr16:69330446-69330996 | Common:3; Rare:235; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr16:69339241-69339364 | Rare:48; Clinvar:1 | ||||
| chr16:69339461-69339845 | Common:2; Rare:170; Clinvar:1; Clinvar (benign):4 | ||||
| chr16:69385895-69386124 | Rare:82 | ||||
| chr16:69424266-69424782 | Common:4; Rare:137 | ||||
| chr16:69425203-69425289 | Common:1; Rare:19 | ||||
| chr16:69565635-69566173 | Common:5; Rare:188 | ||||
| chr16:69566499-69566634 | Rare:33 | ||||
| chr16:69566814-69566966 | Rare:24 |