| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:88811897-88812059 | Common:2; Rare:68; Clinvar (benign):1 | ||||
| chr16:88856917-88857178 | Common:4; Rare:123; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:89217619-89217716 | Common:1; Rare:42 | ||||
| chr16:89508253-89508426 | Common:1; Rare:96; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr16:89560535-89560717 | Rare:77 | ||||
| chr16:89657673-89657863 | Common:1; Rare:101 | ||||
| chr16:89686596-89686702 | Common:6; Rare:51 | ||||
| chr16:89923185-89923352 | Rare:61 | ||||
| chr16:89972474-89972614 | Common:1; Rare:48 | ||||
| chr17:714807-714883 | Common:1; Rare:26 | ||||
| chr17:752146-752339 | Common:2; Rare:74 | ||||
| chr17:1400048-1400356 | Common:3; Rare:126 | ||||
| chr17:1492692-1492796 | Rare:21 | ||||
| chr17:1516636-1516960 | Common:1; Rare:114 | ||||
| chr17:1684802-1685048 | Common:2; Rare:77; Clinvar:3; Clinvar (benign):1 |