| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:86555190-86555329 | Rare:71 | ||||
| chr16:87765940-87766044 | Rare:36 | ||||
| chr16:88570138-88570436 | Common:2; Rare:110 | ||||
| chr16:88856891-88857153 | Common:4; Rare:125; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:89217632-89217749 | Common:1; Rare:52 | ||||
| chr16:89560540-89560712 | Rare:72 | ||||
| chr16:89657664-89657846 | Common:1; Rare:94 | ||||
| chr16:89923145-89923346 | Rare:77 | ||||
| chr16:89948560-89948803 | Common:3; Rare:72 | ||||
| chr16:90022552-90022697 | Rare:57 | ||||
| chr17:1400102-1400427 | Common:3; Rare:141 | ||||
| chr17:1516628-1516960 | Common:1; Rare:118 | ||||
| chr17:1684813-1685067 | Common:2; Rare:80; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:1716206-1716520 | Common:2; Rare:94 | ||||
| chr17:1829805-1830039 | Common:6; Rare:101 |