| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89686613-89686701 | Common:6; Rare:46 | ||||
| chr16:89816625-89816772 | Common:2; Rare:68; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:89873442-89873662 | Common:4; Rare:107 | ||||
| chr16:89923203-89923355 | Rare:60 | ||||
| chr16:89972521-89972609 | Rare:26 | ||||
| chr17:714816-714883 | Common:1; Rare:22 | ||||
| chr17:752146-752347 | Common:2; Rare:78 | ||||
| chr17:1400048-1400311 | Common:2; Rare:102 | ||||
| chr17:1485737-1486059 | Common:4; Rare:106 | ||||
| chr17:1516595-1516955 | Common:1; Rare:125 | ||||
| chr17:1684802-1685038 | Common:2; Rare:77; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:1829779-1830016 | Common:5; Rare:101 | ||||
| chr17:2303736-2303983 | Common:2; Rare:94 | ||||
| chr17:2336428-2336550 | Rare:48 | ||||
| chr17:2511806-2512021 | Common:2; Rare:68 |