| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:8106201-8106358 | Common:2; Rare:31 | ||||
| chr17:8119602-8119766 | Common:8; Rare:64 | ||||
| chr17:8120353-8120437 | Common:2; Rare:54 | ||||
| chr17:8120897-8120942 | Common:2; Rare:38 | ||||
| chr17:8123307-8123512 | Common:1; Rare:44 | ||||
| chr17:8125613-8125753 | Rare:61 | ||||
| chr17:8126346-8126753 | Rare:100 | ||||
| chr17:8126899-8126931 | Rare:3 | ||||
| chr17:8126933-8127025 | Common:2; Rare:22 | ||||
| chr17:8138946-8139159 | Common:6; Rare:92 | ||||
| chr17:8139514-8139539 | Common:1; Rare:15 | ||||
| chr17:8153621-8153867 | Common:1; Rare:44 | ||||
| chr17:8154169-8154480 | Common:1; Rare:66 | ||||
| chr17:8157032-8157129 | Rare:32 | ||||
| chr17:8173379-8173590 | Common:11; Rare:295; Clinvar:3; Clinvar (pathogenic):4 |