| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:9575550-9576240 | Common:16; Rare:233 | ||||
| chr17:9645250-9645610 | Rare:140 | ||||
| chr17:9842134-9842595 | Common:6; Rare:193 | ||||
| chr17:10697473-10697674 | Common:8; Rare:166; Clinvar:8; Clinvar (benign):5 | ||||
| chr17:11997293-11997607 | Rare:161 | ||||
| chr17:12020687-12020886 | Common:2; Rare:85 | ||||
| chr17:12021313-12021659 | Rare:181 | ||||
| chr17:13017602-13017726 | Rare:96; Clinvar (benign):2 | ||||
| chr17:13017928-13018340 | Common:13; Rare:258; Clinvar (benign):4 | ||||
| chr17:14069329-14069593 | Common:4; Rare:185; Clinvar:8; Clinvar (benign):6 | ||||
| chr17:15260700-15261030 | Common:4; Rare:189; Clinvar (benign):8 | ||||
| chr17:15262472-15262699 | Rare:101 | ||||
| chr17:15563421-15563739 | Common:1; Rare:203 | ||||
| chr17:15699440-15699800 | Common:7; Rare:174 | ||||
| chr17:15999554-15999886 | Common:6; Rare:323; Clinvar:10; Clinvar (benign):16; Clinvar (pathogenic):4 |