| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7931906-7932275 | Common:5; Rare:104 | ||||
| chr17:8147236-8147550 | Common:2; Rare:108 | ||||
| chr17:8151141-8151494 | Common:3; Rare:88 | ||||
| chr17:8247925-8248182 | Common:3; Rare:104; Clinvar:6; Clinvar (benign):3 | ||||
| chr17:8249024-8249319 | Common:1; Rare:64 | ||||
| chr17:8295346-8295504 | Common:1; Rare:40 | ||||
| chr17:8435666-8436028 | Common:5; Rare:142 | ||||
| chr17:8450893-8451006 | Common:1; Rare:35 | ||||
| chr17:8965638-8965798 | Common:1; Rare:39 | ||||
| chr17:10019837-10020137 | Common:1; Rare:75 | ||||
| chr17:10114507-10114866 | Common:3; Rare:60 | ||||
| chr17:10697505-10697653 | Common:3; Rare:57; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:11997420-11997640 | Common:3; Rare:83 | ||||
| chr17:14069463-14069547 | Common:2; Rare:27; Clinvar:1; Clinvar (benign):2 | ||||
| chr17:15999589-15999824 | Common:1; Rare:122; Clinvar:4; Clinvar (benign):4 |