| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:5468606-5469002 | Common:2; Rare:151 | ||||
| chr17:5486089-5486652 | Common:6; Rare:192 | ||||
| chr17:5486778-5486943 | Common:4; Rare:51 | ||||
| chr17:6070166-6070407 | Common:2; Rare:52 | ||||
| chr17:6444246-6444502 | Common:2; Rare:84 | ||||
| chr17:6640569-6641226 | Common:9; Rare:208 | ||||
| chr17:6651539-6651768 | Common:1; Rare:80 | ||||
| chr17:6713348-6713528 | Common:3; Rare:38; Clinvar (benign):2 | ||||
| chr17:6995707-6996052 | Common:3; Rare:69 | ||||
| chr17:7012308-7012684 | Rare:130 | ||||
| chr17:7022844-7023102 | Common:3; Rare:58 | ||||
| chr17:7035815-7036042 | Rare:57 | ||||
| chr17:7042982-7043167 | Common:3; Rare:66 | ||||
| chr17:7217584-7217738 | Common:1; Rare:27 | ||||
| chr17:7219728-7220042 | Common:4; Rare:122; Clinvar:6; Clinvar (benign):4; Clinvar (pathogenic):1 |