| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:14300806-14301103 | Common:2; Rare:81 | ||||
| chr17:15260645-15261066 | Common:3; Rare:130; Clinvar:1; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr17:15262448-15262738 | Rare:63 | ||||
| chr17:15475717-15475915 | Common:1; Rare:35 | ||||
| chr17:15699514-15699773 | Common:3; Rare:68 | ||||
| chr17:15999591-15999827 | Common:1; Rare:123; Clinvar:4; Clinvar (benign):4 | ||||
| chr17:16215532-16215650 | Common:1; Rare:51 | ||||
| chr17:16415511-16415818 | Common:4; Rare:78 | ||||
| chr17:16653825-16653924 | Rare:31 | ||||
| chr17:17237133-17237415 | Common:4; Rare:86; Clinvar (benign):2 | ||||
| chr17:17496388-17496575 | Common:2; Rare:51 | ||||
| chr17:17591587-17591926 | Common:2; Rare:96 | ||||
| chr17:18039044-18039422 | Common:4; Rare:97; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:18182958-18183111 | Common:1; Rare:47 | ||||
| chr17:18183261-18183529 | Rare:70 |