| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:15988740-15989041 | Common:4; Rare:67 | ||||
| chr17:16006488-16006665 | Rare:47; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr17:16006890-16007262 | Common:2; Rare:74 | ||||
| chr17:16007739-16007886 | Common:2; Rare:25 | ||||
| chr17:16019829-16020082 | Common:1; Rare:28 | ||||
| chr17:16020637-16020830 | Common:1; Rare:33 | ||||
| chr17:16041558-16041677 | Rare:37 | ||||
| chr17:16045019-16045085 | Rare:13 | ||||
| chr17:16106569-16106781 | Common:1; Rare:40 | ||||
| chr17:16438656-16439110 | Common:1; Rare:125 | ||||
| chr17:16439217-16439773 | Common:8; Rare:213 | ||||
| chr17:16439776-16440037 | Common:1; Rare:55 | ||||
| chr17:16440752-16441146 | Common:4; Rare:108 | ||||
| chr17:16441311-16441553 | Rare:63 | ||||
| chr17:16450958-16450970 | Common:1; Rare:1 |