| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:16022358-16022473 | Common:3; Rare:28 | ||||
| chr17:16026342-16026702 | Rare:91; Clinvar (benign):2 | ||||
| chr17:16034797-16035066 | Rare:62 | ||||
| chr17:16342377-16342608 | Common:1; Rare:42 | ||||
| chr17:16438745-16439057 | Common:1; Rare:85 | ||||
| chr17:16439320-16439359 | Rare:12 | ||||
| chr17:16439445-16439815 | Common:4; Rare:136 | ||||
| chr17:16441174-16441420 | Common:3; Rare:82 | ||||
| chr17:16441475-16441574 | Common:2; Rare:16 | ||||
| chr17:16454080-16454258 | Common:4; Rare:24 | ||||
| chr17:16457420-16457575 | Common:2; Rare:30 | ||||
| chr17:16459144-16459371 | Common:1; Rare:34 | ||||
| chr17:16464640-16464808 | Common:3; Rare:29 | ||||
| chr17:16465985-16466255 | Common:2; Rare:51 | ||||
| chr17:16469604-16469925 | Common:1; Rare:47 |