| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:11996793-11996969 | Rare:40 | ||||
| chr17:11997025-11997073 | Common:1; Rare:13 | ||||
| chr17:11997095-11997200 | Common:2; Rare:22 | ||||
| chr17:11997220-11997811 | Common:4; Rare:178 | ||||
| chr17:12020678-12021002 | Common:2; Rare:128 | ||||
| chr17:12021007-12021063 | Common:1; Rare:10 | ||||
| chr17:12021209-12021419 | Rare:83 | ||||
| chr17:12021450-12021517 | Rare:20 | ||||
| chr17:13016885-13017114 | Common:1; Rare:82; Clinvar (benign):2 | ||||
| chr17:13017363-13017486 | Common:1; Rare:28 | ||||
| chr17:13017588-13017820 | Common:1; Rare:95; Clinvar (benign):3 | ||||
| chr17:13017904-13018377 | Common:8; Rare:157; Clinvar (benign):2 | ||||
| chr17:13018493-13018579 | Rare:18 | ||||
| chr17:13601500-13601577 | Common:1; Rare:27 | ||||
| chr17:13601775-13602185 | Common:3; Rare:121 |