| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:1776871-1777280 | Common:3; Rare:180; Clinvar:1 | ||||
| chr17:1829708-1830127 | Common:26; Rare:461 | ||||
| chr17:2025139-2025550 | Rare:276 | ||||
| chr17:2029977-2030220 | Common:2; Rare:185; Clinvar (pathogenic):2 | ||||
| chr17:2030612-2030784 | Rare:49 | ||||
| chr17:2041380-2042191 | Common:18; Rare:613 | ||||
| chr17:2054488-2054750 | Common:2; Rare:127 | ||||
| chr17:2094999-2095272 | Common:3; Rare:51 | ||||
| chr17:2303100-2304055 | Common:9; Rare:766 | ||||
| chr17:2336404-2336658 | Rare:245 | ||||
| chr17:2337313-2337734 | Common:1; Rare:258 | ||||
| chr17:2337933-2338218 | Common:6; Rare:197 | ||||
| chr17:2392510-2393070 | Common:21; Rare:530 | ||||
| chr17:2393004-2393620 | Common:16; Rare:426 | ||||
| chr17:2393730-2394151 | Common:9; Rare:404 |