| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42387937-42389032 | Common:12; Rare:1132; Clinvar:17 | ||||
| chr17:42423131-42423531 | Common:7; Rare:481; Clinvar:10 | ||||
| chr17:42458617-42459041 | Common:15; Rare:529 | ||||
| chr17:42459603-42459775 | Common:4; Rare:50 | ||||
| chr17:42467927-42468327 | Common:2; Rare:109 | ||||
| chr17:42520071-42520471 | Common:1; Rare:137 | ||||
| chr17:42536041-42537020 | Common:26; Rare:966; Clinvar:46; Clinvar (benign):9; Clinvar (pathogenic):32 | ||||
| chr17:42541245-42541645 | Common:4; Rare:62 | ||||
| chr17:42553250-42553850 | Common:3; Rare:243 | ||||
| chr17:42561870-42562250 | Common:3; Rare:295 | ||||
| chr17:42562691-42563324 | Common:5; Rare:433; Clinvar:4; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr17:42566813-42567213 | Common:18; Rare:552 | ||||
| chr17:42567395-42567795 | Common:1; Rare:156 | ||||
| chr17:42577554-42578349 | Common:9; Rare:1019 | ||||
| chr17:42609255-42609780 | Common:56; Rare:1263; Clinvar (benign):12 |