| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:74431275-74431393 | Rare:31 | ||||
| chr17:74432012-74432107 | Common:1; Rare:42 | ||||
| chr17:74466228-74466406 | Common:2; Rare:36 | ||||
| chr17:74466574-74466706 | Rare:39 | ||||
| chr17:74748407-74748644 | Common:2; Rare:81 | ||||
| chr17:74776250-74776543 | Common:4; Rare:96 | ||||
| chr17:74972695-74972865 | Common:2; Rare:45 | ||||
| chr17:75012536-75012687 | Common:1; Rare:37 | ||||
| chr17:75046929-75047156 | Common:1; Rare:70 | ||||
| chr17:75109800-75109969 | Common:2; Rare:46 | ||||
| chr17:75154484-75154795 | Common:1; Rare:95 | ||||
| chr17:75182836-75183216 | Common:2; Rare:134 | ||||
| chr17:75205384-75205730 | Rare:100 | ||||
| chr17:75261580-75261935 | Common:4; Rare:110; Clinvar (benign):2 | ||||
| chr17:75271146-75271390 | Common:3; Rare:44 |