| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42017531-42017632 | Rare:33 | ||||
| chr17:42017634-42017798 | Rare:35 | ||||
| chr17:42019974-42020183 | Common:1; Rare:64 | ||||
| chr17:42121332-42121454 | Rare:30 | ||||
| chr17:42154896-42155187 | Common:3; Rare:76 | ||||
| chr17:42423103-42423413 | Common:1; Rare:84; Clinvar:2 | ||||
| chr17:42458712-42458960 | Common:3; Rare:92 | ||||
| chr17:42566926-42567210 | Common:3; Rare:101 | ||||
| chr17:42577631-42577864 | Common:1; Rare:112 | ||||
| chr17:42609333-42609775 | Common:8; Rare:178; Clinvar (benign):2 | ||||
| chr17:42659156-42659441 | Rare:87 | ||||
| chr17:42682429-42682561 | Rare:29 | ||||
| chr17:42745013-42745343 | Common:3; Rare:91 | ||||
| chr17:42773360-42773501 | Rare:44 | ||||
| chr17:42833322-42833543 | Rare:73 |