| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:78378464-78378658 | Rare:58 | ||||
| chr17:78840731-78841093 | Common:2; Rare:137 | ||||
| chr17:78979847-78980002 | Common:1; Rare:32 | ||||
| chr17:79009717-79009924 | Common:9; Rare:62; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:80035846-80036034 | Common:1; Rare:65 | ||||
| chr17:80036517-80036715 | Common:2; Rare:64; Clinvar:1; Clinvar (benign):2 | ||||
| chr17:80146897-80147383 | Common:11; Rare:211 | ||||
| chr17:80220311-80220459 | Common:1; Rare:57; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr17:80415067-80415500 | Common:5; Rare:222 | ||||
| chr17:80991750-80991972 | Common:1; Rare:82 | ||||
| chr17:81239025-81239464 | Common:4; Rare:144 | ||||
| chr17:81246996-81247277 | Rare:84 | ||||
| chr17:81295253-81295401 | Common:1; Rare:33 | ||||
| chr17:81395194-81395487 | Common:1; Rare:77 | ||||
| chr17:81552346-81552467 | Common:1; Rare:44 |