| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42566994-42567155 | Common:3; Rare:51 | ||||
| chr17:42577655-42577927 | Common:1; Rare:135 | ||||
| chr17:42609316-42609786 | Common:8; Rare:187; Clinvar (benign):2 | ||||
| chr17:42745018-42745180 | Common:3; Rare:60 | ||||
| chr17:42760582-42760888 | Common:5; Rare:92 | ||||
| chr17:42760913-42761299 | Common:1; Rare:102 | ||||
| chr17:42761306-42761381 | Common:1; Rare:16 | ||||
| chr17:42761596-42761899 | Rare:83 | ||||
| chr17:42798685-42798785 | Rare:28 | ||||
| chr17:42833348-42833516 | Rare:58 | ||||
| chr17:42851052-42851346 | Rare:73 | ||||
| chr17:42852448-42852502 | Common:2; Rare:20 | ||||
| chr17:42964404-42964546 | Rare:66 | ||||
| chr17:42998390-42998478 | Common:3; Rare:35 | ||||
| chr17:43125351-43125621 | Rare:54; Clinvar:3; Clinvar (benign):2 |