| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44829499-44829742 | Common:1; Rare:65 | ||||
| chr17:44829753-44830102 | Common:3; Rare:79 | ||||
| chr17:44830159-44830336 | Common:1; Rare:85 | ||||
| chr17:44830687-44830743 | Rare:4 | ||||
| chr17:44898939-44899197 | Common:3; Rare:58 | ||||
| chr17:44899342-44899833 | Common:4; Rare:138; Clinvar:3; Clinvar (benign):2 | ||||
| chr17:44900118-44900325 | Common:2; Rare:38 | ||||
| chr17:44909589-44909824 | Common:8; Rare:31 | ||||
| chr17:44947278-44947319 | Rare:8 | ||||
| chr17:44947526-44947979 | Common:2; Rare:114 | ||||
| chr17:44968274-44968577 | Rare:83 | ||||
| chr17:45051204-45051552 | Common:1; Rare:87 | ||||
| chr17:45051558-45051709 | Rare:56 | ||||
| chr17:45052061-45052168 | Common:1; Rare:16 | ||||
| chr17:45060742-45060960 | Rare:38 |