| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42682402-42682529 | Rare:29 | ||||
| chr17:42773394-42773501 | Rare:35 | ||||
| chr17:42798661-42798785 | Rare:40 | ||||
| chr17:42833340-42833491 | Rare:57 | ||||
| chr17:42964442-42964536 | Rare:43 | ||||
| chr17:43125317-43125580 | Rare:60; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:43170297-43170511 | Common:2; Rare:43 | ||||
| chr17:43171043-43171267 | Common:1; Rare:72 | ||||
| chr17:43778917-43779057 | Rare:29 | ||||
| chr17:44070620-44070947 | Common:3; Rare:115; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:44186658-44187002 | Common:1; Rare:127 | ||||
| chr17:44187192-44187274 | Rare:20 | ||||
| chr17:44324750-44325003 | Common:2; Rare:93 | ||||
| chr17:44345249-44345321 | Rare:17; Clinvar:1; Clinvar (benign):3 | ||||
| chr17:44503374-44503730 | Rare:137 |