| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:43545594-43545820 | Common:1; Rare:62 | ||||
| chr17:43778925-43779073 | Rare:30 | ||||
| chr17:44070608-44070963 | Common:3; Rare:124; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:44123599-44123863 | Common:3; Rare:76 | ||||
| chr17:44186620-44187011 | Common:1; Rare:140 | ||||
| chr17:44187169-44187294 | Rare:33 | ||||
| chr17:44210419-44210672 | Rare:102 | ||||
| chr17:44221273-44221398 | Rare:38 | ||||
| chr17:44222103-44222414 | Rare:65 | ||||
| chr17:44324774-44324955 | Common:2; Rare:65 | ||||
| chr17:44345072-44345321 | Rare:52; Clinvar:5; Clinvar (benign):3 | ||||
| chr17:44503377-44503714 | Rare:132 | ||||
| chr17:44708728-44708899 | Common:3; Rare:57 | ||||
| chr17:44830167-44830398 | Common:1; Rare:100 | ||||
| chr17:44899367-44899735 | Common:2; Rare:114; Clinvar:1; Clinvar (benign):1 |