| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:35373616-35373749 | Common:2; Rare:31 | ||||
| chr17:35433143-35433465 | Common:5; Rare:73 | ||||
| chr17:35578545-35578721 | Common:1; Rare:45; Clinvar (benign):1 | ||||
| chr17:35587222-35587579 | Rare:87 | ||||
| chr17:35809283-35809543 | Rare:109 | ||||
| chr17:36534211-36534276 | Rare:16 | ||||
| chr17:36534799-36535041 | Common:3; Rare:104 | ||||
| chr17:36544781-36545027 | Common:5; Rare:81 | ||||
| chr17:36601491-36601637 | Rare:47 | ||||
| chr17:36936656-36936796 | Common:1; Rare:26 | ||||
| chr17:36948753-36949107 | Common:3; Rare:121 | ||||
| chr17:37406814-37406935 | Rare:45 | ||||
| chr17:37489678-37489919 | Rare:94 | ||||
| chr17:37491450-37491568 | Common:3; Rare:29 | ||||
| chr17:37609343-37609588 | Common:1; Rare:102 |