| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:35373609-35373749 | Common:2; Rare:32 | ||||
| chr17:35578533-35578722 | Common:1; Rare:48; Clinvar (benign):1 | ||||
| chr17:35587165-35587563 | Rare:99 | ||||
| chr17:35809296-35809552 | Rare:107 | ||||
| chr17:36486502-36486721 | Common:3; Rare:82 | ||||
| chr17:36534787-36535042 | Common:3; Rare:108 | ||||
| chr17:36544787-36545054 | Common:5; Rare:82 | ||||
| chr17:36601331-36601606 | Common:3; Rare:72 | ||||
| chr17:36948820-36949046 | Common:2; Rare:76 | ||||
| chr17:37406792-37406934 | Rare:55 | ||||
| chr17:37489698-37489919 | Rare:87 | ||||
| chr17:37609281-37609625 | Common:1; Rare:141 | ||||
| chr17:38428279-38428503 | Common:8; Rare:80 | ||||
| chr17:38706095-38706149 | Rare:27 | ||||
| chr17:38730057-38730398 | Rare:94 |