| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:81833254-81833371 | Rare:49 | ||||
| chr17:81937233-81937594 | Rare:122 | ||||
| chr17:82037683-82037914 | Common:1; Rare:81 | ||||
| chr17:82051403-82051485 | Common:1; Rare:22 | ||||
| chr17:82051630-82051934 | Common:2; Rare:91 | ||||
| chr17:82273682-82273832 | Common:1; Rare:48 | ||||
| chr17:82450726-82450911 | Common:2; Rare:71 | ||||
| chr18:268015-268103 | Rare:31 | ||||
| chr18:812211-812446 | Common:3; Rare:83 | ||||
| chr18:2571474-2571597 | Rare:34 | ||||
| chr18:3247347-3247507 | Common:1; Rare:48 | ||||
| chr18:3261820-3262211 | Common:6; Rare:127 | ||||
| chr18:3450029-3450200 | Rare:51 | ||||
| chr18:3451505-3451688 | Common:2; Rare:68 | ||||
| chr18:9102494-9102766 | Common:2; Rare:106; Clinvar:6; Clinvar (benign):2 |