| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31033264-31033628 | Common:2; Rare:115 | ||||
| chr16:31074197-31074453 | Common:1; Rare:73 | ||||
| chr16:31094721-31094820 | Rare:36 | ||||
| chr16:31184757-31185005 | Common:4; Rare:88; Clinvar (benign):2 | ||||
| chr16:31188957-31189099 | Common:2; Rare:32 | ||||
| chr16:31202314-31202435 | Common:1; Rare:33 | ||||
| chr16:31459310-31459503 | Common:1; Rare:82 | ||||
| chr16:31508122-31508274 | Common:2; Rare:65 | ||||
| chr16:31508371-31508464 | Common:1; Rare:34 | ||||
| chr16:31527863-31527916 | Rare:13 | ||||
| chr16:46689122-46689317 | Common:1; Rare:73; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46973615-46973801 | Rare:88 | ||||
| chr16:47461043-47461350 | Common:2; Rare:107; Clinvar (benign):2 | ||||
| chr16:48244172-48244320 | Common:2; Rare:42 | ||||
| chr16:48610008-48610375 | Common:3; Rare:117 |