| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31442772-31443059 | Common:1; Rare:47 | ||||
| chr16:31458039-31458314 | Common:1; Rare:65 | ||||
| chr16:31459075-31459168 | Rare:32 | ||||
| chr16:31459273-31459517 | Common:1; Rare:102 | ||||
| chr16:31472113-31472189 | Rare:20 | ||||
| chr16:31508369-31508516 | Common:4; Rare:61 | ||||
| chr16:46689117-46689417 | Common:1; Rare:104; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46689510-46689745 | Common:2; Rare:105; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:46831106-46831323 | Common:2; Rare:85 | ||||
| chr16:46973493-46973801 | Rare:119 | ||||
| chr16:47460986-47461378 | Common:2; Rare:161; Clinvar (benign):2 | ||||
| chr16:47462038-47462210 | Rare:21 | ||||
| chr16:48244248-48244581 | Common:2; Rare:100 | ||||
| chr16:48365885-48366098 | Common:5; Rare:64 | ||||
| chr16:48385264-48385552 | Common:3; Rare:111 |