| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:87765908-87766033 | Rare:49 | ||||
| chr16:88570159-88570439 | Common:2; Rare:100 | ||||
| chr16:88627689-88628024 | Rare:105 | ||||
| chr16:88663048-88663382 | Common:9; Rare:141 | ||||
| chr16:88706338-88706575 | Common:4; Rare:119 | ||||
| chr16:88716271-88716450 | Common:1; Rare:88; Clinvar (benign):1 | ||||
| chr16:88810169-88810215 | Common:2; Rare:12 | ||||
| chr16:88856899-88857182 | Common:4; Rare:140; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:89217333-89217763 | Common:4; Rare:181 | ||||
| chr16:89508272-89508590 | Common:3; Rare:161; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr16:89560532-89560962 | Rare:185 | ||||
| chr16:89562330-89562528 | Common:3; Rare:70 | ||||
| chr16:89657621-89658138 | Common:3; Rare:257 | ||||
| chr16:89686638-89686793 | Common:7; Rare:103 | ||||
| chr16:89686904-89687010 | Rare:49 |