| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:96877308-96877607 | Common:5; Rare:69 | ||||
| chr15:101961464-101961629 | Rare:4 | ||||
| chr16:2603326-2603472 | Common:1; Rare:59 | ||||
| chr16:3026934-3027039 | Common:1; Rare:36 | ||||
| chr16:8847485-8847808 | Rare:133; Clinvar:7; Clinvar (benign):1; Clinvar (pathogenic):8 | ||||
| chr16:8855304-8855592 | Common:5; Rare:108 | ||||
| chr16:9676907-9677215 | Common:14; Rare:60 | ||||
| chr16:9680092-9680349 | Common:2; Rare:62 | ||||
| chr16:11328582-11328780 | Rare:48 | ||||
| chr16:13354060-13354152 | Common:1; Rare:18 | ||||
| chr16:13357671-13357868 | Common:7; Rare:56 | ||||
| chr16:21520394-21520547 | Common:1; Rare:16 | ||||
| chr16:29613697-29613853 | Rare:48 | ||||
| chr16:29709013-29709211 | Common:2; Rare:46 | ||||
| chr16:29709771-29709810 | Rare:6 |