| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:84145110-84145349 | Common:2; Rare:113; Clinvar:5 | ||||
| chr16:84504612-84504861 | Common:8; Rare:109 | ||||
| chr16:85027594-85027819 | Common:1; Rare:125 | ||||
| chr16:85613038-85613327 | Common:1; Rare:109 | ||||
| chr16:85799525-85799748 | Common:2; Rare:64 | ||||
| chr16:86555172-86555327 | Rare:80 | ||||
| chr16:87317394-87317527 | Common:2; Rare:51 | ||||
| chr16:87765906-87766028 | Rare:49 | ||||
| chr16:88570167-88570482 | Common:2; Rare:120 | ||||
| chr16:88663070-88663371 | Common:8; Rare:124 | ||||
| chr16:88706192-88706538 | Common:4; Rare:154 | ||||
| chr16:88856831-88857177 | Common:4; Rare:165; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:89093789-89093943 | Common:3; Rare:70 | ||||
| chr16:89217619-89217749 | Common:1; Rare:61 | ||||
| chr16:89508289-89508428 | Common:1; Rare:77; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 |