| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89686490-89686723 | Common:11; Rare:97 | ||||
| chr16:89686889-89686997 | Rare:47 | ||||
| chr16:89701676-89701813 | Rare:53 | ||||
| chr16:89711814-89711897 | Common:1; Rare:42 | ||||
| chr16:89720848-89720999 | Common:1; Rare:40 | ||||
| chr16:89816568-89816749 | Common:3; Rare:96; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr16:89873474-89873856 | Common:3; Rare:171 | ||||
| chr16:89918559-89918880 | Common:4; Rare:100; Clinvar:3; Clinvar (benign):5 | ||||
| chr16:89921780-89921944 | Rare:53 | ||||
| chr16:89923171-89923378 | Rare:91 | ||||
| chr16:89948559-89948806 | Common:3; Rare:74 | ||||
| chr16:89972462-89972684 | Common:1; Rare:78 | ||||
| chr16:89972828-89972860 | Common:1; Rare:9 | ||||
| chr16:90022529-90022724 | Common:1; Rare:79 | ||||
| chr17:352690-352866 | Common:1; Rare:42 |