| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:68539142-68539379 | Common:2; Rare:109 | ||||
| chr16:68737130-68737426 | Common:3; Rare:99; Clinvar:5; Clinvar (benign):19 | ||||
| chr16:69132486-69132686 | Rare:73 | ||||
| chr16:69187026-69187181 | Rare:57 | ||||
| chr16:69339548-69339823 | Common:1; Rare:112; Clinvar (benign):1 | ||||
| chr16:69424489-69424855 | Common:1; Rare:110 | ||||
| chr16:69565661-69565986 | Common:4; Rare:123 | ||||
| chr16:69726431-69726737 | Common:4; Rare:84 | ||||
| chr16:69754855-69755092 | Common:1; Rare:98 | ||||
| chr16:69762251-69762381 | Common:1; Rare:35 | ||||
| chr16:70114124-70114407 | Common:3; Rare:99 | ||||
| chr16:70299093-70299239 | Common:1; Rare:31 | ||||
| chr16:70346751-70347045 | Common:2; Rare:136 | ||||
| chr16:70523517-70523903 | Common:3; Rare:127; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:70800970-70801268 | Common:2; Rare:95 |