| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:47460960-47461374 | Common:2; Rare:169; Clinvar (benign):2 | ||||
| chr16:48244253-48244423 | Common:2; Rare:58 | ||||
| chr16:50741685-50742139 | Common:7; Rare:130; Clinvar:1 | ||||
| chr16:53098894-53099222 | Rare:65 | ||||
| chr16:53208305-53208525 | Rare:44 | ||||
| chr16:53703809-53704215 | Common:1; Rare:131; Clinvar:4; Clinvar (benign):2 | ||||
| chr16:54286722-54287016 | Common:1; Rare:87 | ||||
| chr16:56191077-56191406 | Common:5; Rare:116 | ||||
| chr16:56191603-56191864 | Common:1; Rare:67 | ||||
| chr16:56192162-56192310 | Rare:31; Clinvar (benign):2 | ||||
| chr16:56451286-56451614 | Common:1; Rare:109 | ||||
| chr16:56519973-56520133 | Common:4; Rare:61; Clinvar:6; Clinvar (benign):5 | ||||
| chr16:56608373-56608694 | Common:2; Rare:98 | ||||
| chr16:56625595-56625817 | Common:1; Rare:68 | ||||
| chr16:56657850-56658043 | Common:2; Rare:55 |