| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89700846-89701246 | Rare:136 | ||||
| chr16:89701511-89702320 | Common:58; Rare:1157 | ||||
| chr16:89709767-89710256 | Common:3; Rare:318 | ||||
| chr16:89711597-89713168 | Common:26; Rare:1231 | ||||
| chr16:89718939-89719701 | Common:22; Rare:657 | ||||
| chr16:89720586-89721169 | Common:19; Rare:771 | ||||
| chr16:89721289-89721716 | Common:15; Rare:585 | ||||
| chr16:89721728-89722712 | Common:5; Rare:565 | ||||
| chr16:89739263-89739663 | Common:9; Rare:287; Clinvar:21; Clinvar (benign):8; Clinvar (pathogenic):6 | ||||
| chr16:89743038-89743599 | Common:7; Rare:211 | ||||
| chr16:89816451-89817051 | Common:47; Rare:1254; Clinvar:30; Clinvar (benign):21; Clinvar (pathogenic):22 | ||||
| chr16:89817529-89817929 | Common:4; Rare:262 | ||||
| chr16:89828000-89828650 | Common:10; Rare:482 | ||||
| chr16:89873346-89873818 | Common:20; Rare:879 | ||||
| chr16:89873840-89874454 | Common:18; Rare:394 |