| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:2086635-2086868 | Common:2; Rare:85; Clinvar:14; Clinvar (benign):27; Clinvar (pathogenic):1 | ||||
| chr16:2673351-2673705 | Common:10; Rare:125 | ||||
| chr16:3048729-3048947 | Common:1; Rare:40 | ||||
| chr16:3051572-3051652 | Common:1; Rare:20 | ||||
| chr16:3053155-3053461 | Common:2; Rare:48 | ||||
| chr16:3053488-3053558 | Rare:11 | ||||
| chr16:3054992-3055111 | Rare:29 | ||||
| chr16:3055990-3056279 | Common:5; Rare:51 | ||||
| chr16:3058236-3058434 | Common:1; Rare:83 | ||||
| chr16:3075040-3075169 | Common:1; Rare:35 | ||||
| chr16:3143983-3144264 | Common:4; Rare:52 | ||||
| chr16:3150480-3150670 | Common:3; Rare:80 | ||||
| chr16:3259201-3259374 | Common:1; Rare:42 | ||||
| chr16:4253783-4253880 | Common:2; Rare:31 | ||||
| chr16:4628348-4628614 | Common:3; Rare:76 |