| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:149718049-149718119 | Common:1; Rare:21 | ||||
| chr6:149749626-149749800 | Rare:99 | ||||
| chr6:150142932-150143258 | Common:1; Rare:109 | ||||
| chr6:151240229-151240421 | Common:1; Rare:51 | ||||
| chr6:151390986-151391077 | Common:1; Rare:26 | ||||
| chr6:151391503-151391764 | Common:3; Rare:67 | ||||
| chr6:151452023-151452548 | Common:5; Rare:188; Clinvar (benign):3 | ||||
| chr6:152302067-152302229 | Rare:55; Clinvar (benign):2 | ||||
| chr6:152983029-152983281 | Common:2; Rare:77 | ||||
| chr6:153002471-153002872 | Common:6; Rare:161 | ||||
| chr6:154510518-154510793 | Common:2; Rare:84 | ||||
| chr6:155314456-155314603 | Common:2; Rare:44 | ||||
| chr6:157323495-157323597 | Common:2; Rare:38 | ||||
| chr6:157381074-157381359 | Rare:79 | ||||
| chr6:158168210-158168388 | Common:2; Rare:63 |