| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:13615139-13615648 | Common:3; Rare:205 | ||||
| chr6:13814018-13814083 | Rare:9 | ||||
| chr6:13814119-13814281 | Common:1; Rare:54 | ||||
| chr6:13814429-13814598 | Common:1; Rare:57 | ||||
| chr6:17393593-17393724 | Rare:32 | ||||
| chr6:17600228-17600368 | Common:2; Rare:52 | ||||
| chr6:17705839-17706159 | Common:1; Rare:85 | ||||
| chr6:17706281-17706480 | Common:2; Rare:86 | ||||
| chr6:17706704-17707232 | Common:1; Rare:128 | ||||
| chr6:18122614-18122776 | Common:1; Rare:37; Clinvar (benign):2 | ||||
| chr6:18155055-18155509 | Common:11; Rare:116; Clinvar:1 | ||||
| chr6:18264433-18264703 | Rare:120 | ||||
| chr6:20401524-20401927 | Common:3; Rare:109 | ||||
| chr6:20402340-20402617 | Common:1; Rare:106 | ||||
| chr6:24357913-24358141 | Common:2; Rare:56 |