| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:21594678-21594863 | Rare:44; Clinvar (pathogenic):1 | ||||
| chr6:21596298-21596449 | Rare:59 | ||||
| chr6:22146018-22146371 | Common:2; Rare:72 | ||||
| chr6:22146538-22146951 | Common:3; Rare:121 | ||||
| chr6:22148420-22148684 | Common:1; Rare:51 | ||||
| chr6:24719338-24719473 | Rare:39 | ||||
| chr6:26122989-26123198 | Common:2; Rare:61 | ||||
| chr6:26521775-26522087 | Common:1; Rare:61 | ||||
| chr6:26537467-26537499 | Common:2; Rare:18 | ||||
| chr6:27020296-27020363 | Rare:17 | ||||
| chr6:27139176-27139311 | Rare:46 | ||||
| chr6:27375203-27375323 | Common:1; Rare:21 | ||||
| chr6:27423086-27423249 | Common:1; Rare:38 | ||||
| chr6:27688140-27688187 | Rare:27 | ||||
| chr6:27694025-27694144 | Rare:21 |