| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:31652417-31652463 | Rare:12 | ||||
| chr6:31664886-31665097 | Common:2; Rare:49 | ||||
| chr6:31665727-31666156 | Common:4; Rare:116 | ||||
| chr6:31703284-31703415 | Rare:43 | ||||
| chr6:31806776-31807061 | Common:1; Rare:117 | ||||
| chr6:31815350-31815550 | Common:1; Rare:65 | ||||
| chr6:31834618-31834924 | Common:3; Rare:69 | ||||
| chr6:31835200-31835444 | Common:3; Rare:104 | ||||
| chr6:31897664-31897782 | Rare:22 | ||||
| chr6:31945917-31946124 | Common:1; Rare:25; Clinvar (benign):1 | ||||
| chr6:31958881-31959189 | Rare:98; Clinvar:8 | ||||
| chr6:32109293-32109496 | Rare:33 | ||||
| chr6:32153757-32154216 | Common:4; Rare:78 | ||||
| chr6:32154376-32154492 | Rare:14 | ||||
| chr6:32176037-32176248 | Common:1; Rare:44 |