| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:3118602-3118743 | Common:2; Rare:47 | ||||
| chr6:4021193-4021422 | Rare:102 | ||||
| chr6:5003644-5003843 | Common:5; Rare:63 | ||||
| chr6:5003998-5004112 | Common:2; Rare:55 | ||||
| chr6:5260696-5261017 | Common:3; Rare:106; Clinvar (benign):4 | ||||
| chr6:5261238-5261559 | Common:9; Rare:82 | ||||
| chr6:7313083-7313380 | Common:5; Rare:111 | ||||
| chr6:7389740-7389875 | Common:1; Rare:40 | ||||
| chr6:8435326-8435659 | Common:4; Rare:114 | ||||
| chr6:10694614-10694988 | Common:4; Rare:97 | ||||
| chr6:10722944-10723237 | Common:5; Rare:111 | ||||
| chr6:10747572-10747881 | Common:4; Rare:116 | ||||
| chr6:11232606-11232806 | Rare:43 | ||||
| chr6:13328515-13328621 | Common:2; Rare:36 | ||||
| chr6:13615159-13615550 | Common:3; Rare:152 |