| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:693039-693169 | Rare:49 | ||||
| chr6:1311767-1312141 | Common:3; Rare:117 | ||||
| chr6:1389376-1389515 | Common:1; Rare:27 | ||||
| chr6:2245438-2245832 | Common:1; Rare:134 | ||||
| chr6:2841846-2842048 | Common:3; Rare:33 | ||||
| chr6:2971533-2971719 | Common:1; Rare:51 | ||||
| chr6:2999621-3000047 | Common:10; Rare:94 | ||||
| chr6:3118591-3118740 | Common:2; Rare:48 | ||||
| chr6:3157524-3157688 | Common:6; Rare:57 | ||||
| chr6:3231730-3231785 | Rare:7 | ||||
| chr6:3849163-3849455 | Common:3; Rare:82 | ||||
| chr6:4021213-4021427 | Rare:97 | ||||
| chr6:5003656-5003843 | Common:5; Rare:58 | ||||
| chr6:5260685-5261059 | Common:5; Rare:131; Clinvar (benign):4 | ||||
| chr6:5261256-5261585 | Common:9; Rare:92 |