| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:2971528-2971717 | Common:1; Rare:51 | ||||
| chr6:2999653-2999999 | Common:10; Rare:70 | ||||
| chr6:3068240-3068563 | Common:1; Rare:102 | ||||
| chr6:3118607-3118737 | Common:2; Rare:40 | ||||
| chr6:3157541-3157662 | Common:6; Rare:45 | ||||
| chr6:3849169-3849455 | Common:3; Rare:82 | ||||
| chr6:4021200-4021432 | Rare:102 | ||||
| chr6:5260679-5261017 | Common:3; Rare:115; Clinvar (benign):4 | ||||
| chr6:7108599-7108674 | Rare:24 | ||||
| chr6:7389564-7389986 | Common:2; Rare:117 | ||||
| chr6:7541374-7541684 | Common:1; Rare:93; Clinvar (benign):1 | ||||
| chr6:7910633-7910925 | Common:3; Rare:115 | ||||
| chr6:8064338-8064576 | Common:4; Rare:71 | ||||
| chr6:8102499-8102706 | Common:1; Rare:70 | ||||
| chr6:8435481-8435659 | Common:3; Rare:71 |