| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:2903307-2903527 | Common:4; Rare:56 | ||||
| chr6:2987846-2987975 | Common:1; Rare:22 | ||||
| chr6:2999621-3000065 | Common:10; Rare:101 | ||||
| chr6:3068209-3068571 | Common:1; Rare:114 | ||||
| chr6:3118581-3118750 | Common:2; Rare:57 | ||||
| chr6:3157536-3157642 | Common:6; Rare:42 | ||||
| chr6:3455991-3456188 | Rare:57 | ||||
| chr6:3849123-3849451 | Common:3; Rare:91 | ||||
| chr6:4021159-4021454 | Common:1; Rare:122 | ||||
| chr6:5003603-5003843 | Common:6; Rare:76 | ||||
| chr6:5004000-5004084 | Common:1; Rare:43 | ||||
| chr6:5260671-5261017 | Common:3; Rare:120; Clinvar (benign):4 | ||||
| chr6:5261253-5261591 | Common:9; Rare:96 | ||||
| chr6:7108337-7108862 | Common:5; Rare:166 | ||||
| chr6:7313047-7313385 | Common:5; Rare:126 |