| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:153131194-153131491 | Rare:125 | ||||
| chr6:155216800-155216811 | Rare:1 | ||||
| chr6:157323501-157323628 | Common:2; Rare:41 | ||||
| chr6:158168166-158168388 | Common:3; Rare:82 | ||||
| chr6:158536309-158536720 | Common:2; Rare:159 | ||||
| chr6:158644710-158644784 | Common:2; Rare:42 | ||||
| chr6:158819333-158819560 | Common:2; Rare:83 | ||||
| chr6:158999752-158999930 | Common:1; Rare:77; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:159693257-159693594 | Common:5; Rare:94 | ||||
| chr6:159726911-159727157 | Common:1; Rare:95 | ||||
| chr6:159761834-159762079 | Common:4; Rare:124 | ||||
| chr6:159762305-159762460 | Common:1; Rare:41 | ||||
| chr6:159789545-159789947 | Common:3; Rare:135 | ||||
| chr6:159790261-159790514 | Common:7; Rare:80 | ||||
| chr6:161273974-161274181 | Rare:39 |