| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:179823988-179824318 | Common:1; Rare:130; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr6:5003610-5003825 | Common:6; Rare:62 | ||||
| chr6:5261245-5261601 | Common:9; Rare:100 | ||||
| chr6:7910777-7910912 | Rare:47 | ||||
| chr6:8435506-8435624 | Common:2; Rare:44 | ||||
| chr6:13615177-13615426 | Common:2; Rare:108 | ||||
| chr6:16761424-16761765 | Common:2; Rare:107 | ||||
| chr6:26123922-26124172 | Common:4; Rare:99 | ||||
| chr6:30061169-30061265 | Rare:19 | ||||
| chr6:30067027-30067280 | Common:2; Rare:49 | ||||
| chr6:30326801-30326918 | Common:1; Rare:25 | ||||
| chr6:30557210-30557347 | Common:1; Rare:49 | ||||
| chr6:30571260-30571482 | Common:1; Rare:74 | ||||
| chr6:30687147-30687494 | Rare:71 | ||||
| chr6:31546584-31546856 | Common:3; Rare:51 |