| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:159761675-159762073 | Common:8; Rare:160 | ||||
| chr6:159789538-159789984 | Common:4; Rare:150 | ||||
| chr6:159790244-159790610 | Common:9; Rare:137 | ||||
| chr6:160991468-160991801 | Common:5; Rare:95 | ||||
| chr6:162727695-162727985 | Rare:107; Clinvar:4 | ||||
| chr6:166342513-166342659 | Common:3; Rare:58 | ||||
| chr6:166862474-166862637 | Common:2; Rare:37 | ||||
| chr6:166956208-166956261 | Rare:9; Clinvar:2 | ||||
| chr6:166956523-166956769 | Common:5; Rare:83; Clinvar:3 | ||||
| chr6:166999086-166999415 | Common:1; Rare:113 | ||||
| chr6:169701993-169702347 | Common:5; Rare:149 | ||||
| chr6:169751515-169751649 | Rare:54; Clinvar (benign):2 | ||||
| chr6:170306559-170306808 | Common:1; Rare:82 | ||||
| chr6:170554211-170554445 | Common:2; Rare:74 | ||||
| chr7:519094-519324 | Rare:56 |