| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:159761771-159762085 | Common:5; Rare:144 | ||||
| chr6:159762339-159762460 | Common:1; Rare:29 | ||||
| chr6:159789520-159790008 | Common:5; Rare:163 | ||||
| chr6:159790272-159790550 | Common:8; Rare:98 | ||||
| chr6:160991659-160991810 | Common:1; Rare:54 | ||||
| chr6:161273976-161274181 | Rare:37 | ||||
| chr6:166342488-166342659 | Common:4; Rare:72 | ||||
| chr6:166999027-166999407 | Common:1; Rare:129 | ||||
| chr6:169701993-169702340 | Common:5; Rare:147 | ||||
| chr6:169751507-169751644 | Rare:49; Clinvar (benign):1 | ||||
| chr6:170306422-170306818 | Common:2; Rare:120 | ||||
| chr6:170553196-170553377 | Common:3; Rare:77 | ||||
| chr6:170554211-170554443 | Common:2; Rare:74 | ||||
| chr7:727231-727258 | Rare:12 | ||||
| chr7:975498-975669 | Common:1; Rare:76 |