| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:159761728-159762085 | Common:6; Rare:153 | ||||
| chr6:159789545-159790008 | Common:5; Rare:155 | ||||
| chr6:159790244-159790550 | Common:8; Rare:105 | ||||
| chr6:161273951-161274272 | Rare:59 | ||||
| chr6:162727757-162727985 | Rare:60; Clinvar:1 | ||||
| chr6:163415122-163415328 | Common:6; Rare:74 | ||||
| chr6:166342458-166342659 | Common:5; Rare:88 | ||||
| chr6:166999086-166999414 | Common:1; Rare:113 | ||||
| chr6:169701935-169702377 | Common:6; Rare:181 | ||||
| chr6:169751433-169751648 | Common:2; Rare:93; Clinvar (benign):2 | ||||
| chr6:170306617-170306808 | Common:1; Rare:55 | ||||
| chr6:170553132-170553354 | Common:2; Rare:96 | ||||
| chr6:170554211-170554435 | Common:1; Rare:70 | ||||
| chr7:519143-519231 | Rare:26 | ||||
| chr7:602598-602838 | Rare:62 |