| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:158999761-158999902 | Common:1; Rare:56; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:159726926-159727198 | Common:1; Rare:98 | ||||
| chr6:159727333-159727624 | Common:5; Rare:125 | ||||
| chr6:159761845-159762077 | Common:4; Rare:116 | ||||
| chr6:159789550-159790008 | Common:5; Rare:155 | ||||
| chr6:159790244-159790516 | Common:7; Rare:88 | ||||
| chr6:162727757-162727954 | Rare:51; Clinvar:1 | ||||
| chr6:163415969-163416110 | Common:2; Rare:34 | ||||
| chr6:166342510-166342659 | Common:3; Rare:59 | ||||
| chr6:166999074-166999424 | Common:1; Rare:118 | ||||
| chr6:169253781-169254108 | Common:1; Rare:58 | ||||
| chr6:169702004-169702138 | Common:1; Rare:55 | ||||
| chr6:169751534-169751645 | Rare:40; Clinvar (benign):1 | ||||
| chr6:170553196-170553368 | Common:2; Rare:76 | ||||
| chr6:170554211-170554452 | Common:2; Rare:75 |