| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:160991598-160991815 | Common:2; Rare:70 | ||||
| chr6:161273981-161274181 | Rare:36 | ||||
| chr6:162726871-162727166 | Common:4; Rare:56 | ||||
| chr6:162727757-162728070 | Common:3; Rare:85; Clinvar:1 | ||||
| chr6:166342477-166342659 | Common:5; Rare:78 | ||||
| chr6:166956197-166956272 | Rare:10; Clinvar:2 | ||||
| chr6:166956529-166956713 | Common:3; Rare:65; Clinvar:3 | ||||
| chr6:166999028-166999454 | Common:2; Rare:148 | ||||
| chr6:167826816-167827235 | Common:2; Rare:193 | ||||
| chr6:169701888-169702377 | Common:8; Rare:195 | ||||
| chr6:169702534-169702662 | Rare:65 | ||||
| chr6:169751515-169751645 | Rare:49; Clinvar (benign):1 | ||||
| chr6:170306563-170306818 | Common:2; Rare:80 | ||||
| chr6:170553132-170553354 | Common:2; Rare:96 | ||||
| chr6:170554211-170554454 | Common:2; Rare:75 |