| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123436425-123436592 | Rare:38 | ||||
| chr12:123584322-123584813 | Common:9; Rare:163 | ||||
| chr12:123602030-123602139 | Common:3; Rare:34 | ||||
| chr12:123633620-123633856 | Common:1; Rare:111; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:124422655-124422792 | Common:2; Rare:36 | ||||
| chr12:130839104-130839375 | Common:2; Rare:98 | ||||
| chr12:130871730-130872110 | Common:4; Rare:159 | ||||
| chr12:131710795-131711131 | Common:1; Rare:93 | ||||
| chr12:132687311-132687451 | Rare:60; Clinvar:5; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr12:132887553-132887845 | Rare:85 | ||||
| chr12:132956280-132956410 | Common:1; Rare:27 | ||||
| chr12:133037218-133037536 | Common:4; Rare:65 | ||||
| chr12:133080679-133080975 | Common:2; Rare:95 | ||||
| chr12:133130238-133130592 | Common:7; Rare:109 | ||||
| chr13:19633355-19633737 | Common:1; Rare:140 |