| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123602023-123602164 | Common:3; Rare:52 | ||||
| chr12:123633620-123633869 | Common:2; Rare:120; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:124422636-124422940 | Common:4; Rare:76 | ||||
| chr12:124914817-124915057 | Common:3; Rare:99 | ||||
| chr12:130871727-130872126 | Common:4; Rare:166 | ||||
| chr12:131710795-131711131 | Common:1; Rare:93 | ||||
| chr12:131949676-131949975 | Common:2; Rare:95 | ||||
| chr12:132687294-132687685 | Common:4; Rare:147; Clinvar:11; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr12:132829026-132829241 | Rare:93 | ||||
| chr12:132887553-132887835 | Rare:82 | ||||
| chr12:132956252-132956426 | Common:1; Rare:38 | ||||
| chr12:133080724-133080943 | Rare:69 | ||||
| chr12:133130242-133130581 | Common:6; Rare:105 | ||||
| chr13:19782918-19783081 | Common:2; Rare:61 | ||||
| chr13:19863441-19863824 | Common:5; Rare:126 |