| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:131911386-131911460 | Common:1; Rare:34 | ||||
| chr11:134224546-134224680 | Rare:48 | ||||
| chr11:134253298-134253601 | Common:2; Rare:103; Clinvar (benign):1 | ||||
| chr12:389249-389360 | Rare:39 | ||||
| chr12:401446-401644 | Rare:53 | ||||
| chr12:643624-643748 | Rare:21 | ||||
| chr12:991101-991318 | Common:3; Rare:99 | ||||
| chr12:2004420-2004669 | Common:2; Rare:80 | ||||
| chr12:2812891-2813017 | Rare:36 | ||||
| chr12:2877038-2877277 | Rare:80 | ||||
| chr12:2959821-2959944 | Common:1; Rare:33 | ||||
| chr12:4275444-4275572 | Common:2; Rare:15 | ||||
| chr12:4320949-4321260 | Common:5; Rare:118 | ||||
| chr12:4538444-4538867 | Common:1; Rare:90 | ||||
| chr12:4649010-4649171 | Common:2; Rare:55; Clinvar (benign):2 |