| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:126211641-126211819 | Rare:82 | ||||
| chr11:126268763-126269184 | Common:1; Rare:161; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:126355545-126355742 | Rare:47 | ||||
| chr11:128522269-128522546 | Common:1; Rare:88 | ||||
| chr11:130314406-130314495 | Common:1; Rare:26 | ||||
| chr11:130448635-130448646 | Rare:3 | ||||
| chr11:134224533-134224685 | Rare:54 | ||||
| chr11:134253286-134253613 | Common:2; Rare:122; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:389249-389347 | Rare:38 | ||||
| chr12:401446-401644 | Rare:53 | ||||
| chr12:643624-643795 | Common:1; Rare:29 | ||||
| chr12:991109-991285 | Common:2; Rare:77 | ||||
| chr12:2004435-2004669 | Common:2; Rare:69 | ||||
| chr12:2812489-2812713 | Common:1; Rare:52 | ||||
| chr12:2812884-2812957 | Rare:27 |