| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:131911351-131911453 | Common:1; Rare:39 | ||||
| chr11:134253291-134253592 | Common:2; Rare:103; Clinvar (benign):1 | ||||
| chr12:389307-389366 | Rare:18 | ||||
| chr12:389557-389694 | Common:4; Rare:74 | ||||
| chr12:401365-401677 | Common:2; Rare:85 | ||||
| chr12:752340-752605 | Common:1; Rare:78 | ||||
| chr12:990425-990565 | Common:1; Rare:35 | ||||
| chr12:991101-991297 | Common:3; Rare:90 | ||||
| chr12:1592395-1592693 | Rare:56 | ||||
| chr12:2004381-2004669 | Common:2; Rare:102 | ||||
| chr12:2794833-2795234 | Common:1; Rare:136 | ||||
| chr12:2798802-2799167 | Common:1; Rare:89 | ||||
| chr12:2800990-2801235 | Common:1; Rare:69 | ||||
| chr12:2812455-2812727 | Common:1; Rare:68 | ||||
| chr12:2877017-2877278 | Rare:87 |