| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:122202959-122203231 | Common:2; Rare:54 | ||||
| chr11:126304261-126304326 | Common:1; Rare:32 | ||||
| chr11:133955622-133955710 | Rare:11 | ||||
| chr11:134037344-134037450 | Common:2; Rare:36 | ||||
| chr12:2264987-2265287 | Rare:58 | ||||
| chr12:2800134-2800441 | Common:1; Rare:68 | ||||
| chr12:4275444-4275542 | Common:2; Rare:11 | ||||
| chr12:6226068-6226331 | Common:1; Rare:45 | ||||
| chr12:6233153-6233486 | Common:1; Rare:73 | ||||
| chr12:6770153-6770698 | Rare:140 | ||||
| chr12:6927548-6927801 | Rare:63 | ||||
| chr12:6935393-6935595 | Common:2; Rare:45 | ||||
| chr12:7088608-7088988 | Common:2; Rare:114; Clinvar (pathogenic):2 | ||||
| chr12:7089291-7089734 | Common:3; Rare:143 | ||||
| chr12:7486685-7486938 | Rare:71 |