| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:7128872-7128973 | Rare:15 | ||||
| chr12:7130250-7130423 | Common:5; Rare:46 | ||||
| chr12:7936167-7936443 | Common:4; Rare:44 | ||||
| chr12:8227599-8227691 | Rare:26 | ||||
| chr12:8697797-8698098 | Common:1; Rare:110 | ||||
| chr12:8914389-8914764 | Common:6; Rare:114 | ||||
| chr12:8949941-8950095 | Common:1; Rare:45 | ||||
| chr12:9079637-9079976 | Common:1; Rare:83; Clinvar (benign):1 | ||||
| chr12:9106495-9106691 | Rare:51 | ||||
| chr12:9115850-9116283 | Common:3; Rare:88 | ||||
| chr12:10613508-10613686 | Common:1; Rare:70 | ||||
| chr12:11171545-11171760 | Common:4; Rare:72 | ||||
| chr12:12356999-12357098 | Common:1; Rare:51 | ||||
| chr12:12560859-12561156 | Common:3; Rare:65 | ||||
| chr12:12611627-12612047 | Common:2; Rare:123 |