| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:134224533-134224671 | Rare:51 | ||||
| chr11:134253277-134253592 | Common:2; Rare:107; Clinvar (benign):1 | ||||
| chr12:389009-389400 | Common:6; Rare:190 | ||||
| chr12:389452-389703 | Common:6; Rare:106 | ||||
| chr12:401420-401677 | Common:2; Rare:73 | ||||
| chr12:752301-752597 | Common:1; Rare:88 | ||||
| chr12:991080-991342 | Common:5; Rare:113 | ||||
| chr12:1690844-1691079 | Common:2; Rare:86 | ||||
| chr12:1970468-1970829 | Common:1; Rare:51 | ||||
| chr12:2004038-2004250 | Common:3; Rare:67 | ||||
| chr12:2004373-2004660 | Common:1; Rare:104 | ||||
| chr12:2794864-2795208 | Common:1; Rare:121 | ||||
| chr12:2796942-2797180 | Rare:58 | ||||
| chr12:2812489-2812713 | Common:1; Rare:52 | ||||
| chr12:2812880-2813057 | Rare:50 |