| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:134224541-134224627 | Rare:26 | ||||
| chr11:134253290-134253608 | Common:2; Rare:117; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:389230-389364 | Rare:49 | ||||
| chr12:401436-401664 | Rare:63 | ||||
| chr12:643624-643744 | Rare:18 | ||||
| chr12:990340-990595 | Common:2; Rare:66 | ||||
| chr12:991101-991296 | Common:3; Rare:90 | ||||
| chr12:2004420-2004645 | Common:1; Rare:78 | ||||
| chr12:2794565-2794604 | Rare:9 | ||||
| chr12:2794861-2795208 | Common:1; Rare:121 | ||||
| chr12:2812580-2812752 | Common:1; Rare:62 | ||||
| chr12:2812885-2813010 | Rare:38 | ||||
| chr12:2877009-2877268 | Rare:81 | ||||
| chr12:3873307-3873514 | Common:4; Rare:44 | ||||
| chr12:4320982-4321266 | Common:5; Rare:109 |