| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:643594-643676 | Rare:14 | ||||
| chr12:949635-949718 | Rare:31 | ||||
| chr12:991101-991311 | Common:3; Rare:95 | ||||
| chr12:2004439-2004487 | Rare:16 | ||||
| chr12:2796919-2797159 | Rare:57 | ||||
| chr12:2812410-2812713 | Common:1; Rare:70 | ||||
| chr12:2876986-2877260 | Rare:83 | ||||
| chr12:2959824-2959980 | Common:1; Rare:39 | ||||
| chr12:3077280-3077439 | Common:5; Rare:72 | ||||
| chr12:3753107-3753249 | Rare:37 | ||||
| chr12:4275454-4275569 | Common:2; Rare:15 | ||||
| chr12:4538479-4538786 | Rare:60 | ||||
| chr12:4649010-4649171 | Common:2; Rare:55; Clinvar (benign):2 | ||||
| chr12:6124460-6124609 | Rare:24; Clinvar:2 | ||||
| chr12:6200005-6200348 | Common:3; Rare:93 |