| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:129279491-129279725 | Common:3; Rare:95 | ||||
| chr11:129815732-129815874 | Common:1; Rare:35 | ||||
| chr11:130069624-130070079 | Common:2; Rare:161 | ||||
| chr11:130314395-130314520 | Common:1; Rare:42 | ||||
| chr11:134224541-134224690 | Rare:54 | ||||
| chr11:134253298-134253597 | Common:2; Rare:101; Clinvar (benign):1 | ||||
| chr12:389242-389358 | Rare:41 | ||||
| chr12:401436-401664 | Rare:63 | ||||
| chr12:643624-643941 | Common:2; Rare:65 | ||||
| chr12:991101-991318 | Common:3; Rare:99 | ||||
| chr12:2004427-2004669 | Common:2; Rare:74 | ||||
| chr12:2796974-2797275 | Rare:75 | ||||
| chr12:2812609-2812731 | Common:1; Rare:44 | ||||
| chr12:3077249-3077429 | Common:6; Rare:79 | ||||
| chr12:3215079-3215324 | Common:4; Rare:56 |