| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:129895535-129895695 | Common:2; Rare:59 | ||||
| chr11:130069624-130069970 | Common:2; Rare:127 | ||||
| chr11:130314395-130314495 | Common:1; Rare:30 | ||||
| chr11:130916411-130916686 | Common:6; Rare:87 | ||||
| chr11:131911357-131911475 | Common:1; Rare:50 | ||||
| chr11:134253298-134253597 | Common:2; Rare:101; Clinvar (benign):1 | ||||
| chr12:389242-389364 | Rare:42 | ||||
| chr12:401446-401664 | Rare:58 | ||||
| chr12:752311-752587 | Common:1; Rare:82 | ||||
| chr12:991101-991322 | Common:3; Rare:100 | ||||
| chr12:1593090-1593163 | Rare:19 | ||||
| chr12:2004418-2004626 | Common:1; Rare:78 | ||||
| chr12:2794864-2795232 | Common:1; Rare:128 | ||||
| chr12:2812475-2812713 | Common:1; Rare:56 | ||||
| chr12:2877031-2877271 | Rare:76 |