| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:119314549-119314908 | Common:1; Rare:121 | ||||
| chr11:122100404-122100528 | Rare:38 | ||||
| chr11:122100788-122100830 | Rare:8 | ||||
| chr11:122101754-122102097 | Rare:77 | ||||
| chr11:122202993-122203214 | Common:1; Rare:48 | ||||
| chr11:134037354-134037635 | Common:3; Rare:89 | ||||
| chr11:134275446-134275583 | Rare:28 | ||||
| chr12:16763-16843 | Common:4; Rare:27 | ||||
| chr12:753886-754012 | Common:1; Rare:56; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:2054308-2054343 | Rare:5 | ||||
| chr12:2054420-2054502 | Rare:12 | ||||
| chr12:2135786-2136003 | Common:10; Rare:78 | ||||
| chr12:2191335-2191564 | Common:1; Rare:50 | ||||
| chr12:2255909-2256001 | Common:3; Rare:1 | ||||
| chr12:2264968-2265287 | Rare:59 |