| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:129895535-129895661 | Common:2; Rare:46 | ||||
| chr11:130002771-130002875 | Common:2; Rare:17 | ||||
| chr11:130069624-130070018 | Common:2; Rare:140 | ||||
| chr11:130314389-130314513 | Common:1; Rare:39 | ||||
| chr11:130915842-130916033 | Common:1; Rare:60 | ||||
| chr11:134224530-134224685 | Rare:55 | ||||
| chr11:134225425-134225526 | Rare:30 | ||||
| chr11:134253298-134253620 | Common:2; Rare:118; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:134276097-134276270 | Common:3; Rare:32 | ||||
| chr11:134276357-134276691 | Common:4; Rare:86 | ||||
| chr12:388964-389398 | Common:6; Rare:210 | ||||
| chr12:401446-401664 | Rare:58 | ||||
| chr12:643616-643923 | Common:2; Rare:65 | ||||
| chr12:752327-752636 | Common:1; Rare:95 | ||||
| chr12:753402-754282 | Common:6; Rare:298; Clinvar:17; Clinvar (benign):16 |