| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:119018620-119018789 | Common:5; Rare:69 | ||||
| chr11:119057073-119057437 | Common:3; Rare:141 | ||||
| chr11:119067665-119067816 | Common:2; Rare:56 | ||||
| chr11:119206211-119206315 | Common:3; Rare:44; Clinvar:5; Clinvar (benign):3 | ||||
| chr11:124673710-124673916 | Common:4; Rare:62 | ||||
| chr11:126211651-126211804 | Rare:70 | ||||
| chr11:126268796-126269145 | Common:1; Rare:130; Clinvar:1 | ||||
| chr11:126303984-126304075 | Rare:51 | ||||
| chr11:126355532-126355763 | Common:1; Rare:64 | ||||
| chr11:134253306-134253584 | Common:2; Rare:89; Clinvar (benign):1 | ||||
| chr12:401446-401664 | Rare:58 | ||||
| chr12:2877022-2877253 | Rare:68 | ||||
| chr12:6452078-6452119 | Common:1; Rare:10 | ||||
| chr12:6493234-6493502 | Common:7; Rare:79 | ||||
| chr12:6493782-6494144 | Common:2; Rare:108 |