| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18012990-18013268 | Common:5; Rare:89 | ||||
| chr11:18237042-18237237 | Common:1; Rare:27 | ||||
| chr11:18248425-18248910 | Common:3; Rare:95 | ||||
| chr11:18266008-18266441 | Common:5; Rare:81 | ||||
| chr11:18266502-18266990 | Common:1; Rare:86 | ||||
| chr11:18322077-18322677 | Common:8; Rare:209; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:18394332-18394633 | Common:1; Rare:120; Clinvar (benign):1 | ||||
| chr11:18396075-18396408 | Common:1; Rare:120 | ||||
| chr11:18526812-18526977 | Rare:75 | ||||
| chr11:18588667-18588839 | Common:2; Rare:56 | ||||
| chr11:18634332-18634570 | Common:2; Rare:74 | ||||
| chr11:20022782-20023126 | Rare:73 | ||||
| chr11:20023218-20023353 | Rare:25 | ||||
| chr11:20363650-20363778 | Common:3; Rare:26 | ||||
| chr11:22625808-22626002 | Common:2; Rare:68; Clinvar:2; Clinvar (benign):1 |