| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:126268731-126269207 | Common:2; Rare:182; Clinvar:2; Clinvar (benign):4 | ||||
| chr11:126283002-126283125 | Common:1; Rare:46 | ||||
| chr11:126303984-126304083 | Rare:56 | ||||
| chr11:126355521-126355742 | Common:2; Rare:59 | ||||
| chr11:128522144-128522606 | Common:4; Rare:143 | ||||
| chr11:128692712-128692985 | Rare:61 | ||||
| chr11:128693797-128694195 | Common:2; Rare:73 | ||||
| chr11:129895535-129895666 | Common:2; Rare:48 | ||||
| chr11:130002780-130002932 | Common:2; Rare:25 | ||||
| chr11:130003015-130003367 | Common:1; Rare:145 | ||||
| chr11:130069558-130069998 | Common:2; Rare:165 | ||||
| chr11:130314395-130314520 | Common:1; Rare:42 | ||||
| chr11:130448430-130448656 | Rare:55 | ||||
| chr11:130916380-130916663 | Common:7; Rare:85 | ||||
| chr11:133957431-133957659 | Rare:46 |