| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:123741606-123741756 | Common:1; Rare:41 | ||||
| chr11:124622791-124622918 | Common:3; Rare:43 | ||||
| chr11:124673712-124673961 | Common:5; Rare:70 | ||||
| chr11:125111690-125111974 | Common:3; Rare:59 | ||||
| chr11:125164496-125164759 | Rare:50 | ||||
| chr11:125496192-125496447 | Rare:59 | ||||
| chr11:125592580-125592932 | Common:6; Rare:115 | ||||
| chr11:125887480-125887749 | Common:2; Rare:89 | ||||
| chr11:126211610-126211822 | Rare:99 | ||||
| chr11:126268533-126268646 | Common:2; Rare:26 | ||||
| chr11:126268802-126269207 | Common:2; Rare:159; Clinvar:2; Clinvar (benign):4 | ||||
| chr11:126304027-126304112 | Rare:55 | ||||
| chr11:126355548-126355730 | Rare:43 | ||||
| chr11:128522242-128522546 | Common:1; Rare:93 | ||||
| chr11:128693646-128693931 | Common:4; Rare:71 |