| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:126268534-126268648 | Common:2; Rare:28 | ||||
| chr11:126268779-126269216 | Common:2; Rare:171; Clinvar:3; Clinvar (benign):5 | ||||
| chr11:126270435-126270667 | Common:2; Rare:33 | ||||
| chr11:126303965-126304090 | Rare:73 | ||||
| chr11:126355548-126355774 | Rare:60 | ||||
| chr11:128905987-128906113 | Rare:23 | ||||
| chr11:130002767-130002955 | Common:3; Rare:34 | ||||
| chr11:130069663-130069932 | Common:2; Rare:90 | ||||
| chr11:130314386-130314477 | Rare:31 | ||||
| chr11:130314732-130315003 | Common:4; Rare:94 | ||||
| chr11:130448408-130448668 | Rare:63 | ||||
| chr11:134223909-134224161 | Common:2; Rare:87 | ||||
| chr11:134253306-134253595 | Common:2; Rare:95; Clinvar (benign):1 | ||||
| chr12:389239-389394 | Common:1; Rare:59 | ||||
| chr12:389482-389687 | Common:5; Rare:92 |