| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:126268829-126269209 | Common:2; Rare:144; Clinvar:2; Clinvar (benign):4 | ||||
| chr11:126304013-126304083 | Rare:38 | ||||
| chr11:126355532-126355760 | Common:1; Rare:62 | ||||
| chr11:127000761-127000956 | Common:1; Rare:31 | ||||
| chr11:129895535-129895677 | Common:2; Rare:54 | ||||
| chr11:130069624-130069932 | Common:2; Rare:111 | ||||
| chr11:130314395-130314489 | Common:1; Rare:30 | ||||
| chr11:130916432-130916627 | Common:5; Rare:61 | ||||
| chr11:131911277-131911471 | Common:1; Rare:66 | ||||
| chr11:133532349-133532456 | Common:1; Rare:21 | ||||
| chr11:134223946-134224103 | Common:1; Rare:43 | ||||
| chr11:134253292-134253608 | Common:2; Rare:115; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:389229-389368 | Rare:53 | ||||
| chr12:401446-401664 | Rare:58 | ||||
| chr12:991101-991322 | Common:3; Rare:100 |