| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:60924321-60924491 | Rare:44 | ||||
| chr11:60924516-60924916 | Common:1; Rare:151 | ||||
| chr11:60951800-60952386 | Common:7; Rare:139 | ||||
| chr11:61160993-61161393 | Rare:102 | ||||
| chr11:61161417-61161818 | Common:1; Rare:109 | ||||
| chr11:61294772-61294952 | Rare:42 | ||||
| chr11:61295024-61295457 | Common:1; Rare:88 | ||||
| chr11:61333052-61333337 | Common:1; Rare:103 | ||||
| chr11:61333687-61334090 | Rare:154 | ||||
| chr11:61361819-61362055 | Common:2; Rare:56; Clinvar:2 | ||||
| chr11:61362165-61362456 | Common:2; Rare:88; Clinvar:8; Clinvar (benign):1 | ||||
| chr11:61392503-61392680 | Common:2; Rare:58; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:61429290-61429550 | Common:4; Rare:91 | ||||
| chr11:61429886-61430193 | Common:2; Rare:132; Clinvar:3; Clinvar (benign):8 | ||||
| chr11:61480891-61482036 | Common:10; Rare:313 |