| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:68030378-68030797 | Common:6; Rare:217; Clinvar:2; Clinvar (benign):4 | ||||
| chr11:68030760-68031100 | Common:8; Rare:130 | ||||
| chr11:68038904-68039120 | Rare:121; Clinvar:2 | ||||
| chr11:68121317-68121650 | Common:9; Rare:219 | ||||
| chr11:68213245-68213386 | Common:2; Rare:102 | ||||
| chr11:68213558-68213979 | Common:2; Rare:479 | ||||
| chr11:68271891-68272206 | Common:4; Rare:260 | ||||
| chr11:68312414-68312760 | Common:1; Rare:122; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68460409-68460836 | Common:6; Rare:235 | ||||
| chr11:68839323-68839501 | Common:2; Rare:83 | ||||
| chr11:68841771-68841932 | Common:1; Rare:54; Clinvar (benign):3 | ||||
| chr11:68843826-68844226 | Common:3; Rare:108 | ||||
| chr11:68903748-68903964 | Common:10; Rare:187; Clinvar:6; Clinvar (benign):14 | ||||
| chr11:69048701-69049003 | Common:12; Rare:201 | ||||
| chr11:69298430-69299000 | Common:10; Rare:190 |