Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:356321-356422 | Rare:28 | ||||
chr11:518762-519064 | Common:8; Rare:165 | ||||
chr11:568373-568947 | Common:4; Rare:218 | ||||
chr11:629337-629422 | Rare:17 | ||||
chr11:748068-748222 | Rare:27 | ||||
chr11:748465-748655 | Common:1; Rare:32 | ||||
chr11:778006-778038 | Rare:7 | ||||
chr11:808543-808850 | Common:3; Rare:72 | ||||
chr11:819727-819850 | Common:1; Rare:31; Clinvar:2; Clinvar (benign):1 | ||||
chr11:819999-820277 | Common:2; Rare:66 | ||||
chr11:1262615-1262872 | Common:3; Rare:69 | ||||
chr11:1336212-1336549 | Common:1; Rare:58 | ||||
chr11:1521896-1522046 | Rare:35 | ||||
chr11:1606041-1606192 | Common:1; Rare:34 | ||||
chr11:1853756-1853987 | Common:5; Rare:42 |