Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:1933789-1934005 | Rare:81; Clinvar:1; Clinvar (benign):2 | ||||
chr11:2137281-2137609 | Common:3; Rare:84 | ||||
chr11:2138235-2138585 | Common:2; Rare:70 | ||||
chr11:2138631-2138702 | Rare:17 | ||||
chr11:2140887-2141158 | Rare:53 | ||||
chr11:2301862-2302141 | Common:2; Rare:73 | ||||
chr11:2444500-2444651 | Rare:21 | ||||
chr11:2884156-2884222 | Common:1; Rare:24 | ||||
chr11:3057354-3057545 | Rare:67 | ||||
chr11:3126596-3126790 | Common:2; Rare:43 | ||||
chr11:3379083-3379314 | Common:3; Rare:59 | ||||
chr11:3641984-3642180 | Common:7; Rare:69 | ||||
chr11:3797449-3797941 | Rare:190 | ||||
chr11:3808507-3808606 | Common:1; Rare:35 | ||||
chr11:3840916-3841096 | Rare:74 |