Item | Value |
---|---|
geneid | 8450 |
ensemblid | ENSG00000158290.19 |
hgncid | 2555 |
symbol | CUL4B |
name | cullin 4B |
refseq_nuc | NM_001079872.2 |
refseq_prot | NP_001073341.1 |
ensembl_nuc | ENST00000371322.11 |
ensembl_prot | ENSP00000360373.5 |
mane_status | MANE Select |
chr | chrX |
start | 120523858 |
end | 120560962 |
strand | - |
ver | v1.2 |
region | chrX:120523858-120560962 |
region5000 | chrX:120518858-120565962 |
regionname0 | CUL4B_chrX_120523858_120560962 |
regionname5000 | CUL4B_chrX_120518858_120565962 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2685 | 274 | 60 | 48 | 129 | 11 | 24 | CUL4B_chrX_120518858_120565962 | CUL4B | ATGTT others(2680): Show |
chrX | 120518858 | 120565962 | ||
a0001c0002 | 0/0 | 2685 | 2 | 2 | 0 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | ATGTT others(2680): Show |
chrX | 120518858 | 120565962 | ||
a0001c0003 | 0/0 | 2685 | 1 | 1 | 0 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | ATGTT others(2680): Show |
chrX | 120518858 | 120565962 | ||
a0001c0004 | 0/0 | 2685 | 1 | 1 | 0 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | ATGTT others(2680): Show |
chrX | 120518858 | 120565962 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 5915 | 235 | 29 | 43 | 126 | 11 | 24 | CUL4B_chrX_120518858_120565962 | CUL4B | AGACT others(5910): Show |
chrX | 120518858 | 120565962 |
a0001c0001t0002 | 0/0 | 5915 | 16 | 12 | 4 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | AGACT others(5910): Show |
chrX | 120518858 | 120565962 |
a0001c0001t0003 | 0/0 | 5915 | 11 | 11 | 0 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | AGACT others(5910): Show |
chrX | 120518858 | 120565962 |
a0001c0001t0004 | 0/0 | 5911 | 4 | 3 | 1 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | AGACT others(5906): Show |
chrX | 120518858 | 120565962 |
a0001c0001t0005 | 0/0 | 5915 | 3 | 3 | 0 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | AGACT others(5910): Show |
chrX | 120518858 | 120565962 |
a0001c0001t0006 | 0/0 | 5915 | 1 | 0 | 0 | 1 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | AGACT others(5910): Show |
chrX | 120518858 | 120565962 |
a0001c0001t0007 | 0/0 | 5915 | 1 | 0 | 0 | 1 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | AGACT others(5910): Show |
chrX | 120518858 | 120565962 |
a0001c0001t0008 | 0/0 | 5915 | 1 | 1 | 0 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | AGACT others(5910): Show |
chrX | 120518858 | 120565962 |
a0001c0001t0009 | 0/0 | 5915 | 1 | 0 | 0 | 1 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | AGACT others(5910): Show |
chrX | 120518858 | 120565962 |
a0001c0001t0010 | 0/0 | 5915 | 1 | 1 | 0 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | AGACT others(5910): Show |
chrX | 120518858 | 120565962 |
a0001c0002t0003 | 0/0 | 5915 | 2 | 2 | 0 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | AGACT others(5910): Show |
chrX | 120518858 | 120565962 |
a0001c0003t0003 | 0/0 | 5915 | 1 | 1 | 0 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | AGACT others(5910): Show |
chrX | 120518858 | 120565962 |
a0001c0004t0003 | 0/0 | 5915 | 1 | 1 | 0 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | AGACT others(5910): Show |
chrX | 120518858 | 120565962 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 30 | 1 | 7 | 22 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0002 | 0/0 | 21 | 0 | 1 | 19 | 0 | 1 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0003 | 0/0 | 13 | 0 | 4 | 4 | 0 | 5 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0004 | 1/0 | 12 | 1 | 2 | 6 | 1 | 1 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0005 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0006 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0007 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0008 | 0/0 | 7 | 0 | 2 | 0 | 2 | 3 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0011 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0013 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0023 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0048 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0002g0009 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0002g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0003g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0003g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0003g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0004g0016 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0005g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0006g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0007g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0008g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0009g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0001t0010g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0002t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0002t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0003t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
a0001c0004t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0068 | EUR | GBR | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0056 | EUR | FIN | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0028 | EUR | FIN | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG00558 | hp1 | a0001 | c0001 | t0009 | g0063 | EAS | CHS | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG00558 | hp2 | a0001 | c0001 | t0006 | g0100 | EAS | CHS | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG00639 | hp2 | a0001 | c0001 | t0004 | g0016 | AMR | PUR | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | IBS | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0030 | EUR | IBS | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0030 | EUR | IBS | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | IBS | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0119 | AFR | ACB | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG01884 | hp2 | a0001 | c0001 | t0004 | g0016 | AFR | ACB | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG01891 | hp1 | a0001 | c0003 | t0003 | g0079 | AFR | ACB | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02055 | hp1 | a0001 | c0001 | t0005 | g0021 | AFR | ACB | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0092 | AFR | ACB | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02258 | hp1 | a0001 | c0001 | t0003 | g0120 | AFR | ACB | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | ACB | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0045 | AFR | ACB | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0094 | AFR | GWD | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | GWD | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02630 | hp2 | a0001 | c0001 | t0003 | g0038 | AFR | GWD | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0121 | AFR | GWD | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02723 | hp1 | a0001 | c0004 | t0003 | g0126 | AFR | GWD | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0026 | AFR | GWD | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0037 | AFR | GWD | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02818 | hp1 | a0001 | c0001 | t0005 | g0046 | AFR | GWD | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0044 | AFR | GWD | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02922 | hp1 | a0001 | c0001 | t0003 | g0038 | AFR | ESN | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02922 | hp2 | a0001 | c0001 | t0005 | g0021 | AFR | ESN | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02976 | hp1 | a0001 | c0001 | t0003 | g0083 | AFR | ESN | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ESN | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG03098 | hp1 | a0001 | c0001 | t0003 | g0037 | AFR | MSL | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ESN | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG03195 | hp2 | a0001 | c0002 | t0003 | g0112 | AFR | ESN | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0123 | AFR | MSL | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0115 | AFR | MSL | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | STU | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | BEB | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | BEB | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | BEB | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | BEB | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | BEB | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | STU | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | STU | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | YRI | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | YRI | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | YRI | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18970 | hp1 | a0001 | c0001 | t0007 | g0059 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA19030 | hp1 | a0001 | c0002 | t0003 | g0081 | AFR | LWK | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA19030 | hp2 | a0001 | c0001 | t0004 | g0042 | AFR | LWK | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | LWK | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0093 | AFR | ASW | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA20129 | hp2 | a0001 | c0001 | t0004 | g0016 | AFR | ASW | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | TSI | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | TSI | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | ACB | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0043 | AFR | ACB | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG02559 | hp2 | a0001 | c0001 | t0010 | g0039 | AFR | ACB | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | MSL | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | USA | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | USA | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0026 | AFR | USA | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA21309 | hp1 | a0001 | c0001 | t0008 | g0125 | AFR | LWK | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | LWK | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0048 | REF | REF | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0004 | REF | REF | CUL4B_chrX_120518858_120565962 | CUL4B | chrX | 120518858 | 120565962 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:120526815 | C | T | 2 | a0001c0002 a0001c0004 |
3 | HG02723.hp1 HG03195.hp2 NA19030.hp1 |
synonymous_variant | LOW | c.2634G>A | p.Arg878Arg | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 20/20 | 2958/5915 | 2634/2688 | 878/895 | chrX | 120526815 | |||
chrX:120544123 | T | C | 1 | a0001c0003 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.1164A>G | p.Gln388Gln | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 7/20 | 1488/5915 | 1164/2688 | 388/895 | chrX | 120544123 | |||
chrX:120560129 | G | A | 1 | a0001c0004 | 1 | HG02723.hp1 | synonymous_variant | LOW | c.510C>T | p.Asn170Asn | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 1/20 | 834/5915 | 510/2688 | 170/895 | chrX | 120560129 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:120523934 | C | T | 9 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(6): Show |
40 | HG00639.hp2 HG00733.hp2 HG01109.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*2827G>A | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 20/20 | 2827 | chrX | 120523934 | ||||||
chrX:120524104 | G | A | 1 | a0001c0001t0008 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2657C>T | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 20/20 | 2657 | chrX | 120524104 | ||||||
chrX:120524513 | A | G | 1 | a0001c0001t0007 | 1 | NA18970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2248T>C | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 20/20 | 2248 | chrX | 120524513 | ||||||
chrX:120525381 | G | A | 1 | a0001c0001t0009 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1380C>T | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 20/20 | 1380 | chrX | 120525381 | ||||||
chrX:120525601 | C | G | 1 | a0001c0001t0006 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1160G>C | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 20/20 | 1160 | chrX | 120525601 | ||||||
chrX:120525918 | A | C | 1 | a0001c0001t0005 | 3 | HG02055.hp1 HG02818.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*843T>G | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 20/20 | 843 | chrX | 120525918 | ||||||
chrX:120526086 | C | T | 4 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(1): Show |
24 | HG00639.hp2 HG00733.hp2 HG01109.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*675G>A | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 20/20 | 675 | chrX | 120526086 | ||||||
chrX:120526286 | G | A | 1 | a0001c0001t0010 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*475C>T | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 20/20 | 475 | chrX | 120526286 | ||||||
chrX:120526425 | GGTGT | G | 1 | a0001c0001t0004 | 4 | HG00639.hp2 HG01884.hp2 NA19030.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*332_*335delACAC | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 20/20 | 332 | chrX | 120526425 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:120526946 | C | T | 13 | a0001c0001t0003g0026 a0001c0001t0003g0037 a0001c0001t0003g0038 others(10): Show |
16 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2593-90G>A | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 19/19 | chrX | 120526946 | |||||||
chrX:120527062 | C | CT | 3 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0060 |
10 | HG01081.hp2 HG01346.hp2 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.2593-207dupA | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 19/19 | chrX | 120527062 | |||||||
chrX:120527082 | C | T | 3 | a0001c0002t0003g0081 a0001c0002t0003g0112 a0001c0004t0003g0126 |
3 | HG02723.hp1 HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2593-226G>A | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 19/19 | chrX | 120527082 | |||||||
chrX:120527120 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2593-264G>A | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 19/19 | chrX | 120527120 | |||||||
chrX:120527348 | G | A | 1 | a0001c0001t0002g0020 | 2 | HG01109.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2593-492C>T | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 19/19 | chrX | 120527348 | |||||||
chrX:120527556 | C | G | 1 | a0001c0001t0001g0027 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.2593-700G>C | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 19/19 | chrX | 120527556 | |||||||
chrX:120527611 | G | C | 1 | a0001c0001t0001g0027 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.2593-755C>G | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 19/19 | chrX | 120527611 | |||||||
chrX:120528232 | C | T | 53 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(50): Show |
136 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.2593-1376G>A | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 19/19 | chrX | 120528232 | |||||||
chrX:120528248 | A | T | 2 | a0001c0001t0005g0021 a0001c0001t0005g0046 |
3 | HG02055.hp1 HG02818.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2593-1392T>A | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 19/19 | chrX | 120528248 | |||||||
chrX:120528383 | G | C | 2 | a0001c0001t0001g0078 a0001c0001t0001g0124 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2593-1527C>G | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 19/19 | chrX | 120528383 | |||||||
chrX:120528550 | G | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0105 a0001c0001t0001g0118 |
4 | HG00735.hp2 HG01069.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.2592+1552C>T | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 19/19 | chrX | 120528550 | |||||||
chrX:120528601 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2592+1501C>T | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 19/19 | chrX | 120528601 | |||||||
chrX:120528672 | G | C | 1 | a0001c0003t0003g0079 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2592+1430C>G | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 19/19 | chrX | 120528672 | |||||||
chrX:120529219 | A | G | 1 | a0001c0001t0001g0028 | 2 | HG00323.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.2592+883T>C | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 19/19 | chrX | 120529219 | |||||||
chrX:120529942 | G | GT | 51 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(48): Show |
134 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.2592+159dupA | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 19/19 | chrX | 120529942 | |||||||
chrX:120530003 | T | C | 1 | a0001c0001t0002g0041 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2592+99A>G | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 19/19 | chrX | 120530003 | |||||||
chrX:120530275 | C | T | 1 | a0001c0001t0002g0094 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2440-21G>A | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 18/19 | chrX | 120530275 | |||||||
chrX:120530690 | C | T | 53 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(50): Show |
136 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.2440-436G>A | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 18/19 | chrX | 120530690 | |||||||
chrX:120530924 | G | A | 1 | a0001c0001t0002g0115 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2440-670C>T | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 18/19 | chrX | 120530924 | |||||||
chrX:120530932 | A | C | 13 | a0001c0001t0003g0026 a0001c0001t0003g0037 a0001c0001t0003g0038 others(10): Show |
16 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2440-678T>G | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 18/19 | chrX | 120530932 | |||||||
chrX:120530955 | A | G | 4 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0094 others(1): Show |
4 | HG02257.hp1 HG02622.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2440-701T>C | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 18/19 | chrX | 120530955 | |||||||
chrX:120530961 | T | C | 7 | a0001c0001t0002g0009 a0001c0001t0002g0020 a0001c0001t0002g0040 others(4): Show |
14 | HG00639.hp2 HG00733.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.2440-707A>G | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 18/19 | chrX | 120530961 | |||||||
chrX:120531083 | G | C | 1 | a0001c0001t0001g0089 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2440-829C>G | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 18/19 | chrX | 120531083 | |||||||
chrX:120531330 | A | T | 4 | a0001c0001t0001g0102 a0001c0002t0003g0081 a0001c0002t0003g0112 others(1): Show |
4 | HG02723.hp1 HG03195.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.2440-1076T>A | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 18/19 | chrX | 120531330 | |||||||
chrX:120531521 | G | A | 1 | a0001c0001t0005g0021 | 2 | HG02055.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2439+901C>T | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 18/19 | chrX | 120531521 | |||||||
chrX:120531563 | G | A | 1 | a0001c0002t0003g0112 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2439+859C>T | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 18/19 | chrX | 120531563 | |||||||
chrX:120531923 | A | G | 10 | a0001c0001t0002g0009 a0001c0001t0002g0020 a0001c0001t0002g0040 others(7): Show |
17 | HG00639.hp2 HG00733.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.2439+499T>C | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 18/19 | chrX | 120531923 | |||||||
chrX:120532120 | T | C | 1 | a0001c0001t0001g0032 | 2 | NA18994.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.2439+302A>G | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 18/19 | chrX | 120532120 | |||||||
chrX:120532153 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2439+269G>A | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 18/19 | chrX | 120532153 | |||||||
chrX:120532322 | T | A | 1 | a0001c0001t0002g0092 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2439+100A>T | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 18/19 | chrX | 120532322 | |||||||
chrX:120533046 | G | A | 1 | a0001c0001t0005g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2267-452C>T | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 17/19 | chrX | 120533046 | |||||||
chrX:120533169 | A | G | 4 | a0001c0001t0001g0024 a0001c0001t0001g0075 a0001c0001t0001g0076 others(1): Show |
5 | HG00673.hp1 HG03834.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.2267-575T>C | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 17/19 | chrX | 120533169 | |||||||
chrX:120533425 | A | G | 1 | a0001c0001t0001g0074 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2267-831T>C | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 17/19 | chrX | 120533425 | |||||||
chrX:120533448 | C | A | 1 | a0001c0001t0001g0033 | 2 | NA19000.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.2267-854G>T | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 17/19 | chrX | 120533448 | |||||||
chrX:120533698 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2266+783A>G | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 17/19 | chrX | 120533698 | |||||||
chrX:120534052 | C | A | 2 | a0001c0001t0005g0021 a0001c0001t0005g0046 |
3 | HG02055.hp1 HG02818.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2266+429G>T | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 17/19 | chrX | 120534052 | |||||||
chrX:120534190 | T | A | 7 | a0001c0001t0002g0009 a0001c0001t0002g0020 a0001c0001t0002g0040 others(4): Show |
14 | HG00639.hp2 HG00733.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.2266+291A>T | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 17/19 | chrX | 120534190 | |||||||
chrX:120534252 | T | A | 1 | a0001c0001t0003g0026 | 2 | HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2266+229A>T | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 17/19 | chrX | 120534252 | |||||||
chrX:120534448 | G | C | 2 | a0001c0001t0003g0026 a0001c0001t0003g0083 |
3 | HG02723.hp2 HG02976.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2266+33C>G | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 17/19 | chrX | 120534448 | |||||||
chrX:120534723 | G | A | 2 | a0001c0001t0001g0078 a0001c0001t0001g0124 |
2 | HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2161-137C>T | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 16/19 | chrX | 120534723 | |||||||
chrX:120534858 | G | T | 1 | a0001c0001t0002g0115 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2161-272C>A | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 16/19 | chrX | 120534858 | |||||||
chrX:120534975 | C | T | 4 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0094 others(1): Show |
4 | HG02257.hp1 HG02622.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2161-389G>A | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 16/19 | chrX | 120534975 | |||||||
chrX:120535008 | C | G | 1 | a0001c0001t0001g0078 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2161-422G>C | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 16/19 | chrX | 120535008 | |||||||
chrX:120535123 | A | C | 13 | a0001c0001t0003g0026 a0001c0001t0003g0037 a0001c0001t0003g0038 others(10): Show |
16 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2161-537T>G | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 16/19 | chrX | 120535123 | |||||||
chrX:120535431 | G | A | 10 | a0001c0001t0002g0009 a0001c0001t0002g0020 a0001c0001t0002g0040 others(7): Show |
17 | HG00639.hp2 HG00733.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.2160+399C>T | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 16/19 | chrX | 120535431 | |||||||
chrX:120535475 | C | T | 2 | a0001c0001t0003g0026 a0001c0001t0003g0083 |
3 | HG02723.hp2 HG02976.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2160+355G>A | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 16/19 | chrX | 120535475 | |||||||
chrX:120535703 | T | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0065 |
4 | HG01256.hp1 HG01361.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.2160+127A>T | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 16/19 | chrX | 120535703 | |||||||
chrX:120535704 | C | CA | 44 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(41): Show |
123 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.2160+125dupT | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 16/19 | chrX | 120535704 | |||||||
chrX:120535704 | C | CAA | 10 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0090 others(7): Show |
12 | HG00609.hp1 HG01168.hp1 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.2160+124_2160+125d others(4): Show |
CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 16/19 | chrX | 120535704 | |||||||
chrX:120535704 | CA | C | 18 | a0001c0001t0001g0014 a0001c0001t0001g0053 a0001c0001t0001g0058 others(15): Show |
29 | HG00438.hp1 HG00639.hp2 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.2160+125delT | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 16/19 | chrX | 120535704 | |||||||
chrX:120535704 | CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0001g0075 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2160+112_2160+125d others(16): Show |
CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 16/19 | chrX | 120535704 | |||||||
chrX:120535726 | A | G | 1 | a0001c0001t0002g0043 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2160+104T>C | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 16/19 | chrX | 120535726 | |||||||
chrX:120536416 | T | A | 1 | a0001c0001t0001g0091 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2047-473A>T | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 15/19 | chrX | 120536416 | |||||||
chrX:120536509 | T | C | 2 | a0001c0001t0003g0038 a0001c0001t0003g0119 |
3 | HG01884.hp1 HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2046+418A>G | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 15/19 | chrX | 120536509 | |||||||
chrX:120536852 | A | G | 1 | a0001c0001t0002g0045 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2046+75T>C | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 15/19 | chrX | 120536852 | |||||||
chrX:120537270 | C | T | 1 | a0001c0003t0003g0079 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1939-236G>A | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 14/19 | chrX | 120537270 | |||||||
chrX:120537392 | T | G | 2 | a0001c0001t0002g0093 a0001c0001t0002g0094 |
2 | HG02622.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1939-358A>C | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 14/19 | chrX | 120537392 | |||||||
chrX:120537436 | A | C | 2 | a0001c0002t0003g0112 a0001c0004t0003g0126 |
2 | HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1939-402T>G | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 14/19 | chrX | 120537436 | |||||||
chrX:120537613 | G | C | 1 | a0001c0001t0001g0066 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1938+511C>G | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 14/19 | chrX | 120537613 | |||||||
chrX:120537703 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1938+421A>G | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 14/19 | chrX | 120537703 | |||||||
chrX:120537832 | G | T | 1 | a0001c0001t0001g0110 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1938+292C>A | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 14/19 | chrX | 120537832 | |||||||
chrX:120537993 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1938+131A>G | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 14/19 | chrX | 120537993 | |||||||
chrX:120538238 | A | T | 1 | a0001c0001t0003g0026 | 2 | HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1853-29T>A | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 13/19 | chrX | 120538238 | |||||||
chrX:120538246 | G | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0067 |
5 | HG02148.hp1 NA18975.hp1 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.1853-37C>T | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 13/19 | chrX | 120538246 | |||||||
chrX:120538417 | G | A | 1 | a0001c0001t0001g0024 | 2 | NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1853-208C>T | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 13/19 | chrX | 120538417 | |||||||
chrX:120539889 | C | T | 1 | a0001c0001t0001g0072 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1636+481G>A | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 11/19 | chrX | 120539889 | |||||||
chrX:120540311 | G | C | 1 | a0001c0001t0001g0068 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1636+59C>G | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 11/19 | chrX | 120540311 | |||||||
chrX:120540359 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1636+11C>T | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 11/19 | chrX | 120540359 | |||||||
chrX:120540702 | T | C | 6 | a0001c0001t0002g0009 a0001c0001t0002g0020 a0001c0001t0002g0040 others(3): Show |
13 | HG00639.hp2 HG01109.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.1444-140A>G | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 10/19 | chrX | 120540702 | |||||||
chrX:120540945 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1444-383C>T | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 10/19 | chrX | 120540945 | |||||||
chrX:120541082 | A | C | 1 | a0001c0001t0001g0116 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1443+520T>G | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 10/19 | chrX | 120541082 | |||||||
chrX:120541454 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1443+148C>T | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 10/19 | chrX | 120541454 | |||||||
chrX:120542012 | T | C | 2 | a0001c0001t0001g0029 a0001c0001t0001g0030 |
4 | HG01168.hp1 HG01516.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.1325-292A>G | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 9/19 | chrX | 120542012 | |||||||
chrX:120542636 | A | G | 1 | a0001c0001t0001g0024 | 2 | NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1324+330T>C | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 9/19 | chrX | 120542636 | |||||||
chrX:120542951 | C | T | 12 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0022 others(9): Show |
25 | HG00438.hp1 HG01934.hp1 HG02027.hp1 others(22): Show |
intron_variant | MODIFIER | c.1324+15G>A | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 9/19 | chrX | 120542951 | |||||||
chrX:120543383 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1256+344G>A | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 8/19 | chrX | 120543383 | |||||||
chrX:120543495 | AAC | A | 3 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0050 |
3 | HG02647.hp1 NA18906.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.1256+230_1256+231d others(4): Show |
CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 8/19 | chrX | 120543495 | |||||||
chrX:120543495 | AACAC | A | 35 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(32): Show |
62 | HG00438.hp1 HG00639.hp2 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.1256+228_1256+231d others(6): Show |
CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 8/19 | chrX | 120543495 | |||||||
chrX:120543495 | AACACAC | A | 11 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0001t0002g0041 others(8): Show |
15 | HG00733.hp2 HG02258.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1256+226_1256+231d others(8): Show |
CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 8/19 | chrX | 120543495 | |||||||
chrX:120543495 | AACACACA others(1): Show |
A | 59 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(56): Show |
133 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.1256+224_1256+231d others(10): Show |
CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 8/19 | chrX | 120543495 | |||||||
chrX:120543495 | AACACACA others(3): Show |
A | 1 | a0001c0001t0005g0021 | 2 | HG02055.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1256+222_1256+231d others(12): Show |
CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 8/19 | chrX | 120543495 | |||||||
chrX:120543495 | AACACACA others(11): Show |
A | 1 | a0001c0001t0002g0092 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1256+214_1256+231d others(20): Show |
CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 8/19 | chrX | 120543495 | |||||||
chrX:120543532 | A | C | 13 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(10): Show |
23 | HG00438.hp1 HG01934.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.1256+195T>G | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 8/19 | chrX | 120543532 | |||||||
chrX:120543680 | G | A | 4 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0094 others(1): Show |
4 | HG02257.hp1 HG02622.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1256+47C>T | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 8/19 | chrX | 120543680 | |||||||
chrX:120543700 | CTA | C | 14 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0015 others(11): Show |
51 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.1256+25_1256+26del others(2): Show |
CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 8/19 | chrX | 120543700 | |||||||
chrX:120543829 | C | T | 29 | a0001c0001t0002g0009 a0001c0001t0002g0020 a0001c0001t0002g0040 others(26): Show |
40 | HG00639.hp2 HG00733.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.1174-20G>A | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 7/19 | chrX | 120543829 | |||||||
chrX:120544033 | T | C | 5 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0055 others(2): Show |
17 | HG02056.hp1 HG02165.hp2 HG02523.hp1 others(14): Show |
intron_variant | MODIFIER | c.1173+81A>G | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 7/19 | chrX | 120544033 | |||||||
chrX:120544733 | A | C | 7 | a0001c0001t0002g0009 a0001c0001t0002g0020 a0001c0001t0002g0040 others(4): Show |
14 | HG00639.hp2 HG00733.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.921-90T>G | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 5/19 | chrX | 120544733 | |||||||
chrX:120544963 | A | C | 5 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0055 others(2): Show |
17 | HG02056.hp1 HG02165.hp2 HG02523.hp1 others(14): Show |
intron_variant | MODIFIER | c.921-320T>G | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 5/19 | chrX | 120544963 | |||||||
chrX:120545108 | G | A | 1 | a0001c0001t0002g0040 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.920+336C>T | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 5/19 | chrX | 120545108 | |||||||
chrX:120545125 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.920+319A>G | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 5/19 | chrX | 120545125 | |||||||
chrX:120545870 | G | T | 1 | a0001c0001t0003g0120 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.847-353C>A | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 4/19 | chrX | 120545870 | |||||||
chrX:120546249 | G | A | 1 | a0001c0001t0001g0018 | 3 | HG00733.hp1 HG01255.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.846+298C>T | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 4/19 | chrX | 120546249 | |||||||
chrX:120546491 | T | C | 1 | a0001c0001t0002g0043 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.846+56A>G | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 4/19 | chrX | 120546491 | |||||||
chrX:120546520 | C | T | 1 | a0001c0001t0002g0043 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.846+27G>A | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 4/19 | chrX | 120546520 | |||||||
chrX:120546628 | G | A | 3 | a0001c0002t0003g0081 a0001c0002t0003g0112 a0001c0004t0003g0126 |
3 | HG02723.hp1 HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.777-12C>T | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 3/19 | chrX | 120546628 | |||||||
chrX:120546638 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.777-22A>G | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 3/19 | chrX | 120546638 | |||||||
chrX:120546875 | A | G | 1 | a0001c0001t0008g0125 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.777-259T>C | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 3/19 | chrX | 120546875 | |||||||
chrX:120546951 | C | T | 12 | a0001c0001t0002g0009 a0001c0001t0002g0020 a0001c0001t0002g0040 others(9): Show |
20 | HG00639.hp2 HG00733.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.776+185G>A | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 3/19 | chrX | 120546951 | |||||||
chrX:120547123 | T | C | 1 | a0001c0001t0002g0094 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.776+13A>G | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 3/19 | chrX | 120547123 | |||||||
chrX:120547124 | T | C | 1 | a0001c0001t0001g0027 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.776+12A>G | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 3/19 | chrX | 120547124 | |||||||
chrX:120547124 | T | TA | 10 | a0001c0001t0002g0009 a0001c0001t0002g0020 a0001c0001t0002g0040 others(7): Show |
17 | HG00639.hp2 HG00733.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.776+11dupT | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 3/19 | chrX | 120547124 | |||||||
chrX:120547629 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.673-390G>A | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120547629 | |||||||
chrX:120547663 | T | C | 4 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0094 others(1): Show |
4 | HG02257.hp1 HG02622.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.673-424A>G | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120547663 | |||||||
chrX:120547851 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.673-612G>A | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120547851 | |||||||
chrX:120548001 | C | G | 12 | a0001c0001t0002g0009 a0001c0001t0002g0020 a0001c0001t0002g0040 others(9): Show |
20 | HG00639.hp2 HG00733.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.673-762G>C | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120548001 | |||||||
chrX:120548330 | T | C | 1 | a0001c0001t0001g0056 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.673-1091A>G | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120548330 | |||||||
chrX:120548419 | G | A | 1 | a0001c0003t0003g0079 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.673-1180C>T | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120548419 | |||||||
chrX:120548536 | A | G | 3 | a0001c0001t0001g0082 a0001c0001t0001g0086 a0001c0001t0001g0108 |
3 | HG00639.hp1 HG00741.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.673-1297T>C | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120548536 | |||||||
chrX:120548653 | G | A | 6 | a0001c0001t0002g0009 a0001c0001t0002g0020 a0001c0001t0002g0040 others(3): Show |
13 | HG00639.hp2 HG01109.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.673-1414C>T | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120548653 | |||||||
chrX:120548748 | T | C | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(84): Show |
182 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.673-1509A>G | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120548748 | |||||||
chrX:120548770 | G | C | 1 | a0001c0001t0002g0043 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.673-1531C>G | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120548770 | |||||||
chrX:120548914 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.673-1675G>A | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120548914 | |||||||
chrX:120549000 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.673-1761T>C | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120549000 | |||||||
chrX:120549359 | C | T | 2 | a0001c0001t0003g0026 a0001c0001t0003g0083 |
3 | HG02723.hp2 HG02976.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.673-2120G>A | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120549359 | |||||||
chrX:120549418 | G | A | 4 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0094 others(1): Show |
4 | HG02257.hp1 HG02622.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.673-2179C>T | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120549418 | |||||||
chrX:120549492 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.673-2253C>T | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120549492 | |||||||
chrX:120549566 | AAGAGCAG others(3): Show |
A | 1 | a0001c0001t0001g0070 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.673-2337_673-2328d others(12): Show |
CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120549566 | |||||||
chrX:120549647 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.673-2408G>A | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120549647 | |||||||
chrX:120549753 | A | G | 2 | a0001c0001t0003g0026 a0001c0001t0003g0083 |
3 | HG02723.hp2 HG02976.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.673-2514T>C | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120549753 | |||||||
chrX:120550173 | T | C | 1 | a0001c0001t0001g0071 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.673-2934A>G | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120550173 | |||||||
chrX:120550385 | A | G | 1 | a0001c0001t0001g0025 | 2 | HG02257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.673-3146T>C | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120550385 | |||||||
chrX:120550417 | G | A | 1 | a0001c0001t0001g0030 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.673-3178C>T | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120550417 | |||||||
chrX:120550648 | G | C | 1 | a0001c0001t0001g0013 | 4 | HG01106.hp1 HG01891.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.673-3409C>G | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120550648 | |||||||
chrX:120550702 | C | T | 4 | a0001c0001t0001g0024 a0001c0001t0001g0075 a0001c0001t0001g0076 others(1): Show |
5 | HG00673.hp1 HG03834.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.673-3463G>A | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120550702 | |||||||
chrX:120551757 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.673-4518C>T | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120551757 | |||||||
chrX:120551919 | C | A | 1 | a0001c0001t0002g0044 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.673-4680G>T | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120551919 | |||||||
chrX:120552013 | C | G | 16 | a0001c0001t0002g0009 a0001c0001t0002g0020 a0001c0001t0002g0040 others(13): Show |
24 | HG00639.hp2 HG00733.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.673-4774G>C | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120552013 | |||||||
chrX:120552059 | T | G | 2 | a0001c0001t0002g0044 a0001c0001t0002g0045 |
2 | HG02451.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.673-4820A>C | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120552059 | |||||||
chrX:120552126 | C | T | 1 | a0001c0001t0001g0019 | 3 | HG02280.hp2 HG02895.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.673-4887G>A | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120552126 | |||||||
chrX:120552127 | G | A | 5 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0119 others(2): Show |
7 | HG01884.hp1 HG02258.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.673-4888C>T | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120552127 | |||||||
chrX:120552243 | GTTCAACC others(4): Show |
G | 16 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0028 others(13): Show |
32 | HG00323.hp2 HG00408.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.673-5015_673-5005d others(13): Show |
CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120552243 | |||||||
chrX:120552282 | G | A | 1 | a0001c0001t0003g0120 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.673-5043C>T | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120552282 | |||||||
chrX:120552438 | G | C | 1 | a0001c0001t0001g0034 | 2 | NA19070.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.673-5199C>G | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120552438 | |||||||
chrX:120552693 | T | A | 2 | a0001c0001t0001g0029 a0001c0001t0001g0030 |
4 | HG01168.hp1 HG01516.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.672+5231A>T | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120552693 | |||||||
chrX:120553492 | C | T | 1 | a0001c0001t0001g0011 | 4 | HG02148.hp1 NA18975.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.672+4432G>A | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120553492 | |||||||
chrX:120553506 | G | T | 1 | a0001c0001t0001g0055 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.672+4418C>A | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120553506 | |||||||
chrX:120553860 | C | T | 1 | a0001c0001t0001g0095 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.672+4064G>A | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120553860 | |||||||
chrX:120553985 | G | A | 4 | a0001c0001t0002g0092 a0001c0001t0002g0093 a0001c0001t0002g0094 others(1): Show |
4 | HG02257.hp1 HG02622.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.672+3939C>T | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120553985 | |||||||
chrX:120554040 | C | A | 3 | a0001c0002t0003g0081 a0001c0002t0003g0112 a0001c0004t0003g0126 |
3 | HG02723.hp1 HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.672+3884G>T | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120554040 | |||||||
chrX:120554074 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.672+3850A>G | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120554074 | |||||||
chrX:120554121 | T | G | 1 | a0001c0001t0001g0107 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.672+3803A>C | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120554121 | |||||||
chrX:120554216 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.672+3708G>A | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120554216 | |||||||
chrX:120554724 | G | A | 31 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(28): Show |
94 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.672+3200C>T | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120554724 | |||||||
chrX:120554758 | A | G | 4 | a0001c0001t0001g0007 a0001c0001t0001g0052 a0001c0001t0001g0053 others(1): Show |
10 | HG01496.hp2 HG02572.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.672+3166T>C | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120554758 | |||||||
chrX:120555542 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.672+2382G>A | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120555542 | |||||||
chrX:120555864 | C | G | 1 | a0001c0001t0001g0113 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.672+2060G>C | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120555864 | |||||||
chrX:120555941 | C | CA | 12 | a0001c0001t0001g0023 a0001c0001t0001g0035 a0001c0001t0001g0072 others(9): Show |
14 | HG00733.hp2 HG01071.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.672+1982dupT | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120555941 | |||||||
chrX:120555941 | CA | C | 14 | a0001c0001t0001g0080 a0001c0001t0003g0037 a0001c0001t0003g0038 others(11): Show |
17 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.672+1982delT | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120555941 | |||||||
chrX:120556557 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.672+1367G>A | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120556557 | |||||||
chrX:120556598 | G | T | 1 | a0001c0001t0001g0074 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.672+1326C>A | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120556598 | |||||||
chrX:120556734 | T | C | 2 | a0001c0001t0002g0044 a0001c0001t0002g0045 |
2 | HG02451.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.672+1190A>G | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120556734 | |||||||
chrX:120556762 | C | A | 1 | a0001c0001t0001g0074 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.672+1162G>T | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120556762 | |||||||
chrX:120556824 | C | T | 1 | a0001c0003t0003g0079 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.672+1100G>A | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120556824 | |||||||
chrX:120556903 | GTA | G | 63 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(60): Show |
146 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.672+1019_672+1020d others(4): Show |
CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120556903 | |||||||
chrX:120556910 | TA | T | 2 | a0001c0001t0005g0021 a0001c0001t0005g0046 |
3 | HG02055.hp1 HG02818.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.672+1013delT | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120556910 | |||||||
chrX:120556910 | TATA | T | 7 | a0001c0001t0002g0009 a0001c0001t0002g0020 a0001c0001t0002g0040 others(4): Show |
14 | HG00639.hp2 HG00733.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.672+1011_672+1013d others(5): Show |
CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120556910 | |||||||
chrX:120556912 | TA | T | 34 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(31): Show |
84 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.672+1011delT | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120556912 | |||||||
chrX:120556913 | A | T | 5 | a0001c0001t0001g0049 a0001c0001t0001g0070 a0001c0001t0001g0109 others(2): Show |
6 | HG02055.hp1 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.672+1011T>A | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120556913 | |||||||
chrX:120556913 | AT | A | 10 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0015 others(7): Show |
14 | HG00438.hp1 HG02145.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.672+1010delA | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120556913 | |||||||
chrX:120556913 | ATT | A | 8 | a0001c0001t0001g0015 a0001c0001t0001g0036 a0001c0001t0001g0114 others(5): Show |
9 | HG00735.hp2 HG01258.hp1 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.672+1009_672+1010d others(4): Show |
CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120556913 | |||||||
chrX:120556988 | C | T | 1 | a0001c0001t0001g0025 | 2 | HG02257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.672+936G>A | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120556988 | |||||||
chrX:120556989 | G | A | 6 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0119 others(3): Show |
8 | HG01884.hp1 HG02258.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.672+935C>T | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120556989 | |||||||
chrX:120557207 | G | A | 1 | a0001c0001t0003g0038 | 2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.672+717C>T | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120557207 | |||||||
chrX:120557216 | T | C | 1 | a0001c0001t0001g0122 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.672+708A>G | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120557216 | |||||||
chrX:120557451 | C | T | 1 | a0001c0001t0001g0078 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.672+473G>A | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120557451 | |||||||
chrX:120557623 | C | A | 1 | a0001c0001t0003g0123 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.672+301G>T | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120557623 | |||||||
chrX:120557653 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.672+271A>G | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120557653 | |||||||
chrX:120557736 | T | C | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(79): Show |
176 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.672+188A>G | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 2/19 | chrX | 120557736 | |||||||
chrX:120558779 | T | C | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(84): Show |
185 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.557-740A>G | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 1/19 | chrX | 120558779 | |||||||
chrX:120559306 | C | G | 1 | a0001c0001t0001g0047 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.556+777G>C | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 1/19 | chrX | 120559306 | |||||||
chrX:120559365 | A | G | 10 | a0001c0001t0002g0009 a0001c0001t0002g0020 a0001c0001t0002g0040 others(7): Show |
17 | HG00639.hp2 HG00733.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.556+718T>C | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 1/19 | chrX | 120559365 | |||||||
chrX:120559782 | C | T | 12 | a0001c0001t0002g0009 a0001c0001t0002g0020 a0001c0001t0002g0040 others(9): Show |
20 | HG00639.hp2 HG00733.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.556+301G>A | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 1/19 | chrX | 120559782 | |||||||
chrX:120559883 | G | C | 1 | a0001c0001t0008g0125 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.556+200C>G | CUL4B | ENSG00000158290.19 | transcript | ENST00000371322.11 | protein_coding | 1/19 | chrX | 120559883 |