Item | Value |
---|---|
geneid | 221477 |
ensemblid | ENSG00000198663.17 |
hgncid | 21114 |
symbol | C6orf89 |
name | chromosome 6 open reading frame 89 |
refseq_nuc | NM_001286635.2 |
refseq_prot | NP_001273564.1 |
ensembl_nuc | ENST00000480824.7 |
ensembl_prot | ENSP00000475947.1 |
mane_status | MANE Select |
chr | chr6 |
start | 36885952 |
end | 36928964 |
strand | + |
ver | v1.2 |
region | chr6:36885952-36928964 |
region5000 | chr6:36880952-36933964 |
regionname0 | C6orf89_chr6_36885952_36928964 |
regionname5000 | C6orf89_chr6_36880952_36933964 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 347 | 393 | 92 | 71 | 179 | 12 | 37 | 141 | C6orf89_chr6_36880952_36933964 | C6orf89 | MDLAA others(342): Show |
chr6 | 36880952 | 36933964 |
a0002 | 0/0 | 347 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | MDLAA others(342): Show |
chr6 | 36880952 | 36933964 |
a0003 | 0/0 | 347 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | MDLAA others(342): Show |
chr6 | 36880952 | 36933964 |
a0004 | 0/0 | 347 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | C6orf89_chr6_36880952_36933964 | C6orf89 | MDLAA others(342): Show |
chr6 | 36880952 | 36933964 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1041 | 242 | 48 | 50 | 108 | 7 | 27 | C6orf89_chr6_36880952_36933964 | C6orf89 | ATGGA others(1036): Show |
chr6 | 36880952 | 36933964 | ||
a0001c0002 | 0/0 | 1041 | 110 | 26 | 14 | 62 | 3 | 5 | C6orf89_chr6_36880952_36933964 | C6orf89 | ATGGA others(1036): Show |
chr6 | 36880952 | 36933964 | ||
a0001c0003 | 0/0 | 1041 | 20 | 4 | 6 | 3 | 2 | 5 | C6orf89_chr6_36880952_36933964 | C6orf89 | ATGGA others(1036): Show |
chr6 | 36880952 | 36933964 | ||
a0001c0004 | 0/0 | 1041 | 14 | 14 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | ATGGA others(1036): Show |
chr6 | 36880952 | 36933964 | ||
a0001c0005 | 0/0 | 1041 | 7 | 0 | 1 | 6 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | ATGGA others(1036): Show |
chr6 | 36880952 | 36933964 | ||
a0002c0006 | 0/0 | 1041 | 1 | 0 | 1 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | ATGGA others(1036): Show |
chr6 | 36880952 | 36933964 | ||
a0003c0007 | 0/0 | 1041 | 1 | 0 | 0 | 0 | 0 | 1 | C6orf89_chr6_36880952_36933964 | C6orf89 | ATGGA others(1036): Show |
chr6 | 36880952 | 36933964 | ||
a0004c0008 | 0/0 | 1041 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | ATGGA others(1036): Show |
chr6 | 36880952 | 36933964 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 6763 | 84 | 3 | 22 | 45 | 4 | 9 | C6orf89_chr6_36880952_36933964 | C6orf89 | AGGAA others(6758): Show |
chr6 | 36880952 | 36933964 |
a0001c0001t0002 | 0/0 | 6763 | 78 | 6 | 17 | 45 | 2 | 8 | C6orf89_chr6_36880952_36933964 | C6orf89 | AGGAA others(6758): Show |
chr6 | 36880952 | 36933964 |
a0001c0001t0004 | 0/0 | 6763 | 35 | 21 | 6 | 4 | 1 | 3 | C6orf89_chr6_36880952_36933964 | C6orf89 | AGGAA others(6758): Show |
chr6 | 36880952 | 36933964 |
a0001c0001t0008 | 0/0 | 6763 | 12 | 7 | 1 | 0 | 0 | 4 | C6orf89_chr6_36880952_36933964 | C6orf89 | AGGAA others(6758): Show |
chr6 | 36880952 | 36933964 |
a0001c0001t0011 | 0/0 | 6763 | 8 | 0 | 0 | 8 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | AGGAA others(6758): Show |
chr6 | 36880952 | 36933964 |
a0001c0001t0015 | 0/0 | 6759 | 5 | 5 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | AGGAA others(6754): Show |
chr6 | 36880952 | 36933964 |
a0001c0001t0017 | 0/0 | 6763 | 4 | 2 | 1 | 0 | 0 | 1 | C6orf89_chr6_36880952_36933964 | C6orf89 | AGGAA others(6758): Show |
chr6 | 36880952 | 36933964 |
a0001c0001t0024 | 0/0 | 6763 | 2 | 0 | 0 | 2 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | AGGAA others(6758): Show |
chr6 | 36880952 | 36933964 |
a0001c0001t0025 | 0/0 | 6759 | 2 | 2 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | AGGAA others(6754): Show |
chr6 | 36880952 | 36933964 |
a0001c0001t0026 | 0/0 | 6763 | 2 | 2 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | AGGAA others(6758): Show |
chr6 | 36880952 | 36933964 |
a0001c0001t0038 | 0/0 | 6763 | 1 | 0 | 0 | 0 | 0 | 1 | C6orf89_chr6_36880952_36933964 | C6orf89 | AGGAA others(6758): Show |
chr6 | 36880952 | 36933964 |
a0001c0001t0039 | 0/0 | 6763 | 1 | 0 | 1 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | AGGAA others(6758): Show |
chr6 | 36880952 | 36933964 |
a0001c0001t0040 | 0/0 | 6763 | 1 | 0 | 1 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | AGGAA others(6758): Show |
chr6 | 36880952 | 36933964 |
a0001c0001t0041 | 0/0 | 6763 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | AGGAA others(6758): Show |
chr6 | 36880952 | 36933964 |
a0001c0001t0042 | 0/0 | 6763 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | AGGAA others(6758): Show |
chr6 | 36880952 | 36933964 |
a0001c0001t0043 | 0/0 | 6763 | 1 | 0 | 0 | 0 | 0 | 1 | C6orf89_chr6_36880952_36933964 | C6orf89 | AGGAA others(6758): Show |
chr6 | 36880952 | 36933964 |
a0001c0001t0044 | 0/0 | 6763 | 1 | 0 | 1 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | AGGAA others(6758): Show |
chr6 | 36880952 | 36933964 |
a0001c0001t0045 | 0/0 | 6763 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | AGGAA others(6758): Show |
chr6 | 36880952 | 36933964 |
a0001c0001t0046 | 0/0 | 6763 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | AGGAA others(6758): Show |
chr6 | 36880952 | 36933964 |
a0001c0001t0048 | 0/1 | 6764 | 1 | 0 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | AGGAA others(6759): Show |
chr6 | 36880952 | 36933964 |
a0001c0002t0003 | 0/0 | 6760 | 36 | 1 | 0 | 33 | 0 | 2 | C6orf89_chr6_36880952_36933964 | C6orf89 | AGGAA others(6755): Show |
chr6 | 36880952 | 36933964 |
a0001c0002t0005 | 0/0 | 6761 | 19 | 3 | 6 | 4 | 3 | 3 | C6orf89_chr6_36880952_36933964 | C6orf89 | AGGAA others(6756): Show |
chr6 | 36880952 | 36933964 |
a0001c0002t0009 | 0/0 | 6761 | 9 | 0 | 7 | 2 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | AGGAA others(6756): Show |
chr6 | 36880952 | 36933964 |
a0001c0002t0010 | 0/0 | 6760 | 10 | 0 | 0 | 10 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | AGGAA others(6755): Show |
chr6 | 36880952 | 36933964 |
a0001c0002t0013 | 0/0 | 6756 | 5 | 5 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | AGGAA others(6751): Show |
chr6 | 36880952 | 36933964 |
a0001c0002t0014 | 0/0 | 6760 | 5 | 0 | 0 | 5 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | AGGAA others(6755): Show |
chr6 | 36880952 | 36933964 |
a0001c0002t0016 | 0/0 | 6760 | 4 | 4 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | AGGAA others(6755): Show |
chr6 | 36880952 | 36933964 |
a0001c0002t0018 | 0/0 | 6760 | 3 | 0 | 0 | 3 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | AGGAA others(6755): Show |
chr6 | 36880952 | 36933964 |
a0001c0002t0019 | 0/0 | 6756 | 3 | 3 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | AGGAA others(6751): Show |
chr6 | 36880952 | 36933964 |
a0001c0002t0020 | 0/0 | 6760 | 2 | 2 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | AGGAA others(6755): Show |
chr6 | 36880952 | 36933964 |
a0001c0002t0021 | 0/0 | 6760 | 2 | 1 | 1 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | AGGAA others(6755): Show |
chr6 | 36880952 | 36933964 |
a0001c0002t0023 | 0/0 | 6760 | 2 | 2 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | AGGAA others(6755): Show |
chr6 | 36880952 | 36933964 |
a0001c0002t0027 | 0/0 | 6760 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | AGGAA others(6755): Show |
chr6 | 36880952 | 36933964 |
a0001c0002t0028 | 0/0 | 6760 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | AGGAA others(6755): Show |
chr6 | 36880952 | 36933964 |
a0001c0002t0029 | 0/0 | 6760 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | AGGAA others(6755): Show |
chr6 | 36880952 | 36933964 |
a0001c0002t0030 | 0/0 | 6761 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | AGGAA others(6756): Show |
chr6 | 36880952 | 36933964 |
a0001c0002t0031 | 0/0 | 6756 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | AGGAA others(6751): Show |
chr6 | 36880952 | 36933964 |
a0001c0002t0032 | 0/0 | 6760 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | AGGAA others(6755): Show |
chr6 | 36880952 | 36933964 |
a0001c0002t0033 | 0/0 | 6760 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | AGGAA others(6755): Show |
chr6 | 36880952 | 36933964 |
a0001c0002t0035 | 0/0 | 6760 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | AGGAA others(6755): Show |
chr6 | 36880952 | 36933964 |
a0001c0002t0037 | 0/0 | 6756 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | AGGAA others(6751): Show |
chr6 | 36880952 | 36933964 |
a0001c0002t0047 | 0/0 | 6760 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | AGGAA others(6755): Show |
chr6 | 36880952 | 36933964 |
a0001c0003t0006 | 0/0 | 6760 | 17 | 4 | 4 | 2 | 2 | 5 | C6orf89_chr6_36880952_36933964 | C6orf89 | AGGAA others(6755): Show |
chr6 | 36880952 | 36933964 |
a0001c0003t0022 | 0/0 | 6760 | 2 | 0 | 2 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | AGGAA others(6755): Show |
chr6 | 36880952 | 36933964 |
a0001c0003t0036 | 0/0 | 6760 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | AGGAA others(6755): Show |
chr6 | 36880952 | 36933964 |
a0001c0004t0007 | 0/0 | 6760 | 13 | 13 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | AGGAA others(6755): Show |
chr6 | 36880952 | 36933964 |
a0001c0004t0034 | 0/0 | 6760 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | AGGAA others(6755): Show |
chr6 | 36880952 | 36933964 |
a0001c0005t0012 | 0/0 | 6764 | 7 | 0 | 1 | 6 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | AGGAA others(6759): Show |
chr6 | 36880952 | 36933964 |
a0002c0006t0009 | 0/0 | 6761 | 1 | 0 | 1 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | AGGAA others(6756): Show |
chr6 | 36880952 | 36933964 |
a0003c0007t0001 | 0/0 | 6763 | 1 | 0 | 0 | 0 | 0 | 1 | C6orf89_chr6_36880952_36933964 | C6orf89 | AGGAA others(6758): Show |
chr6 | 36880952 | 36933964 |
a0004c0008t0003 | 0/0 | 6760 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | AGGAA others(6755): Show |
chr6 | 36880952 | 36933964 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 9 | 0 | 2 | 7 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0005 | 0/0 | 6 | 0 | 1 | 4 | 0 | 1 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0046 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0144 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0002g0001 | 0/0 | 14 | 0 | 2 | 10 | 0 | 2 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0002g0009 | 0/0 | 5 | 0 | 2 | 0 | 0 | 3 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0002g0010 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0002g0011 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0002g0012 | 0/0 | 5 | 0 | 0 | 3 | 2 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0002g0018 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0002g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0002g0040 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0002g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0002g0053 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0002g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0002g0057 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0004g0006 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0004g0025 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0004g0026 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0004g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0004g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0004g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0004g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0004g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0004g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0004g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0004g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0004g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0004g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0004g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0004g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0004g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0008g0024 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0008g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0008g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0008g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0008g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0008g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0008g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0008g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0008g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0011g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0011g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0011g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0015g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0015g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0017g0030 | 0/0 | 3 | 2 | 0 | 0 | 0 | 1 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0017g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0024g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0024g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0025g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0025g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0026g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0026g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0038g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0039g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0040g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0041g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0042g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0043g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0044g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0045g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0046g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0001t0048g0059 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0003g0002 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0003g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0003g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0003g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0003g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0005g0004 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0005g0028 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0005g0029 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0005g0058 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0005g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0005g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0005g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0005g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0005g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0005g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0005g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0005g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0009g0004 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0009g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0009g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0009g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0009g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0010g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0010g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0010g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0010g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0010g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0013g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0013g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0014g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0014g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0014g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0014g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0016g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0016g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0016g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0018g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0019g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0019g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0019g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0020g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0021g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0021g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0023g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0023g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0027g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0028g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0029g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0030g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0031g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0032g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0033g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0035g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0037g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0002t0047g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0003t0006g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0003t0006g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0003t0006g0032 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0003t0006g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0003t0006g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0003t0006g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0003t0006g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0003t0006g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0003t0006g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0003t0006g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0003t0006g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0003t0006g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0003t0006g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0003t0006g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0003t0022g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0003t0036g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0004t0007g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0004t0007g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0004t0007g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0004t0007g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0004t0007g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0004t0007g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0004t0007g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0004t0007g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0004t0007g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0004t0007g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0004t0034g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0005t0012g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0001c0005t0012g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0002c0006t0009g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0003c0007t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
a0004c0008t0003g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0002 | t0005 | g0004 | EUR | GBR | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG00140 | hp2 | a0001 | c0003 | t0006 | g0071 | EUR | GBR | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG00323 | hp1 | a0001 | c0003 | t0006 | g0032 | EUR | FIN | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0134 | EUR | FIN | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG00423 | hp1 | a0001 | c0002 | t0014 | g0034 | EAS | CHS | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG00438 | hp1 | a0001 | c0002 | t0003 | g0078 | EAS | CHS | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | CHS | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG00544 | hp1 | a0001 | c0002 | t0003 | g0008 | EAS | CHS | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG00544 | hp2 | a0001 | c0002 | t0018 | g0023 | EAS | CHS | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG00558 | hp1 | a0001 | c0001 | t0045 | g0152 | EAS | CHS | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG00597 | hp1 | a0001 | c0002 | t0010 | g0088 | EAS | CHS | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | CHS | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG00609 | hp1 | a0001 | c0001 | t0042 | g0241 | EAS | CHS | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0205 | AMR | PUR | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG00673 | hp2 | a0001 | c0002 | t0010 | g0036 | EAS | CHS | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG00733 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | PUR | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG00735 | hp1 | a0001 | c0003 | t0022 | g0017 | AMR | PUR | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG00735 | hp2 | a0001 | c0002 | t0009 | g0004 | AMR | PUR | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG00741 | hp1 | a0001 | c0001 | t0004 | g0133 | AMR | PUR | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG00741 | hp2 | a0001 | c0001 | t0040 | g0219 | AMR | PUR | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01069 | hp2 | a0001 | c0001 | t0044 | g0130 | AMR | PUR | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01074 | hp1 | a0001 | c0002 | t0005 | g0166 | AMR | PUR | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01106 | hp1 | a0001 | c0001 | t0017 | g0156 | AMR | PUR | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01106 | hp2 | a0001 | c0002 | t0005 | g0028 | AMR | PUR | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01109 | hp2 | a0001 | c0003 | t0006 | g0068 | AMR | PUR | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01168 | hp1 | a0001 | c0003 | t0006 | g0062 | AMR | PUR | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01168 | hp2 | a0001 | c0002 | t0005 | g0028 | AMR | PUR | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01169 | hp2 | a0001 | c0002 | t0005 | g0028 | AMR | PUR | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01175 | hp1 | a0001 | c0002 | t0005 | g0239 | AMR | PUR | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01192 | hp1 | a0001 | c0003 | t0006 | g0031 | AMR | PUR | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | PUR | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01243 | hp2 | a0001 | c0003 | t0006 | g0017 | AMR | PUR | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01255 | hp2 | a0001 | c0003 | t0022 | g0017 | AMR | CLM | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0214 | AMR | CLM | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0096 | AMR | CLM | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01261 | hp1 | a0001 | c0002 | t0009 | g0234 | AMR | CLM | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01261 | hp2 | a0001 | c0005 | t0012 | g0194 | AMR | CLM | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01346 | hp1 | a0001 | c0001 | t0004 | g0025 | AMR | CLM | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01346 | hp2 | a0001 | c0002 | t0009 | g0231 | AMR | CLM | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01358 | hp1 | a0001 | c0001 | t0004 | g0178 | AMR | CLM | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01358 | hp2 | a0001 | c0002 | t0009 | g0235 | AMR | CLM | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01361 | hp1 | a0001 | c0002 | t0021 | g0228 | AMR | CLM | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0204 | AMR | CLM | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01433 | hp1 | a0002 | c0006 | t0009 | g0232 | AMR | CLM | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01496 | hp1 | a0001 | c0001 | t0008 | g0185 | AMR | CLM | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0097 | AMR | CLM | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0122 | EUR | IBS | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0222 | EUR | IBS | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01516 | hp1 | a0001 | c0002 | t0005 | g0233 | EUR | IBS | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0012 | EUR | IBS | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0012 | EUR | IBS | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0046 | EUR | IBS | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01884 | hp1 | a0001 | c0001 | t0008 | g0039 | AFR | ACB | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01884 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | ACB | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01891 | hp1 | a0001 | c0001 | t0004 | g0183 | AFR | ACB | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01891 | hp2 | a0001 | c0001 | t0008 | g0039 | AFR | ACB | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | PEL | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01934 | hp1 | a0001 | c0002 | t0009 | g0004 | AMR | PEL | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0215 | AMR | PEL | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01943 | hp1 | a0001 | c0001 | t0004 | g0180 | AMR | PEL | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02004 | hp2 | a0001 | c0002 | t0009 | g0004 | AMR | PEL | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02015 | hp1 | a0001 | c0002 | t0047 | g0081 | EAS | KHV | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02015 | hp2 | a0001 | c0002 | t0003 | g0073 | EAS | KHV | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | KHV | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02040 | hp2 | a0001 | c0002 | t0005 | g0238 | EAS | KHV | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02055 | hp1 | a0001 | c0002 | t0037 | g0103 | AFR | ACB | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02055 | hp2 | a0001 | c0001 | t0004 | g0148 | AFR | ACB | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02056 | hp1 | a0001 | c0002 | t0003 | g0086 | EAS | KHV | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02056 | hp2 | a0001 | c0003 | t0006 | g0065 | EAS | KHV | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02071 | hp1 | a0001 | c0002 | t0030 | g0171 | EAS | KHV | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02071 | hp2 | a0001 | c0003 | t0006 | g0064 | EAS | KHV | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02080 | hp1 | a0001 | c0002 | t0005 | g0237 | EAS | KHV | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | KHV | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | KHV | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | KHV | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | KHV | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02129 | hp2 | a0001 | c0002 | t0005 | g0058 | EAS | KHV | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02132 | hp1 | a0001 | c0001 | t0041 | g0011 | EAS | KHV | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | KHV | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02145 | hp1 | a0001 | c0001 | t0008 | g0176 | AFR | ACB | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02145 | hp2 | a0001 | c0004 | t0007 | g0118 | AFR | ACB | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02148 | hp1 | a0001 | c0001 | t0004 | g0025 | AMR | PEL | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | CDX | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02165 | hp2 | a0001 | c0002 | t0010 | g0002 | EAS | CDX | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02258 | hp1 | a0001 | c0004 | t0007 | g0015 | AFR | ACB | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02258 | hp2 | a0001 | c0002 | t0005 | g0029 | AFR | ACB | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PEL | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02280 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | ACB | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02280 | hp2 | a0001 | c0004 | t0007 | g0163 | AFR | ACB | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02293 | hp2 | a0001 | c0002 | t0005 | g0004 | AMR | PEL | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0217 | AMR | PEL | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02300 | hp2 | a0001 | c0002 | t0009 | g0230 | AMR | PEL | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02451 | hp1 | a0001 | c0002 | t0021 | g0117 | AFR | ACB | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02451 | hp2 | a0001 | c0002 | t0033 | g0227 | AFR | ACB | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02572 | hp1 | a0001 | c0002 | t0005 | g0029 | AFR | GWD | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02572 | hp2 | a0001 | c0002 | t0035 | g0172 | AFR | GWD | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02615 | hp1 | a0001 | c0002 | t0028 | g0069 | AFR | GWD | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02615 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | GWD | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02622 | hp1 | a0001 | c0004 | t0034 | g0015 | AFR | GWD | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02622 | hp2 | a0001 | c0002 | t0016 | g0226 | AFR | GWD | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02630 | hp1 | a0001 | c0002 | t0019 | g0105 | AFR | GWD | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02630 | hp2 | a0001 | c0004 | t0007 | g0119 | AFR | GWD | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02647 | hp1 | a0001 | c0001 | t0015 | g0016 | AFR | GWD | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02647 | hp2 | a0001 | c0001 | t0008 | g0175 | AFR | GWD | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02683 | hp2 | a0001 | c0002 | t0005 | g0004 | SAS | PJL | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02698 | hp1 | a0001 | c0001 | t0004 | g0187 | SAS | PJL | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02717 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | GWD | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02717 | hp2 | a0001 | c0001 | t0004 | g0038 | AFR | GWD | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02738 | hp1 | a0001 | c0003 | t0006 | g0101 | SAS | PJL | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02809 | hp1 | a0001 | c0002 | t0016 | g0055 | AFR | GWD | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02809 | hp2 | a0001 | c0004 | t0007 | g0120 | AFR | GWD | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02886 | hp1 | a0001 | c0004 | t0007 | g0245 | AFR | GWD | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02886 | hp2 | a0001 | c0003 | t0006 | g0100 | AFR | GWD | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0072 | AFR | GWD | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02895 | hp2 | a0001 | c0003 | t0006 | g0033 | AFR | GWD | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02896 | hp1 | a0001 | c0002 | t0016 | g0225 | AFR | GWD | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02896 | hp2 | a0001 | c0001 | t0017 | g0030 | AFR | GWD | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02897 | hp1 | a0001 | c0003 | t0006 | g0033 | AFR | GWD | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02897 | hp2 | a0001 | c0001 | t0017 | g0030 | AFR | GWD | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0048 | AFR | ESN | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02922 | hp2 | a0001 | c0002 | t0013 | g0013 | AFR | ESN | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02965 | hp1 | a0001 | c0001 | t0026 | g0196 | AFR | ESN | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02965 | hp2 | a0001 | c0002 | t0013 | g0060 | AFR | ESN | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02970 | hp1 | a0001 | c0001 | t0004 | g0121 | AFR | ESN | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ESN | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02976 | hp1 | a0001 | c0001 | t0008 | g0114 | AFR | ESN | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0116 | AFR | ESN | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG03041 | hp1 | a0001 | c0004 | t0007 | g0112 | AFR | GWD | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG03041 | hp2 | a0001 | c0001 | t0026 | g0197 | AFR | GWD | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG03130 | hp1 | a0001 | c0002 | t0020 | g0056 | AFR | ESN | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG03130 | hp2 | a0001 | c0001 | t0015 | g0016 | AFR | ESN | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG03139 | hp1 | a0001 | c0001 | t0008 | g0174 | AFR | ESN | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ESN | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG03195 | hp1 | a0001 | c0001 | t0015 | g0016 | AFR | ESN | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG03195 | hp2 | a0001 | c0001 | t0025 | g0168 | AFR | ESN | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG03209 | hp1 | a0001 | c0004 | t0007 | g0049 | AFR | MSL | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG03209 | hp2 | a0001 | c0002 | t0019 | g0111 | AFR | MSL | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG03225 | hp1 | a0001 | c0001 | t0004 | g0184 | AFR | MSL | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG03225 | hp2 | a0001 | c0003 | t0006 | g0066 | AFR | MSL | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG03239 | hp1 | a0001 | c0002 | t0005 | g0236 | SAS | PJL | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG03453 | hp1 | a0001 | c0001 | t0004 | g0048 | AFR | MSL | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG03453 | hp2 | a0001 | c0002 | t0013 | g0013 | AFR | MSL | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG03486 | hp1 | a0001 | c0002 | t0019 | g0104 | AFR | MSL | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG03486 | hp2 | a0001 | c0001 | t0004 | g0182 | AFR | MSL | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG03490 | hp1 | a0003 | c0007 | t0001 | g0005 | SAS | PJL | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0223 | SAS | PJL | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG03516 | hp1 | a0001 | c0001 | t0004 | g0181 | AFR | ESN | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG03516 | hp2 | a0001 | c0001 | t0015 | g0016 | AFR | ESN | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG03540 | hp1 | a0001 | c0001 | t0025 | g0169 | AFR | GWD | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG03540 | hp2 | a0001 | c0001 | t0004 | g0160 | AFR | GWD | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0147 | AFR | MSL | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG03579 | hp2 | a0001 | c0002 | t0003 | g0080 | AFR | MSL | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG03688 | hp1 | a0001 | c0002 | t0003 | g0002 | SAS | STU | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG03688 | hp2 | a0001 | c0001 | t0008 | g0173 | SAS | STU | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG03704 | hp1 | a0001 | c0001 | t0004 | g0189 | SAS | PJL | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG03704 | hp2 | a0001 | c0003 | t0006 | g0032 | SAS | PJL | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG03710 | hp1 | a0001 | c0001 | t0008 | g0024 | SAS | PJL | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG03831 | hp1 | a0001 | c0002 | t0003 | g0087 | SAS | BEB | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0011 | SAS | BEB | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG03834 | hp1 | a0001 | c0001 | t0008 | g0024 | SAS | BEB | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | BEB | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | BEB | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG03927 | hp2 | a0001 | c0001 | t0043 | g0021 | SAS | BEB | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG03942 | hp1 | a0001 | c0001 | t0038 | g0022 | SAS | BEB | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG03942 | hp2 | a0001 | c0003 | t0006 | g0031 | SAS | BEB | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG04115 | hp1 | a0001 | c0001 | t0017 | g0030 | SAS | STU | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG04115 | hp2 | a0001 | c0003 | t0006 | g0067 | SAS | STU | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG04184 | hp1 | a0001 | c0001 | t0004 | g0188 | SAS | BEB | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG04184 | hp2 | a0001 | c0002 | t0005 | g0244 | SAS | BEB | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | STU | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0198 | SAS | STU | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0113 | AFR | YRI | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18522 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | YRI | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | CHB | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18612 | hp2 | a0001 | c0002 | t0003 | g0075 | EAS | CHB | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | CHB | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18747 | hp2 | a0001 | c0002 | t0018 | g0023 | EAS | CHB | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18906 | hp1 | a0001 | c0001 | t0004 | g0038 | AFR | YRI | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18906 | hp2 | a0001 | c0002 | t0023 | g0106 | AFR | YRI | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18939 | hp2 | a0001 | c0002 | t0014 | g0034 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18940 | hp2 | a0001 | c0002 | t0010 | g0082 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18942 | hp1 | a0001 | c0001 | t0046 | g0022 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18943 | hp1 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18943 | hp2 | a0001 | c0002 | t0003 | g0077 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18944 | hp1 | a0001 | c0002 | t0010 | g0036 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18944 | hp2 | a0001 | c0002 | t0003 | g0008 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18946 | hp2 | a0001 | c0002 | t0003 | g0094 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18947 | hp2 | a0001 | c0002 | t0032 | g0002 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18950 | hp1 | a0001 | c0002 | t0014 | g0095 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18952 | hp1 | a0001 | c0002 | t0003 | g0008 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18956 | hp1 | a0001 | c0001 | t0024 | g0202 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18957 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18959 | hp2 | a0001 | c0002 | t0031 | g0014 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18960 | hp1 | a0001 | c0002 | t0029 | g0035 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18960 | hp2 | a0001 | c0001 | t0011 | g0052 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18961 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18962 | hp2 | a0001 | c0002 | t0003 | g0091 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18964 | hp2 | a0001 | c0001 | t0011 | g0001 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18965 | hp2 | a0001 | c0002 | t0003 | g0167 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18967 | hp2 | a0001 | c0002 | t0014 | g0076 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18968 | hp2 | a0001 | c0002 | t0003 | g0014 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18969 | hp1 | a0001 | c0002 | t0010 | g0002 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18971 | hp1 | a0001 | c0002 | t0003 | g0014 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18972 | hp2 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18973 | hp2 | a0001 | c0002 | t0018 | g0023 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18975 | hp1 | a0001 | c0002 | t0003 | g0074 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18975 | hp2 | a0001 | c0001 | t0011 | g0001 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18979 | hp1 | a0001 | c0001 | t0004 | g0025 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18982 | hp2 | a0001 | c0002 | t0010 | g0002 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18983 | hp1 | a0001 | c0001 | t0011 | g0001 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18983 | hp2 | a0001 | c0002 | t0003 | g0037 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18984 | hp1 | a0001 | c0005 | t0012 | g0007 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18984 | hp2 | a0001 | c0002 | t0003 | g0099 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18990 | hp1 | a0004 | c0008 | t0003 | g0002 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18991 | hp1 | a0001 | c0002 | t0009 | g0004 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18991 | hp2 | a0001 | c0002 | t0010 | g0002 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18992 | hp2 | a0001 | c0001 | t0011 | g0001 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18993 | hp1 | a0001 | c0005 | t0012 | g0007 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18994 | hp2 | a0001 | c0002 | t0005 | g0240 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18998 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA18999 | hp2 | a0001 | c0002 | t0003 | g0008 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19000 | hp1 | a0001 | c0002 | t0014 | g0098 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19000 | hp2 | a0001 | c0002 | t0010 | g0102 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19004 | hp1 | a0001 | c0002 | t0003 | g0037 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19005 | hp1 | a0001 | c0002 | t0010 | g0002 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19007 | hp1 | a0001 | c0002 | t0003 | g0014 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19009 | hp1 | a0001 | c0005 | t0012 | g0007 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19009 | hp2 | a0001 | c0001 | t0011 | g0001 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19030 | hp1 | a0001 | c0004 | t0007 | g0195 | AFR | LWK | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | LWK | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | LWK | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19043 | hp2 | a0001 | c0001 | t0004 | g0115 | AFR | LWK | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19055 | hp1 | a0001 | c0001 | t0011 | g0224 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19055 | hp2 | a0001 | c0001 | t0004 | g0186 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19056 | hp2 | a0001 | c0002 | t0003 | g0085 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19058 | hp2 | a0001 | c0002 | t0003 | g0035 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19062 | hp2 | a0001 | c0005 | t0012 | g0007 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19063 | hp2 | a0001 | c0002 | t0003 | g0083 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19064 | hp1 | a0001 | c0002 | t0003 | g0008 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19066 | hp1 | a0001 | c0003 | t0036 | g0063 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19068 | hp1 | a0001 | c0002 | t0009 | g0004 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19070 | hp1 | a0001 | c0005 | t0012 | g0007 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19072 | hp1 | a0001 | c0002 | t0003 | g0089 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19074 | hp2 | a0001 | c0002 | t0003 | g0093 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19075 | hp2 | a0001 | c0002 | t0003 | g0084 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19077 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19078 | hp2 | a0001 | c0001 | t0024 | g0201 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19080 | hp1 | a0001 | c0002 | t0003 | g0090 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19084 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19084 | hp2 | a0001 | c0005 | t0012 | g0007 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19089 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19089 | hp2 | a0001 | c0002 | t0003 | g0092 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19090 | hp1 | a0001 | c0001 | t0011 | g0052 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19240 | hp1 | a0001 | c0002 | t0016 | g0055 | AFR | YRI | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA19240 | hp2 | a0001 | c0002 | t0013 | g0013 | AFR | YRI | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA20129 | hp1 | a0001 | c0001 | t0004 | g0190 | AFR | ASW | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | ASW | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA20752 | hp1 | a0001 | c0001 | t0004 | g0179 | EUR | TSI | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA20752 | hp2 | a0001 | c0002 | t0005 | g0058 | EUR | TSI | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA20905 | hp1 | a0001 | c0003 | t0006 | g0061 | SAS | GIH | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA20905 | hp2 | a0001 | c0001 | t0008 | g0024 | SAS | GIH | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG01123 | hp2 | a0001 | c0001 | t0039 | g0206 | AMR | CLM | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02109 | hp1 | a0001 | c0002 | t0005 | g0029 | AFR | ACB | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02109 | hp2 | a0001 | c0002 | t0023 | g0107 | AFR | ACB | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02486 | hp1 | a0001 | c0002 | t0020 | g0056 | AFR | ACB | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02486 | hp2 | a0001 | c0004 | t0007 | g0049 | AFR | ACB | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0199 | AFR | ACB | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG02559 | hp2 | a0001 | c0001 | t0008 | g0177 | AFR | ACB | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG03471 | hp1 | a0001 | c0004 | t0007 | g0015 | AFR | MSL | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG03471 | hp2 | a0001 | c0002 | t0013 | g0013 | AFR | MSL | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG06807 | hp1 | a0001 | c0004 | t0007 | g0164 | AFR | USA | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
HG06807 | hp2 | a0001 | c0002 | t0027 | g0070 | AFR | USA | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA20300 | hp1 | a0001 | c0001 | t0004 | g0026 | AFR | USA | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA20300 | hp2 | a0001 | c0004 | t0007 | g0015 | AFR | USA | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA21309 | hp1 | a0001 | c0001 | t0015 | g0170 | AFR | LWK | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
NA21309 | hp2 | a0001 | c0001 | t0004 | g0191 | AFR | LWK | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
homoSapiens | chm13v2 | a0001 | c0001 | t0048 | g0059 | REF | REF | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0144 | REF | REF | C6orf89_chr6_36880952_36933964 | C6orf89 | chr6 | 36880952 | 36933964 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:36914322 | G | C | 1 | a0002 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.442G>C | p.Glu148Gln | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 5/9 | 638/6763 | 442/1044 | 148/347 | chr6 | 36914322 | |||
chr6:36923391 | G | A | 1 | a0004 | 1 | NA18990.hp1 | missense_variant | MODERATE | c.994G>A | p.Gly332Arg | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 1190/6763 | 994/1044 | 332/347 | chr6 | 36923391 | |||
chr6:36923394 | G | A | 1 | a0003 | 1 | HG03490.hp1 | missense_variant | MODERATE | c.997G>A | p.Val333Ile | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 1193/6763 | 997/1044 | 333/347 | chr6 | 36923394 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:36899600 | C | T | 1 | a0001c0005 | 7 | HG01261.hp2 NA18984.hp1 NA18993.hp1 others(4): Show |
synonymous_variant | LOW | c.156C>T | p.Pro52Pro | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/9 | 352/6763 | 156/1044 | 52/347 | chr6 | 36899600 | |||
chr6:36914577 | A | G | 4 | a0001c0002 a0001c0003 a0002c0006 others(1): Show |
132 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(129): Show |
synonymous_variant | LOW | c.579A>G | p.Glu193Glu | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 6/9 | 775/6763 | 579/1044 | 193/347 | chr6 | 36914577 | |||
chr6:36919700 | C | T | 2 | a0001c0003 a0001c0004 |
34 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(31): Show |
splice_region_variant&synonymous_variant | LOW | c.948C>T | p.Ile316Ile | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 8/9 | 1144/6763 | 948/1044 | 316/347 | chr6 | 36919700 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:36886008 | C | T | 1 | a0001c0001t0026 | 2 | HG02965.hp1 HG03041.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-140C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/9 | chr6 | 36886008 | |||||||
chr6:36923532 | G | A | 1 | a0001c0001t0026 | 2 | HG02965.hp1 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*91G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 91 | chr6 | 36923532 | ||||||
chr6:36923706 | C | T | 2 | a0001c0002t0010 a0001c0002t0047 |
11 | HG00597.hp1 HG00673.hp2 HG02015.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*265C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 265 | chr6 | 36923706 | ||||||
chr6:36923868 | T | C | 29 | a0001c0002t0003 a0001c0002t0005 a0001c0002t0009 others(26): Show |
146 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(143): Show |
3_prime_UTR_variant | MODIFIER | c.*427T>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 427 | chr6 | 36923868 | ||||||
chr6:36923948 | G | T | 1 | a0001c0001t0046 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*507G>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 507 | chr6 | 36923948 | ||||||
chr6:36924004 | A | G | 1 | a0001c0002t0023 | 2 | HG02109.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*563A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 563 | chr6 | 36924004 | ||||||
chr6:36924167 | G | A | 1 | a0001c0002t0027 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*726G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 726 | chr6 | 36924167 | ||||||
chr6:36924340 | T | C | 2 | a0001c0002t0016 a0001c0002t0028 |
5 | HG02615.hp1 HG02622.hp2 HG02809.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*899T>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 899 | chr6 | 36924340 | ||||||
chr6:36924445 | A | G | 29 | a0001c0002t0003 a0001c0002t0005 a0001c0002t0009 others(26): Show |
146 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(143): Show |
3_prime_UTR_variant | MODIFIER | c.*1004A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 1004 | chr6 | 36924445 | ||||||
chr6:36924755 | C | G | 1 | a0001c0002t0037 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1314C>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 1314 | chr6 | 36924755 | ||||||
chr6:36924795 | C | G | 3 | a0001c0002t0005 a0001c0002t0009 a0002c0006t0009 |
29 | HG00140.hp1 HG00735.hp2 HG01074.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1354C>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 1354 | chr6 | 36924795 | ||||||
chr6:36924896 | C | A | 1 | a0001c0002t0029 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1455C>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 1455 | chr6 | 36924896 | ||||||
chr6:36925001 | T | C | 1 | a0001c0002t0023 | 2 | HG02109.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1560T>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 1560 | chr6 | 36925001 | ||||||
chr6:36925026 | G | C | 1 | a0001c0002t0029 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1585G>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 1585 | chr6 | 36925026 | ||||||
chr6:36925063 | A | AT | 29 | a0001c0002t0003 a0001c0002t0005 a0001c0002t0009 others(26): Show |
146 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(143): Show |
3_prime_UTR_variant | MODIFIER | c.*1628dupT | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 1629 | INFO_REALIGN_3_PRIME | chr6 | 36925063 | |||||
chr6:36925252 | G | A | 1 | a0001c0001t0008 | 12 | HG01496.hp1 HG01884.hp1 HG01891.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1811G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 1811 | chr6 | 36925252 | ||||||
chr6:36925307 | A | G | 32 | a0001c0001t0015 a0001c0001t0025 a0001c0001t0026 others(29): Show |
155 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(152): Show |
3_prime_UTR_variant | MODIFIER | c.*1866A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 1866 | chr6 | 36925307 | ||||||
chr6:36925470 | C | T | 1 | a0001c0001t0017 | 4 | HG01106.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2029C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 2029 | chr6 | 36925470 | ||||||
chr6:36925498 | A | G | 1 | a0001c0001t0025 | 2 | HG03195.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2057A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 2057 | chr6 | 36925498 | ||||||
chr6:36925685 | G | C | 1 | a0001c0001t0026 | 2 | HG02965.hp1 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2244G>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 2244 | chr6 | 36925685 | ||||||
chr6:36925762 | G | A | 2 | a0001c0002t0018 a0001c0002t0030 |
4 | HG00544.hp2 HG02071.hp1 NA18747.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2321G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 2321 | chr6 | 36925762 | ||||||
chr6:36925830 | C | T | 1 | a0001c0001t0024 | 2 | NA18956.hp1 NA19078.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2389C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 2389 | chr6 | 36925830 | ||||||
chr6:36925843 | A | T | 25 | a0001c0002t0003 a0001c0002t0005 a0001c0002t0009 others(22): Show |
136 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*2402A>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 2402 | chr6 | 36925843 | ||||||
chr6:36925983 | C | T | 1 | a0001c0003t0036 | 1 | NA19066.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2542C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 2542 | chr6 | 36925983 | ||||||
chr6:36925998 | G | T | 1 | a0001c0003t0022 | 2 | HG00735.hp1 HG01255.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2557G>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 2557 | chr6 | 36925998 | ||||||
chr6:36926058 | G | A | 1 | a0001c0001t0026 | 2 | HG02965.hp1 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2617G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 2617 | chr6 | 36926058 | ||||||
chr6:36926099 | G | T | 3 | a0001c0003t0006 a0001c0003t0022 a0001c0003t0036 |
20 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2658G>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 2658 | chr6 | 36926099 | ||||||
chr6:36926219 | G | A | 2 | a0001c0002t0013 a0001c0002t0037 |
6 | HG02055.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2778G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 2778 | chr6 | 36926219 | ||||||
chr6:36926242 | A | G | 1 | a0001c0001t0026 | 2 | HG02965.hp1 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2801A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 2801 | chr6 | 36926242 | ||||||
chr6:36926408 | C | T | 2 | a0001c0001t0015 a0001c0001t0025 |
7 | HG02647.hp1 HG03130.hp2 HG03195.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2967C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 2967 | chr6 | 36926408 | ||||||
chr6:36926472 | G | A | 2 | a0001c0002t0009 a0002c0006t0009 |
10 | HG00735.hp2 HG01261.hp1 HG01346.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3031G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 3031 | chr6 | 36926472 | ||||||
chr6:36926494 | C | G | 1 | a0001c0002t0047 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3053C>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 3053 | chr6 | 36926494 | ||||||
chr6:36926549 | G | GA | 1 | a0001c0005t0012 | 7 | HG01261.hp2 NA18984.hp1 NA18993.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3119dupA | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 3120 | INFO_REALIGN_3_PRIME | chr6 | 36926549 | |||||
chr6:36926559 | AAGAG | A | 26 | a0001c0002t0003 a0001c0002t0005 a0001c0002t0009 others(23): Show |
139 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(136): Show |
3_prime_UTR_variant | MODIFIER | c.*3126_*3129delGAGA | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 3126 | INFO_REALIGN_3_PRIME | chr6 | 36926559 | |||||
chr6:36926559 | AAGAGAGA others(1): Show |
A | 3 | a0001c0002t0013 a0001c0002t0031 a0001c0002t0037 |
7 | HG02055.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3122_*3129delGAGA others(4): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 3122 | INFO_REALIGN_3_PRIME | chr6 | 36926559 | |||||
chr6:36926592 | AAAGGG | A | 24 | a0001c0002t0003 a0001c0002t0010 a0001c0002t0013 others(21): Show |
115 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*3158_*3162delAGGG others(1): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 3158 | INFO_REALIGN_3_PRIME | chr6 | 36926592 | |||||
chr6:36926593 | A | AGGGGAGG others(2): Show |
4 | a0001c0002t0005 a0001c0002t0009 a0001c0002t0030 others(1): Show |
29 | HG00140.hp1 HG00735.hp2 HG01074.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*3152_*3153insGGGG others(5): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 3153 | chr6 | 36926593 | ||||||
chr6:36926594 | A | G | 3 | a0001c0001t0015 a0001c0001t0025 a0001c0001t0026 |
9 | HG02647.hp1 HG02965.hp1 HG03041.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3153A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 3153 | chr6 | 36926594 | ||||||
chr6:36926599 | A | AG | 4 | a0001c0002t0005 a0001c0002t0009 a0001c0002t0030 others(1): Show |
30 | HG00140.hp1 HG00735.hp2 HG01074.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*3161dupG | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 3162 | INFO_REALIGN_3_PRIME | chr6 | 36926599 | |||||
chr6:36926599 | A | G | 25 | a0001c0002t0003 a0001c0002t0010 a0001c0002t0013 others(22): Show |
116 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*3158A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 3158 | chr6 | 36926599 | ||||||
chr6:36926601 | G | A | 1 | a0001c0001t0038 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3160G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 3160 | chr6 | 36926601 | ||||||
chr6:36926607 | G | A | 1 | a0001c0002t0032 | 1 | NA18947.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3166G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 3166 | chr6 | 36926607 | ||||||
chr6:36926637 | G | T | 2 | a0001c0002t0016 a0001c0002t0028 |
5 | HG02615.hp1 HG02622.hp2 HG02809.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3196G>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 3196 | chr6 | 36926637 | ||||||
chr6:36926665 | G | A | 29 | a0001c0002t0003 a0001c0002t0005 a0001c0002t0009 others(26): Show |
146 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(143): Show |
3_prime_UTR_variant | MODIFIER | c.*3224G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 3224 | chr6 | 36926665 | ||||||
chr6:36926680 | A | G | 1 | a0001c0001t0011 | 8 | NA18960.hp2 NA18964.hp2 NA18975.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3239A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 3239 | chr6 | 36926680 | ||||||
chr6:36926901 | T | C | 43 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0008 others(40): Show |
305 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(302): Show |
3_prime_UTR_variant | MODIFIER | c.*3460T>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 3460 | chr6 | 36926901 | ||||||
chr6:36926909 | G | A | 26 | a0001c0002t0003 a0001c0002t0005 a0001c0002t0009 others(23): Show |
135 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*3468G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 3468 | chr6 | 36926909 | ||||||
chr6:36926935 | A | C | 1 | a0001c0001t0042 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3494A>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 3494 | chr6 | 36926935 | ||||||
chr6:36926951 | C | T | 1 | a0001c0002t0016 | 4 | HG02622.hp2 HG02809.hp1 HG02896.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3510C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 3510 | chr6 | 36926951 | ||||||
chr6:36927074 | A | G | 1 | a0001c0001t0041 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3633A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 3633 | chr6 | 36927074 | ||||||
chr6:36927202 | A | T | 1 | a0001c0001t0040 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3761A>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 3761 | chr6 | 36927202 | ||||||
chr6:36927356 | G | A | 1 | a0001c0001t0043 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3915G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 3915 | chr6 | 36927356 | ||||||
chr6:36927445 | C | T | 1 | a0001c0002t0035 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4004C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 4004 | chr6 | 36927445 | ||||||
chr6:36927566 | A | G | 1 | a0001c0002t0013 | 5 | HG02922.hp2 HG02965.hp2 HG03453.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4125A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 4125 | chr6 | 36927566 | ||||||
chr6:36927613 | C | T | 1 | a0001c0002t0021 | 2 | HG01361.hp1 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4172C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 4172 | chr6 | 36927613 | ||||||
chr6:36927752 | G | A | 5 | a0001c0002t0019 a0001c0002t0020 a0001c0002t0021 others(2): Show |
9 | HG01361.hp1 HG02451.hp1 HG02451.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4311G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 4311 | chr6 | 36927752 | ||||||
chr6:36927764 | A | G | 9 | a0001c0001t0045 a0001c0002t0003 a0001c0002t0010 others(6): Show |
57 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*4323A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 4323 | chr6 | 36927764 | ||||||
chr6:36927942 | G | T | 1 | a0001c0001t0044 | 1 | HG01069.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4501G>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 4501 | chr6 | 36927942 | ||||||
chr6:36927967 | G | C | 1 | a0001c0002t0023 | 2 | HG02109.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4526G>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 4526 | chr6 | 36927967 | ||||||
chr6:36928059 | C | T | 29 | a0001c0002t0003 a0001c0002t0005 a0001c0002t0009 others(26): Show |
146 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(143): Show |
3_prime_UTR_variant | MODIFIER | c.*4618C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 4618 | chr6 | 36928059 | ||||||
chr6:36928095 | C | T | 1 | a0001c0002t0020 | 2 | HG02486.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4654C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 4654 | chr6 | 36928095 | ||||||
chr6:36928262 | G | A | 1 | a0001c0004t0034 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4821G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 4821 | chr6 | 36928262 | ||||||
chr6:36928359 | A | G | 2 | a0001c0002t0016 a0001c0002t0028 |
5 | HG02615.hp1 HG02622.hp2 HG02809.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4918A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 4918 | chr6 | 36928359 | ||||||
chr6:36928416 | TACTC | T | 3 | a0001c0001t0015 a0001c0001t0025 a0001c0002t0019 |
10 | HG02630.hp1 HG02647.hp1 HG03130.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4978_*4981delTCAC | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 4978 | INFO_REALIGN_3_PRIME | chr6 | 36928416 | |||||
chr6:36928454 | C | G | 1 | a0001c0001t0026 | 2 | HG02965.hp1 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5013C>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 5013 | chr6 | 36928454 | ||||||
chr6:36928655 | G | A | 1 | a0001c0001t0039 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5214G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 5214 | chr6 | 36928655 | ||||||
chr6:36928661 | T | G | 41 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0011 others(38): Show |
263 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(260): Show |
3_prime_UTR_variant | MODIFIER | c.*5220T>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 5220 | chr6 | 36928661 | ||||||
chr6:36928696 | G | A | 1 | a0001c0001t0026 | 2 | HG02965.hp1 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5255G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 9/9 | 5255 | chr6 | 36928696 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:36886293 | G | T | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | NA18965.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.-120+265G>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36886293 | |||||||
chr6:36886319 | A | G | 1 | a0001c0004t0007g0245 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-120+291A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36886319 | |||||||
chr6:36886328 | G | C | 67 | a0001c0001t0002g0018 a0001c0001t0002g0072 a0001c0001t0002g0079 others(64): Show |
94 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.-120+300G>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36886328 | |||||||
chr6:36886907 | C | T | 1 | a0001c0002t0003g0037 | 2 | NA18983.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.-120+879C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36886907 | |||||||
chr6:36886917 | A | G | 68 | a0001c0001t0001g0218 a0001c0001t0001g0222 a0001c0001t0002g0001 others(65): Show |
122 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.-120+889A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36886917 | |||||||
chr6:36886992 | CAAGACCT others(6): Show |
C | 2 | a0001c0001t0026g0196 a0001c0001t0026g0197 |
2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-120+967_-120+979d others(15): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr6 | 36886992 | ||||||
chr6:36887110 | C | G | 4 | a0001c0002t0019g0104 a0001c0002t0019g0105 a0001c0002t0023g0106 others(1): Show |
4 | HG02109.hp2 HG02630.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-120+1082C>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36887110 | |||||||
chr6:36887119 | G | GT | 28 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0002g0242 others(25): Show |
44 | HG00733.hp1 HG01261.hp2 HG01346.hp1 others(41): Show |
intron_variant | MODIFIER | c.-120+1104dupT | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr6 | 36887119 | ||||||
chr6:36887119 | G | T | 1 | a0001c0002t0037g0103 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-120+1091G>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36887119 | |||||||
chr6:36887135 | G | T | 1 | a0001c0002t0037g0103 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-120+1107G>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36887135 | |||||||
chr6:36887207 | C | T | 1 | a0001c0001t0042g0241 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-120+1179C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36887207 | |||||||
chr6:36887315 | A | G | 4 | a0001c0001t0008g0174 a0001c0001t0008g0175 a0001c0001t0008g0176 others(1): Show |
4 | HG02145.hp1 HG02559.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-120+1287A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36887315 | |||||||
chr6:36887398 | G | A | 2 | a0001c0001t0026g0196 a0001c0001t0026g0197 |
2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-120+1370G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36887398 | |||||||
chr6:36887606 | G | C | 68 | a0001c0001t0001g0218 a0001c0001t0001g0222 a0001c0001t0002g0001 others(65): Show |
122 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.-120+1578G>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36887606 | |||||||
chr6:36887608 | A | G | 17 | a0001c0002t0005g0004 a0001c0002t0005g0028 a0001c0002t0005g0029 others(14): Show |
28 | HG00140.hp1 HG00735.hp2 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.-120+1580A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36887608 | |||||||
chr6:36887640 | T | G | 1 | a0001c0001t0008g0174 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-120+1612T>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36887640 | |||||||
chr6:36887843 | A | G | 1 | a0001c0001t0001g0050 | 2 | HG00642.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.-120+1815A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36887843 | |||||||
chr6:36887947 | A | G | 5 | a0001c0001t0008g0024 a0001c0001t0008g0173 a0001c0001t0026g0196 others(2): Show |
7 | HG02572.hp2 HG02965.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.-120+1919A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36887947 | |||||||
chr6:36887966 | C | G | 2 | a0001c0002t0018g0023 a0001c0002t0030g0171 |
4 | HG00544.hp2 HG02071.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.-120+1938C>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36887966 | |||||||
chr6:36887982 | C | T | 2 | a0001c0002t0018g0023 a0001c0002t0030g0171 |
4 | HG00544.hp2 HG02071.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.-120+1954C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36887982 | |||||||
chr6:36888090 | A | G | 2 | a0001c0001t0002g0057 a0001c0001t0002g0229 |
3 | NA18950.hp2 NA18972.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.-120+2062A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36888090 | |||||||
chr6:36888354 | G | A | 9 | a0001c0002t0005g0004 a0001c0002t0005g0233 a0001c0002t0005g0236 others(6): Show |
15 | HG00140.hp1 HG00735.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.-120+2326G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36888354 | |||||||
chr6:36888505 | G | A | 3 | a0001c0001t0008g0024 a0001c0001t0008g0173 a0001c0002t0035g0172 |
5 | HG02572.hp2 HG03688.hp2 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.-120+2477G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36888505 | |||||||
chr6:36888566 | A | G | 146 | a0001c0001t0001g0218 a0001c0001t0001g0222 a0001c0001t0002g0001 others(143): Show |
234 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.-120+2538A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36888566 | |||||||
chr6:36888620 | G | A | 2 | a0001c0001t0026g0196 a0001c0001t0026g0197 |
2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-120+2592G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36888620 | |||||||
chr6:36888655 | G | A | 45 | a0001c0001t0001g0218 a0001c0001t0001g0222 a0001c0001t0002g0001 others(42): Show |
86 | HG00438.hp2 HG00558.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.-120+2627G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36888655 | |||||||
chr6:36888681 | G | A | 4 | a0001c0001t0004g0025 a0001c0001t0004g0178 a0001c0001t0004g0179 others(1): Show |
6 | HG01346.hp1 HG01358.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.-120+2653G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36888681 | |||||||
chr6:36888743 | A | G | 1 | a0001c0003t0006g0100 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-120+2715A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36888743 | |||||||
chr6:36888862 | A | G | 5 | a0001c0001t0008g0024 a0001c0001t0008g0173 a0001c0001t0026g0196 others(2): Show |
7 | HG02572.hp2 HG02965.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.-120+2834A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36888862 | |||||||
chr6:36888870 | A | C | 1 | a0001c0002t0003g0099 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-120+2842A>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36888870 | |||||||
chr6:36888963 | C | T | 138 | a0001c0001t0001g0218 a0001c0001t0001g0222 a0001c0001t0002g0001 others(135): Show |
221 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.-120+2935C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36888963 | |||||||
chr6:36888966 | A | T | 42 | a0001c0001t0002g0018 a0001c0001t0002g0079 a0001c0001t0002g0096 others(39): Show |
62 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.-120+2938A>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36888966 | |||||||
chr6:36889057 | G | C | 3 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 |
3 | HG01257.hp1 HG01943.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.-120+3029G>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36889057 | |||||||
chr6:36889143 | C | T | 1 | a0001c0002t0014g0098 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-120+3115C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36889143 | |||||||
chr6:36889144 | G | A | 5 | a0001c0001t0004g0006 a0001c0001t0004g0181 a0001c0001t0004g0182 others(2): Show |
10 | HG00733.hp1 HG01884.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.-120+3116G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36889144 | |||||||
chr6:36889181 | G | A | 6 | a0001c0002t0013g0013 a0001c0002t0013g0060 a0001c0002t0019g0104 others(3): Show |
9 | HG02109.hp2 HG02630.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.-120+3153G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36889181 | |||||||
chr6:36889197 | G | A | 2 | a0001c0002t0018g0023 a0001c0002t0030g0171 |
4 | HG00544.hp2 HG02071.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.-120+3169G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36889197 | |||||||
chr6:36889309 | G | T | 1 | a0001c0002t0005g0029 | 3 | HG02109.hp1 HG02258.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.-120+3281G>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36889309 | |||||||
chr6:36889391 | C | G | 2 | a0001c0002t0013g0013 a0001c0002t0013g0060 |
5 | HG02922.hp2 HG02965.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.-120+3363C>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36889391 | |||||||
chr6:36889422 | A | G | 2 | a0001c0002t0018g0023 a0001c0002t0030g0171 |
4 | HG00544.hp2 HG02071.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.-120+3394A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36889422 | |||||||
chr6:36889453 | G | A | 1 | a0001c0002t0009g0230 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-120+3425G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36889453 | |||||||
chr6:36889510 | A | C | 20 | a0001c0002t0005g0004 a0001c0002t0005g0028 a0001c0002t0005g0029 others(17): Show |
32 | HG00140.hp1 HG00735.hp2 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.-120+3482A>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36889510 | |||||||
chr6:36889582 | C | CAAAAAAA | 58 | a0001c0001t0002g0079 a0001c0002t0003g0002 a0001c0002t0003g0008 others(55): Show |
91 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.-120+3559_-120+356 others(11): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr6 | 36889582 | ||||||
chr6:36889582 | C | CAAAAAAA others(1): Show |
24 | a0001c0002t0003g0073 a0001c0002t0003g0074 a0001c0002t0003g0167 others(21): Show |
27 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.-120+3558_-120+356 others(12): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr6 | 36889582 | ||||||
chr6:36889582 | C | CAAAAAAA others(4): Show |
2 | a0001c0001t0026g0196 a0001c0001t0026g0197 |
2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-120+3555_-120+356 others(15): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr6 | 36889582 | ||||||
chr6:36889588 | A | C | 6 | a0001c0001t0001g0165 a0001c0004t0007g0049 a0001c0004t0007g0163 others(3): Show |
7 | HG01255.hp1 HG02280.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-120+3560A>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36889588 | |||||||
chr6:36889724 | T | G | 1 | a0001c0001t0001g0108 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-120+3696T>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36889724 | |||||||
chr6:36889820 | G | A | 96 | a0001c0001t0002g0079 a0001c0001t0025g0168 a0001c0001t0025g0169 others(93): Show |
136 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.-120+3792G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36889820 | |||||||
chr6:36889829 | C | T | 2 | a0001c0001t0025g0168 a0001c0001t0025g0169 |
2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-120+3801C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36889829 | |||||||
chr6:36890170 | A | G | 23 | a0001c0002t0005g0004 a0001c0002t0005g0028 a0001c0002t0005g0029 others(20): Show |
35 | HG00140.hp1 HG00735.hp2 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.-120+4142A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36890170 | |||||||
chr6:36890216 | T | C | 2 | a0001c0001t0026g0196 a0001c0001t0026g0197 |
2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-120+4188T>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36890216 | |||||||
chr6:36890217 | G | A | 88 | a0001c0001t0002g0079 a0001c0002t0003g0002 a0001c0002t0003g0008 others(85): Show |
125 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.-120+4189G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36890217 | |||||||
chr6:36890318 | C | A | 1 | a0001c0001t0004g0038 | 2 | HG02717.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-119-4186C>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36890318 | |||||||
chr6:36890390 | C | T | 39 | a0001c0001t0002g0079 a0001c0002t0003g0002 a0001c0002t0003g0008 others(36): Show |
57 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.-119-4114C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36890390 | |||||||
chr6:36890438 | G | A | 2 | a0001c0002t0018g0023 a0001c0002t0030g0171 |
4 | HG00544.hp2 HG02071.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.-119-4066G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36890438 | |||||||
chr6:36890447 | G | T | 1 | a0001c0002t0021g0228 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-119-4057G>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36890447 | |||||||
chr6:36890529 | TA | T | 5 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0002g0223 others(2): Show |
5 | HG03490.hp2 HG03540.hp1 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.-119-3965delA | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr6 | 36890529 | ||||||
chr6:36890539 | A | AT | 87 | a0001c0001t0002g0079 a0001c0002t0003g0002 a0001c0002t0003g0008 others(84): Show |
123 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.-119-3961dupT | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr6 | 36890539 | ||||||
chr6:36890638 | A | G | 4 | a0001c0002t0021g0228 a0001c0002t0027g0070 a0001c0002t0033g0227 others(1): Show |
4 | HG01361.hp1 HG02451.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.-119-3866A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36890638 | |||||||
chr6:36890900 | G | A | 4 | a0001c0002t0021g0228 a0001c0002t0027g0070 a0001c0002t0033g0227 others(1): Show |
4 | HG01361.hp1 HG02451.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.-119-3604G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36890900 | |||||||
chr6:36890917 | G | T | 2 | a0001c0001t0026g0196 a0001c0001t0026g0197 |
2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-119-3587G>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36890917 | |||||||
chr6:36890989 | ACTTTTT | A | 73 | a0001c0001t0001g0218 a0001c0001t0002g0001 a0001c0001t0002g0009 others(70): Show |
123 | HG00438.hp2 HG00558.hp2 HG00597.hp2 others(120): Show |
intron_variant | MODIFIER | c.-119-3508_-119-350 others(10): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr6 | 36890989 | ||||||
chr6:36891101 | C | T | 2 | a0001c0005t0012g0007 a0001c0005t0012g0194 |
7 | HG01261.hp2 NA18984.hp1 NA18993.hp1 others(4): Show |
intron_variant | MODIFIER | c.-119-3403C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36891101 | |||||||
chr6:36891148 | C | A | 1 | a0001c0001t0002g0198 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-119-3356C>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36891148 | |||||||
chr6:36891247 | G | T | 1 | a0001c0001t0011g0224 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-119-3257G>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36891247 | |||||||
chr6:36891262 | C | G | 5 | a0001c0002t0020g0056 a0001c0002t0021g0228 a0001c0002t0027g0070 others(2): Show |
6 | HG01361.hp1 HG02451.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-119-3242C>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36891262 | |||||||
chr6:36891276 | A | G | 2 | a0001c0002t0019g0111 a0001c0002t0037g0103 |
2 | HG02055.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-119-3228A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36891276 | |||||||
chr6:36891428 | A | G | 1 | a0001c0002t0020g0056 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-119-3076A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36891428 | |||||||
chr6:36891435 | A | G | 5 | a0001c0002t0020g0056 a0001c0002t0021g0228 a0001c0002t0027g0070 others(2): Show |
6 | HG01361.hp1 HG02451.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-119-3069A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36891435 | |||||||
chr6:36891529 | C | G | 1 | a0001c0001t0002g0072 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-119-2975C>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36891529 | |||||||
chr6:36891661 | A | G | 2 | a0001c0002t0018g0023 a0001c0002t0030g0171 |
4 | HG00544.hp2 HG02071.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.-119-2843A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36891661 | |||||||
chr6:36891664 | C | T | 1 | a0001c0002t0010g0036 | 2 | HG00673.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.-119-2840C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36891664 | |||||||
chr6:36891665 | A | G | 4 | a0001c0002t0016g0055 a0001c0002t0016g0225 a0001c0002t0016g0226 others(1): Show |
5 | HG02615.hp1 HG02622.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-119-2839A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36891665 | |||||||
chr6:36891667 | A | G | 2 | a0001c0001t0004g0048 a0001c0001t0004g0160 |
3 | HG02922.hp1 HG03453.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-119-2837A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36891667 | |||||||
chr6:36891781 | T | G | 1 | a0001c0001t0004g0121 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-119-2723T>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36891781 | |||||||
chr6:36891907 | G | C | 88 | a0001c0001t0002g0079 a0001c0002t0003g0002 a0001c0002t0003g0008 others(85): Show |
125 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.-119-2597G>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36891907 | |||||||
chr6:36891961 | T | C | 9 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0178 others(6): Show |
13 | HG01346.hp1 HG01358.hp1 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.-119-2543T>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36891961 | |||||||
chr6:36891996 | C | G | 2 | a0001c0002t0018g0023 a0001c0002t0030g0171 |
4 | HG00544.hp2 HG02071.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.-119-2508C>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36891996 | |||||||
chr6:36892153 | C | A | 5 | a0001c0002t0020g0056 a0001c0002t0021g0228 a0001c0002t0027g0070 others(2): Show |
6 | HG01361.hp1 HG02451.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-119-2351C>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36892153 | |||||||
chr6:36892201 | C | T | 2 | a0001c0001t0025g0168 a0001c0001t0025g0169 |
2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-119-2303C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36892201 | |||||||
chr6:36892204 | C | T | 2 | a0001c0002t0005g0028 a0001c0002t0005g0239 |
4 | HG01106.hp2 HG01168.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.-119-2300C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36892204 | |||||||
chr6:36892290 | CTT | C | 2 | a0001c0002t0018g0023 a0001c0002t0030g0171 |
4 | HG00544.hp2 HG02071.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.-119-2212_-119-221 others(6): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr6 | 36892290 | ||||||
chr6:36892316 | C | T | 81 | a0001c0001t0002g0079 a0001c0002t0003g0002 a0001c0002t0003g0008 others(78): Show |
115 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.-119-2188C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36892316 | |||||||
chr6:36892341 | T | A | 81 | a0001c0001t0002g0079 a0001c0002t0003g0002 a0001c0002t0003g0008 others(78): Show |
115 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.-119-2163T>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36892341 | |||||||
chr6:36892473 | C | G | 16 | a0001c0003t0006g0017 a0001c0003t0006g0031 a0001c0003t0006g0032 others(13): Show |
20 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.-119-2031C>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36892473 | |||||||
chr6:36892550 | A | G | 2 | a0001c0002t0018g0023 a0001c0002t0030g0171 |
4 | HG00544.hp2 HG02071.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.-119-1954A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36892550 | |||||||
chr6:36892611 | T | A | 1 | a0002c0006t0009g0232 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-119-1893T>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36892611 | |||||||
chr6:36892658 | A | G | 88 | a0001c0001t0002g0079 a0001c0002t0003g0002 a0001c0002t0003g0008 others(85): Show |
125 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.-119-1846A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36892658 | |||||||
chr6:36892811 | C | T | 1 | a0001c0001t0004g0160 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-119-1693C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36892811 | |||||||
chr6:36892896 | A | G | 2 | a0001c0002t0018g0023 a0001c0002t0030g0171 |
4 | HG00544.hp2 HG02071.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.-119-1608A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36892896 | |||||||
chr6:36892908 | T | C | 2 | a0001c0005t0012g0007 a0001c0005t0012g0194 |
7 | HG01261.hp2 NA18984.hp1 NA18993.hp1 others(4): Show |
intron_variant | MODIFIER | c.-119-1596T>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36892908 | |||||||
chr6:36892937 | AT | A | 65 | a0001c0001t0001g0122 a0001c0001t0002g0079 a0001c0002t0003g0002 others(62): Show |
91 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.-119-1552delT | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr6 | 36892937 | ||||||
chr6:36892937 | ATT | A | 18 | a0001c0002t0005g0004 a0001c0002t0005g0028 a0001c0002t0005g0029 others(15): Show |
29 | HG00140.hp1 HG00735.hp2 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.-119-1553_-119-155 others(6): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr6 | 36892937 | ||||||
chr6:36892974 | G | A | 16 | a0001c0003t0006g0017 a0001c0003t0006g0031 a0001c0003t0006g0032 others(13): Show |
20 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.-119-1530G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36892974 | |||||||
chr6:36893044 | C | T | 18 | a0001c0002t0005g0004 a0001c0002t0005g0028 a0001c0002t0005g0029 others(15): Show |
29 | HG00140.hp1 HG00735.hp2 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.-119-1460C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36893044 | |||||||
chr6:36893045 | C | T | 2 | a0001c0002t0013g0013 a0001c0002t0013g0060 |
5 | HG02922.hp2 HG02965.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.-119-1459C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36893045 | |||||||
chr6:36893058 | C | A | 1 | a0001c0002t0035g0172 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-119-1446C>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36893058 | |||||||
chr6:36893180 | C | T | 1 | a0001c0003t0006g0067 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-119-1324C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36893180 | |||||||
chr6:36893190 | T | C | 82 | a0001c0001t0002g0079 a0001c0002t0003g0002 a0001c0002t0003g0008 others(79): Show |
116 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.-119-1314T>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36893190 | |||||||
chr6:36893192 | C | A | 82 | a0001c0001t0002g0079 a0001c0002t0003g0002 a0001c0002t0003g0008 others(79): Show |
116 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.-119-1312C>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36893192 | |||||||
chr6:36893212 | G | A | 1 | a0001c0002t0020g0056 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-119-1292G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36893212 | |||||||
chr6:36893225 | C | T | 4 | a0001c0002t0016g0055 a0001c0002t0016g0225 a0001c0002t0016g0226 others(1): Show |
5 | HG02615.hp1 HG02622.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-119-1279C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36893225 | |||||||
chr6:36893229 | C | T | 1 | a0001c0002t0035g0172 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-119-1275C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36893229 | |||||||
chr6:36893307 | T | A | 82 | a0001c0001t0002g0079 a0001c0002t0003g0002 a0001c0002t0003g0008 others(79): Show |
116 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.-119-1197T>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36893307 | |||||||
chr6:36893328 | A | G | 2 | a0001c0002t0018g0023 a0001c0002t0030g0171 |
4 | HG00544.hp2 HG02071.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.-119-1176A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36893328 | |||||||
chr6:36893770 | A | G | 2 | a0001c0001t0002g0220 a0001c0001t0002g0221 |
2 | HG02083.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.-119-734A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36893770 | |||||||
chr6:36893939 | G | A | 2 | a0001c0001t0026g0196 a0001c0001t0026g0197 |
2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-119-565G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36893939 | |||||||
chr6:36893993 | C | T | 1 | a0001c0002t0014g0095 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-119-511C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36893993 | |||||||
chr6:36894005 | C | T | 4 | a0001c0002t0020g0056 a0001c0002t0021g0228 a0001c0002t0033g0227 others(1): Show |
5 | HG01361.hp1 HG02451.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-119-499C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36894005 | |||||||
chr6:36894023 | C | CA | 6 | a0001c0001t0001g0019 a0001c0001t0001g0123 a0001c0001t0004g0178 others(3): Show |
8 | HG00642.hp2 HG01109.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.-119-466dupA | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr6 | 36894023 | ||||||
chr6:36894023 | CA | C | 5 | a0001c0004t0007g0015 a0001c0004t0007g0118 a0001c0004t0007g0119 others(2): Show |
7 | HG02145.hp2 HG02258.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-119-466delA | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr6 | 36894023 | ||||||
chr6:36894168 | C | T | 2 | a0001c0001t0026g0196 a0001c0001t0026g0197 |
2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-119-336C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36894168 | |||||||
chr6:36894216 | T | C | 2 | a0001c0001t0026g0196 a0001c0001t0026g0197 |
2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-119-288T>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36894216 | |||||||
chr6:36894290 | C | T | 1 | a0001c0002t0028g0069 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-119-214C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 1/8 | chr6 | 36894290 | |||||||
chr6:36894725 | G | A | 1 | a0001c0001t0015g0016 | 4 | HG02647.hp1 HG03130.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+122G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | chr6 | 36894725 | |||||||
chr6:36894790 | G | T | 1 | a0001c0001t0040g0219 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-20+187G>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | chr6 | 36894790 | |||||||
chr6:36894799 | C | T | 92 | a0001c0001t0002g0079 a0001c0002t0003g0002 a0001c0002t0003g0008 others(89): Show |
132 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.-20+196C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | chr6 | 36894799 | |||||||
chr6:36895103 | A | G | 1 | a0001c0001t0002g0072 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-20+500A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | chr6 | 36895103 | |||||||
chr6:36895304 | A | G | 18 | a0001c0002t0005g0004 a0001c0002t0005g0028 a0001c0002t0005g0029 others(15): Show |
29 | HG00140.hp1 HG00735.hp2 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.-20+701A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | chr6 | 36895304 | |||||||
chr6:36895344 | T | C | 2 | a0001c0001t0026g0196 a0001c0001t0026g0197 |
2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-20+741T>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | chr6 | 36895344 | |||||||
chr6:36895375 | C | T | 1 | a0001c0002t0005g0236 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-20+772C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | chr6 | 36895375 | |||||||
chr6:36895583 | A | G | 1 | a0001c0001t0002g0116 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-20+980A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | chr6 | 36895583 | |||||||
chr6:36895627 | C | T | 79 | a0001c0001t0002g0079 a0001c0002t0003g0002 a0001c0002t0003g0008 others(76): Show |
113 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.-20+1024C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | chr6 | 36895627 | |||||||
chr6:36895691 | T | C | 1 | a0001c0001t0001g0050 | 2 | HG00642.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.-20+1088T>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | chr6 | 36895691 | |||||||
chr6:36895747 | C | T | 1 | a0001c0002t0005g0244 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-20+1144C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | chr6 | 36895747 | |||||||
chr6:36895775 | T | C | 11 | a0001c0002t0013g0013 a0001c0002t0013g0060 a0001c0002t0019g0104 others(8): Show |
14 | HG01361.hp1 HG02055.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.-20+1172T>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | chr6 | 36895775 | |||||||
chr6:36895886 | A | G | 3 | a0001c0002t0003g0035 a0001c0002t0003g0099 a0001c0002t0029g0035 |
3 | NA18960.hp1 NA18984.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.-20+1283A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | chr6 | 36895886 | |||||||
chr6:36895912 | C | T | 2 | a0001c0002t0018g0023 a0001c0002t0030g0171 |
4 | HG00544.hp2 HG02071.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20+1309C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | chr6 | 36895912 | |||||||
chr6:36895936 | A | G | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-20+1333A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | chr6 | 36895936 | |||||||
chr6:36896058 | T | G | 80 | a0001c0001t0002g0079 a0001c0002t0003g0002 a0001c0002t0003g0008 others(77): Show |
114 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.-20+1455T>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | chr6 | 36896058 | |||||||
chr6:36896079 | T | C | 1 | a0001c0002t0003g0075 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-20+1476T>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | chr6 | 36896079 | |||||||
chr6:36896108 | C | A | 171 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(168): Show |
269 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.-20+1505C>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | chr6 | 36896108 | |||||||
chr6:36896112 | G | A | 1 | a0001c0001t0025g0169 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-20+1509G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | chr6 | 36896112 | |||||||
chr6:36896166 | G | C | 2 | a0001c0001t0026g0196 a0001c0001t0026g0197 |
2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-20+1563G>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | chr6 | 36896166 | |||||||
chr6:36896635 | C | A | 1 | a0001c0001t0002g0199 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-20+2032C>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | chr6 | 36896635 | |||||||
chr6:36896767 | C | T | 4 | a0001c0003t0006g0033 a0001c0003t0006g0066 a0001c0003t0006g0068 others(1): Show |
5 | HG01109.hp2 HG02886.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20+2164C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | chr6 | 36896767 | |||||||
chr6:36896807 | T | A | 2 | a0001c0002t0013g0013 a0001c0002t0013g0060 |
5 | HG02922.hp2 HG02965.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20+2204T>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | chr6 | 36896807 | |||||||
chr6:36896965 | T | C | 1 | a0001c0002t0005g0239 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-20+2362T>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | chr6 | 36896965 | |||||||
chr6:36897060 | C | T | 2 | a0001c0001t0026g0196 a0001c0001t0026g0197 |
2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-19-2366C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | chr6 | 36897060 | |||||||
chr6:36897129 | C | CA | 7 | a0001c0001t0001g0124 a0001c0001t0004g0115 a0001c0001t0004g0182 others(4): Show |
12 | HG01261.hp2 HG02683.hp1 HG03486.hp2 others(9): Show |
intron_variant | MODIFIER | c.-19-2275dupA | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 36897129 | ||||||
chr6:36897129 | CA | C | 139 | a0001c0001t0001g0047 a0001c0001t0002g0001 a0001c0001t0002g0009 others(136): Show |
227 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.-19-2275delA | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 36897129 | ||||||
chr6:36897129 | CAA | C | 18 | a0001c0001t0008g0114 a0001c0001t0011g0224 a0001c0001t0025g0168 others(15): Show |
21 | HG01361.hp1 HG02055.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.-19-2276_-19-2275d others(4): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 36897129 | ||||||
chr6:36897147 | A | G | 20 | a0001c0001t0001g0157 a0001c0002t0005g0004 a0001c0002t0005g0028 others(17): Show |
31 | HG00140.hp1 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-19-2279A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | chr6 | 36897147 | |||||||
chr6:36897182 | T | G | 93 | a0001c0001t0002g0079 a0001c0002t0003g0002 a0001c0002t0003g0008 others(90): Show |
133 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.-19-2244T>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | chr6 | 36897182 | |||||||
chr6:36897229 | A | T | 2 | a0001c0004t0007g0118 a0001c0004t0007g0120 |
2 | HG02145.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-19-2197A>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | chr6 | 36897229 | |||||||
chr6:36897302 | C | T | 80 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0014 others(77): Show |
115 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.-19-2124C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | chr6 | 36897302 | |||||||
chr6:36897401 | C | T | 169 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(166): Show |
262 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.-19-2025C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | chr6 | 36897401 | |||||||
chr6:36897438 | C | T | 4 | a0001c0001t0001g0046 a0001c0001t0001g0122 a0001c0001t0001g0155 others(1): Show |
5 | HG01106.hp1 HG01433.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19-1988C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | chr6 | 36897438 | |||||||
chr6:36897866 | C | CAT | 92 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0014 others(89): Show |
132 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.-19-1560_-19-1559i others(4): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | chr6 | 36897866 | |||||||
chr6:36898156 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-19-1270C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | chr6 | 36898156 | |||||||
chr6:36898171 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-19-1255C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | chr6 | 36898171 | |||||||
chr6:36898281 | TTC | T | 78 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0014 others(75): Show |
112 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.-19-1143_-19-1142d others(4): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 36898281 | ||||||
chr6:36898282 | TC | T | 12 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0002t0013g0013 others(9): Show |
16 | HG01361.hp1 HG02055.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.-19-1143delC | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | chr6 | 36898282 | |||||||
chr6:36898283 | C | T | 80 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(77): Show |
133 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(130): Show |
intron_variant | MODIFIER | c.-19-1143C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | chr6 | 36898283 | |||||||
chr6:36898340 | C | T | 4 | a0001c0002t0013g0013 a0001c0002t0013g0060 a0001c0002t0019g0111 others(1): Show |
7 | HG02055.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19-1086C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | chr6 | 36898340 | |||||||
chr6:36898341 | G | A | 2 | a0001c0002t0023g0106 a0001c0002t0023g0107 |
2 | HG02109.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-19-1085G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | chr6 | 36898341 | |||||||
chr6:36898381 | G | A | 92 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0014 others(89): Show |
132 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.-19-1045G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | chr6 | 36898381 | |||||||
chr6:36898582 | G | A | 1 | a0001c0001t0001g0161 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-19-844G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | chr6 | 36898582 | |||||||
chr6:36898602 | A | G | 4 | a0001c0001t0001g0046 a0001c0001t0001g0122 a0001c0001t0001g0155 others(1): Show |
5 | HG01106.hp1 HG01433.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19-824A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | chr6 | 36898602 | |||||||
chr6:36898623 | C | G | 1 | a0001c0003t0006g0064 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-19-803C>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | chr6 | 36898623 | |||||||
chr6:36898632 | C | T | 92 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0014 others(89): Show |
132 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.-19-794C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | chr6 | 36898632 | |||||||
chr6:36898776 | T | A | 18 | a0001c0002t0005g0004 a0001c0002t0005g0028 a0001c0002t0005g0029 others(15): Show |
29 | HG00140.hp1 HG00735.hp2 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.-19-650T>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | chr6 | 36898776 | |||||||
chr6:36898781 | A | G | 10 | a0001c0002t0003g0014 a0001c0002t0003g0073 a0001c0002t0003g0074 others(7): Show |
12 | HG00438.hp1 HG02015.hp2 NA18946.hp2 others(9): Show |
intron_variant | MODIFIER | c.-19-645A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | chr6 | 36898781 | |||||||
chr6:36898906 | T | C | 9 | a0001c0001t0008g0024 a0001c0001t0008g0039 a0001c0001t0008g0114 others(6): Show |
12 | HG01496.hp1 HG01884.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.-19-520T>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | chr6 | 36898906 | |||||||
chr6:36899139 | G | A | 2 | a0001c0005t0012g0007 a0001c0005t0012g0194 |
7 | HG01261.hp2 NA18984.hp1 NA18993.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19-287G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | chr6 | 36899139 | |||||||
chr6:36899146 | T | C | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG02602.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.-19-280T>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | chr6 | 36899146 | |||||||
chr6:36899222 | C | G | 1 | a0001c0001t0045g0152 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-19-204C>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | chr6 | 36899222 | |||||||
chr6:36899311 | A | G | 2 | a0001c0001t0025g0168 a0001c0001t0025g0169 |
2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-19-115A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | chr6 | 36899311 | |||||||
chr6:36899415 | G | A | 1 | a0001c0001t0015g0016 | 4 | HG02647.hp1 HG03130.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-11G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 2/8 | chr6 | 36899415 | |||||||
chr6:36899703 | A | G | 1 | a0001c0001t0008g0185 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.189+70A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | chr6 | 36899703 | |||||||
chr6:36899910 | G | A | 15 | a0001c0001t0004g0006 a0001c0001t0004g0025 a0001c0001t0004g0026 others(12): Show |
24 | HG00733.hp1 HG01346.hp1 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.189+277G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | chr6 | 36899910 | |||||||
chr6:36899948 | C | T | 10 | a0001c0002t0013g0013 a0001c0002t0013g0060 a0001c0002t0019g0104 others(7): Show |
13 | HG01361.hp1 HG02055.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.189+315C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | chr6 | 36899948 | |||||||
chr6:36899957 | G | A | 14 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0127 others(11): Show |
19 | HG01361.hp1 HG02055.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.189+324G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | chr6 | 36899957 | |||||||
chr6:36900014 | G | A | 98 | a0001c0001t0015g0016 a0001c0001t0015g0170 a0001c0001t0025g0168 others(95): Show |
141 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.189+381G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | chr6 | 36900014 | |||||||
chr6:36900035 | G | A | 2 | a0001c0002t0018g0023 a0001c0002t0030g0171 |
4 | HG00544.hp2 HG02071.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.189+402G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | chr6 | 36900035 | |||||||
chr6:36900079 | T | G | 94 | a0001c0001t0026g0196 a0001c0001t0026g0197 a0001c0002t0003g0002 others(91): Show |
134 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.189+446T>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | chr6 | 36900079 | |||||||
chr6:36900087 | A | G | 2 | a0001c0002t0023g0106 a0001c0002t0023g0107 |
2 | HG02109.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.189+454A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | chr6 | 36900087 | |||||||
chr6:36900167 | G | A | 1 | a0001c0002t0003g0080 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.189+534G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | chr6 | 36900167 | |||||||
chr6:36900196 | G | GT | 14 | a0001c0002t0003g0090 a0001c0002t0013g0013 a0001c0002t0013g0060 others(11): Show |
19 | HG00544.hp2 HG01361.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.189+572dupT | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 36900196 | ||||||
chr6:36900219 | T | G | 1 | a0001c0001t0001g0128 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.189+586T>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | chr6 | 36900219 | |||||||
chr6:36900262 | C | T | 2 | a0001c0001t0026g0196 a0001c0001t0026g0197 |
2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.189+629C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | chr6 | 36900262 | |||||||
chr6:36900335 | G | A | 1 | a0001c0001t0001g0041 | 2 | NA19066.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.189+702G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | chr6 | 36900335 | |||||||
chr6:36900402 | A | G | 1 | a0001c0002t0033g0227 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.189+769A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | chr6 | 36900402 | |||||||
chr6:36900457 | T | C | 3 | a0001c0001t0002g0200 a0001c0001t0024g0201 a0001c0001t0024g0202 |
3 | NA18956.hp1 NA18968.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.189+824T>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | chr6 | 36900457 | |||||||
chr6:36900499 | A | G | 98 | a0001c0001t0015g0016 a0001c0001t0015g0170 a0001c0001t0025g0168 others(95): Show |
141 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.189+866A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | chr6 | 36900499 | |||||||
chr6:36900700 | C | T | 18 | a0001c0001t0026g0196 a0001c0001t0026g0197 a0001c0003t0006g0017 others(15): Show |
22 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.189+1067C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | chr6 | 36900700 | |||||||
chr6:36900767 | C | CT | 2 | a0001c0002t0018g0023 a0001c0002t0030g0171 |
4 | HG00544.hp2 HG02071.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.189+1135dupT | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 36900767 | ||||||
chr6:36900797 | C | T | 2 | a0001c0002t0018g0023 a0001c0002t0030g0171 |
4 | HG00544.hp2 HG02071.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.189+1164C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | chr6 | 36900797 | |||||||
chr6:36900992 | A | G | 1 | a0001c0002t0020g0056 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.190-1229A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | chr6 | 36900992 | |||||||
chr6:36901066 | G | A | 1 | a0001c0003t0006g0071 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.190-1155G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | chr6 | 36901066 | |||||||
chr6:36901278 | G | A | 6 | a0001c0001t0001g0020 a0001c0001t0001g0047 a0001c0001t0001g0129 others(3): Show |
9 | HG01069.hp2 NA18954.hp1 NA18956.hp2 others(6): Show |
intron_variant | MODIFIER | c.190-943G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | chr6 | 36901278 | |||||||
chr6:36901289 | G | GTAT | 9 | a0001c0001t0001g0043 a0001c0001t0001g0132 a0001c0001t0001g0154 others(6): Show |
10 | HG00738.hp1 HG01106.hp1 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.190-900_190-898dup others(3): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 36901289 | ||||||
chr6:36901312 | A | T | 80 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0014 others(77): Show |
117 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.190-909A>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | chr6 | 36901312 | |||||||
chr6:36901315 | A | AT | 5 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0193 others(2): Show |
6 | HG01123.hp1 HG01167.hp2 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.190-904dupT | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 36901315 | ||||||
chr6:36901315 | A | ATT | 5 | a0001c0001t0002g0012 a0001c0001t0002g0198 a0001c0001t0002g0214 others(2): Show |
9 | HG01256.hp1 HG01516.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.190-905_190-904dup others(2): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 36901315 | ||||||
chr6:36901315 | A | ATTT | 3 | a0001c0001t0002g0040 a0001c0001t0002g0054 a0001c0001t0008g0176 |
5 | HG01243.hp1 HG02145.hp1 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.190-904_190-903ins others(3): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 36901315 | ||||||
chr6:36901315 | A | T | 5 | a0001c0001t0002g0079 a0001c0001t0002g0217 a0001c0001t0002g0221 others(2): Show |
5 | HG02015.hp1 HG02300.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.190-906A>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | chr6 | 36901315 | |||||||
chr6:36901315 | ATTATTAT others(7): Show |
A | 10 | a0001c0002t0013g0013 a0001c0002t0013g0060 a0001c0002t0019g0104 others(7): Show |
13 | HG01361.hp1 HG02055.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.190-903_190-890del others(14): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 36901315 | ||||||
chr6:36901317 | TA | T | 3 | a0001c0001t0001g0003 a0001c0001t0001g0045 a0001c0001t0004g0048 |
3 | HG02922.hp1 NA19072.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.190-903delA | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | chr6 | 36901317 | |||||||
chr6:36901318 | A | AT | 11 | a0001c0001t0001g0125 a0001c0001t0001g0165 a0001c0001t0002g0010 others(8): Show |
12 | HG00741.hp2 HG01255.hp1 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.190-901dupT | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 36901318 | ||||||
chr6:36901318 | A | ATT | 9 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0018 others(6): Show |
17 | HG00558.hp2 HG01074.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.190-902_190-901dup others(2): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 36901318 | ||||||
chr6:36901318 | A | ATTT | 10 | a0001c0001t0002g0001 a0001c0001t0002g0113 a0001c0001t0002g0200 others(7): Show |
17 | HG00597.hp2 HG00621.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.190-901_190-900ins others(3): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 36901318 | ||||||
chr6:36901318 | A | ATTTT | 3 | a0001c0001t0002g0204 a0001c0001t0008g0174 a0001c0001t0024g0202 |
3 | HG01361.hp2 HG03139.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.190-901_190-900ins others(4): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 36901318 | ||||||
chr6:36901318 | A | T | 21 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0045 others(18): Show |
28 | HG01070.hp2 HG01123.hp1 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.190-903A>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | chr6 | 36901318 | |||||||
chr6:36901318 | ATTATTTT others(13): Show |
A | 80 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0014 others(77): Show |
117 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.190-900_190-881del others(20): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 36901318 | ||||||
chr6:36901320 | TA | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0131 a0001c0001t0004g0048 others(2): Show |
5 | HG00738.hp2 HG01069.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.190-900delA | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | chr6 | 36901320 | |||||||
chr6:36901321 | A | AT | 18 | a0001c0001t0001g0044 a0001c0001t0001g0123 a0001c0001t0001g0140 others(15): Show |
22 | HG00673.hp1 HG01175.hp2 HG02040.hp1 others(19): Show |
intron_variant | MODIFIER | c.190-869dupT | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 36901321 | ||||||
chr6:36901321 | A | ATT | 15 | a0001c0001t0001g0003 a0001c0001t0002g0001 a0001c0001t0002g0009 others(12): Show |
16 | HG00438.hp2 HG00609.hp1 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.190-870_190-869dup others(2): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 36901321 | ||||||
chr6:36901321 | A | ATTT | 6 | a0001c0001t0001g0046 a0001c0001t0001g0122 a0001c0001t0002g0009 others(3): Show |
7 | HG01433.hp2 HG01515.hp1 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.190-871_190-869dup others(3): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 36901321 | ||||||
chr6:36901321 | A | ATTTT | 6 | a0001c0001t0001g0003 a0001c0001t0002g0229 a0001c0001t0008g0039 others(3): Show |
6 | HG01884.hp1 HG02280.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.190-872_190-869dup others(4): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 36901321 | ||||||
chr6:36901321 | A | T | 70 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(67): Show |
100 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.190-900A>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | chr6 | 36901321 | |||||||
chr6:36901321 | AT | A | 10 | a0001c0001t0001g0005 a0001c0001t0001g0041 a0001c0001t0001g0042 others(7): Show |
12 | HG01256.hp2 HG01943.hp2 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.190-869delT | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 36901321 | ||||||
chr6:36901321 | ATTTTTTT others(10): Show |
A | 1 | a0001c0002t0047g0081 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.190-885_190-869del others(17): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 36901321 | ||||||
chr6:36901322 | T | TTATTATT others(5): Show |
1 | a0001c0001t0015g0016 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.190-898_190-897ins others(12): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 36901322 | ||||||
chr6:36901323 | T | TA | 9 | a0001c0001t0001g0128 a0001c0001t0001g0158 a0001c0001t0001g0159 others(6): Show |
9 | HG01070.hp1 HG01071.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.190-898_190-897ins others(1): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | chr6 | 36901323 | |||||||
chr6:36901323 | T | TATTATTA others(1): Show |
3 | a0001c0001t0015g0016 a0001c0001t0015g0170 a0001c0001t0025g0169 |
3 | HG03130.hp2 HG03540.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.190-898_190-897ins others(8): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | chr6 | 36901323 | |||||||
chr6:36901323 | T | TATTATTA others(4): Show |
1 | a0001c0001t0015g0016 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.190-898_190-897ins others(11): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | chr6 | 36901323 | |||||||
chr6:36901323 | T | TATTATTA others(7): Show |
1 | a0001c0001t0015g0016 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.190-898_190-897ins others(14): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | chr6 | 36901323 | |||||||
chr6:36901324 | T | A | 14 | a0001c0001t0001g0005 a0001c0001t0001g0108 a0001c0001t0001g0110 others(11): Show |
15 | HG00423.hp2 HG01257.hp1 HG02293.hp1 others(12): Show |
intron_variant | MODIFIER | c.190-897T>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | chr6 | 36901324 | |||||||
chr6:36901325 | T | A | 5 | a0001c0001t0001g0109 a0001c0001t0001g0153 a0001c0001t0015g0016 others(2): Show |
7 | HG01943.hp2 HG02165.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.190-896T>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | chr6 | 36901325 | |||||||
chr6:36901326 | T | A | 2 | a0001c0001t0002g0027 a0001c0002t0033g0227 |
2 | HG02451.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.190-895T>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | chr6 | 36901326 | |||||||
chr6:36901327 | T | A | 3 | a0001c0001t0001g0139 a0001c0001t0004g0115 a0001c0001t0004g0190 |
3 | NA19030.hp2 NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.190-894T>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | chr6 | 36901327 | |||||||
chr6:36901328 | T | A | 1 | a0001c0001t0001g0153 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.190-893T>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | chr6 | 36901328 | |||||||
chr6:36901329 | T | A | 1 | a0001c0002t0033g0227 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.190-892T>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | chr6 | 36901329 | |||||||
chr6:36901332 | T | A | 2 | a0001c0001t0004g0038 a0001c0001t0004g0133 |
3 | HG00741.hp1 HG02717.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.190-889T>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | chr6 | 36901332 | |||||||
chr6:36901335 | T | A | 11 | a0001c0002t0013g0013 a0001c0002t0013g0060 a0001c0002t0019g0104 others(8): Show |
14 | HG01361.hp1 HG02055.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.190-886T>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | chr6 | 36901335 | |||||||
chr6:36901338 | T | A | 11 | a0001c0002t0013g0013 a0001c0002t0013g0060 a0001c0002t0019g0104 others(8): Show |
14 | HG01361.hp1 HG02055.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.190-883T>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | chr6 | 36901338 | |||||||
chr6:36901345 | T | A | 92 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0014 others(89): Show |
132 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.190-876T>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | chr6 | 36901345 | |||||||
chr6:36901413 | C | A | 4 | a0001c0002t0014g0034 a0001c0002t0014g0076 a0001c0002t0014g0095 others(1): Show |
5 | HG00423.hp1 NA18939.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.190-808C>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | chr6 | 36901413 | |||||||
chr6:36901570 | G | A | 1 | a0001c0001t0002g0214 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.190-651G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | chr6 | 36901570 | |||||||
chr6:36901676 | A | AT | 34 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0014 others(31): Show |
51 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.190-535dupT | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 36901676 | ||||||
chr6:36901676 | A | T | 3 | a0001c0001t0001g0149 a0001c0001t0008g0176 a0001c0001t0008g0177 |
3 | HG02145.hp1 HG02559.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.190-545A>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | chr6 | 36901676 | |||||||
chr6:36901757 | G | A | 77 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0014 others(74): Show |
113 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.190-464G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | chr6 | 36901757 | |||||||
chr6:36901862 | G | A | 1 | a0001c0001t0008g0173 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.190-359G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | chr6 | 36901862 | |||||||
chr6:36901918 | G | A | 1 | a0001c0002t0003g0167 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.190-303G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | chr6 | 36901918 | |||||||
chr6:36901922 | C | T | 2 | a0001c0001t0026g0196 a0001c0001t0026g0197 |
2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.190-299C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 3/8 | chr6 | 36901922 | |||||||
chr6:36902480 | G | A | 1 | a0001c0002t0020g0056 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.403+46G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36902480 | |||||||
chr6:36902482 | A | G | 2 | a0001c0001t0026g0196 a0001c0001t0026g0197 |
2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.403+48A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36902482 | |||||||
chr6:36902583 | G | A | 1 | a0001c0002t0003g0091 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.403+149G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36902583 | |||||||
chr6:36902597 | G | A | 94 | a0001c0001t0015g0016 a0001c0001t0015g0170 a0001c0001t0025g0168 others(91): Show |
136 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.403+163G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36902597 | |||||||
chr6:36902817 | C | T | 1 | a0001c0001t0002g0116 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.403+383C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36902817 | |||||||
chr6:36902837 | A | G | 88 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0014 others(85): Show |
127 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.403+403A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36902837 | |||||||
chr6:36902950 | A | G | 1 | a0001c0001t0004g0179 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.403+516A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36902950 | |||||||
chr6:36902975 | A | T | 90 | a0001c0001t0026g0196 a0001c0001t0026g0197 a0001c0002t0003g0002 others(87): Show |
129 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.403+541A>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36902975 | |||||||
chr6:36903068 | GT | G | 88 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0014 others(85): Show |
127 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.403+636delT | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr6 | 36903068 | ||||||
chr6:36903118 | G | T | 4 | a0001c0001t0004g0038 a0001c0001t0004g0121 a0001c0001t0004g0133 others(1): Show |
5 | HG00741.hp1 HG02055.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.403+684G>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36903118 | |||||||
chr6:36903225 | T | TTG | 3 | a0001c0001t0001g0045 a0001c0001t0025g0168 a0001c0001t0025g0169 |
4 | HG03195.hp2 HG03540.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.403+811_403+812dup others(2): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr6 | 36903225 | ||||||
chr6:36903225 | TTG | T | 83 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0014 others(80): Show |
121 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.403+811_403+812del others(2): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr6 | 36903225 | ||||||
chr6:36903407 | A | C | 92 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0014 others(89): Show |
132 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.403+973A>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36903407 | |||||||
chr6:36903490 | C | T | 1 | a0001c0001t0001g0045 | 2 | NA19005.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.403+1056C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36903490 | |||||||
chr6:36903499 | G | A | 1 | a0001c0002t0035g0172 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.403+1065G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36903499 | |||||||
chr6:36903621 | G | A | 7 | a0001c0002t0019g0104 a0001c0002t0019g0105 a0001c0002t0021g0117 others(4): Show |
7 | HG01361.hp1 HG02451.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.403+1187G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36903621 | |||||||
chr6:36903663 | G | C | 1 | a0001c0002t0010g0082 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.403+1229G>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36903663 | |||||||
chr6:36903781 | G | T | 1 | a0001c0001t0004g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.403+1347G>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36903781 | |||||||
chr6:36903819 | T | G | 1 | a0001c0001t0002g0096 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.403+1385T>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36903819 | |||||||
chr6:36903860 | T | A | 4 | a0001c0001t0001g0050 a0001c0001t0025g0169 a0001c0002t0005g0238 others(1): Show |
5 | HG00642.hp1 HG01256.hp2 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.403+1426T>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36903860 | |||||||
chr6:36903912 | T | A | 1 | a0001c0001t0001g0134 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.403+1478T>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36903912 | |||||||
chr6:36903956 | C | A | 18 | a0001c0002t0005g0004 a0001c0002t0005g0028 a0001c0002t0005g0029 others(15): Show |
29 | HG00140.hp1 HG00735.hp2 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.403+1522C>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36903956 | |||||||
chr6:36903957 | T | TA | 4 | a0001c0001t0002g0203 a0001c0002t0005g0240 a0001c0005t0012g0007 others(1): Show |
9 | HG01261.hp2 NA18984.hp1 NA18993.hp1 others(6): Show |
intron_variant | MODIFIER | c.403+1536dupA | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr6 | 36903957 | ||||||
chr6:36903996 | G | T | 1 | a0001c0001t0002g0116 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.403+1562G>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36903996 | |||||||
chr6:36904044 | C | T | 1 | a0001c0001t0002g0212 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.403+1610C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36904044 | |||||||
chr6:36904125 | A | G | 1 | a0001c0001t0002g0213 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.403+1691A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36904125 | |||||||
chr6:36904155 | A | G | 11 | a0001c0002t0013g0013 a0001c0002t0013g0060 a0001c0002t0019g0104 others(8): Show |
14 | HG01361.hp1 HG02055.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.403+1721A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36904155 | |||||||
chr6:36904198 | G | A | 2 | a0001c0002t0018g0023 a0001c0002t0030g0171 |
4 | HG00544.hp2 HG02071.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.403+1764G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36904198 | |||||||
chr6:36904218 | G | A | 2 | a0001c0002t0018g0023 a0001c0002t0030g0171 |
4 | HG00544.hp2 HG02071.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.403+1784G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36904218 | |||||||
chr6:36904222 | A | G | 13 | a0001c0002t0013g0013 a0001c0002t0013g0060 a0001c0002t0018g0023 others(10): Show |
18 | HG00544.hp2 HG01361.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.403+1788A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36904222 | |||||||
chr6:36904294 | T | C | 88 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0014 others(85): Show |
127 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.403+1860T>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36904294 | |||||||
chr6:36904321 | T | C | 1 | a0001c0002t0033g0227 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.403+1887T>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36904321 | |||||||
chr6:36904534 | C | T | 88 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0014 others(85): Show |
127 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.403+2100C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36904534 | |||||||
chr6:36904562 | A | G | 94 | a0001c0001t0015g0016 a0001c0001t0015g0170 a0001c0001t0025g0168 others(91): Show |
136 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.403+2128A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36904562 | |||||||
chr6:36904658 | AT | A | 88 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0014 others(85): Show |
127 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.403+2230delT | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr6 | 36904658 | ||||||
chr6:36904778 | G | A | 1 | a0001c0003t0006g0068 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.403+2344G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36904778 | |||||||
chr6:36904803 | C | T | 2 | a0001c0002t0021g0117 a0001c0002t0021g0228 |
2 | HG01361.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.403+2369C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36904803 | |||||||
chr6:36904871 | T | C | 3 | a0001c0001t0002g0009 a0001c0001t0002g0199 a0001c0001t0002g0204 |
7 | HG01074.hp2 HG01361.hp2 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.403+2437T>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36904871 | |||||||
chr6:36904881 | A | G | 11 | a0001c0002t0013g0013 a0001c0002t0013g0060 a0001c0002t0019g0104 others(8): Show |
14 | HG01361.hp1 HG02055.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.403+2447A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36904881 | |||||||
chr6:36905055 | C | A | 2 | a0001c0001t0026g0196 a0001c0001t0026g0197 |
2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.403+2621C>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36905055 | |||||||
chr6:36905129 | G | T | 2 | a0001c0001t0026g0196 a0001c0001t0026g0197 |
2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.403+2695G>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36905129 | |||||||
chr6:36905179 | G | A | 2 | a0001c0002t0018g0023 a0001c0002t0030g0171 |
4 | HG00544.hp2 HG02071.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.403+2745G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36905179 | |||||||
chr6:36905255 | G | A | 1 | a0001c0002t0003g0091 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.403+2821G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36905255 | |||||||
chr6:36905290 | G | A | 1 | a0001c0001t0002g0205 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.403+2856G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36905290 | |||||||
chr6:36905459 | T | C | 1 | a0001c0002t0033g0227 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.403+3025T>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36905459 | |||||||
chr6:36905568 | C | T | 18 | a0001c0002t0005g0004 a0001c0002t0005g0028 a0001c0002t0005g0029 others(15): Show |
29 | HG00140.hp1 HG00735.hp2 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.403+3134C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36905568 | |||||||
chr6:36905985 | C | T | 2 | a0001c0002t0023g0106 a0001c0002t0023g0107 |
2 | HG02109.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.403+3551C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36905985 | |||||||
chr6:36906011 | T | G | 221 | a0001c0001t0001g0005 a0001c0001t0001g0044 a0001c0001t0001g0045 others(218): Show |
338 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(335): Show |
intron_variant | MODIFIER | c.403+3577T>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36906011 | |||||||
chr6:36906185 | G | A | 6 | a0001c0001t0001g0044 a0001c0001t0001g0135 a0001c0001t0001g0136 others(3): Show |
7 | NA18965.hp1 NA18966.hp1 NA18988.hp2 others(4): Show |
intron_variant | MODIFIER | c.403+3751G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36906185 | |||||||
chr6:36906550 | A | G | 10 | a0001c0002t0003g0014 a0001c0002t0003g0073 a0001c0002t0003g0074 others(7): Show |
12 | HG00438.hp1 HG02015.hp2 NA18946.hp2 others(9): Show |
intron_variant | MODIFIER | c.403+4116A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36906550 | |||||||
chr6:36906576 | A | G | 1 | a0001c0002t0010g0088 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.403+4142A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36906576 | |||||||
chr6:36906610 | A | G | 88 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0014 others(85): Show |
127 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.403+4176A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36906610 | |||||||
chr6:36906652 | C | T | 16 | a0001c0003t0006g0017 a0001c0003t0006g0031 a0001c0003t0006g0032 others(13): Show |
20 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.403+4218C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36906652 | |||||||
chr6:36906665 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.403+4231C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36906665 | |||||||
chr6:36906672 | G | A | 67 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(64): Show |
115 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.403+4238G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36906672 | |||||||
chr6:36906726 | G | A | 3 | a0001c0002t0016g0055 a0001c0002t0016g0225 a0001c0002t0016g0226 |
4 | HG02622.hp2 HG02809.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.403+4292G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36906726 | |||||||
chr6:36907042 | C | G | 2 | a0001c0002t0018g0023 a0001c0002t0030g0171 |
4 | HG00544.hp2 HG02071.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.403+4608C>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36907042 | |||||||
chr6:36907173 | A | G | 2 | a0001c0002t0018g0023 a0001c0002t0030g0171 |
4 | HG00544.hp2 HG02071.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.403+4739A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36907173 | |||||||
chr6:36907275 | C | CTTTTG | 13 | a0001c0001t0001g0157 a0001c0001t0004g0121 a0001c0001t0004g0133 others(10): Show |
19 | HG00423.hp2 HG00741.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.403+4876_403+4880d others(7): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr6 | 36907275 | ||||||
chr6:36907275 | C | CTTTTGTT others(8): Show |
2 | a0001c0002t0019g0111 a0001c0002t0037g0103 |
2 | HG02055.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.403+4866_403+4880d others(17): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr6 | 36907275 | ||||||
chr6:36907275 | C | CTTTTGTT others(18): Show |
2 | a0001c0002t0019g0104 a0001c0002t0019g0105 |
2 | HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.403+4856_403+4880d others(27): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr6 | 36907275 | ||||||
chr6:36907275 | CTTTTG | C | 81 | a0001c0001t0002g0229 a0001c0001t0004g0184 a0001c0001t0026g0196 others(78): Show |
115 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.403+4876_403+4880d others(7): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr6 | 36907275 | ||||||
chr6:36907275 | CTTTTGTT others(3): Show |
C | 3 | a0001c0001t0001g0131 a0001c0002t0018g0023 a0001c0002t0030g0171 |
5 | HG00544.hp2 HG02071.hp1 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.403+4871_403+4880d others(12): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr6 | 36907275 | ||||||
chr6:36907546 | T | G | 1 | a0001c0002t0003g0083 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.403+5112T>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36907546 | |||||||
chr6:36907633 | G | A | 1 | a0001c0001t0002g0215 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.403+5199G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36907633 | |||||||
chr6:36907673 | T | TA | 88 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0014 others(85): Show |
127 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.403+5245dupA | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr6 | 36907673 | ||||||
chr6:36907841 | T | C | 6 | a0001c0001t0001g0044 a0001c0001t0001g0135 a0001c0001t0001g0136 others(3): Show |
7 | NA18965.hp1 NA18966.hp1 NA18988.hp2 others(4): Show |
intron_variant | MODIFIER | c.403+5407T>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36907841 | |||||||
chr6:36907964 | G | A | 34 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0014 others(31): Show |
51 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.403+5530G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36907964 | |||||||
chr6:36907967 | A | C | 2 | a0001c0001t0004g0121 a0001c0001t0004g0133 |
2 | HG00741.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.403+5533A>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36907967 | |||||||
chr6:36907983 | G | T | 2 | a0001c0001t0026g0196 a0001c0001t0026g0197 |
2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.403+5549G>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36907983 | |||||||
chr6:36907984 | A | T | 2 | a0001c0001t0026g0196 a0001c0001t0026g0197 |
2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.403+5550A>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36907984 | |||||||
chr6:36908052 | A | G | 90 | a0001c0001t0026g0196 a0001c0001t0026g0197 a0001c0002t0003g0002 others(87): Show |
129 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.403+5618A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36908052 | |||||||
chr6:36908074 | C | T | 2 | a0001c0002t0021g0117 a0001c0002t0021g0228 |
2 | HG01361.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.403+5640C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36908074 | |||||||
chr6:36908089 | G | A | 2 | a0001c0004t0007g0015 a0001c0004t0034g0015 |
4 | HG02258.hp1 HG02622.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.403+5655G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36908089 | |||||||
chr6:36908107 | C | T | 10 | a0001c0002t0013g0013 a0001c0002t0013g0060 a0001c0002t0019g0104 others(7): Show |
13 | HG01361.hp1 HG02055.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.403+5673C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36908107 | |||||||
chr6:36908274 | C | A | 10 | a0001c0002t0013g0013 a0001c0002t0013g0060 a0001c0002t0019g0104 others(7): Show |
13 | HG01361.hp1 HG02055.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.403+5840C>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36908274 | |||||||
chr6:36908288 | CT | C | 75 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0014 others(72): Show |
108 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.403+5855delT | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36908288 | |||||||
chr6:36908353 | A | G | 4 | a0001c0002t0016g0055 a0001c0002t0016g0225 a0001c0002t0016g0226 others(1): Show |
5 | HG02615.hp1 HG02622.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.403+5919A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36908353 | |||||||
chr6:36908456 | A | T | 1 | a0001c0002t0028g0069 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.404-5828A>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36908456 | |||||||
chr6:36908460 | ATACT | A | 88 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0014 others(85): Show |
127 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.404-5821_404-5818d others(6): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr6 | 36908460 | ||||||
chr6:36908478 | T | A | 1 | a0001c0001t0002g0215 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.404-5806T>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36908478 | |||||||
chr6:36908486 | A | T | 1 | a0001c0001t0001g0218 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.404-5798A>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36908486 | |||||||
chr6:36908566 | A | G | 76 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0014 others(73): Show |
110 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.404-5718A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36908566 | |||||||
chr6:36908616 | C | T | 2 | a0001c0002t0018g0023 a0001c0002t0030g0171 |
4 | HG00544.hp2 HG02071.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.404-5668C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36908616 | |||||||
chr6:36908663 | T | C | 1 | a0001c0002t0018g0023 | 3 | HG00544.hp2 NA18747.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.404-5621T>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36908663 | |||||||
chr6:36908691 | G | A | 2 | a0001c0001t0015g0016 a0001c0001t0015g0170 |
5 | HG02647.hp1 HG03130.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.404-5593G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36908691 | |||||||
chr6:36908773 | TA | T | 2 | a0001c0002t0013g0013 a0001c0002t0013g0060 |
5 | HG02922.hp2 HG02965.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.404-5510delA | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36908773 | |||||||
chr6:36908783 | T | C | 88 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0014 others(85): Show |
127 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.404-5501T>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36908783 | |||||||
chr6:36908905 | C | A | 4 | a0001c0002t0016g0055 a0001c0002t0016g0225 a0001c0002t0016g0226 others(1): Show |
5 | HG02615.hp1 HG02622.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.404-5379C>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36908905 | |||||||
chr6:36909026 | T | C | 1 | a0001c0002t0033g0227 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.404-5258T>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36909026 | |||||||
chr6:36909095 | A | G | 2 | a0001c0002t0019g0111 a0001c0002t0037g0103 |
2 | HG02055.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.404-5189A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36909095 | |||||||
chr6:36909181 | G | GT | 64 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0123 others(61): Show |
96 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.404-5089dupT | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr6 | 36909181 | ||||||
chr6:36909181 | G | GTT | 22 | a0001c0002t0003g0087 a0001c0002t0003g0092 a0001c0002t0003g0094 others(19): Show |
26 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.404-5090_404-5089d others(4): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr6 | 36909181 | ||||||
chr6:36909181 | G | GTTT | 9 | a0001c0002t0013g0013 a0001c0002t0013g0060 a0001c0002t0019g0104 others(6): Show |
13 | HG01192.hp1 HG01361.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.404-5091_404-5089d others(5): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr6 | 36909181 | ||||||
chr6:36909374 | A | G | 2 | a0001c0002t0018g0023 a0001c0002t0030g0171 |
4 | HG00544.hp2 HG02071.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.404-4910A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36909374 | |||||||
chr6:36909411 | T | A | 1 | a0001c0001t0045g0152 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.404-4873T>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36909411 | |||||||
chr6:36909511 | G | A | 2 | a0001c0002t0019g0104 a0001c0002t0019g0105 |
2 | HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.404-4773G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36909511 | |||||||
chr6:36909636 | G | A | 1 | a0001c0001t0001g0161 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.404-4648G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36909636 | |||||||
chr6:36909692 | GGATCACC others(5): Show |
G | 2 | a0001c0001t0001g0137 a0001c0001t0001g0150 |
2 | HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.404-4591_404-4580d others(14): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36909692 | |||||||
chr6:36909706 | C | T | 2 | a0001c0001t0001g0137 a0001c0001t0001g0150 |
2 | HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.404-4578C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36909706 | |||||||
chr6:36909732 | G | A | 3 | a0001c0001t0026g0196 a0001c0001t0026g0197 a0001c0001t0045g0152 |
3 | HG00558.hp1 HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.404-4552G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36909732 | |||||||
chr6:36909782 | C | CA | 9 | a0001c0001t0001g0123 a0001c0001t0001g0141 a0001c0001t0001g0162 others(6): Show |
10 | HG01123.hp2 HG01175.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.404-4484dupA | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr6 | 36909782 | ||||||
chr6:36909782 | CAA | C | 78 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0014 others(75): Show |
115 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.404-4485_404-4484d others(4): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr6 | 36909782 | ||||||
chr6:36909836 | G | C | 2 | a0001c0002t0003g0008 a0001c0002t0003g0092 |
6 | HG00544.hp1 NA18944.hp2 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.404-4448G>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36909836 | |||||||
chr6:36909857 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.404-4427G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36909857 | |||||||
chr6:36909858 | T | G | 1 | a0001c0002t0033g0227 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.404-4426T>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36909858 | |||||||
chr6:36910258 | T | G | 79 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0014 others(76): Show |
113 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.404-4026T>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36910258 | |||||||
chr6:36910362 | C | A | 2 | a0001c0002t0013g0013 a0001c0002t0013g0060 |
5 | HG02922.hp2 HG02965.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.404-3922C>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36910362 | |||||||
chr6:36910370 | T | C | 1 | a0001c0002t0005g0166 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.404-3914T>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36910370 | |||||||
chr6:36910486 | G | C | 2 | a0001c0002t0018g0023 a0001c0002t0030g0171 |
4 | HG00544.hp2 HG02071.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.404-3798G>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36910486 | |||||||
chr6:36910618 | C | T | 1 | a0001c0002t0033g0227 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.404-3666C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36910618 | |||||||
chr6:36910665 | C | T | 2 | a0001c0001t0025g0168 a0001c0001t0025g0169 |
2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.404-3619C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36910665 | |||||||
chr6:36910677 | G | C | 4 | a0001c0001t0015g0016 a0001c0001t0015g0170 a0001c0001t0025g0168 others(1): Show |
7 | HG02647.hp1 HG03130.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.404-3607G>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36910677 | |||||||
chr6:36910726 | C | CT | 2 | a0001c0001t0015g0016 a0001c0001t0015g0170 |
5 | HG02647.hp1 HG03130.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.404-3557dupT | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr6 | 36910726 | ||||||
chr6:36910734 | A | C | 1 | a0001c0001t0001g0136 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.404-3550A>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36910734 | |||||||
chr6:36910760 | G | A | 6 | a0001c0001t0001g0020 a0001c0001t0001g0047 a0001c0001t0001g0129 others(3): Show |
9 | HG01069.hp2 NA18954.hp1 NA18956.hp2 others(6): Show |
intron_variant | MODIFIER | c.404-3524G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36910760 | |||||||
chr6:36910834 | A | G | 1 | a0001c0003t0006g0071 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.404-3450A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36910834 | |||||||
chr6:36910979 | C | A | 4 | a0001c0002t0013g0013 a0001c0002t0013g0060 a0001c0002t0019g0111 others(1): Show |
7 | HG02055.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.404-3305C>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36910979 | |||||||
chr6:36911047 | C | T | 10 | a0001c0002t0013g0013 a0001c0002t0013g0060 a0001c0002t0019g0104 others(7): Show |
13 | HG01361.hp1 HG02055.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.404-3237C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911047 | |||||||
chr6:36911215 | C | T | 1 | a0001c0002t0027g0070 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.404-3069C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911215 | |||||||
chr6:36911218 | A | C | 1 | a0001c0001t0001g0222 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.404-3066A>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911218 | |||||||
chr6:36911219 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.404-3065G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911219 | |||||||
chr6:36911223 | C | G | 1 | a0001c0001t0001g0222 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.404-3061C>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911223 | |||||||
chr6:36911224 | T | C | 1 | a0001c0001t0001g0222 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.404-3060T>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911224 | |||||||
chr6:36911227 | C | A | 1 | a0001c0001t0001g0222 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.404-3057C>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911227 | |||||||
chr6:36911230 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.404-3054C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911230 | |||||||
chr6:36911239 | CAGCACTT others(17): Show |
C | 1 | a0001c0001t0001g0222 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.404-3044_404-3021d others(26): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911239 | |||||||
chr6:36911247 | T | C | 1 | a0001c0001t0041g0011 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.404-3037T>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911247 | |||||||
chr6:36911264 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.404-3020C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911264 | |||||||
chr6:36911271 | T | G | 1 | a0001c0001t0001g0222 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.404-3013T>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911271 | |||||||
chr6:36911282 | G | C | 1 | a0001c0001t0001g0222 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.404-3002G>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911282 | |||||||
chr6:36911284 | G | T | 1 | a0001c0001t0001g0222 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.404-3000G>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911284 | |||||||
chr6:36911285 | T | A | 1 | a0001c0001t0001g0222 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.404-2999T>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911285 | |||||||
chr6:36911293 | C | G | 1 | a0001c0001t0001g0222 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.404-2991C>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911293 | |||||||
chr6:36911295 | G | C | 1 | a0001c0001t0001g0222 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.404-2989G>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911295 | |||||||
chr6:36911296 | C | A | 1 | a0001c0001t0001g0222 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.404-2988C>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911296 | |||||||
chr6:36911308 | G | C | 1 | a0001c0001t0001g0222 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.404-2976G>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911308 | |||||||
chr6:36911313 | A | C | 1 | a0001c0001t0001g0222 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.404-2971A>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911313 | |||||||
chr6:36911324 | T | C | 1 | a0001c0001t0001g0222 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.404-2960T>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911324 | |||||||
chr6:36911327 | T | A | 1 | a0001c0001t0001g0222 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.404-2957T>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911327 | |||||||
chr6:36911332 | A | C | 1 | a0001c0001t0001g0222 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.404-2952A>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911332 | |||||||
chr6:36911333 | T | C | 1 | a0001c0001t0001g0222 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.404-2951T>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911333 | |||||||
chr6:36911335 | C | A | 1 | a0001c0001t0004g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.404-2949C>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911335 | |||||||
chr6:36911338 | A | C | 1 | a0001c0001t0001g0222 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.404-2946A>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911338 | |||||||
chr6:36911352 | T | C | 1 | a0001c0001t0001g0222 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.404-2932T>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911352 | |||||||
chr6:36911353 | C | A | 1 | a0001c0001t0001g0222 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.404-2931C>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911353 | |||||||
chr6:36911354 | G | A | 3 | a0001c0001t0001g0019 a0001c0001t0001g0123 a0001c0001t0001g0146 |
5 | HG00642.hp2 HG01167.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.404-2930G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911354 | |||||||
chr6:36911354 | G | T | 1 | a0001c0001t0001g0222 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.404-2930G>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911354 | |||||||
chr6:36911355 | T | C | 1 | a0001c0001t0001g0222 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.404-2929T>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911355 | |||||||
chr6:36911365 | C | A | 1 | a0001c0001t0001g0222 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.404-2919C>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911365 | |||||||
chr6:36911384 | G | C | 1 | a0001c0001t0001g0222 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.404-2900G>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911384 | |||||||
chr6:36911385 | G | T | 1 | a0001c0001t0001g0222 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.404-2899G>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911385 | |||||||
chr6:36911390 | T | A | 1 | a0001c0001t0001g0222 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.404-2894T>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911390 | |||||||
chr6:36911397 | G | T | 1 | a0001c0001t0001g0222 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.404-2887G>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911397 | |||||||
chr6:36911399 | A | C | 1 | a0001c0001t0001g0222 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.404-2885A>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911399 | |||||||
chr6:36911401 | A | C | 1 | a0001c0001t0001g0222 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.404-2883A>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911401 | |||||||
chr6:36911403 | T | C | 1 | a0001c0001t0001g0222 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.404-2881T>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911403 | |||||||
chr6:36911404 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.404-2880C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911404 | |||||||
chr6:36911406 | C | A | 1 | a0001c0001t0001g0222 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.404-2878C>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911406 | |||||||
chr6:36911407 | T | C | 1 | a0001c0001t0001g0222 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.404-2877T>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911407 | |||||||
chr6:36911468 | C | T | 2 | a0001c0001t0025g0168 a0001c0001t0025g0169 |
2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.404-2816C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911468 | |||||||
chr6:36911490 | CA | C | 4 | a0001c0002t0016g0055 a0001c0002t0016g0225 a0001c0002t0016g0226 others(1): Show |
5 | HG02615.hp1 HG02622.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.404-2786delA | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr6 | 36911490 | ||||||
chr6:36911496 | A | T | 3 | a0001c0001t0004g0191 a0001c0002t0018g0023 a0001c0002t0030g0171 |
5 | HG00544.hp2 HG02071.hp1 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.404-2788A>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911496 | |||||||
chr6:36911499 | T | A | 12 | a0001c0001t0025g0168 a0001c0001t0025g0169 a0001c0002t0013g0013 others(9): Show |
15 | HG01361.hp1 HG02055.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.404-2785T>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911499 | |||||||
chr6:36911525 | A | G | 1 | a0001c0002t0020g0056 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.404-2759A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911525 | |||||||
chr6:36911542 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.404-2742C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911542 | |||||||
chr6:36911567 | C | T | 1 | a0001c0001t0002g0221 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.404-2717C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911567 | |||||||
chr6:36911602 | G | A | 2 | a0001c0002t0023g0106 a0001c0002t0023g0107 |
2 | HG02109.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.404-2682G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911602 | |||||||
chr6:36911688 | G | A | 80 | a0001c0001t0001g0046 a0001c0001t0001g0122 a0001c0001t0001g0128 others(77): Show |
131 | HG00438.hp2 HG00558.hp2 HG00597.hp2 others(128): Show |
intron_variant | MODIFIER | c.404-2596G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911688 | |||||||
chr6:36911821 | C | T | 1 | a0001c0002t0027g0070 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.404-2463C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911821 | |||||||
chr6:36911930 | A | AC | 51 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0019 others(48): Show |
79 | HG00323.hp2 HG00609.hp2 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.404-2342dupC | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr6 | 36911930 | ||||||
chr6:36911930 | A | ACC | 19 | a0001c0001t0001g0021 a0001c0001t0001g0123 a0001c0001t0001g0125 others(16): Show |
22 | HG00423.hp2 HG00558.hp1 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.404-2343_404-2342d others(4): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr6 | 36911930 | ||||||
chr6:36911930 | AC | A | 64 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(61): Show |
115 | HG00438.hp2 HG00558.hp2 HG00597.hp2 others(112): Show |
intron_variant | MODIFIER | c.404-2342delC | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr6 | 36911930 | ||||||
chr6:36911932 | C | A | 4 | a0001c0001t0004g0038 a0001c0001t0004g0121 a0001c0001t0004g0133 others(1): Show |
5 | HG00741.hp1 HG02055.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.404-2352C>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911932 | |||||||
chr6:36911934 | C | A | 2 | a0001c0001t0015g0016 a0001c0001t0015g0170 |
5 | HG02647.hp1 HG03130.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.404-2350C>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911934 | |||||||
chr6:36911936 | C | A | 79 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0014 others(76): Show |
116 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.404-2348C>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911936 | |||||||
chr6:36911938 | C | G | 2 | a0001c0002t0013g0013 a0001c0002t0013g0060 |
5 | HG02922.hp2 HG02965.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.404-2346C>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911938 | |||||||
chr6:36911938 | C | T | 1 | a0001c0002t0037g0103 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.404-2346C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36911938 | |||||||
chr6:36912054 | C | T | 2 | a0001c0002t0018g0023 a0001c0002t0030g0171 |
4 | HG00544.hp2 HG02071.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.404-2230C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36912054 | |||||||
chr6:36912055 | G | A | 2 | a0001c0001t0026g0196 a0001c0001t0026g0197 |
2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.404-2229G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36912055 | |||||||
chr6:36912368 | A | G | 1 | a0001c0002t0027g0070 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.404-1916A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36912368 | |||||||
chr6:36912394 | C | G | 5 | a0001c0004t0007g0015 a0001c0004t0007g0118 a0001c0004t0007g0119 others(2): Show |
7 | HG02145.hp2 HG02258.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.404-1890C>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36912394 | |||||||
chr6:36912515 | A | C | 96 | a0001c0001t0025g0168 a0001c0001t0025g0169 a0001c0001t0026g0196 others(93): Show |
136 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.404-1769A>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36912515 | |||||||
chr6:36912693 | C | T | 1 | a0001c0001t0001g0042 | 2 | NA18982.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.404-1591C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36912693 | |||||||
chr6:36912695 | A | G | 92 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0014 others(89): Show |
132 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.404-1589A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36912695 | |||||||
chr6:36912746 | A | C | 1 | a0001c0001t0001g0045 | 2 | NA19005.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.404-1538A>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36912746 | |||||||
chr6:36912747 | T | C | 2 | a0001c0002t0023g0106 a0001c0002t0023g0107 |
2 | HG02109.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.404-1537T>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36912747 | |||||||
chr6:36912782 | C | T | 4 | a0001c0001t0015g0016 a0001c0001t0015g0170 a0001c0001t0025g0168 others(1): Show |
7 | HG02647.hp1 HG03130.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.404-1502C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36912782 | |||||||
chr6:36912974 | A | G | 2 | a0001c0002t0018g0023 a0001c0002t0030g0171 |
4 | HG00544.hp2 HG02071.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.404-1310A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36912974 | |||||||
chr6:36913006 | C | G | 1 | a0001c0001t0004g0183 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.404-1278C>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36913006 | |||||||
chr6:36913025 | C | T | 10 | a0001c0002t0013g0013 a0001c0002t0013g0060 a0001c0002t0019g0104 others(7): Show |
13 | HG01361.hp1 HG02055.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.404-1259C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36913025 | |||||||
chr6:36913079 | C | G | 1 | a0001c0002t0020g0056 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.404-1205C>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36913079 | |||||||
chr6:36913117 | A | G | 2 | a0001c0002t0023g0106 a0001c0002t0023g0107 |
2 | HG02109.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.404-1167A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36913117 | |||||||
chr6:36913245 | A | ACT | 6 | a0001c0001t0015g0016 a0001c0001t0015g0170 a0001c0001t0025g0168 others(3): Show |
9 | HG02647.hp1 HG02965.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.404-1038_404-1037i others(4): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr6 | 36913245 | ||||||
chr6:36913458 | G | A | 2 | a0001c0001t0025g0168 a0001c0001t0025g0169 |
2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.404-826G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36913458 | |||||||
chr6:36913504 | A | C | 2 | a0001c0002t0023g0106 a0001c0002t0023g0107 |
2 | HG02109.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.404-780A>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36913504 | |||||||
chr6:36913546 | T | C | 2 | a0001c0001t0025g0168 a0001c0001t0025g0169 |
2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.404-738T>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36913546 | |||||||
chr6:36913620 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.404-664A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36913620 | |||||||
chr6:36913759 | A | G | 20 | a0001c0002t0005g0004 a0001c0002t0005g0028 a0001c0002t0005g0029 others(17): Show |
31 | HG00140.hp1 HG00735.hp2 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.404-525A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36913759 | |||||||
chr6:36913833 | AGCGGTCT others(1): Show |
A | 33 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0014 others(30): Show |
50 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.404-450_404-443del others(8): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36913833 | |||||||
chr6:36913842 | C | A | 33 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0014 others(30): Show |
50 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.404-442C>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36913842 | |||||||
chr6:36913844 | G | A | 1 | a0001c0002t0003g0089 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.404-440G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36913844 | |||||||
chr6:36913844 | G | T | 49 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0027 others(46): Show |
77 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.404-440G>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36913844 | |||||||
chr6:36913846 | G | T | 34 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0014 others(31): Show |
51 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.404-438G>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36913846 | |||||||
chr6:36913847 | C | T | 34 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0014 others(31): Show |
51 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.404-437C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36913847 | |||||||
chr6:36913849 | T | A | 34 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0014 others(31): Show |
51 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.404-435T>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36913849 | |||||||
chr6:36913851 | T | A | 34 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0014 others(31): Show |
51 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.404-433T>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36913851 | |||||||
chr6:36913852 | C | A | 34 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0014 others(31): Show |
51 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.404-432C>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36913852 | |||||||
chr6:36913856 | G | A | 34 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0014 others(31): Show |
51 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.404-428G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36913856 | |||||||
chr6:36913858 | T | TCA | 34 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0014 others(31): Show |
51 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.404-426_404-425ins others(2): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36913858 | |||||||
chr6:36913859 | T | A | 34 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0014 others(31): Show |
51 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.404-425T>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36913859 | |||||||
chr6:36914018 | A | G | 34 | a0001c0002t0005g0004 a0001c0002t0005g0028 a0001c0002t0005g0029 others(31): Show |
49 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.404-266A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36914018 | |||||||
chr6:36914019 | T | C | 1 | a0001c0001t0001g0143 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.404-265T>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36914019 | |||||||
chr6:36914034 | G | A | 2 | a0001c0002t0013g0013 a0001c0002t0013g0060 |
5 | HG02922.hp2 HG02965.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.404-250G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36914034 | |||||||
chr6:36914215 | T | C | 92 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0014 others(89): Show |
132 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.404-69T>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 4/8 | chr6 | 36914215 | |||||||
chr6:36914495 | C | T | 1 | a0001c0002t0035g0172 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.556-59C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 5/8 | chr6 | 36914495 | |||||||
chr6:36914782 | G | A | 2 | a0001c0002t0021g0117 a0001c0002t0021g0228 |
2 | HG01361.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.695+89G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 6/8 | chr6 | 36914782 | |||||||
chr6:36914828 | A | G | 1 | a0001c0001t0044g0130 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.695+135A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 6/8 | chr6 | 36914828 | |||||||
chr6:36914882 | C | G | 4 | a0001c0002t0013g0013 a0001c0002t0013g0060 a0001c0002t0019g0111 others(1): Show |
7 | HG02055.hp1 HG02922.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.695+189C>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 6/8 | chr6 | 36914882 | |||||||
chr6:36914944 | C | T | 1 | a0001c0002t0003g0086 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.695+251C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 6/8 | chr6 | 36914944 | |||||||
chr6:36914950 | A | G | 2 | a0001c0002t0013g0013 a0001c0002t0013g0060 |
5 | HG02922.hp2 HG02965.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.695+257A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 6/8 | chr6 | 36914950 | |||||||
chr6:36914978 | A | G | 1 | a0001c0001t0002g0211 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.695+285A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 6/8 | chr6 | 36914978 | |||||||
chr6:36915013 | G | T | 1 | a0001c0001t0001g0110 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.695+320G>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 6/8 | chr6 | 36915013 | |||||||
chr6:36915079 | G | A | 2 | a0001c0002t0023g0106 a0001c0002t0023g0107 |
2 | HG02109.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.695+386G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 6/8 | chr6 | 36915079 | |||||||
chr6:36915170 | G | A | 92 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0014 others(89): Show |
132 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.695+477G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 6/8 | chr6 | 36915170 | |||||||
chr6:36915366 | C | T | 7 | a0001c0001t0001g0046 a0001c0001t0001g0122 a0001c0001t0001g0128 others(4): Show |
8 | HG01070.hp1 HG01071.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.695+673C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 6/8 | chr6 | 36915366 | |||||||
chr6:36915377 | T | A | 2 | a0001c0004t0007g0118 a0001c0004t0007g0120 |
2 | HG02145.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.695+684T>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 6/8 | chr6 | 36915377 | |||||||
chr6:36915536 | G | T | 1 | a0001c0001t0002g0210 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.695+843G>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 6/8 | chr6 | 36915536 | |||||||
chr6:36915565 | G | A | 2 | a0001c0004t0007g0118 a0001c0004t0007g0120 |
2 | HG02145.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.695+872G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 6/8 | chr6 | 36915565 | |||||||
chr6:36915729 | G | A | 2 | a0001c0002t0019g0111 a0001c0002t0037g0103 |
2 | HG02055.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.696-716G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 6/8 | chr6 | 36915729 | |||||||
chr6:36915738 | A | G | 2 | a0001c0002t0018g0023 a0001c0002t0030g0171 |
4 | HG00544.hp2 HG02071.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.696-707A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 6/8 | chr6 | 36915738 | |||||||
chr6:36915764 | A | G | 176 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(173): Show |
275 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(272): Show |
intron_variant | MODIFIER | c.696-681A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 6/8 | chr6 | 36915764 | |||||||
chr6:36915839 | C | T | 1 | a0001c0002t0005g0244 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.696-606C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 6/8 | chr6 | 36915839 | |||||||
chr6:36915972 | A | G | 17 | a0001c0002t0027g0070 a0001c0003t0006g0017 a0001c0003t0006g0031 others(14): Show |
21 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.696-473A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 6/8 | chr6 | 36915972 | |||||||
chr6:36915983 | A | G | 92 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0014 others(89): Show |
132 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.696-462A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 6/8 | chr6 | 36915983 | |||||||
chr6:36916028 | G | A | 1 | a0001c0002t0019g0104 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.696-417G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 6/8 | chr6 | 36916028 | |||||||
chr6:36916063 | A | C | 2 | a0001c0002t0023g0106 a0001c0002t0023g0107 |
2 | HG02109.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.696-382A>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 6/8 | chr6 | 36916063 | |||||||
chr6:36916092 | C | A | 1 | a0001c0001t0002g0203 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.696-353C>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 6/8 | chr6 | 36916092 | |||||||
chr6:36916095 | T | C | 39 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0014 others(36): Show |
57 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.696-350T>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 6/8 | chr6 | 36916095 | |||||||
chr6:36916116 | G | A | 2 | a0001c0001t0025g0168 a0001c0001t0025g0169 |
2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.696-329G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 6/8 | chr6 | 36916116 | |||||||
chr6:36916210 | C | T | 79 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0014 others(76): Show |
113 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.696-235C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 6/8 | chr6 | 36916210 | |||||||
chr6:36916252 | C | CTGTG | 2 | a0001c0001t0004g0048 a0001c0001t0004g0160 |
3 | HG02922.hp1 HG03453.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.696-187_696-184dup others(4): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 36916252 | ||||||
chr6:36916266 | A | G | 168 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(165): Show |
258 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.696-179A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 6/8 | chr6 | 36916266 | |||||||
chr6:36916290 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.696-155A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 6/8 | chr6 | 36916290 | |||||||
chr6:36916331 | A | G | 1 | a0001c0001t0002g0212 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.696-114A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 6/8 | chr6 | 36916331 | |||||||
chr6:36916345 | A | G | 18 | a0001c0002t0005g0004 a0001c0002t0005g0028 a0001c0002t0005g0029 others(15): Show |
29 | HG00140.hp1 HG00735.hp2 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.696-100A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 6/8 | chr6 | 36916345 | |||||||
chr6:36916588 | A | G | 1 | a0001c0002t0003g0167 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.825+14A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 7/8 | chr6 | 36916588 | |||||||
chr6:36916598 | GA | G | 16 | a0001c0003t0006g0017 a0001c0003t0006g0031 a0001c0003t0006g0032 others(13): Show |
20 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.825+25delA | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 7/8 | chr6 | 36916598 | |||||||
chr6:36916714 | C | T | 78 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0010 others(75): Show |
131 | HG00438.hp2 HG00558.hp2 HG00597.hp2 others(128): Show |
intron_variant | MODIFIER | c.825+140C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 7/8 | chr6 | 36916714 | |||||||
chr6:36916729 | G | T | 1 | a0001c0002t0035g0172 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.825+155G>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 7/8 | chr6 | 36916729 | |||||||
chr6:36916751 | A | C | 2 | a0001c0002t0013g0013 a0001c0002t0013g0060 |
5 | HG02922.hp2 HG02965.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.825+177A>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 7/8 | chr6 | 36916751 | |||||||
chr6:36916793 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.825+219G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 7/8 | chr6 | 36916793 | |||||||
chr6:36916794 | C | A | 2 | a0001c0002t0021g0117 a0001c0002t0021g0228 |
2 | HG01361.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.825+220C>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 7/8 | chr6 | 36916794 | |||||||
chr6:36916832 | C | T | 1 | a0001c0001t0002g0216 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.825+258C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 7/8 | chr6 | 36916832 | |||||||
chr6:36916905 | C | T | 87 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0014 others(84): Show |
122 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.825+331C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 7/8 | chr6 | 36916905 | |||||||
chr6:36916945 | G | A | 2 | a0001c0001t0025g0169 a0001c0002t0005g0238 |
2 | HG02040.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.825+371G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 7/8 | chr6 | 36916945 | |||||||
chr6:36917028 | A | G | 2 | a0001c0001t0015g0016 a0001c0001t0015g0170 |
5 | HG02647.hp1 HG03130.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.825+454A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 7/8 | chr6 | 36917028 | |||||||
chr6:36917136 | T | C | 98 | a0001c0001t0015g0016 a0001c0001t0015g0170 a0001c0001t0025g0168 others(95): Show |
141 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.825+562T>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 7/8 | chr6 | 36917136 | |||||||
chr6:36917712 | T | TGCCTCAG others(1): Show |
87 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0014 others(84): Show |
122 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.825+1139_825+1146d others(10): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 36917712 | ||||||
chr6:36917807 | G | GC | 92 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0014 others(89): Show |
132 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.825+1234dupC | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 36917807 | ||||||
chr6:36917816 | T | C | 2 | a0001c0002t0023g0106 a0001c0002t0023g0107 |
2 | HG02109.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.825+1242T>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 7/8 | chr6 | 36917816 | |||||||
chr6:36917860 | C | T | 2 | a0001c0005t0012g0007 a0001c0005t0012g0194 |
7 | HG01261.hp2 NA18984.hp1 NA18993.hp1 others(4): Show |
intron_variant | MODIFIER | c.825+1286C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 7/8 | chr6 | 36917860 | |||||||
chr6:36917909 | C | G | 1 | a0001c0001t0002g0208 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.825+1335C>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 7/8 | chr6 | 36917909 | |||||||
chr6:36917932 | G | A | 2 | a0001c0002t0019g0105 a0001c0002t0019g0111 |
2 | HG02630.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.825+1358G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 7/8 | chr6 | 36917932 | |||||||
chr6:36918043 | C | T | 1 | a0001c0002t0003g0085 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.825+1469C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 7/8 | chr6 | 36918043 | |||||||
chr6:36918292 | C | T | 3 | a0001c0002t0013g0013 a0001c0002t0013g0060 a0001c0002t0037g0103 |
6 | HG02055.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.826-1286C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 7/8 | chr6 | 36918292 | |||||||
chr6:36918317 | T | C | 3 | a0001c0002t0013g0013 a0001c0002t0013g0060 a0001c0002t0037g0103 |
6 | HG02055.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.826-1261T>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 7/8 | chr6 | 36918317 | |||||||
chr6:36918453 | A | G | 2 | a0001c0002t0018g0023 a0001c0002t0030g0171 |
4 | HG00544.hp2 HG02071.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.826-1125A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 7/8 | chr6 | 36918453 | |||||||
chr6:36918460 | G | A | 4 | a0001c0001t0002g0027 a0001c0001t0002g0242 a0001c0001t0026g0196 others(1): Show |
6 | HG00438.hp2 HG02965.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.826-1118G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 7/8 | chr6 | 36918460 | |||||||
chr6:36918495 | T | C | 3 | a0001c0002t0013g0013 a0001c0002t0013g0060 a0001c0002t0037g0103 |
6 | HG02055.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.826-1083T>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 7/8 | chr6 | 36918495 | |||||||
chr6:36918545 | A | AGAT | 4 | a0001c0002t0016g0055 a0001c0002t0016g0225 a0001c0002t0016g0226 others(1): Show |
5 | HG02615.hp1 HG02622.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.826-1031_826-1029d others(5): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr6 | 36918545 | ||||||
chr6:36918776 | C | T | 1 | a0001c0002t0020g0056 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.826-802C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 7/8 | chr6 | 36918776 | |||||||
chr6:36918832 | C | T | 2 | a0001c0001t0026g0196 a0001c0001t0026g0197 |
2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.826-746C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 7/8 | chr6 | 36918832 | |||||||
chr6:36918864 | T | G | 103 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0014 others(100): Show |
146 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.826-714T>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 7/8 | chr6 | 36918864 | |||||||
chr6:36918913 | T | G | 3 | a0001c0002t0013g0013 a0001c0002t0013g0060 a0001c0002t0037g0103 |
6 | HG02055.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.826-665T>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 7/8 | chr6 | 36918913 | |||||||
chr6:36919009 | T | C | 1 | a0001c0002t0035g0172 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.826-569T>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 7/8 | chr6 | 36919009 | |||||||
chr6:36919108 | T | G | 2 | a0001c0002t0018g0023 a0001c0002t0030g0171 |
4 | HG00544.hp2 HG02071.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.826-470T>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 7/8 | chr6 | 36919108 | |||||||
chr6:36919221 | T | C | 3 | a0001c0002t0013g0013 a0001c0002t0013g0060 a0001c0002t0037g0103 |
6 | HG02055.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.826-357T>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 7/8 | chr6 | 36919221 | |||||||
chr6:36919359 | A | C | 3 | a0001c0002t0013g0013 a0001c0002t0013g0060 a0001c0002t0037g0103 |
6 | HG02055.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.826-219A>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 7/8 | chr6 | 36919359 | |||||||
chr6:36919374 | C | G | 1 | a0001c0002t0009g0234 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.826-204C>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 7/8 | chr6 | 36919374 | |||||||
chr6:36919384 | C | G | 1 | a0001c0001t0001g0139 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.826-194C>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 7/8 | chr6 | 36919384 | |||||||
chr6:36919389 | C | T | 3 | a0001c0002t0013g0013 a0001c0002t0013g0060 a0001c0002t0037g0103 |
6 | HG02055.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.826-189C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 7/8 | chr6 | 36919389 | |||||||
chr6:36919406 | T | G | 10 | a0001c0002t0003g0014 a0001c0002t0003g0073 a0001c0002t0003g0074 others(7): Show |
12 | HG00438.hp1 HG02015.hp2 NA18946.hp2 others(9): Show |
intron_variant | MODIFIER | c.826-172T>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 7/8 | chr6 | 36919406 | |||||||
chr6:36919451 | T | C | 1 | a0001c0003t0006g0062 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.826-127T>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 7/8 | chr6 | 36919451 | |||||||
chr6:36919532 | G | A | 88 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0014 others(85): Show |
127 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.826-46G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 7/8 | chr6 | 36919532 | |||||||
chr6:36919921 | C | T | 1 | a0001c0001t0002g0204 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.949+220C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 8/8 | chr6 | 36919921 | |||||||
chr6:36919937 | A | G | 18 | a0001c0002t0005g0004 a0001c0002t0005g0028 a0001c0002t0005g0029 others(15): Show |
29 | HG00140.hp1 HG00735.hp2 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.949+236A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 8/8 | chr6 | 36919937 | |||||||
chr6:36919988 | C | T | 2 | a0001c0001t0002g0220 a0001c0001t0002g0221 |
2 | HG02083.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.949+287C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 8/8 | chr6 | 36919988 | |||||||
chr6:36920064 | C | T | 2 | a0001c0001t0026g0196 a0001c0001t0026g0197 |
2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.949+363C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 8/8 | chr6 | 36920064 | |||||||
chr6:36920082 | T | C | 4 | a0001c0002t0016g0055 a0001c0002t0016g0225 a0001c0002t0016g0226 others(1): Show |
5 | HG02615.hp1 HG02622.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.949+381T>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 8/8 | chr6 | 36920082 | |||||||
chr6:36920383 | T | A | 27 | a0001c0003t0006g0017 a0001c0003t0006g0031 a0001c0003t0006g0032 others(24): Show |
34 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.949+682T>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 8/8 | chr6 | 36920383 | |||||||
chr6:36920551 | T | G | 86 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0002t0003g0002 others(83): Show |
122 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.949+850T>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 8/8 | chr6 | 36920551 | |||||||
chr6:36920565 | G | C | 4 | a0001c0002t0021g0117 a0001c0002t0021g0228 a0001c0002t0027g0070 others(1): Show |
4 | HG01361.hp1 HG02451.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.949+864G>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 8/8 | chr6 | 36920565 | |||||||
chr6:36920612 | ATAAC | A | 34 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0014 others(31): Show |
51 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.949+913_949+916del others(4): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr6 | 36920612 | ||||||
chr6:36920904 | C | G | 2 | a0001c0002t0023g0106 a0001c0002t0023g0107 |
2 | HG02109.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.949+1203C>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 8/8 | chr6 | 36920904 | |||||||
chr6:36920978 | TA | T | 82 | a0001c0001t0002g0096 a0001c0001t0026g0197 a0001c0002t0003g0002 others(79): Show |
113 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.949+1289delA | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr6 | 36920978 | ||||||
chr6:36920979 | A | T | 1 | a0001c0001t0001g0138 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.949+1278A>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 8/8 | chr6 | 36920979 | |||||||
chr6:36921096 | T | G | 1 | a0001c0001t0008g0174 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.949+1395T>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 8/8 | chr6 | 36921096 | |||||||
chr6:36921121 | A | G | 1 | a0001c0002t0027g0070 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.949+1420A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 8/8 | chr6 | 36921121 | |||||||
chr6:36921441 | A | C | 1 | a0001c0001t0040g0219 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.949+1740A>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 8/8 | chr6 | 36921441 | |||||||
chr6:36921463 | G | A | 2 | a0001c0001t0026g0196 a0001c0001t0026g0197 |
2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.949+1762G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 8/8 | chr6 | 36921463 | |||||||
chr6:36921693 | ATGAGATC others(48): Show |
A | 1 | a0001c0001t0001g0153 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.950-1649_950-1595d others(57): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr6 | 36921693 | ||||||
chr6:36921736 | C | T | 13 | a0001c0002t0005g0004 a0001c0002t0005g0028 a0001c0002t0005g0058 others(10): Show |
21 | HG00140.hp1 HG00735.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.950-1611C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 8/8 | chr6 | 36921736 | |||||||
chr6:36921896 | C | T | 2 | a0001c0002t0023g0106 a0001c0002t0023g0107 |
2 | HG02109.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.950-1451C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 8/8 | chr6 | 36921896 | |||||||
chr6:36921905 | G | A | 4 | a0001c0001t0015g0016 a0001c0001t0015g0170 a0001c0001t0025g0168 others(1): Show |
7 | HG02647.hp1 HG03130.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.950-1442G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 8/8 | chr6 | 36921905 | |||||||
chr6:36921933 | T | C | 5 | a0001c0002t0013g0013 a0001c0002t0013g0060 a0001c0002t0018g0023 others(2): Show |
10 | HG00544.hp2 HG02055.hp1 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.950-1414T>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 8/8 | chr6 | 36921933 | |||||||
chr6:36921973 | A | AGCTATGA others(17): Show |
7 | a0001c0001t0002g0011 a0001c0001t0002g0027 a0001c0001t0002g0203 others(4): Show |
12 | HG00438.hp2 HG02132.hp1 HG03831.hp2 others(9): Show |
intron_variant | MODIFIER | c.950-1373_950-1350d others(26): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr6 | 36921973 | ||||||
chr6:36922014 | C | T | 2 | a0001c0001t0002g0207 a0001c0001t0002g0243 |
2 | NA18966.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.950-1333C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 8/8 | chr6 | 36922014 | |||||||
chr6:36922047 | A | T | 3 | a0001c0002t0013g0013 a0001c0002t0013g0060 a0001c0002t0037g0103 |
6 | HG02055.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.950-1300A>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 8/8 | chr6 | 36922047 | |||||||
chr6:36922110 | G | A | 1 | a0001c0002t0035g0172 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.950-1237G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 8/8 | chr6 | 36922110 | |||||||
chr6:36922210 | T | G | 1 | a0001c0002t0003g0090 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.950-1137T>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 8/8 | chr6 | 36922210 | |||||||
chr6:36922237 | G | A | 2 | a0001c0002t0023g0106 a0001c0002t0023g0107 |
2 | HG02109.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.950-1110G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 8/8 | chr6 | 36922237 | |||||||
chr6:36922288 | C | T | 1 | a0001c0002t0005g0029 | 3 | HG02109.hp1 HG02258.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.950-1059C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 8/8 | chr6 | 36922288 | |||||||
chr6:36922305 | A | G | 2 | a0001c0001t0026g0196 a0001c0001t0026g0197 |
2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.950-1042A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 8/8 | chr6 | 36922305 | |||||||
chr6:36922344 | AAAAAAAA others(5): Show |
A | 3 | a0001c0002t0013g0013 a0001c0002t0013g0060 a0001c0002t0037g0103 |
6 | HG02055.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.950-992_950-981del others(12): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr6 | 36922344 | ||||||
chr6:36922461 | A | C | 1 | a0001c0001t0002g0198 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.950-886A>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 8/8 | chr6 | 36922461 | |||||||
chr6:36922464 | C | G | 3 | a0001c0002t0013g0013 a0001c0002t0013g0060 a0001c0002t0037g0103 |
6 | HG02055.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.950-883C>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 8/8 | chr6 | 36922464 | |||||||
chr6:36922549 | T | C | 1 | a0001c0002t0005g0237 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.950-798T>C | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 8/8 | chr6 | 36922549 | |||||||
chr6:36922605 | A | G | 1 | a0001c0001t0002g0209 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.950-742A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 8/8 | chr6 | 36922605 | |||||||
chr6:36922713 | C | T | 1 | a0001c0002t0014g0076 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.950-634C>T | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 8/8 | chr6 | 36922713 | |||||||
chr6:36922740 | G | A | 1 | a0001c0002t0013g0060 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.950-607G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 8/8 | chr6 | 36922740 | |||||||
chr6:36922789 | A | G | 1 | a0001c0002t0020g0056 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.950-558A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 8/8 | chr6 | 36922789 | |||||||
chr6:36922906 | A | G | 1 | a0001c0003t0006g0064 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.950-441A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 8/8 | chr6 | 36922906 | |||||||
chr6:36922957 | G | A | 2 | a0001c0001t0026g0196 a0001c0001t0026g0197 |
2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.950-390G>A | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 8/8 | chr6 | 36922957 | |||||||
chr6:36923007 | T | G | 90 | a0001c0002t0003g0002 a0001c0002t0003g0008 a0001c0002t0003g0014 others(87): Show |
127 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.950-340T>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 8/8 | chr6 | 36923007 | |||||||
chr6:36923107 | A | G | 105 | a0001c0001t0026g0196 a0001c0001t0026g0197 a0001c0002t0003g0002 others(102): Show |
148 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.950-240A>G | C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 8/8 | chr6 | 36923107 | |||||||
chr6:36923155 | A | ACC | 2 | a0001c0001t0015g0016 a0001c0001t0015g0170 |
5 | HG02647.hp1 HG03130.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.950-189_950-188dup others(2): Show |
C6orf89 | ENSG00000198663.17 | transcript | ENST00000480824.7 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr6 | 36923155 |