Item | Value |
---|---|
geneid | 8530 |
ensemblid | ENSG00000077984.6 |
hgncid | 2479 |
symbol | CST7 |
name | cystatin F |
refseq_nuc | NM_003650.4 |
refseq_prot | NP_003641.3 |
ensembl_nuc | ENST00000480798.2 |
ensembl_prot | ENSP00000420384.1 |
mane_status | MANE Select |
chr | chr20 |
start | 24949269 |
end | 24959928 |
strand | + |
ver | v1.2 |
region | chr20:24949269-24959928 |
region5000 | chr20:24944269-24964928 |
regionname0 | CST7_chr20_24949269_24959928 |
regionname5000 | CST7_chr20_24944269_24964928 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 145 | 345 | 90 | 70 | 126 | 16 | 41 | 94 | CST7_chr20_24944269_24964928 | CST7 | MRAAG others(140): Show |
chr20 | 24944269 | 24964928 |
a0002 | 0/0 | 1 | 2 | 1 | 0 | 1 | 0 | 0 | 1 | CST7_chr20_24944269_24964928 | CST7 | M | chr20 | 24944269 | 24964928 |
a0003 | 0/0 | 145 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | MQAAG others(140): Show |
chr20 | 24944269 | 24964928 |
a0004 | 0/0 | 145 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CST7_chr20_24944269_24964928 | CST7 | MRAAG others(140): Show |
chr20 | 24944269 | 24964928 |
a0005 | 0/0 | 145 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CST7_chr20_24944269_24964928 | CST7 | MRAAG others(140): Show |
chr20 | 24944269 | 24964928 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 435 | 202 | 23 | 36 | 107 | 9 | 27 | CST7_chr20_24944269_24964928 | CST7 | ATGCG others(430): Show |
chr20 | 24944269 | 24964928 | ||
a0001c0002 | 1/1 | 435 | 140 | 64 | 34 | 19 | 7 | 14 | CST7_chr20_24944269_24964928 | CST7 | ATGCG others(430): Show |
chr20 | 24944269 | 24964928 | ||
a0001c0003 | 0/0 | 435 | 3 | 3 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | ATGCG others(430): Show |
chr20 | 24944269 | 24964928 | ||
a0002c0007 | 0/0 | 435 | 1 | 0 | 0 | 1 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | ATGTG others(430): Show |
chr20 | 24944269 | 24964928 | ||
a0002c0008 | 0/0 | 435 | 1 | 1 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | ATGTG others(430): Show |
chr20 | 24944269 | 24964928 | ||
a0003c0004 | 0/0 | 435 | 1 | 1 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | ATGCA others(430): Show |
chr20 | 24944269 | 24964928 | ||
a0004c0005 | 0/0 | 435 | 1 | 0 | 0 | 0 | 0 | 1 | CST7_chr20_24944269_24964928 | CST7 | ATGCG others(430): Show |
chr20 | 24944269 | 24964928 | ||
a0005c0006 | 0/0 | 435 | 1 | 0 | 0 | 1 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | ATGCG others(430): Show |
chr20 | 24944269 | 24964928 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 891 | 195 | 17 | 36 | 106 | 9 | 27 | CST7_chr20_24944269_24964928 | CST7 | ACTGT others(886): Show |
chr20 | 24944269 | 24964928 |
a0001c0001t0007 | 0/0 | 891 | 2 | 2 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | ACTGT others(886): Show |
chr20 | 24944269 | 24964928 |
a0001c0001t0010 | 0/0 | 891 | 2 | 2 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | ACTGT others(886): Show |
chr20 | 24944269 | 24964928 |
a0001c0001t0011 | 0/0 | 891 | 1 | 0 | 0 | 1 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | ACTGT others(886): Show |
chr20 | 24944269 | 24964928 |
a0001c0001t0012 | 0/0 | 891 | 1 | 1 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | ACTGT others(886): Show |
chr20 | 24944269 | 24964928 |
a0001c0001t0013 | 0/0 | 891 | 1 | 1 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | ACTGT others(886): Show |
chr20 | 24944269 | 24964928 |
a0001c0002t0002 | 1/0 | 891 | 67 | 39 | 15 | 0 | 3 | 9 | CST7_chr20_24944269_24964928 | CST7 | ACTGT others(886): Show |
chr20 | 24944269 | 24964928 |
a0001c0002t0003 | 0/1 | 891 | 33 | 4 | 8 | 15 | 1 | 4 | CST7_chr20_24944269_24964928 | CST7 | ACTGT others(886): Show |
chr20 | 24944269 | 24964928 |
a0001c0002t0004 | 0/0 | 891 | 25 | 10 | 11 | 0 | 3 | 1 | CST7_chr20_24944269_24964928 | CST7 | ACTGT others(886): Show |
chr20 | 24944269 | 24964928 |
a0001c0002t0005 | 0/0 | 888 | 7 | 7 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | ACTGT others(883): Show |
chr20 | 24944269 | 24964928 |
a0001c0002t0006 | 0/0 | 891 | 4 | 0 | 0 | 4 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | ACTGT others(886): Show |
chr20 | 24944269 | 24964928 |
a0001c0002t0008 | 0/0 | 891 | 2 | 2 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | ACTGT others(886): Show |
chr20 | 24944269 | 24964928 |
a0001c0002t0009 | 0/0 | 891 | 2 | 2 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | ACTGT others(886): Show |
chr20 | 24944269 | 24964928 |
a0001c0003t0005 | 0/0 | 888 | 3 | 3 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | ACTGT others(883): Show |
chr20 | 24944269 | 24964928 |
a0002c0007t0001 | 0/0 | 891 | 1 | 0 | 0 | 1 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | ACTGT others(886): Show |
chr20 | 24944269 | 24964928 |
a0002c0008t0002 | 0/0 | 891 | 1 | 1 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | ACTGT others(886): Show |
chr20 | 24944269 | 24964928 |
a0003c0004t0003 | 0/0 | 891 | 1 | 1 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | ACTGT others(886): Show |
chr20 | 24944269 | 24964928 |
a0004c0005t0002 | 0/0 | 891 | 1 | 0 | 0 | 0 | 0 | 1 | CST7_chr20_24944269_24964928 | CST7 | ACTGT others(886): Show |
chr20 | 24944269 | 24964928 |
a0005c0006t0003 | 0/0 | 891 | 1 | 0 | 0 | 1 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | ACTGT others(886): Show |
chr20 | 24944269 | 24964928 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 118 | 12 | 21 | 61 | 9 | 15 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0001t0001g0003 | 0/0 | 11 | 0 | 0 | 8 | 0 | 3 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0001t0001g0009 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0001t0001g0011 | 0/0 | 5 | 1 | 4 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0001t0001g0013 | 0/0 | 5 | 2 | 3 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0001t0007g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0001t0010g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0001t0010g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0001t0011g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0001t0012g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0001t0013g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0002g0004 | 0/0 | 12 | 11 | 1 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0002g0005 | 0/0 | 11 | 2 | 7 | 0 | 1 | 1 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0002g0008 | 0/0 | 6 | 0 | 2 | 0 | 0 | 4 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0002g0012 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0002g0015 | 0/0 | 4 | 0 | 1 | 0 | 0 | 3 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0002g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0002g0019 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0002g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0002g0092 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0003g0002 | 0/0 | 18 | 0 | 4 | 11 | 0 | 3 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0003g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0003g0016 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0003g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0003g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0003g0035 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0003g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0004g0006 | 0/0 | 12 | 2 | 7 | 0 | 3 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0004g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0004g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0004g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0004g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0004g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0004g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0004g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0005g0007 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0006g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0008g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0008g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0002t0009g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0003t0005g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0001c0003t0005g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0002c0007t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0002c0008t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0003c0004t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0004c0005t0002g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
a0005c0006t0003g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG00140 | hp1 | a0001 | c0002 | t0002 | g0005 | EUR | GBR | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG00323 | hp1 | a0001 | c0002 | t0002 | g0019 | EUR | FIN | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | CHS | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG00639 | hp2 | a0001 | c0002 | t0003 | g0048 | AMR | PUR | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG00642 | hp1 | a0001 | c0002 | t0002 | g0019 | AMR | PUR | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG00642 | hp2 | a0001 | c0002 | t0004 | g0006 | AMR | PUR | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG00673 | hp1 | a0001 | c0001 | t0011 | g0001 | EAS | CHS | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG00735 | hp1 | a0001 | c0002 | t0004 | g0006 | AMR | PUR | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG00738 | hp2 | a0001 | c0002 | t0004 | g0101 | AMR | PUR | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG00741 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | PUR | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01069 | hp2 | a0001 | c0002 | t0004 | g0104 | AMR | PUR | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01070 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PUR | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01071 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PUR | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01074 | hp1 | a0001 | c0002 | t0002 | g0034 | AMR | PUR | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01074 | hp2 | a0001 | c0002 | t0004 | g0006 | AMR | PUR | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01081 | hp1 | a0001 | c0002 | t0004 | g0006 | AMR | PUR | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01081 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PUR | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01106 | hp1 | a0001 | c0002 | t0004 | g0006 | AMR | PUR | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01109 | hp1 | a0001 | c0002 | t0002 | g0069 | AMR | PUR | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01109 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PUR | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01168 | hp2 | a0001 | c0002 | t0003 | g0002 | AMR | PUR | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01175 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | PUR | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01192 | hp1 | a0001 | c0002 | t0003 | g0016 | AMR | PUR | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01243 | hp2 | a0001 | c0002 | t0002 | g0079 | AMR | PUR | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01256 | hp1 | a0001 | c0002 | t0003 | g0002 | AMR | CLM | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01257 | hp1 | a0001 | c0002 | t0002 | g0015 | AMR | CLM | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01257 | hp2 | a0001 | c0002 | t0004 | g0006 | AMR | CLM | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01258 | hp1 | a0001 | c0002 | t0004 | g0006 | AMR | CLM | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01258 | hp2 | a0001 | c0002 | t0003 | g0002 | AMR | CLM | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01346 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | CLM | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01346 | hp2 | a0001 | c0002 | t0004 | g0040 | AMR | CLM | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01358 | hp2 | a0001 | c0002 | t0003 | g0022 | AMR | CLM | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01515 | hp1 | a0001 | c0002 | t0004 | g0006 | EUR | IBS | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01515 | hp2 | a0001 | c0002 | t0003 | g0016 | EUR | IBS | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01516 | hp1 | a0001 | c0002 | t0004 | g0006 | EUR | IBS | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01517 | hp1 | a0001 | c0002 | t0004 | g0006 | EUR | IBS | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01884 | hp1 | a0001 | c0002 | t0002 | g0089 | AFR | ACB | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01884 | hp2 | a0001 | c0002 | t0003 | g0047 | AFR | ACB | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01934 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01981 | hp1 | a0001 | c0002 | t0002 | g0008 | AMR | PEL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02055 | hp1 | a0001 | c0002 | t0002 | g0078 | AFR | ACB | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02055 | hp2 | a0001 | c0002 | t0004 | g0102 | AFR | ACB | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02145 | hp1 | a0001 | c0003 | t0005 | g0105 | AFR | ACB | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02145 | hp2 | a0001 | c0002 | t0004 | g0020 | AFR | ACB | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02257 | hp2 | a0001 | c0002 | t0002 | g0019 | AFR | ACB | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02258 | hp1 | a0001 | c0002 | t0002 | g0030 | AFR | ACB | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02258 | hp2 | a0001 | c0002 | t0002 | g0012 | AFR | ACB | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02280 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | ACB | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02293 | hp1 | a0001 | c0002 | t0003 | g0002 | AMR | PEL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02300 | hp2 | a0001 | c0002 | t0004 | g0100 | AMR | PEL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02451 | hp1 | a0001 | c0002 | t0002 | g0004 | AFR | ACB | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02451 | hp2 | a0001 | c0002 | t0002 | g0090 | AFR | ACB | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02572 | hp1 | a0001 | c0001 | t0012 | g0098 | AFR | GWD | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02572 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | GWD | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02602 | hp1 | a0001 | c0002 | t0003 | g0002 | SAS | PJL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02615 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | GWD | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02630 | hp1 | a0001 | c0002 | t0004 | g0103 | AFR | GWD | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02630 | hp2 | a0001 | c0002 | t0002 | g0018 | AFR | GWD | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02717 | hp1 | a0001 | c0002 | t0002 | g0004 | AFR | GWD | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02717 | hp2 | a0001 | c0002 | t0004 | g0107 | AFR | GWD | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02723 | hp1 | a0001 | c0002 | t0002 | g0087 | AFR | GWD | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02723 | hp2 | a0001 | c0002 | t0005 | g0007 | AFR | GWD | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02735 | hp2 | a0001 | c0002 | t0003 | g0045 | SAS | PJL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02738 | hp1 | a0001 | c0002 | t0002 | g0015 | SAS | PJL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02809 | hp1 | a0001 | c0002 | t0004 | g0020 | AFR | GWD | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02809 | hp2 | a0001 | c0002 | t0002 | g0012 | AFR | GWD | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02818 | hp1 | a0001 | c0002 | t0002 | g0083 | AFR | GWD | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02818 | hp2 | a0001 | c0002 | t0008 | g0051 | AFR | GWD | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02886 | hp2 | a0001 | c0002 | t0002 | g0091 | AFR | GWD | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02895 | hp1 | a0001 | c0002 | t0002 | g0018 | AFR | GWD | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02896 | hp1 | a0001 | c0002 | t0005 | g0007 | AFR | GWD | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02896 | hp2 | a0001 | c0001 | t0007 | g0001 | AFR | GWD | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02897 | hp1 | a0001 | c0002 | t0002 | g0018 | AFR | GWD | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02897 | hp2 | a0001 | c0002 | t0005 | g0007 | AFR | GWD | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02922 | hp1 | a0001 | c0002 | t0002 | g0030 | AFR | ESN | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02922 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | ESN | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02965 | hp1 | a0001 | c0002 | t0005 | g0007 | AFR | ESN | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02965 | hp2 | a0001 | c0001 | t0010 | g0097 | AFR | ESN | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02970 | hp1 | a0001 | c0002 | t0002 | g0005 | AFR | ESN | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02970 | hp2 | a0001 | c0001 | t0007 | g0001 | AFR | ESN | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02976 | hp1 | a0001 | c0002 | t0002 | g0004 | AFR | ESN | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02976 | hp2 | a0003 | c0004 | t0003 | g0041 | AFR | ESN | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG03017 | hp1 | a0001 | c0002 | t0002 | g0015 | SAS | PJL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG03041 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | GWD | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG03098 | hp1 | a0001 | c0002 | t0002 | g0071 | AFR | MSL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG03098 | hp2 | a0001 | c0001 | t0010 | g0096 | AFR | MSL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG03130 | hp1 | a0001 | c0002 | t0005 | g0007 | AFR | ESN | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG03130 | hp2 | a0001 | c0002 | t0002 | g0080 | AFR | ESN | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG03139 | hp1 | a0001 | c0002 | t0002 | g0084 | AFR | ESN | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG03139 | hp2 | a0001 | c0002 | t0002 | g0005 | AFR | ESN | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG03195 | hp1 | a0001 | c0002 | t0002 | g0012 | AFR | ESN | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG03195 | hp2 | a0001 | c0002 | t0005 | g0007 | AFR | ESN | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG03209 | hp1 | a0001 | c0002 | t0002 | g0082 | AFR | MSL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG03209 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | MSL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG03225 | hp1 | a0002 | c0008 | t0002 | g0088 | AFR | MSL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG03225 | hp2 | a0001 | c0002 | t0002 | g0072 | AFR | MSL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG03453 | hp1 | a0001 | c0002 | t0002 | g0012 | AFR | MSL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG03453 | hp2 | a0001 | c0002 | t0003 | g0049 | AFR | MSL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG03486 | hp1 | a0001 | c0002 | t0002 | g0004 | AFR | MSL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG03486 | hp2 | a0001 | c0002 | t0002 | g0012 | AFR | MSL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ESN | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG03516 | hp2 | a0001 | c0002 | t0002 | g0085 | AFR | ESN | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG03579 | hp1 | a0001 | c0002 | t0002 | g0086 | AFR | MSL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG03579 | hp2 | a0001 | c0002 | t0004 | g0032 | AFR | MSL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG03654 | hp1 | a0004 | c0005 | t0002 | g0005 | SAS | PJL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG03654 | hp2 | a0001 | c0002 | t0003 | g0002 | SAS | PJL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG03669 | hp1 | a0001 | c0002 | t0004 | g0099 | SAS | PJL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG03688 | hp1 | a0001 | c0002 | t0002 | g0008 | SAS | STU | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG03710 | hp2 | a0001 | c0002 | t0002 | g0095 | SAS | PJL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG03831 | hp2 | a0001 | c0002 | t0002 | g0005 | SAS | BEB | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | BEB | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG03927 | hp1 | a0001 | c0002 | t0002 | g0008 | SAS | BEB | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG03927 | hp2 | a0001 | c0002 | t0003 | g0002 | SAS | BEB | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG03942 | hp1 | a0001 | c0002 | t0002 | g0008 | SAS | BEB | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | STU | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG04228 | hp2 | a0001 | c0002 | t0002 | g0015 | SAS | STU | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18522 | hp1 | a0001 | c0003 | t0005 | g0033 | AFR | YRI | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | CHB | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18906 | hp2 | a0001 | c0002 | t0009 | g0031 | AFR | YRI | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18948 | hp2 | a0001 | c0002 | t0003 | g0050 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18954 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18956 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18965 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18973 | hp2 | a0001 | c0002 | t0006 | g0010 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18976 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18976 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18977 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18979 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18995 | hp1 | a0005 | c0006 | t0003 | g0002 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18995 | hp2 | a0001 | c0002 | t0006 | g0010 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18998 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA19009 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA19030 | hp1 | a0001 | c0002 | t0008 | g0056 | AFR | LWK | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA19043 | hp1 | a0001 | c0003 | t0005 | g0033 | AFR | LWK | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA19043 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | LWK | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA19054 | hp2 | a0001 | c0002 | t0006 | g0010 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA19057 | hp1 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA19065 | hp1 | a0002 | c0007 | t0001 | g0053 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA19066 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA19068 | hp1 | a0001 | c0002 | t0003 | g0023 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA19070 | hp2 | a0001 | c0002 | t0003 | g0023 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA19079 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA19084 | hp1 | a0001 | c0002 | t0003 | g0010 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA19085 | hp2 | a0001 | c0002 | t0006 | g0010 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA19087 | hp2 | a0001 | c0002 | t0003 | g0002 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA19240 | hp1 | a0001 | c0002 | t0004 | g0006 | AFR | YRI | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA19240 | hp2 | a0001 | c0002 | t0009 | g0031 | AFR | YRI | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA20129 | hp2 | a0001 | c0002 | t0004 | g0006 | AFR | ASW | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA20752 | hp1 | a0001 | c0002 | t0002 | g0094 | EUR | TSI | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA20905 | hp1 | a0001 | c0002 | t0002 | g0008 | SAS | GIH | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01123 | hp1 | a0001 | c0002 | t0002 | g0008 | AMR | CLM | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG01123 | hp2 | a0001 | c0002 | t0003 | g0022 | AMR | CLM | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02109 | hp1 | a0001 | c0002 | t0003 | g0046 | AFR | ACB | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02109 | hp2 | a0001 | c0001 | t0013 | g0003 | AFR | ACB | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02486 | hp2 | a0001 | c0002 | t0004 | g0020 | AFR | ACB | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG03471 | hp2 | a0001 | c0002 | t0005 | g0007 | AFR | MSL | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG06807 | hp1 | a0001 | c0002 | t0003 | g0016 | AFR | USA | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
HG06807 | hp2 | a0001 | c0002 | t0004 | g0032 | AFR | USA | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | USA | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA21309 | hp1 | a0001 | c0002 | t0002 | g0070 | AFR | LWK | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
NA21309 | hp2 | a0001 | c0002 | t0002 | g0081 | AFR | LWK | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
homoSapiens | chm13v2 | a0001 | c0002 | t0003 | g0035 | REF | REF | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0092 | REF | REF | CST7_chr20_24944269_24964928 | CST7 | chr20 | 24944269 | 24964928 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:24949509 | C | T | 1 | a0002 | 2 | HG03225.hp1 NA19065.hp1 |
stop_gained | HIGH | c.4C>T | p.Arg2* | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/4 | 241/891 | 4/438 | 2/145 | chr20 | 24949509 | |||
chr20:24949510 | G | A | 1 | a0003 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.5G>A | p.Arg2Gln | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/4 | 242/891 | 5/438 | 2/145 | chr20 | 24949510 | |||
chr20:24957446 | G | C | 1 | a0004 | 1 | HG03654.hp1 | missense_variant | MODERATE | c.230G>C | p.Arg77Thr | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 2/4 | 467/891 | 230/438 | 77/145 | chr20 | 24957446 | |||
chr20:24959686 | G | A | 1 | a0005 | 1 | NA18995.hp1 | missense_variant | MODERATE | c.412G>A | p.Glu138Lys | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 4/4 | 649/891 | 412/438 | 138/145 | chr20 | 24959686 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:24957411 | C | T | 1 | a0001c0003 | 3 | HG02145.hp1 NA18522.hp1 NA19043.hp1 |
synonymous_variant | LOW | c.195C>T | p.Asn65Asn | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 2/4 | 432/891 | 195/438 | 65/145 | chr20 | 24957411 | |||
chr20:24958954 | G | C | 2 | a0001c0001 a0002c0007 |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(200): Show |
synonymous_variant | LOW | c.270G>C | p.Leu90Leu | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 3/4 | 507/891 | 270/438 | 90/145 | chr20 | 24958954 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:24949275 | C | T | 1 | a0001c0001t0013 | 1 | HG02109.hp2 | 5_prime_UTR_variant | MODIFIER | c.-231C>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/4 | 231 | chr20 | 24949275 | ||||||
chr20:24949277 | A | G | 4 | a0001c0001t0010 a0001c0001t0012 a0001c0002t0004 others(1): Show |
30 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(27): Show |
5_prime_UTR_variant | MODIFIER | c.-229A>G | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/4 | 229 | chr20 | 24949277 | ||||||
chr20:24949311 | C | T | 4 | a0001c0002t0003 a0001c0002t0006 a0003c0004t0003 others(1): Show |
38 | HG00639.hp2 HG01123.hp2 HG01168.hp2 others(35): Show |
5_prime_UTR_variant | MODIFIER | c.-195C>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/4 | 195 | chr20 | 24949311 | ||||||
chr20:24949384 | C | T | 2 | a0001c0001t0010 a0001c0001t0012 |
3 | HG02572.hp1 HG02965.hp2 HG03098.hp2 |
5_prime_UTR_variant | MODIFIER | c.-122C>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/4 | 122 | chr20 | 24949384 | ||||||
chr20:24949410 | C | T | 1 | a0001c0001t0012 | 1 | HG02572.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-96C>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/4 | chr20 | 24949410 | |||||||
chr20:24949419 | A | C | 1 | a0001c0002t0009 | 2 | NA18906.hp2 NA19240.hp2 |
5_prime_UTR_variant | MODIFIER | c.-87A>C | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/4 | 87 | chr20 | 24949419 | ||||||
chr20:24949449 | G | A | 4 | a0001c0002t0003 a0001c0002t0006 a0003c0004t0003 others(1): Show |
38 | HG00639.hp2 HG01123.hp2 HG01168.hp2 others(35): Show |
5_prime_UTR_variant | MODIFIER | c.-57G>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/4 | 57 | chr20 | 24949449 | ||||||
chr20:24949501 | C | T | 1 | a0001c0002t0006 | 4 | NA18973.hp2 NA18995.hp2 NA19054.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-5C>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/4 | 5 | chr20 | 24949501 | ||||||
chr20:24959719 | C | A | 1 | a0001c0001t0011 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7C>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 4/4 | 7 | chr20 | 24959719 | ||||||
chr20:24959781 | C | T | 1 | a0001c0002t0008 | 2 | HG02818.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*69C>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 4/4 | 69 | chr20 | 24959781 | ||||||
chr20:24959831 | C | G | 2 | a0001c0002t0004 a0001c0002t0009 |
27 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*119C>G | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 4/4 | 119 | chr20 | 24959831 | ||||||
chr20:24959855 | G | A | 1 | a0001c0001t0007 | 2 | HG02896.hp2 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*143G>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 4/4 | 143 | chr20 | 24959855 | ||||||
chr20:24959885 | A | G | 9 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0010 others(6): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
3_prime_UTR_variant | MODIFIER | c.*173A>G | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 4/4 | 173 | chr20 | 24959885 | ||||||
chr20:24959885 | ACCT | A | 2 | a0001c0002t0005 a0001c0003t0005 |
10 | HG02145.hp1 HG02723.hp2 HG02896.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*177_*179delCCT | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 4/4 | 177 | INFO_REALIGN_3_PRIME | chr20 | 24959885 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:24949585 | G | A | 2 | a0001c0002t0002g0008 a0001c0002t0002g0034 |
7 | HG01074.hp1 HG01123.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.70+10G>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24949585 | |||||||
chr20:24949605 | C | T | 1 | a0001c0002t0004g0107 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.70+30C>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24949605 | |||||||
chr20:24949766 | G | A | 1 | a0001c0001t0001g0036 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.70+191G>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24949766 | |||||||
chr20:24949894 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.70+319C>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24949894 | |||||||
chr20:24949895 | G | A | 4 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(1): Show |
4 | HG01256.hp2 HG01346.hp2 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.70+320G>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24949895 | |||||||
chr20:24949994 | C | T | 2 | a0001c0003t0005g0033 a0001c0003t0005g0105 |
3 | HG02145.hp1 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.70+419C>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24949994 | |||||||
chr20:24950006 | C | T | 12 | a0001c0002t0004g0006 a0001c0002t0004g0020 a0001c0002t0004g0032 others(9): Show |
27 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.70+431C>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24950006 | |||||||
chr20:24950082 | A | C | 12 | a0001c0002t0004g0006 a0001c0002t0004g0020 a0001c0002t0004g0032 others(9): Show |
27 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.70+507A>C | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24950082 | |||||||
chr20:24950138 | CAA | C | 3 | a0001c0001t0010g0096 a0001c0001t0010g0097 a0001c0001t0012g0098 |
3 | HG02572.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.70+564_70+565delAA | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24950138 | |||||||
chr20:24950165 | T | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(82): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.70+590T>C | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24950165 | |||||||
chr20:24950199 | G | A | 1 | a0003c0004t0003g0041 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.70+624G>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24950199 | |||||||
chr20:24950420 | G | C | 1 | a0001c0001t0001g0042 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.70+845G>C | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24950420 | |||||||
chr20:24950521 | G | A | 13 | a0001c0001t0001g0043 a0001c0002t0004g0006 a0001c0002t0004g0020 others(10): Show |
28 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.70+946G>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24950521 | |||||||
chr20:24950629 | T | C | 1 | a0001c0001t0001g0021 | 2 | HG02083.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.70+1054T>C | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24950629 | |||||||
chr20:24950663 | A | G | 1 | a0001c0002t0002g0095 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.70+1088A>G | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24950663 | |||||||
chr20:24950668 | G | A | 1 | a0001c0002t0003g0022 | 2 | HG01123.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.70+1093G>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24950668 | |||||||
chr20:24950675 | A | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0017 |
8 | HG00738.hp1 HG00741.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.70+1100A>G | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24950675 | |||||||
chr20:24950709 | C | CCTT | 15 | a0001c0001t0010g0096 a0001c0001t0010g0097 a0001c0001t0012g0098 others(12): Show |
30 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.70+1138_70+1140dup others(3): Show |
CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr20 | 24950709 | ||||||
chr20:24950810 | T | C | 101 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(98): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.70+1235T>C | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24950810 | |||||||
chr20:24950875 | T | C | 13 | a0001c0001t0010g0096 a0001c0002t0004g0006 a0001c0002t0004g0020 others(10): Show |
28 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.70+1300T>C | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24950875 | |||||||
chr20:24950901 | C | T | 1 | a0001c0002t0004g0104 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.70+1326C>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24950901 | |||||||
chr20:24950949 | T | G | 12 | a0001c0002t0004g0006 a0001c0002t0004g0020 a0001c0002t0004g0032 others(9): Show |
27 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.70+1374T>G | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24950949 | |||||||
chr20:24951026 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.70+1451C>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24951026 | |||||||
chr20:24951029 | T | C | 2 | a0001c0001t0010g0097 a0001c0001t0012g0098 |
2 | HG02572.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.70+1454T>C | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24951029 | |||||||
chr20:24951048 | C | T | 3 | a0001c0001t0010g0096 a0001c0001t0010g0097 a0001c0001t0012g0098 |
3 | HG02572.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.70+1473C>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24951048 | |||||||
chr20:24951050 | G | A | 1 | a0001c0001t0001g0014 | 4 | HG00597.hp2 HG00621.hp2 HG02074.hp1 others(1): Show |
intron_variant | MODIFIER | c.70+1475G>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24951050 | |||||||
chr20:24951086 | T | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(82): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.70+1511T>C | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24951086 | |||||||
chr20:24951157 | G | A | 3 | a0001c0001t0010g0096 a0001c0001t0010g0097 a0001c0001t0012g0098 |
3 | HG02572.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.70+1582G>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24951157 | |||||||
chr20:24951178 | A | G | 1 | a0001c0001t0010g0096 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.70+1603A>G | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24951178 | |||||||
chr20:24951211 | G | C | 1 | a0001c0001t0001g0044 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.70+1636G>C | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24951211 | |||||||
chr20:24951213 | G | A | 1 | a0001c0002t0002g0078 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.70+1638G>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24951213 | |||||||
chr20:24951219 | T | C | 13 | a0001c0002t0003g0002 a0001c0002t0003g0010 a0001c0002t0003g0016 others(10): Show |
37 | HG00639.hp2 HG01123.hp2 HG01168.hp2 others(34): Show |
intron_variant | MODIFIER | c.70+1644T>C | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24951219 | |||||||
chr20:24951281 | G | A | 3 | a0001c0001t0010g0096 a0001c0001t0010g0097 a0001c0001t0012g0098 |
3 | HG02572.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.70+1706G>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24951281 | |||||||
chr20:24951328 | T | C | 15 | a0001c0001t0010g0096 a0001c0001t0010g0097 a0001c0001t0012g0098 others(12): Show |
30 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.70+1753T>C | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24951328 | |||||||
chr20:24951392 | A | G | 29 | a0001c0001t0010g0096 a0001c0001t0010g0097 a0001c0001t0012g0098 others(26): Show |
68 | HG00639.hp2 HG00642.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.70+1817A>G | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24951392 | |||||||
chr20:24951555 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.70+1980G>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24951555 | |||||||
chr20:24951568 | T | C | 15 | a0001c0001t0010g0096 a0001c0001t0010g0097 a0001c0001t0012g0098 others(12): Show |
30 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.70+1993T>C | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24951568 | |||||||
chr20:24951641 | G | A | 2 | a0001c0001t0010g0097 a0001c0001t0012g0098 |
2 | HG02572.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.70+2066G>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24951641 | |||||||
chr20:24951682 | G | A | 1 | a0001c0002t0008g0051 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.70+2107G>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24951682 | |||||||
chr20:24951801 | C | T | 1 | a0001c0002t0008g0051 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.70+2226C>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24951801 | |||||||
chr20:24951805 | C | T | 14 | a0001c0002t0003g0002 a0001c0002t0003g0010 a0001c0002t0003g0016 others(11): Show |
38 | HG00639.hp2 HG01123.hp2 HG01168.hp2 others(35): Show |
intron_variant | MODIFIER | c.70+2230C>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24951805 | |||||||
chr20:24951837 | C | G | 6 | a0001c0002t0002g0004 a0001c0002t0002g0030 a0001c0002t0002g0087 others(3): Show |
18 | HG01109.hp2 HG01884.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.70+2262C>G | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24951837 | |||||||
chr20:24951861 | G | A | 1 | a0001c0002t0002g0087 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.70+2286G>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24951861 | |||||||
chr20:24951913 | C | T | 3 | a0001c0001t0010g0096 a0001c0001t0010g0097 a0001c0001t0012g0098 |
3 | HG02572.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.70+2338C>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24951913 | |||||||
chr20:24952068 | G | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0052 |
3 | NA18968.hp2 NA18982.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.70+2493G>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24952068 | |||||||
chr20:24952081 | C | T | 1 | a0001c0001t0001g0076 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.70+2506C>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24952081 | |||||||
chr20:24952084 | G | T | 12 | a0001c0002t0004g0006 a0001c0002t0004g0020 a0001c0002t0004g0032 others(9): Show |
27 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.70+2509G>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24952084 | |||||||
chr20:24952151 | T | G | 1 | a0002c0007t0001g0053 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.70+2576T>G | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24952151 | |||||||
chr20:24952203 | T | G | 1 | a0001c0001t0001g0054 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.70+2628T>G | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24952203 | |||||||
chr20:24952205 | C | T | 3 | a0001c0002t0005g0007 a0001c0003t0005g0033 a0001c0003t0005g0105 |
10 | HG02145.hp1 HG02723.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.70+2630C>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24952205 | |||||||
chr20:24952234 | T | C | 2 | a0001c0001t0001g0055 a0001c0002t0004g0099 |
2 | HG02738.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.70+2659T>C | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24952234 | |||||||
chr20:24952254 | C | T | 3 | a0001c0001t0010g0096 a0001c0001t0010g0097 a0001c0001t0012g0098 |
3 | HG02572.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.70+2679C>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24952254 | |||||||
chr20:24952365 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.70+2790C>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24952365 | |||||||
chr20:24952422 | T | C | 1 | a0001c0002t0008g0056 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.70+2847T>C | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24952422 | |||||||
chr20:24952430 | T | C | 1 | a0001c0002t0005g0007 | 7 | HG02723.hp2 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.70+2855T>C | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24952430 | |||||||
chr20:24952435 | TCCG | T | 3 | a0001c0002t0002g0079 a0001c0002t0002g0080 a0001c0002t0002g0081 |
3 | HG01243.hp2 HG03130.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.70+2863_70+2865del others(3): Show |
CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr20 | 24952435 | ||||||
chr20:24952458 | G | C | 1 | a0001c0001t0001g0057 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.70+2883G>C | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24952458 | |||||||
chr20:24952482 | G | A | 12 | a0001c0002t0004g0006 a0001c0002t0004g0020 a0001c0002t0004g0032 others(9): Show |
27 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.70+2907G>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24952482 | |||||||
chr20:24952491 | A | G | 5 | a0001c0002t0004g0020 a0001c0002t0004g0032 a0001c0002t0004g0102 others(2): Show |
8 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.70+2916A>G | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24952491 | |||||||
chr20:24952568 | A | C | 1 | a0001c0002t0009g0031 | 2 | NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.70+2993A>C | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24952568 | |||||||
chr20:24952571 | C | T | 1 | a0001c0002t0002g0086 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.70+2996C>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24952571 | |||||||
chr20:24952701 | C | G | 3 | a0001c0001t0001g0029 a0001c0001t0001g0073 a0001c0001t0001g0074 |
4 | NA18940.hp1 NA18976.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.70+3126C>G | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24952701 | |||||||
chr20:24952726 | G | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(46): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.70+3151G>C | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24952726 | |||||||
chr20:24952746 | A | G | 1 | a0001c0002t0004g0103 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.70+3171A>G | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24952746 | |||||||
chr20:24952866 | A | C | 3 | a0001c0001t0010g0096 a0001c0001t0010g0097 a0001c0001t0012g0098 |
3 | HG02572.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.70+3291A>C | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24952866 | |||||||
chr20:24952887 | G | A | 1 | a0001c0002t0002g0091 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.70+3312G>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24952887 | |||||||
chr20:24952972 | C | CTT | 110 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(107): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.70+3397_70+3398ins others(2): Show |
CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24952972 | |||||||
chr20:24952978 | G | A | 3 | a0001c0001t0010g0096 a0001c0001t0010g0097 a0001c0001t0012g0098 |
3 | HG02572.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.70+3403G>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24952978 | |||||||
chr20:24952984 | T | C | 1 | a0001c0002t0004g0102 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.70+3409T>C | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24952984 | |||||||
chr20:24953056 | C | CT | 3 | a0001c0002t0002g0018 a0001c0002t0002g0078 a0001c0002t0002g0086 |
5 | HG02055.hp1 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.70+3482dupT | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr20 | 24953056 | ||||||
chr20:24953065 | A | G | 3 | a0001c0001t0010g0096 a0001c0001t0010g0097 a0001c0001t0012g0098 |
3 | HG02572.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.70+3490A>G | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24953065 | |||||||
chr20:24953139 | T | C | 2 | a0001c0003t0005g0033 a0001c0003t0005g0105 |
3 | HG02145.hp1 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.70+3564T>C | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24953139 | |||||||
chr20:24953163 | G | A | 1 | a0001c0002t0002g0095 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.70+3588G>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24953163 | |||||||
chr20:24953166 | C | T | 15 | a0001c0001t0010g0096 a0001c0001t0010g0097 a0001c0001t0012g0098 others(12): Show |
30 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.70+3591C>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24953166 | |||||||
chr20:24953195 | A | C | 101 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(98): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.70+3620A>C | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24953195 | |||||||
chr20:24953207 | A | G | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(46): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.70+3632A>G | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24953207 | |||||||
chr20:24953211 | G | A | 1 | a0003c0004t0003g0041 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.70+3636G>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24953211 | |||||||
chr20:24953239 | G | C | 1 | a0001c0002t0005g0007 | 7 | HG02723.hp2 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.70+3664G>C | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24953239 | |||||||
chr20:24953285 | C | T | 1 | a0001c0001t0001g0028 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.70+3710C>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24953285 | |||||||
chr20:24953287 | G | A | 12 | a0001c0002t0004g0006 a0001c0002t0004g0020 a0001c0002t0004g0032 others(9): Show |
27 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.70+3712G>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24953287 | |||||||
chr20:24953373 | A | C | 1 | a0001c0001t0001g0068 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.70+3798A>C | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24953373 | |||||||
chr20:24953460 | A | AG | 3 | a0001c0001t0010g0096 a0001c0001t0010g0097 a0001c0001t0012g0098 |
3 | HG02572.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.71-3826dupG | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr20 | 24953460 | ||||||
chr20:24953534 | A | C | 3 | a0001c0001t0010g0096 a0001c0001t0010g0097 a0001c0001t0012g0098 |
3 | HG02572.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.71-3753A>C | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24953534 | |||||||
chr20:24953690 | G | A | 1 | a0001c0002t0002g0079 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.71-3597G>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24953690 | |||||||
chr20:24953697 | A | T | 1 | a0001c0001t0001g0076 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.71-3590A>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24953697 | |||||||
chr20:24953702 | G | C | 3 | a0001c0001t0010g0096 a0001c0001t0010g0097 a0001c0001t0012g0098 |
3 | HG02572.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.71-3585G>C | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24953702 | |||||||
chr20:24953727 | C | T | 1 | a0001c0002t0002g0081 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.71-3560C>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24953727 | |||||||
chr20:24953765 | C | T | 1 | a0001c0002t0009g0031 | 2 | NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.71-3522C>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24953765 | |||||||
chr20:24953882 | G | A | 3 | a0001c0001t0010g0096 a0001c0001t0010g0097 a0001c0001t0012g0098 |
3 | HG02572.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.71-3405G>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24953882 | |||||||
chr20:24953884 | C | CA | 3 | a0001c0002t0002g0069 a0001c0002t0008g0051 a0001c0002t0008g0056 |
3 | HG01109.hp1 HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.71-3402dupA | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr20 | 24953884 | ||||||
chr20:24953889 | C | T | 6 | a0001c0002t0002g0018 a0001c0002t0002g0078 a0001c0002t0002g0079 others(3): Show |
8 | HG01243.hp2 HG02055.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.71-3398C>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24953889 | |||||||
chr20:24953947 | A | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0075 |
6 | HG01175.hp2 HG01433.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.71-3340A>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24953947 | |||||||
chr20:24954103 | G | T | 2 | a0001c0001t0010g0097 a0001c0001t0012g0098 |
2 | HG02572.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.71-3184G>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24954103 | |||||||
chr20:24954150 | C | G | 1 | a0001c0001t0001g0039 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.71-3137C>G | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24954150 | |||||||
chr20:24954156 | G | T | 2 | a0001c0001t0010g0097 a0001c0001t0012g0098 |
2 | HG02572.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.71-3131G>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24954156 | |||||||
chr20:24954193 | T | C | 3 | a0001c0002t0002g0079 a0001c0002t0002g0080 a0001c0002t0002g0081 |
3 | HG01243.hp2 HG03130.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.71-3094T>C | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24954193 | |||||||
chr20:24954287 | A | G | 4 | a0001c0001t0010g0096 a0001c0001t0010g0097 a0001c0001t0012g0098 others(1): Show |
4 | HG01109.hp1 HG02572.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-3000A>G | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24954287 | |||||||
chr20:24954295 | C | A | 1 | a0001c0002t0002g0070 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.71-2992C>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24954295 | |||||||
chr20:24954318 | A | ATC | 7 | a0001c0001t0010g0096 a0001c0001t0010g0097 a0001c0001t0012g0098 others(4): Show |
9 | HG01109.hp1 HG02055.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.71-2969_71-2968ins others(2): Show |
CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24954318 | |||||||
chr20:24954334 | C | T | 11 | a0001c0002t0004g0006 a0001c0002t0004g0020 a0001c0002t0004g0040 others(8): Show |
25 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.71-2953C>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24954334 | |||||||
chr20:24954381 | G | A | 1 | a0001c0002t0003g0016 | 3 | HG01192.hp1 HG01515.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.71-2906G>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24954381 | |||||||
chr20:24954399 | T | C | 1 | a0001c0001t0001g0058 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.71-2888T>C | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24954399 | |||||||
chr20:24954412 | T | G | 65 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(62): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.71-2875T>G | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24954412 | |||||||
chr20:24954437 | C | T | 4 | a0001c0002t0002g0082 a0001c0002t0002g0083 a0001c0002t0002g0084 others(1): Show |
4 | HG02818.hp1 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.71-2850C>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24954437 | |||||||
chr20:24954456 | T | C | 92 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(89): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.71-2831T>C | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24954456 | |||||||
chr20:24954530 | T | C | 1 | a0001c0002t0003g0045 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.71-2757T>C | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24954530 | |||||||
chr20:24954555 | ATAGGTTT others(3): Show |
A | 1 | a0001c0001t0001g0066 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.71-2730_71-2721del others(10): Show |
CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr20 | 24954555 | ||||||
chr20:24954873 | T | C | 1 | a0001c0001t0001g0025 | 2 | NA18944.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.71-2414T>C | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24954873 | |||||||
chr20:24954981 | T | G | 47 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(44): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.71-2306T>G | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24954981 | |||||||
chr20:24955040 | C | A | 1 | a0001c0001t0012g0098 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.71-2247C>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24955040 | |||||||
chr20:24955043 | C | A | 2 | a0001c0001t0010g0096 a0001c0001t0010g0097 |
2 | HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.71-2244C>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24955043 | |||||||
chr20:24955047 | A | G | 3 | a0001c0002t0002g0083 a0001c0002t0002g0084 a0001c0002t0002g0085 |
3 | HG02818.hp1 HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.71-2240A>G | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24955047 | |||||||
chr20:24955051 | AC | A | 6 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0002t0002g0082 others(3): Show |
11 | HG00673.hp2 HG02027.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.71-2235delC | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24955051 | |||||||
chr20:24955053 | AAC | A | 6 | a0001c0001t0012g0098 a0001c0002t0002g0004 a0001c0002t0002g0087 others(3): Show |
17 | HG01109.hp2 HG01884.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.71-2232_71-2231del others(2): Show |
CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr20 | 24955053 | ||||||
chr20:24955054 | AC | A | 71 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(68): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.71-2232delC | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24955054 | |||||||
chr20:24955055 | C | A | 23 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0026 others(20): Show |
45 | HG00642.hp2 HG00673.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.71-2232C>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24955055 | |||||||
chr20:24955055 | CA | C | 4 | a0001c0001t0001g0054 a0001c0002t0002g0012 a0001c0002t0002g0071 others(1): Show |
6 | HG02809.hp2 HG03098.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.71-2223delA | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr20 | 24955055 | ||||||
chr20:24955112 | T | C | 108 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(105): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.71-2175T>C | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24955112 | |||||||
chr20:24955190 | T | G | 62 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(59): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.71-2097T>G | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24955190 | |||||||
chr20:24955265 | A | C | 15 | a0001c0001t0010g0096 a0001c0001t0010g0097 a0001c0001t0012g0098 others(12): Show |
30 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.71-2022A>C | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24955265 | |||||||
chr20:24955392 | C | T | 12 | a0001c0002t0004g0006 a0001c0002t0004g0020 a0001c0002t0004g0032 others(9): Show |
27 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.71-1895C>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24955392 | |||||||
chr20:24955439 | C | G | 2 | a0001c0001t0001g0009 a0001c0001t0001g0065 |
7 | HG00597.hp1 HG00609.hp2 NA18962.hp2 others(4): Show |
intron_variant | MODIFIER | c.71-1848C>G | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24955439 | |||||||
chr20:24955446 | C | CT | 9 | a0001c0001t0001g0003 a0001c0001t0001g0036 a0001c0001t0001g0058 others(6): Show |
19 | HG01109.hp1 HG02109.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.71-1822dupT | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr20 | 24955446 | ||||||
chr20:24955446 | CT | C | 18 | a0001c0001t0001g0065 a0001c0002t0002g0071 a0001c0002t0002g0082 others(15): Show |
34 | HG00642.hp2 HG00735.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.71-1822delT | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr20 | 24955446 | ||||||
chr20:24955580 | C | G | 86 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(83): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.71-1707C>G | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24955580 | |||||||
chr20:24955593 | G | C | 2 | a0001c0001t0010g0097 a0001c0001t0012g0098 |
2 | HG02572.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.71-1694G>C | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24955593 | |||||||
chr20:24955598 | C | T | 3 | a0001c0002t0002g0018 a0001c0002t0002g0078 a0001c0002t0002g0086 |
5 | HG02055.hp1 HG02630.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-1689C>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24955598 | |||||||
chr20:24955696 | G | A | 7 | a0001c0002t0002g0012 a0001c0002t0002g0069 a0001c0002t0002g0070 others(4): Show |
11 | HG01109.hp1 HG02258.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.71-1591G>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24955696 | |||||||
chr20:24955829 | G | A | 12 | a0001c0002t0004g0006 a0001c0002t0004g0020 a0001c0002t0004g0032 others(9): Show |
27 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.71-1458G>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24955829 | |||||||
chr20:24955870 | G | A | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | NA18940.hp1 NA18976.hp1 |
intron_variant | MODIFIER | c.71-1417G>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24955870 | |||||||
chr20:24955906 | G | C | 1 | a0001c0001t0001g0037 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.71-1381G>C | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24955906 | |||||||
chr20:24955958 | C | G | 11 | a0001c0002t0003g0002 a0001c0002t0003g0010 a0001c0002t0003g0016 others(8): Show |
35 | HG00639.hp2 HG01123.hp2 HG01168.hp2 others(32): Show |
intron_variant | MODIFIER | c.71-1329C>G | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24955958 | |||||||
chr20:24956066 | C | T | 3 | a0001c0001t0010g0096 a0001c0001t0010g0097 a0001c0001t0012g0098 |
3 | HG02572.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.71-1221C>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24956066 | |||||||
chr20:24956068 | G | T | 2 | a0001c0001t0010g0097 a0001c0001t0012g0098 |
2 | HG02572.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.71-1219G>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24956068 | |||||||
chr20:24956128 | C | T | 1 | a0001c0002t0003g0049 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.71-1159C>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24956128 | |||||||
chr20:24956152 | G | T | 1 | a0003c0004t0003g0041 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.71-1135G>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24956152 | |||||||
chr20:24956287 | C | T | 2 | a0001c0002t0003g0046 a0001c0002t0003g0047 |
2 | HG01884.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.71-1000C>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24956287 | |||||||
chr20:24956292 | G | A | 2 | a0001c0001t0010g0097 a0001c0001t0012g0098 |
2 | HG02572.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.71-995G>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24956292 | |||||||
chr20:24956359 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.71-928C>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24956359 | |||||||
chr20:24956432 | C | T | 1 | a0001c0002t0005g0007 | 7 | HG02723.hp2 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.71-855C>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24956432 | |||||||
chr20:24956436 | C | T | 1 | a0001c0001t0001g0052 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.71-851C>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24956436 | |||||||
chr20:24956486 | C | A | 1 | a0001c0001t0001g0017 | 3 | HG00738.hp1 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.71-801C>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24956486 | |||||||
chr20:24956505 | A | G | 2 | a0001c0001t0010g0097 a0001c0001t0012g0098 |
2 | HG02572.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.71-782A>G | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24956505 | |||||||
chr20:24956636 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.71-651C>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24956636 | |||||||
chr20:24956649 | A | C | 15 | a0001c0001t0010g0096 a0001c0001t0010g0097 a0001c0001t0012g0098 others(12): Show |
30 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.71-638A>C | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24956649 | |||||||
chr20:24956662 | G | A | 3 | a0001c0001t0010g0096 a0001c0001t0010g0097 a0001c0001t0012g0098 |
3 | HG02572.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.71-625G>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24956662 | |||||||
chr20:24956717 | A | G | 3 | a0001c0001t0010g0096 a0001c0001t0010g0097 a0001c0001t0012g0098 |
3 | HG02572.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.71-570A>G | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24956717 | |||||||
chr20:24956731 | G | A | 12 | a0001c0002t0004g0006 a0001c0002t0004g0020 a0001c0002t0004g0032 others(9): Show |
27 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.71-556G>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24956731 | |||||||
chr20:24956758 | G | T | 2 | a0001c0002t0008g0051 a0001c0002t0008g0056 |
2 | HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.71-529G>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24956758 | |||||||
chr20:24956772 | A | T | 3 | a0001c0001t0010g0096 a0001c0001t0010g0097 a0001c0001t0012g0098 |
3 | HG02572.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.71-515A>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24956772 | |||||||
chr20:24956798 | G | A | 1 | a0001c0002t0002g0083 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.71-489G>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24956798 | |||||||
chr20:24956831 | C | T | 4 | a0001c0001t0001g0043 a0001c0001t0010g0096 a0001c0001t0010g0097 others(1): Show |
4 | HG02572.hp1 HG02965.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-456C>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24956831 | |||||||
chr20:24956858 | T | C | 1 | a0001c0002t0002g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.71-429T>C | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24956858 | |||||||
chr20:24956953 | A | G | 12 | a0001c0002t0004g0006 a0001c0002t0004g0020 a0001c0002t0004g0032 others(9): Show |
27 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.71-334A>G | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24956953 | |||||||
chr20:24956971 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.71-316C>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24956971 | |||||||
chr20:24956977 | A | G | 1 | a0001c0002t0002g0072 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.71-310A>G | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24956977 | |||||||
chr20:24957013 | G | GGGGAGCA others(7): Show |
6 | a0001c0002t0004g0020 a0001c0002t0004g0032 a0001c0002t0004g0102 others(3): Show |
10 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.71-271_71-270insAG others(12): Show |
CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr20 | 24957013 | ||||||
chr20:24957017 | G | A | 7 | a0001c0002t0002g0091 a0001c0002t0004g0006 a0001c0002t0004g0040 others(4): Show |
18 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.71-270G>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24957017 | |||||||
chr20:24957026 | G | GA | 6 | a0001c0002t0004g0006 a0001c0002t0004g0040 a0001c0002t0004g0099 others(3): Show |
17 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.71-261_71-260insA | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24957026 | |||||||
chr20:24957026 | G | GAGGGGGC others(33): Show |
4 | a0001c0001t0010g0096 a0001c0001t0010g0097 a0001c0001t0012g0098 others(1): Show |
4 | HG02572.hp1 HG02886.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-261_71-260insAG others(38): Show |
CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24957026 | |||||||
chr20:24957028 | G | GA | 6 | a0001c0002t0004g0020 a0001c0002t0004g0032 a0001c0002t0004g0102 others(3): Show |
10 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.71-259_71-258insA | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24957028 | |||||||
chr20:24957030 | A | G | 10 | a0001c0001t0010g0096 a0001c0001t0010g0097 a0001c0001t0012g0098 others(7): Show |
21 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.71-257A>G | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24957030 | |||||||
chr20:24957038 | A | AG | 4 | a0001c0001t0010g0096 a0001c0001t0010g0097 a0001c0001t0012g0098 others(1): Show |
4 | HG02572.hp1 HG02886.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-248dupG | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr20 | 24957038 | ||||||
chr20:24957040 | A | G | 6 | a0001c0002t0004g0006 a0001c0002t0004g0040 a0001c0002t0004g0099 others(3): Show |
17 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.71-247A>G | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24957040 | |||||||
chr20:24957042 | G | A | 6 | a0001c0002t0004g0006 a0001c0002t0004g0040 a0001c0002t0004g0099 others(3): Show |
17 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.71-245G>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24957042 | |||||||
chr20:24957044 | G | A | 6 | a0001c0002t0004g0006 a0001c0002t0004g0040 a0001c0002t0004g0099 others(3): Show |
17 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.71-243G>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24957044 | |||||||
chr20:24957045 | G | A | 6 | a0001c0002t0004g0006 a0001c0002t0004g0040 a0001c0002t0004g0099 others(3): Show |
17 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.71-242G>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24957045 | |||||||
chr20:24957055 | GA | G | 6 | a0001c0002t0004g0006 a0001c0002t0004g0040 a0001c0002t0004g0099 others(3): Show |
17 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.71-231delA | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24957055 | |||||||
chr20:24957058 | A | C | 1 | a0001c0001t0001g0027 | 2 | NA19078.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.71-229A>C | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24957058 | |||||||
chr20:24957058 | A | G | 6 | a0001c0002t0004g0006 a0001c0002t0004g0040 a0001c0002t0004g0099 others(3): Show |
17 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.71-229A>G | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24957058 | |||||||
chr20:24957059 | A | ACAGGTGA others(6): Show |
79 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(76): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.71-216_71-215insGC others(11): Show |
CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr20 | 24957059 | ||||||
chr20:24957059 | A | AGGTGAGA others(32): Show |
1 | a0001c0001t0001g0027 | 2 | NA19078.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.71-228_71-227insGG others(37): Show |
CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24957059 | |||||||
chr20:24957059 | A | G | 6 | a0001c0002t0004g0006 a0001c0002t0004g0040 a0001c0002t0004g0099 others(3): Show |
17 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.71-228A>G | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24957059 | |||||||
chr20:24957065 | G | GGGGGGCA others(99): Show |
3 | a0001c0001t0010g0096 a0001c0001t0010g0097 a0001c0001t0012g0098 |
3 | HG02572.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.71-222_71-221insGG others(104): Show |
CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24957065 | |||||||
chr20:24957065 | G | GGGGGGCA others(99): Show |
1 | a0001c0002t0002g0091 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.71-222_71-221insGG others(104): Show |
CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24957065 | |||||||
chr20:24957066 | A | AG | 21 | a0001c0002t0002g0004 a0001c0002t0002g0005 a0001c0002t0002g0008 others(18): Show |
55 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.71-216dupG | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr20 | 24957066 | ||||||
chr20:24957077 | GA | G | 4 | a0001c0001t0010g0096 a0001c0001t0010g0097 a0001c0001t0012g0098 others(1): Show |
4 | HG02572.hp1 HG02886.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-209delA | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24957077 | |||||||
chr20:24957078 | A | AGGAGGGG others(139): Show |
46 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(43): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.71-207_71-206insAG others(144): Show |
CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr20 | 24957078 | ||||||
chr20:24957078 | A | AGGAGGGG others(140): Show |
1 | a0001c0001t0001g0036 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.71-207_71-206insAG others(145): Show |
CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr20 | 24957078 | ||||||
chr20:24957078 | A | AGGAGGGG others(139): Show |
38 | a0001c0002t0002g0012 a0001c0002t0002g0069 a0001c0002t0002g0070 others(35): Show |
88 | HG00639.hp2 HG00642.hp2 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.71-207_71-206insAG others(144): Show |
CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr20 | 24957078 | ||||||
chr20:24957078 | A | AGGAGGGG others(137): Show |
1 | a0001c0002t0002g0080 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.71-207_71-206insAG others(142): Show |
CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr20 | 24957078 | ||||||
chr20:24957078 | A | AGGAGGGG others(139): Show |
1 | a0001c0001t0001g0024 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.71-207_71-206insAG others(144): Show |
CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr20 | 24957078 | ||||||
chr20:24957078 | A | AGGGGGCA others(166): Show |
1 | a0001c0002t0008g0051 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.71-204_71-203insCA others(171): Show |
CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr20 | 24957078 | ||||||
chr20:24957078 | A | AGGGGGCA others(151): Show |
5 | a0001c0002t0002g0004 a0001c0002t0002g0030 a0001c0002t0002g0087 others(2): Show |
14 | HG01109.hp2 HG01884.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.71-204_71-203insCA others(156): Show |
CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr20 | 24957078 | ||||||
chr20:24957078 | A | AGGGGGCA others(151): Show |
8 | a0001c0002t0002g0004 a0001c0002t0002g0018 a0001c0002t0002g0078 others(5): Show |
12 | HG02055.hp1 HG02630.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.71-204_71-203insCA others(156): Show |
CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr20 | 24957078 | ||||||
chr20:24957078 | A | AGGGGGCA others(151): Show |
7 | a0001c0002t0002g0005 a0001c0002t0002g0008 a0001c0002t0002g0015 others(4): Show |
27 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.71-204_71-203insCA others(156): Show |
CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr20 | 24957078 | ||||||
chr20:24957078 | A | AGGGGGCA others(256): Show |
1 | a0001c0002t0002g0094 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.71-204_71-203insCA others(261): Show |
CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr20 | 24957078 | ||||||
chr20:24957186 | C | T | 12 | a0001c0002t0004g0006 a0001c0002t0004g0020 a0001c0002t0004g0032 others(9): Show |
27 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.71-101C>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 1/3 | chr20 | 24957186 | |||||||
chr20:24957470 | G | C | 1 | a0001c0002t0002g0089 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.243+11G>C | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 2/3 | chr20 | 24957470 | |||||||
chr20:24957485 | A | G | 15 | a0001c0001t0010g0096 a0001c0001t0010g0097 a0001c0001t0012g0098 others(12): Show |
30 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.243+26A>G | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 2/3 | chr20 | 24957485 | |||||||
chr20:24957521 | G | A | 1 | a0001c0002t0004g0101 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.243+62G>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 2/3 | chr20 | 24957521 | |||||||
chr20:24957523 | G | A | 12 | a0001c0002t0004g0006 a0001c0002t0004g0020 a0001c0002t0004g0032 others(9): Show |
27 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.243+64G>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 2/3 | chr20 | 24957523 | |||||||
chr20:24957537 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.243+78C>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 2/3 | chr20 | 24957537 | |||||||
chr20:24957543 | G | A | 3 | a0001c0001t0010g0096 a0001c0001t0010g0097 a0001c0001t0012g0098 |
3 | HG02572.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.243+84G>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 2/3 | chr20 | 24957543 | |||||||
chr20:24957559 | C | T | 47 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(44): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.243+100C>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 2/3 | chr20 | 24957559 | |||||||
chr20:24957630 | C | G | 14 | a0001c0002t0003g0002 a0001c0002t0003g0010 a0001c0002t0003g0016 others(11): Show |
38 | HG00639.hp2 HG01123.hp2 HG01168.hp2 others(35): Show |
intron_variant | MODIFIER | c.243+171C>G | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 2/3 | chr20 | 24957630 | |||||||
chr20:24957636 | T | C | 3 | a0001c0001t0010g0096 a0001c0001t0010g0097 a0001c0001t0012g0098 |
3 | HG02572.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.243+177T>C | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 2/3 | chr20 | 24957636 | |||||||
chr20:24957652 | G | A | 15 | a0001c0001t0010g0096 a0001c0001t0010g0097 a0001c0001t0012g0098 others(12): Show |
30 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.243+193G>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 2/3 | chr20 | 24957652 | |||||||
chr20:24957653 | C | T | 3 | a0001c0001t0010g0096 a0001c0001t0010g0097 a0001c0001t0012g0098 |
3 | HG02572.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.243+194C>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 2/3 | chr20 | 24957653 | |||||||
chr20:24957750 | G | A | 3 | a0001c0001t0010g0096 a0001c0001t0010g0097 a0001c0001t0012g0098 |
3 | HG02572.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.243+291G>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 2/3 | chr20 | 24957750 | |||||||
chr20:24957751 | G | C | 3 | a0001c0001t0010g0096 a0001c0001t0010g0097 a0001c0001t0012g0098 |
3 | HG02572.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.243+292G>C | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 2/3 | chr20 | 24957751 | |||||||
chr20:24957770 | A | T | 1 | a0001c0001t0001g0026 | 2 | NA19003.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.243+311A>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 2/3 | chr20 | 24957770 | |||||||
chr20:24957784 | G | C | 1 | a0001c0002t0002g0079 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.243+325G>C | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 2/3 | chr20 | 24957784 | |||||||
chr20:24957880 | T | C | 3 | a0001c0001t0010g0096 a0001c0001t0010g0097 a0001c0001t0012g0098 |
3 | HG02572.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.243+421T>C | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 2/3 | chr20 | 24957880 | |||||||
chr20:24957890 | G | C | 3 | a0001c0001t0010g0096 a0001c0001t0010g0097 a0001c0001t0012g0098 |
3 | HG02572.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.243+431G>C | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 2/3 | chr20 | 24957890 | |||||||
chr20:24957964 | G | A | 3 | a0001c0001t0010g0096 a0001c0001t0010g0097 a0001c0001t0012g0098 |
3 | HG02572.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.243+505G>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 2/3 | chr20 | 24957964 | |||||||
chr20:24958080 | G | A | 3 | a0001c0001t0010g0096 a0001c0001t0010g0097 a0001c0001t0012g0098 |
3 | HG02572.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.243+621G>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 2/3 | chr20 | 24958080 | |||||||
chr20:24958130 | G | A | 6 | a0001c0002t0002g0004 a0001c0002t0002g0030 a0001c0002t0002g0087 others(3): Show |
18 | HG01109.hp2 HG01884.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.243+671G>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 2/3 | chr20 | 24958130 | |||||||
chr20:24958196 | A | G | 29 | a0001c0001t0010g0096 a0001c0001t0010g0097 a0001c0001t0012g0098 others(26): Show |
68 | HG00639.hp2 HG00642.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.244-732A>G | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 2/3 | chr20 | 24958196 | |||||||
chr20:24958247 | T | C | 14 | a0001c0001t0010g0097 a0001c0001t0012g0098 a0001c0002t0004g0006 others(11): Show |
29 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.244-681T>C | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 2/3 | chr20 | 24958247 | |||||||
chr20:24958297 | C | A | 13 | a0001c0002t0003g0002 a0001c0002t0003g0010 a0001c0002t0003g0016 others(10): Show |
37 | HG00639.hp2 HG01123.hp2 HG01168.hp2 others(34): Show |
intron_variant | MODIFIER | c.244-631C>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 2/3 | chr20 | 24958297 | |||||||
chr20:24958333 | T | G | 15 | a0001c0001t0010g0096 a0001c0001t0010g0097 a0001c0001t0012g0098 others(12): Show |
30 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.244-595T>G | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 2/3 | chr20 | 24958333 | |||||||
chr20:24958465 | C | A | 1 | a0001c0001t0001g0059 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.244-463C>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 2/3 | chr20 | 24958465 | |||||||
chr20:24958482 | C | T | 2 | a0001c0002t0004g0100 a0001c0002t0004g0104 |
2 | HG01069.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.244-446C>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 2/3 | chr20 | 24958482 | |||||||
chr20:24958514 | C | G | 3 | a0001c0002t0002g0012 a0001c0002t0002g0071 a0001c0002t0002g0072 |
7 | HG02258.hp2 HG02809.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.244-414C>G | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 2/3 | chr20 | 24958514 | |||||||
chr20:24958569 | C | A | 47 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(44): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.244-359C>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 2/3 | chr20 | 24958569 | |||||||
chr20:24958581 | C | T | 1 | a0001c0002t0003g0048 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.244-347C>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 2/3 | chr20 | 24958581 | |||||||
chr20:24958634 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.244-294G>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 2/3 | chr20 | 24958634 | |||||||
chr20:24958710 | T | A | 3 | a0001c0001t0010g0096 a0001c0001t0010g0097 a0001c0001t0012g0098 |
3 | HG02572.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.244-218T>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 2/3 | chr20 | 24958710 | |||||||
chr20:24958712 | T | C | 3 | a0001c0001t0010g0096 a0001c0001t0010g0097 a0001c0001t0012g0098 |
3 | HG02572.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.244-216T>C | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 2/3 | chr20 | 24958712 | |||||||
chr20:24958740 | G | C | 1 | a0001c0002t0003g0046 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.244-188G>C | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 2/3 | chr20 | 24958740 | |||||||
chr20:24959128 | C | T | 11 | a0001c0002t0003g0002 a0001c0002t0003g0010 a0001c0002t0003g0016 others(8): Show |
35 | HG00639.hp2 HG01123.hp2 HG01168.hp2 others(32): Show |
intron_variant | MODIFIER | c.360+84C>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 3/3 | chr20 | 24959128 | |||||||
chr20:24959194 | T | C | 3 | a0001c0001t0010g0096 a0001c0001t0010g0097 a0001c0001t0012g0098 |
3 | HG02572.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.360+150T>C | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 3/3 | chr20 | 24959194 | |||||||
chr20:24959203 | G | A | 2 | a0001c0002t0002g0087 a0001c0002t0002g0090 |
2 | HG02451.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.360+159G>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 3/3 | chr20 | 24959203 | |||||||
chr20:24959256 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.360+212G>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 3/3 | chr20 | 24959256 | |||||||
chr20:24959355 | G | A | 3 | a0001c0001t0010g0096 a0001c0001t0010g0097 a0001c0001t0012g0098 |
3 | HG02572.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.361-280G>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 3/3 | chr20 | 24959355 | |||||||
chr20:24959461 | G | A | 3 | a0001c0001t0010g0096 a0001c0001t0010g0097 a0001c0001t0012g0098 |
3 | HG02572.hp1 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.361-174G>A | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 3/3 | chr20 | 24959461 | |||||||
chr20:24959569 | C | T | 7 | a0001c0002t0002g0012 a0001c0002t0002g0069 a0001c0002t0002g0070 others(4): Show |
11 | HG01109.hp1 HG02258.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.361-66C>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 3/3 | chr20 | 24959569 | |||||||
chr20:24959574 | C | T | 1 | a0001c0002t0002g0069 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.361-61C>T | CST7 | ENSG00000077984.6 | transcript | ENST00000480798.2 | protein_coding | 3/3 | chr20 | 24959574 |