Item | Value |
---|---|
geneid | 153918 |
ensemblid | ENSG00000118491.10 |
hgncid | 21174 |
symbol | ZC2HC1B |
name | zinc finger C2HC-type containing 1B |
refseq_nuc | NM_001013623.3 |
refseq_prot | NP_001013645.1 |
ensembl_nuc | ENST00000237275.9 |
ensembl_prot | ENSP00000237275.6 |
mane_status | MANE Select |
chr | chr6 |
start | 143864474 |
end | 143938343 |
strand | + |
ver | v1.2 |
region | chr6:143864474-143938343 |
region5000 | chr6:143859474-143943343 |
regionname0 | ZC2HC1B_chr6_143864474_143938343 |
regionname5000 | ZC2HC1B_chr6_143859474_143943343 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 222 | 315 | 72 | 54 | 143 | 6 | 38 | 109 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | MAGAE others(217): Show |
chr6 | 143859474 | 143943343 |
a0002 | 0/0 | 222 | 11 | 11 | 0 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | MAGAE others(217): Show |
chr6 | 143859474 | 143943343 |
a0003 | 0/0 | 222 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | MAGAE others(217): Show |
chr6 | 143859474 | 143943343 |
a0004 | 0/0 | 222 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | MAGAE others(217): Show |
chr6 | 143859474 | 143943343 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 666 | 315 | 72 | 54 | 143 | 6 | 38 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | ATGGC others(661): Show |
chr6 | 143859474 | 143943343 | ||
a0002c0002 | 0/0 | 666 | 11 | 11 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | ATGGC others(661): Show |
chr6 | 143859474 | 143943343 | ||
a0003c0003 | 0/0 | 666 | 3 | 3 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | ATGGC others(661): Show |
chr6 | 143859474 | 143943343 | ||
a0004c0004 | 0/0 | 666 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | ATGGC others(661): Show |
chr6 | 143859474 | 143943343 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 951 | 315 | 72 | 54 | 143 | 6 | 38 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | AGTAT others(946): Show |
chr6 | 143859474 | 143943343 |
a0002c0002t0001 | 0/0 | 951 | 11 | 11 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | AGTAT others(946): Show |
chr6 | 143859474 | 143943343 |
a0003c0003t0001 | 0/0 | 951 | 3 | 3 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | AGTAT others(946): Show |
chr6 | 143859474 | 143943343 |
a0004c0004t0001 | 0/0 | 951 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | AGTAT others(946): Show |
chr6 | 143859474 | 143943343 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0216 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0227 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0002c0002t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0002c0002t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0002c0002t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0002c0002t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0002c0002t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0002c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0002c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0002c0002t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0002c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0002c0002t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0002c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0003c0003t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0003c0003t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0003c0003t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
a0004c0004t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0047 | EUR | GBR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0245 | EUR | GBR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0226 | EUR | GBR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0147 | EUR | GBR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | CHS | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | CHS | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | CHS | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | CHS | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | CHS | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | CHS | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | CHS | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | CHS | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0314 | AMR | PUR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | CHS | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0310 | AMR | PUR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0309 | AMR | PUR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | CLM | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | PEL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | KHV | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | KHV | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02145 | hp1 | a0002 | c0002 | t0001 | g0029 | AFR | ACB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | ACB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0317 | AMR | PEL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | ACB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PEL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02647 | hp2 | a0002 | c0002 | t0001 | g0026 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02717 | hp1 | a0002 | c0002 | t0001 | g0024 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02723 | hp1 | a0002 | c0002 | t0001 | g0025 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02818 | hp2 | a0003 | c0003 | t0001 | g0039 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02895 | hp2 | a0002 | c0002 | t0001 | g0020 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02897 | hp1 | a0002 | c0002 | t0001 | g0019 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | ESN | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ESN | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | ESN | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03041 | hp2 | a0002 | c0002 | t0001 | g0021 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | MSL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03098 | hp2 | a0002 | c0002 | t0001 | g0028 | AFR | MSL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | ESN | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ESN | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03209 | hp1 | a0002 | c0002 | t0001 | g0023 | AFR | MSL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | MSL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | MSL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | MSL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | MSL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | MSL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | MSL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | ESN | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03540 | hp1 | a0003 | c0003 | t0001 | g0038 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | GWD | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | MSL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | MSL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | STU | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | STU | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | BEB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | BEB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | BEB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | BEB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | BEB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | BEB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | BEB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0274 | SAS | BEB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | STU | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | STU | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | BEB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | BEB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | STU | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | STU | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | STU | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | STU | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | STU | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | STU | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | YRI | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | YRI | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | CHB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | CHB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | CHB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CHB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18965 | hp2 | a0004 | c0004 | t0001 | g0088 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | LWK | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | LWK | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | YRI | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | YRI | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA20129 | hp1 | a0002 | c0002 | t0001 | g0027 | AFR | ASW | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | ASW | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0162 | EUR | TSI | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0177 | EUR | TSI | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | GIH | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | GIH | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02109 | hp1 | a0003 | c0003 | t0001 | g0037 | AFR | ACB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ACB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | ACB | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | MSL | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG06807 | hp1 | a0002 | c0002 | t0001 | g0022 | AFR | USA | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | USA | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | USA | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | USA | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | LWK | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | LWK | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0216 | REF | REF | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0227 | REF | REF | ZC2HC1B_chr6_143859474_143943343 | ZC2HC1B | chr6 | 143859474 | 143943343 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:143864555 | C | T | 1 | a0002 | 11 | HG02145.hp1 HG02647.hp2 HG02717.hp1 others(8): Show |
missense_variant | MODERATE | c.16C>T | p.Pro6Ser | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/8 | 82/951 | 16/669 | 6/222 | chr6 | 143864555 | |||
chr6:143886128 | G | C | 1 | a0003 | 3 | HG02109.hp1 HG02818.hp2 HG03540.hp1 |
missense_variant | MODERATE | c.187G>C | p.Val63Leu | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 3/8 | 253/951 | 187/669 | 63/222 | chr6 | 143886128 | |||
chr6:143886132 | A | C | 1 | a0004 | 1 | NA18965.hp2 | missense_variant | MODERATE | c.191A>C | p.Lys64Thr | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 3/8 | 257/951 | 191/669 | 64/222 | chr6 | 143886132 |
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 |
---|
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 |
---|
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:143864781 | T | G | 5 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(2): Show |
5 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.28+214T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143864781 | |||||||
chr6:143864844 | A | AG | 4 | a0001c0001t0001g0009 a0001c0001t0001g0319 a0001c0001t0001g0320 others(1): Show |
5 | HG00408.hp2 HG02071.hp2 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.28+278dupG | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143864844 | ||||||
chr6:143864862 | A | G | 5 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(2): Show |
5 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.28+295A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143864862 | |||||||
chr6:143864910 | T | C | 2 | a0001c0001t0001g0015 a0001c0001t0001g0016 |
2 | HG02572.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.28+343T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143864910 | |||||||
chr6:143865116 | T | G | 5 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(2): Show |
5 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.28+549T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143865116 | |||||||
chr6:143865196 | T | G | 2 | a0001c0001t0001g0017 a0001c0001t0001g0018 |
2 | NA18983.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.28+629T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143865196 | |||||||
chr6:143865374 | T | C | 5 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(2): Show |
5 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.28+807T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143865374 | |||||||
chr6:143865385 | C | A | 11 | a0002c0002t0001g0019 a0002c0002t0001g0020 a0002c0002t0001g0021 others(8): Show |
11 | HG02145.hp1 HG02647.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.28+818C>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143865385 | |||||||
chr6:143865385 | C | T | 1 | a0001c0001t0001g0318 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.28+818C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143865385 | |||||||
chr6:143865407 | A | G | 1 | a0001c0001t0001g0317 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.28+840A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143865407 | |||||||
chr6:143865638 | G | A | 1 | a0001c0001t0001g0010 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.28+1071G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143865638 | |||||||
chr6:143865640 | G | A | 5 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(2): Show |
5 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.28+1073G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143865640 | |||||||
chr6:143865720 | T | TAGAA | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(143): Show |
150 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.28+1154_28+1157dup others(4): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143865720 | ||||||
chr6:143865812 | A | G | 5 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(2): Show |
5 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.28+1245A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143865812 | |||||||
chr6:143865853 | G | T | 5 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(2): Show |
5 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.28+1286G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143865853 | |||||||
chr6:143865859 | G | A | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG00738.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.28+1292G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143865859 | |||||||
chr6:143865982 | A | AT | 5 | a0001c0001t0001g0003 a0001c0001t0001g0155 a0001c0001t0001g0156 others(2): Show |
6 | HG03927.hp1 NA18952.hp1 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.28+1420dupT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143865982 | ||||||
chr6:143866102 | G | A | 5 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(2): Show |
5 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.28+1535G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143866102 | |||||||
chr6:143866145 | A | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(155): Show |
162 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.28+1578A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143866145 | |||||||
chr6:143866176 | C | T | 36 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(33): Show |
37 | HG00140.hp2 HG00673.hp1 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.28+1609C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143866176 | |||||||
chr6:143866255 | C | T | 1 | a0001c0001t0001g0315 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.28+1688C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143866255 | |||||||
chr6:143866350 | C | T | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(143): Show |
150 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.28+1783C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143866350 | |||||||
chr6:143866384 | A | G | 36 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(33): Show |
37 | HG00140.hp2 HG00673.hp1 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.28+1817A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143866384 | |||||||
chr6:143866393 | C | T | 1 | a0001c0001t0001g0314 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.28+1826C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143866393 | |||||||
chr6:143866491 | C | T | 86 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0015 others(83): Show |
88 | HG00099.hp1 HG00408.hp2 HG00733.hp1 others(85): Show |
intron_variant | MODIFIER | c.28+1924C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143866491 | |||||||
chr6:143866588 | A | G | 13 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0111 others(10): Show |
13 | HG00733.hp1 HG01258.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.28+2021A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143866588 | |||||||
chr6:143866815 | ATATT | A | 3 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0318 |
3 | HG02109.hp2 HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.28+2251_28+2254del others(4): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143866815 | ||||||
chr6:143867039 | T | A | 5 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(2): Show |
5 | HG02055.hp2 HG02630.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.28+2472T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143867039 | |||||||
chr6:143867091 | T | C | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(138): Show |
145 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.28+2524T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143867091 | |||||||
chr6:143867098 | G | T | 1 | a0001c0001t0001g0010 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.28+2531G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143867098 | |||||||
chr6:143867355 | A | G | 13 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0111 others(10): Show |
13 | HG00733.hp1 HG01258.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.28+2788A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143867355 | |||||||
chr6:143867410 | C | T | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
186 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.28+2843C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143867410 | |||||||
chr6:143867427 | C | T | 5 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(2): Show |
5 | HG02055.hp2 HG02630.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.28+2860C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143867427 | |||||||
chr6:143867580 | C | T | 8 | a0001c0001t0001g0001 a0001c0001t0001g0040 a0001c0001t0001g0041 others(5): Show |
9 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.28+3013C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143867580 | |||||||
chr6:143867628 | T | C | 11 | a0002c0002t0001g0019 a0002c0002t0001g0020 a0002c0002t0001g0021 others(8): Show |
11 | HG02145.hp1 HG02647.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.28+3061T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143867628 | |||||||
chr6:143867668 | A | G | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(143): Show |
150 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.28+3101A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143867668 | |||||||
chr6:143867808 | T | G | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG02602.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.28+3241T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143867808 | |||||||
chr6:143868006 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.28+3439T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143868006 | |||||||
chr6:143868095 | A | G | 2 | a0001c0001t0001g0290 a0001c0001t0001g0291 |
2 | HG00673.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.28+3528A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143868095 | |||||||
chr6:143868318 | C | T | 2 | a0001c0001t0001g0288 a0001c0001t0001g0289 |
2 | HG00609.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.28+3751C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143868318 | |||||||
chr6:143868335 | A | C | 5 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(2): Show |
5 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.28+3768A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143868335 | |||||||
chr6:143868368 | A | C | 5 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(2): Show |
5 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.28+3801A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143868368 | |||||||
chr6:143868375 | A | G | 3 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0318 |
3 | HG02109.hp2 HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.28+3808A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143868375 | |||||||
chr6:143868423 | G | A | 1 | a0001c0001t0001g0161 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.28+3856G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143868423 | |||||||
chr6:143868466 | A | AC | 13 | a0001c0001t0001g0001 a0001c0001t0001g0032 a0001c0001t0001g0033 others(10): Show |
14 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.28+3899_28+3900ins others(1): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143868466 | |||||||
chr6:143868466 | A | AT | 115 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(112): Show |
118 | HG00408.hp2 HG00423.hp1 HG00733.hp1 others(115): Show |
intron_variant | MODIFIER | c.28+3909dupT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143868466 | ||||||
chr6:143868466 | A | ATT | 33 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(30): Show |
34 | HG00140.hp2 HG00673.hp1 HG01978.hp1 others(31): Show |
intron_variant | MODIFIER | c.28+3908_28+3909dup others(2): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143868466 | ||||||
chr6:143868581 | C | T | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(138): Show |
145 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.28+4014C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143868581 | |||||||
chr6:143868758 | T | C | 1 | a0001c0001t0001g0132 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.28+4191T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143868758 | |||||||
chr6:143869193 | A | G | 26 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(23): Show |
27 | HG00140.hp2 HG00673.hp1 HG01978.hp1 others(24): Show |
intron_variant | MODIFIER | c.28+4626A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143869193 | |||||||
chr6:143869208 | C | T | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01081.hp2 HG02258.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.28+4641C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143869208 | |||||||
chr6:143869315 | A | T | 1 | a0001c0001t0001g0036 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.28+4748A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143869315 | |||||||
chr6:143869449 | C | T | 1 | a0001c0001t0001g0286 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.28+4882C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143869449 | |||||||
chr6:143869535 | ATAAGGCA others(3): Show |
A | 1 | a0001c0001t0001g0285 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.28+4971_28+4980del others(10): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143869535 | ||||||
chr6:143869874 | C | T | 67 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0047 others(64): Show |
69 | HG00099.hp1 HG00408.hp2 HG01123.hp1 others(66): Show |
intron_variant | MODIFIER | c.28+5307C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143869874 | |||||||
chr6:143870100 | A | G | 11 | a0002c0002t0001g0019 a0002c0002t0001g0020 a0002c0002t0001g0021 others(8): Show |
11 | HG02145.hp1 HG02647.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.28+5533A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143870100 | |||||||
chr6:143870219 | G | T | 1 | a0001c0001t0001g0284 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.28+5652G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143870219 | |||||||
chr6:143870357 | C | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0014 |
2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.28+5790C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143870357 | |||||||
chr6:143870479 | A | G | 2 | a0001c0001t0001g0312 a0001c0001t0001g0313 |
2 | HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.28+5912A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143870479 | |||||||
chr6:143870568 | A | G | 5 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(2): Show |
5 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.28+6001A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143870568 | |||||||
chr6:143870608 | T | C | 1 | a0001c0001t0001g0010 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.28+6041T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143870608 | |||||||
chr6:143870803 | C | T | 11 | a0002c0002t0001g0019 a0002c0002t0001g0020 a0002c0002t0001g0021 others(8): Show |
11 | HG02145.hp1 HG02647.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.28+6236C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143870803 | |||||||
chr6:143870809 | C | T | 111 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(108): Show |
114 | HG00099.hp1 HG00408.hp2 HG00733.hp1 others(111): Show |
intron_variant | MODIFIER | c.28+6242C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143870809 | |||||||
chr6:143870829 | A | G | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG00738.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.28+6262A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143870829 | |||||||
chr6:143871072 | A | T | 3 | a0003c0003t0001g0037 a0003c0003t0001g0038 a0003c0003t0001g0039 |
3 | HG02109.hp1 HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.28+6505A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143871072 | |||||||
chr6:143871258 | A | G | 1 | a0001c0001t0001g0283 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.28+6691A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143871258 | |||||||
chr6:143871271 | G | C | 1 | a0001c0001t0001g0162 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.28+6704G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143871271 | |||||||
chr6:143871450 | G | A | 1 | a0001c0001t0001g0054 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.28+6883G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143871450 | |||||||
chr6:143871518 | T | G | 92 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0013 others(89): Show |
94 | HG00099.hp1 HG00408.hp2 HG00733.hp1 others(91): Show |
intron_variant | MODIFIER | c.28+6951T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143871518 | |||||||
chr6:143871592 | C | G | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01081.hp2 HG02258.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.28+7025C>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143871592 | |||||||
chr6:143871773 | C | T | 5 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(2): Show |
5 | HG02055.hp2 HG02630.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.28+7206C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143871773 | |||||||
chr6:143871779 | A | G | 1 | a0001c0001t0001g0282 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.28+7212A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143871779 | |||||||
chr6:143871944 | T | G | 13 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(10): Show |
13 | HG01261.hp1 HG01361.hp2 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.28+7377T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143871944 | |||||||
chr6:143871969 | G | A | 1 | a0001c0001t0001g0174 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.28+7402G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143871969 | |||||||
chr6:143872013 | ACATCAGC others(14): Show |
A | 2 | a0001c0001t0001g0048 a0001c0001t0001g0049 |
2 | HG03098.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.28+7449_28+7469del others(21): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143872013 | ||||||
chr6:143872070 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.28+7503C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143872070 | |||||||
chr6:143872216 | C | T | 7 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0048 others(4): Show |
7 | HG01884.hp1 HG02451.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.28+7649C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143872216 | |||||||
chr6:143872296 | C | T | 7 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0048 others(4): Show |
7 | HG01884.hp1 HG02451.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.28+7729C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143872296 | |||||||
chr6:143872338 | A | G | 2 | a0001c0001t0001g0011 a0001c0001t0001g0012 |
2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.28+7771A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143872338 | |||||||
chr6:143872446 | C | T | 1 | a0001c0001t0001g0281 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.28+7879C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143872446 | |||||||
chr6:143872480 | G | C | 9 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0155 others(6): Show |
11 | HG00408.hp2 HG02071.hp2 HG03927.hp1 others(8): Show |
intron_variant | MODIFIER | c.28+7913G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143872480 | |||||||
chr6:143872501 | C | T | 1 | a0001c0001t0001g0108 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.28+7934C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143872501 | |||||||
chr6:143872555 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.28+7988G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143872555 | |||||||
chr6:143872656 | G | T | 1 | a0001c0001t0001g0311 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.28+8089G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143872656 | |||||||
chr6:143872668 | A | G | 2 | a0001c0001t0001g0312 a0001c0001t0001g0313 |
2 | HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.28+8101A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143872668 | |||||||
chr6:143872673 | A | G | 2 | a0001c0001t0001g0312 a0001c0001t0001g0313 |
2 | HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.28+8106A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143872673 | |||||||
chr6:143872680 | A | T | 2 | a0001c0001t0001g0312 a0001c0001t0001g0313 |
2 | HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.28+8113A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143872680 | |||||||
chr6:143872683 | A | T | 2 | a0001c0001t0001g0312 a0001c0001t0001g0313 |
2 | HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.28+8116A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143872683 | |||||||
chr6:143872695 | G | A | 2 | a0001c0001t0001g0312 a0001c0001t0001g0313 |
2 | HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.28+8128G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143872695 | |||||||
chr6:143872810 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.28+8243G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143872810 | |||||||
chr6:143872925 | A | C | 4 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 others(1): Show |
4 | HG01928.hp1 HG01934.hp2 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.28+8358A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143872925 | |||||||
chr6:143872949 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.28+8382A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143872949 | |||||||
chr6:143873097 | A | G | 13 | a0001c0001t0001g0008 a0001c0001t0001g0299 a0001c0001t0001g0300 others(10): Show |
14 | HG01099.hp1 HG01123.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.28+8530A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143873097 | |||||||
chr6:143873108 | G | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0299 a0001c0001t0001g0300 others(1): Show |
5 | HG01123.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.28+8541G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143873108 | |||||||
chr6:143873184 | A | T | 3 | a0001c0001t0001g0002 a0001c0001t0001g0153 a0001c0001t0001g0154 |
4 | NA18948.hp2 NA18957.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.28+8617A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143873184 | |||||||
chr6:143873422 | G | T | 2 | a0001c0001t0001g0309 a0001c0001t0001g0310 |
2 | HG01099.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.28+8855G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143873422 | |||||||
chr6:143873458 | C | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(85): Show |
91 | HG00140.hp2 HG00558.hp1 HG00673.hp1 others(88): Show |
intron_variant | MODIFIER | c.28+8891C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143873458 | |||||||
chr6:143873480 | T | C | 102 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(99): Show |
105 | HG00140.hp2 HG00558.hp1 HG00673.hp1 others(102): Show |
intron_variant | MODIFIER | c.28+8913T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143873480 | |||||||
chr6:143873552 | T | C | 2 | a0001c0001t0001g0312 a0001c0001t0001g0313 |
2 | HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.28+8985T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143873552 | |||||||
chr6:143873579 | C | T | 13 | a0001c0001t0001g0001 a0001c0001t0001g0032 a0001c0001t0001g0033 others(10): Show |
14 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.28+9012C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143873579 | |||||||
chr6:143873772 | A | G | 6 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 others(3): Show |
6 | HG02280.hp2 HG02622.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.28+9205A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143873772 | |||||||
chr6:143873812 | C | T | 2 | a0001c0001t0001g0297 a0001c0001t0001g0298 |
2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.28+9245C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143873812 | |||||||
chr6:143873850 | G | C | 2 | a0001c0001t0001g0312 a0001c0001t0001g0313 |
2 | HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.28+9283G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143873850 | |||||||
chr6:143873973 | C | T | 102 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(99): Show |
105 | HG00140.hp2 HG00558.hp1 HG00673.hp1 others(102): Show |
intron_variant | MODIFIER | c.28+9406C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143873973 | |||||||
chr6:143874045 | T | C | 13 | a0001c0001t0001g0008 a0001c0001t0001g0299 a0001c0001t0001g0300 others(10): Show |
14 | HG01099.hp1 HG01123.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.28+9478T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143874045 | |||||||
chr6:143874130 | T | C | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.28+9563T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143874130 | |||||||
chr6:143874154 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.28+9587C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143874154 | |||||||
chr6:143874192 | CAA | C | 11 | a0002c0002t0001g0019 a0002c0002t0001g0020 a0002c0002t0001g0021 others(8): Show |
11 | HG02145.hp1 HG02647.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.28+9626_28+9627del others(2): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143874192 | |||||||
chr6:143874246 | A | G | 1 | a0001c0001t0001g0274 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.28+9679A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143874246 | |||||||
chr6:143874313 | T | C | 2 | a0001c0001t0001g0056 a0001c0001t0001g0057 |
2 | HG04115.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.28+9746T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143874313 | |||||||
chr6:143874335 | A | G | 3 | a0003c0003t0001g0037 a0003c0003t0001g0038 a0003c0003t0001g0039 |
3 | HG02109.hp1 HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.28+9768A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143874335 | |||||||
chr6:143874348 | C | T | 1 | a0001c0001t0001g0315 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.28+9781C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143874348 | |||||||
chr6:143874416 | G | A | 1 | a0001c0001t0001g0176 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.28+9849G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143874416 | |||||||
chr6:143874497 | C | A | 1 | a0001c0001t0001g0177 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.29-9807C>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143874497 | |||||||
chr6:143874587 | T | C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(85): Show |
91 | HG00140.hp2 HG00558.hp1 HG00673.hp1 others(88): Show |
intron_variant | MODIFIER | c.29-9717T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143874587 | |||||||
chr6:143874763 | G | A | 13 | a0001c0001t0001g0008 a0001c0001t0001g0299 a0001c0001t0001g0300 others(10): Show |
14 | HG01099.hp1 HG01123.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.29-9541G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143874763 | |||||||
chr6:143874800 | A | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 |
3 | HG02055.hp1 HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.29-9504A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143874800 | |||||||
chr6:143874808 | A | G | 3 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0318 |
3 | HG02109.hp2 HG02451.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.29-9496A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143874808 | |||||||
chr6:143874845 | G | C | 1 | a0001c0001t0001g0316 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.29-9459G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143874845 | |||||||
chr6:143874891 | G | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0012 |
2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.29-9413G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143874891 | |||||||
chr6:143874927 | G | A | 41 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(38): Show |
42 | HG00140.hp2 HG00558.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.29-9377G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143874927 | |||||||
chr6:143874945 | G | A | 1 | a0001c0001t0001g0058 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.29-9359G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143874945 | |||||||
chr6:143874952 | C | A | 3 | a0003c0003t0001g0037 a0003c0003t0001g0038 a0003c0003t0001g0039 |
3 | HG02109.hp1 HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.29-9352C>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143874952 | |||||||
chr6:143875005 | G | A | 1 | a0001c0001t0001g0178 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.29-9299G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143875005 | |||||||
chr6:143875038 | G | A | 2 | a0001c0001t0001g0288 a0001c0001t0001g0289 |
2 | HG00609.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.29-9266G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143875038 | |||||||
chr6:143875053 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.29-9251G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143875053 | |||||||
chr6:143875078 | C | T | 1 | a0001c0001t0001g0010 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.29-9226C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143875078 | |||||||
chr6:143875086 | G | C | 1 | a0001c0001t0001g0048 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.29-9218G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143875086 | |||||||
chr6:143875221 | A | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(178): Show |
186 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.29-9083A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143875221 | |||||||
chr6:143875316 | TCTAAAGT others(3418): Show |
T | 14 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0111 others(11): Show |
14 | HG00733.hp1 HG01258.hp1 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.29-8983_29-5559del | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143875316 | ||||||
chr6:143875576 | C | A | 3 | a0001c0001t0001g0162 a0001c0001t0001g0191 a0001c0001t0001g0200 |
3 | HG01884.hp2 NA20752.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.29-8728C>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143875576 | |||||||
chr6:143875721 | T | A | 1 | a0001c0001t0001g0005 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.29-8583T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143875721 | |||||||
chr6:143875769 | T | G | 2 | a0001c0001t0001g0124 a0001c0001t0001g0125 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.29-8535T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143875769 | |||||||
chr6:143875838 | C | T | 2 | a0002c0002t0001g0025 a0002c0002t0001g0029 |
2 | HG02145.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.29-8466C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143875838 | |||||||
chr6:143875853 | A | C | 1 | a0001c0001t0001g0010 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.29-8451A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143875853 | |||||||
chr6:143875868 | C | T | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(163): Show |
171 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.29-8436C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143875868 | |||||||
chr6:143875874 | G | A | 1 | a0002c0002t0001g0027 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.29-8430G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143875874 | |||||||
chr6:143876175 | C | G | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(84): Show |
90 | HG00140.hp2 HG00558.hp1 HG00673.hp1 others(87): Show |
intron_variant | MODIFIER | c.29-8129C>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143876175 | |||||||
chr6:143876238 | A | C | 2 | a0001c0001t0001g0312 a0001c0001t0001g0313 |
2 | HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.29-8066A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143876238 | |||||||
chr6:143876265 | A | G | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(84): Show |
90 | HG00140.hp2 HG00558.hp1 HG00673.hp1 others(87): Show |
intron_variant | MODIFIER | c.29-8039A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143876265 | |||||||
chr6:143876281 | C | A | 11 | a0002c0002t0001g0019 a0002c0002t0001g0020 a0002c0002t0001g0021 others(8): Show |
11 | HG02145.hp1 HG02647.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.29-8023C>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143876281 | |||||||
chr6:143876339 | A | G | 13 | a0001c0001t0001g0008 a0001c0001t0001g0299 a0001c0001t0001g0300 others(10): Show |
14 | HG01099.hp1 HG01123.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.29-7965A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143876339 | |||||||
chr6:143876441 | G | C | 1 | a0001c0001t0001g0316 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.29-7863G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143876441 | |||||||
chr6:143876444 | T | C | 1 | a0001c0001t0001g0316 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.29-7860T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143876444 | |||||||
chr6:143876544 | T | G | 11 | a0002c0002t0001g0019 a0002c0002t0001g0020 a0002c0002t0001g0021 others(8): Show |
11 | HG02145.hp1 HG02647.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.29-7760T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143876544 | |||||||
chr6:143876605 | G | T | 1 | a0001c0001t0001g0010 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.29-7699G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143876605 | |||||||
chr6:143876918 | T | G | 1 | a0001c0001t0001g0170 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.29-7386T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143876918 | |||||||
chr6:143876941 | T | TA | 4 | a0001c0001t0001g0008 a0001c0001t0001g0299 a0001c0001t0001g0300 others(1): Show |
5 | HG01123.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.29-7361dupA | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143876941 | ||||||
chr6:143876952 | G | A | 1 | a0001c0001t0001g0005 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.29-7352G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143876952 | |||||||
chr6:143877005 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.29-7299G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143877005 | |||||||
chr6:143877044 | A | G | 13 | a0001c0001t0001g0001 a0001c0001t0001g0032 a0001c0001t0001g0033 others(10): Show |
14 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.29-7260A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143877044 | |||||||
chr6:143877140 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.29-7164G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143877140 | |||||||
chr6:143877272 | C | CT | 36 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0055 others(33): Show |
36 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(33): Show |
intron_variant | MODIFIER | c.29-7005dupT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143877272 | ||||||
chr6:143877272 | C | CTT | 46 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(43): Show |
47 | HG01123.hp1 HG01243.hp2 HG01943.hp1 others(44): Show |
intron_variant | MODIFIER | c.29-7006_29-7005dup others(2): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143877272 | ||||||
chr6:143877272 | C | CTTT | 29 | a0001c0001t0001g0009 a0001c0001t0001g0052 a0001c0001t0001g0053 others(26): Show |
30 | HG00408.hp2 HG01358.hp1 HG02027.hp1 others(27): Show |
intron_variant | MODIFIER | c.29-7007_29-7005dup others(3): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143877272 | ||||||
chr6:143877272 | C | CTTTTTTT others(3): Show |
7 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 others(4): Show |
7 | HG01081.hp2 HG02258.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.29-7014_29-7005dup others(10): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143877272 | ||||||
chr6:143877272 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0132 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.29-7015_29-7005dup others(11): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143877272 | ||||||
chr6:143877272 | CT | C | 30 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0030 others(27): Show |
30 | HG01099.hp1 HG01168.hp2 HG01258.hp2 others(27): Show |
intron_variant | MODIFIER | c.29-7005delT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143877272 | ||||||
chr6:143877272 | CTTTTTTT others(1): Show |
C | 33 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0017 others(30): Show |
35 | HG00140.hp2 HG00673.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.29-7012_29-7005del others(8): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143877272 | ||||||
chr6:143877342 | G | A | 13 | a0001c0001t0001g0001 a0001c0001t0001g0032 a0001c0001t0001g0033 others(10): Show |
14 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.29-6962G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143877342 | |||||||
chr6:143877352 | A | G | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(73): Show |
78 | HG00140.hp2 HG00558.hp1 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.29-6952A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143877352 | |||||||
chr6:143877361 | A | C | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(73): Show |
78 | HG00140.hp2 HG00558.hp1 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.29-6943A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143877361 | |||||||
chr6:143877511 | A | G | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(73): Show |
78 | HG00140.hp2 HG00558.hp1 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.29-6793A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143877511 | |||||||
chr6:143877562 | C | T | 11 | a0001c0001t0001g0292 a0001c0001t0001g0293 a0001c0001t0001g0294 others(8): Show |
11 | HG02572.hp2 HG02615.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.29-6742C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143877562 | |||||||
chr6:143877576 | C | T | 13 | a0001c0001t0001g0001 a0001c0001t0001g0032 a0001c0001t0001g0033 others(10): Show |
14 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.29-6728C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143877576 | |||||||
chr6:143878075 | C | T | 2 | a0001c0001t0001g0052 a0001c0001t0001g0053 |
2 | HG02451.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.29-6229C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143878075 | |||||||
chr6:143878174 | C | T | 1 | a0001c0001t0001g0316 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.29-6130C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143878174 | |||||||
chr6:143878345 | G | T | 4 | a0001c0001t0001g0198 a0001c0001t0001g0205 a0001c0001t0001g0251 others(1): Show |
4 | NA18956.hp1 NA18964.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.29-5959G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143878345 | |||||||
chr6:143878393 | G | A | 34 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(31): Show |
35 | HG00140.hp2 HG00558.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.29-5911G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143878393 | |||||||
chr6:143878479 | A | G | 1 | a0001c0001t0001g0268 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.29-5825A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143878479 | |||||||
chr6:143878483 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.29-5821C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143878483 | |||||||
chr6:143878514 | T | G | 89 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(86): Show |
92 | HG00140.hp2 HG00558.hp1 HG00673.hp1 others(89): Show |
intron_variant | MODIFIER | c.29-5790T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143878514 | |||||||
chr6:143878940 | C | T | 1 | a0001c0001t0001g0035 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.29-5364C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143878940 | |||||||
chr6:143879018 | G | A | 10 | a0001c0001t0001g0292 a0001c0001t0001g0293 a0001c0001t0001g0294 others(7): Show |
10 | HG02572.hp2 HG02615.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.29-5286G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143879018 | |||||||
chr6:143879033 | C | T | 1 | a0001c0001t0001g0010 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.29-5271C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143879033 | |||||||
chr6:143879095 | G | A | 1 | a0001c0001t0001g0316 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.29-5209G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143879095 | |||||||
chr6:143879112 | C | T | 14 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0111 others(11): Show |
14 | HG00733.hp1 HG01258.hp1 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.29-5192C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143879112 | |||||||
chr6:143879674 | C | T | 1 | a0001c0001t0001g0296 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.29-4630C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143879674 | |||||||
chr6:143879791 | G | GT | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(179): Show |
187 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.29-4500dupT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143879791 | ||||||
chr6:143879824 | A | AT | 25 | a0001c0001t0001g0016 a0001c0001t0001g0111 a0001c0001t0001g0112 others(22): Show |
25 | HG00733.hp1 HG00738.hp1 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.29-4455dupT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143879824 | ||||||
chr6:143879824 | A | ATTTT | 8 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 others(5): Show |
8 | HG01081.hp2 HG02258.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.29-4458_29-4455dup others(4): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143879824 | ||||||
chr6:143879824 | A | ATTTTT | 20 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0127 others(17): Show |
21 | HG00140.hp2 HG00558.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.29-4459_29-4455dup others(5): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143879824 | ||||||
chr6:143879824 | AT | A | 91 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(88): Show |
94 | HG00099.hp1 HG00408.hp2 HG00738.hp2 others(91): Show |
intron_variant | MODIFIER | c.29-4455delT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143879824 | ||||||
chr6:143879861 | T | C | 12 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(9): Show |
12 | HG01884.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.29-4443T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143879861 | |||||||
chr6:143879878 | A | G | 1 | a0001c0001t0001g0259 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.29-4426A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143879878 | |||||||
chr6:143880002 | T | G | 1 | a0003c0003t0001g0037 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.29-4302T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143880002 | |||||||
chr6:143880016 | A | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0014 |
2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.29-4288A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143880016 | |||||||
chr6:143880236 | G | C | 10 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0030 others(7): Show |
10 | HG01884.hp1 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.29-4068G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143880236 | |||||||
chr6:143880565 | TA | T | 5 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(2): Show |
5 | HG02683.hp2 HG03239.hp2 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.29-3734delA | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143880565 | ||||||
chr6:143880687 | G | A | 13 | a0001c0001t0001g0001 a0001c0001t0001g0032 a0001c0001t0001g0033 others(10): Show |
14 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.29-3617G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143880687 | |||||||
chr6:143880828 | C | T | 1 | a0001c0001t0001g0036 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.29-3476C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143880828 | |||||||
chr6:143880993 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.29-3311C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143880993 | |||||||
chr6:143881054 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.29-3250C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143881054 | |||||||
chr6:143881111 | T | G | 1 | a0001c0001t0001g0030 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.29-3193T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143881111 | |||||||
chr6:143881133 | A | G | 48 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0017 others(45): Show |
50 | HG00140.hp2 HG00558.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.29-3171A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143881133 | |||||||
chr6:143881166 | G | A | 1 | a0001c0001t0001g0010 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.29-3138G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143881166 | |||||||
chr6:143881302 | A | G | 14 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0111 others(11): Show |
14 | HG00733.hp1 HG01258.hp1 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.29-3002A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143881302 | |||||||
chr6:143881498 | C | T | 3 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0307 |
3 | HG02486.hp2 HG02622.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.29-2806C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143881498 | |||||||
chr6:143881550 | C | CA | 48 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0032 others(45): Show |
49 | HG00423.hp1 HG00423.hp2 HG01071.hp1 others(46): Show |
intron_variant | MODIFIER | c.29-2727dupA | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143881550 | ||||||
chr6:143881550 | C | CAAAA | 7 | a0001c0001t0001g0302 a0001c0001t0001g0303 a0001c0001t0001g0305 others(4): Show |
7 | HG01099.hp1 HG01192.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.29-2730_29-2727dup others(4): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143881550 | ||||||
chr6:143881550 | CA | C | 6 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0179 others(3): Show |
6 | HG00609.hp1 HG01168.hp2 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.29-2727delA | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143881550 | ||||||
chr6:143881550 | CAAAAAA | C | 7 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(4): Show |
7 | HG01081.hp2 HG02135.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.29-2732_29-2727del others(6): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143881550 | ||||||
chr6:143881550 | CAAAAAAA | C | 38 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(35): Show |
39 | HG00140.hp2 HG00558.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.29-2733_29-2727del others(7): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143881550 | ||||||
chr6:143881570 | A | G | 2 | a0001c0001t0001g0011 a0001c0001t0001g0012 |
2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.29-2734A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143881570 | |||||||
chr6:143881574 | A | G | 1 | a0001c0001t0001g0253 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.29-2730A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143881574 | |||||||
chr6:143881608 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.29-2696A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143881608 | |||||||
chr6:143881714 | T | A | 2 | a0001c0001t0001g0164 a0001c0001t0001g0317 |
2 | HG01928.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.29-2590T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143881714 | |||||||
chr6:143881864 | T | C | 1 | a0001c0001t0001g0292 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.29-2440T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143881864 | |||||||
chr6:143881882 | T | C | 3 | a0001c0001t0001g0180 a0001c0001t0001g0188 a0001c0001t0001g0189 |
3 | NA18963.hp1 NA18984.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.29-2422T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143881882 | |||||||
chr6:143881968 | G | A | 1 | a0001c0001t0001g0010 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.29-2336G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143881968 | |||||||
chr6:143882046 | G | C | 3 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 |
3 | HG02886.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.29-2258G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143882046 | |||||||
chr6:143882221 | T | C | 48 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0017 others(45): Show |
50 | HG00140.hp2 HG00558.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.29-2083T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143882221 | |||||||
chr6:143882250 | G | C | 1 | a0001c0001t0001g0062 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.29-2054G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143882250 | |||||||
chr6:143882325 | T | TTA | 5 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0309 others(2): Show |
5 | HG01192.hp1 HG02109.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.29-1975_29-1974dup others(2): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882325 | ||||||
chr6:143882329 | A | AT | 21 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0065 others(18): Show |
23 | HG00408.hp2 HG01952.hp1 HG02027.hp1 others(20): Show |
intron_variant | MODIFIER | c.29-1969dupT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882329 | ||||||
chr6:143882329 | ATT | A | 8 | a0001c0001t0001g0183 a0001c0001t0001g0185 a0001c0001t0001g0220 others(5): Show |
8 | HG01433.hp1 HG02895.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.29-1970_29-1969del others(2): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882329 | ||||||
chr6:143882331 | T | A | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(90): Show |
96 | HG00140.hp2 HG00558.hp1 HG00673.hp1 others(93): Show |
intron_variant | MODIFIER | c.29-1973T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143882331 | |||||||
chr6:143882332 | T | A | 2 | a0001c0001t0001g0309 a0001c0001t0001g0310 |
2 | HG01099.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.29-1972T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143882332 | |||||||
chr6:143882332 | T | TTA | 7 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 others(4): Show |
7 | HG02027.hp2 HG02080.hp1 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.29-1971_29-1970ins others(2): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882332 | ||||||
chr6:143882332 | T | TTATA | 11 | a0001c0001t0001g0059 a0001c0001t0001g0196 a0001c0001t0001g0197 others(8): Show |
11 | HG00438.hp1 HG01884.hp2 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.29-1971_29-1970ins others(4): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882332 | ||||||
chr6:143882332 | T | TTATATA | 5 | a0001c0001t0001g0162 a0001c0001t0001g0181 a0001c0001t0001g0194 others(2): Show |
5 | HG00423.hp1 NA18949.hp1 NA19068.hp2 others(2): Show |
intron_variant | MODIFIER | c.29-1971_29-1970ins others(6): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882332 | ||||||
chr6:143882332 | T | TTATATAT others(3): Show |
3 | a0001c0001t0001g0193 a0001c0001t0001g0265 a0001c0001t0001g0292 |
3 | HG02040.hp1 HG03516.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.29-1971_29-1970ins others(10): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882332 | ||||||
chr6:143882332 | T | TTATATAT others(5): Show |
2 | a0001c0001t0001g0191 a0001c0001t0001g0192 |
2 | HG01109.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.29-1971_29-1970ins others(12): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882332 | ||||||
chr6:143882332 | T | TTATATAT others(7): Show |
1 | a0001c0001t0001g0298 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.29-1971_29-1970ins others(14): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882332 | ||||||
chr6:143882332 | T | TTATATAT others(9): Show |
1 | a0001c0001t0001g0190 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.29-1971_29-1970ins others(16): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882332 | ||||||
chr6:143882332 | T | TTATATAT others(11): Show |
2 | a0001c0001t0001g0165 a0001c0001t0001g0311 |
2 | HG01261.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.29-1971_29-1970ins others(18): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882332 | ||||||
chr6:143882332 | T | TTATATAT others(13): Show |
1 | a0001c0001t0001g0297 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.29-1971_29-1970ins others(20): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882332 | ||||||
chr6:143882332 | TTTTATAT others(13): Show |
T | 1 | a0001c0001t0001g0293 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.29-1970_29-1951del others(20): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882332 | ||||||
chr6:143882333 | T | A | 5 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 others(2): Show |
5 | HG02895.hp1 HG02896.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.29-1971T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143882333 | |||||||
chr6:143882334 | T | A | 75 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0018 others(72): Show |
76 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.29-1970T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143882334 | |||||||
chr6:143882334 | T | TATATATA others(2): Show |
3 | a0001c0001t0001g0044 a0001c0001t0001g0067 a0001c0001t0001g0068 |
3 | HG04204.hp2 NA19068.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.29-1970_29-1969ins others(9): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143882334 | |||||||
chr6:143882334 | T | TATATATA others(4): Show |
1 | a0001c0001t0001g0066 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.29-1970_29-1969ins others(11): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143882334 | |||||||
chr6:143882334 | T | TTA | 7 | a0001c0001t0001g0123 a0001c0001t0001g0161 a0001c0001t0001g0180 others(4): Show |
7 | HG01106.hp2 HG02630.hp2 NA18963.hp1 others(4): Show |
intron_variant | MODIFIER | c.29-1936_29-1935dup others(2): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | ||||||
chr6:143882334 | T | TTATA | 7 | a0001c0001t0001g0004 a0001c0001t0001g0043 a0001c0001t0001g0140 others(4): Show |
8 | HG01934.hp1 HG01943.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.29-1938_29-1935dup others(4): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | ||||||
chr6:143882334 | T | TTATATA | 9 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0036 others(6): Show |
10 | HG01106.hp1 HG01361.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.29-1940_29-1935dup others(6): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | ||||||
chr6:143882334 | T | TTATATAT others(1): Show |
4 | a0001c0001t0001g0033 a0001c0001t0001g0221 a0001c0001t0001g0222 others(1): Show |
4 | HG03579.hp1 HG04184.hp2 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.29-1942_29-1935dup others(8): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | ||||||
chr6:143882334 | T | TTATATAT others(3): Show |
9 | a0001c0001t0001g0012 a0001c0001t0001g0032 a0001c0001t0001g0035 others(6): Show |
9 | HG02258.hp1 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.29-1944_29-1935dup others(10): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | ||||||
chr6:143882334 | T | TTATATAT others(5): Show |
4 | a0001c0001t0001g0011 a0001c0001t0001g0115 a0001c0001t0001g0120 others(1): Show |
4 | HG01081.hp2 HG01258.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.29-1946_29-1935dup others(12): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | ||||||
chr6:143882334 | T | TTATATAT others(9): Show |
2 | a0001c0001t0001g0050 a0002c0002t0001g0029 |
2 | HG02145.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.29-1950_29-1935dup others(16): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | ||||||
chr6:143882334 | T | TTATATAT others(11): Show |
8 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0111 others(5): Show |
8 | HG01884.hp1 HG02602.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.29-1952_29-1935dup others(18): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | ||||||
chr6:143882334 | T | TTATATAT others(13): Show |
1 | a0001c0001t0001g0128 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.29-1954_29-1935dup others(20): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | ||||||
chr6:143882334 | T | TTATATAT others(15): Show |
8 | a0001c0001t0001g0016 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
8 | HG02145.hp2 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.29-1956_29-1935dup others(22): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | ||||||
chr6:143882334 | T | TTATATAT others(17): Show |
3 | a0001c0001t0001g0132 a0001c0001t0001g0295 a0002c0002t0001g0024 |
3 | HG02717.hp1 HG03540.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.29-1958_29-1935dup others(24): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | ||||||
chr6:143882334 | T | TTATATAT others(19): Show |
5 | a0001c0001t0001g0048 a0001c0001t0001g0117 a0001c0001t0001g0294 others(2): Show |
5 | HG00733.hp1 HG02717.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.29-1960_29-1935dup others(26): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | ||||||
chr6:143882334 | T | TTATATAT others(21): Show |
1 | a0001c0001t0001g0046 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.29-1962_29-1935dup others(28): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | ||||||
chr6:143882334 | T | TTATATAT others(23): Show |
2 | a0001c0001t0001g0030 a0002c0002t0001g0021 |
2 | HG02451.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.29-1964_29-1935dup others(30): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | ||||||
chr6:143882334 | T | TTATATAT others(27): Show |
2 | a0002c0002t0001g0019 a0002c0002t0001g0020 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.29-1968_29-1935dup others(34): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | ||||||
chr6:143882334 | T | TTATATAT others(14): Show |
2 | a0003c0003t0001g0038 a0003c0003t0001g0039 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.29-1963_29-1962ins others(21): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | ||||||
chr6:143882334 | T | TTATATAT others(26): Show |
1 | a0001c0001t0001g0316 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.29-1963_29-1962ins others(33): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | ||||||
chr6:143882334 | T | TTTA | 17 | a0001c0001t0001g0047 a0001c0001t0001g0055 a0001c0001t0001g0057 others(14): Show |
17 | HG00099.hp1 HG00738.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.29-1969_29-1968ins others(3): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | ||||||
chr6:143882334 | T | TTTATATA | 7 | a0001c0001t0001g0056 a0001c0001t0001g0078 a0001c0001t0001g0079 others(4): Show |
7 | HG01168.hp1 HG04115.hp2 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.29-1969_29-1968ins others(7): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | ||||||
chr6:143882334 | T | TTTATATA others(2): Show |
7 | a0001c0001t0001g0054 a0001c0001t0001g0063 a0001c0001t0001g0075 others(4): Show |
7 | HG01243.hp2 HG02080.hp2 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.29-1969_29-1968ins others(9): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | ||||||
chr6:143882334 | T | TTTATATA others(4): Show |
5 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(2): Show |
5 | NA18942.hp1 NA18956.hp2 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.29-1969_29-1968ins others(11): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | ||||||
chr6:143882334 | T | TTTATATA others(6): Show |
1 | a0001c0001t0001g0061 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.29-1969_29-1968ins others(13): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | ||||||
chr6:143882334 | T | TTTATATA others(12): Show |
1 | a0001c0001t0001g0070 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.29-1969_29-1968ins others(19): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | ||||||
chr6:143882334 | T | TTTTATAT others(9): Show |
1 | a0001c0001t0001g0121 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.29-1969_29-1968ins others(16): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | ||||||
chr6:143882334 | T | TTTTATAT others(11): Show |
1 | a0001c0001t0001g0126 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.29-1969_29-1968ins others(18): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | ||||||
chr6:143882334 | T | TTTTATAT others(15): Show |
1 | a0001c0001t0001g0031 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.29-1969_29-1968ins others(22): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | ||||||
chr6:143882334 | T | TTTTATAT others(17): Show |
2 | a0001c0001t0001g0124 a0001c0001t0001g0125 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.29-1969_29-1968ins others(24): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | ||||||
chr6:143882334 | TTA | T | 55 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0127 others(52): Show |
57 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.29-1936_29-1935del others(2): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | ||||||
chr6:143882334 | TTATATAT others(11): Show |
T | 1 | a0001c0001t0001g0015 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.29-1952_29-1935del others(18): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143882334 | ||||||
chr6:143882335 | TATATATA others(6): Show |
T | 1 | a0001c0001t0001g0097 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.29-1968_29-1956del others(13): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143882335 | |||||||
chr6:143882336 | A | T | 4 | a0001c0001t0001g0009 a0001c0001t0001g0319 a0001c0001t0001g0320 others(1): Show |
5 | HG00408.hp2 HG02071.hp2 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.29-1968A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143882336 | |||||||
chr6:143882340 | A | T | 1 | a0001c0001t0001g0010 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.29-1964A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143882340 | |||||||
chr6:143882369 | T | TATATATA others(10): Show |
1 | a0001c0001t0001g0171 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.29-1935_29-1934ins others(17): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143882369 | |||||||
chr6:143882467 | A | G | 10 | a0001c0001t0001g0178 a0001c0001t0001g0193 a0001c0001t0001g0201 others(7): Show |
10 | HG00438.hp1 HG02027.hp2 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.29-1837A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143882467 | |||||||
chr6:143882504 | T | C | 13 | a0001c0001t0001g0001 a0001c0001t0001g0032 a0001c0001t0001g0033 others(10): Show |
14 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.29-1800T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143882504 | |||||||
chr6:143882640 | A | G | 14 | a0001c0001t0001g0008 a0001c0001t0001g0121 a0001c0001t0001g0299 others(11): Show |
15 | HG01099.hp1 HG01123.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.29-1664A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143882640 | |||||||
chr6:143882905 | C | T | 1 | a0001c0001t0001g0318 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.29-1399C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143882905 | |||||||
chr6:143883051 | A | G | 37 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(34): Show |
38 | HG00140.hp2 HG00558.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.29-1253A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143883051 | |||||||
chr6:143883186 | C | T | 59 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0162 others(56): Show |
59 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.29-1118C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143883186 | |||||||
chr6:143883231 | A | G | 1 | a0001c0001t0001g0132 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.29-1073A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143883231 | |||||||
chr6:143883258 | C | T | 8 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0048 others(5): Show |
8 | HG01884.hp1 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.29-1046C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143883258 | |||||||
chr6:143883265 | T | C | 68 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(65): Show |
70 | HG00733.hp1 HG01099.hp1 HG01106.hp1 others(67): Show |
intron_variant | MODIFIER | c.29-1039T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143883265 | |||||||
chr6:143883473 | T | C | 41 | a0001c0001t0001g0001 a0001c0001t0001g0032 a0001c0001t0001g0033 others(38): Show |
42 | HG00733.hp1 HG01106.hp1 HG01258.hp1 others(39): Show |
intron_variant | MODIFIER | c.29-831T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143883473 | |||||||
chr6:143883538 | C | CT | 9 | a0001c0001t0001g0302 a0001c0001t0001g0303 a0001c0001t0001g0304 others(6): Show |
9 | HG01099.hp1 HG01192.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.29-759dupT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 143883538 | ||||||
chr6:143883679 | A | G | 1 | a0001c0001t0001g0217 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.29-625A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143883679 | |||||||
chr6:143883781 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.29-523A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143883781 | |||||||
chr6:143883942 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.29-362A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143883942 | |||||||
chr6:143884058 | A | G | 2 | a0001c0001t0001g0292 a0001c0001t0001g0293 |
2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.29-246A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 1/7 | chr6 | 143884058 | |||||||
chr6:143884454 | A | G | 11 | a0002c0002t0001g0019 a0002c0002t0001g0020 a0002c0002t0001g0021 others(8): Show |
11 | HG02145.hp1 HG02647.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.90+89A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 2/7 | chr6 | 143884454 | |||||||
chr6:143884558 | C | G | 1 | a0001c0001t0001g0184 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.90+193C>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 2/7 | chr6 | 143884558 | |||||||
chr6:143884622 | C | T | 13 | a0001c0001t0001g0007 a0001c0001t0001g0174 a0001c0001t0001g0179 others(10): Show |
14 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(11): Show |
intron_variant | MODIFIER | c.90+257C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 2/7 | chr6 | 143884622 | |||||||
chr6:143884644 | A | G | 29 | a0001c0001t0001g0001 a0001c0001t0001g0032 a0001c0001t0001g0033 others(26): Show |
30 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(27): Show |
intron_variant | MODIFIER | c.90+279A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 2/7 | chr6 | 143884644 | |||||||
chr6:143884733 | A | G | 1 | a0001c0001t0001g0299 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.90+368A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 2/7 | chr6 | 143884733 | |||||||
chr6:143884816 | G | A | 2 | a0001c0001t0001g0056 a0001c0001t0001g0057 |
2 | HG04115.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.90+451G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 2/7 | chr6 | 143884816 | |||||||
chr6:143884891 | A | G | 1 | a0003c0003t0001g0039 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.90+526A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 2/7 | chr6 | 143884891 | |||||||
chr6:143885002 | G | C | 1 | a0001c0001t0001g0144 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.90+637G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 2/7 | chr6 | 143885002 | |||||||
chr6:143885158 | G | A | 1 | a0001c0001t0001g0065 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.90+793G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 2/7 | chr6 | 143885158 | |||||||
chr6:143885299 | C | CCACCAGG others(10): Show |
1 | a0001c0001t0001g0317 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.91-727_91-726insGG others(15): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 143885299 | ||||||
chr6:143885306 | T | A | 1 | a0001c0001t0001g0174 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.91-726T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 2/7 | chr6 | 143885306 | |||||||
chr6:143885328 | A | C | 62 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(59): Show |
63 | HG00733.hp1 HG01099.hp1 HG01106.hp1 others(60): Show |
intron_variant | MODIFIER | c.91-704A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 2/7 | chr6 | 143885328 | |||||||
chr6:143885363 | C | A | 12 | a0001c0001t0001g0010 a0001c0001t0001g0111 a0001c0001t0001g0112 others(9): Show |
12 | HG00733.hp1 HG01258.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.91-669C>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 2/7 | chr6 | 143885363 | |||||||
chr6:143885517 | C | A | 13 | a0001c0001t0001g0001 a0001c0001t0001g0032 a0001c0001t0001g0033 others(10): Show |
14 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.91-515C>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 2/7 | chr6 | 143885517 | |||||||
chr6:143885540 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.91-492T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 2/7 | chr6 | 143885540 | |||||||
chr6:143885552 | T | G | 25 | a0001c0001t0001g0001 a0001c0001t0001g0032 a0001c0001t0001g0033 others(22): Show |
26 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(23): Show |
intron_variant | MODIFIER | c.91-480T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 2/7 | chr6 | 143885552 | |||||||
chr6:143885634 | T | C | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG02602.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.91-398T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 2/7 | chr6 | 143885634 | |||||||
chr6:143885713 | A | C | 2 | a0001c0001t0001g0300 a0001c0001t0001g0301 |
2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.91-319A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 2/7 | chr6 | 143885713 | |||||||
chr6:143885714 | A | G | 3 | a0001c0001t0001g0219 a0001c0001t0001g0260 a0001c0001t0001g0273 |
3 | NA18951.hp2 NA18987.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.91-318A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 2/7 | chr6 | 143885714 | |||||||
chr6:143885742 | GGAGTA | G | 12 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0001g0301 others(9): Show |
12 | HG01099.hp1 HG01192.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.91-289_91-285delGA others(3): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 2/7 | chr6 | 143885742 | |||||||
chr6:143886394 | A | C | 70 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0050 others(67): Show |
72 | HG00408.hp2 HG00738.hp2 HG01123.hp1 others(69): Show |
intron_variant | MODIFIER | c.210+243A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 3/7 | chr6 | 143886394 | |||||||
chr6:143886425 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.211-258A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 3/7 | chr6 | 143886425 | |||||||
chr6:143886460 | A | AT | 3 | a0003c0003t0001g0037 a0003c0003t0001g0038 a0003c0003t0001g0039 |
3 | HG02109.hp1 HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.211-218dupT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 143886460 | ||||||
chr6:143886526 | T | C | 1 | a0001c0001t0001g0064 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.211-157T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 3/7 | chr6 | 143886526 | |||||||
chr6:143886975 | A | G | 1 | a0001c0001t0001g0065 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.349+154A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143886975 | |||||||
chr6:143887042 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.349+221A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143887042 | |||||||
chr6:143887216 | A | G | 1 | a0001c0001t0001g0285 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.349+395A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143887216 | |||||||
chr6:143887275 | T | C | 1 | a0001c0001t0001g0141 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.349+454T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143887275 | |||||||
chr6:143887517 | T | G | 8 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0048 others(5): Show |
8 | HG01884.hp1 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.349+696T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143887517 | |||||||
chr6:143887608 | C | T | 1 | a0001c0001t0001g0318 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.349+787C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143887608 | |||||||
chr6:143887716 | T | A | 24 | a0001c0001t0001g0010 a0001c0001t0001g0111 a0001c0001t0001g0112 others(21): Show |
24 | HG00733.hp1 HG01099.hp1 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.349+895T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143887716 | |||||||
chr6:143887900 | C | T | 13 | a0001c0001t0001g0001 a0001c0001t0001g0032 a0001c0001t0001g0033 others(10): Show |
14 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.349+1079C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143887900 | |||||||
chr6:143888251 | A | G | 1 | a0001c0001t0001g0010 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.349+1430A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143888251 | |||||||
chr6:143888367 | T | C | 63 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(60): Show |
64 | HG00733.hp1 HG01099.hp1 HG01106.hp1 others(61): Show |
intron_variant | MODIFIER | c.349+1546T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143888367 | |||||||
chr6:143888368 | G | A | 12 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0001g0301 others(9): Show |
12 | HG01099.hp1 HG01192.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.349+1547G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143888368 | |||||||
chr6:143888493 | A | G | 1 | a0001c0001t0001g0245 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.349+1672A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143888493 | |||||||
chr6:143888527 | A | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0012 |
2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.349+1706A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143888527 | |||||||
chr6:143888545 | AT | A | 4 | a0001c0001t0001g0316 a0003c0003t0001g0037 a0003c0003t0001g0038 others(1): Show |
4 | HG02109.hp1 HG02818.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.349+1727delT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 143888545 | ||||||
chr6:143888550 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.349+1729C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143888550 | |||||||
chr6:143889065 | A | G | 14 | a0001c0001t0001g0001 a0001c0001t0001g0032 a0001c0001t0001g0033 others(11): Show |
15 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.349+2244A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143889065 | |||||||
chr6:143889106 | A | G | 34 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(31): Show |
35 | HG00140.hp2 HG00558.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.349+2285A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143889106 | |||||||
chr6:143889182 | CT | C | 11 | a0002c0002t0001g0019 a0002c0002t0001g0020 a0002c0002t0001g0021 others(8): Show |
11 | HG02145.hp1 HG02647.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.349+2362delT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143889182 | |||||||
chr6:143889216 | T | C | 3 | a0003c0003t0001g0037 a0003c0003t0001g0038 a0003c0003t0001g0039 |
3 | HG02109.hp1 HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.349+2395T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143889216 | |||||||
chr6:143889521 | A | AG | 25 | a0001c0001t0001g0001 a0001c0001t0001g0032 a0001c0001t0001g0033 others(22): Show |
26 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(23): Show |
intron_variant | MODIFIER | c.349+2701dupG | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 143889521 | ||||||
chr6:143889562 | G | C | 1 | a0001c0001t0001g0179 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.349+2741G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143889562 | |||||||
chr6:143889601 | A | G | 11 | a0002c0002t0001g0019 a0002c0002t0001g0020 a0002c0002t0001g0021 others(8): Show |
11 | HG02145.hp1 HG02647.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.349+2780A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143889601 | |||||||
chr6:143889721 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.349+2900A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143889721 | |||||||
chr6:143889778 | A | T | 4 | a0001c0001t0001g0316 a0003c0003t0001g0037 a0003c0003t0001g0038 others(1): Show |
4 | HG02109.hp1 HG02818.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.349+2957A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143889778 | |||||||
chr6:143889834 | C | A | 3 | a0001c0001t0001g0219 a0001c0001t0001g0260 a0001c0001t0001g0273 |
3 | NA18951.hp2 NA18987.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.349+3013C>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143889834 | |||||||
chr6:143889931 | A | G | 2 | a0001c0001t0001g0095 a0001c0001t0001g0105 |
2 | HG02027.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.349+3110A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143889931 | |||||||
chr6:143890058 | C | T | 1 | a0001c0001t0001g0274 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.349+3237C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143890058 | |||||||
chr6:143890135 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.349+3314G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143890135 | |||||||
chr6:143890398 | C | CA | 11 | a0001c0001t0001g0100 a0001c0001t0001g0108 a0001c0001t0001g0116 others(8): Show |
11 | HG02074.hp1 HG02145.hp2 HG02965.hp2 others(8): Show |
intron_variant | MODIFIER | c.349+3594dupA | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 143890398 | ||||||
chr6:143890398 | CA | C | 35 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(32): Show |
36 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(33): Show |
intron_variant | MODIFIER | c.349+3594delA | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 143890398 | ||||||
chr6:143890493 | T | C | 2 | a0001c0001t0001g0272 a0001c0001t0001g0282 |
2 | NA19075.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.349+3672T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143890493 | |||||||
chr6:143890706 | G | T | 4 | a0001c0001t0001g0316 a0003c0003t0001g0037 a0003c0003t0001g0038 others(1): Show |
4 | HG02109.hp1 HG02818.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.349+3885G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143890706 | |||||||
chr6:143890855 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.349+4034C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143890855 | |||||||
chr6:143890912 | G | A | 2 | a0001c0001t0001g0030 a0001c0001t0001g0031 |
2 | HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.349+4091G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143890912 | |||||||
chr6:143890926 | G | A | 3 | a0001c0001t0001g0197 a0001c0001t0001g0206 a0001c0001t0001g0207 |
3 | HG03017.hp2 HG03834.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.349+4105G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143890926 | |||||||
chr6:143891130 | C | CA | 27 | a0001c0001t0001g0010 a0001c0001t0001g0102 a0001c0001t0001g0111 others(24): Show |
27 | HG00639.hp1 HG00733.hp1 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.349+4324dupA | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 143891130 | ||||||
chr6:143891130 | CA | C | 24 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(21): Show |
25 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.349+4324delA | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 143891130 | ||||||
chr6:143891251 | A | T | 2 | a0001c0001t0001g0288 a0001c0001t0001g0289 |
2 | HG00609.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.349+4430A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143891251 | |||||||
chr6:143891356 | A | G | 2 | a0003c0003t0001g0038 a0003c0003t0001g0039 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.349+4535A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143891356 | |||||||
chr6:143891438 | C | T | 13 | a0001c0001t0001g0001 a0001c0001t0001g0032 a0001c0001t0001g0033 others(10): Show |
14 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.349+4617C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143891438 | |||||||
chr6:143891466 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.349+4645C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143891466 | |||||||
chr6:143891686 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.349+4865T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143891686 | |||||||
chr6:143891693 | CA | C | 26 | a0001c0001t0001g0001 a0001c0001t0001g0032 a0001c0001t0001g0033 others(23): Show |
27 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.349+4887delA | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 143891693 | ||||||
chr6:143891705 | A | G | 1 | a0001c0001t0001g0315 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.349+4884A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143891705 | |||||||
chr6:143891876 | A | AT | 38 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(35): Show |
39 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(36): Show |
intron_variant | MODIFIER | c.349+5056dupT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 143891876 | ||||||
chr6:143892297 | C | CT | 16 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(13): Show |
17 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.349+5492dupT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 143892297 | ||||||
chr6:143892297 | CT | C | 18 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0100 others(15): Show |
18 | HG01884.hp1 HG02145.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.349+5492delT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 143892297 | ||||||
chr6:143892367 | C | G | 2 | a0001c0001t0001g0007 a0001c0001t0001g0250 |
3 | NA18983.hp2 NA19084.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.349+5546C>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143892367 | |||||||
chr6:143892734 | A | C | 2 | a0003c0003t0001g0038 a0003c0003t0001g0039 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.350-5818A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143892734 | |||||||
chr6:143892905 | T | A | 1 | a0001c0001t0001g0286 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.350-5647T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143892905 | |||||||
chr6:143892906 | A | T | 10 | a0001c0001t0001g0035 a0001c0001t0001g0111 a0001c0001t0001g0112 others(7): Show |
10 | HG00733.hp1 HG01258.hp1 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.350-5646A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143892906 | |||||||
chr6:143893002 | GA | G | 16 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(13): Show |
16 | HG01884.hp1 HG01978.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.350-5539delA | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 143893002 | ||||||
chr6:143893002 | GAA | G | 24 | a0001c0001t0001g0001 a0001c0001t0001g0032 a0001c0001t0001g0033 others(21): Show |
25 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.350-5540_350-5539d others(4): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 143893002 | ||||||
chr6:143893028 | A | T | 6 | a0001c0001t0001g0294 a0001c0001t0001g0295 a0001c0001t0001g0296 others(3): Show |
6 | HG02572.hp2 HG02615.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.350-5524A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143893028 | |||||||
chr6:143893048 | C | T | 1 | a0001c0001t0001g0315 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.350-5504C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143893048 | |||||||
chr6:143893337 | G | A | 12 | a0001c0001t0001g0010 a0001c0001t0001g0111 a0001c0001t0001g0112 others(9): Show |
12 | HG00733.hp1 HG01258.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.350-5215G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143893337 | |||||||
chr6:143893340 | G | A | 3 | a0003c0003t0001g0037 a0003c0003t0001g0038 a0003c0003t0001g0039 |
3 | HG02109.hp1 HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.350-5212G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143893340 | |||||||
chr6:143893353 | C | T | 13 | a0001c0001t0001g0001 a0001c0001t0001g0032 a0001c0001t0001g0033 others(10): Show |
14 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.350-5199C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143893353 | |||||||
chr6:143893355 | G | A | 3 | a0003c0003t0001g0037 a0003c0003t0001g0038 a0003c0003t0001g0039 |
3 | HG02109.hp1 HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.350-5197G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143893355 | |||||||
chr6:143893380 | C | G | 24 | a0001c0001t0001g0001 a0001c0001t0001g0032 a0001c0001t0001g0033 others(21): Show |
25 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.350-5172C>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143893380 | |||||||
chr6:143893417 | A | G | 2 | a0001c0001t0001g0095 a0001c0001t0001g0105 |
2 | HG02027.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.350-5135A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143893417 | |||||||
chr6:143893417 | A | T | 1 | a0001c0001t0001g0287 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.350-5135A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143893417 | |||||||
chr6:143893422 | G | A | 1 | a0001c0001t0001g0032 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.350-5130G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143893422 | |||||||
chr6:143893443 | C | T | 1 | a0001c0001t0001g0309 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.350-5109C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143893443 | |||||||
chr6:143893721 | C | G | 1 | a0001c0001t0001g0315 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.350-4831C>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143893721 | |||||||
chr6:143893780 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.350-4772A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143893780 | |||||||
chr6:143893787 | C | T | 35 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(32): Show |
36 | HG00140.hp2 HG00558.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.350-4765C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143893787 | |||||||
chr6:143893832 | A | G | 7 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0122 others(4): Show |
7 | HG01433.hp1 HG02055.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.350-4720A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143893832 | |||||||
chr6:143893832 | A | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0012 |
2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.350-4720A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143893832 | |||||||
chr6:143893925 | A | C | 3 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0001g0301 |
3 | HG02723.hp2 HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.350-4627A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143893925 | |||||||
chr6:143893950 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.350-4602T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143893950 | |||||||
chr6:143893954 | G | A | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01081.hp2 HG02258.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.350-4598G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143893954 | |||||||
chr6:143893978 | G | A | 1 | a0001c0001t0001g0246 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.350-4574G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143893978 | |||||||
chr6:143893992 | G | A | 1 | a0001c0001t0001g0316 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.350-4560G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143893992 | |||||||
chr6:143894166 | TAAAC | T | 24 | a0001c0001t0001g0001 a0001c0001t0001g0032 a0001c0001t0001g0033 others(21): Show |
25 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.350-4384_350-4381d others(6): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 143894166 | ||||||
chr6:143894278 | T | C | 2 | a0001c0001t0001g0030 a0001c0001t0001g0031 |
2 | HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.350-4274T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143894278 | |||||||
chr6:143894362 | T | C | 1 | a0001c0001t0001g0315 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.350-4190T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143894362 | |||||||
chr6:143894398 | T | C | 1 | a0001c0001t0001g0304 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.350-4154T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143894398 | |||||||
chr6:143894418 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.350-4134G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143894418 | |||||||
chr6:143894585 | C | T | 1 | a0001c0001t0001g0214 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.350-3967C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143894585 | |||||||
chr6:143894978 | A | G | 14 | a0001c0001t0001g0001 a0001c0001t0001g0032 a0001c0001t0001g0033 others(11): Show |
15 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.350-3574A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143894978 | |||||||
chr6:143895004 | C | T | 1 | a0001c0001t0001g0316 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.350-3548C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143895004 | |||||||
chr6:143895076 | C | A | 1 | a0001c0001t0001g0215 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.350-3476C>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143895076 | |||||||
chr6:143895077 | A | T | 1 | a0001c0001t0001g0215 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.350-3475A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143895077 | |||||||
chr6:143895079 | G | A | 1 | a0001c0001t0001g0316 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.350-3473G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143895079 | |||||||
chr6:143895311 | C | T | 6 | a0001c0001t0001g0114 a0001c0001t0001g0116 a0001c0001t0001g0118 others(3): Show |
6 | HG01928.hp1 HG02145.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-3241C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143895311 | |||||||
chr6:143895408 | A | C | 60 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(57): Show |
61 | HG01099.hp1 HG01106.hp1 HG01192.hp1 others(58): Show |
intron_variant | MODIFIER | c.350-3144A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143895408 | |||||||
chr6:143895414 | C | T | 42 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0030 others(39): Show |
43 | HG00140.hp2 HG00558.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.350-3138C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143895414 | |||||||
chr6:143895458 | C | T | 6 | a0001c0001t0001g0064 a0001c0001t0001g0069 a0001c0001t0001g0085 others(3): Show |
6 | NA18959.hp1 NA18979.hp1 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.350-3094C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143895458 | |||||||
chr6:143895608 | T | C | 13 | a0001c0001t0001g0001 a0001c0001t0001g0032 a0001c0001t0001g0033 others(10): Show |
14 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.350-2944T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143895608 | |||||||
chr6:143895708 | A | G | 14 | a0001c0001t0001g0001 a0001c0001t0001g0032 a0001c0001t0001g0033 others(11): Show |
15 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.350-2844A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143895708 | |||||||
chr6:143895726 | A | G | 2 | a0001c0001t0001g0011 a0001c0001t0001g0012 |
2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.350-2826A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143895726 | |||||||
chr6:143895741 | T | C | 14 | a0001c0001t0001g0001 a0001c0001t0001g0032 a0001c0001t0001g0033 others(11): Show |
15 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.350-2811T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143895741 | |||||||
chr6:143895836 | G | A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(55): Show |
59 | HG01106.hp1 HG01192.hp1 HG01258.hp1 others(56): Show |
intron_variant | MODIFIER | c.350-2716G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143895836 | |||||||
chr6:143895942 | G | A | 13 | a0001c0001t0001g0001 a0001c0001t0001g0032 a0001c0001t0001g0033 others(10): Show |
14 | HG01106.hp1 HG01358.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.350-2610G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143895942 | |||||||
chr6:143896050 | A | G | 11 | a0002c0002t0001g0019 a0002c0002t0001g0020 a0002c0002t0001g0021 others(8): Show |
11 | HG02145.hp1 HG02647.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.350-2502A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143896050 | |||||||
chr6:143896068 | G | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0012 |
2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.350-2484G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143896068 | |||||||
chr6:143896100 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0012 |
2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.350-2452C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143896100 | |||||||
chr6:143896614 | G | A | 1 | a0001c0001t0001g0272 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.350-1938G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143896614 | |||||||
chr6:143896657 | T | A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(55): Show |
59 | HG01106.hp1 HG01192.hp1 HG01258.hp1 others(56): Show |
intron_variant | MODIFIER | c.350-1895T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143896657 | |||||||
chr6:143896765 | A | G | 10 | a0001c0001t0001g0292 a0001c0001t0001g0293 a0001c0001t0001g0294 others(7): Show |
10 | HG02572.hp2 HG02615.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.350-1787A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143896765 | |||||||
chr6:143897001 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.350-1551G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143897001 | |||||||
chr6:143897090 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.350-1462C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143897090 | |||||||
chr6:143897190 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.350-1362C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143897190 | |||||||
chr6:143897457 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.350-1095C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143897457 | |||||||
chr6:143897475 | T | G | 3 | a0003c0003t0001g0037 a0003c0003t0001g0038 a0003c0003t0001g0039 |
3 | HG02109.hp1 HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.350-1077T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143897475 | |||||||
chr6:143897505 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.350-1047T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143897505 | |||||||
chr6:143897510 | T | A | 11 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0114 others(8): Show |
11 | HG00733.hp1 HG01258.hp1 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.350-1042T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143897510 | |||||||
chr6:143897667 | T | A | 1 | a0001c0001t0001g0217 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.350-885T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143897667 | |||||||
chr6:143897842 | C | G | 6 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(3): Show |
6 | NA18965.hp2 NA18998.hp1 NA19009.hp2 others(3): Show |
intron_variant | MODIFIER | c.350-710C>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143897842 | |||||||
chr6:143897926 | C | A | 12 | a0001c0001t0001g0132 a0002c0002t0001g0019 a0002c0002t0001g0020 others(9): Show |
12 | HG02145.hp1 HG02647.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.350-626C>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143897926 | |||||||
chr6:143897958 | A | G | 8 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0048 others(5): Show |
8 | HG01884.hp1 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.350-594A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143897958 | |||||||
chr6:143898103 | C | T | 1 | a0001c0001t0001g0315 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.350-449C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143898103 | |||||||
chr6:143898233 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.350-319G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143898233 | |||||||
chr6:143898539 | T | C | 3 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 |
3 | HG02886.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.350-13T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 4/7 | chr6 | 143898539 | |||||||
chr6:143899127 | A | G | 1 | a0001c0001t0001g0318 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.489+436A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143899127 | |||||||
chr6:143899267 | C | T | 53 | a0001c0001t0001g0008 a0001c0001t0001g0059 a0001c0001t0001g0060 others(50): Show |
54 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.489+576C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143899267 | |||||||
chr6:143899398 | CAG | C | 5 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0220 others(2): Show |
5 | HG01433.hp1 HG02055.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+708_489+709del others(2): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143899398 | |||||||
chr6:143899492 | C | T | 11 | a0002c0002t0001g0019 a0002c0002t0001g0020 a0002c0002t0001g0021 others(8): Show |
11 | HG02145.hp1 HG02647.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.489+801C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143899492 | |||||||
chr6:143899532 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.489+841C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143899532 | |||||||
chr6:143899774 | G | A | 1 | a0001c0001t0001g0316 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.489+1083G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143899774 | |||||||
chr6:143900070 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.489+1379G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143900070 | |||||||
chr6:143900092 | C | T | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG02602.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.489+1401C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143900092 | |||||||
chr6:143900222 | T | C | 6 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(3): Show |
6 | NA18965.hp2 NA18998.hp1 NA19009.hp2 others(3): Show |
intron_variant | MODIFIER | c.489+1531T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143900222 | |||||||
chr6:143900262 | G | C | 4 | a0001c0001t0001g0316 a0003c0003t0001g0037 a0003c0003t0001g0038 others(1): Show |
4 | HG02109.hp1 HG02818.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+1571G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143900262 | |||||||
chr6:143900390 | C | CA | 122 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(119): Show |
125 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.489+1714dupA | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 143900390 | ||||||
chr6:143900433 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.489+1742G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143900433 | |||||||
chr6:143900556 | GACAGGTC others(8): Show |
G | 2 | a0001c0001t0001g0011 a0001c0001t0001g0012 |
2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.489+1893_489+1907d others(17): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 143900556 | ||||||
chr6:143900597 | G | C | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01081.hp2 HG02258.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+1906G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143900597 | |||||||
chr6:143900619 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.489+1928G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143900619 | |||||||
chr6:143900795 | G | A | 3 | a0001c0001t0001g0245 a0001c0001t0001g0263 a0001c0001t0001g0268 |
3 | HG00099.hp2 HG00738.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.489+2104G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143900795 | |||||||
chr6:143900864 | A | T | 15 | a0001c0001t0001g0316 a0002c0002t0001g0019 a0002c0002t0001g0020 others(12): Show |
15 | HG02109.hp1 HG02145.hp1 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.489+2173A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143900864 | |||||||
chr6:143900874 | T | C | 2 | a0001c0001t0001g0011 a0001c0001t0001g0012 |
2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.490-2170T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143900874 | |||||||
chr6:143900925 | G | A | 6 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(3): Show |
6 | NA18965.hp2 NA18998.hp1 NA19009.hp2 others(3): Show |
intron_variant | MODIFIER | c.490-2119G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143900925 | |||||||
chr6:143900941 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.490-2103C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143900941 | |||||||
chr6:143900942 | G | A | 1 | a0001c0001t0001g0284 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.490-2102G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143900942 | |||||||
chr6:143900956 | A | G | 10 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0001g0301 others(7): Show |
10 | HG01192.hp1 HG02486.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.490-2088A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143900956 | |||||||
chr6:143900981 | A | G | 188 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(185): Show |
191 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(188): Show |
intron_variant | MODIFIER | c.490-2063A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143900981 | |||||||
chr6:143901048 | A | G | 32 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(29): Show |
32 | HG00733.hp1 HG01192.hp1 HG01258.hp1 others(29): Show |
intron_variant | MODIFIER | c.490-1996A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143901048 | |||||||
chr6:143901081 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.490-1963C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143901081 | |||||||
chr6:143901177 | G | A | 1 | a0002c0002t0001g0025 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.490-1867G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143901177 | |||||||
chr6:143901250 | C | CT | 86 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0017 others(83): Show |
87 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.490-1767dupT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 143901250 | ||||||
chr6:143901250 | C | CTT | 32 | a0001c0001t0001g0010 a0001c0001t0001g0049 a0001c0001t0001g0051 others(29): Show |
32 | HG00733.hp1 HG01192.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.490-1768_490-1767d others(4): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 143901250 | ||||||
chr6:143901250 | C | CTTT | 12 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0048 others(9): Show |
12 | HG01258.hp1 HG01884.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.490-1769_490-1767d others(5): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 143901250 | ||||||
chr6:143901250 | CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0196 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.490-1780_490-1767d others(16): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 143901250 | ||||||
chr6:143901250 | CTTTTTTT others(8): Show |
C | 3 | a0001c0001t0001g0094 a0001c0001t0001g0099 a0001c0001t0001g0109 |
3 | HG02074.hp2 NA18948.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.490-1781_490-1767d others(17): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 143901250 | ||||||
chr6:143901317 | T | C | 2 | a0001c0001t0001g0011 a0001c0001t0001g0012 |
2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.490-1727T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143901317 | |||||||
chr6:143901424 | T | C | 11 | a0002c0002t0001g0019 a0002c0002t0001g0020 a0002c0002t0001g0021 others(8): Show |
11 | HG02145.hp1 HG02647.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.490-1620T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143901424 | |||||||
chr6:143901550 | G | A | 6 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(3): Show |
6 | NA18965.hp2 NA18998.hp1 NA19009.hp2 others(3): Show |
intron_variant | MODIFIER | c.490-1494G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143901550 | |||||||
chr6:143901563 | G | A | 2 | a0001c0001t0001g0300 a0001c0001t0001g0301 |
2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.490-1481G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143901563 | |||||||
chr6:143901793 | G | A | 27 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(24): Show |
27 | HG01192.hp1 HG01258.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.490-1251G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143901793 | |||||||
chr6:143901884 | G | T | 52 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(49): Show |
52 | HG01192.hp1 HG01258.hp1 HG01884.hp1 others(49): Show |
intron_variant | MODIFIER | c.490-1160G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143901884 | |||||||
chr6:143902477 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.490-567C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143902477 | |||||||
chr6:143902526 | A | C | 1 | a0001c0001t0001g0056 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.490-518A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143902526 | |||||||
chr6:143902707 | T | A | 9 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0114 others(6): Show |
9 | HG00733.hp1 HG01258.hp1 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.490-337T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143902707 | |||||||
chr6:143902750 | T | C | 2 | a0001c0001t0001g0030 a0001c0001t0001g0031 |
2 | HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.490-294T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143902750 | |||||||
chr6:143902772 | T | C | 10 | a0001c0001t0001g0292 a0001c0001t0001g0293 a0001c0001t0001g0294 others(7): Show |
10 | HG02572.hp2 HG02615.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.490-272T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143902772 | |||||||
chr6:143902889 | G | A | 3 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0004c0004t0001g0088 |
3 | NA18965.hp2 NA18998.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.490-155G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143902889 | |||||||
chr6:143902947 | T | C | 6 | a0001c0001t0001g0070 a0001c0001t0001g0073 a0001c0001t0001g0078 others(3): Show |
6 | NA18747.hp2 NA18951.hp1 NA18994.hp2 others(3): Show |
intron_variant | MODIFIER | c.490-97T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143902947 | |||||||
chr6:143902988 | A | C | 1 | a0001c0001t0001g0056 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.490-56A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143902988 | |||||||
chr6:143903031 | T | C | 3 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0004c0004t0001g0088 |
3 | NA18965.hp2 NA18998.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.490-13T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 5/7 | chr6 | 143903031 | |||||||
chr6:143903175 | T | G | 32 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0034 others(29): Show |
32 | HG01192.hp1 HG01884.hp1 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.598+23T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143903175 | |||||||
chr6:143903334 | A | G | 1 | a0001c0001t0001g0004 | 2 | HG01943.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.598+182A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143903334 | |||||||
chr6:143903444 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0012 |
2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.598+292C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143903444 | |||||||
chr6:143903486 | T | C | 1 | a0001c0001t0001g0078 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.598+334T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143903486 | |||||||
chr6:143903587 | A | T | 1 | a0001c0001t0001g0240 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.598+435A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143903587 | |||||||
chr6:143903743 | C | T | 2 | a0001c0001t0001g0106 a0001c0001t0001g0161 |
2 | NA18960.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.598+591C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143903743 | |||||||
chr6:143904224 | A | C | 2 | a0001c0001t0001g0304 a0001c0001t0001g0312 |
2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.598+1072A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143904224 | |||||||
chr6:143904474 | A | G | 9 | a0002c0002t0001g0019 a0002c0002t0001g0020 a0002c0002t0001g0021 others(6): Show |
9 | HG02647.hp2 HG02717.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.598+1322A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143904474 | |||||||
chr6:143904533 | T | A | 1 | a0001c0001t0001g0046 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.598+1381T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143904533 | |||||||
chr6:143904543 | G | A | 9 | a0002c0002t0001g0019 a0002c0002t0001g0020 a0002c0002t0001g0021 others(6): Show |
9 | HG02647.hp2 HG02717.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.598+1391G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143904543 | |||||||
chr6:143904633 | T | G | 1 | a0001c0001t0001g0050 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.598+1481T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143904633 | |||||||
chr6:143904727 | G | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0192 |
3 | HG01109.hp1 HG01123.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.598+1575G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143904727 | |||||||
chr6:143904745 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.598+1593G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143904745 | |||||||
chr6:143904950 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.598+1798C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143904950 | |||||||
chr6:143905166 | A | G | 5 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0270 others(2): Show |
5 | NA18940.hp2 NA18965.hp2 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.598+2014A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143905166 | |||||||
chr6:143905373 | A | G | 2 | a0001c0001t0001g0052 a0001c0001t0001g0053 |
2 | HG02451.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.598+2221A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143905373 | |||||||
chr6:143905570 | G | C | 4 | a0001c0001t0001g0185 a0001c0001t0001g0196 a0001c0001t0001g0215 others(1): Show |
4 | HG02486.hp1 HG04184.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.598+2418G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143905570 | |||||||
chr6:143905787 | G | A | 1 | a0001c0001t0001g0132 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.598+2635G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143905787 | |||||||
chr6:143905878 | C | T | 7 | a0001c0001t0001g0302 a0001c0001t0001g0303 a0001c0001t0001g0305 others(4): Show |
7 | HG01192.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.598+2726C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143905878 | |||||||
chr6:143905994 | A | G | 254 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(251): Show |
258 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(255): Show |
intron_variant | MODIFIER | c.598+2842A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143905994 | |||||||
chr6:143906091 | G | C | 5 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0036 others(2): Show |
5 | HG03490.hp1 HG03710.hp2 NA19009.hp2 others(2): Show |
intron_variant | MODIFIER | c.598+2939G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143906091 | |||||||
chr6:143906160 | C | T | 2 | a0001c0001t0001g0034 a0004c0004t0001g0088 |
2 | NA18965.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.598+3008C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143906160 | |||||||
chr6:143906340 | C | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0048 a0001c0001t0001g0049 others(1): Show |
4 | HG02055.hp1 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.598+3188C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143906340 | |||||||
chr6:143906362 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.598+3210A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143906362 | |||||||
chr6:143906367 | A | G | 4 | a0001c0001t0001g0010 a0001c0001t0001g0048 a0001c0001t0001g0049 others(1): Show |
4 | HG02055.hp1 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.598+3215A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143906367 | |||||||
chr6:143906370 | G | T | 9 | a0002c0002t0001g0019 a0002c0002t0001g0020 a0002c0002t0001g0021 others(6): Show |
9 | HG02647.hp2 HG02717.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.598+3218G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143906370 | |||||||
chr6:143906424 | T | G | 1 | a0001c0001t0001g0308 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.598+3272T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143906424 | |||||||
chr6:143906424 | TTTTTAA | T | 8 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0137 others(5): Show |
8 | NA19003.hp2 NA19011.hp2 NA19056.hp1 others(5): Show |
intron_variant | MODIFIER | c.598+3289_598+3294d others(8): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143906424 | ||||||
chr6:143906683 | A | G | 77 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0018 others(74): Show |
79 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.598+3531A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143906683 | |||||||
chr6:143906747 | CT | C | 134 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(131): Show |
136 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.598+3609delT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143906747 | ||||||
chr6:143906747 | CTT | C | 13 | a0001c0001t0001g0082 a0001c0001t0001g0114 a0001c0001t0001g0116 others(10): Show |
13 | HG00140.hp2 HG00639.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.598+3608_598+3609d others(4): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143906747 | ||||||
chr6:143906748 | T | A | 1 | a0001c0001t0001g0262 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.598+3596T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143906748 | |||||||
chr6:143906818 | A | G | 54 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0041 others(51): Show |
55 | HG00408.hp1 HG00438.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.598+3666A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143906818 | |||||||
chr6:143907091 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.598+3939T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143907091 | |||||||
chr6:143907234 | A | G | 2 | a0001c0001t0001g0141 a0001c0001t0001g0143 |
2 | NA18942.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.598+4082A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143907234 | |||||||
chr6:143907515 | A | C | 2 | a0003c0003t0001g0038 a0003c0003t0001g0039 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.598+4363A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143907515 | |||||||
chr6:143907517 | T | G | 2 | a0001c0001t0001g0113 a0001c0001t0001g0217 |
2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.598+4365T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143907517 | |||||||
chr6:143907675 | T | A | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(209): Show |
216 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.598+4523T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143907675 | |||||||
chr6:143907895 | T | G | 3 | a0001c0001t0001g0034 a0001c0001t0001g0258 a0004c0004t0001g0088 |
3 | NA18965.hp2 NA18998.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.598+4743T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143907895 | |||||||
chr6:143908252 | T | C | 12 | a0001c0001t0001g0052 a0001c0001t0001g0275 a0001c0001t0001g0279 others(9): Show |
12 | HG02451.hp1 HG02622.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.598+5100T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143908252 | |||||||
chr6:143908253 | A | C | 22 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0115 others(19): Show |
23 | HG00558.hp1 HG01258.hp1 HG01978.hp1 others(20): Show |
intron_variant | MODIFIER | c.598+5101A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143908253 | |||||||
chr6:143908291 | A | G | 4 | a0001c0001t0001g0005 a0001c0001t0001g0186 a0001c0001t0001g0229 others(1): Show |
5 | HG00733.hp2 HG01106.hp2 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.598+5139A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143908291 | |||||||
chr6:143908292 | G | GT | 224 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(221): Show |
228 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(225): Show |
intron_variant | MODIFIER | c.598+5146dupT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143908292 | ||||||
chr6:143908320 | A | G | 77 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0018 others(74): Show |
79 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.598+5168A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143908320 | |||||||
chr6:143908347 | A | T | 2 | a0001c0001t0001g0030 a0001c0001t0001g0031 |
2 | HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.598+5195A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143908347 | |||||||
chr6:143908393 | T | C | 1 | a0001c0001t0001g0063 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.598+5241T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143908393 | |||||||
chr6:143908408 | G | A | 13 | a0001c0001t0001g0082 a0001c0001t0001g0114 a0001c0001t0001g0116 others(10): Show |
13 | HG00140.hp2 HG00639.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.598+5256G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143908408 | |||||||
chr6:143908465 | A | G | 2 | a0001c0001t0001g0030 a0001c0001t0001g0031 |
2 | HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.598+5313A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143908465 | |||||||
chr6:143908570 | C | T | 1 | a0001c0001t0001g0316 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.598+5418C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143908570 | |||||||
chr6:143908779 | G | T | 2 | a0001c0001t0001g0304 a0001c0001t0001g0312 |
2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.598+5627G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143908779 | |||||||
chr6:143908811 | A | G | 1 | a0001c0001t0001g0312 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.598+5659A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143908811 | |||||||
chr6:143909285 | T | A | 1 | a0001c0001t0001g0313 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.598+6133T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143909285 | |||||||
chr6:143909382 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.598+6230G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143909382 | |||||||
chr6:143909421 | G | T | 2 | a0001c0001t0001g0304 a0001c0001t0001g0312 |
2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.598+6269G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143909421 | |||||||
chr6:143909422 | G | T | 2 | a0001c0001t0001g0304 a0001c0001t0001g0312 |
2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.598+6270G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143909422 | |||||||
chr6:143909498 | T | A | 253 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(250): Show |
257 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(254): Show |
intron_variant | MODIFIER | c.598+6346T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143909498 | |||||||
chr6:143909530 | C | CT | 34 | a0001c0001t0001g0052 a0001c0001t0001g0061 a0001c0001t0001g0111 others(31): Show |
34 | HG01884.hp2 HG02451.hp1 HG02572.hp2 others(31): Show |
intron_variant | MODIFIER | c.598+6395dupT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143909530 | ||||||
chr6:143909530 | CT | C | 20 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(17): Show |
21 | HG01081.hp2 HG01168.hp1 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.598+6395delT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143909530 | ||||||
chr6:143909547 | T | C | 1 | a0001c0001t0001g0226 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.598+6395T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143909547 | |||||||
chr6:143909666 | A | G | 1 | a0001c0001t0001g0222 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.598+6514A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143909666 | |||||||
chr6:143909689 | A | G | 8 | a0001c0001t0001g0182 a0001c0001t0001g0302 a0001c0001t0001g0303 others(5): Show |
8 | HG01192.hp1 HG02486.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.598+6537A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143909689 | |||||||
chr6:143909695 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.598+6543A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143909695 | |||||||
chr6:143909794 | C | A | 1 | a0001c0001t0001g0316 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.598+6642C>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143909794 | |||||||
chr6:143910066 | C | T | 1 | a0001c0001t0001g0309 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.598+6914C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143910066 | |||||||
chr6:143910367 | G | T | 1 | a0001c0001t0001g0030 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.598+7215G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143910367 | |||||||
chr6:143910419 | C | A | 1 | a0001c0001t0001g0116 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.598+7267C>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143910419 | |||||||
chr6:143910420 | A | G | 1 | a0001c0001t0001g0053 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.598+7268A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143910420 | |||||||
chr6:143910428 | G | T | 3 | a0003c0003t0001g0037 a0003c0003t0001g0038 a0003c0003t0001g0039 |
3 | HG02109.hp1 HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.598+7276G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143910428 | |||||||
chr6:143910499 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.598+7347A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143910499 | |||||||
chr6:143910739 | G | T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0299 others(2): Show |
5 | HG01884.hp1 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.598+7587G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143910739 | |||||||
chr6:143910894 | G | A | 253 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(250): Show |
257 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(254): Show |
intron_variant | MODIFIER | c.598+7742G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143910894 | |||||||
chr6:143910992 | A | T | 1 | a0001c0001t0001g0097 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.598+7840A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143910992 | |||||||
chr6:143911300 | G | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0012 |
2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.598+8148G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143911300 | |||||||
chr6:143911718 | A | G | 1 | a0003c0003t0001g0037 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.598+8566A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143911718 | |||||||
chr6:143911826 | T | C | 3 | a0003c0003t0001g0037 a0003c0003t0001g0038 a0003c0003t0001g0039 |
3 | HG02109.hp1 HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.598+8674T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143911826 | |||||||
chr6:143912059 | C | T | 3 | a0001c0001t0001g0034 a0001c0001t0001g0258 a0004c0004t0001g0088 |
3 | NA18965.hp2 NA18998.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.598+8907C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143912059 | |||||||
chr6:143912091 | T | C | 3 | a0001c0001t0001g0034 a0001c0001t0001g0258 a0004c0004t0001g0088 |
3 | NA18965.hp2 NA18998.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.598+8939T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143912091 | |||||||
chr6:143912097 | G | A | 1 | a0001c0001t0001g0016 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.598+8945G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143912097 | |||||||
chr6:143912228 | G | A | 3 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 |
3 | HG03927.hp1 NA18952.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.598+9076G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143912228 | |||||||
chr6:143912374 | A | G | 3 | a0003c0003t0001g0037 a0003c0003t0001g0038 a0003c0003t0001g0039 |
3 | HG02109.hp1 HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.598+9222A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143912374 | |||||||
chr6:143912521 | T | C | 3 | a0001c0001t0001g0008 a0001c0001t0001g0192 a0001c0001t0001g0220 |
4 | HG01109.hp1 HG01123.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.598+9369T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143912521 | |||||||
chr6:143912693 | C | T | 2 | a0001c0001t0001g0197 a0001c0001t0001g0206 |
2 | HG03017.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.598+9541C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143912693 | |||||||
chr6:143912804 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0012 |
2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.598+9652C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143912804 | |||||||
chr6:143913052 | G | T | 1 | a0001c0001t0001g0093 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.598+9900G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143913052 | |||||||
chr6:143913229 | T | TACC | 6 | a0001c0001t0001g0054 a0001c0001t0001g0067 a0001c0001t0001g0076 others(3): Show |
6 | HG02083.hp1 HG02083.hp2 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.598+10078_598+1008 others(7): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143913229 | ||||||
chr6:143913422 | G | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0012 |
2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.598+10270G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143913422 | |||||||
chr6:143913557 | C | T | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01081.hp2 HG02258.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.598+10405C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143913557 | |||||||
chr6:143913651 | T | A | 1 | a0001c0001t0001g0312 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.598+10499T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143913651 | |||||||
chr6:143913756 | T | C | 4 | a0001c0001t0001g0010 a0001c0001t0001g0048 a0001c0001t0001g0049 others(1): Show |
4 | HG02055.hp1 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.598+10604T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143913756 | |||||||
chr6:143913763 | T | C | 16 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0162 others(13): Show |
16 | HG01261.hp1 HG01361.hp2 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.598+10611T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143913763 | |||||||
chr6:143913829 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.598+10677G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143913829 | |||||||
chr6:143913881 | C | G | 7 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0137 others(4): Show |
7 | NA19003.hp2 NA19011.hp2 NA19056.hp1 others(4): Show |
intron_variant | MODIFIER | c.598+10729C>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143913881 | |||||||
chr6:143913937 | T | A | 7 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0137 others(4): Show |
7 | NA19003.hp2 NA19011.hp2 NA19056.hp1 others(4): Show |
intron_variant | MODIFIER | c.598+10785T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143913937 | |||||||
chr6:143914000 | A | G | 2 | a0001c0001t0001g0011 a0001c0001t0001g0012 |
2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.598+10848A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143914000 | |||||||
chr6:143914092 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.598+10940C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143914092 | |||||||
chr6:143914150 | G | A | 10 | a0001c0001t0001g0146 a0002c0002t0001g0019 a0002c0002t0001g0020 others(7): Show |
10 | HG02647.hp2 HG02717.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.598+10998G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143914150 | |||||||
chr6:143914411 | A | T | 7 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0137 others(4): Show |
7 | NA19003.hp2 NA19011.hp2 NA19056.hp1 others(4): Show |
intron_variant | MODIFIER | c.598+11259A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143914411 | |||||||
chr6:143914493 | G | T | 1 | a0001c0001t0001g0062 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.598+11341G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143914493 | |||||||
chr6:143914563 | A | T | 318 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(315): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.598+11411A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143914563 | |||||||
chr6:143914773 | C | T | 1 | a0001c0001t0001g0307 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.598+11621C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143914773 | |||||||
chr6:143915132 | C | T | 29 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0115 others(26): Show |
30 | HG00558.hp1 HG01081.hp2 HG01258.hp1 others(27): Show |
intron_variant | MODIFIER | c.598+11980C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143915132 | |||||||
chr6:143915203 | A | G | 3 | a0003c0003t0001g0037 a0003c0003t0001g0038 a0003c0003t0001g0039 |
3 | HG02109.hp1 HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.598+12051A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143915203 | |||||||
chr6:143915356 | A | G | 1 | a0001c0001t0001g0238 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.598+12204A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143915356 | |||||||
chr6:143915401 | C | T | 3 | a0001c0001t0001g0094 a0001c0001t0001g0099 a0001c0001t0001g0109 |
3 | HG02074.hp2 NA18948.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.598+12249C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143915401 | |||||||
chr6:143915444 | G | C | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0299 others(2): Show |
5 | HG01884.hp1 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.598+12292G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143915444 | |||||||
chr6:143915454 | C | T | 1 | a0001c0001t0001g0318 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.598+12302C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143915454 | |||||||
chr6:143915461 | A | G | 1 | a0003c0003t0001g0037 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.598+12309A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143915461 | |||||||
chr6:143915486 | A | G | 1 | a0001c0001t0001g0313 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.598+12334A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143915486 | |||||||
chr6:143915593 | T | G | 8 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0137 others(5): Show |
8 | HG03486.hp2 NA19003.hp2 NA19011.hp2 others(5): Show |
intron_variant | MODIFIER | c.598+12441T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143915593 | |||||||
chr6:143915728 | G | A | 5 | a0001c0001t0001g0068 a0001c0001t0001g0071 a0001c0001t0001g0072 others(2): Show |
5 | NA18942.hp1 NA18956.hp2 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.598+12576G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143915728 | |||||||
chr6:143915819 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.598+12667A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143915819 | |||||||
chr6:143916084 | G | A | 2 | a0001c0001t0001g0194 a0001c0001t0001g0203 |
2 | HG02080.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.598+12932G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143916084 | |||||||
chr6:143916239 | C | T | 7 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0137 others(4): Show |
7 | NA19003.hp2 NA19011.hp2 NA19056.hp1 others(4): Show |
intron_variant | MODIFIER | c.598+13087C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143916239 | |||||||
chr6:143916260 | G | A | 7 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0137 others(4): Show |
7 | NA19003.hp2 NA19011.hp2 NA19056.hp1 others(4): Show |
intron_variant | MODIFIER | c.598+13108G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143916260 | |||||||
chr6:143916340 | A | G | 254 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(251): Show |
258 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(255): Show |
intron_variant | MODIFIER | c.598+13188A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143916340 | |||||||
chr6:143916413 | G | C | 1 | a0001c0001t0001g0158 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.598+13261G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143916413 | |||||||
chr6:143916478 | C | T | 77 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0018 others(74): Show |
79 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.598+13326C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143916478 | |||||||
chr6:143916540 | G | A | 6 | a0001c0001t0001g0115 a0001c0001t0001g0120 a0001c0001t0001g0139 others(3): Show |
6 | HG01258.hp1 HG02257.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.598+13388G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143916540 | |||||||
chr6:143916750 | G | T | 8 | a0001c0001t0001g0182 a0001c0001t0001g0302 a0001c0001t0001g0303 others(5): Show |
8 | HG01192.hp1 HG02486.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.598+13598G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143916750 | |||||||
chr6:143916942 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.598+13790T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143916942 | |||||||
chr6:143917054 | T | C | 1 | a0001c0001t0001g0318 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.598+13902T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143917054 | |||||||
chr6:143917376 | A | C | 1 | a0001c0001t0001g0060 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.598+14224A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143917376 | |||||||
chr6:143917385 | G | A | 112 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0015 others(109): Show |
114 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(111): Show |
intron_variant | MODIFIER | c.598+14233G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143917385 | |||||||
chr6:143917595 | A | G | 1 | a0001c0001t0001g0212 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.598+14443A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143917595 | |||||||
chr6:143917636 | C | T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0299 others(2): Show |
5 | HG01884.hp1 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.598+14484C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143917636 | |||||||
chr6:143917644 | T | C | 3 | a0001c0001t0001g0034 a0001c0001t0001g0258 a0004c0004t0001g0088 |
3 | NA18965.hp2 NA18998.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.598+14492T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143917644 | |||||||
chr6:143917735 | T | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0012 |
2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.598+14583T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143917735 | |||||||
chr6:143917857 | G | A | 13 | a0001c0001t0001g0082 a0001c0001t0001g0114 a0001c0001t0001g0116 others(10): Show |
13 | HG00140.hp2 HG00639.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.598+14705G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143917857 | |||||||
chr6:143917929 | G | A | 14 | a0001c0001t0001g0034 a0001c0001t0001g0134 a0001c0001t0001g0135 others(11): Show |
14 | HG02109.hp1 HG02818.hp2 HG03486.hp2 others(11): Show |
intron_variant | MODIFIER | c.598+14777G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143917929 | |||||||
chr6:143918169 | C | T | 72 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(69): Show |
73 | HG00438.hp1 HG00609.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.598+15017C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143918169 | |||||||
chr6:143918200 | T | TA | 91 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0018 others(88): Show |
93 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.598+15048_598+1504 others(5): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143918200 | |||||||
chr6:143918209 | A | C | 1 | a0001c0001t0001g0139 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.598+15057A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143918209 | |||||||
chr6:143918257 | C | G | 7 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0137 others(4): Show |
7 | NA19003.hp2 NA19011.hp2 NA19056.hp1 others(4): Show |
intron_variant | MODIFIER | c.598+15105C>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143918257 | |||||||
chr6:143918333 | A | G | 1 | a0001c0001t0001g0116 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.598+15181A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143918333 | |||||||
chr6:143918428 | C | T | 2 | a0001c0001t0001g0139 a0001c0001t0001g0148 |
2 | HG03831.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.598+15276C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143918428 | |||||||
chr6:143918512 | G | A | 22 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0115 others(19): Show |
23 | HG00558.hp1 HG01258.hp1 HG01978.hp1 others(20): Show |
intron_variant | MODIFIER | c.598+15360G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143918512 | |||||||
chr6:143918645 | C | T | 1 | a0001c0001t0001g0288 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.598+15493C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143918645 | |||||||
chr6:143918844 | A | G | 12 | a0001c0001t0001g0052 a0001c0001t0001g0275 a0001c0001t0001g0279 others(9): Show |
12 | HG02451.hp1 HG02622.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.598+15692A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143918844 | |||||||
chr6:143918921 | C | G | 16 | a0001c0001t0001g0082 a0001c0001t0001g0111 a0001c0001t0001g0112 others(13): Show |
16 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.598+15769C>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143918921 | |||||||
chr6:143918939 | G | T | 112 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0015 others(109): Show |
114 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.598+15787G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143918939 | |||||||
chr6:143918946 | G | T | 87 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0018 others(84): Show |
89 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.598+15794G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143918946 | |||||||
chr6:143918958 | G | C | 3 | a0001c0001t0001g0034 a0001c0001t0001g0258 a0004c0004t0001g0088 |
3 | NA18965.hp2 NA18998.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.598+15806G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143918958 | |||||||
chr6:143919215 | CTCTG | C | 4 | a0001c0001t0001g0065 a0001c0001t0001g0159 a0001c0001t0001g0160 others(1): Show |
4 | HG00438.hp2 HG00738.hp2 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.598+16065_598+1606 others(8): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143919215 | ||||||
chr6:143919215 | CTCTGTG | C | 13 | a0001c0001t0001g0018 a0001c0001t0001g0058 a0001c0001t0001g0062 others(10): Show |
13 | HG01123.hp1 HG01168.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.598+16065_598+1607 others(10): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143919215 | ||||||
chr6:143919215 | CTCTGTGT others(1): Show |
C | 45 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0054 others(42): Show |
47 | HG00408.hp2 HG00423.hp1 HG01943.hp1 others(44): Show |
intron_variant | MODIFIER | c.598+16065_598+1607 others(12): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143919215 | ||||||
chr6:143919215 | CTCTGTGT others(3): Show |
C | 6 | a0001c0001t0001g0061 a0001c0001t0001g0064 a0001c0001t0001g0080 others(3): Show |
6 | NA18940.hp2 NA18949.hp1 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.598+16065_598+1607 others(14): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143919215 | ||||||
chr6:143919215 | CTCTGTGT others(5): Show |
C | 5 | a0001c0001t0001g0069 a0001c0001t0001g0085 a0001c0001t0001g0086 others(2): Show |
5 | NA18959.hp1 NA18979.hp1 NA19006.hp2 others(2): Show |
intron_variant | MODIFIER | c.598+16065_598+1607 others(16): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143919215 | ||||||
chr6:143919217 | C | CTCTG | 3 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0307 |
3 | HG02486.hp2 HG02622.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.598+16066_598+1606 others(8): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143919217 | ||||||
chr6:143919217 | C | CTG | 37 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0066 others(34): Show |
37 | HG00673.hp1 HG01099.hp1 HG02027.hp2 others(34): Show |
intron_variant | MODIFIER | c.598+16113_598+1611 others(6): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143919217 | ||||||
chr6:143919217 | C | CTGTG | 13 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0128 others(10): Show |
13 | HG01884.hp1 HG02258.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.598+16111_598+1611 others(8): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143919217 | ||||||
chr6:143919217 | C | CTGTGTG | 7 | a0001c0001t0001g0015 a0001c0001t0001g0034 a0001c0001t0001g0119 others(4): Show |
7 | HG02572.hp1 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.598+16109_598+1611 others(10): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143919217 | ||||||
chr6:143919217 | C | CTGTGTGT others(1): Show |
4 | a0001c0001t0001g0258 a0001c0001t0001g0300 a0001c0001t0001g0301 others(1): Show |
4 | HG02895.hp1 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.598+16107_598+1611 others(12): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143919217 | ||||||
chr6:143919217 | C | CTGTGTGT others(5): Show |
1 | a0001c0001t0001g0152 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.598+16103_598+1611 others(16): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143919217 | ||||||
chr6:143919217 | C | CTGTGTGT others(9): Show |
2 | a0001c0001t0001g0127 a0001c0001t0001g0280 |
2 | HG00558.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.598+16099_598+1611 others(20): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143919217 | ||||||
chr6:143919217 | CTG | C | 30 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(27): Show |
31 | HG00438.hp1 HG00609.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.598+16113_598+1611 others(6): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143919217 | ||||||
chr6:143919217 | CTGTG | C | 68 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(65): Show |
71 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(68): Show |
intron_variant | MODIFIER | c.598+16111_598+1611 others(8): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143919217 | ||||||
chr6:143919217 | CTGTGTG | C | 7 | a0001c0001t0001g0040 a0001c0001t0001g0046 a0001c0001t0001g0132 others(4): Show |
7 | HG00639.hp2 HG00673.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.598+16109_598+1611 others(10): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143919217 | ||||||
chr6:143919217 | CTGTGTGT others(1): Show |
C | 8 | a0001c0001t0001g0010 a0001c0001t0001g0048 a0001c0001t0001g0049 others(5): Show |
8 | HG00733.hp2 HG02055.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.598+16107_598+1611 others(12): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143919217 | ||||||
chr6:143919217 | CTGTGTGT others(3): Show |
C | 4 | a0001c0001t0001g0052 a0001c0001t0001g0275 a0001c0001t0001g0279 others(1): Show |
4 | HG02451.hp1 HG02622.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.598+16105_598+1611 others(14): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143919217 | ||||||
chr6:143919217 | CTGTGTGT others(5): Show |
C | 2 | a0003c0003t0001g0038 a0003c0003t0001g0039 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.598+16103_598+1611 others(16): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143919217 | ||||||
chr6:143919217 | CTGTGTGT others(17): Show |
C | 2 | a0001c0001t0001g0191 a0001c0001t0001g0200 |
2 | HG01884.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.598+16091_598+1611 others(28): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143919217 | ||||||
chr6:143919263 | G | A | 3 | a0001c0001t0001g0032 a0001c0001t0001g0140 a0001c0001t0001g0230 |
3 | HG03490.hp1 HG03710.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.598+16111G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143919263 | |||||||
chr6:143919347 | C | T | 20 | a0001c0001t0001g0010 a0001c0001t0001g0048 a0001c0001t0001g0049 others(17): Show |
20 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.598+16195C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143919347 | |||||||
chr6:143919389 | G | GT | 73 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(70): Show |
74 | HG00408.hp1 HG00438.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.598+16243dupT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143919389 | ||||||
chr6:143919620 | T | C | 8 | a0001c0001t0001g0182 a0001c0001t0001g0302 a0001c0001t0001g0303 others(5): Show |
8 | HG01192.hp1 HG02486.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.598+16468T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143919620 | |||||||
chr6:143919645 | T | C | 2 | a0001c0001t0001g0290 a0001c0001t0001g0291 |
2 | HG00673.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.598+16493T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143919645 | |||||||
chr6:143919691 | T | G | 1 | a0001c0001t0001g0278 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.598+16539T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143919691 | |||||||
chr6:143919762 | G | C | 1 | a0001c0001t0001g0209 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.598+16610G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143919762 | |||||||
chr6:143919824 | C | T | 8 | a0001c0001t0001g0182 a0001c0001t0001g0302 a0001c0001t0001g0303 others(5): Show |
8 | HG01192.hp1 HG02486.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.598+16672C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143919824 | |||||||
chr6:143919856 | T | C | 2 | a0001c0001t0001g0011 a0001c0001t0001g0012 |
2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.598+16704T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143919856 | |||||||
chr6:143919866 | G | A | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0299 others(2): Show |
5 | HG01884.hp1 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.598+16714G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143919866 | |||||||
chr6:143919941 | A | G | 12 | a0001c0001t0001g0052 a0001c0001t0001g0275 a0001c0001t0001g0279 others(9): Show |
12 | HG02451.hp1 HG02622.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.598+16789A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143919941 | |||||||
chr6:143919985 | T | C | 1 | a0001c0001t0001g0132 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.598+16833T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143919985 | |||||||
chr6:143920001 | G | GA | 14 | a0001c0001t0001g0034 a0001c0001t0001g0134 a0001c0001t0001g0135 others(11): Show |
14 | HG02109.hp1 HG02818.hp2 HG03486.hp2 others(11): Show |
intron_variant | MODIFIER | c.598+16858dupA | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143920001 | ||||||
chr6:143920318 | T | C | 2 | a0001c0001t0001g0115 a0001c0001t0001g0120 |
2 | HG01258.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.598+17166T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143920318 | |||||||
chr6:143920420 | C | T | 12 | a0001c0001t0001g0052 a0001c0001t0001g0275 a0001c0001t0001g0279 others(9): Show |
12 | HG02451.hp1 HG02622.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.599-17229C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143920420 | |||||||
chr6:143920509 | A | G | 2 | a0001c0001t0001g0030 a0001c0001t0001g0031 |
2 | HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.599-17140A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143920509 | |||||||
chr6:143920638 | T | C | 254 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(251): Show |
258 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(255): Show |
intron_variant | MODIFIER | c.599-17011T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143920638 | |||||||
chr6:143920684 | G | A | 2 | a0001c0001t0001g0030 a0001c0001t0001g0031 |
2 | HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.599-16965G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143920684 | |||||||
chr6:143920733 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.599-16916C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143920733 | |||||||
chr6:143920736 | C | T | 1 | a0001c0001t0001g0087 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.599-16913C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143920736 | |||||||
chr6:143920762 | G | T | 9 | a0001c0001t0001g0277 a0001c0001t0001g0292 a0001c0001t0001g0293 others(6): Show |
9 | HG02572.hp2 HG02615.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.599-16887G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143920762 | |||||||
chr6:143920849 | A | G | 3 | a0001c0001t0001g0034 a0001c0001t0001g0258 a0004c0004t0001g0088 |
3 | NA18965.hp2 NA18998.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.599-16800A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143920849 | |||||||
chr6:143920906 | C | CA | 6 | a0001c0001t0001g0017 a0001c0001t0001g0173 a0001c0001t0001g0221 others(3): Show |
6 | HG01934.hp2 HG02109.hp1 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.599-16725dupA | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143920906 | ||||||
chr6:143920906 | CA | C | 128 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0011 others(125): Show |
130 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.599-16725delA | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143920906 | ||||||
chr6:143920906 | CAA | C | 9 | a0001c0001t0001g0010 a0001c0001t0001g0034 a0001c0001t0001g0048 others(6): Show |
9 | HG02055.hp1 HG02300.hp1 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.599-16726_599-1672 others(6): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143920906 | ||||||
chr6:143921085 | C | G | 6 | a0001c0001t0001g0277 a0001c0001t0001g0294 a0001c0001t0001g0295 others(3): Show |
6 | HG02572.hp2 HG02615.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.599-16564C>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143921085 | |||||||
chr6:143921213 | T | A | 2 | a0001c0001t0001g0030 a0001c0001t0001g0031 |
2 | HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.599-16436T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143921213 | |||||||
chr6:143921392 | T | C | 1 | a0001c0001t0001g0136 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.599-16257T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143921392 | |||||||
chr6:143921541 | C | A | 1 | a0001c0001t0001g0316 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.599-16108C>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143921541 | |||||||
chr6:143921871 | A | C | 2 | a0001c0001t0001g0292 a0001c0001t0001g0293 |
2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.599-15778A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143921871 | |||||||
chr6:143922148 | G | A | 2 | a0001c0001t0001g0256 a0001c0001t0001g0310 |
2 | HG01099.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.599-15501G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143922148 | |||||||
chr6:143922176 | A | G | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0299 others(2): Show |
5 | HG01884.hp1 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.599-15473A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143922176 | |||||||
chr6:143922199 | A | G | 1 | a0001c0001t0001g0018 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.599-15450A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143922199 | |||||||
chr6:143922372 | G | A | 4 | a0001c0001t0001g0053 a0001c0001t0001g0304 a0001c0001t0001g0312 others(1): Show |
4 | HG02257.hp2 HG02615.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.599-15277G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143922372 | |||||||
chr6:143922442 | G | A | 6 | a0001c0001t0001g0138 a0001c0001t0001g0142 a0001c0001t0001g0219 others(3): Show |
6 | HG00673.hp1 HG02027.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.599-15207G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143922442 | |||||||
chr6:143923079 | G | A | 242 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(239): Show |
246 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(243): Show |
intron_variant | MODIFIER | c.599-14570G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143923079 | |||||||
chr6:143923154 | C | A | 8 | a0001c0001t0001g0182 a0001c0001t0001g0302 a0001c0001t0001g0303 others(5): Show |
8 | HG01192.hp1 HG02486.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.599-14495C>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143923154 | |||||||
chr6:143923736 | T | G | 12 | a0001c0001t0001g0052 a0001c0001t0001g0275 a0001c0001t0001g0279 others(9): Show |
12 | HG02451.hp1 HG02622.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.599-13913T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143923736 | |||||||
chr6:143923807 | G | A | 2 | a0001c0001t0001g0056 a0001c0001t0001g0057 |
2 | HG04115.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.599-13842G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143923807 | |||||||
chr6:143923968 | T | C | 8 | a0001c0001t0001g0277 a0001c0001t0001g0292 a0001c0001t0001g0293 others(5): Show |
8 | HG02572.hp2 HG02615.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.599-13681T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143923968 | |||||||
chr6:143924089 | C | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0048 a0001c0001t0001g0049 others(1): Show |
4 | HG02055.hp1 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.599-13560C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143924089 | |||||||
chr6:143924153 | G | A | 1 | a0001c0001t0001g0065 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.599-13496G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143924153 | |||||||
chr6:143924276 | A | G | 2 | a0001c0001t0001g0030 a0001c0001t0001g0031 |
2 | HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.599-13373A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143924276 | |||||||
chr6:143924296 | A | G | 3 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 |
3 | HG02886.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.599-13353A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143924296 | |||||||
chr6:143924349 | T | TTA | 6 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0051 others(3): Show |
6 | HG01884.hp1 HG02723.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.599-13286_599-1328 others(6): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143924349 | ||||||
chr6:143924474 | A | C | 20 | a0001c0001t0001g0010 a0001c0001t0001g0048 a0001c0001t0001g0049 others(17): Show |
20 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.599-13175A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143924474 | |||||||
chr6:143924679 | G | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0258 |
2 | NA18998.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.599-12970G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143924679 | |||||||
chr6:143924760 | GA | G | 7 | a0001c0001t0001g0138 a0001c0001t0001g0142 a0001c0001t0001g0196 others(4): Show |
7 | HG00673.hp1 HG02027.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.599-12886delA | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143924760 | ||||||
chr6:143924769 | A | G | 27 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0034 others(24): Show |
27 | HG02109.hp1 HG02109.hp2 HG02451.hp1 others(24): Show |
intron_variant | MODIFIER | c.599-12880A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143924769 | |||||||
chr6:143924977 | G | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0258 |
2 | NA18998.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.599-12672G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143924977 | |||||||
chr6:143925165 | C | CT | 49 | a0001c0001t0001g0010 a0001c0001t0001g0034 a0001c0001t0001g0061 others(46): Show |
49 | HG00423.hp1 HG00423.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.599-12456dupT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143925165 | ||||||
chr6:143925165 | C | CTT | 20 | a0001c0001t0001g0002 a0001c0001t0001g0086 a0001c0001t0001g0110 others(17): Show |
21 | HG00558.hp1 HG01258.hp1 HG02129.hp2 others(18): Show |
intron_variant | MODIFIER | c.599-12457_599-1245 others(6): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143925165 | ||||||
chr6:143925165 | C | CTTT | 7 | a0001c0001t0001g0017 a0001c0001t0001g0115 a0001c0001t0001g0136 others(4): Show |
7 | HG01978.hp1 HG02257.hp1 HG04199.hp1 others(4): Show |
intron_variant | MODIFIER | c.599-12458_599-1245 others(7): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143925165 | ||||||
chr6:143925165 | CT | C | 27 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0048 others(24): Show |
27 | HG00733.hp1 HG01109.hp2 HG01928.hp1 others(24): Show |
intron_variant | MODIFIER | c.599-12456delT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143925165 | ||||||
chr6:143925165 | CTT | C | 19 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(16): Show |
19 | HG00140.hp2 HG00639.hp2 HG01258.hp2 others(16): Show |
intron_variant | MODIFIER | c.599-12457_599-1245 others(6): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143925165 | ||||||
chr6:143925165 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0184 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.599-12468_599-1245 others(17): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143925165 | ||||||
chr6:143925165 | CTTTTTTT others(7): Show |
C | 72 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(69): Show |
73 | HG00408.hp1 HG00438.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.599-12469_599-1245 others(18): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143925165 | ||||||
chr6:143925171 | T | C | 12 | a0001c0001t0001g0052 a0001c0001t0001g0275 a0001c0001t0001g0279 others(9): Show |
12 | HG02451.hp1 HG02622.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.599-12478T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143925171 | |||||||
chr6:143925214 | C | T | 4 | a0001c0001t0001g0053 a0001c0001t0001g0304 a0001c0001t0001g0312 others(1): Show |
4 | HG02257.hp2 HG02615.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.599-12435C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143925214 | |||||||
chr6:143925224 | G | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0012 |
2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.599-12425G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143925224 | |||||||
chr6:143925237 | G | A | 1 | a0001c0001t0001g0316 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.599-12412G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143925237 | |||||||
chr6:143925265 | TC | T | 3 | a0001c0001t0001g0094 a0001c0001t0001g0099 a0001c0001t0001g0109 |
3 | HG02074.hp2 NA18948.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.599-12381delC | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143925265 | ||||||
chr6:143925289 | C | A | 1 | a0002c0002t0001g0025 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.599-12360C>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143925289 | |||||||
chr6:143925290 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.599-12359G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143925290 | |||||||
chr6:143925290 | G | C | 3 | a0001c0001t0001g0094 a0001c0001t0001g0099 a0001c0001t0001g0109 |
3 | HG02074.hp2 NA18948.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.599-12359G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143925290 | |||||||
chr6:143925300 | C | T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0299 others(2): Show |
5 | HG01884.hp1 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.599-12349C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143925300 | |||||||
chr6:143925301 | G | A | 4 | a0001c0001t0001g0094 a0001c0001t0001g0099 a0001c0001t0001g0109 others(1): Show |
4 | HG02074.hp2 HG03540.hp2 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.599-12348G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143925301 | |||||||
chr6:143925304 | C | T | 3 | a0001c0001t0001g0094 a0001c0001t0001g0099 a0001c0001t0001g0109 |
3 | HG02074.hp2 NA18948.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.599-12345C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143925304 | |||||||
chr6:143925313 | G | C | 3 | a0001c0001t0001g0094 a0001c0001t0001g0099 a0001c0001t0001g0109 |
3 | HG02074.hp2 NA18948.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.599-12336G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143925313 | |||||||
chr6:143925316 | T | C | 3 | a0001c0001t0001g0094 a0001c0001t0001g0099 a0001c0001t0001g0109 |
3 | HG02074.hp2 NA18948.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.599-12333T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143925316 | |||||||
chr6:143925321 | A | G | 3 | a0001c0001t0001g0094 a0001c0001t0001g0099 a0001c0001t0001g0109 |
3 | HG02074.hp2 NA18948.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.599-12328A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143925321 | |||||||
chr6:143925410 | C | T | 2 | a0001c0001t0001g0304 a0001c0001t0001g0312 |
2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.599-12239C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143925410 | |||||||
chr6:143925418 | G | A | 26 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0115 others(23): Show |
27 | HG00438.hp1 HG00558.hp1 HG01258.hp1 others(24): Show |
intron_variant | MODIFIER | c.599-12231G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143925418 | |||||||
chr6:143925527 | T | G | 1 | a0001c0001t0001g0060 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.599-12122T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143925527 | |||||||
chr6:143925536 | C | CTT | 11 | a0001c0001t0001g0052 a0001c0001t0001g0275 a0002c0002t0001g0019 others(8): Show |
11 | HG02451.hp1 HG02622.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.599-12097_599-1209 others(6): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143925536 | ||||||
chr6:143925536 | CT | C | 218 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(215): Show |
222 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(219): Show |
intron_variant | MODIFIER | c.599-12096delT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143925536 | ||||||
chr6:143925542 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.599-12107T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143925542 | |||||||
chr6:143925558 | C | T | 1 | a0001c0001t0001g0212 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.599-12091C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143925558 | |||||||
chr6:143925578 | C | G | 1 | a0001c0001t0001g0318 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.599-12071C>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143925578 | |||||||
chr6:143925591 | T | C | 1 | a0001c0001t0001g0240 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.599-12058T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143925591 | |||||||
chr6:143925605 | C | T | 73 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(70): Show |
74 | HG00408.hp1 HG00438.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.599-12044C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143925605 | |||||||
chr6:143926082 | A | T | 1 | a0001c0001t0001g0105 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.599-11567A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143926082 | |||||||
chr6:143926249 | C | T | 1 | a0001c0001t0001g0307 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.599-11400C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143926249 | |||||||
chr6:143926250 | G | A | 1 | a0001c0001t0001g0305 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.599-11399G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143926250 | |||||||
chr6:143926250 | G | T | 3 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0051 |
3 | HG03098.hp1 HG03195.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.599-11399G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143926250 | |||||||
chr6:143926283 | T | G | 76 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0018 others(73): Show |
78 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.599-11366T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143926283 | |||||||
chr6:143926366 | C | T | 7 | a0001c0001t0001g0001 a0001c0001t0001g0040 a0001c0001t0001g0043 others(4): Show |
8 | HG01106.hp1 HG01358.hp2 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.599-11283C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143926366 | |||||||
chr6:143926390 | T | C | 1 | a0001c0001t0001g0316 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.599-11259T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143926390 | |||||||
chr6:143926408 | T | C | 5 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0172 others(2): Show |
5 | HG01433.hp2 HG01934.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.599-11241T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143926408 | |||||||
chr6:143926413 | G | A | 12 | a0001c0001t0001g0052 a0001c0001t0001g0275 a0001c0001t0001g0279 others(9): Show |
12 | HG02451.hp1 HG02622.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.599-11236G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143926413 | |||||||
chr6:143926431 | CTGT | C | 73 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0018 others(70): Show |
75 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.599-11213_599-1121 others(7): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143926431 | ||||||
chr6:143926493 | A | AT | 124 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0015 others(121): Show |
126 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.599-11146dupT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143926493 | ||||||
chr6:143926533 | A | G | 1 | a0001c0001t0001g0132 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.599-11116A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143926533 | |||||||
chr6:143926577 | T | C | 3 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 |
3 | HG02886.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.599-11072T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143926577 | |||||||
chr6:143926624 | T | G | 1 | a0001c0001t0001g0316 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.599-11025T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143926624 | |||||||
chr6:143926627 | G | A | 1 | a0001c0001t0001g0296 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.599-11022G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143926627 | |||||||
chr6:143926695 | A | G | 7 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0137 others(4): Show |
7 | NA19003.hp2 NA19011.hp2 NA19056.hp1 others(4): Show |
intron_variant | MODIFIER | c.599-10954A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143926695 | |||||||
chr6:143926774 | ATATATAA others(1): Show |
A | 7 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0137 others(4): Show |
7 | NA19003.hp2 NA19011.hp2 NA19056.hp1 others(4): Show |
intron_variant | MODIFIER | c.599-10873_599-1086 others(12): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143926774 | ||||||
chr6:143926779 | T | G | 4 | a0001c0001t0001g0316 a0003c0003t0001g0037 a0003c0003t0001g0038 others(1): Show |
4 | HG02109.hp1 HG02818.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.599-10870T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143926779 | |||||||
chr6:143926828 | C | CT | 33 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0015 others(30): Show |
34 | HG00408.hp1 HG01123.hp1 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.599-10795dupT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143926828 | ||||||
chr6:143926828 | CT | C | 27 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0048 others(24): Show |
27 | HG01192.hp1 HG01952.hp2 HG02486.hp2 others(24): Show |
intron_variant | MODIFIER | c.599-10795delT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143926828 | ||||||
chr6:143926828 | CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 |
3 | HG02886.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.599-10806_599-1079 others(16): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143926828 | ||||||
chr6:143926860 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.599-10789G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143926860 | |||||||
chr6:143926885 | G | A | 1 | a0002c0002t0001g0022 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.599-10764G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143926885 | |||||||
chr6:143926898 | C | T | 2 | a0001c0001t0001g0030 a0001c0001t0001g0031 |
2 | HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.599-10751C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143926898 | |||||||
chr6:143926920 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0258 |
2 | NA18998.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.599-10729C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143926920 | |||||||
chr6:143926936 | G | A | 1 | a0001c0001t0001g0035 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.599-10713G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143926936 | |||||||
chr6:143926953 | G | GGCGCCCG others(5): Show |
144 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(141): Show |
146 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.599-10689_599-1068 others(16): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143926953 | ||||||
chr6:143926955 | C | CGCCCGCC others(5): Show |
1 | a0001c0001t0001g0231 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.599-10689_599-1068 others(16): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143926955 | ||||||
chr6:143927007 | C | A | 145 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(142): Show |
147 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.599-10642C>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143927007 | |||||||
chr6:143927078 | G | A | 3 | a0003c0003t0001g0037 a0003c0003t0001g0038 a0003c0003t0001g0039 |
3 | HG02109.hp1 HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.599-10571G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143927078 | |||||||
chr6:143927094 | G | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0012 |
2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.599-10555G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143927094 | |||||||
chr6:143927111 | C | T | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG00738.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.599-10538C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143927111 | |||||||
chr6:143927117 | G | A | 12 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0034 others(9): Show |
12 | HG01884.hp1 HG02257.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.599-10532G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143927117 | |||||||
chr6:143927216 | T | C | 3 | a0001c0001t0001g0187 a0001c0001t0001g0264 a0001c0001t0001g0314 |
3 | HG00642.hp1 HG01071.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.599-10433T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143927216 | |||||||
chr6:143927332 | C | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0250 |
3 | NA18983.hp2 NA19084.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.599-10317C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143927332 | |||||||
chr6:143927472 | G | T | 2 | a0001c0001t0001g0141 a0001c0001t0001g0143 |
2 | NA18942.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.599-10177G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143927472 | |||||||
chr6:143927512 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.599-10137A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143927512 | |||||||
chr6:143927565 | T | G | 7 | a0001c0001t0001g0138 a0001c0001t0001g0142 a0001c0001t0001g0196 others(4): Show |
7 | HG00673.hp1 HG02027.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.599-10084T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143927565 | |||||||
chr6:143927835 | A | G | 4 | a0001c0001t0001g0127 a0001c0001t0001g0133 a0001c0001t0001g0136 others(1): Show |
4 | HG00558.hp1 HG02129.hp2 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.599-9814A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143927835 | |||||||
chr6:143928084 | TTGTC | T | 3 | a0001c0001t0001g0180 a0001c0001t0001g0188 a0001c0001t0001g0189 |
3 | NA18963.hp1 NA18984.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.599-9559_599-9556d others(6): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143928084 | ||||||
chr6:143928252 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.599-9397C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143928252 | |||||||
chr6:143928345 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.599-9304C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143928345 | |||||||
chr6:143928347 | A | G | 25 | a0001c0001t0001g0010 a0001c0001t0001g0048 a0001c0001t0001g0049 others(22): Show |
25 | HG00140.hp2 HG00639.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.599-9302A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143928347 | |||||||
chr6:143928405 | G | A | 137 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(134): Show |
139 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.599-9244G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143928405 | |||||||
chr6:143928460 | T | C | 2 | a0001c0001t0001g0011 a0001c0001t0001g0012 |
2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.599-9189T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143928460 | |||||||
chr6:143928548 | G | C | 1 | a0001c0001t0001g0311 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.599-9101G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143928548 | |||||||
chr6:143928565 | G | A | 5 | a0001c0001t0001g0064 a0001c0001t0001g0069 a0001c0001t0001g0085 others(2): Show |
5 | NA18959.hp1 NA18979.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.599-9084G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143928565 | |||||||
chr6:143928595 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.599-9054G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143928595 | |||||||
chr6:143928795 | A | G | 1 | a0001c0001t0001g0237 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.599-8854A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143928795 | |||||||
chr6:143928824 | G | GT | 22 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0030 others(19): Show |
22 | HG01884.hp1 HG02109.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.599-8814dupT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143928824 | ||||||
chr6:143928824 | G | GTT | 224 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(221): Show |
228 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(225): Show |
intron_variant | MODIFIER | c.599-8815_599-8814d others(4): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143928824 | ||||||
chr6:143928824 | G | GTTT | 7 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0053 others(4): Show |
7 | HG01884.hp2 HG02258.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.599-8816_599-8814d others(5): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143928824 | ||||||
chr6:143929069 | G | A | 1 | a0002c0002t0001g0025 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.599-8580G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143929069 | |||||||
chr6:143929078 | T | G | 3 | a0001c0001t0001g0009 a0001c0001t0001g0319 a0001c0001t0001g0320 |
4 | HG00408.hp2 NA18971.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.599-8571T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143929078 | |||||||
chr6:143929200 | C | T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0299 others(2): Show |
5 | HG01884.hp1 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.599-8449C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143929200 | |||||||
chr6:143929231 | A | G | 2 | a0001c0001t0001g0304 a0001c0001t0001g0312 |
2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.599-8418A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143929231 | |||||||
chr6:143929283 | C | T | 1 | a0001c0001t0001g0010 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.599-8366C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143929283 | |||||||
chr6:143929330 | T | C | 2 | a0001c0001t0001g0141 a0001c0001t0001g0143 |
2 | NA18942.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.599-8319T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143929330 | |||||||
chr6:143929374 | G | C | 1 | a0001c0001t0001g0315 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.599-8275G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143929374 | |||||||
chr6:143929375 | A | T | 1 | a0001c0001t0001g0315 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.599-8274A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143929375 | |||||||
chr6:143929465 | G | A | 2 | a0001c0001t0001g0292 a0001c0001t0001g0293 |
2 | HG03516.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.599-8184G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143929465 | |||||||
chr6:143929498 | A | T | 23 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0034 others(20): Show |
23 | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.599-8151A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143929498 | |||||||
chr6:143929509 | A | G | 1 | a0001c0001t0001g0298 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.599-8140A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143929509 | |||||||
chr6:143929516 | T | G | 1 | a0001c0001t0001g0170 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.599-8133T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143929516 | |||||||
chr6:143929571 | T | C | 1 | a0001c0001t0001g0091 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.599-8078T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143929571 | |||||||
chr6:143929604 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.599-8045G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143929604 | |||||||
chr6:143929682 | G | A | 7 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0137 others(4): Show |
7 | NA19003.hp2 NA19011.hp2 NA19056.hp1 others(4): Show |
intron_variant | MODIFIER | c.599-7967G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143929682 | |||||||
chr6:143929683 | A | C | 1 | a0001c0001t0001g0239 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.599-7966A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143929683 | |||||||
chr6:143929705 | TTTGTTG | T | 7 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 others(4): Show |
7 | HG01081.hp2 HG02258.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.599-7929_599-7924d others(8): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143929705 | ||||||
chr6:143929892 | T | C | 229 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(226): Show |
233 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(230): Show |
intron_variant | MODIFIER | c.599-7757T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143929892 | |||||||
chr6:143929995 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.599-7654G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143929995 | |||||||
chr6:143930224 | C | A | 158 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(155): Show |
160 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.599-7425C>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143930224 | |||||||
chr6:143930237 | T | C | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG00738.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.599-7412T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143930237 | |||||||
chr6:143930367 | A | G | 2 | a0001c0001t0001g0034 a0001c0001t0001g0258 |
2 | NA18998.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.599-7282A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143930367 | |||||||
chr6:143930381 | CT | C | 164 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(161): Show |
167 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.599-7248delT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143930381 | ||||||
chr6:143930381 | CTT | C | 78 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(75): Show |
79 | HG00408.hp1 HG00438.hp1 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.599-7249_599-7248d others(4): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143930381 | ||||||
chr6:143930385 | T | C | 1 | a0001c0001t0001g0223 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.599-7264T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143930385 | |||||||
chr6:143930386 | T | C | 20 | a0001c0001t0001g0010 a0001c0001t0001g0048 a0001c0001t0001g0049 others(17): Show |
20 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.599-7263T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143930386 | |||||||
chr6:143930426 | G | A | 9 | a0001c0001t0001g0277 a0001c0001t0001g0292 a0001c0001t0001g0293 others(6): Show |
9 | HG02572.hp2 HG02615.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.599-7223G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143930426 | |||||||
chr6:143930449 | C | T | 1 | a0001c0001t0001g0281 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.599-7200C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143930449 | |||||||
chr6:143930450 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.599-7199G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143930450 | |||||||
chr6:143930473 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.599-7176G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143930473 | |||||||
chr6:143930545 | G | A | 137 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(134): Show |
139 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.599-7104G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143930545 | |||||||
chr6:143930549 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.599-7100G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143930549 | |||||||
chr6:143930591 | G | A | 251 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(248): Show |
255 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(252): Show |
intron_variant | MODIFIER | c.599-7058G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143930591 | |||||||
chr6:143930651 | A | T | 1 | a0001c0001t0001g0047 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.599-6998A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143930651 | |||||||
chr6:143930882 | A | G | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0299 others(2): Show |
5 | HG01884.hp1 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.599-6767A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143930882 | |||||||
chr6:143931221 | A | G | 2 | a0001c0001t0001g0211 a0001c0001t0001g0213 |
2 | HG00408.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.599-6428A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143931221 | |||||||
chr6:143931239 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.599-6410C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143931239 | |||||||
chr6:143931255 | A | G | 1 | a0001c0001t0001g0032 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.599-6394A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143931255 | |||||||
chr6:143931280 | T | G | 2 | a0001c0001t0001g0011 a0001c0001t0001g0012 |
2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.599-6369T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143931280 | |||||||
chr6:143931365 | C | T | 2 | a0001c0001t0001g0030 a0001c0001t0001g0031 |
2 | HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.599-6284C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143931365 | |||||||
chr6:143931404 | A | C | 1 | a0001c0001t0001g0316 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.599-6245A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143931404 | |||||||
chr6:143931462 | G | T | 1 | a0001c0001t0001g0229 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.599-6187G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143931462 | |||||||
chr6:143931506 | T | C | 12 | a0001c0001t0001g0052 a0001c0001t0001g0275 a0001c0001t0001g0279 others(9): Show |
12 | HG02451.hp1 HG02622.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.599-6143T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143931506 | |||||||
chr6:143931603 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0258 |
2 | NA18998.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.599-6046C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143931603 | |||||||
chr6:143931709 | T | A | 226 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(223): Show |
230 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(227): Show |
intron_variant | MODIFIER | c.599-5940T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143931709 | |||||||
chr6:143931756 | A | G | 1 | a0001c0001t0001g0236 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.599-5893A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143931756 | |||||||
chr6:143931811 | A | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0048 a0001c0001t0001g0049 others(1): Show |
4 | HG02055.hp1 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.599-5838A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143931811 | |||||||
chr6:143931844 | T | C | 140 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(137): Show |
142 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.599-5805T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143931844 | |||||||
chr6:143931848 | ACTT | A | 5 | a0001c0001t0001g0085 a0001c0001t0001g0094 a0001c0001t0001g0106 others(2): Show |
5 | HG03017.hp2 HG03579.hp1 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.599-5785_599-5783d others(5): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143931848 | ||||||
chr6:143931862 | TTC | T | 208 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(205): Show |
212 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.599-5785_599-5784d others(4): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143931862 | ||||||
chr6:143931863 | TC | T | 25 | a0001c0001t0001g0052 a0001c0001t0001g0067 a0001c0001t0001g0134 others(22): Show |
25 | HG02109.hp1 HG02451.hp1 HG02602.hp2 others(22): Show |
intron_variant | MODIFIER | c.599-5785delC | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143931863 | |||||||
chr6:143931864 | CTT | C | 11 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0132 others(8): Show |
11 | HG01192.hp1 HG02258.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.599-5768_599-5767d others(4): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143931864 | ||||||
chr6:143931884 | A | G | 2 | a0001c0001t0001g0304 a0001c0001t0001g0312 |
2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.599-5765A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143931884 | |||||||
chr6:143931903 | G | A | 1 | a0002c0002t0001g0026 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.599-5746G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143931903 | |||||||
chr6:143931943 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0258 |
2 | NA18998.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.599-5706C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143931943 | |||||||
chr6:143931958 | A | G | 140 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(137): Show |
142 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.599-5691A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143931958 | |||||||
chr6:143931967 | C | T | 1 | a0001c0001t0001g0161 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.599-5682C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143931967 | |||||||
chr6:143932094 | C | T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0299 others(2): Show |
5 | HG01884.hp1 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.599-5555C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143932094 | |||||||
chr6:143932095 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.599-5554G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143932095 | |||||||
chr6:143932211 | T | C | 140 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(137): Show |
142 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.599-5438T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143932211 | |||||||
chr6:143932250 | T | G | 1 | a0001c0001t0001g0218 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.599-5399T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143932250 | |||||||
chr6:143932447 | G | T | 140 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(137): Show |
142 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.599-5202G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143932447 | |||||||
chr6:143932636 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0012 |
2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.599-5013C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143932636 | |||||||
chr6:143932823 | T | G | 75 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0018 others(72): Show |
77 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.599-4826T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143932823 | |||||||
chr6:143932824 | G | C | 2 | a0001c0001t0001g0034 a0001c0001t0001g0258 |
2 | NA18998.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.599-4825G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143932824 | |||||||
chr6:143932844 | C | T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0299 others(2): Show |
5 | HG01884.hp1 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.599-4805C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143932844 | |||||||
chr6:143932884 | G | A | 8 | a0001c0001t0001g0182 a0001c0001t0001g0302 a0001c0001t0001g0303 others(5): Show |
8 | HG01192.hp1 HG02486.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.599-4765G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143932884 | |||||||
chr6:143932976 | G | A | 2 | a0001c0001t0001g0030 a0001c0001t0001g0031 |
2 | HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.599-4673G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143932976 | |||||||
chr6:143933143 | A | G | 1 | a0001c0001t0001g0235 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.599-4506A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143933143 | |||||||
chr6:143933156 | C | T | 139 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(136): Show |
141 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.599-4493C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143933156 | |||||||
chr6:143933459 | T | C | 2 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
2 | HG01081.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.599-4190T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143933459 | |||||||
chr6:143933607 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.599-4042C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143933607 | |||||||
chr6:143933608 | G | A | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0299 others(2): Show |
5 | HG01884.hp1 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.599-4041G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143933608 | |||||||
chr6:143933674 | G | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0012 |
2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.599-3975G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143933674 | |||||||
chr6:143933808 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.599-3841C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143933808 | |||||||
chr6:143933858 | C | T | 85 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0011 others(82): Show |
87 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.599-3791C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143933858 | |||||||
chr6:143933910 | T | A | 112 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0015 others(109): Show |
114 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.599-3739T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143933910 | |||||||
chr6:143933965 | G | A | 2 | a0001c0001t0001g0030 a0001c0001t0001g0031 |
2 | HG02109.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.599-3684G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143933965 | |||||||
chr6:143933980 | A | G | 1 | a0001c0001t0001g0316 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.599-3669A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143933980 | |||||||
chr6:143934074 | C | A | 7 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0137 others(4): Show |
7 | NA19003.hp2 NA19011.hp2 NA19056.hp1 others(4): Show |
intron_variant | MODIFIER | c.599-3575C>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143934074 | |||||||
chr6:143934115 | G | A | 226 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(223): Show |
230 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(227): Show |
intron_variant | MODIFIER | c.599-3534G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143934115 | |||||||
chr6:143934255 | G | C | 2 | a0001c0001t0001g0300 a0001c0001t0001g0301 |
2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.599-3394G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143934255 | |||||||
chr6:143934329 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.599-3320G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143934329 | |||||||
chr6:143934358 | T | A | 226 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(223): Show |
230 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(227): Show |
intron_variant | MODIFIER | c.599-3291T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143934358 | |||||||
chr6:143934375 | T | A | 1 | a0001c0001t0001g0204 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.599-3274T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143934375 | |||||||
chr6:143934597 | A | G | 4 | a0001c0001t0001g0097 a0001c0001t0001g0111 a0001c0001t0001g0112 others(1): Show |
4 | HG00733.hp1 HG02602.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.599-3052A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143934597 | |||||||
chr6:143934683 | C | T | 1 | a0001c0001t0001g0010 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.599-2966C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143934683 | |||||||
chr6:143934756 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.599-2893G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143934756 | |||||||
chr6:143935088 | C | T | 230 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(227): Show |
234 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(231): Show |
intron_variant | MODIFIER | c.599-2561C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143935088 | |||||||
chr6:143935122 | C | T | 22 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0115 others(19): Show |
23 | HG00558.hp1 HG01258.hp1 HG01978.hp1 others(20): Show |
intron_variant | MODIFIER | c.599-2527C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143935122 | |||||||
chr6:143935140 | T | TGGTGGGC others(2): Show |
230 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(227): Show |
234 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(231): Show |
intron_variant | MODIFIER | c.599-2503_599-2502i others(11): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143935140 | ||||||
chr6:143935255 | T | G | 2 | a0001c0001t0001g0034 a0001c0001t0001g0258 |
2 | NA18998.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.599-2394T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143935255 | |||||||
chr6:143935326 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.599-2323A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143935326 | |||||||
chr6:143935400 | C | T | 79 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0018 others(76): Show |
81 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.599-2249C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143935400 | |||||||
chr6:143935431 | G | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0258 |
2 | NA18998.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.599-2218G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143935431 | |||||||
chr6:143935446 | C | T | 7 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0137 others(4): Show |
7 | NA19003.hp2 NA19011.hp2 NA19056.hp1 others(4): Show |
intron_variant | MODIFIER | c.599-2203C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143935446 | |||||||
chr6:143935581 | T | G | 1 | a0001c0001t0001g0318 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.599-2068T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143935581 | |||||||
chr6:143935616 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.599-2033A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143935616 | |||||||
chr6:143935619 | C | A | 20 | a0001c0001t0001g0052 a0001c0001t0001g0134 a0001c0001t0001g0135 others(17): Show |
20 | HG02451.hp1 HG02622.hp1 HG02647.hp2 others(17): Show |
intron_variant | MODIFIER | c.599-2030C>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143935619 | |||||||
chr6:143935625 | T | A | 7 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0137 others(4): Show |
7 | NA19003.hp2 NA19011.hp2 NA19056.hp1 others(4): Show |
intron_variant | MODIFIER | c.599-2024T>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143935625 | |||||||
chr6:143935628 | A | G | 8 | a0001c0001t0001g0055 a0001c0001t0001g0080 a0001c0001t0001g0089 others(5): Show |
8 | HG01943.hp1 HG01952.hp1 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.599-2021A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143935628 | |||||||
chr6:143935646 | C | CT | 29 | a0001c0001t0001g0034 a0001c0001t0001g0041 a0001c0001t0001g0045 others(26): Show |
29 | HG00140.hp2 HG00609.hp2 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.599-1975dupT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143935646 | ||||||
chr6:143935646 | C | CTT | 11 | a0001c0001t0001g0060 a0001c0001t0001g0116 a0001c0001t0001g0118 others(8): Show |
11 | HG01099.hp1 HG02040.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.599-1976_599-1975d others(4): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143935646 | ||||||
chr6:143935646 | C | CTTT | 60 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(57): Show |
61 | HG00408.hp1 HG00438.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.599-1977_599-1975d others(5): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143935646 | ||||||
chr6:143935646 | C | CTTTT | 11 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0066 others(8): Show |
11 | HG01109.hp1 HG01433.hp2 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.599-1978_599-1975d others(6): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143935646 | ||||||
chr6:143935646 | C | CTTTTT | 18 | a0001c0001t0001g0002 a0001c0001t0001g0032 a0001c0001t0001g0033 others(15): Show |
19 | HG01081.hp2 HG01258.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.599-1979_599-1975d others(7): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143935646 | ||||||
chr6:143935646 | C | CTTTTTT | 10 | a0001c0001t0001g0115 a0001c0001t0001g0124 a0001c0001t0001g0125 others(7): Show |
10 | HG01978.hp1 HG02129.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.599-1980_599-1975d others(8): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143935646 | ||||||
chr6:143935646 | C | CTTTTTTT | 6 | a0001c0001t0001g0017 a0001c0001t0001g0133 a0001c0001t0001g0136 others(3): Show |
6 | NA18940.hp1 NA18963.hp1 NA19012.hp2 others(3): Show |
intron_variant | MODIFIER | c.599-1981_599-1975d others(9): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143935646 | ||||||
chr6:143935646 | CT | C | 8 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0040 others(5): Show |
8 | HG00558.hp2 HG02109.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.599-1975delT | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143935646 | ||||||
chr6:143935646 | CTT | C | 7 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0050 others(4): Show |
7 | HG02109.hp1 HG02258.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.599-1976_599-1975d others(4): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143935646 | ||||||
chr6:143935646 | CTTT | C | 6 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0144 others(3): Show |
6 | NA19011.hp2 NA19056.hp1 NA19062.hp2 others(3): Show |
intron_variant | MODIFIER | c.599-1977_599-1975d others(5): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143935646 | ||||||
chr6:143935646 | CTTTTT | C | 11 | a0001c0001t0001g0052 a0001c0001t0001g0275 a0001c0001t0001g0279 others(8): Show |
11 | HG02451.hp1 HG02622.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.599-1979_599-1975d others(7): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143935646 | ||||||
chr6:143935646 | CTTTTTTT others(4): Show |
C | 4 | a0001c0001t0001g0010 a0001c0001t0001g0048 a0001c0001t0001g0049 others(1): Show |
4 | HG02055.hp1 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.599-1985_599-1975d others(13): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143935646 | ||||||
chr6:143935646 | CTTTTTTT others(7): Show |
C | 13 | a0001c0001t0001g0061 a0001c0001t0001g0065 a0001c0001t0001g0070 others(10): Show |
13 | HG02080.hp2 HG02135.hp2 NA18747.hp2 others(10): Show |
intron_variant | MODIFIER | c.599-1988_599-1975d others(16): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143935646 | ||||||
chr6:143935674 | T | G | 20 | a0001c0001t0001g0050 a0001c0001t0001g0053 a0001c0001t0001g0061 others(17): Show |
20 | HG02080.hp2 HG02135.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.599-1975T>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143935674 | |||||||
chr6:143935674 | T | TTG | 42 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0013 others(39): Show |
44 | HG00408.hp2 HG00438.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.599-1975_599-1974i others(4): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143935674 | |||||||
chr6:143935674 | T | TTTG | 20 | a0001c0001t0001g0055 a0001c0001t0001g0058 a0001c0001t0001g0062 others(17): Show |
20 | HG01358.hp1 HG01943.hp1 HG01952.hp1 others(17): Show |
intron_variant | MODIFIER | c.599-1975_599-1974i others(5): Show |
ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143935674 | |||||||
chr6:143935687 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0012 |
2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.599-1962C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143935687 | |||||||
chr6:143935728 | C | G | 2 | a0001c0001t0001g0034 a0001c0001t0001g0258 |
2 | NA18998.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.599-1921C>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143935728 | |||||||
chr6:143935777 | C | A | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG00738.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.599-1872C>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143935777 | |||||||
chr6:143935884 | A | C | 2 | a0001c0001t0001g0011 a0001c0001t0001g0012 |
2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.599-1765A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143935884 | |||||||
chr6:143935960 | G | A | 230 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(227): Show |
234 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(231): Show |
intron_variant | MODIFIER | c.599-1689G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143935960 | |||||||
chr6:143935992 | A | T | 230 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(227): Show |
234 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(231): Show |
intron_variant | MODIFIER | c.599-1657A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143935992 | |||||||
chr6:143936105 | A | G | 2 | a0001c0001t0001g0091 a0001c0001t0001g0092 |
2 | NA18950.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.599-1544A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143936105 | |||||||
chr6:143936133 | C | T | 232 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(229): Show |
236 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(233): Show |
intron_variant | MODIFIER | c.599-1516C>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143936133 | |||||||
chr6:143936202 | A | G | 1 | a0001c0001t0001g0159 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.599-1447A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143936202 | |||||||
chr6:143936227 | T | C | 1 | a0001c0001t0001g0174 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.599-1422T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143936227 | |||||||
chr6:143936307 | G | A | 113 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0015 others(110): Show |
115 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.599-1342G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143936307 | |||||||
chr6:143936315 | A | G | 1 | a0001c0001t0001g0240 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.599-1334A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143936315 | |||||||
chr6:143936415 | A | T | 1 | a0001c0001t0001g0237 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.599-1234A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143936415 | |||||||
chr6:143936502 | A | C | 22 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0115 others(19): Show |
23 | HG00558.hp1 HG01258.hp1 HG01978.hp1 others(20): Show |
intron_variant | MODIFIER | c.599-1147A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143936502 | |||||||
chr6:143937107 | T | C | 141 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(138): Show |
143 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.599-542T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143937107 | |||||||
chr6:143937216 | T | C | 1 | a0001c0001t0001g0316 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.599-433T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143937216 | |||||||
chr6:143937222 | T | C | 254 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(251): Show |
258 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(255): Show |
intron_variant | MODIFIER | c.599-427T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143937222 | |||||||
chr6:143937249 | G | A | 12 | a0001c0001t0001g0052 a0001c0001t0001g0275 a0001c0001t0001g0279 others(9): Show |
12 | HG02451.hp1 HG02622.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.599-400G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143937249 | |||||||
chr6:143937314 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.599-335G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143937314 | |||||||
chr6:143937445 | G | C | 136 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(133): Show |
138 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.599-204G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143937445 | |||||||
chr6:143937482 | G | A | 232 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(229): Show |
236 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(233): Show |
intron_variant | MODIFIER | c.599-167G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143937482 | |||||||
chr6:143937513 | C | A | 254 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(251): Show |
258 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(255): Show |
intron_variant | MODIFIER | c.599-136C>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143937513 | |||||||
chr6:143937533 | C | CA | 253 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(250): Show |
257 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(254): Show |
intron_variant | MODIFIER | c.599-108dupA | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 143937533 | ||||||
chr6:143937585 | A | T | 1 | a0001c0001t0001g0050 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.599-64A>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143937585 | |||||||
chr6:143937639 | G | A | 1 | a0001c0001t0001g0205 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.599-10G>A | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 6/7 | chr6 | 143937639 | |||||||
chr6:143937744 | A | G | 7 | a0001c0001t0001g0063 a0001c0001t0001g0081 a0001c0001t0001g0101 others(4): Show |
7 | HG00738.hp2 HG01123.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.*14+11A>G | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 7/7 | chr6 | 143937744 | |||||||
chr6:143937753 | G | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0258 |
2 | NA18998.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.*14+20G>T | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 7/7 | chr6 | 143937753 | |||||||
chr6:143937761 | A | C | 1 | a0001c0001t0001g0214 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.*14+28A>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 7/7 | chr6 | 143937761 | |||||||
chr6:143937793 | G | C | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG01081.hp2 HG02258.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.*14+60G>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 7/7 | chr6 | 143937793 | |||||||
chr6:143937882 | T | C | 1 | a0001c0001t0001g0132 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.*14+149T>C | ZC2HC1B | ENSG00000118491.10 | transcript | ENST00000237275.9 | protein_coding | 7/7 | chr6 | 143937882 |