geneid | 84668 |
---|---|
ensemblid | ENSG00000122591.13 |
hgncid | 24587 |
symbol | HYCC1 |
name | hyccin PI4KA lipid kinase complex subunit 1 |
refseq_nuc | NM_032581.4 |
refseq_prot | NP_115970.2 |
ensembl_nuc | ENST00000432176.7 |
ensembl_prot | ENSP00000403396.2 |
mane_status | MANE Select |
chr | chr7 |
start | 22934211 |
end | 23014130 |
strand | - |
ver | v1.2 |
region | chr7:22934211-23014130 |
region5000 | chr7:22929211-23019130 |
regionname0 | HYCC1_chr7_22934211_23014130 |
regionname5000 | HYCC1_chr7_22929211_23019130 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 521 | 376 | 77 | 69 | 173 | 13 | 42 | 143 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0002 | 0/0 | 521 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0003 | 0/0 | 521 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0004 | 0/0 | 521 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0005 | 0/0 | 521 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0006 | 0/0 | 521 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0007 | 0/0 | 521 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0008 | 0/0 | 521 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1566 | 230 | 45 | 49 | 94 | 10 | 30 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
c0002 | 0/0 | 1566 | 144 | 32 | 20 | 77 | 3 | 12 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
c0003 | 0/0 | 1566 | 2 | 2 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
c0004 | 0/0 | 1566 | 2 | 2 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
c0005 | 0/0 | 1566 | 2 | 0 | 0 | 2 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
c0006 | 0/0 | 1566 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
c0007 | 0/0 | 1566 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
c0008 | 0/0 | 1566 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
c0009 | 0/0 | 1566 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
c0010 | 0/0 | 1566 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
c0011 | 0/0 | 1566 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 11599 | 31 | 1 | 3 | 24 | 1 | 2 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0002 | 0/0 | 11613 | 28 | 8 | 8 | 4 | 5 | 3 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0003 | 0/0 | 11614 | 26 | 2 | 6 | 16 | 0 | 2 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0004 | 0/0 | 11599 | 24 | 0 | 3 | 21 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0005 | 0/0 | 11599 | 24 | 0 | 2 | 17 | 1 | 4 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0006 | 0/0 | 11615 | 19 | 1 | 2 | 14 | 1 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0007 | 0/0 | 11601 | 18 | 0 | 3 | 15 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0008 | 0/0 | 11599 | 14 | 0 | 9 | 0 | 2 | 3 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0009 | 0/0 | 11616 | 13 | 1 | 0 | 11 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0010 | 0/1 | 11599 | 10 | 3 | 4 | 0 | 0 | 2 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0011 | 0/0 | 11605 | 10 | 5 | 4 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0012 | 0/0 | 11601 | 9 | 9 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0013 | 0/0 | 11604 | 9 | 3 | 1 | 4 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0014 | 0/0 | 11605 | 7 | 0 | 0 | 0 | 0 | 7 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0015 | 0/0 | 11610 | 6 | 0 | 4 | 0 | 1 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0016 | 0/0 | 11617 | 6 | 2 | 2 | 2 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0017 | 0/0 | 11602 | 4 | 0 | 0 | 4 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0018 | 0/0 | 11587 | 4 | 0 | 0 | 4 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0019 | 0/0 | 11605 | 3 | 2 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0020 | 0/0 | 11612 | 3 | 2 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0021 | 0/0 | 11602 | 3 | 3 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0022 | 0/0 | 11606 | 3 | 1 | 1 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0023 | 0/0 | 11587 | 3 | 0 | 0 | 3 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0024 | 0/0 | 11593 | 2 | 1 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0025 | 0/0 | 11617 | 2 | 0 | 0 | 2 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0026 | 0/0 | 11600 | 2 | 0 | 0 | 0 | 0 | 2 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0027 | 0/0 | 11615 | 2 | 0 | 2 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0028 | 0/0 | 11604 | 2 | 0 | 0 | 2 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0029 | 0/0 | 11613 | 2 | 2 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0030 | 0/0 | 11600 | 2 | 2 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0031 | 0/0 | 11614 | 2 | 0 | 0 | 2 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0032 | 0/0 | 11608 | 2 | 1 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0033 | 0/0 | 11606 | 2 | 2 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0034 | 0/0 | 11610 | 2 | 2 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0035 | 0/0 | 11604 | 2 | 0 | 1 | 0 | 1 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0036 | 0/0 | 11606 | 2 | 2 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0037 | 0/0 | 11600 | 2 | 0 | 0 | 1 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0038 | 0/0 | 11600 | 2 | 0 | 0 | 2 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0039 | 0/0 | 11599 | 2 | 0 | 1 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0040 | 0/0 | 11600 | 2 | 0 | 1 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0041 | 0/0 | 11604 | 2 | 0 | 0 | 2 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0042 | 0/0 | 11593 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0043 | 0/0 | 11592 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0044 | 0/0 | 11613 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0045 | 0/0 | 11607 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0046 | 0/0 | 11618 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0047 | 0/0 | 11619 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0048 | 0/0 | 11618 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0049 | 0/0 | 11603 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0050 | 0/0 | 11598 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0051 | 0/0 | 11599 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0052 | 0/0 | 11602 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0053 | 0/0 | 11608 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0054 | 0/0 | 11609 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0055 | 0/0 | 11609 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0056 | 0/0 | 11615 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0057 | 0/0 | 11614 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0058 | 0/0 | 11615 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0059 | 0/0 | 11606 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0060 | 0/0 | 11609 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0061 | 0/0 | 11615 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0062 | 0/0 | 11613 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0063 | 1/0 | 11613 | 1 | 0 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0064 | 0/0 | 11597 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0065 | 0/0 | 11606 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0066 | 0/0 | 11613 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0067 | 0/0 | 11605 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0068 | 0/0 | 11605 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0069 | 0/0 | 11606 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0070 | 0/0 | 11605 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0071 | 0/0 | 11603 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0072 | 0/0 | 11615 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0073 | 0/0 | 11598 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0074 | 0/0 | 11605 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0075 | 0/0 | 11613 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0076 | 0/0 | 11614 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0077 | 0/0 | 11613 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0078 | 0/0 | 11609 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0079 | 0/0 | 11613 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0080 | 0/0 | 11608 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0081 | 0/0 | 11608 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0082 | 0/0 | 11598 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0083 | 0/0 | 11605 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0084 | 0/0 | 11604 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0085 | 0/0 | 11601 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0086 | 0/0 | 11602 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0087 | 0/0 | 11605 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0088 | 0/0 | 11602 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0089 | 0/0 | 11605 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0090 | 0/0 | 11601 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0091 | 0/0 | 11607 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0092 | 0/0 | 11608 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0093 | 0/0 | 11609 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0094 | 0/0 | 11604 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0095 | 0/0 | 11607 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0096 | 0/0 | 11604 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0097 | 0/0 | 11608 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0098 | 0/0 | 11601 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0099 | 0/0 | 11606 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0100 | 0/0 | 11601 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0101 | 0/0 | 11602 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0102 | 0/0 | 11604 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0103 | 0/0 | 11599 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0104 | 0/0 | 11602 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0105 | 0/0 | 11599 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0106 | 0/0 | 11598 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0107 | 0/0 | 11600 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0108 | 0/0 | 11600 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0109 | 0/0 | 11599 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0110 | 0/0 | 11600 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0111 | 0/0 | 11599 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0112 | 0/0 | 11605 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0113 | 0/0 | 11599 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
t0114 | 0/0 | 11614 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0002 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0003 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0004 | 0/0 | 4 | 1 | 1 | 2 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0005 | 0/1 | 3 | 1 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0007 | 0/0 | 3 | 1 | 0 | 0 | 1 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0017 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0023 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0033 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1566 | 230 | 45 | 49 | 94 | 10 | 30 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0002 | 0/0 | 1566 | 144 | 32 | 20 | 77 | 3 | 12 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0006 | 0/0 | 1566 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0011 | 0/0 | 1566 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0002c0004 | 0/0 | 1566 | 2 | 2 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0003c0003 | 0/0 | 1566 | 2 | 2 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0004c0005 | 0/0 | 1566 | 2 | 0 | 0 | 2 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0005c0008 | 0/0 | 1566 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0006c0010 | 0/0 | 1566 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0007c0009 | 0/0 | 1566 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0008c0007 | 0/0 | 1566 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/0 | 13178 | 27 | 8 | 7 | 4 | 5 | 3 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0003 | 0/0 | 13179 | 26 | 2 | 6 | 16 | 0 | 2 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0004 | 0/0 | 13164 | 24 | 0 | 3 | 21 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0006 | 0/0 | 13180 | 17 | 1 | 2 | 12 | 1 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0007 | 0/0 | 13166 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0008 | 0/0 | 13164 | 13 | 0 | 9 | 0 | 1 | 3 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0009 | 0/0 | 13181 | 13 | 1 | 0 | 11 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0010 | 0/1 | 13164 | 10 | 3 | 4 | 0 | 0 | 2 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0013 | 0/0 | 13169 | 8 | 3 | 1 | 3 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0014 | 0/0 | 13170 | 7 | 0 | 0 | 0 | 0 | 7 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0015 | 0/0 | 13175 | 6 | 0 | 4 | 0 | 1 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0016 | 0/0 | 13182 | 6 | 2 | 2 | 2 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0017 | 0/0 | 13167 | 4 | 0 | 0 | 4 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0019 | 0/0 | 13170 | 3 | 2 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0020 | 0/0 | 13177 | 3 | 2 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0024 | 0/0 | 13158 | 2 | 1 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0025 | 0/0 | 13182 | 2 | 0 | 0 | 2 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0026 | 0/0 | 13165 | 2 | 0 | 0 | 0 | 0 | 2 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0027 | 0/0 | 13180 | 2 | 0 | 2 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0028 | 0/0 | 13169 | 2 | 0 | 0 | 2 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0030 | 0/0 | 13165 | 2 | 2 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0031 | 0/0 | 13179 | 2 | 0 | 0 | 2 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0032 | 0/0 | 13173 | 2 | 1 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0035 | 0/0 | 13169 | 2 | 0 | 1 | 0 | 1 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0036 | 0/0 | 13171 | 2 | 2 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0042 | 0/0 | 13158 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0043 | 0/0 | 13157 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0044 | 0/0 | 13178 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0046 | 0/0 | 13183 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0047 | 0/0 | 13184 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0048 | 0/0 | 13183 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0049 | 0/0 | 13168 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0050 | 0/0 | 13163 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0051 | 0/0 | 13164 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0052 | 0/0 | 13167 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0053 | 0/0 | 13173 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0054 | 0/0 | 13174 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0055 | 0/0 | 13174 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0056 | 0/0 | 13180 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0057 | 0/0 | 13179 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0058 | 0/0 | 13180 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0059 | 0/0 | 13171 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0060 | 0/0 | 13174 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0061 | 0/0 | 13180 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0062 | 0/0 | 13178 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0063 | 1/0 | 13178 | 1 | 0 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0064 | 0/0 | 13162 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0065 | 0/0 | 13171 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0066 | 0/0 | 13178 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0067 | 0/0 | 13170 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0068 | 0/0 | 13170 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0069 | 0/0 | 13171 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0070 | 0/0 | 13170 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0071 | 0/0 | 13168 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0072 | 0/0 | 13180 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0073 | 0/0 | 13163 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0076 | 0/0 | 13179 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0077 | 0/0 | 13178 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0078 | 0/0 | 13174 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0079 | 0/0 | 13178 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0080 | 0/0 | 13173 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0082 | 0/0 | 13163 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0083 | 0/0 | 13170 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0086 | 0/0 | 13167 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0087 | 0/0 | 13170 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0094 | 0/0 | 13169 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0001t0114 | 0/0 | 13179 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0002t0001 | 0/0 | 13164 | 29 | 1 | 3 | 22 | 1 | 2 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0002t0005 | 0/0 | 13164 | 24 | 0 | 2 | 17 | 1 | 4 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0002t0007 | 0/0 | 13166 | 17 | 0 | 3 | 14 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0002t0011 | 0/0 | 13170 | 10 | 5 | 4 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0002t0012 | 0/0 | 13166 | 9 | 9 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0002t0018 | 0/0 | 13152 | 4 | 0 | 0 | 4 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0002t0021 | 0/0 | 13167 | 3 | 3 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0002t0022 | 0/0 | 13171 | 3 | 1 | 1 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0002t0023 | 0/0 | 13152 | 3 | 0 | 0 | 3 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0002t0033 | 0/0 | 13171 | 2 | 2 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0002t0034 | 0/0 | 13175 | 2 | 2 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0002t0037 | 0/0 | 13165 | 2 | 0 | 0 | 1 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0002t0038 | 0/0 | 13165 | 2 | 0 | 0 | 2 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0002t0039 | 0/0 | 13164 | 2 | 0 | 1 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0002t0040 | 0/0 | 13165 | 2 | 0 | 1 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0002t0041 | 0/0 | 13169 | 2 | 0 | 0 | 2 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0002t0045 | 0/0 | 13172 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0002t0084 | 0/0 | 13169 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0002t0085 | 0/0 | 13166 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0002t0088 | 0/0 | 13167 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0002t0089 | 0/0 | 13170 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0002t0090 | 0/0 | 13166 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0002t0091 | 0/0 | 13172 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0002t0092 | 0/0 | 13173 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0002t0093 | 0/0 | 13174 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0002t0095 | 0/0 | 13172 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0002t0096 | 0/0 | 13169 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0002t0097 | 0/0 | 13173 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0002t0098 | 0/0 | 13166 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0002t0099 | 0/0 | 13171 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0002t0100 | 0/0 | 13166 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0002t0101 | 0/0 | 13167 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0002t0102 | 0/0 | 13169 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0002t0103 | 0/0 | 13164 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0002t0104 | 0/0 | 13167 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0002t0105 | 0/0 | 13164 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0002t0106 | 0/0 | 13163 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0002t0107 | 0/0 | 13165 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0002t0108 | 0/0 | 13165 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0002t0109 | 0/0 | 13164 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0002t0110 | 0/0 | 13165 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0002t0111 | 0/0 | 13164 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0002t0112 | 0/0 | 13170 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0002t0113 | 0/0 | 13164 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0006t0006 | 0/0 | 13180 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0001c0011t0006 | 0/0 | 13180 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0002c0004t0029 | 0/0 | 13178 | 2 | 2 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0003c0003t0075 | 0/0 | 13178 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0003c0003t0081 | 0/0 | 13173 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0004c0005t0001 | 0/0 | 13164 | 2 | 0 | 0 | 2 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0005c0008t0008 | 0/0 | 13164 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0006c0010t0002 | 0/0 | 13178 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0007c0009t0074 | 0/0 | 13170 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
a0008c0007t0013 | 0/0 | 13169 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | copy fasta | chr7 | 22929211 | 23019130 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0002g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0003g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0003g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0003g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0004g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0004g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0004g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0004g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0004g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0004g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0004g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0004g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0004g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0004g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0004g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0004g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0004g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0004g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0004g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0004g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0006g0004 | 0/0 | 4 | 1 | 1 | 2 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0006g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0006g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0006g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0006g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0006g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0006g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0006g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0006g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0006g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0006g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0006g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0006g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0006g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0007g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0008g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0008g0023 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0008g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0008g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0008g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0008g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0008g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0008g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0008g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0008g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0008g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0009g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0009g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0009g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0009g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0009g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0009g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0009g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0009g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0009g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0009g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0009g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0009g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0009g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0010g0003 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0010g0005 | 0/1 | 3 | 1 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0010g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0010g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0010g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0013g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0013g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0013g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0013g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0013g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0013g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0013g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0013g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0014g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0014g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0014g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0014g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0014g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0014g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0014g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0015g0002 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0015g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0015g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0016g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0016g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0016g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0016g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0016g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0016g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0017g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0017g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0017g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0017g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0019g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0019g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0019g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0020g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0020g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0020g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0024g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0024g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0025g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0025g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0026g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0026g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0027g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0028g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0028g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0030g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0030g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0031g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0031g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0032g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0032g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0035g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0035g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0036g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0036g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0042g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0043g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0044g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0046g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0047g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0048g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0049g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0050g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0051g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0052g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0053g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0054g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0055g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0056g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0057g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0058g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0059g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0060g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0061g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0062g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0063g0033 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0064g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0065g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0066g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0067g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0068g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0069g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0070g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0071g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0072g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0073g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0076g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0077g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0078g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0079g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0080g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0082g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0083g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0086g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0087g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0094g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0001t0114g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0001g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0001g0007 | 0/0 | 3 | 1 | 0 | 0 | 1 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0005g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0005g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0005g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0005g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0005g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0005g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0005g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0005g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0005g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0005g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0005g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0005g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0005g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0005g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0005g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0005g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0005g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0005g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0005g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0005g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0005g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0005g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0007g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0007g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0007g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0007g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0007g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0007g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0007g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0007g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0007g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0007g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0007g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0007g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0007g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0007g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0007g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0011g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0011g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0011g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0011g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0011g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0011g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0011g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0011g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0011g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0012g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0012g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0012g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0012g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0012g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0012g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0012g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0012g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0012g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0018g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0018g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0018g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0021g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0021g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0021g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0022g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0022g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0022g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0023g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0023g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0033g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0033g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0034g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0034g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0037g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0037g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0038g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0038g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0039g0017 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0040g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0040g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0041g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0041g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0045g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0084g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0085g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0088g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0089g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0090g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0091g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0092g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0093g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0095g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0096g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0097g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0098g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0099g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0100g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0101g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0102g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0103g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0104g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0105g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0106g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0107g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0108g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0109g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0110g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0111g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0112g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0002t0113g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0006t0006g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0001c0011t0006g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0002c0004t0029g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0003c0003t0075g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0003c0003t0081g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0004c0005t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0005c0008t0008g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0006c0010t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0007c0009t0074g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
a0008c0007t0013g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0035 | g0109 | EUR | GBR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0112 | EUR | GBR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG00140 | hp1 | a0001 | c0002 | t0001 | g0007 | EUR | GBR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0125 | EUR | GBR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG00280 | hp1 | a0001 | c0001 | t0044 | g0029 | EUR | FIN | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG00280 | hp2 | a0001 | c0002 | t0005 | g0291 | EUR | FIN | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG00423 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | CHS | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG00423 | hp2 | a0001 | c0002 | t0001 | g0245 | EAS | CHS | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG00438 | hp1 | a0001 | c0001 | t0009 | g0178 | EAS | CHS | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG00438 | hp2 | a0001 | c0001 | t0009 | g0060 | EAS | CHS | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG00544 | hp1 | a0001 | c0001 | t0013 | g0175 | EAS | CHS | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG00544 | hp2 | a0001 | c0001 | t0049 | g0310 | EAS | CHS | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG00558 | hp1 | a0004 | c0005 | t0001 | g0016 | EAS | CHS | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG00558 | hp2 | a0001 | c0001 | t0003 | g0177 | EAS | CHS | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG00639 | hp1 | a0001 | c0001 | t0057 | g0096 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG00639 | hp2 | a0001 | c0001 | t0016 | g0065 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0297 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG00642 | hp2 | a0001 | c0001 | t0008 | g0021 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG00673 | hp1 | a0001 | c0001 | t0009 | g0144 | EAS | CHS | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG00673 | hp2 | a0001 | c0002 | t0001 | g0236 | EAS | CHS | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG00733 | hp1 | a0001 | c0002 | t0011 | g0018 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG00733 | hp2 | a0001 | c0001 | t0056 | g0094 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG00738 | hp1 | a0001 | c0001 | t0010 | g0003 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG00738 | hp2 | a0001 | c0001 | t0015 | g0038 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01069 | hp1 | a0001 | c0001 | t0008 | g0326 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01069 | hp2 | a0001 | c0001 | t0019 | g0083 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0338 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01070 | hp2 | a0001 | c0002 | t0001 | g0271 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01071 | hp1 | a0001 | c0001 | t0059 | g0084 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0339 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01074 | hp1 | a0001 | c0002 | t0011 | g0018 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01074 | hp2 | a0001 | c0002 | t0039 | g0017 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01081 | hp1 | a0001 | c0001 | t0013 | g0306 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01081 | hp2 | a0001 | c0001 | t0032 | g0048 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01099 | hp1 | a0001 | c0001 | t0006 | g0004 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01099 | hp2 | a0001 | c0002 | t0011 | g0299 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01106 | hp1 | a0001 | c0001 | t0010 | g0005 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0202 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01109 | hp1 | a0001 | c0002 | t0022 | g0300 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0071 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01168 | hp1 | a0001 | c0001 | t0008 | g0324 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01168 | hp2 | a0001 | c0001 | t0015 | g0002 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01169 | hp1 | a0001 | c0002 | t0007 | g0223 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01169 | hp2 | a0001 | c0001 | t0015 | g0002 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0108 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01175 | hp2 | a0001 | c0002 | t0107 | g0225 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01192 | hp1 | a0001 | c0002 | t0084 | g0260 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01192 | hp2 | a0001 | c0001 | t0008 | g0021 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0068 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01243 | hp2 | a0001 | c0002 | t0099 | g0269 | AMR | PUR | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01255 | hp1 | a0006 | c0010 | t0002 | g0187 | AMR | CLM | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01255 | hp2 | a0001 | c0001 | t0016 | g0342 | AMR | CLM | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01256 | hp1 | a0001 | c0002 | t0005 | g0024 | AMR | CLM | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01256 | hp2 | a0001 | c0001 | t0008 | g0318 | AMR | CLM | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01257 | hp1 | a0001 | c0001 | t0027 | g0013 | AMR | CLM | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01257 | hp2 | a0001 | c0002 | t0011 | g0230 | AMR | CLM | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01258 | hp1 | a0001 | c0001 | t0027 | g0013 | AMR | CLM | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01258 | hp2 | a0001 | c0002 | t0005 | g0024 | AMR | CLM | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0118 | AMR | CLM | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01261 | hp2 | a0001 | c0001 | t0010 | g0312 | AMR | CLM | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01358 | hp1 | a0001 | c0001 | t0010 | g0003 | AMR | CLM | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01358 | hp2 | a0001 | c0001 | t0003 | g0157 | AMR | CLM | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01361 | hp1 | a0001 | c0002 | t0001 | g0258 | AMR | CLM | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01361 | hp2 | a0001 | c0001 | t0024 | g0027 | AMR | CLM | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0091 | AMR | CLM | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01433 | hp2 | a0001 | c0001 | t0015 | g0002 | AMR | CLM | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0234 | AMR | CLM | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01496 | hp2 | a0001 | c0001 | t0006 | g0337 | AMR | CLM | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01515 | hp1 | a0001 | c0001 | t0015 | g0002 | EUR | IBS | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0127 | EUR | IBS | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01516 | hp1 | a0005 | c0008 | t0008 | g0045 | EUR | IBS | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0126 | EUR | IBS | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01884 | hp1 | a0001 | c0002 | t0012 | g0200 | AFR | ACB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01884 | hp2 | a0001 | c0001 | t0010 | g0043 | AFR | ACB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01891 | hp1 | a0001 | c0001 | t0009 | g0155 | AFR | ACB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01891 | hp2 | a0001 | c0001 | t0013 | g0070 | AFR | ACB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01928 | hp1 | a0001 | c0001 | t0004 | g0046 | AMR | PEL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01928 | hp2 | a0001 | c0002 | t0040 | g0254 | AMR | PEL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01943 | hp1 | a0001 | c0001 | t0008 | g0333 | AMR | PEL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0343 | AMR | PEL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01978 | hp1 | a0001 | c0001 | t0004 | g0022 | AMR | PEL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01978 | hp2 | a0001 | c0001 | t0071 | g0040 | AMR | PEL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01993 | hp1 | a0001 | c0001 | t0035 | g0069 | AMR | PEL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG01993 | hp2 | a0001 | c0001 | t0020 | g0105 | AMR | PEL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02004 | hp1 | a0001 | c0002 | t0007 | g0217 | AMR | PEL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02004 | hp2 | a0001 | c0001 | t0004 | g0022 | AMR | PEL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02015 | hp1 | a0001 | c0001 | t0004 | g0330 | EAS | KHV | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02015 | hp2 | a0001 | c0001 | t0003 | g0203 | EAS | KHV | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02040 | hp1 | a0001 | c0006 | t0006 | g0160 | EAS | KHV | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02040 | hp2 | a0001 | c0002 | t0103 | g0280 | EAS | KHV | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02055 | hp1 | a0001 | c0002 | t0034 | g0057 | AFR | ACB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02055 | hp2 | a0001 | c0001 | t0077 | g0052 | AFR | ACB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02056 | hp1 | a0001 | c0002 | t0005 | g0289 | EAS | KHV | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02056 | hp2 | a0001 | c0001 | t0006 | g0174 | EAS | KHV | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02071 | hp1 | a0001 | c0001 | t0094 | g0111 | EAS | KHV | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02071 | hp2 | a0001 | c0002 | t0005 | g0019 | EAS | KHV | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | KHV | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02074 | hp2 | a0001 | c0002 | t0005 | g0284 | EAS | KHV | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02083 | hp1 | a0001 | c0002 | t0005 | g0286 | EAS | KHV | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02083 | hp2 | a0001 | c0001 | t0003 | g0167 | EAS | KHV | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02132 | hp1 | a0001 | c0002 | t0041 | g0249 | EAS | KHV | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02132 | hp2 | a0008 | c0007 | t0013 | g0058 | EAS | KHV | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02135 | hp1 | a0001 | c0001 | t0013 | g0169 | EAS | KHV | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02135 | hp2 | a0001 | c0002 | t0038 | g0285 | EAS | KHV | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02145 | hp1 | a0001 | c0001 | t0070 | g0074 | AFR | ACB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02145 | hp2 | a0003 | c0003 | t0075 | g0051 | AFR | ACB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02148 | hp1 | a0001 | c0001 | t0003 | g0161 | AMR | PEL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02148 | hp2 | a0001 | c0001 | t0003 | g0093 | AMR | PEL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02155 | hp1 | a0001 | c0002 | t0037 | g0274 | EAS | CDX | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02155 | hp2 | a0001 | c0002 | t0007 | g0215 | EAS | CDX | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0135 | EAS | CDX | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02165 | hp2 | a0001 | c0002 | t0005 | g0288 | EAS | CDX | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02257 | hp1 | a0001 | c0002 | t0011 | g0262 | AFR | ACB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02257 | hp2 | a0001 | c0001 | t0010 | g0044 | AFR | ACB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0097 | AFR | ACB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02258 | hp2 | a0001 | c0001 | t0010 | g0005 | AFR | ACB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02273 | hp1 | a0001 | c0002 | t0101 | g0205 | AMR | PEL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02273 | hp2 | a0001 | c0001 | t0008 | g0321 | AMR | PEL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02293 | hp1 | a0001 | c0001 | t0008 | g0315 | AMR | PEL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02293 | hp2 | a0001 | c0002 | t0090 | g0199 | AMR | PEL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02300 | hp1 | a0001 | c0002 | t0007 | g0209 | AMR | PEL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02300 | hp2 | a0001 | c0001 | t0008 | g0325 | AMR | PEL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02572 | hp1 | a0001 | c0002 | t0012 | g0201 | AFR | GWD | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02572 | hp2 | a0001 | c0002 | t0091 | g0259 | AFR | GWD | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02602 | hp1 | a0001 | c0002 | t0039 | g0017 | SAS | PJL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0114 | SAS | PJL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02622 | hp1 | a0001 | c0001 | t0032 | g0047 | AFR | GWD | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02622 | hp2 | a0001 | c0001 | t0076 | g0345 | AFR | GWD | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02630 | hp1 | a0001 | c0001 | t0079 | g0054 | AFR | GWD | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02630 | hp2 | a0001 | c0002 | t0095 | g0227 | AFR | GWD | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0076 | SAS | PJL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02698 | hp2 | a0001 | c0001 | t0086 | g0081 | SAS | PJL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02717 | hp1 | a0001 | c0002 | t0012 | g0194 | AFR | GWD | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0066 | AFR | GWD | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02735 | hp1 | a0001 | c0001 | t0055 | g0039 | SAS | PJL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02735 | hp2 | a0001 | c0001 | t0010 | g0003 | SAS | PJL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02738 | hp1 | a0001 | c0001 | t0006 | g0149 | SAS | PJL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02738 | hp2 | a0001 | c0001 | t0008 | g0320 | SAS | PJL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02809 | hp1 | a0001 | c0002 | t0089 | g0266 | AFR | GWD | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0063 | AFR | GWD | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02818 | hp1 | a0002 | c0004 | t0029 | g0011 | AFR | GWD | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02818 | hp2 | a0001 | c0002 | t0011 | g0235 | AFR | GWD | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02886 | hp1 | a0001 | c0002 | t0033 | g0303 | AFR | GWD | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02886 | hp2 | a0001 | c0002 | t0021 | g0192 | AFR | GWD | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02896 | hp1 | a0001 | c0002 | t0012 | g0296 | AFR | GWD | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02896 | hp2 | a0001 | c0001 | t0036 | g0031 | AFR | GWD | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02897 | hp1 | a0001 | c0001 | t0020 | g0130 | AFR | GWD | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02897 | hp2 | a0001 | c0002 | t0012 | g0295 | AFR | GWD | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02922 | hp1 | a0001 | c0001 | t0013 | g0134 | AFR | ESN | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02922 | hp2 | a0001 | c0001 | t0016 | g0171 | AFR | ESN | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02965 | hp1 | a0001 | c0001 | t0030 | g0115 | AFR | ESN | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0116 | AFR | ESN | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02970 | hp1 | a0001 | c0002 | t0045 | g0036 | AFR | ESN | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02970 | hp2 | a0001 | c0002 | t0012 | g0198 | AFR | ESN | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02976 | hp1 | a0001 | c0001 | t0043 | g0028 | AFR | ESN | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02976 | hp2 | a0007 | c0009 | t0074 | g0344 | AFR | ESN | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03017 | hp1 | a0001 | c0001 | t0015 | g0037 | SAS | PJL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03017 | hp2 | a0001 | c0001 | t0066 | g0168 | SAS | PJL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0064 | AFR | GWD | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03041 | hp2 | a0001 | c0002 | t0011 | g0267 | AFR | GWD | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03098 | hp1 | a0003 | c0003 | t0081 | g0050 | AFR | MSL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03098 | hp2 | a0001 | c0002 | t0021 | g0233 | AFR | MSL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03130 | hp1 | a0001 | c0001 | t0003 | g0055 | AFR | ESN | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03130 | hp2 | a0001 | c0001 | t0069 | g0073 | AFR | ESN | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03139 | hp1 | a0001 | c0001 | t0019 | g0341 | AFR | ESN | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03139 | hp2 | a0001 | c0002 | t0085 | g0197 | AFR | ESN | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03195 | hp1 | a0001 | c0001 | t0060 | g0067 | AFR | ESN | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03195 | hp2 | a0001 | c0001 | t0068 | g0087 | AFR | ESN | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03209 | hp1 | a0001 | c0002 | t0092 | g0056 | AFR | MSL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03209 | hp2 | a0001 | c0002 | t0012 | g0189 | AFR | MSL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03239 | hp1 | a0001 | c0001 | t0083 | g0123 | SAS | PJL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03239 | hp2 | a0001 | c0002 | t0005 | g0275 | SAS | PJL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0163 | AFR | MSL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03453 | hp2 | a0001 | c0002 | t0021 | g0261 | AFR | MSL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03486 | hp1 | a0001 | c0001 | t0082 | g0188 | AFR | MSL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03486 | hp2 | a0001 | c0002 | t0098 | g0193 | AFR | MSL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03490 | hp1 | a0001 | c0001 | t0014 | g0090 | SAS | PJL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0113 | SAS | PJL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0124 | SAS | PJL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03491 | hp2 | a0001 | c0001 | t0026 | g0317 | SAS | PJL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03492 | hp1 | a0001 | c0001 | t0026 | g0327 | SAS | PJL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03492 | hp2 | a0001 | c0001 | t0014 | g0080 | SAS | PJL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03540 | hp1 | a0002 | c0004 | t0029 | g0011 | AFR | GWD | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03540 | hp2 | a0001 | c0001 | t0078 | g0049 | AFR | GWD | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03579 | hp1 | a0001 | c0002 | t0011 | g0264 | AFR | MSL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03579 | hp2 | a0001 | c0001 | t0042 | g0025 | AFR | MSL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03688 | hp1 | a0001 | c0001 | t0087 | g0086 | SAS | STU | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03688 | hp2 | a0001 | c0001 | t0008 | g0322 | SAS | STU | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03704 | hp1 | a0001 | c0001 | t0064 | g0078 | SAS | PJL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03704 | hp2 | a0001 | c0002 | t0096 | g0232 | SAS | PJL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0129 | SAS | PJL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03710 | hp2 | a0001 | c0001 | t0013 | g0103 | SAS | PJL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03831 | hp1 | a0001 | c0002 | t0037 | g0298 | SAS | BEB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03831 | hp2 | a0001 | c0002 | t0022 | g0268 | SAS | BEB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03834 | hp1 | a0001 | c0001 | t0014 | g0101 | SAS | BEB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03834 | hp2 | a0001 | c0002 | t0005 | g0292 | SAS | BEB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03927 | hp1 | a0001 | c0002 | t0005 | g0277 | SAS | BEB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03927 | hp2 | a0001 | c0001 | t0053 | g0041 | SAS | BEB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03942 | hp1 | a0001 | c0001 | t0014 | g0100 | SAS | BEB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03942 | hp2 | a0001 | c0001 | t0009 | g0150 | SAS | BEB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG04115 | hp1 | a0001 | c0001 | t0014 | g0110 | SAS | STU | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG04115 | hp2 | a0001 | c0002 | t0005 | g0278 | SAS | STU | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG04184 | hp1 | a0001 | c0001 | t0010 | g0003 | SAS | BEB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0244 | SAS | BEB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG04199 | hp1 | a0001 | c0001 | t0014 | g0102 | SAS | STU | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG04199 | hp2 | a0001 | c0001 | t0008 | g0023 | SAS | STU | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG04204 | hp1 | a0001 | c0001 | t0014 | g0082 | SAS | STU | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0007 | SAS | STU | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG04228 | hp1 | a0001 | c0002 | t0011 | g0301 | SAS | STU | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG04228 | hp2 | a0001 | c0002 | t0100 | g0218 | SAS | STU | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18522 | hp1 | a0001 | c0001 | t0036 | g0032 | AFR | YRI | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0088 | AFR | YRI | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18612 | hp1 | a0001 | c0001 | t0013 | g0059 | EAS | CHB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18612 | hp2 | a0001 | c0001 | t0051 | g0329 | EAS | CHB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18906 | hp1 | a0001 | c0002 | t0011 | g0265 | AFR | YRI | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18906 | hp2 | a0001 | c0002 | t0012 | g0190 | AFR | YRI | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18939 | hp1 | a0001 | c0001 | t0006 | g0179 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18939 | hp2 | a0001 | c0001 | t0025 | g0186 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18941 | hp1 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18941 | hp2 | a0001 | c0001 | t0007 | g0221 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18942 | hp1 | a0001 | c0001 | t0028 | g0147 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18942 | hp2 | a0001 | c0001 | t0028 | g0121 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18943 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18943 | hp2 | a0001 | c0002 | t0018 | g0015 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18946 | hp1 | a0001 | c0002 | t0001 | g0252 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18946 | hp2 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18952 | hp1 | a0001 | c0001 | t0031 | g0307 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0152 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18954 | hp1 | a0001 | c0002 | t0110 | g0239 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18954 | hp2 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18956 | hp1 | a0001 | c0002 | t0007 | g0006 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18960 | hp1 | a0001 | c0002 | t0007 | g0214 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18960 | hp2 | a0001 | c0001 | t0004 | g0335 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18961 | hp1 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18961 | hp2 | a0001 | c0002 | t0005 | g0276 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18963 | hp1 | a0001 | c0001 | t0004 | g0332 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18963 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18965 | hp1 | a0001 | c0002 | t0005 | g0294 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18965 | hp2 | a0001 | c0001 | t0017 | g0131 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18966 | hp1 | a0001 | c0002 | t0005 | g0030 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18966 | hp2 | a0001 | c0001 | t0004 | g0020 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18968 | hp1 | a0001 | c0002 | t0005 | g0273 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18968 | hp2 | a0001 | c0001 | t0009 | g0145 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18970 | hp2 | a0001 | c0002 | t0007 | g0309 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18971 | hp1 | a0001 | c0002 | t0001 | g0238 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18972 | hp1 | a0001 | c0002 | t0001 | g0253 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18972 | hp2 | a0001 | c0001 | t0004 | g0020 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18973 | hp1 | a0001 | c0001 | t0061 | g0146 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18973 | hp2 | a0001 | c0001 | t0004 | g0331 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18975 | hp1 | a0001 | c0002 | t0001 | g0257 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18975 | hp2 | a0001 | c0001 | t0009 | g0139 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18977 | hp1 | a0001 | c0002 | t0007 | g0006 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18977 | hp2 | a0001 | c0001 | t0006 | g0004 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18978 | hp1 | a0001 | c0001 | t0009 | g0158 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18978 | hp2 | a0001 | c0002 | t0038 | g0283 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18979 | hp1 | a0001 | c0001 | t0006 | g0099 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18979 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18981 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18982 | hp2 | a0001 | c0001 | t0004 | g0334 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18983 | hp1 | a0001 | c0002 | t0088 | g0208 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18983 | hp2 | a0001 | c0002 | t0001 | g0231 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18984 | hp1 | a0001 | c0001 | t0017 | g0122 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18984 | hp2 | a0001 | c0002 | t0023 | g0014 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18985 | hp1 | a0001 | c0001 | t0009 | g0176 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18985 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18986 | hp1 | a0001 | c0002 | t0001 | g0270 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18986 | hp2 | a0001 | c0001 | t0050 | g0328 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18987 | hp1 | a0001 | c0001 | t0004 | g0316 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18987 | hp2 | a0001 | c0002 | t0104 | g0293 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18988 | hp1 | a0001 | c0001 | t0031 | g0308 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18988 | hp2 | a0001 | c0002 | t0007 | g0212 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18989 | hp1 | a0001 | c0002 | t0007 | g0216 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18989 | hp2 | a0001 | c0002 | t0001 | g0246 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18990 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18990 | hp2 | a0001 | c0001 | t0006 | g0004 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18991 | hp1 | a0001 | c0001 | t0009 | g0173 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18991 | hp2 | a0001 | c0002 | t0109 | g0255 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18992 | hp1 | a0004 | c0005 | t0001 | g0016 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18992 | hp2 | a0001 | c0002 | t0102 | g0213 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0165 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18994 | hp2 | a0001 | c0002 | t0007 | g0220 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18998 | hp1 | a0001 | c0002 | t0040 | g0228 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18998 | hp2 | a0001 | c0002 | t0007 | g0006 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18999 | hp1 | a0001 | c0001 | t0017 | g0119 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA18999 | hp2 | a0001 | c0001 | t0004 | g0319 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19000 | hp1 | a0001 | c0002 | t0007 | g0207 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19000 | hp2 | a0001 | c0001 | t0006 | g0170 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19001 | hp1 | a0001 | c0001 | t0073 | g0336 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19001 | hp2 | a0001 | c0001 | t0004 | g0313 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19002 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19003 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19003 | hp2 | a0001 | c0011 | t0006 | g0154 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19004 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19004 | hp2 | a0001 | c0002 | t0007 | g0206 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19005 | hp1 | a0001 | c0002 | t0018 | g0211 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19005 | hp2 | a0001 | c0002 | t0005 | g0272 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19007 | hp1 | a0001 | c0002 | t0001 | g0241 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19007 | hp2 | a0001 | c0001 | t0006 | g0098 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19009 | hp1 | a0001 | c0001 | t0006 | g0159 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19009 | hp2 | a0001 | c0002 | t0001 | g0226 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19010 | hp1 | a0001 | c0001 | t0046 | g0185 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19010 | hp2 | a0001 | c0001 | t0052 | g0311 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19012 | hp1 | a0001 | c0002 | t0005 | g0282 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19012 | hp2 | a0001 | c0002 | t0007 | g0219 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19043 | hp1 | a0001 | c0002 | t0097 | g0195 | AFR | LWK | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0132 | AFR | LWK | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19054 | hp1 | a0001 | c0002 | t0005 | g0279 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19054 | hp2 | a0001 | c0001 | t0004 | g0314 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19056 | hp1 | a0001 | c0001 | t0009 | g0106 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19056 | hp2 | a0001 | c0001 | t0025 | g0136 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19058 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19058 | hp2 | a0001 | c0002 | t0023 | g0222 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19059 | hp1 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19059 | hp2 | a0001 | c0001 | t0006 | g0104 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19062 | hp1 | a0001 | c0002 | t0023 | g0014 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19062 | hp2 | a0001 | c0001 | t0048 | g0137 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19065 | hp1 | a0001 | c0002 | t0007 | g0210 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19065 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19066 | hp1 | a0001 | c0002 | t0005 | g0281 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19066 | hp2 | a0001 | c0002 | t0018 | g0224 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19067 | hp1 | a0001 | c0002 | t0005 | g0302 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19068 | hp1 | a0001 | c0002 | t0018 | g0015 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19068 | hp2 | a0001 | c0001 | t0017 | g0117 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19070 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19070 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19074 | hp1 | a0001 | c0001 | t0114 | g0347 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19074 | hp2 | a0001 | c0001 | t0004 | g0323 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19076 | hp1 | a0001 | c0002 | t0007 | g0204 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19076 | hp2 | a0001 | c0002 | t0005 | g0290 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19077 | hp1 | a0001 | c0002 | t0106 | g0034 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19077 | hp2 | a0001 | c0001 | t0058 | g0140 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19079 | hp1 | a0001 | c0002 | t0105 | g0035 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19079 | hp2 | a0001 | c0001 | t0062 | g0148 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19081 | hp1 | a0001 | c0002 | t0041 | g0243 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19081 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19082 | hp1 | a0001 | c0001 | t0047 | g0184 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19083 | hp1 | a0001 | c0001 | t0016 | g0180 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19083 | hp2 | a0001 | c0002 | t0111 | g0247 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19084 | hp1 | a0001 | c0001 | t0006 | g0153 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19084 | hp2 | a0001 | c0002 | t0005 | g0287 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19085 | hp1 | a0001 | c0002 | t0001 | g0251 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19085 | hp2 | a0001 | c0001 | t0006 | g0181 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19086 | hp1 | a0001 | c0001 | t0009 | g0142 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19086 | hp2 | a0001 | c0002 | t0108 | g0240 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19087 | hp1 | a0001 | c0001 | t0016 | g0143 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19087 | hp2 | a0001 | c0002 | t0001 | g0256 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19088 | hp1 | a0001 | c0002 | t0001 | g0248 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19088 | hp2 | a0001 | c0001 | t0009 | g0172 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19089 | hp1 | a0001 | c0001 | t0072 | g0107 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19089 | hp2 | a0001 | c0002 | t0001 | g0250 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19090 | hp1 | a0001 | c0001 | t0006 | g0162 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19090 | hp2 | a0001 | c0002 | t0113 | g0346 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19091 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19091 | hp2 | a0001 | c0002 | t0005 | g0019 | EAS | JPT | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19240 | hp1 | a0001 | c0001 | t0020 | g0079 | AFR | YRI | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA19240 | hp2 | a0001 | c0002 | t0012 | g0191 | AFR | YRI | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0077 | AFR | ASW | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA20129 | hp2 | a0001 | c0002 | t0022 | g0263 | AFR | ASW | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0128 | EUR | TSI | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA20752 | hp2 | a0001 | c0002 | t0112 | g0304 | EUR | TSI | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA20805 | hp1 | a0001 | c0001 | t0008 | g0023 | EUR | TSI | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA20805 | hp2 | a0001 | c0001 | t0006 | g0156 | EUR | TSI | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02109 | hp1 | a0001 | c0001 | t0054 | g0042 | AFR | ACB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02109 | hp2 | a0001 | c0001 | t0030 | g0120 | AFR | ACB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02486 | hp1 | a0001 | c0001 | t0080 | g0053 | AFR | ACB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02486 | hp2 | a0001 | c0002 | t0093 | g0196 | AFR | ACB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02559 | hp1 | a0001 | c0001 | t0067 | g0072 | AFR | ACB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG02559 | hp2 | a0001 | c0001 | t0024 | g0026 | AFR | ACB | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03471 | hp1 | a0001 | c0001 | t0019 | g0340 | AFR | MSL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG03471 | hp2 | a0001 | c0002 | t0033 | g0229 | AFR | MSL | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG06807 | hp1 | a0001 | c0002 | t0034 | g0305 | AFR | USA | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
HG06807 | hp2 | a0001 | c0002 | t0001 | g0007 | AFR | USA | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA20300 | hp1 | a0001 | c0001 | t0065 | g0075 | AFR | USA | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA20300 | hp2 | a0001 | c0001 | t0006 | g0004 | AFR | USA | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA21309 | hp1 | a0001 | c0001 | t0016 | g0085 | AFR | LWK | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
NA21309 | hp2 | a0001 | c0001 | t0013 | g0133 | AFR | LWK | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0010 | g0005 | REF | REF | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0063 | g0033 | REF | REF | HYCC1_chr7_22929211_23019130 | HYCC1 | chr7 | 22929211 | 23019130 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:22945600
|
A | G | 1 | a0003 | 2 | HG02145.hp2 HG03098.hp1 |
missense_variant | MODERATE | c.1555T>C | p.Ser519Pro | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 1789/13178 | 1555/1566 | 519/521 | chr7 | 22945600 | ||
chr7:22945636
|
C | G | 1 | a0006 | 1 | HG01255.hp1 | missense_variant | MODERATE | c.1519G>C | p.Gly507Arg | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 1753/13178 | 1519/1566 | 507/521 | chr7 | 22945636 | ||
chr7:22945663
|
T | C | 1 | a0002 | 2 | HG02818.hp1 HG03540.hp1 |
missense_variant | MODERATE | c.1492A>G | p.Thr498Ala | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 1726/13178 | 1492/1566 | 498/521 | chr7 | 22945663 | ||
chr7:22945740
|
C | T | 1 | a0007 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.1415G>A | p.Cys472Tyr | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 1649/13178 | 1415/1566 | 472/521 | chr7 | 22945740 | ||
chr7:22945812
|
G | T | 1 | a0005 | 1 | HG01516.hp1 | missense_variant | MODERATE | c.1343C>A | p.Thr448Asn | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 1577/13178 | 1343/1566 | 448/521 | chr7 | 22945812 | ||
chr7:22945816
|
C | T | 1 | a0004 | 2 | HG00558.hp1 NA18992.hp1 |
missense_variant | MODERATE | c.1339G>A | p.Ala447Thr | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 1573/13178 | 1339/1566 | 447/521 | chr7 | 22945816 | ||
chr7:22945984
|
C | G | 1 | a0008 | 1 | HG02132.hp2 | missense_variant | MODERATE | c.1171G>C | p.Gly391Arg | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 1405/13178 | 1171/1566 | 391/521 | chr7 | 22945984 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:22960413
|
A | C | 1 | a0001c0006 | 1 | HG02040.hp1 | splice_region_variant&synonymous_variant | LOW | c.834T>G | p.Val278Val | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/11 | 1068/13178 | 834/1566 | 278/521 | chr7 | 22960413 | ||
chr7:22976212
|
T | C | 2 | a0001c0002a0004c0005 | 146 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(143): Show |
splice_region_variant&synonymous_variant | LOW | c.624A>G | p.Ser208Ser | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/11 | 858/13178 | 624/1566 | 208/521 | chr7 | 22976212 | ||
chr7:22976221
|
T | C | 1 | a0001c0011 | 1 | NA19003.hp2 | synonymous_variant | LOW | c.615A>G | p.Gln205Gln | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/11 | 849/13178 | 615/1566 | 205/521 | chr7 | 22976221 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:22934233
|
T | C | 1 | a0001c0001t0082 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11356A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 11356 | chr7 | 22934233 | |||||
chr7:22934234
|
T | C | 19 | a0001c0001t0004a0001c0001t0008a0001c0001t0010others(16): Show | 66 | HG00423.hp1 HG00642.hp2 HG00738.hp1 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*11355A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 11355 | chr7 | 22934234 | |||||
chr7:22934234
|
T | TC | 11 | a0001c0001t0047a0001c0001t0048a0001c0001t0054others(8): Show | 21 | HG00733.hp1 HG01074.hp1 HG01099.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*11354dupG | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 11354 | chr7 | 22934234 | |||||
chr7:22934234
|
T | TTC | 6 | a0001c0001t0015a0001c0001t0055a0001c0002t0022others(3): Show | 14 | HG00738.hp2 HG01109.hp1 HG01168.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*11354_*11355insGA | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 11354 | chr7 | 22934234 | |||||
chr7:22934258
|
T | TCAG | 6 | a0001c0002t0034a0001c0002t0091a0001c0002t0092others(3): Show | 7 | HG02055.hp1 HG02486.hp2 HG02572.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*11328_*11330dupCT others(1): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 11330 | chr7 | 22934258 | |||||
chr7:22934697
|
C | A | 1 | a0007c0009t0074 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10892G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 10892 | chr7 | 22934697 | |||||
chr7:22934948
|
G | A | 1 | a0001c0001t0031 | 2 | NA18952.hp1 NA18988.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10641C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 10641 | chr7 | 22934948 | |||||
chr7:22934976
|
G | C | 1 | a0001c0002t0045 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10613C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 10613 | chr7 | 22934976 | |||||
chr7:22935224
|
T | G | 1 | a0001c0001t0073 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10365A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 10365 | chr7 | 22935224 | |||||
chr7:22935293
|
T | G | 79 | a0001c0001t0004a0001c0001t0007a0001c0001t0008others(76): Show | 246 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(243): Show |
3_prime_UTR_variant | MODIFIER | c.*10296A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 10296 | chr7 | 22935293 | |||||
chr7:22935385
|
C | T | 44 | a0001c0001t0004a0001c0001t0008a0001c0001t0010others(41): Show | 123 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*10204G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 10204 | chr7 | 22935385 | |||||
chr7:22935426
|
C | T | 80 | a0001c0001t0004a0001c0001t0007a0001c0001t0008others(77): Show | 247 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(244): Show |
3_prime_UTR_variant | MODIFIER | c.*10163G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 10163 | chr7 | 22935426 | |||||
chr7:22935650
|
T | C | 1 | a0001c0001t0094 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9939A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 9939 | chr7 | 22935650 | |||||
chr7:22935688
|
C | T | 3 | a0001c0001t0024a0001c0001t0042a0001c0001t0043 | 4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*9901G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 9901 | chr7 | 22935688 | |||||
chr7:22935710
|
A | G | 33 | a0001c0001t0007a0001c0001t0036a0001c0001t0049others(30): Show | 121 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*9879T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 9879 | chr7 | 22935710 | |||||
chr7:22935864
|
G | A | 1 | a0001c0002t0095 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9725C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 9725 | chr7 | 22935864 | |||||
chr7:22935873
|
TTC | T | 10 | a0001c0001t0049a0001c0001t0052a0001c0002t0001others(7): Show | 40 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*9714_*9715delGA | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 9714 | chr7 | 22935873 | |||||
chr7:22936030
|
G | T | 1 | a0001c0001t0076 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9559C>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 9559 | chr7 | 22936030 | |||||
chr7:22936040
|
G | A | 56 | a0001c0001t0007a0001c0001t0013a0001c0001t0014others(53): Show | 172 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(169): Show |
3_prime_UTR_variant | MODIFIER | c.*9549C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 9549 | chr7 | 22936040 | |||||
chr7:22936289
|
G | A | 20 | a0001c0001t0004a0001c0001t0008a0001c0001t0010others(17): Show | 71 | HG00423.hp1 HG00642.hp2 HG00738.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*9300C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 9300 | chr7 | 22936289 | |||||
chr7:22936322
|
C | T | 4 | a0001c0001t0014a0001c0001t0035a0001c0001t0083others(1): Show | 11 | HG00099.hp1 HG01993.hp1 HG02698.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*9267G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 9267 | chr7 | 22936322 | |||||
chr7:22936960
|
G | A | 120 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(117): Show | 385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
3_prime_UTR_variant | MODIFIER | c.*8629C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 8629 | chr7 | 22936960 | |||||
chr7:22937006
|
G | C | 1 | a0001c0001t0073 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8583C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 8583 | chr7 | 22937006 | |||||
chr7:22937079
|
G | A | 5 | a0001c0001t0024a0001c0001t0042a0001c0001t0043others(2): Show | 6 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*8510C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 8510 | chr7 | 22937079 | |||||
chr7:22937175
|
T | C | 7 | a0001c0001t0032a0001c0001t0077a0001c0001t0078others(4): Show | 8 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*8414A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 8414 | chr7 | 22937175 | |||||
chr7:22937193
|
G | A | 1 | a0001c0001t0044 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8396C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 8396 | chr7 | 22937193 | |||||
chr7:22937226
|
A | T | 1 | a0001c0002t0089 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8363T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 8363 | chr7 | 22937226 | |||||
chr7:22937250
|
C | A | 60 | a0001c0001t0007a0001c0001t0013a0001c0001t0014others(57): Show | 177 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(174): Show |
3_prime_UTR_variant | MODIFIER | c.*8339G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 8339 | chr7 | 22937250 | |||||
chr7:22937268
|
C | CA | 17 | a0001c0001t0004a0001c0001t0008a0001c0001t0010others(14): Show | 68 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*8320dupT | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 8320 | chr7 | 22937268 | |||||
chr7:22937489
|
A | C | 1 | a0001c0002t0107 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8100T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 8100 | chr7 | 22937489 | |||||
chr7:22937493
|
A | G | 1 | a0001c0001t0067 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8096T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 8096 | chr7 | 22937493 | |||||
chr7:22937535
|
G | C | 2 | a0001c0001t0073a0007c0009t0074 | 2 | HG02976.hp2 NA19001.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8054C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 8054 | chr7 | 22937535 | |||||
chr7:22937537
|
G | A | 1 | a0001c0002t0096 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8052C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 8052 | chr7 | 22937537 | |||||
chr7:22937633
|
G | C | 1 | a0001c0001t0061 | 1 | NA18973.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7956C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 7956 | chr7 | 22937633 | |||||
chr7:22937902
|
T | C | 1 | a0001c0001t0073 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7687A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 7687 | chr7 | 22937902 | |||||
chr7:22937904
|
C | T | 1 | a0001c0001t0043 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7685G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 7685 | chr7 | 22937904 | |||||
chr7:22938049
|
T | G | 55 | a0001c0001t0007a0001c0001t0013a0001c0001t0014others(52): Show | 171 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*7540A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 7540 | chr7 | 22938049 | |||||
chr7:22938069
|
T | C | 1 | a0001c0002t0039 | 2 | HG01074.hp2 HG02602.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7520A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 7520 | chr7 | 22938069 | |||||
chr7:22938160
|
A | T | 1 | a0001c0001t0086 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7429T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 7429 | chr7 | 22938160 | |||||
chr7:22938193
|
G | A | 3 | a0001c0001t0024a0001c0001t0042a0001c0001t0043 | 4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7396C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 7396 | chr7 | 22938193 | |||||
chr7:22938294
|
C | T | 1 | a0001c0001t0062 | 1 | NA19079.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7295G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 7295 | chr7 | 22938294 | |||||
chr7:22938350
|
A | G | 4 | a0001c0001t0024a0001c0001t0042a0001c0001t0043others(1): Show | 5 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*7239T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 7239 | chr7 | 22938350 | |||||
chr7:22938527
|
A | C | 55 | a0001c0001t0007a0001c0001t0013a0001c0001t0014others(52): Show | 171 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*7062T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 7062 | chr7 | 22938527 | |||||
chr7:22938567
|
T | C | 55 | a0001c0001t0007a0001c0001t0013a0001c0001t0014others(52): Show | 171 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*7022A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 7022 | chr7 | 22938567 | |||||
chr7:22938675
|
C | G | 1 | a0001c0002t0111 | 1 | NA19083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6914G>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 6914 | chr7 | 22938675 | |||||
chr7:22938756
|
A | T | 26 | a0001c0001t0004a0001c0001t0008a0001c0001t0010others(23): Show | 78 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*6833T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 6833 | chr7 | 22938756 | |||||
chr7:22938796
|
A | G | 1 | a0001c0001t0077 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6793T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 6793 | chr7 | 22938796 | |||||
chr7:22938836
|
TCA | T | 54 | a0001c0001t0007a0001c0001t0013a0001c0001t0014others(51): Show | 169 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(166): Show |
3_prime_UTR_variant | MODIFIER | c.*6751_*6752delTG | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 6751 | chr7 | 22938836 | |||||
chr7:22938888
|
T | A | 1 | a0001c0002t0097 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6701A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 6701 | chr7 | 22938888 | |||||
chr7:22938920
|
T | C | 2 | a0001c0002t0105a0001c0002t0106 | 2 | NA19077.hp1 NA19079.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6669A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 6669 | chr7 | 22938920 | |||||
chr7:22938968
|
G | A | 61 | a0001c0001t0007a0001c0001t0013a0001c0001t0014others(58): Show | 178 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(175): Show |
3_prime_UTR_variant | MODIFIER | c.*6621C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 6621 | chr7 | 22938968 | |||||
chr7:22939307
|
A | G | 55 | a0001c0001t0007a0001c0001t0013a0001c0001t0014others(52): Show | 171 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*6282T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 6282 | chr7 | 22939307 | |||||
chr7:22939478
|
A | G | 55 | a0001c0001t0007a0001c0001t0013a0001c0001t0014others(52): Show | 171 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*6111T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 6111 | chr7 | 22939478 | |||||
chr7:22939503
|
T | C | 1 | a0001c0002t0098 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6086A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 6086 | chr7 | 22939503 | |||||
chr7:22939519
|
C | T | 1 | a0001c0001t0027 | 2 | HG01257.hp1 HG01258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6070G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 6070 | chr7 | 22939519 | |||||
chr7:22939536
|
C | T | 1 | a0001c0001t0079 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6053G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 6053 | chr7 | 22939536 | |||||
chr7:22939622
|
C | T | 1 | a0001c0002t0100 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5967G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5967 | chr7 | 22939622 | |||||
chr7:22939779
|
C | A | 22 | a0001c0001t0004a0001c0001t0008a0001c0001t0010others(19): Show | 73 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*5810G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5810 | chr7 | 22939779 | |||||
chr7:22939914
|
G | A | 2 | a0001c0001t0056a0001c0001t0057 | 2 | HG00639.hp1 HG00733.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5675C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5675 | chr7 | 22939914 | |||||
chr7:22939924
|
T | A | 1 | a0001c0002t0045 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5665A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5665 | chr7 | 22939924 | |||||
chr7:22940013
|
T | C | 8 | a0001c0001t0007a0001c0002t0007a0001c0002t0018others(5): Show | 29 | HG01169.hp1 HG02004.hp1 HG02155.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*5576A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5576 | chr7 | 22940013 | |||||
chr7:22940090
|
C | A | 1 | a0001c0002t0099 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5499G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5499 | chr7 | 22940090 | |||||
chr7:22940094
|
T | G | 1 | a0001c0001t0073 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5495A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5495 | chr7 | 22940094 | |||||
chr7:22940167
|
A | C | 1 | a0001c0001t0076 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5422T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5422 | chr7 | 22940167 | |||||
chr7:22940220
|
T | C | 8 | a0001c0001t0007a0001c0002t0007a0001c0002t0018others(5): Show | 29 | HG01169.hp1 HG02004.hp1 HG02155.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*5369A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5369 | chr7 | 22940220 | |||||
chr7:22940236
|
G | GT | 6 | a0001c0001t0003a0001c0001t0031a0001c0001t0057others(3): Show | 32 | HG00558.hp2 HG00639.hp1 HG01070.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*5352dupA | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5352 | chr7 | 22940236 | |||||
chr7:22940236
|
G | GTT | 8 | a0001c0001t0006a0001c0001t0027a0001c0001t0056others(5): Show | 25 | HG00733.hp2 HG01099.hp1 HG01257.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*5351_*5352dupAA | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5352 | chr7 | 22940236 | |||||
chr7:22940236
|
G | GTTT | 4 | a0001c0001t0009a0001c0001t0025a0001c0001t0048others(1): Show | 17 | HG00438.hp1 HG00438.hp2 HG00673.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*5350_*5352dupAAA | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5352 | chr7 | 22940236 | |||||
chr7:22940236
|
G | GTTTT | 3 | a0001c0001t0016a0001c0001t0046a0001c0001t0047 | 8 | HG00639.hp2 HG01255.hp2 HG02922.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5349_*5352dupAAAA | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5352 | chr7 | 22940236 | |||||
chr7:22940236
|
GT | G | 2 | a0001c0001t0019a0001c0001t0020 | 6 | HG01069.hp2 HG01993.hp2 HG02897.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5352delA | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5352 | chr7 | 22940236 | |||||
chr7:22940236
|
GTTTTT | G | 6 | a0001c0001t0026a0001c0001t0032a0001c0001t0078others(3): Show | 8 | HG01081.hp2 HG02486.hp1 HG02622.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5348_*5352delAAAA others(1): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5348 | chr7 | 22940236 | |||||
chr7:22940236
|
GTTTTTT | G | 12 | a0001c0001t0004a0001c0001t0008a0001c0001t0010others(9): Show | 61 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*5347_*5352delAAAA others(2): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5347 | chr7 | 22940236 | |||||
chr7:22940236
|
GTTTTTTT others(1): Show |
G | 13 | a0001c0001t0014a0001c0001t0073a0001c0001t0083others(10): Show | 24 | HG02055.hp1 HG02155.hp1 HG02698.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*5345_*5352delAAAA others(4): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5345 | chr7 | 22940236 | |||||
chr7:22940236
|
GTTTTTTT others(2): Show |
G | 45 | a0001c0001t0007a0001c0001t0013a0001c0001t0024others(42): Show | 147 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(144): Show |
3_prime_UTR_variant | MODIFIER | c.*5344_*5352delAAAA others(5): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5344 | chr7 | 22940236 | |||||
chr7:22940236
|
GTTTTTTT others(3): Show |
G | 1 | a0001c0002t0106 | 1 | NA19077.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5343_*5352delAAAA others(6): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5343 | chr7 | 22940236 | |||||
chr7:22940236
|
GTTTTTTT others(4): Show |
G | 1 | a0001c0001t0017 | 4 | NA18965.hp2 NA18984.hp1 NA18999.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5342_*5352delAAAA others(7): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5342 | chr7 | 22940236 | |||||
chr7:22940236
|
GTTTTTTT others(6): Show |
G | 1 | a0001c0001t0030 | 2 | HG02109.hp2 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5340_*5352delAAAA others(9): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5340 | chr7 | 22940236 | |||||
chr7:22940236
|
GTTTTTTT others(9): Show |
G | 1 | a0001c0001t0064 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5337_*5352delAAAA others(12): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5337 | chr7 | 22940236 | |||||
chr7:22940236
|
GTTTTTTT others(16): Show |
G | 2 | a0001c0002t0018a0001c0002t0023 | 7 | NA18943.hp2 NA18984.hp2 NA19005.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5330_*5352delAAAA others(19): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5330 | chr7 | 22940236 | |||||
chr7:22940238
|
T | G | 1 | a0001c0001t0070 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5351A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5351 | chr7 | 22940238 | |||||
chr7:22940250
|
T | G | 3 | a0001c0001t0024a0001c0001t0042a0001c0001t0043 | 4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5339A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5339 | chr7 | 22940250 | |||||
chr7:22940252
|
T | G | 1 | a0001c0001t0026 | 2 | HG03491.hp2 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5337A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5337 | chr7 | 22940252 | |||||
chr7:22940253
|
T | G | 11 | a0001c0001t0004a0001c0001t0008a0001c0001t0010others(8): Show | 60 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*5336A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5336 | chr7 | 22940253 | |||||
chr7:22940256
|
T | G | 1 | a0002c0004t0029 | 2 | HG02818.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5333A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5333 | chr7 | 22940256 | |||||
chr7:22940338
|
G | A | 1 | a0001c0001t0082 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5251C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5251 | chr7 | 22940338 | |||||
chr7:22940400
|
C | T | 1 | a0001c0001t0042 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5189G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5189 | chr7 | 22940400 | |||||
chr7:22940542
|
G | A | 55 | a0001c0001t0007a0001c0001t0013a0001c0001t0014others(52): Show | 171 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*5047C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5047 | chr7 | 22940542 | |||||
chr7:22940552
|
A | G | 2 | a0001c0001t0019a0001c0001t0059 | 4 | HG01069.hp2 HG01071.hp1 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5037T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 5037 | chr7 | 22940552 | |||||
chr7:22940641
|
G | A | 55 | a0001c0001t0007a0001c0001t0013a0001c0001t0014others(52): Show | 171 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*4948C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 4948 | chr7 | 22940641 | |||||
chr7:22940659
|
C | T | 4 | a0001c0001t0015a0001c0001t0053a0001c0001t0054others(1): Show | 9 | HG00738.hp2 HG01168.hp2 HG01169.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4930G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 4930 | chr7 | 22940659 | |||||
chr7:22940679
|
C | A | 8 | a0001c0001t0032a0001c0001t0076a0001c0001t0077others(5): Show | 9 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4910G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 4910 | chr7 | 22940679 | |||||
chr7:22940743
|
G | A | 1 | a0001c0002t0023 | 3 | NA18984.hp2 NA19058.hp2 NA19062.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4846C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 4846 | chr7 | 22940743 | |||||
chr7:22940750
|
G | T | 1 | a0001c0002t0085 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4839C>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 4839 | chr7 | 22940750 | |||||
chr7:22940797
|
T | C | 1 | a0001c0001t0073 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4792A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 4792 | chr7 | 22940797 | |||||
chr7:22940819
|
CT | C | 8 | a0001c0001t0050a0001c0001t0055a0001c0001t0065others(5): Show | 8 | HG02145.hp1 HG02559.hp1 HG02735.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4769delA | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 4769 | chr7 | 22940819 | |||||
chr7:22940875
|
A | G | 1 | a0001c0002t0084 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4714T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 4714 | chr7 | 22940875 | |||||
chr7:22941019
|
C | A | 22 | a0001c0001t0004a0001c0001t0008a0001c0001t0010others(19): Show | 73 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*4570G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 4570 | chr7 | 22941019 | |||||
chr7:22941221
|
T | C | 1 | a0001c0001t0030 | 2 | HG02109.hp2 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4368A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 4368 | chr7 | 22941221 | |||||
chr7:22941234
|
A | G | 1 | a0001c0001t0058 | 1 | NA19077.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4355T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 4355 | chr7 | 22941234 | |||||
chr7:22941310
|
A | AAC | 55 | a0001c0001t0007a0001c0001t0013a0001c0001t0014others(52): Show | 171 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*4278_*4279insGT | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 4278 | chr7 | 22941310 | |||||
chr7:22941368
|
C | G | 2 | a0001c0002t0108a0001c0002t0109 | 2 | NA18991.hp2 NA19086.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4221G>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 4221 | chr7 | 22941368 | |||||
chr7:22941672
|
T | C | 1 | a0007c0009t0074 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3917A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 3917 | chr7 | 22941672 | |||||
chr7:22941702
|
A | C | 1 | a0001c0001t0079 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3887T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 3887 | chr7 | 22941702 | |||||
chr7:22941785
|
T | G | 27 | a0001c0001t0004a0001c0001t0008a0001c0001t0010others(24): Show | 79 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*3804A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 3804 | chr7 | 22941785 | |||||
chr7:22941909
|
T | C | 55 | a0001c0001t0007a0001c0001t0013a0001c0001t0014others(52): Show | 171 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*3680A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 3680 | chr7 | 22941909 | |||||
chr7:22942081
|
T | C | 1 | a0001c0001t0072 | 1 | NA19089.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3508A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 3508 | chr7 | 22942081 | |||||
chr7:22942323
|
G | A | 1 | a0001c0001t0010 | 10 | HG00738.hp1 HG01106.hp1 HG01261.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3266C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 3266 | chr7 | 22942323 | |||||
chr7:22942323
|
G | T | 1 | a0001c0002t0103 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3266C>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 3266 | chr7 | 22942323 | |||||
chr7:22942588
|
T | C | 55 | a0001c0001t0007a0001c0001t0013a0001c0001t0014others(52): Show | 171 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*3001A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 3001 | chr7 | 22942588 | |||||
chr7:22942613
|
C | A | 4 | a0001c0001t0015a0001c0001t0053a0001c0001t0054others(1): Show | 9 | HG00738.hp2 HG01168.hp2 HG01169.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2976G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 2976 | chr7 | 22942613 | |||||
chr7:22942711
|
A | C | 1 | a0001c0001t0031 | 2 | NA18952.hp1 NA18988.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2878T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 2878 | chr7 | 22942711 | |||||
chr7:22942893
|
T | C | 1 | a0007c0009t0074 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2696A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 2696 | chr7 | 22942893 | |||||
chr7:22942905
|
T | C | 1 | a0001c0001t0051 | 1 | NA18612.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2684A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 2684 | chr7 | 22942905 | |||||
chr7:22942928
|
G | A | 22 | a0001c0001t0004a0001c0001t0008a0001c0001t0010others(19): Show | 73 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*2661C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 2661 | chr7 | 22942928 | |||||
chr7:22943130
|
G | T | 4 | a0001c0001t0015a0001c0001t0053a0001c0001t0054others(1): Show | 9 | HG00738.hp2 HG01168.hp2 HG01169.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2459C>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 2459 | chr7 | 22943130 | |||||
chr7:22943206
|
CAT | C | 9 | a0001c0002t0005a0001c0002t0037a0001c0002t0038others(6): Show | 35 | HG00280.hp2 HG01074.hp2 HG01175.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*2381_*2382delAT | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 2381 | chr7 | 22943206 | |||||
chr7:22943391
|
T | C | 1 | a0001c0002t0107 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2198A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 2198 | chr7 | 22943391 | |||||
chr7:22943481
|
C | T | 1 | a0001c0001t0031 | 2 | NA18952.hp1 NA18988.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2108G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 2108 | chr7 | 22943481 | |||||
chr7:22943620
|
C | T | 8 | a0001c0001t0015a0001c0001t0032a0001c0001t0053others(5): Show | 14 | HG00738.hp2 HG01081.hp2 HG01168.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1969G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 1969 | chr7 | 22943620 | |||||
chr7:22943777
|
G | T | 1 | a0001c0001t0031 | 2 | NA18952.hp1 NA18988.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1812C>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 1812 | chr7 | 22943777 | |||||
chr7:22943981
|
T | C | 26 | a0001c0001t0004a0001c0001t0008a0001c0001t0010others(23): Show | 78 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*1608A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 1608 | chr7 | 22943981 | |||||
chr7:22944083
|
A | T | 83 | a0001c0001t0004a0001c0001t0007a0001c0001t0008others(80): Show | 252 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(249): Show |
3_prime_UTR_variant | MODIFIER | c.*1506T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 1506 | chr7 | 22944083 | |||||
chr7:22944161
|
A | G | 1 | a0001c0001t0083 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1428T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 1428 | chr7 | 22944161 | |||||
chr7:22944235
|
T | C | 10 | a0001c0001t0052a0001c0002t0001a0001c0002t0040others(7): Show | 41 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1354A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 1354 | chr7 | 22944235 | |||||
chr7:22944271
|
T | C | 85 | a0001c0001t0004a0001c0001t0007a0001c0001t0008others(82): Show | 254 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(251): Show |
3_prime_UTR_variant | MODIFIER | c.*1318A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 1318 | chr7 | 22944271 | |||||
chr7:22944281
|
A | G | 1 | a0003c0003t0075 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1308T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 1308 | chr7 | 22944281 | |||||
chr7:22944341
|
A | G | 1 | a0001c0002t0112 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1248T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 1248 | chr7 | 22944341 | |||||
chr7:22944731
|
A | T | 3 | a0001c0001t0024a0001c0001t0042a0001c0001t0043 | 4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*858T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 858 | chr7 | 22944731 | |||||
chr7:22945006
|
T | C | 1 | a0001c0001t0082 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*583A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 583 | chr7 | 22945006 | |||||
chr7:22945137
|
C | A | 1 | a0001c0001t0031 | 2 | NA18952.hp1 NA18988.hp1 |
3_prime_UTR_variant | MODIFIER | c.*452G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 452 | chr7 | 22945137 | |||||
chr7:22945152
|
C | T | 3 | a0001c0001t0024a0001c0001t0042a0001c0001t0043 | 4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*437G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 437 | chr7 | 22945152 | |||||
chr7:22945153
|
A | C | 55 | a0001c0001t0007a0001c0001t0013a0001c0001t0014others(52): Show | 171 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*436T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 436 | chr7 | 22945153 | |||||
chr7:22945154
|
G | A | 55 | a0001c0001t0007a0001c0001t0013a0001c0001t0014others(52): Show | 171 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*435C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 435 | chr7 | 22945154 | |||||
chr7:22945205
|
T | C | 81 | a0001c0001t0004a0001c0001t0007a0001c0001t0008others(78): Show | 249 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(246): Show |
3_prime_UTR_variant | MODIFIER | c.*384A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 384 | chr7 | 22945205 | |||||
chr7:22945217
|
C | G | 2 | a0001c0001t0056a0001c0001t0057 | 2 | HG00639.hp1 HG00733.hp2 |
3_prime_UTR_variant | MODIFIER | c.*372G>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 372 | chr7 | 22945217 | |||||
chr7:22945348
|
A | G | 19 | a0001c0001t0004a0001c0001t0008a0001c0001t0010others(16): Show | 71 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*241T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 241 | chr7 | 22945348 | |||||
chr7:22945391
|
A | C | 10 | a0001c0001t0004a0001c0001t0010a0001c0001t0025others(7): Show | 43 | HG00423.hp1 HG00544.hp2 HG00738.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*198T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 198 | chr7 | 22945391 | |||||
chr7:22945512
|
G | C | 1 | a0001c0002t0112 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*77C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 77 | chr7 | 22945512 | |||||
chr7:22945523
|
C | T | 1 | a0001c0002t0045 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*66G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 11/11 | 66 | chr7 | 22945523 | |||||
chr7:23014007
|
C | T | 1 | a0001c0001t0044 | 1 | HG00280.hp1 | 5_prime_UTR_variant | MODIFIER | c.-111G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/11 | 22896 | chr7 | 23014007 | |||||
chr7:23014059
|
T | G | 1 | a0001c0002t0113 | 1 | NA19090.hp2 | 5_prime_UTR_variant | MODIFIER | c.-163A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/11 | 22948 | chr7 | 23014059 | |||||
chr7:23014078
|
TCTCA | T | 3 | a0001c0001t0024a0001c0001t0042a0001c0001t0043 | 4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-186_-183delTGAG | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/11 | 22968 | chr7 | 23014078 | |||||
chr7:23014098
|
G | A | 1 | a0001c0001t0114 | 1 | NA19074.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-202C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/11 | chr7 | 23014098 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:22946174
|
A | C | 5 | a0001c0001t0065g0075a0001c0001t0067g0072a0001c0001t0068g0087others(2): Show | 5 | HG02145.hp1 HG02559.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.992-11T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22946174 | ||||||
chr7:22946249
|
T | C | 61 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(58): Show | 79 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.992-86A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22946249 | ||||||
chr7:22946332
|
G | A | 1 | a0001c0001t0077g0052 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.992-169C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22946332 | ||||||
chr7:22946342
|
C | G | 57 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(54): Show | 75 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.992-179G>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22946342 | ||||||
chr7:22946460
|
T | C | 1 | a0001c0001t0073g0336 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.992-297A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22946460 | ||||||
chr7:22946488
|
G | A | 30 | a0001c0002t0005g0019a0001c0002t0005g0024a0001c0002t0005g0030others(27): Show | 33 | HG00280.hp2 HG01074.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.992-325C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22946488 | ||||||
chr7:22946498
|
C | T | 6 | a0001c0001t0002g0064a0001c0001t0002g0066a0001c0001t0002g0068others(3): Show | 6 | HG00639.hp2 HG01243.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.992-335G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22946498 | ||||||
chr7:22946748
|
A | G | 1 | a0001c0001t0079g0054 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.992-585T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22946748 | ||||||
chr7:22946829
|
A | G | 344 | a0001c0001t0002g0063a0001c0001t0002g0064a0001c0001t0002g0066others(341): Show | 383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.992-666T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22946829 | ||||||
chr7:22946886
|
T | C | 1 | a0001c0002t0040g0228 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.992-723A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22946886 | ||||||
chr7:22947160
|
G | A | 1 | a0001c0002t0001g0248 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.992-997C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22947160 | ||||||
chr7:22947171
|
G | A | 1 | a0001c0002t0005g0302 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.992-1008C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22947171 | ||||||
chr7:22947511
|
A | G | 1 | a0001c0002t0095g0227 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.992-1348T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22947511 | ||||||
chr7:22947741
|
A | AGT | 223 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(220): Show | 256 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.992-1579_992-1578i others(4): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22947741 | ||||||
chr7:22947870
|
A | G | 27 | a0001c0001t0007g0221a0001c0002t0007g0006a0001c0002t0007g0204others(24): Show | 31 | HG01169.hp1 HG02004.hp1 HG02155.hp2 others(28): Show |
intron_variant | MODIFIER | c.992-1707T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22947870 | ||||||
chr7:22947881
|
G | A | 169 | a0001c0001t0007g0221a0001c0001t0013g0059a0001c0001t0013g0070others(166): Show | 187 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.992-1718C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22947881 | ||||||
chr7:22948343
|
T | C | 50 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(47): Show | 68 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.992-2180A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22948343 | ||||||
chr7:22948608
|
G | A | 1 | a0001c0002t0007g0223 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.992-2445C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22948608 | ||||||
chr7:22948704
|
G | C | 1 | a0001c0002t0099g0269 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.992-2541C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22948704 | ||||||
chr7:22948762
|
A | G | 86 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(83): Show | 111 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.992-2599T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22948762 | ||||||
chr7:22948969
|
G | C | 153 | a0001c0001t0007g0221a0001c0001t0013g0059a0001c0001t0013g0070others(150): Show | 168 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.992-2806C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22948969 | ||||||
chr7:22949201
|
A | G | 207 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(204): Show | 240 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.992-3038T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22949201 | ||||||
chr7:22949224
|
T | C | 1 | a0001c0002t0001g0245 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.992-3061A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22949224 | ||||||
chr7:22949283
|
A | G | 4 | a0001c0001t0024g0026a0001c0001t0024g0027a0001c0001t0042g0025others(1): Show | 4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.992-3120T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22949283 | ||||||
chr7:22949386
|
A | G | 1 | a0001c0002t0007g0204 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.992-3223T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22949386 | ||||||
chr7:22949469
|
T | C | 2 | a0001c0001t0036g0031a0001c0001t0036g0032 | 2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.992-3306A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22949469 | ||||||
chr7:22949521
|
C | T | 51 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(48): Show | 69 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.992-3358G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22949521 | ||||||
chr7:22949522
|
G | A | 1 | a0001c0001t0086g0081 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.992-3359C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22949522 | ||||||
chr7:22949585
|
A | T | 218 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(215): Show | 251 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.992-3422T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22949585 | ||||||
chr7:22949623
|
G | A | 2 | a0001c0002t0007g0309a0001c0002t0088g0208 | 2 | NA18970.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.992-3460C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22949623 | ||||||
chr7:22949722
|
A | G | 2 | a0001c0001t0009g0144a0001c0001t0062g0148 | 2 | HG00673.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.992-3559T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22949722 | ||||||
chr7:22949800
|
C | A | 2 | a0001c0002t0108g0240a0001c0002t0109g0255 | 2 | NA18991.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.992-3637G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22949800 | ||||||
chr7:22950027
|
A | C | 9 | a0001c0001t0032g0047a0001c0001t0032g0048a0001c0001t0076g0345others(6): Show | 9 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.992-3864T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22950027 | ||||||
chr7:22950141
|
T | A | 2 | a0001c0001t0032g0048a0001c0001t0078g0049 | 2 | HG01081.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.992-3978A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22950141 | ||||||
chr7:22950257
|
C | T | 1 | a0003c0003t0081g0050 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.992-4094G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22950257 | ||||||
chr7:22950339
|
T | C | 12 | a0001c0002t0005g0019a0001c0002t0005g0030a0001c0002t0005g0272others(9): Show | 13 | HG02040.hp2 HG02056.hp1 HG02071.hp2 others(10): Show |
intron_variant | MODIFIER | c.992-4176A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22950339 | ||||||
chr7:22950365
|
T | A | 57 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(54): Show | 75 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.992-4202A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22950365 | ||||||
chr7:22950426
|
T | C | 50 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(47): Show | 68 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.992-4263A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22950426 | ||||||
chr7:22950654
|
G | A | 1 | a0001c0001t0073g0336 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.992-4491C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22950654 | ||||||
chr7:22950840
|
T | C | 1 | a0001c0001t0035g0069 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.992-4677A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22950840 | ||||||
chr7:22950989
|
C | T | 5 | a0001c0001t0015g0002a0001c0001t0015g0037a0001c0001t0015g0038others(2): Show | 8 | HG00738.hp2 HG01168.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.992-4826G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22950989 | ||||||
chr7:22950996
|
T | C | 1 | a0001c0001t0004g0332 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.992-4833A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22950996 | ||||||
chr7:22951033
|
A | G | 1 | a0001c0001t0082g0188 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.992-4870T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22951033 | ||||||
chr7:22951228
|
C | T | 1 | a0001c0001t0009g0172 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.992-5065G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22951228 | ||||||
chr7:22951356
|
C | T | 1 | a0001c0001t0008g0315 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.992-5193G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22951356 | ||||||
chr7:22951491
|
A | G | 7 | a0001c0001t0015g0002a0001c0001t0015g0037a0001c0001t0015g0038others(4): Show | 10 | HG00738.hp2 HG01168.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.992-5328T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22951491 | ||||||
chr7:22951543
|
T | A | 3 | a0001c0001t0032g0047a0001c0001t0032g0048a0001c0001t0078g0049 | 3 | HG01081.hp2 HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.992-5380A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22951543 | ||||||
chr7:22951569
|
C | CATAAA | 158 | a0001c0001t0007g0221a0001c0001t0013g0059a0001c0001t0013g0070others(155): Show | 173 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.992-5407_992-5406i others(7): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22951569 | ||||||
chr7:22951783
|
C | G | 1 | a0001c0001t0004g0020 | 2 | NA18966.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.992-5620G>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22951783 | ||||||
chr7:22952195
|
G | A | 1 | a0001c0002t0001g0244 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.992-6032C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22952195 | ||||||
chr7:22952263
|
A | G | 156 | a0001c0001t0007g0221a0001c0001t0013g0059a0001c0001t0013g0070others(153): Show | 171 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.992-6100T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22952263 | ||||||
chr7:22952342
|
T | C | 1 | a0001c0001t0016g0143 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.992-6179A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22952342 | ||||||
chr7:22952366
|
A | G | 106 | a0001c0001t0007g0221a0001c0001t0052g0311a0001c0002t0001g0001others(103): Show | 120 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.992-6203T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22952366 | ||||||
chr7:22952421
|
C | T | 34 | a0001c0001t0052g0311a0001c0002t0001g0001a0001c0002t0001g0007others(31): Show | 41 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.992-6258G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22952421 | ||||||
chr7:22952466
|
G | A | 1 | a0001c0001t0065g0075 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.992-6303C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22952466 | ||||||
chr7:22952692
|
C | T | 1 | a0001c0001t0003g0077 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.992-6529G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22952692 | ||||||
chr7:22952909
|
T | A | 1 | a0007c0009t0074g0344 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.992-6746A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22952909 | ||||||
chr7:22952999
|
C | T | 154 | a0001c0001t0007g0221a0001c0001t0013g0059a0001c0001t0013g0070others(151): Show | 169 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.992-6836G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22952999 | ||||||
chr7:22953010
|
A | G | 10 | a0001c0001t0008g0023a0001c0001t0008g0315a0001c0001t0008g0318others(7): Show | 11 | HG01256.hp2 HG01516.hp1 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.992-6847T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22953010 | ||||||
chr7:22953076
|
T | C | 4 | a0001c0001t0024g0026a0001c0001t0024g0027a0001c0001t0042g0025others(1): Show | 4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.992-6913A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22953076 | ||||||
chr7:22953168
|
C | A | 154 | a0001c0001t0007g0221a0001c0001t0013g0059a0001c0001t0013g0070others(151): Show | 169 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.992-7005G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22953168 | ||||||
chr7:22953224
|
G | A | 161 | a0001c0001t0007g0221a0001c0001t0013g0059a0001c0001t0013g0070others(158): Show | 176 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.991+7032C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22953224 | ||||||
chr7:22953338
|
G | A | 34 | a0001c0001t0052g0311a0001c0002t0001g0001a0001c0002t0001g0007others(31): Show | 41 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.991+6918C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22953338 | ||||||
chr7:22953349
|
T | C | 4 | a0001c0002t0011g0018a0001c0002t0011g0299a0001c0002t0022g0300others(1): Show | 5 | HG00733.hp1 HG01074.hp1 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.991+6907A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22953349 | ||||||
chr7:22953509
|
C | T | 1 | a0007c0009t0074g0344 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.991+6747G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22953509 | ||||||
chr7:22953714
|
T | C | 154 | a0001c0001t0007g0221a0001c0001t0013g0059a0001c0001t0013g0070others(151): Show | 169 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.991+6542A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22953714 | ||||||
chr7:22953864
|
C | T | 1 | a0001c0001t0003g0113 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.991+6392G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22953864 | ||||||
chr7:22953874
|
T | A | 134 | a0001c0001t0007g0221a0001c0001t0052g0311a0001c0002t0001g0001others(131): Show | 149 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.991+6382A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22953874 | ||||||
chr7:22953885
|
A | T | 134 | a0001c0001t0007g0221a0001c0001t0052g0311a0001c0002t0001g0001others(131): Show | 149 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.991+6371T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22953885 | ||||||
chr7:22954136
|
G | T | 1 | a0001c0001t0082g0188 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.991+6120C>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22954136 | ||||||
chr7:22954155
|
C | A | 4 | a0001c0001t0024g0026a0001c0001t0024g0027a0001c0001t0042g0025others(1): Show | 4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.991+6101G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22954155 | ||||||
chr7:22954322
|
A | T | 8 | a0001c0001t0032g0047a0001c0001t0032g0048a0001c0001t0077g0052others(5): Show | 8 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.991+5934T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22954322 | ||||||
chr7:22954348
|
T | G | 1 | a0001c0001t0073g0336 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.991+5908A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22954348 | ||||||
chr7:22954458
|
T | C | 5 | a0001c0001t0015g0002a0001c0001t0015g0037a0001c0001t0015g0038others(2): Show | 8 | HG00738.hp2 HG01168.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.991+5798A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22954458 | ||||||
chr7:22954486
|
A | T | 1 | a0001c0002t0007g0220 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.991+5770T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22954486 | ||||||
chr7:22954567
|
T | G | 1 | a0001c0002t0005g0024 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.991+5689A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22954567 | ||||||
chr7:22954715
|
CATT | C | 154 | a0001c0001t0007g0221a0001c0001t0013g0059a0001c0001t0013g0070others(151): Show | 169 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.991+5538_991+5540d others(5): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22954715 | ||||||
chr7:22954771
|
T | C | 1 | a0007c0009t0074g0344 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.991+5485A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22954771 | ||||||
chr7:22954811
|
AATTAAAT others(173): Show |
A | 1 | a0001c0002t0011g0265 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.991+5265_991+5444d others(2): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22954811 | ||||||
chr7:22955138
|
C | T | 1 | a0001c0001t0004g0335 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.991+5118G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22955138 | ||||||
chr7:22955261
|
T | C | 1 | a0001c0002t0100g0218 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.991+4995A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22955261 | ||||||
chr7:22955300
|
T | C | 163 | a0001c0001t0007g0221a0001c0001t0013g0059a0001c0001t0013g0070others(160): Show | 178 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.991+4956A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22955300 | ||||||
chr7:22955335
|
T | C | 34 | a0001c0001t0052g0311a0001c0002t0001g0001a0001c0002t0001g0007others(31): Show | 41 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.991+4921A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22955335 | ||||||
chr7:22955337
|
C | CTTAA | 156 | a0001c0001t0007g0221a0001c0001t0013g0059a0001c0001t0013g0070others(153): Show | 171 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.991+4915_991+4918d others(6): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22955337 | ||||||
chr7:22955358
|
A | G | 1 | a0001c0001t0004g0316 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.991+4898T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22955358 | ||||||
chr7:22955420
|
C | G | 1 | a0001c0002t0045g0036 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.991+4836G>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22955420 | ||||||
chr7:22955565
|
CA | C | 3 | a0001c0001t0036g0031a0001c0001t0036g0032a0001c0001t0073g0336 | 3 | HG02896.hp2 NA18522.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.991+4690delT | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22955565 | ||||||
chr7:22955859
|
C | T | 1 | a0001c0001t0003g0095 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.991+4397G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22955859 | ||||||
chr7:22955907
|
A | G | 4 | a0001c0001t0006g0153a0001c0001t0006g0159a0001c0001t0009g0142others(1): Show | 4 | NA18978.hp1 NA19009.hp1 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.991+4349T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22955907 | ||||||
chr7:22956094
|
T | C | 1 | a0001c0001t0004g0323 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.991+4162A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22956094 | ||||||
chr7:22956111
|
C | T | 160 | a0001c0001t0007g0221a0001c0001t0013g0070a0001c0001t0013g0103others(157): Show | 175 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.991+4145G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22956111 | ||||||
chr7:22956219
|
C | T | 6 | a0001c0001t0015g0002a0001c0001t0015g0037a0001c0001t0015g0038others(3): Show | 9 | HG00738.hp2 HG01168.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.991+4037G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22956219 | ||||||
chr7:22956327
|
G | A | 1 | a0001c0002t0001g0245 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.991+3929C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22956327 | ||||||
chr7:22956447
|
ATTAAG | A | 8 | a0001c0001t0032g0047a0001c0001t0032g0048a0001c0001t0077g0052others(5): Show | 8 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.991+3804_991+3808d others(7): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22956447 | ||||||
chr7:22956464
|
C | T | 1 | a0001c0001t0076g0345 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.991+3792G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22956464 | ||||||
chr7:22956541
|
CA | C | 152 | a0001c0001t0007g0221a0001c0001t0013g0059a0001c0001t0013g0070others(149): Show | 167 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.991+3714delT | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22956541 | ||||||
chr7:22956814
|
A | T | 1 | a0001c0002t0045g0036 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.991+3442T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22956814 | ||||||
chr7:22956892
|
T | A | 1 | a0001c0001t0082g0188 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.991+3364A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22956892 | ||||||
chr7:22957013
|
G | A | 2 | a0001c0002t0012g0189a0001c0002t0012g0190 | 2 | HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.991+3243C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22957013 | ||||||
chr7:22957042
|
T | A | 1 | a0001c0002t0091g0259 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.991+3214A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22957042 | ||||||
chr7:22957064
|
G | A | 1 | a0001c0002t0045g0036 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.991+3192C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22957064 | ||||||
chr7:22957174
|
A | G | 344 | a0001c0001t0002g0063a0001c0001t0002g0064a0001c0001t0002g0066others(341): Show | 383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.991+3082T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22957174 | ||||||
chr7:22957197
|
T | C | 1 | a0001c0001t0082g0188 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.991+3059A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22957197 | ||||||
chr7:22957206
|
C | T | 16 | a0001c0001t0003g0012a0001c0001t0003g0138a0001c0001t0003g0141others(13): Show | 17 | HG02015.hp2 HG02056.hp2 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.991+3050G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22957206 | ||||||
chr7:22957302
|
GA | G | 342 | a0001c0001t0002g0063a0001c0001t0002g0064a0001c0001t0002g0066others(339): Show | 381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.991+2953delT | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22957302 | ||||||
chr7:22957476
|
A | G | 1 | a0001c0001t0094g0111 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.991+2780T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22957476 | ||||||
chr7:22957493
|
A | G | 1 | a0001c0002t0045g0036 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.991+2763T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22957493 | ||||||
chr7:22957545
|
G | A | 167 | a0001c0001t0007g0221a0001c0001t0013g0059a0001c0001t0013g0070others(164): Show | 182 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.991+2711C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22957545 | ||||||
chr7:22957690
|
T | C | 1 | a0001c0001t0008g0325 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.991+2566A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22957690 | ||||||
chr7:22957820
|
G | A | 1 | a0001c0001t0002g0116 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.991+2436C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22957820 | ||||||
chr7:22957829
|
T | C | 6 | a0001c0001t0015g0002a0001c0001t0015g0037a0001c0001t0015g0038others(3): Show | 9 | HG00738.hp2 HG01168.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.991+2427A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22957829 | ||||||
chr7:22957842
|
TGA | T | 6 | a0001c0001t0015g0002a0001c0001t0015g0037a0001c0001t0015g0038others(3): Show | 9 | HG00738.hp2 HG01168.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.991+2412_991+2413d others(4): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22957842 | ||||||
chr7:22957986
|
A | C | 2 | a0001c0001t0003g0338a0001c0001t0003g0339 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.991+2270T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22957986 | ||||||
chr7:22957990
|
T | C | 3 | a0001c0001t0032g0047a0001c0001t0032g0048a0001c0001t0078g0049 | 3 | HG01081.hp2 HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.991+2266A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22957990 | ||||||
chr7:22958023
|
C | A | 47 | a0001c0002t0005g0019a0001c0002t0005g0024a0001c0002t0005g0030others(44): Show | 50 | HG00280.hp2 HG01074.hp2 HG01175.hp2 others(47): Show |
intron_variant | MODIFIER | c.991+2233G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22958023 | ||||||
chr7:22958329
|
G | T | 52 | a0001c0001t0002g0164a0001c0001t0002g0182a0001c0001t0003g0012others(49): Show | 57 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.991+1927C>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22958329 | ||||||
chr7:22958523
|
G | A | 3 | a0001c0001t0032g0047a0001c0001t0032g0048a0001c0001t0078g0049 | 3 | HG01081.hp2 HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.991+1733C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22958523 | ||||||
chr7:22958716
|
G | A | 2 | a0001c0001t0036g0031a0001c0001t0036g0032 | 2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.991+1540C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22958716 | ||||||
chr7:22958771
|
G | A | 1 | a0001c0001t0002g0163 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.991+1485C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22958771 | ||||||
chr7:22958855
|
G | A | 2 | a0001c0001t0036g0031a0001c0001t0036g0032 | 2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.991+1401C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22958855 | ||||||
chr7:22959014
|
A | G | 1 | a0001c0002t0103g0280 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.991+1242T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22959014 | ||||||
chr7:22959015
|
T | C | 6 | a0001c0001t0002g0202a0001c0001t0002g0343a0001c0001t0003g0093others(3): Show | 6 | HG00438.hp2 HG01106.hp2 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.991+1241A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22959015 | ||||||
chr7:22959192
|
T | G | 1 | a0001c0002t0005g0030 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.991+1064A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22959192 | ||||||
chr7:22959261
|
T | C | 4 | a0001c0001t0024g0026a0001c0001t0024g0027a0001c0001t0042g0025others(1): Show | 4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.991+995A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22959261 | ||||||
chr7:22959268
|
C | T | 199 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(196): Show | 229 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.991+988G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22959268 | ||||||
chr7:22959291
|
G | A | 150 | a0001c0001t0013g0059a0001c0001t0013g0070a0001c0001t0013g0103others(147): Show | 165 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.991+965C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22959291 | ||||||
chr7:22959357
|
T | C | 1 | a0001c0001t0003g0077 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.991+899A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22959357 | ||||||
chr7:22959453
|
T | C | 4 | a0001c0002t0011g0230a0001c0002t0022g0268a0001c0002t0084g0260others(1): Show | 4 | HG01192.hp1 HG01257.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.991+803A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22959453 | ||||||
chr7:22959588
|
A | G | 80 | a0001c0002t0001g0001a0001c0002t0001g0007a0001c0002t0001g0226others(77): Show | 90 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.991+668T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22959588 | ||||||
chr7:22959649
|
T | A | 1 | a0001c0001t0073g0336 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.991+607A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22959649 | ||||||
chr7:22959649
|
T | C | 1 | a0001c0001t0003g0077 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.991+607A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22959649 | ||||||
chr7:22959764
|
C | A | 7 | a0001c0001t0024g0026a0001c0001t0024g0027a0001c0001t0036g0031others(4): Show | 7 | HG01361.hp2 HG02559.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.991+492G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22959764 | ||||||
chr7:22960002
|
T | C | 1 | a0001c0002t0001g0246 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.991+254A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 10/10 | chr7 | 22960002 | ||||||
chr7:22960457
|
A | AAGATCAA others(3): Show |
4 | a0001c0001t0024g0026a0001c0001t0024g0027a0001c0001t0042g0025others(1): Show | 4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.832-43_832-42insAT others(8): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 9/10 | chr7 | 22960457 | ||||||
chr7:22960483
|
G | A | 1 | a0001c0001t0006g0099 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.832-68C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 9/10 | chr7 | 22960483 | ||||||
chr7:22960515
|
A | C | 3 | a0001c0001t0014g0100a0001c0001t0014g0102a0001c0001t0083g0123 | 3 | HG03239.hp1 HG03942.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.832-100T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 9/10 | chr7 | 22960515 | ||||||
chr7:22960572
|
G | A | 1 | a0001c0001t0010g0312 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.832-157C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 9/10 | chr7 | 22960572 | ||||||
chr7:22960787
|
C | T | 1 | a0001c0001t0049g0310 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.832-372G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 9/10 | chr7 | 22960787 | ||||||
chr7:22961042
|
A | C | 1 | a0007c0009t0074g0344 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.831+193T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 9/10 | chr7 | 22961042 | ||||||
chr7:22961062
|
T | A | 4 | a0001c0001t0024g0026a0001c0001t0024g0027a0001c0001t0042g0025others(1): Show | 4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+173A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 9/10 | chr7 | 22961062 | ||||||
chr7:22961064
|
A | T | 2 | a0001c0002t0005g0281a0001c0002t0103g0280 | 2 | HG02040.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.831+171T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 9/10 | chr7 | 22961064 | ||||||
chr7:22961081
|
A | G | 1 | a0001c0002t0099g0269 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.831+154T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 9/10 | chr7 | 22961081 | ||||||
chr7:22961164
|
G | GCTCT | 229 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(226): Show | 263 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.831+67_831+70dupAG others(2): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 9/10 | chr7 | 22961164 | ||||||
chr7:22961767
|
T | C | 1 | a0007c0009t0074g0344 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.744-445A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22961767 | ||||||
chr7:22961869
|
G | C | 1 | a0001c0001t0003g0129 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.744-547C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22961869 | ||||||
chr7:22961969
|
T | A | 1 | a0001c0001t0002g0297 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.744-647A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22961969 | ||||||
chr7:22962025
|
C | G | 1 | a0001c0001t0069g0073 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.744-703G>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22962025 | ||||||
chr7:22962034
|
T | C | 33 | a0001c0002t0001g0001a0001c0002t0001g0007a0001c0002t0001g0226others(30): Show | 40 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.744-712A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22962034 | ||||||
chr7:22962076
|
G | A | 2 | a0001c0001t0002g0071a0001c0001t0002g0132 | 2 | HG01109.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.744-754C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22962076 | ||||||
chr7:22962078
|
T | G | 1 | a0001c0002t0099g0269 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.744-756A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22962078 | ||||||
chr7:22962081
|
TC | T | 151 | a0001c0001t0013g0070a0001c0001t0013g0103a0001c0001t0013g0133others(148): Show | 166 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.744-760delG | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22962081 | ||||||
chr7:22962188
|
C | T | 1 | a0007c0009t0074g0344 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.744-866G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22962188 | ||||||
chr7:22962204
|
T | G | 2 | a0001c0001t0014g0080a0001c0001t0014g0090 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.744-882A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22962204 | ||||||
chr7:22962235
|
T | A | 4 | a0001c0002t0001g0007a0001c0002t0001g0258a0001c0002t0001g0271others(1): Show | 6 | HG00140.hp1 HG01070.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.744-913A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22962235 | ||||||
chr7:22962248
|
A | G | 1 | a0001c0001t0028g0147 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.744-926T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22962248 | ||||||
chr7:22962288
|
G | A | 4 | a0001c0002t0001g0007a0001c0002t0001g0258a0001c0002t0001g0271others(1): Show | 6 | HG00140.hp1 HG01070.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.744-966C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22962288 | ||||||
chr7:22962537
|
C | T | 33 | a0001c0002t0001g0001a0001c0002t0001g0007a0001c0002t0001g0226others(30): Show | 40 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.744-1215G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22962537 | ||||||
chr7:22962545
|
A | T | 164 | a0001c0001t0013g0070a0001c0001t0013g0103a0001c0001t0013g0133others(161): Show | 179 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.744-1223T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22962545 | ||||||
chr7:22962564
|
G | A | 3 | a0001c0001t0024g0026a0001c0001t0024g0027a0001c0001t0042g0025 | 3 | HG01361.hp2 HG02559.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.744-1242C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22962564 | ||||||
chr7:22962578
|
G | GA | 151 | a0001c0001t0009g0142a0001c0001t0009g0150a0001c0001t0013g0070others(148): Show | 166 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.744-1257dupT | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22962578 | ||||||
chr7:22962735
|
C | T | 47 | a0001c0002t0005g0019a0001c0002t0005g0024a0001c0002t0005g0030others(44): Show | 50 | HG00280.hp2 HG01074.hp2 HG01175.hp2 others(47): Show |
intron_variant | MODIFIER | c.744-1413G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22962735 | ||||||
chr7:22962741
|
C | A | 3 | a0001c0001t0002g0089a0001c0001t0002g0092a0001c0001t0003g0095 | 3 | NA18956.hp2 NA18981.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.744-1419G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22962741 | ||||||
chr7:22962754
|
T | C | 153 | a0001c0001t0013g0059a0001c0001t0013g0070a0001c0001t0013g0103others(150): Show | 168 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.744-1432A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22962754 | ||||||
chr7:22962757
|
C | A | 150 | a0001c0001t0013g0070a0001c0001t0013g0103a0001c0001t0013g0133others(147): Show | 165 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.744-1435G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22962757 | ||||||
chr7:22962779
|
G | T | 40 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(37): Show | 55 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.744-1457C>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22962779 | ||||||
chr7:22962805
|
C | T | 1 | a0001c0001t0082g0188 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.744-1483G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22962805 | ||||||
chr7:22962874
|
C | T | 151 | a0001c0001t0013g0070a0001c0001t0013g0103a0001c0001t0013g0133others(148): Show | 166 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.743+1541G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22962874 | ||||||
chr7:22962960
|
A | C | 1 | a0001c0002t0011g0265 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.743+1455T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22962960 | ||||||
chr7:22963138
|
C | A | 1 | a0001c0001t0076g0345 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.743+1277G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22963138 | ||||||
chr7:22963154
|
C | A | 3 | a0001c0001t0036g0031a0001c0001t0036g0032a0001c0001t0054g0042 | 3 | HG02109.hp1 HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.743+1261G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22963154 | ||||||
chr7:22963170
|
C | T | 1 | a0001c0001t0082g0188 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.743+1245G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22963170 | ||||||
chr7:22963171
|
A | G | 1 | a0001c0001t0077g0052 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.743+1244T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22963171 | ||||||
chr7:22963401
|
C | T | 1 | a0001c0001t0002g0163 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.743+1014G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22963401 | ||||||
chr7:22963409
|
G | A | 1 | a0001c0001t0003g0135 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.743+1006C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22963409 | ||||||
chr7:22963487
|
T | C | 12 | a0001c0002t0001g0001a0001c0002t0001g0226a0001c0002t0001g0237others(9): Show | 16 | NA18946.hp1 NA18954.hp1 NA18963.hp2 others(13): Show |
intron_variant | MODIFIER | c.743+928A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22963487 | ||||||
chr7:22963503
|
C | T | 1 | a0001c0002t0011g0301 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.743+912G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22963503 | ||||||
chr7:22963646
|
C | A | 1 | a0001c0001t0073g0336 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.743+769G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22963646 | ||||||
chr7:22963647
|
G | A | 4 | a0001c0001t0024g0026a0001c0001t0024g0027a0001c0001t0042g0025others(1): Show | 4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.743+768C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22963647 | ||||||
chr7:22963719
|
A | G | 22 | a0001c0001t0013g0059a0001c0001t0013g0070a0001c0001t0013g0103others(19): Show | 22 | HG00099.hp1 HG00544.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.743+696T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22963719 | ||||||
chr7:22963869
|
T | C | 1 | a0001c0002t0041g0249 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.743+546A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22963869 | ||||||
chr7:22964109
|
C | CA | 107 | a0001c0001t0003g0077a0001c0001t0009g0150a0001c0002t0001g0001others(104): Show | 121 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.743+305dupT | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22964109 | ||||||
chr7:22964395
|
G | A | 2 | a0003c0003t0075g0051a0003c0003t0081g0050 | 2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.743+20C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 8/10 | chr7 | 22964395 | ||||||
chr7:22964754
|
A | G | 210 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(207): Show | 240 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.627-223T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22964754 | ||||||
chr7:22964768
|
C | A | 1 | a0001c0001t0061g0146 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.627-237G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22964768 | ||||||
chr7:22964783
|
G | A | 162 | a0001c0001t0013g0059a0001c0001t0013g0070a0001c0001t0013g0103others(159): Show | 177 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.627-252C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22964783 | ||||||
chr7:22964834
|
C | T | 3 | a0001c0002t0007g0209a0001c0002t0007g0217a0001c0002t0101g0205 | 3 | HG02004.hp1 HG02273.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.627-303G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22964834 | ||||||
chr7:22964895
|
G | A | 2 | a0001c0001t0076g0345a0001c0001t0079g0054 | 2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.627-364C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22964895 | ||||||
chr7:22965012
|
T | C | 1 | a0001c0001t0027g0013 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.627-481A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22965012 | ||||||
chr7:22965129
|
A | AT | 8 | a0001c0001t0006g0104a0001c0001t0009g0106a0001c0001t0017g0117others(5): Show | 8 | NA18942.hp2 NA18965.hp2 NA18984.hp1 others(5): Show |
intron_variant | MODIFIER | c.627-599dupA | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22965129 | ||||||
chr7:22965131
|
TA | T | 197 | a0001c0001t0003g0077a0001c0001t0004g0008a0001c0001t0004g0009others(194): Show | 227 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.627-601delT | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22965131 | ||||||
chr7:22965144
|
A | G | 5 | a0001c0002t0007g0006a0001c0002t0007g0206a0001c0002t0007g0207others(2): Show | 7 | NA18956.hp1 NA18960.hp1 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.627-613T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22965144 | ||||||
chr7:22965219
|
T | G | 2 | a0001c0001t0026g0317a0001c0001t0026g0327 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.627-688A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22965219 | ||||||
chr7:22965421
|
A | G | 1 | a0001c0001t0080g0053 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.627-890T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22965421 | ||||||
chr7:22965431
|
G | T | 3 | a0001c0001t0004g0022a0001c0001t0004g0046a0001c0001t0051g0329 | 4 | HG01928.hp1 HG01978.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.627-900C>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22965431 | ||||||
chr7:22965457
|
C | T | 24 | a0001c0002t0007g0006a0001c0002t0007g0204a0001c0002t0007g0206others(21): Show | 28 | HG01169.hp1 HG02004.hp1 HG02155.hp2 others(25): Show |
intron_variant | MODIFIER | c.627-926G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22965457 | ||||||
chr7:22965483
|
T | G | 1 | a0007c0009t0074g0344 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.627-952A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22965483 | ||||||
chr7:22965528
|
C | T | 4 | a0001c0001t0019g0083a0001c0001t0019g0340a0001c0001t0019g0341others(1): Show | 4 | HG01069.hp2 HG01071.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.627-997G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22965528 | ||||||
chr7:22965594
|
T | TA | 38 | a0001c0001t0004g0008a0001c0001t0004g0331a0001c0001t0008g0324others(35): Show | 44 | HG01168.hp1 HG01169.hp1 HG01175.hp2 others(41): Show |
intron_variant | MODIFIER | c.627-1064dupT | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22965594 | ||||||
chr7:22965594
|
TA | T | 6 | a0001c0001t0006g0104a0001c0001t0019g0083a0001c0001t0028g0147others(3): Show | 6 | HG01069.hp2 NA18942.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.627-1064delT | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22965594 | ||||||
chr7:22965606
|
A | C | 2 | a0001c0001t0002g0071a0001c0001t0002g0132 | 2 | HG01109.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.627-1075T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22965606 | ||||||
chr7:22965746
|
C | T | 2 | a0001c0001t0076g0345a0001c0001t0079g0054 | 2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.627-1215G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22965746 | ||||||
chr7:22965881
|
G | A | 1 | a0001c0001t0016g0085 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.627-1350C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22965881 | ||||||
chr7:22966217
|
A | G | 1 | a0001c0001t0010g0043 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.627-1686T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22966217 | ||||||
chr7:22966301
|
T | C | 2 | a0001c0001t0002g0071a0001c0001t0002g0132 | 2 | HG01109.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.627-1770A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22966301 | ||||||
chr7:22966339
|
T | C | 46 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(43): Show | 61 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.627-1808A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22966339 | ||||||
chr7:22966364
|
T | C | 1 | a0001c0001t0082g0188 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.627-1833A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22966364 | ||||||
chr7:22966471
|
T | C | 26 | a0001c0002t0007g0006a0001c0002t0007g0204a0001c0002t0007g0206others(23): Show | 30 | HG01169.hp1 HG02004.hp1 HG02155.hp2 others(27): Show |
intron_variant | MODIFIER | c.627-1940A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22966471 | ||||||
chr7:22966534
|
T | C | 3 | a0001c0001t0032g0047a0001c0001t0032g0048a0001c0001t0078g0049 | 3 | HG01081.hp2 HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.627-2003A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22966534 | ||||||
chr7:22966615
|
T | C | 1 | a0001c0002t0113g0346 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.627-2084A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22966615 | ||||||
chr7:22966633
|
T | A | 1 | a0001c0002t0023g0222 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.627-2102A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22966633 | ||||||
chr7:22966674
|
A | G | 1 | a0001c0002t0001g0231 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.627-2143T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22966674 | ||||||
chr7:22966686
|
T | C | 1 | a0001c0002t0001g0231 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.627-2155A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22966686 | ||||||
chr7:22966933
|
A | G | 5 | a0001c0001t0002g0202a0001c0001t0002g0343a0001c0001t0003g0093others(2): Show | 5 | HG01106.hp2 HG01943.hp2 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.627-2402T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22966933 | ||||||
chr7:22967035
|
G | A | 2 | a0001c0001t0003g0167a0001c0001t0006g0174 | 2 | HG02056.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.627-2504C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22967035 | ||||||
chr7:22967051
|
T | C | 1 | a0001c0001t0020g0079 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.627-2520A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22967051 | ||||||
chr7:22967276
|
G | A | 3 | a0001c0001t0076g0345a0001c0001t0079g0054a0001c0001t0083g0123 | 3 | HG02622.hp2 HG02630.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.627-2745C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22967276 | ||||||
chr7:22967537
|
G | A | 39 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(36): Show | 54 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.627-3006C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22967537 | ||||||
chr7:22967588
|
T | C | 9 | a0001c0002t0011g0018a0001c0002t0011g0230a0001c0002t0011g0299others(6): Show | 10 | HG00733.hp1 HG01074.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.627-3057A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22967588 | ||||||
chr7:22967594
|
T | G | 40 | a0001c0001t0006g0153a0001c0001t0006g0159a0001c0001t0009g0139others(37): Show | 47 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.627-3063A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22967594 | ||||||
chr7:22967612
|
G | A | 3 | a0001c0002t0011g0018a0001c0002t0011g0299a0001c0002t0022g0300 | 4 | HG00733.hp1 HG01074.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.627-3081C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22967612 | ||||||
chr7:22967710
|
G | A | 2 | a0001c0001t0014g0100a0001c0001t0014g0102 | 2 | HG03942.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.627-3179C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22967710 | ||||||
chr7:22967897
|
C | T | 3 | a0001c0001t0080g0053a0003c0003t0075g0051a0003c0003t0081g0050 | 3 | HG02145.hp2 HG02486.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.627-3366G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22967897 | ||||||
chr7:22967898
|
G | A | 1 | a0001c0001t0016g0171 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.627-3367C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22967898 | ||||||
chr7:22967934
|
C | G | 3 | a0001c0002t0021g0233a0001c0002t0033g0229a0001c0002t0033g0303 | 3 | HG02886.hp1 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.627-3403G>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22967934 | ||||||
chr7:22968080
|
A | G | 9 | a0001c0001t0032g0047a0001c0001t0032g0048a0001c0001t0076g0345others(6): Show | 9 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.627-3549T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22968080 | ||||||
chr7:22968365
|
C | T | 1 | a0007c0009t0074g0344 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.627-3834G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22968365 | ||||||
chr7:22968371
|
A | T | 51 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(48): Show | 69 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.627-3840T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22968371 | ||||||
chr7:22968420
|
T | C | 1 | a0001c0001t0077g0052 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.627-3889A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22968420 | ||||||
chr7:22968566
|
A | T | 1 | a0001c0002t0045g0036 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.627-4035T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22968566 | ||||||
chr7:22968576
|
T | C | 5 | a0001c0001t0065g0075a0001c0001t0067g0072a0001c0001t0068g0087others(2): Show | 5 | HG02145.hp1 HG02559.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.627-4045A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22968576 | ||||||
chr7:22968589
|
T | C | 206 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(203): Show | 239 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(236): Show |
intron_variant | MODIFIER | c.627-4058A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22968589 | ||||||
chr7:22968598
|
A | C | 1 | a0001c0001t0061g0146 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.627-4067T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22968598 | ||||||
chr7:22968604
|
G | A | 1 | a0001c0001t0082g0188 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.627-4073C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22968604 | ||||||
chr7:22968698
|
C | T | 1 | a0001c0001t0077g0052 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.627-4167G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22968698 | ||||||
chr7:22968704
|
A | G | 1 | a0001c0001t0008g0315 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.627-4173T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22968704 | ||||||
chr7:22968751
|
G | A | 1 | a0001c0001t0009g0150 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.627-4220C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22968751 | ||||||
chr7:22968837
|
T | C | 137 | a0001c0001t0006g0153a0001c0001t0006g0159a0001c0001t0009g0139others(134): Show | 152 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.627-4306A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22968837 | ||||||
chr7:22968901
|
G | A | 1 | a0001c0002t0005g0277 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.627-4370C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22968901 | ||||||
chr7:22968985
|
C | T | 1 | a0001c0002t0001g0241 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.627-4454G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22968985 | ||||||
chr7:22969197
|
T | C | 2 | a0001c0002t0005g0287a0001c0002t0104g0293 | 2 | NA18987.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.627-4666A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22969197 | ||||||
chr7:22969305
|
G | A | 137 | a0001c0001t0006g0153a0001c0001t0006g0159a0001c0001t0009g0139others(134): Show | 152 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.627-4774C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22969305 | ||||||
chr7:22969318
|
T | TTG | 11 | a0001c0001t0032g0047a0001c0001t0032g0048a0001c0001t0076g0345others(8): Show | 11 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.627-4789_627-4788d others(4): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22969318 | ||||||
chr7:22969448
|
G | A | 7 | a0001c0001t0003g0157a0001c0001t0003g0338a0001c0001t0003g0339others(4): Show | 8 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.627-4917C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22969448 | ||||||
chr7:22969471
|
G | C | 1 | a0001c0001t0043g0028 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.627-4940C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22969471 | ||||||
chr7:22969507
|
T | C | 1 | a0001c0002t0005g0275 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.627-4976A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22969507 | ||||||
chr7:22969524
|
G | T | 3 | a0001c0001t0036g0031a0001c0001t0036g0032a0001c0001t0073g0336 | 3 | HG02896.hp2 NA18522.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.627-4993C>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22969524 | ||||||
chr7:22969525
|
G | GT | 8 | a0001c0001t0002g0126a0001c0001t0002g0164a0001c0001t0003g0093others(5): Show | 8 | HG00438.hp2 HG01516.hp2 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.627-4995dupA | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22969525 | ||||||
chr7:22969525
|
GT | G | 193 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(190): Show | 226 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(223): Show |
intron_variant | MODIFIER | c.627-4995delA | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22969525 | ||||||
chr7:22969526
|
T | G | 4 | a0001c0001t0036g0031a0001c0001t0036g0032a0001c0001t0073g0336others(1): Show | 4 | HG02896.hp2 NA18522.hp1 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.627-4995A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22969526 | ||||||
chr7:22970012
|
T | C | 3 | a0001c0001t0032g0047a0001c0001t0032g0048a0001c0001t0078g0049 | 3 | HG01081.hp2 HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.627-5481A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22970012 | ||||||
chr7:22970111
|
C | CACATGAA others(82): Show |
6 | a0001c0001t0015g0002a0001c0001t0015g0037a0001c0001t0015g0038others(3): Show | 9 | HG00738.hp2 HG01168.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.627-5669_627-5581d others(91): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22970111 | ||||||
chr7:22970135
|
T | C | 6 | a0001c0001t0002g0064a0001c0001t0002g0066a0001c0001t0002g0068others(3): Show | 6 | HG00639.hp2 HG01243.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.627-5604A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22970135 | ||||||
chr7:22970196
|
A | G | 1 | a0001c0002t0012g0194 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.627-5665T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22970196 | ||||||
chr7:22970276
|
T | C | 137 | a0001c0001t0006g0153a0001c0001t0006g0159a0001c0001t0009g0139others(134): Show | 152 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.627-5745A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22970276 | ||||||
chr7:22970342
|
T | C | 4 | a0001c0001t0024g0026a0001c0001t0024g0027a0001c0001t0042g0025others(1): Show | 4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.627-5811A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22970342 | ||||||
chr7:22970444
|
T | C | 177 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(174): Show | 207 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(204): Show |
intron_variant | MODIFIER | c.626+5766A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22970444 | ||||||
chr7:22970457
|
A | G | 1 | a0001c0001t0008g0021 | 2 | HG00642.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.626+5753T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22970457 | ||||||
chr7:22970525
|
C | CA | 4 | a0001c0001t0024g0026a0001c0001t0024g0027a0001c0001t0042g0025others(1): Show | 4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.626+5684dupT | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22970525 | ||||||
chr7:22970806
|
C | T | 2 | a0003c0003t0075g0051a0003c0003t0081g0050 | 2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.626+5404G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22970806 | ||||||
chr7:22970837
|
C | T | 1 | a0001c0002t0088g0208 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.626+5373G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22970837 | ||||||
chr7:22970859
|
G | A | 1 | a0001c0002t0011g0267 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.626+5351C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22970859 | ||||||
chr7:22970926
|
T | C | 80 | a0001c0002t0001g0001a0001c0002t0001g0007a0001c0002t0001g0226others(77): Show | 90 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.626+5284A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22970926 | ||||||
chr7:22971135
|
T | C | 1 | a0001c0001t0013g0306 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.626+5075A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22971135 | ||||||
chr7:22971210
|
C | T | 1 | a0001c0001t0094g0111 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.626+5000G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22971210 | ||||||
chr7:22971217
|
G | A | 3 | a0001c0001t0032g0047a0001c0001t0032g0048a0001c0001t0078g0049 | 3 | HG01081.hp2 HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.626+4993C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22971217 | ||||||
chr7:22971225
|
C | T | 4 | a0001c0001t0019g0083a0001c0001t0019g0340a0001c0001t0019g0341others(1): Show | 4 | HG01069.hp2 HG01071.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.626+4985G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22971225 | ||||||
chr7:22971418
|
A | G | 177 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(174): Show | 207 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(204): Show |
intron_variant | MODIFIER | c.626+4792T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22971418 | ||||||
chr7:22971573
|
C | T | 1 | a0001c0002t0098g0193 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.626+4637G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22971573 | ||||||
chr7:22971598
|
C | T | 3 | a0001c0002t0034g0057a0001c0002t0045g0036a0001c0002t0092g0056 | 3 | HG02055.hp1 HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.626+4612G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22971598 | ||||||
chr7:22971638
|
T | C | 15 | a0001c0001t0015g0002a0001c0001t0015g0037a0001c0001t0015g0038others(12): Show | 18 | HG00738.hp2 HG01081.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.626+4572A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22971638 | ||||||
chr7:22971657
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.626+4553G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22971657 | ||||||
chr7:22971677
|
C | CA | 6 | a0001c0001t0014g0100a0001c0001t0014g0102a0001c0001t0031g0307others(3): Show | 6 | HG01978.hp2 HG03942.hp1 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.626+4532dupT | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22971677 | ||||||
chr7:22971677
|
CA | C | 176 | a0001c0001t0002g0064a0001c0001t0002g0124a0001c0001t0003g0138others(173): Show | 206 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(203): Show |
intron_variant | MODIFIER | c.626+4532delT | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22971677 | ||||||
chr7:22971803
|
G | A | 131 | a0001c0002t0001g0001a0001c0002t0001g0007a0001c0002t0001g0226others(128): Show | 146 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.626+4407C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22971803 | ||||||
chr7:22971843
|
C | T | 43 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(40): Show | 58 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.626+4367G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22971843 | ||||||
chr7:22971954
|
G | A | 2 | a0001c0001t0006g0149a0001c0001t0009g0150 | 2 | HG02738.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.626+4256C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22971954 | ||||||
chr7:22972006
|
G | C | 4 | a0001c0001t0017g0117a0001c0001t0017g0119a0001c0001t0017g0122others(1): Show | 4 | NA18942.hp2 NA18984.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.626+4204C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22972006 | ||||||
chr7:22972036
|
A | G | 2 | a0001c0001t0036g0031a0001c0001t0036g0032 | 2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.626+4174T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22972036 | ||||||
chr7:22972057
|
A | T | 1 | a0001c0002t0005g0289 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.626+4153T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22972057 | ||||||
chr7:22972153
|
T | C | 1 | a0007c0009t0074g0344 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.626+4057A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22972153 | ||||||
chr7:22972238
|
GC | G | 4 | a0001c0001t0024g0026a0001c0001t0024g0027a0001c0001t0042g0025others(1): Show | 4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.626+3971delG | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22972238 | ||||||
chr7:22972312
|
A | T | 1 | a0001c0001t0082g0188 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.626+3898T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22972312 | ||||||
chr7:22972720
|
T | A | 1 | a0001c0002t0007g0212 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.626+3490A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22972720 | ||||||
chr7:22972796
|
C | T | 2 | a0001c0002t0007g0206a0001c0002t0007g0207 | 2 | NA19000.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.626+3414G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22972796 | ||||||
chr7:22972885
|
G | T | 12 | a0001c0002t0012g0189a0001c0002t0012g0190a0001c0002t0012g0194others(9): Show | 12 | HG01884.hp1 HG02293.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.626+3325C>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22972885 | ||||||
chr7:22972960
|
C | G | 1 | a0001c0001t0003g0151 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.626+3250G>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22972960 | ||||||
chr7:22972976
|
T | C | 2 | a0001c0001t0026g0317a0001c0001t0026g0327 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.626+3234A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22972976 | ||||||
chr7:22973143
|
T | C | 4 | a0001c0001t0024g0026a0001c0001t0024g0027a0001c0001t0042g0025others(1): Show | 4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.626+3067A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22973143 | ||||||
chr7:22973259
|
C | A | 1 | a0001c0001t0066g0168 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.626+2951G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22973259 | ||||||
chr7:22973354
|
A | G | 4 | a0001c0001t0077g0052a0001c0001t0080g0053a0003c0003t0075g0051others(1): Show | 4 | HG02055.hp2 HG02145.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.626+2856T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22973354 | ||||||
chr7:22973452
|
A | G | 3 | a0001c0002t0021g0233a0001c0002t0033g0229a0001c0002t0033g0303 | 3 | HG02886.hp1 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.626+2758T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22973452 | ||||||
chr7:22973499
|
T | C | 1 | a0001c0001t0071g0040 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.626+2711A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22973499 | ||||||
chr7:22973617
|
C | T | 199 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(196): Show | 232 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(229): Show |
intron_variant | MODIFIER | c.626+2593G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22973617 | ||||||
chr7:22973758
|
T | C | 1 | a0001c0001t0003g0055 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.626+2452A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22973758 | ||||||
chr7:22973799
|
T | G | 1 | a0002c0004t0029g0011 | 2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.626+2411A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22973799 | ||||||
chr7:22974066
|
T | C | 177 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(174): Show | 207 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(204): Show |
intron_variant | MODIFIER | c.626+2144A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22974066 | ||||||
chr7:22974229
|
C | T | 177 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(174): Show | 207 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(204): Show |
intron_variant | MODIFIER | c.626+1981G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22974229 | ||||||
chr7:22974736
|
C | T | 6 | a0001c0001t0015g0002a0001c0001t0015g0037a0001c0001t0015g0038others(3): Show | 9 | HG00738.hp2 HG01168.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.626+1474G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22974736 | ||||||
chr7:22974791
|
C | T | 44 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(41): Show | 59 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.626+1419G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22974791 | ||||||
chr7:22974828
|
G | C | 28 | a0001c0002t0001g0007a0001c0002t0001g0258a0001c0002t0001g0271others(25): Show | 34 | HG00140.hp1 HG01070.hp2 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.626+1382C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22974828 | ||||||
chr7:22974905
|
T | C | 4 | a0001c0001t0024g0026a0001c0001t0024g0027a0001c0001t0042g0025others(1): Show | 4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.626+1305A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22974905 | ||||||
chr7:22974931
|
C | T | 1 | a0001c0001t0009g0178 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.626+1279G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22974931 | ||||||
chr7:22975197
|
T | A | 50 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(47): Show | 68 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.626+1013A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22975197 | ||||||
chr7:22975201
|
TTTTG | T | 131 | a0001c0001t0082g0188a0001c0002t0001g0001a0001c0002t0001g0007others(128): Show | 146 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.626+1005_626+1008d others(6): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22975201 | ||||||
chr7:22975378
|
A | G | 1 | a0001c0002t0005g0294 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.626+832T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22975378 | ||||||
chr7:22975810
|
G | A | 2 | a0001c0001t0076g0345a0001c0001t0079g0054 | 2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.626+400C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22975810 | ||||||
chr7:22975862
|
G | A | 47 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(44): Show | 65 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.626+348C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22975862 | ||||||
chr7:22975896
|
T | C | 1 | a0001c0001t0076g0345 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.626+314A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22975896 | ||||||
chr7:22975955
|
C | T | 1 | a0001c0001t0073g0336 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.626+255G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22975955 | ||||||
chr7:22975974
|
G | A | 46 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(43): Show | 64 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.626+236C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22975974 | ||||||
chr7:22976063
|
A | G | 1 | a0001c0002t0005g0278 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.626+147T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22976063 | ||||||
chr7:22976170
|
C | T | 1 | a0001c0001t0006g0170 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.626+40G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 7/10 | chr7 | 22976170 | ||||||
chr7:22976340
|
T | C | 2 | a0001c0001t0013g0059a0008c0007t0013g0058 | 2 | HG02132.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.531-35A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 6/10 | chr7 | 22976340 | ||||||
chr7:22976418
|
A | G | 2 | a0001c0001t0036g0031a0001c0001t0036g0032 | 2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.531-113T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 6/10 | chr7 | 22976418 | ||||||
chr7:22976496
|
T | G | 3 | a0001c0001t0032g0047a0001c0001t0032g0048a0001c0001t0078g0049 | 3 | HG01081.hp2 HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.531-191A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 6/10 | chr7 | 22976496 | ||||||
chr7:22976548
|
G | C | 1 | a0001c0001t0002g0076 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.530+145C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 6/10 | chr7 | 22976548 | ||||||
chr7:22976665
|
G | C | 2 | a0001c0001t0030g0115a0001c0001t0030g0120 | 2 | HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.530+28C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 6/10 | chr7 | 22976665 | ||||||
chr7:22976911
|
A | G | 132 | a0001c0002t0001g0001a0001c0002t0001g0007a0001c0002t0001g0226others(129): Show | 147 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.415-103T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 5/10 | chr7 | 22976911 | ||||||
chr7:22977028
|
T | C | 132 | a0001c0002t0001g0001a0001c0002t0001g0007a0001c0002t0001g0226others(129): Show | 147 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.415-220A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 5/10 | chr7 | 22977028 | ||||||
chr7:22977074
|
A | G | 1 | a0001c0001t0002g0124 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.415-266T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 5/10 | chr7 | 22977074 | ||||||
chr7:22977268
|
A | G | 1 | a0001c0002t0022g0268 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.414+73T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 5/10 | chr7 | 22977268 | ||||||
chr7:22977322
|
G | A | 14 | a0001c0001t0024g0026a0001c0001t0024g0027a0001c0001t0032g0047others(11): Show | 14 | HG01081.hp2 HG01361.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.414+19C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 5/10 | chr7 | 22977322 | ||||||
chr7:22977572
|
T | C | 1 | a0001c0001t0002g0182 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.334-151A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 4/10 | chr7 | 22977572 | ||||||
chr7:22977599
|
T | C | 2 | a0001c0002t0005g0276a0001c0002t0005g0288 | 2 | HG02165.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.334-178A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 4/10 | chr7 | 22977599 | ||||||
chr7:22977848
|
T | C | 9 | a0001c0001t0032g0047a0001c0001t0032g0048a0001c0001t0076g0345others(6): Show | 9 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.333+421A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 4/10 | chr7 | 22977848 | ||||||
chr7:22977950
|
C | A | 1 | a0001c0001t0002g0088 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.333+319G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 4/10 | chr7 | 22977950 | ||||||
chr7:22978477
|
G | T | 2 | a0001c0001t0019g0083a0001c0001t0059g0084 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.154-29C>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22978477 | ||||||
chr7:22978602
|
C | G | 1 | a0001c0001t0086g0081 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.154-154G>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22978602 | ||||||
chr7:22978604
|
T | C | 1 | a0001c0001t0008g0325 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.154-156A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22978604 | ||||||
chr7:22978699
|
G | A | 7 | a0001c0001t0003g0157a0001c0001t0003g0338a0001c0001t0003g0339others(4): Show | 8 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.154-251C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22978699 | ||||||
chr7:22979014
|
G | A | 4 | a0001c0001t0019g0083a0001c0001t0019g0340a0001c0001t0019g0341others(1): Show | 4 | HG01069.hp2 HG01071.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.154-566C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22979014 | ||||||
chr7:22979096
|
C | T | 1 | a0001c0001t0016g0171 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.154-648G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22979096 | ||||||
chr7:22979182
|
G | T | 1 | a0001c0002t0001g0270 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.154-734C>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22979182 | ||||||
chr7:22979278
|
G | C | 1 | a0001c0002t0001g0250 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.154-830C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22979278 | ||||||
chr7:22979418
|
T | C | 1 | a0001c0001t0058g0140 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.154-970A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22979418 | ||||||
chr7:22979506
|
G | A | 20 | a0001c0001t0013g0070a0001c0001t0013g0103a0001c0001t0013g0133others(17): Show | 20 | HG00099.hp1 HG00544.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.154-1058C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22979506 | ||||||
chr7:22979587
|
C | T | 139 | a0001c0001t0024g0026a0001c0001t0024g0027a0001c0001t0036g0031others(136): Show | 154 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.154-1139G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22979587 | ||||||
chr7:22979771
|
A | G | 1 | a0001c0001t0073g0336 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.154-1323T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22979771 | ||||||
chr7:22979782
|
G | C | 1 | a0001c0001t0076g0345 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.154-1334C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22979782 | ||||||
chr7:22979792
|
C | T | 4 | a0001c0001t0024g0026a0001c0001t0024g0027a0001c0001t0042g0025others(1): Show | 4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.154-1344G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22979792 | ||||||
chr7:22979804
|
C | G | 23 | a0001c0002t0007g0006a0001c0002t0007g0204a0001c0002t0007g0206others(20): Show | 27 | HG01169.hp1 HG02004.hp1 HG02155.hp2 others(24): Show |
intron_variant | MODIFIER | c.154-1356G>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22979804 | ||||||
chr7:22979828
|
G | A | 1 | a0001c0001t0017g0122 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.154-1380C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22979828 | ||||||
chr7:22979977
|
T | A | 1 | a0001c0001t0004g0046 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.154-1529A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22979977 | ||||||
chr7:22980006
|
T | G | 1 | a0001c0001t0073g0336 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.154-1558A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22980006 | ||||||
chr7:22980158
|
T | C | 2 | a0001c0001t0031g0307a0001c0001t0031g0308 | 2 | NA18952.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.154-1710A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22980158 | ||||||
chr7:22980191
|
A | G | 132 | a0001c0001t0042g0025a0001c0002t0001g0001a0001c0002t0001g0007others(129): Show | 147 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.154-1743T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22980191 | ||||||
chr7:22980274
|
G | GT | 15 | a0001c0001t0013g0169a0001c0001t0014g0100a0001c0001t0014g0102others(12): Show | 15 | HG01069.hp2 HG01071.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.154-1827dupA | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22980274 | ||||||
chr7:22980274
|
G | GTT | 126 | a0001c0002t0001g0001a0001c0002t0001g0007a0001c0002t0001g0226others(123): Show | 141 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.154-1828_154-1827d others(4): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22980274 | ||||||
chr7:22980274
|
GT | G | 14 | a0001c0001t0002g0063a0001c0001t0002g0064a0001c0001t0002g0066others(11): Show | 14 | HG00639.hp1 HG00639.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.154-1827delA | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22980274 | ||||||
chr7:22980314
|
T | C | 1 | a0001c0001t0008g0326 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.154-1866A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22980314 | ||||||
chr7:22980677
|
G | A | 1 | a0001c0001t0086g0081 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.154-2229C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22980677 | ||||||
chr7:22980692
|
C | T | 2 | a0001c0001t0076g0345a0007c0009t0074g0344 | 2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.154-2244G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22980692 | ||||||
chr7:22980890
|
G | A | 1 | a0001c0001t0004g0332 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.154-2442C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22980890 | ||||||
chr7:22980894
|
C | T | 337 | a0001c0001t0002g0063a0001c0001t0002g0064a0001c0001t0002g0066others(334): Show | 376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.154-2446G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22980894 | ||||||
chr7:22980939
|
T | A | 1 | a0007c0009t0074g0344 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.154-2491A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22980939 | ||||||
chr7:22980953
|
C | A | 1 | a0001c0002t0045g0036 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.154-2505G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22980953 | ||||||
chr7:22981053
|
G | A | 130 | a0001c0002t0001g0001a0001c0002t0001g0007a0001c0002t0001g0226others(127): Show | 145 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.154-2605C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22981053 | ||||||
chr7:22981090
|
T | G | 1 | a0001c0002t0007g0216 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.154-2642A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22981090 | ||||||
chr7:22981176
|
A | C | 9 | a0001c0002t0011g0018a0001c0002t0011g0230a0001c0002t0011g0299others(6): Show | 10 | HG00733.hp1 HG01074.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.154-2728T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22981176 | ||||||
chr7:22981258
|
C | T | 3 | a0001c0001t0003g0061a0001c0001t0003g0062a0001c0001t0003g0135 | 3 | HG02074.hp1 HG02165.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.153+2686G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22981258 | ||||||
chr7:22981369
|
A | G | 130 | a0001c0002t0001g0001a0001c0002t0001g0007a0001c0002t0001g0226others(127): Show | 145 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.153+2575T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22981369 | ||||||
chr7:22981463
|
A | C | 195 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(192): Show | 228 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(225): Show |
intron_variant | MODIFIER | c.153+2481T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22981463 | ||||||
chr7:22981519
|
A | C | 1 | a0001c0002t0012g0200 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.153+2425T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22981519 | ||||||
chr7:22981582
|
A | C | 2 | a0001c0002t0001g0007a0001c0002t0001g0271 | 4 | HG00140.hp1 HG01070.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.153+2362T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22981582 | ||||||
chr7:22981773
|
C | T | 1 | a0001c0002t0104g0293 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.153+2171G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22981773 | ||||||
chr7:22981836
|
T | C | 55 | a0001c0001t0002g0163a0001c0001t0002g0164a0001c0001t0002g0182others(52): Show | 60 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.153+2108A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22981836 | ||||||
chr7:22981843
|
C | T | 2 | a0001c0001t0036g0031a0001c0001t0036g0032 | 2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.153+2101G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22981843 | ||||||
chr7:22981888
|
A | C | 130 | a0001c0002t0001g0001a0001c0002t0001g0007a0001c0002t0001g0226others(127): Show | 145 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.153+2056T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22981888 | ||||||
chr7:22981896
|
A | G | 3 | a0001c0001t0032g0047a0001c0001t0032g0048a0001c0001t0078g0049 | 3 | HG01081.hp2 HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.153+2048T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22981896 | ||||||
chr7:22982034
|
G | A | 41 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(38): Show | 56 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.153+1910C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22982034 | ||||||
chr7:22982053
|
C | T | 1 | a0001c0001t0073g0336 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.153+1891G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22982053 | ||||||
chr7:22982110
|
T | TA | 9 | a0001c0001t0032g0047a0001c0001t0032g0048a0001c0001t0077g0052others(6): Show | 9 | HG01081.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.153+1833dupT | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22982110 | ||||||
chr7:22982140
|
C | G | 3 | a0001c0001t0003g0161a0001c0001t0003g0183a0001c0001t0006g0004 | 6 | HG01099.hp1 HG02148.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.153+1804G>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22982140 | ||||||
chr7:22982178
|
G | T | 7 | a0001c0001t0015g0002a0001c0001t0015g0037a0001c0001t0015g0038others(4): Show | 10 | HG00738.hp2 HG01168.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.153+1766C>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22982178 | ||||||
chr7:22982291
|
G | A | 1 | a0001c0001t0076g0345 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.153+1653C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22982291 | ||||||
chr7:22982422
|
T | C | 1 | a0001c0001t0082g0188 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.153+1522A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22982422 | ||||||
chr7:22982565
|
T | G | 1 | a0001c0002t0001g0251 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.153+1379A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22982565 | ||||||
chr7:22982828
|
T | C | 202 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(199): Show | 235 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.153+1116A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22982828 | ||||||
chr7:22982845
|
T | TC | 46 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(43): Show | 61 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.153+1098dupG | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22982845 | ||||||
chr7:22982895
|
T | C | 2 | a0001c0002t0001g0258a0001c0002t0040g0254 | 2 | HG01361.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.153+1049A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22982895 | ||||||
chr7:22982926
|
C | A | 1 | a0001c0001t0002g0089 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.153+1018G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22982926 | ||||||
chr7:22982953
|
T | C | 1 | a0001c0001t0002g0108 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.153+991A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22982953 | ||||||
chr7:22983066
|
T | C | 3 | a0001c0002t0021g0233a0001c0002t0033g0229a0001c0002t0033g0303 | 3 | HG02886.hp1 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.153+878A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22983066 | ||||||
chr7:22983092
|
G | C | 1 | a0001c0002t0045g0036 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.153+852C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22983092 | ||||||
chr7:22983185
|
C | T | 1 | a0001c0001t0014g0102 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.153+759G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22983185 | ||||||
chr7:22983198
|
G | A | 53 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(50): Show | 71 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.153+746C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22983198 | ||||||
chr7:22983212
|
C | T | 25 | a0001c0001t0007g0221a0001c0002t0007g0006a0001c0002t0007g0204others(22): Show | 29 | HG01169.hp1 HG02004.hp1 HG02155.hp2 others(26): Show |
intron_variant | MODIFIER | c.153+732G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22983212 | ||||||
chr7:22983320
|
C | A | 1 | a0001c0001t0073g0336 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.153+624G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22983320 | ||||||
chr7:22983328
|
C | CA | 54 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(51): Show | 69 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.153+615dupT | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22983328 | ||||||
chr7:22983381
|
T | C | 4 | a0001c0001t0024g0026a0001c0001t0024g0027a0001c0001t0042g0025others(1): Show | 4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.153+563A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22983381 | ||||||
chr7:22983415
|
C | T | 1 | a0001c0002t0007g0223 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.153+529G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22983415 | ||||||
chr7:22983529
|
C | T | 1 | a0001c0002t0045g0036 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.153+415G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22983529 | ||||||
chr7:22983547
|
T | C | 1 | a0001c0001t0086g0081 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.153+397A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22983547 | ||||||
chr7:22983662
|
G | A | 2 | a0001c0002t0034g0057a0001c0002t0092g0056 | 2 | HG02055.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.153+282C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22983662 | ||||||
chr7:22983845
|
C | T | 1 | a0001c0002t0045g0036 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.153+99G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 3/10 | chr7 | 22983845 | ||||||
chr7:22984074
|
C | T | 1 | a0001c0001t0006g0337 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.52-29G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22984074 | ||||||
chr7:22984202
|
G | A | 1 | a0001c0002t0099g0269 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.52-157C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22984202 | ||||||
chr7:22984210
|
C | A | 1 | a0001c0002t0084g0260 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.52-165G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22984210 | ||||||
chr7:22984335
|
A | C | 4 | a0001c0001t0024g0026a0001c0001t0024g0027a0001c0001t0042g0025others(1): Show | 4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.52-290T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22984335 | ||||||
chr7:22984339
|
TAAAAC | T | 3 | a0001c0002t0011g0262a0001c0002t0021g0261a0001c0002t0022g0263 | 3 | HG02257.hp1 HG03453.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.52-299_52-295delGT others(3): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22984339 | ||||||
chr7:22984648
|
G | A | 1 | a0001c0001t0014g0110 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.52-603C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22984648 | ||||||
chr7:22984657
|
C | T | 1 | a0001c0001t0003g0055 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.52-612G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22984657 | ||||||
chr7:22984658
|
G | A | 1 | a0001c0001t0073g0336 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.52-613C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22984658 | ||||||
chr7:22984716
|
G | C | 1 | a0001c0001t0002g0132 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.52-671C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22984716 | ||||||
chr7:22984731
|
G | A | 1 | a0001c0001t0073g0336 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.52-686C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22984731 | ||||||
chr7:22984789
|
G | A | 1 | a0007c0009t0074g0344 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.52-744C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22984789 | ||||||
chr7:22984929
|
A | G | 1 | a0001c0001t0073g0336 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.52-884T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22984929 | ||||||
chr7:22984944
|
TA | T | 5 | a0001c0001t0065g0075a0001c0001t0067g0072a0001c0001t0068g0087others(2): Show | 5 | HG02145.hp1 HG02559.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.52-900delT | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22984944 | ||||||
chr7:22985107
|
CCT | C | 3 | a0001c0001t0032g0047a0001c0001t0032g0048a0001c0001t0078g0049 | 3 | HG01081.hp2 HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.52-1064_52-1063del others(2): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22985107 | ||||||
chr7:22985111
|
CAG | C | 3 | a0001c0001t0032g0047a0001c0001t0032g0048a0001c0001t0078g0049 | 3 | HG01081.hp2 HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.52-1068_52-1067del others(2): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22985111 | ||||||
chr7:22985117
|
G | C | 3 | a0001c0001t0032g0047a0001c0001t0032g0048a0001c0001t0078g0049 | 3 | HG01081.hp2 HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.52-1072C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22985117 | ||||||
chr7:22985118
|
T | C | 3 | a0001c0001t0032g0047a0001c0001t0032g0048a0001c0001t0078g0049 | 3 | HG01081.hp2 HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.52-1073A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22985118 | ||||||
chr7:22985176
|
A | G | 52 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(49): Show | 70 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.52-1131T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22985176 | ||||||
chr7:22985301
|
C | A | 131 | a0001c0001t0007g0221a0001c0002t0001g0001a0001c0002t0001g0007others(128): Show | 146 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.52-1256G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22985301 | ||||||
chr7:22985337
|
A | C | 1 | a0001c0001t0002g0164 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.52-1292T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22985337 | ||||||
chr7:22985388
|
A | C | 1 | a0001c0001t0013g0306 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.52-1343T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22985388 | ||||||
chr7:22985389
|
A | C | 3 | a0001c0001t0036g0031a0001c0001t0036g0032a0001c0001t0073g0336 | 3 | HG02896.hp2 NA18522.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.52-1344T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22985389 | ||||||
chr7:22985460
|
T | C | 132 | a0001c0001t0007g0221a0001c0002t0001g0001a0001c0002t0001g0007others(129): Show | 147 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.52-1415A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22985460 | ||||||
chr7:22985556
|
C | G | 1 | a0001c0002t0005g0275 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.52-1511G>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22985556 | ||||||
chr7:22985600
|
C | T | 1 | a0001c0002t0007g0204 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.52-1555G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22985600 | ||||||
chr7:22985621
|
T | C | 1 | a0001c0001t0006g0104 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.52-1576A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22985621 | ||||||
chr7:22985641
|
C | T | 1 | a0001c0002t0092g0056 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.52-1596G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22985641 | ||||||
chr7:22985669
|
A | G | 2 | a0001c0002t0091g0259a0001c0002t0095g0227 | 2 | HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.52-1624T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22985669 | ||||||
chr7:22985688
|
C | A | 2 | a0001c0002t0001g0253a0001c0002t0001g0257 | 2 | NA18972.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.52-1643G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22985688 | ||||||
chr7:22985740
|
G | C | 1 | a0007c0009t0074g0344 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.52-1695C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22985740 | ||||||
chr7:22985822
|
T | C | 1 | a0001c0001t0014g0102 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.52-1777A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22985822 | ||||||
chr7:22985964
|
T | C | 2 | a0001c0002t0001g0241a0001c0002t0001g0252 | 2 | NA18946.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.52-1919A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22985964 | ||||||
chr7:22986028
|
T | TTA | 127 | a0001c0001t0007g0221a0001c0002t0001g0001a0001c0002t0001g0226others(124): Show | 140 | HG00280.hp2 HG00423.hp2 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.52-1985_52-1984dup others(2): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22986028 | ||||||
chr7:22986028
|
T | TTATA | 5 | a0001c0002t0001g0007a0001c0002t0001g0258a0001c0002t0001g0271others(2): Show | 7 | HG00140.hp1 HG01070.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.52-1987_52-1984dup others(4): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22986028 | ||||||
chr7:22986061
|
G | C | 1 | a0001c0001t0064g0078 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.52-2016C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22986061 | ||||||
chr7:22986100
|
T | C | 1 | a0001c0002t0001g0238 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.52-2055A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22986100 | ||||||
chr7:22986272
|
C | A | 4 | a0001c0001t0024g0026a0001c0001t0024g0027a0001c0001t0042g0025others(1): Show | 4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.52-2227G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22986272 | ||||||
chr7:22986511
|
T | C | 46 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(43): Show | 61 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.52-2466A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22986511 | ||||||
chr7:22986569
|
T | A | 26 | a0001c0002t0011g0018a0001c0002t0011g0230a0001c0002t0011g0235others(23): Show | 27 | HG00733.hp1 HG01074.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.52-2524A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22986569 | ||||||
chr7:22986576
|
G | A | 1 | a0001c0002t0011g0301 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.52-2531C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22986576 | ||||||
chr7:22986635
|
C | T | 1 | a0001c0001t0002g0092 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.52-2590G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22986635 | ||||||
chr7:22986706
|
T | C | 1 | a0001c0001t0073g0336 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.52-2661A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22986706 | ||||||
chr7:22986817
|
C | T | 4 | a0001c0001t0024g0026a0001c0001t0024g0027a0001c0001t0042g0025others(1): Show | 4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.52-2772G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22986817 | ||||||
chr7:22986849
|
A | G | 1 | a0002c0004t0029g0011 | 2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.52-2804T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22986849 | ||||||
chr7:22986946
|
G | C | 4 | a0001c0001t0024g0026a0001c0001t0024g0027a0001c0001t0042g0025others(1): Show | 4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.52-2901C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22986946 | ||||||
chr7:22987028
|
C | T | 132 | a0001c0001t0007g0221a0001c0002t0001g0001a0001c0002t0001g0007others(129): Show | 147 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.52-2983G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22987028 | ||||||
chr7:22987166
|
T | C | 2 | a0001c0002t0001g0253a0001c0002t0001g0257 | 2 | NA18972.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.52-3121A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22987166 | ||||||
chr7:22987219
|
T | C | 1 | a0001c0001t0002g0163 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.52-3174A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22987219 | ||||||
chr7:22987228
|
C | T | 1 | a0001c0002t0001g0241 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.52-3183G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22987228 | ||||||
chr7:22987233
|
A | G | 1 | a0001c0002t0011g0264 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.52-3188T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22987233 | ||||||
chr7:22987274
|
C | T | 1 | a0001c0002t0005g0277 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.52-3229G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22987274 | ||||||
chr7:22987289
|
G | A | 48 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(45): Show | 66 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.52-3244C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22987289 | ||||||
chr7:22987309
|
A | T | 131 | a0001c0001t0007g0221a0001c0002t0001g0001a0001c0002t0001g0007others(128): Show | 146 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.52-3264T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22987309 | ||||||
chr7:22987323
|
G | A | 3 | a0001c0001t0003g0061a0001c0001t0003g0062a0001c0001t0003g0135 | 3 | HG02074.hp1 HG02165.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.52-3278C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22987323 | ||||||
chr7:22987374
|
C | A | 15 | a0001c0002t0012g0189a0001c0002t0012g0190a0001c0002t0012g0191others(12): Show | 15 | HG01884.hp1 HG02293.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.52-3329G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22987374 | ||||||
chr7:22987401
|
A | G | 1 | a0001c0002t0005g0291 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.52-3356T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22987401 | ||||||
chr7:22987431
|
C | T | 1 | a0001c0002t0101g0205 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.52-3386G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22987431 | ||||||
chr7:22987438
|
C | T | 1 | a0001c0001t0009g0144 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.52-3393G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22987438 | ||||||
chr7:22987473
|
A | G | 132 | a0001c0001t0007g0221a0001c0002t0001g0001a0001c0002t0001g0007others(129): Show | 147 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.52-3428T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22987473 | ||||||
chr7:22987694
|
A | C | 1 | a0001c0002t0107g0225 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.51+3367T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22987694 | ||||||
chr7:22987867
|
T | A | 1 | a0007c0009t0074g0344 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.51+3194A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22987867 | ||||||
chr7:22987878
|
T | C | 44 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(41): Show | 59 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.51+3183A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22987878 | ||||||
chr7:22987928
|
T | C | 1 | a0001c0006t0006g0160 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.51+3133A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22987928 | ||||||
chr7:22988064
|
G | A | 1 | a0001c0001t0065g0075 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.51+2997C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22988064 | ||||||
chr7:22988076
|
TTTTGCCT others(7): Show |
T | 132 | a0001c0001t0007g0221a0001c0002t0001g0001a0001c0002t0001g0007others(129): Show | 147 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.51+2971_51+2984del others(14): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22988076 | ||||||
chr7:22988108
|
CAT | C | 4 | a0001c0002t0005g0292a0001c0002t0034g0305a0001c0002t0091g0259others(1): Show | 4 | HG02572.hp2 HG02630.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.51+2951_51+2952del others(2): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22988108 | ||||||
chr7:22988422
|
T | C | 196 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(193): Show | 229 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(226): Show |
intron_variant | MODIFIER | c.51+2639A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22988422 | ||||||
chr7:22988434
|
T | C | 1 | a0001c0002t0045g0036 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.51+2627A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22988434 | ||||||
chr7:22988465
|
A | G | 1 | a0001c0001t0013g0103 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.51+2596T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22988465 | ||||||
chr7:22988632
|
C | T | 9 | a0001c0002t0011g0235a0001c0002t0011g0262a0001c0002t0011g0264others(6): Show | 9 | HG01243.hp2 HG02257.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.51+2429G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22988632 | ||||||
chr7:22988686
|
C | T | 161 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(158): Show | 190 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.51+2375G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22988686 | ||||||
chr7:22988716
|
C | T | 1 | a0001c0002t0045g0036 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.51+2345G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22988716 | ||||||
chr7:22988891
|
C | T | 1 | a0001c0001t0073g0336 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.51+2170G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22988891 | ||||||
chr7:22988991
|
G | T | 39 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(36): Show | 54 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.51+2070C>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22988991 | ||||||
chr7:22989007
|
T | C | 13 | a0001c0002t0012g0189a0001c0002t0012g0190a0001c0002t0012g0191others(10): Show | 13 | HG01884.hp1 HG02293.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.51+2054A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989007 | ||||||
chr7:22989131
|
C | T | 2 | a0001c0001t0036g0031a0001c0001t0036g0032 | 2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.51+1930G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989131 | ||||||
chr7:22989168
|
A | G | 1 | a0001c0001t0076g0345 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.51+1893T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989168 | ||||||
chr7:22989230
|
C | CA | 198 | a0001c0001t0003g0055a0001c0001t0004g0008a0001c0001t0004g0009others(195): Show | 231 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.51+1830dupT | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989230 | ||||||
chr7:22989253
|
C | T | 1 | a0001c0002t0005g0276 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.51+1808G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989253 | ||||||
chr7:22989268
|
A | G | 1 | a0001c0001t0076g0345 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.51+1793T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989268 | ||||||
chr7:22989285
|
A | AAC | 94 | a0001c0001t0002g0076a0001c0001t0002g0088a0001c0001t0002g0089others(91): Show | 99 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.51+1774_51+1775dup others(2): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989285 | ||||||
chr7:22989285
|
A | AACAC | 10 | a0001c0001t0002g0063a0001c0001t0003g0091a0001c0001t0006g0149others(7): Show | 10 | HG01433.hp1 HG02132.hp2 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.51+1772_51+1775dup others(4): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989285 | ||||||
chr7:22989285
|
A | AACACAC | 4 | a0001c0001t0003g0141a0001c0001t0003g0161a0001c0001t0009g0144others(1): Show | 4 | HG00673.hp1 HG02148.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.51+1770_51+1775dup others(6): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989285 | ||||||
chr7:22989285
|
A | AACACACA others(3): Show |
2 | a0001c0001t0002g0182a0001c0001t0009g0145 | 2 | NA18968.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.51+1766_51+1775dup others(10): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989285 | ||||||
chr7:22989285
|
A | AACACACA others(5): Show |
1 | a0001c0001t0002g0164 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.51+1764_51+1775dup others(12): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989285 | ||||||
chr7:22989285
|
AAC | A | 5 | a0001c0001t0002g0132a0001c0001t0053g0041a0001c0001t0071g0040others(2): Show | 5 | HG01978.hp2 HG02071.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.51+1774_51+1775del others(2): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989285 | ||||||
chr7:22989285
|
AACAC | A | 14 | a0001c0001t0013g0103a0001c0001t0013g0134a0001c0001t0015g0002others(11): Show | 17 | HG00738.hp2 HG01081.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.51+1772_51+1775del others(4): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989285 | ||||||
chr7:22989285
|
AACACAC | A | 13 | a0001c0001t0003g0055a0001c0001t0024g0027a0001c0001t0030g0115others(10): Show | 13 | HG01361.hp2 HG02055.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.51+1770_51+1775del others(6): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989285 | ||||||
chr7:22989285
|
AACACACA others(5): Show |
A | 1 | a0001c0002t0093g0196 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.51+1764_51+1775del others(12): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989285 | ||||||
chr7:22989285
|
AACACACA others(7): Show |
A | 2 | a0001c0002t0108g0240a0001c0002t0109g0255 | 2 | NA18991.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.51+1762_51+1775del others(14): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989285 | ||||||
chr7:22989285
|
AACACACA others(9): Show |
A | 169 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(166): Show | 199 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(196): Show |
intron_variant | MODIFIER | c.51+1760_51+1775del others(16): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989285 | ||||||
chr7:22989285
|
AACACACA others(11): Show |
A | 1 | a0001c0002t0045g0036 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.51+1758_51+1775del others(18): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989285 | ||||||
chr7:22989287
|
C | T | 3 | a0001c0001t0002g0125a0001c0001t0002g0127a0006c0010t0002g0187 | 3 | HG00140.hp2 HG01255.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.51+1774G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989287 | ||||||
chr7:22989402
|
C | G | 1 | a0001c0002t0005g0275 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.51+1659G>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989402 | ||||||
chr7:22989413
|
C | T | 212 | a0001c0001t0002g0064a0001c0001t0002g0066a0001c0001t0002g0068others(209): Show | 245 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(242): Show |
intron_variant | MODIFIER | c.51+1648G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989413 | ||||||
chr7:22989428
|
A | T | 197 | a0001c0001t0003g0055a0001c0001t0004g0008a0001c0001t0004g0009others(194): Show | 230 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(227): Show |
intron_variant | MODIFIER | c.51+1633T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989428 | ||||||
chr7:22989467
|
C | T | 1 | a0001c0002t0045g0036 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.51+1594G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989467 | ||||||
chr7:22989526
|
AT | A | 197 | a0001c0001t0003g0055a0001c0001t0004g0008a0001c0001t0004g0009others(194): Show | 230 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(227): Show |
intron_variant | MODIFIER | c.51+1534delA | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989526 | ||||||
chr7:22989530
|
T | A | 42 | a0001c0001t0002g0063a0001c0001t0002g0088a0001c0001t0002g0089others(39): Show | 42 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.51+1531A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989530 | ||||||
chr7:22989531
|
T | A | 5 | a0001c0001t0015g0037a0001c0001t0015g0038a0001c0001t0036g0031others(2): Show | 5 | HG00738.hp2 HG02896.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.51+1530A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989531 | ||||||
chr7:22989534
|
T | A | 1 | a0001c0001t0064g0078 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.51+1527A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989534 | ||||||
chr7:22989610
|
T | C | 202 | a0001c0001t0003g0055a0001c0001t0004g0008a0001c0001t0004g0009others(199): Show | 235 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.51+1451A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989610 | ||||||
chr7:22989775
|
A | T | 2 | a0001c0001t0036g0031a0001c0001t0036g0032 | 2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.51+1286T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989775 | ||||||
chr7:22989778
|
C | T | 1 | a0001c0001t0009g0144 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.51+1283G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989778 | ||||||
chr7:22989789
|
T | C | 4 | a0001c0002t0005g0024a0001c0002t0005g0291a0001c0002t0005g0292others(1): Show | 5 | HG00280.hp2 HG01175.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.51+1272A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989789 | ||||||
chr7:22989847
|
G | A | 1 | a0001c0002t0045g0036 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.51+1214C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989847 | ||||||
chr7:22989888
|
A | G | 131 | a0001c0001t0007g0221a0001c0002t0001g0001a0001c0002t0001g0007others(128): Show | 146 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.51+1173T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989888 | ||||||
chr7:22989950
|
A | G | 1 | a0001c0002t0045g0036 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.51+1111T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22989950 | ||||||
chr7:22990341
|
A | G | 2 | a0001c0001t0019g0340a0001c0001t0019g0341 | 2 | HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.51+720T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22990341 | ||||||
chr7:22990356
|
T | C | 1 | a0001c0001t0020g0130 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.51+705A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22990356 | ||||||
chr7:22990546
|
C | T | 39 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(36): Show | 54 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.51+515G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22990546 | ||||||
chr7:22990610
|
G | T | 1 | a0001c0002t0007g0204 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.51+451C>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22990610 | ||||||
chr7:22990613
|
C | T | 198 | a0001c0001t0003g0055a0001c0001t0004g0008a0001c0001t0004g0009others(195): Show | 231 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.51+448G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22990613 | ||||||
chr7:22990984
|
A | T | 4 | a0001c0002t0011g0235a0001c0002t0011g0265a0001c0002t0011g0267others(1): Show | 4 | HG02809.hp1 HG02818.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.51+77T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 2/10 | chr7 | 22990984 | ||||||
chr7:22991168
|
G | A | 1 | a0001c0001t0076g0345 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-28-29C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22991168 | ||||||
chr7:22991396
|
A | G | 1 | a0001c0002t0007g0204 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-28-257T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22991396 | ||||||
chr7:22991505
|
C | G | 74 | a0001c0001t0002g0163a0001c0001t0002g0164a0001c0001t0002g0182others(71): Show | 79 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.-28-366G>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22991505 | ||||||
chr7:22991645
|
T | C | 1 | a0001c0002t0045g0036 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-28-506A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22991645 | ||||||
chr7:22991714
|
G | A | 197 | a0001c0001t0003g0055a0001c0001t0004g0008a0001c0001t0004g0009others(194): Show | 230 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(227): Show |
intron_variant | MODIFIER | c.-28-575C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22991714 | ||||||
chr7:22991759
|
T | C | 2 | a0001c0001t0036g0031a0001c0001t0036g0032 | 2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-28-620A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22991759 | ||||||
chr7:22991812
|
T | C | 1 | a0001c0001t0004g0313 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-28-673A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22991812 | ||||||
chr7:22992043
|
C | A | 2 | a0001c0001t0026g0317a0001c0001t0026g0327 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-28-904G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22992043 | ||||||
chr7:22992144
|
T | TTAC | 133 | a0001c0001t0007g0221a0001c0002t0001g0001a0001c0002t0001g0007others(130): Show | 148 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.-28-1006_-28-1005i others(5): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22992144 | ||||||
chr7:22992207
|
G | A | 1 | a0001c0002t0005g0302 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-28-1068C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22992207 | ||||||
chr7:22992287
|
T | A | 2 | a0001c0001t0036g0031a0001c0001t0036g0032 | 2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-28-1148A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22992287 | ||||||
chr7:22992331
|
C | T | 1 | a0001c0001t0016g0180 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-28-1192G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22992331 | ||||||
chr7:22992378
|
G | A | 40 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(37): Show | 55 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.-28-1239C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22992378 | ||||||
chr7:22992467
|
A | G | 1 | a0001c0001t0073g0336 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-28-1328T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22992467 | ||||||
chr7:22992676
|
T | C | 26 | a0001c0002t0011g0018a0001c0002t0011g0230a0001c0002t0011g0235others(23): Show | 27 | HG00733.hp1 HG01074.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.-28-1537A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22992676 | ||||||
chr7:22992802
|
G | C | 1 | a0001c0002t0091g0259 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-28-1663C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22992802 | ||||||
chr7:22993086
|
T | A | 133 | a0001c0001t0007g0221a0001c0002t0001g0001a0001c0002t0001g0007others(130): Show | 148 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.-28-1947A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22993086 | ||||||
chr7:22993120
|
T | C | 2 | a0001c0001t0008g0315a0001c0001t0008g0318 | 2 | HG01256.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.-28-1981A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22993120 | ||||||
chr7:22993151
|
A | G | 3 | a0001c0002t0011g0262a0001c0002t0021g0261a0001c0002t0022g0263 | 3 | HG02257.hp1 HG03453.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-28-2012T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22993151 | ||||||
chr7:22993250
|
T | C | 13 | a0001c0001t0004g0009a0001c0001t0004g0020a0001c0001t0004g0022others(10): Show | 17 | HG00423.hp1 HG01928.hp1 HG01978.hp1 others(14): Show |
intron_variant | MODIFIER | c.-28-2111A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22993250 | ||||||
chr7:22993341
|
G | T | 1 | a0001c0001t0071g0040 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-28-2202C>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22993341 | ||||||
chr7:22993506
|
A | G | 6 | a0001c0001t0002g0064a0001c0001t0002g0066a0001c0001t0002g0068others(3): Show | 6 | HG00639.hp2 HG01243.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.-28-2367T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22993506 | ||||||
chr7:22993610
|
G | A | 3 | a0001c0002t0011g0262a0001c0002t0021g0261a0001c0002t0022g0263 | 3 | HG02257.hp1 HG03453.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-28-2471C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22993610 | ||||||
chr7:22993685
|
A | AAC | 11 | a0001c0001t0003g0055a0001c0001t0008g0318a0001c0001t0032g0047others(8): Show | 11 | HG01081.hp2 HG01256.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-28-2548_-28-2547d others(4): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22993685 | ||||||
chr7:22993707
|
T | C | 1 | a0001c0001t0013g0103 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-28-2568A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22993707 | ||||||
chr7:22993807
|
G | A | 1 | a0001c0001t0002g0182 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-28-2668C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22993807 | ||||||
chr7:22994046
|
C | T | 202 | a0001c0001t0003g0055a0001c0001t0004g0008a0001c0001t0004g0009others(199): Show | 235 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.-28-2907G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22994046 | ||||||
chr7:22994128
|
G | C | 1 | a0001c0002t0007g0219 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-28-2989C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22994128 | ||||||
chr7:22994198
|
G | A | 346 | a0001c0001t0002g0063a0001c0001t0002g0064a0001c0001t0002g0066others(343): Show | 385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.-28-3059C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22994198 | ||||||
chr7:22994208
|
G | A | 2 | a0001c0001t0002g0097a0001c0001t0002g0116 | 2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-28-3069C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22994208 | ||||||
chr7:22994323
|
G | A | 1 | a0001c0002t0091g0259 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-28-3184C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22994323 | ||||||
chr7:22994372
|
G | A | 50 | a0001c0001t0002g0164a0001c0001t0002g0182a0001c0001t0003g0012others(47): Show | 55 | HG00438.hp1 HG00558.hp2 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.-28-3233C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22994372 | ||||||
chr7:22994496
|
T | C | 106 | a0001c0002t0001g0001a0001c0002t0001g0007a0001c0002t0001g0226others(103): Show | 117 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.-28-3357A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22994496 | ||||||
chr7:22994662
|
C | T | 1 | a0001c0002t0110g0239 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-28-3523G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22994662 | ||||||
chr7:22994678
|
T | C | 87 | a0001c0001t0003g0055a0001c0001t0004g0008a0001c0001t0004g0009others(84): Show | 109 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(106): Show |
intron_variant | MODIFIER | c.-28-3539A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22994678 | ||||||
chr7:22994901
|
C | T | 5 | a0001c0001t0015g0002a0001c0001t0015g0037a0001c0001t0015g0038others(2): Show | 8 | HG00738.hp2 HG01168.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.-28-3762G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22994901 | ||||||
chr7:22995180
|
C | A | 80 | a0001c0002t0001g0001a0001c0002t0001g0007a0001c0002t0001g0226others(77): Show | 90 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.-28-4041G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22995180 | ||||||
chr7:22995255
|
C | T | 6 | a0001c0001t0003g0055a0001c0001t0077g0052a0001c0001t0079g0054others(3): Show | 6 | HG02055.hp2 HG02145.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28-4116G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22995255 | ||||||
chr7:22995256
|
G | A | 1 | a0001c0001t0016g0171 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-28-4117C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22995256 | ||||||
chr7:22995344
|
A | T | 8 | a0001c0001t0010g0312a0001c0001t0015g0002a0001c0001t0015g0037others(5): Show | 11 | HG00738.hp2 HG01168.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.-28-4205T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22995344 | ||||||
chr7:22995376
|
A | T | 133 | a0001c0001t0007g0221a0001c0002t0001g0001a0001c0002t0001g0007others(130): Show | 148 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.-28-4237T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22995376 | ||||||
chr7:22995431
|
T | C | 202 | a0001c0001t0003g0055a0001c0001t0004g0008a0001c0001t0004g0009others(199): Show | 235 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.-28-4292A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22995431 | ||||||
chr7:22995487
|
T | C | 1 | a0001c0002t0011g0264 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-28-4348A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22995487 | ||||||
chr7:22995513
|
T | C | 1 | a0001c0002t0007g0220 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-28-4374A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22995513 | ||||||
chr7:22995641
|
G | A | 4 | a0001c0001t0024g0026a0001c0001t0024g0027a0001c0001t0042g0025others(1): Show | 4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-4502C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22995641 | ||||||
chr7:22995646
|
T | A | 4 | a0001c0002t0001g0007a0001c0002t0001g0258a0001c0002t0001g0271others(1): Show | 6 | HG00140.hp1 HG01070.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28-4507A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22995646 | ||||||
chr7:22995650
|
CAT | C | 107 | a0001c0002t0001g0001a0001c0002t0001g0007a0001c0002t0001g0226others(104): Show | 118 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.-28-4513_-28-4512d others(4): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22995650 | ||||||
chr7:22995675
|
A | G | 107 | a0001c0002t0001g0001a0001c0002t0001g0007a0001c0002t0001g0226others(104): Show | 118 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.-28-4536T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22995675 | ||||||
chr7:22995724
|
T | G | 1 | a0001c0001t0008g0333 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-28-4585A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22995724 | ||||||
chr7:22995725
|
G | A | 3 | a0001c0002t0021g0233a0001c0002t0033g0229a0001c0002t0033g0303 | 3 | HG02886.hp1 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-28-4586C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22995725 | ||||||
chr7:22995781
|
G | A | 1 | a0007c0009t0074g0344 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-28-4642C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22995781 | ||||||
chr7:22995843
|
T | C | 4 | a0001c0002t0011g0235a0001c0002t0011g0265a0001c0002t0011g0267others(1): Show | 4 | HG02809.hp1 HG02818.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-28-4704A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22995843 | ||||||
chr7:22995898
|
G | A | 1 | a0001c0001t0002g0112 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-28-4759C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22995898 | ||||||
chr7:22995970
|
C | T | 1 | a0001c0002t0045g0036 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-28-4831G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22995970 | ||||||
chr7:22996033
|
G | A | 108 | a0001c0002t0001g0001a0001c0002t0001g0007a0001c0002t0001g0226others(105): Show | 119 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.-28-4894C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22996033 | ||||||
chr7:22996125
|
T | G | 10 | a0001c0001t0015g0002a0001c0001t0015g0037a0001c0001t0015g0038others(7): Show | 13 | HG00738.hp2 HG01168.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.-28-4986A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22996125 | ||||||
chr7:22996196
|
G | C | 44 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(41): Show | 59 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.-28-5057C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22996196 | ||||||
chr7:22996288
|
G | A | 2 | a0001c0002t0091g0259a0001c0002t0095g0227 | 2 | HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-28-5149C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22996288 | ||||||
chr7:22996292
|
CA | C | 8 | a0001c0001t0002g0116a0001c0001t0002g0126a0001c0001t0004g0316others(5): Show | 8 | HG01516.hp2 HG02965.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.-28-5154delT | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22996292 | ||||||
chr7:22996454
|
G | T | 1 | a0001c0001t0077g0052 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-28-5315C>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22996454 | ||||||
chr7:22996469
|
T | C | 4 | a0001c0001t0024g0026a0001c0001t0024g0027a0001c0001t0042g0025others(1): Show | 4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-5330A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22996469 | ||||||
chr7:22996476
|
T | C | 2 | a0001c0001t0006g0098a0001c0001t0006g0099 | 2 | NA18979.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.-28-5337A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22996476 | ||||||
chr7:22996582
|
G | A | 2 | a0001c0002t0012g0295a0001c0002t0012g0296 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-28-5443C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22996582 | ||||||
chr7:22996597
|
T | TA | 12 | a0001c0001t0002g0125a0001c0001t0002g0182a0001c0001t0003g0161others(9): Show | 12 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(9): Show |
intron_variant | MODIFIER | c.-28-5459dupT | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22996597 | ||||||
chr7:22996597
|
T | TAAAA | 8 | a0001c0002t0001g0234a0001c0002t0001g0237a0001c0002t0001g0238others(5): Show | 8 | HG01070.hp2 HG01496.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.-28-5462_-28-5459d others(6): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22996597 | ||||||
chr7:22996597
|
T | TAAAAA | 32 | a0001c0002t0001g0001a0001c0002t0001g0007a0001c0002t0001g0226others(29): Show | 39 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.-28-5463_-28-5459d others(7): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22996597 | ||||||
chr7:22996597
|
T | TAAAAAA | 31 | a0001c0002t0001g0256a0001c0002t0001g0257a0001c0002t0001g0258others(28): Show | 32 | HG00733.hp1 HG01074.hp1 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.-28-5464_-28-5459d others(8): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22996597 | ||||||
chr7:22996597
|
TA | T | 61 | a0001c0001t0002g0063a0001c0001t0002g0066a0001c0001t0002g0068others(58): Show | 61 | HG00438.hp2 HG00639.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.-28-5459delT | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22996597 | ||||||
chr7:22996597
|
TAA | T | 60 | a0001c0001t0002g0064a0001c0001t0002g0089a0001c0001t0002g0343others(57): Show | 67 | HG00280.hp2 HG01074.hp2 HG01169.hp1 others(64): Show |
intron_variant | MODIFIER | c.-28-5460_-28-5459d others(4): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22996597 | ||||||
chr7:22996597
|
TAAAAA | T | 6 | a0001c0001t0015g0002a0001c0001t0015g0037a0001c0001t0015g0038others(3): Show | 9 | HG00738.hp2 HG01168.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.-28-5463_-28-5459d others(7): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22996597 | ||||||
chr7:22996597
|
TAAAAAAA others(1): Show |
T | 40 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(37): Show | 54 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.-28-5466_-28-5459d others(10): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22996597 | ||||||
chr7:22996597
|
TAAAAAAA others(4): Show |
T | 1 | a0001c0002t0112g0304 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-28-5469_-28-5459d others(13): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22996597 | ||||||
chr7:22996770
|
C | T | 1 | a0001c0002t0045g0036 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-28-5631G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22996770 | ||||||
chr7:22996829
|
C | T | 1 | a0001c0002t0037g0274 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-28-5690G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22996829 | ||||||
chr7:22996849
|
T | C | 1 | a0001c0001t0076g0345 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-28-5710A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22996849 | ||||||
chr7:22997005
|
G | A | 1 | a0001c0001t0002g0163 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-28-5866C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22997005 | ||||||
chr7:22997072
|
A | G | 40 | a0001c0001t0002g0088a0001c0001t0003g0055a0001c0001t0007g0221others(37): Show | 44 | HG01081.hp2 HG01169.hp1 HG01361.hp2 others(41): Show |
intron_variant | MODIFIER | c.-28-5933T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22997072 | ||||||
chr7:22997152
|
C | T | 1 | a0001c0002t0045g0036 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-28-6013G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22997152 | ||||||
chr7:22997170
|
A | T | 1 | a0001c0002t0012g0189 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-28-6031T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22997170 | ||||||
chr7:22997173
|
A | G | 26 | a0001c0002t0011g0018a0001c0002t0011g0230a0001c0002t0011g0235others(23): Show | 27 | HG00733.hp1 HG01074.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.-28-6034T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22997173 | ||||||
chr7:22997281
|
A | G | 1 | a0001c0001t0008g0315 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-28-6142T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22997281 | ||||||
chr7:22997297
|
C | T | 197 | a0001c0001t0003g0055a0001c0001t0004g0008a0001c0001t0004g0009others(194): Show | 230 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(227): Show |
intron_variant | MODIFIER | c.-28-6158G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22997297 | ||||||
chr7:22997867
|
T | C | 1 | a0001c0001t0079g0054 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-28-6728A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22997867 | ||||||
chr7:22997875
|
G | C | 1 | a0001c0001t0073g0336 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-28-6736C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22997875 | ||||||
chr7:22997940
|
T | G | 7 | a0001c0001t0015g0002a0001c0001t0015g0037a0001c0001t0015g0038others(4): Show | 10 | HG00738.hp2 HG01168.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-28-6801A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22997940 | ||||||
chr7:22997960
|
T | C | 1 | a0001c0001t0068g0087 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-28-6821A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22997960 | ||||||
chr7:22997986
|
AATTAGAA others(21): Show |
A | 5 | a0001c0001t0002g0064a0001c0001t0002g0066a0001c0001t0002g0068others(2): Show | 5 | HG00639.hp2 HG01243.hp1 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.-28-6875_-28-6848d others(30): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22997986 | ||||||
chr7:22997992
|
A | T | 4 | a0001c0001t0004g0009a0001c0001t0004g0020a0001c0001t0004g0313others(1): Show | 7 | HG00423.hp1 NA18966.hp2 NA18972.hp2 others(4): Show |
intron_variant | MODIFIER | c.-28-6853T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22997992 | ||||||
chr7:22998040
|
T | G | 1 | a0001c0002t0022g0268 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-28-6901A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22998040 | ||||||
chr7:22998208
|
C | T | 1 | a0001c0001t0010g0312 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-28-7069G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22998208 | ||||||
chr7:22998334
|
T | C | 1 | a0001c0001t0043g0028 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-28-7195A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22998334 | ||||||
chr7:22998405
|
T | C | 109 | a0001c0001t0002g0297a0001c0002t0001g0001a0001c0002t0001g0007others(106): Show | 120 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.-28-7266A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22998405 | ||||||
chr7:22998496
|
T | C | 2 | a0001c0001t0036g0031a0001c0001t0036g0032 | 2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-28-7357A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22998496 | ||||||
chr7:22998532
|
A | G | 108 | a0001c0001t0002g0297a0001c0002t0001g0001a0001c0002t0001g0007others(105): Show | 119 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.-28-7393T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22998532 | ||||||
chr7:22998566
|
A | G | 3 | a0001c0001t0032g0047a0001c0001t0032g0048a0001c0001t0078g0049 | 3 | HG01081.hp2 HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-28-7427T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22998566 | ||||||
chr7:22998607
|
T | G | 5 | a0001c0001t0065g0075a0001c0001t0067g0072a0001c0001t0068g0087others(2): Show | 5 | HG02145.hp1 HG02559.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-28-7468A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22998607 | ||||||
chr7:22998690
|
C | T | 1 | a0001c0002t0005g0273 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-28-7551G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22998690 | ||||||
chr7:22998782
|
T | C | 108 | a0001c0001t0002g0297a0001c0002t0001g0001a0001c0002t0001g0007others(105): Show | 119 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.-28-7643A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22998782 | ||||||
chr7:22998804
|
C | T | 1 | a0001c0002t0095g0227 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-28-7665G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22998804 | ||||||
chr7:22998900
|
A | G | 4 | a0001c0001t0024g0026a0001c0001t0024g0027a0001c0001t0042g0025others(1): Show | 4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-7761T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22998900 | ||||||
chr7:22999006
|
T | C | 1 | a0001c0001t0002g0068 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-28-7867A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22999006 | ||||||
chr7:22999031
|
T | C | 1 | a0001c0002t0045g0036 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-28-7892A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22999031 | ||||||
chr7:22999294
|
A | C | 1 | a0001c0002t0011g0018 | 2 | HG00733.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.-28-8155T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22999294 | ||||||
chr7:22999381
|
C | G | 1 | a0001c0002t0011g0230 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-28-8242G>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22999381 | ||||||
chr7:22999447
|
C | A | 1 | a0001c0001t0073g0336 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-28-8308G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22999447 | ||||||
chr7:22999469
|
A | G | 44 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(41): Show | 59 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.-28-8330T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22999469 | ||||||
chr7:22999501
|
G | C | 108 | a0001c0001t0002g0297a0001c0002t0001g0001a0001c0002t0001g0007others(105): Show | 119 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.-28-8362C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22999501 | ||||||
chr7:22999507
|
T | C | 2 | a0001c0001t0036g0031a0001c0001t0036g0032 | 2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-28-8368A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22999507 | ||||||
chr7:22999624
|
A | G | 132 | a0001c0001t0002g0297a0001c0001t0007g0221a0001c0002t0001g0001others(129): Show | 147 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.-28-8485T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22999624 | ||||||
chr7:22999846
|
C | A | 4 | a0001c0001t0024g0026a0001c0001t0024g0027a0001c0001t0042g0025others(1): Show | 4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-8707G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22999846 | ||||||
chr7:22999938
|
A | C | 1 | a0007c0009t0074g0344 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-28-8799T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 22999938 | ||||||
chr7:23000001
|
A | T | 1 | a0001c0001t0013g0169 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-28-8862T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23000001 | ||||||
chr7:23000098
|
T | G | 2 | a0001c0001t0003g0177a0001c0001t0009g0176 | 2 | HG00558.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.-28-8959A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23000098 | ||||||
chr7:23000102
|
G | A | 1 | a0001c0002t0040g0228 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-28-8963C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23000102 | ||||||
chr7:23000159
|
T | A | 1 | a0001c0001t0031g0308 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-28-9020A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23000159 | ||||||
chr7:23000340
|
A | G | 1 | a0001c0001t0002g0076 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-28-9201T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23000340 | ||||||
chr7:23000442
|
A | G | 1 | a0001c0001t0076g0345 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-28-9303T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23000442 | ||||||
chr7:23000451
|
T | C | 2 | a0001c0002t0023g0014a0001c0002t0023g0222 | 3 | NA18984.hp2 NA19058.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.-28-9312A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23000451 | ||||||
chr7:23000476
|
A | G | 1 | a0001c0001t0036g0032 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-28-9337T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23000476 | ||||||
chr7:23000553
|
T | C | 2 | a0001c0002t0018g0015a0001c0002t0018g0224 | 3 | NA18943.hp2 NA19066.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.-28-9414A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23000553 | ||||||
chr7:23000572
|
A | T | 1 | a0001c0001t0073g0336 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-28-9433T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23000572 | ||||||
chr7:23000584
|
T | A | 1 | a0001c0002t0099g0269 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-28-9445A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23000584 | ||||||
chr7:23000589
|
T | C | 1 | a0001c0002t0037g0298 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-28-9450A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23000589 | ||||||
chr7:23000690
|
T | C | 1 | a0001c0002t0001g0234 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-28-9551A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23000690 | ||||||
chr7:23000754
|
G | T | 1 | a0006c0010t0002g0187 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-28-9615C>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23000754 | ||||||
chr7:23000812
|
G | C | 4 | a0001c0001t0024g0026a0001c0001t0024g0027a0001c0001t0042g0025others(1): Show | 4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-9673C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23000812 | ||||||
chr7:23000849
|
C | T | 81 | a0001c0001t0002g0297a0001c0002t0001g0001a0001c0002t0001g0007others(78): Show | 91 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.-28-9710G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23000849 | ||||||
chr7:23000896
|
T | G | 1 | a0001c0001t0066g0168 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-28-9757A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23000896 | ||||||
chr7:23000920
|
GT | G | 201 | a0001c0001t0002g0297a0001c0001t0003g0055a0001c0001t0004g0008others(198): Show | 234 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(231): Show |
intron_variant | MODIFIER | c.-28-9782delA | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23000920 | ||||||
chr7:23001088
|
A | G | 1 | a0001c0002t0001g0271 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-28-9949T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23001088 | ||||||
chr7:23001536
|
T | G | 3 | a0001c0001t0036g0031a0001c0001t0036g0032a0001c0002t0045g0036 | 3 | HG02896.hp2 HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-28-10397A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23001536 | ||||||
chr7:23001593
|
T | C | 1 | a0001c0001t0043g0028 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-28-10454A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23001593 | ||||||
chr7:23001801
|
G | A | 44 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(41): Show | 59 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.-28-10662C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23001801 | ||||||
chr7:23001895
|
A | AT | 137 | a0001c0001t0002g0297a0001c0001t0007g0221a0001c0001t0024g0026others(134): Show | 152 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.-28-10757dupA | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23001895 | ||||||
chr7:23001895
|
A | T | 7 | a0001c0001t0015g0002a0001c0001t0015g0037a0001c0001t0015g0038others(4): Show | 10 | HG00738.hp2 HG01168.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-28-10756T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23001895 | ||||||
chr7:23002136
|
G | GTA | 3 | a0001c0001t0006g0179a0001c0001t0017g0122a0001c0001t0028g0121 | 3 | NA18939.hp1 NA18942.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.-28-10999_-28-1099 others(6): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002136 | ||||||
chr7:23002136
|
G | GTATATAT others(3): Show |
1 | a0001c0001t0016g0180 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-28-11007_-28-1099 others(14): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002136 | ||||||
chr7:23002136
|
G | GTATATAT others(5): Show |
1 | a0001c0001t0083g0123 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-28-11009_-28-1099 others(16): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002136 | ||||||
chr7:23002136
|
GTATA | G | 4 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0001t0020g0130others(1): Show | 4 | HG00140.hp2 HG01255.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-11001_-28-1099 others(8): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002136 | ||||||
chr7:23002153
|
T | C | 45 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(42): Show | 59 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.-28-11014A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002153 | ||||||
chr7:23002153
|
TATATATA others(17): Show |
T | 1 | a0001c0001t0035g0069 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-28-11038_-28-1101 others(28): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002153 | ||||||
chr7:23002155
|
T | A | 44 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(41): Show | 58 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.-28-11016A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002155 | ||||||
chr7:23002155
|
T | C | 3 | a0001c0001t0008g0023a0001c0001t0076g0345a0007c0009t0074g0344 | 4 | HG02622.hp2 HG02976.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.-28-11016A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002155 | ||||||
chr7:23002156
|
A | T | 44 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(41): Show | 58 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.-28-11017T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002156 | ||||||
chr7:23002157
|
T | A | 2 | a0001c0001t0008g0023a0007c0009t0074g0344 | 3 | HG02976.hp2 HG04199.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-28-11018A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002157 | ||||||
chr7:23002157
|
T | C | 79 | a0001c0001t0007g0221a0001c0001t0073g0336a0001c0001t0076g0345others(76): Show | 90 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.-28-11018A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002157 | ||||||
chr7:23002158
|
A | T | 2 | a0001c0001t0008g0023a0007c0009t0074g0344 | 3 | HG02976.hp2 HG04199.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-28-11019T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002158 | ||||||
chr7:23002159
|
T | A | 55 | a0001c0001t0073g0336a0001c0001t0076g0345a0001c0002t0001g0001others(52): Show | 62 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.-28-11020A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002159 | ||||||
chr7:23002159
|
T | C | 77 | a0001c0001t0002g0297a0001c0001t0007g0221a0001c0001t0036g0031others(74): Show | 84 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(81): Show |
intron_variant | MODIFIER | c.-28-11020A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002159 | ||||||
chr7:23002160
|
A | T | 54 | a0001c0001t0076g0345a0001c0002t0001g0001a0001c0002t0001g0007others(51): Show | 61 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.-28-11021T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002160 | ||||||
chr7:23002161
|
T | A | 75 | a0001c0001t0002g0297a0001c0001t0007g0221a0001c0002t0001g0271others(72): Show | 82 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.-28-11022A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002161 | ||||||
chr7:23002161
|
T | C | 5 | a0001c0001t0036g0031a0001c0001t0036g0032a0001c0002t0005g0019others(2): Show | 6 | HG01169.hp1 HG02071.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-28-11022A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002161 | ||||||
chr7:23002161
|
TATATATA others(9): Show |
T | 2 | a0001c0001t0013g0070a0001c0001t0013g0133 | 2 | HG01891.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-28-11038_-28-1102 others(20): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002161 | ||||||
chr7:23002162
|
A | ATATATAC others(3): Show |
1 | a0001c0001t0015g0037 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-28-11024_-28-1102 others(14): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002162 | ||||||
chr7:23002162
|
A | ATATATAT others(5): Show |
3 | a0001c0001t0015g0002a0001c0001t0015g0038a0001c0001t0055g0039 | 6 | HG00738.hp2 HG01168.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.-28-11024_-28-1102 others(16): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002162 | ||||||
chr7:23002162
|
A | ATATATAT others(7): Show |
2 | a0001c0001t0053g0041a0001c0001t0071g0040 | 2 | HG01978.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-28-11024_-28-1102 others(18): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002162 | ||||||
chr7:23002162
|
A | T | 75 | a0001c0001t0002g0297a0001c0001t0007g0221a0001c0002t0001g0271others(72): Show | 82 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.-28-11023T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002162 | ||||||
chr7:23002163
|
T | A | 3 | a0001c0001t0036g0031a0001c0002t0005g0019a0001c0002t0005g0302 | 4 | HG02071.hp2 HG02896.hp2 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-11024A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002163 | ||||||
chr7:23002163
|
T | C | 6 | a0001c0001t0032g0047a0001c0001t0032g0048a0001c0001t0078g0049others(3): Show | 6 | HG01081.hp2 HG01169.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28-11024A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002163 | ||||||
chr7:23002163
|
TATATATA others(7): Show |
T | 2 | a0001c0001t0013g0134a0001c0001t0031g0307 | 2 | HG02922.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.-28-11038_-28-1102 others(18): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002163 | ||||||
chr7:23002164
|
A | AAT | 3 | a0001c0002t0007g0223a0001c0002t0012g0200a0001c0002t0012g0201 | 3 | HG01169.hp1 HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.-28-11026_-28-1102 others(6): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002164 | ||||||
chr7:23002164
|
A | ACAATTAT others(29): Show |
3 | a0001c0001t0032g0047a0001c0001t0032g0048a0001c0001t0078g0049 | 3 | HG01081.hp2 HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-28-11026_-28-1102 others(40): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002164 | ||||||
chr7:23002164
|
A | ATACAAT | 3 | a0001c0001t0024g0026a0001c0001t0024g0027a0001c0001t0042g0025 | 3 | HG01361.hp2 HG02559.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-28-11026_-28-1102 others(10): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002164 | ||||||
chr7:23002164
|
A | ATACACAA others(1): Show |
3 | a0001c0001t0080g0053a0003c0003t0075g0051a0003c0003t0081g0050 | 3 | HG02145.hp2 HG02486.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-28-11026_-28-1102 others(12): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002164 | ||||||
chr7:23002164
|
A | ATATATAC others(3): Show |
1 | a0001c0001t0043g0028 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-28-11026_-28-1102 others(14): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002164 | ||||||
chr7:23002164
|
A | T | 3 | a0001c0001t0036g0031a0001c0002t0005g0019a0001c0002t0005g0302 | 4 | HG02071.hp2 HG02896.hp2 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-11025T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002164 | ||||||
chr7:23002165
|
TATATATA others(5): Show |
T | 3 | a0001c0001t0002g0071a0001c0001t0009g0139a0001c0001t0058g0140 | 3 | HG01109.hp2 NA18975.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.-28-11038_-28-1102 others(16): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002165 | ||||||
chr7:23002167
|
TATATATA others(3): Show |
T | 37 | a0001c0001t0002g0132a0001c0001t0002g0163a0001c0001t0002g0182others(34): Show | 42 | HG00673.hp1 HG01070.hp1 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.-28-11038_-28-1102 others(14): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002167 | ||||||
chr7:23002169
|
TATATATA others(1): Show |
T | 67 | a0001c0001t0002g0064a0001c0001t0002g0066a0001c0001t0002g0076others(64): Show | 81 | HG00423.hp1 HG00544.hp2 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.-28-11038_-28-1103 others(12): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002169 | ||||||
chr7:23002171
|
TATATAC | T | 32 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0092others(29): Show | 33 | HG00544.hp1 HG00639.hp1 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.-28-11038_-28-1103 others(10): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002171 | ||||||
chr7:23002173
|
TATAC | T | 69 | a0001c0001t0002g0063a0001c0001t0002g0068a0001c0001t0002g0108others(66): Show | 76 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(73): Show |
intron_variant | MODIFIER | c.-28-11038_-28-1103 others(8): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002173 | ||||||
chr7:23002175
|
T | C | 1 | a0001c0001t0020g0130 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-28-11036A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002175 | ||||||
chr7:23002175
|
TAC | T | 82 | a0001c0001t0002g0114a0001c0001t0002g0116a0001c0001t0002g0297others(79): Show | 89 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(86): Show |
intron_variant | MODIFIER | c.-28-11038_-28-1103 others(6): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002175 | ||||||
chr7:23002177
|
C | CAAATATA others(49): Show |
1 | a0001c0001t0073g0336 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-28-11039_-28-1103 others(60): Show |
HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002177 | ||||||
chr7:23002177
|
C | T | 40 | a0001c0001t0002g0118a0001c0001t0003g0055a0001c0001t0006g0179others(37): Show | 44 | HG00438.hp1 HG00438.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.-28-11038G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002177 | ||||||
chr7:23002186
|
T | A | 1 | a0001c0001t0073g0336 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-28-11047A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002186 | ||||||
chr7:23002189
|
G | A | 25 | a0001c0001t0007g0221a0001c0002t0007g0006a0001c0002t0007g0204others(22): Show | 29 | HG01169.hp1 HG02004.hp1 HG02155.hp2 others(26): Show |
intron_variant | MODIFIER | c.-28-11050C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002189 | ||||||
chr7:23002521
|
A | T | 1 | a0001c0002t0021g0233 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-28-11382T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002521 | ||||||
chr7:23002692
|
T | C | 80 | a0001c0001t0003g0055a0001c0001t0004g0008a0001c0001t0004g0009others(77): Show | 99 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.-29+11233A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002692 | ||||||
chr7:23002757
|
T | C | 44 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(41): Show | 59 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.-29+11168A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002757 | ||||||
chr7:23002925
|
T | C | 3 | a0001c0001t0003g0055a0003c0003t0075g0051a0003c0003t0081g0050 | 3 | HG02145.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-29+11000A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002925 | ||||||
chr7:23002960
|
C | T | 1 | a0001c0001t0073g0336 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-29+10965G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23002960 | ||||||
chr7:23003468
|
A | C | 1 | a0001c0001t0076g0345 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-29+10457T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23003468 | ||||||
chr7:23003553
|
C | T | 1 | a0001c0002t0096g0232 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-29+10372G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23003553 | ||||||
chr7:23003633
|
C | T | 1 | a0001c0002t0001g0231 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-29+10292G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23003633 | ||||||
chr7:23003768
|
A | G | 1 | a0001c0002t0012g0191 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-29+10157T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23003768 | ||||||
chr7:23003923
|
C | T | 1 | a0001c0001t0003g0138 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-29+10002G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23003923 | ||||||
chr7:23003974
|
TA | T | 7 | a0001c0001t0015g0002a0001c0001t0015g0037a0001c0001t0015g0038others(4): Show | 10 | HG00738.hp2 HG01168.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-29+9950delT | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23003974 | ||||||
chr7:23004035
|
T | C | 1 | a0001c0001t0017g0131 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-29+9890A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23004035 | ||||||
chr7:23004361
|
T | C | 1 | a0001c0001t0002g0132 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-29+9564A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23004361 | ||||||
chr7:23004531
|
T | C | 1 | a0001c0002t0033g0303 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-29+9394A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23004531 | ||||||
chr7:23004535
|
T | A | 1 | a0001c0001t0077g0052 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-29+9390A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23004535 | ||||||
chr7:23004537
|
A | G | 7 | a0001c0001t0015g0002a0001c0001t0015g0037a0001c0001t0015g0038others(4): Show | 10 | HG00738.hp2 HG01168.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-29+9388T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23004537 | ||||||
chr7:23004809
|
T | C | 1 | a0001c0001t0080g0053 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-29+9116A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23004809 | ||||||
chr7:23004936
|
G | C | 2 | a0001c0001t0013g0133a0001c0001t0013g0134 | 2 | HG02922.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-29+8989C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23004936 | ||||||
chr7:23004936
|
G | T | 6 | a0001c0001t0002g0064a0001c0001t0002g0066a0001c0001t0002g0068others(3): Show | 6 | HG00639.hp2 HG01243.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.-29+8989C>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23004936 | ||||||
chr7:23004951
|
A | G | 190 | a0001c0001t0002g0297a0001c0001t0003g0055a0001c0001t0004g0008others(187): Show | 220 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(217): Show |
intron_variant | MODIFIER | c.-29+8974T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23004951 | ||||||
chr7:23004964
|
C | T | 2 | a0001c0002t0012g0189a0001c0002t0012g0190 | 2 | HG03209.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-29+8961G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23004964 | ||||||
chr7:23005003
|
C | T | 1 | a0001c0001t0076g0345 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-29+8922G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23005003 | ||||||
chr7:23005026
|
C | A | 1 | a0001c0001t0006g0181 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-29+8899G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23005026 | ||||||
chr7:23005051
|
C | T | 25 | a0001c0001t0007g0221a0001c0002t0007g0006a0001c0002t0007g0204others(22): Show | 29 | HG01169.hp1 HG02004.hp1 HG02155.hp2 others(26): Show |
intron_variant | MODIFIER | c.-29+8874G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23005051 | ||||||
chr7:23005093
|
C | T | 3 | a0001c0001t0032g0047a0001c0001t0032g0048a0001c0001t0078g0049 | 3 | HG01081.hp2 HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-29+8832G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23005093 | ||||||
chr7:23005252
|
T | C | 1 | a0001c0002t0045g0036 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-29+8673A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23005252 | ||||||
chr7:23005320
|
G | A | 95 | a0001c0001t0002g0297a0001c0002t0001g0001a0001c0002t0001g0007others(92): Show | 106 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.-29+8605C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23005320 | ||||||
chr7:23005547
|
T | C | 1 | a0001c0001t0003g0055 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-29+8378A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23005547 | ||||||
chr7:23005636
|
T | C | 1 | a0001c0001t0079g0054 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-29+8289A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23005636 | ||||||
chr7:23005746
|
C | T | 1 | a0001c0001t0082g0188 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-29+8179G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23005746 | ||||||
chr7:23005831
|
A | C | 1 | a0001c0002t0011g0230 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-29+8094T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23005831 | ||||||
chr7:23005957
|
C | G | 1 | a0001c0002t0033g0229 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-29+7968G>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23005957 | ||||||
chr7:23006052
|
C | A | 1 | a0001c0002t0112g0304 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-29+7873G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23006052 | ||||||
chr7:23006220
|
A | G | 1 | a0001c0002t0092g0056 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-29+7705T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23006220 | ||||||
chr7:23006328
|
A | G | 203 | a0001c0001t0002g0297a0001c0001t0003g0055a0001c0001t0004g0008others(200): Show | 236 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.-29+7597T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23006328 | ||||||
chr7:23006352
|
T | C | 5 | a0001c0001t0024g0026a0001c0001t0024g0027a0001c0001t0042g0025others(2): Show | 5 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-29+7573A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23006352 | ||||||
chr7:23006508
|
C | G | 1 | a0001c0001t0002g0063 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-29+7417G>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23006508 | ||||||
chr7:23006562
|
C | T | 3 | a0001c0001t0003g0061a0001c0001t0003g0062a0001c0001t0003g0135 | 3 | HG02074.hp1 HG02165.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.-29+7363G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23006562 | ||||||
chr7:23006687
|
A | T | 7 | a0001c0001t0015g0002a0001c0001t0015g0037a0001c0001t0015g0038others(4): Show | 10 | HG00738.hp2 HG01168.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-29+7238T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23006687 | ||||||
chr7:23006756
|
G | A | 1 | a0001c0001t0002g0182 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-29+7169C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23006756 | ||||||
chr7:23006802
|
C | T | 2 | a0001c0001t0036g0031a0001c0001t0036g0032 | 2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-29+7123G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23006802 | ||||||
chr7:23006850
|
G | A | 1 | a0001c0001t0003g0135 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-29+7075C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23006850 | ||||||
chr7:23007261
|
C | A | 1 | a0001c0001t0003g0183 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-29+6664G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23007261 | ||||||
chr7:23007281
|
C | T | 1 | a0001c0001t0019g0340 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-29+6644G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23007281 | ||||||
chr7:23007442
|
T | A | 61 | a0001c0001t0002g0163a0001c0001t0002g0164a0001c0001t0002g0182others(58): Show | 66 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.-29+6483A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23007442 | ||||||
chr7:23007520
|
A | C | 1 | a0001c0002t0107g0225 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-29+6405T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23007520 | ||||||
chr7:23007848
|
A | G | 1 | a0001c0001t0009g0060 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-29+6077T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23007848 | ||||||
chr7:23007850
|
C | G | 1 | a0007c0009t0074g0344 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-29+6075G>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23007850 | ||||||
chr7:23008119
|
C | T | 198 | a0001c0001t0002g0297a0001c0001t0003g0055a0001c0001t0004g0008others(195): Show | 231 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.-29+5806G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23008119 | ||||||
chr7:23008151
|
T | C | 108 | a0001c0001t0002g0297a0001c0002t0001g0001a0001c0002t0001g0007others(105): Show | 119 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.-29+5774A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23008151 | ||||||
chr7:23008200
|
A | G | 30 | a0001c0001t0007g0221a0001c0001t0024g0026a0001c0001t0024g0027others(27): Show | 34 | HG01169.hp1 HG01361.hp2 HG02004.hp1 others(31): Show |
intron_variant | MODIFIER | c.-29+5725T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23008200 | ||||||
chr7:23008227
|
C | T | 1 | a0007c0009t0074g0344 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-29+5698G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23008227 | ||||||
chr7:23008236
|
T | G | 62 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(59): Show | 76 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.-29+5689A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23008236 | ||||||
chr7:23008342
|
G | A | 1 | a0001c0001t0003g0055 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-29+5583C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23008342 | ||||||
chr7:23008398
|
A | T | 4 | a0001c0001t0024g0026a0001c0001t0024g0027a0001c0001t0042g0025others(1): Show | 4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+5527T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23008398 | ||||||
chr7:23008692
|
T | A | 84 | a0001c0001t0003g0055a0001c0001t0004g0008a0001c0001t0004g0009others(81): Show | 106 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(103): Show |
intron_variant | MODIFIER | c.-29+5233A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23008692 | ||||||
chr7:23008856
|
T | C | 1 | a0001c0002t0107g0225 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-29+5069A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23008856 | ||||||
chr7:23008878
|
G | T | 1 | a0001c0002t0040g0228 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-29+5047C>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23008878 | ||||||
chr7:23009133
|
A | T | 108 | a0001c0001t0002g0297a0001c0002t0001g0001a0001c0002t0001g0007others(105): Show | 119 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.-29+4792T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23009133 | ||||||
chr7:23009281
|
T | C | 4 | a0001c0001t0024g0026a0001c0001t0024g0027a0001c0001t0042g0025others(1): Show | 4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+4644A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23009281 | ||||||
chr7:23009367
|
T | C | 1 | a0001c0001t0073g0336 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-29+4558A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23009367 | ||||||
chr7:23009383
|
T | G | 4 | a0001c0001t0024g0026a0001c0001t0024g0027a0001c0001t0042g0025others(1): Show | 4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+4542A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23009383 | ||||||
chr7:23009432
|
C | T | 1 | a0001c0001t0082g0188 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-29+4493G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23009432 | ||||||
chr7:23009443
|
A | C | 2 | a0001c0001t0013g0059a0008c0007t0013g0058 | 2 | HG02132.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.-29+4482T>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23009443 | ||||||
chr7:23009472
|
A | G | 1 | a0001c0002t0095g0227 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-29+4453T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23009472 | ||||||
chr7:23009483
|
C | T | 1 | a0001c0002t0001g0226 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-29+4442G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23009483 | ||||||
chr7:23009509
|
C | G | 1 | a0001c0001t0076g0345 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-29+4416G>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23009509 | ||||||
chr7:23009599
|
G | A | 1 | a0001c0002t0018g0224 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-29+4326C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23009599 | ||||||
chr7:23009680
|
G | A | 1 | a0001c0002t0005g0024 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-29+4245C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23009680 | ||||||
chr7:23009762
|
G | C | 3 | a0001c0001t0025g0186a0001c0001t0046g0185a0001c0001t0047g0184 | 3 | NA18939.hp2 NA19010.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.-29+4163C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23009762 | ||||||
chr7:23009774
|
A | G | 2 | a0001c0001t0010g0005a0001c0001t0010g0044 | 4 | HG01106.hp1 HG02257.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.-29+4151T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23009774 | ||||||
chr7:23009966
|
G | T | 1 | a0001c0002t0107g0225 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-29+3959C>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23009966 | ||||||
chr7:23009967
|
T | A | 94 | a0001c0001t0002g0297a0001c0002t0001g0001a0001c0002t0001g0007others(91): Show | 105 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.-29+3958A>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23009967 | ||||||
chr7:23009984
|
T | C | 1 | a0006c0010t0002g0187 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-29+3941A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23009984 | ||||||
chr7:23010074
|
T | G | 1 | a0001c0001t0010g0044 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-29+3851A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23010074 | ||||||
chr7:23010121
|
T | C | 4 | a0001c0001t0024g0026a0001c0001t0024g0027a0001c0001t0042g0025others(1): Show | 4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+3804A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23010121 | ||||||
chr7:23010213
|
T | C | 200 | a0001c0001t0002g0202a0001c0001t0002g0297a0001c0001t0003g0055others(197): Show | 233 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(230): Show |
intron_variant | MODIFIER | c.-29+3712A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23010213 | ||||||
chr7:23010510
|
C | G | 4 | a0001c0001t0024g0026a0001c0001t0024g0027a0001c0001t0042g0025others(1): Show | 4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+3415G>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23010510 | ||||||
chr7:23010566
|
T | G | 1 | a0001c0001t0013g0306 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-29+3359A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23010566 | ||||||
chr7:23010638
|
T | G | 2 | a0001c0001t0031g0307a0001c0001t0031g0308 | 2 | NA18952.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.-29+3287A>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23010638 | ||||||
chr7:23010669
|
T | C | 35 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(32): Show | 45 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.-29+3256A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23010669 | ||||||
chr7:23010779
|
T | C | 1 | a0001c0002t0045g0036 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-29+3146A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23010779 | ||||||
chr7:23010794
|
A | G | 2 | a0001c0002t0034g0057a0001c0002t0092g0056 | 2 | HG02055.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-29+3131T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23010794 | ||||||
chr7:23011086
|
C | T | 3 | a0001c0001t0004g0008a0001c0001t0049g0310a0001c0001t0052g0311 | 5 | HG00544.hp2 NA19010.hp2 NA19065.hp2 others(2): Show |
intron_variant | MODIFIER | c.-29+2839G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23011086 | ||||||
chr7:23011104
|
G | A | 1 | a0001c0001t0076g0345 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-29+2821C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23011104 | ||||||
chr7:23011186
|
T | C | 1 | a0001c0002t0007g0309 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-29+2739A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23011186 | ||||||
chr7:23011537
|
G | A | 1 | a0001c0001t0073g0336 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-29+2388C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23011537 | ||||||
chr7:23011743
|
G | A | 1 | a0001c0001t0043g0028 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-29+2182C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23011743 | ||||||
chr7:23011884
|
C | A | 35 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0010others(32): Show | 45 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.-29+2041G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23011884 | ||||||
chr7:23011910
|
G | C | 1 | a0001c0001t0073g0336 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-29+2015C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23011910 | ||||||
chr7:23011920
|
T | C | 4 | a0001c0001t0024g0026a0001c0001t0024g0027a0001c0001t0042g0025others(1): Show | 4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+2005A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23011920 | ||||||
chr7:23012026
|
G | C | 1 | a0001c0001t0006g0337 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-29+1899C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23012026 | ||||||
chr7:23012417
|
C | G | 14 | a0001c0001t0003g0055a0001c0001t0024g0026a0001c0001t0024g0027others(11): Show | 14 | HG01081.hp2 HG01361.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-29+1508G>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23012417 | ||||||
chr7:23012467
|
G | C | 2 | a0001c0001t0003g0338a0001c0001t0003g0339 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-29+1458C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23012467 | ||||||
chr7:23012512
|
G | A | 4 | a0001c0001t0024g0026a0001c0001t0024g0027a0001c0001t0042g0025others(1): Show | 4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+1413C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23012512 | ||||||
chr7:23012535
|
T | C | 2 | a0001c0001t0019g0340a0001c0001t0019g0341 | 2 | HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-29+1390A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23012535 | ||||||
chr7:23012548
|
A | G | 1 | a0001c0001t0004g0046 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-29+1377T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23012548 | ||||||
chr7:23012642
|
T | C | 1 | a0001c0001t0016g0342 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-29+1283A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23012642 | ||||||
chr7:23012718
|
C | T | 1 | a0005c0008t0008g0045 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-29+1207G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23012718 | ||||||
chr7:23012807
|
A | T | 11 | a0001c0001t0010g0003a0001c0001t0010g0005a0001c0001t0010g0043others(8): Show | 19 | HG00738.hp1 HG00738.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.-29+1118T>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23012807 | ||||||
chr7:23012897
|
T | C | 1 | a0001c0001t0002g0343 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-29+1028A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23012897 | ||||||
chr7:23012993
|
A | G | 11 | a0001c0001t0010g0003a0001c0001t0010g0005a0001c0001t0010g0043others(8): Show | 19 | HG00738.hp1 HG00738.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.-29+932T>C | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23012993 | ||||||
chr7:23012994
|
G | C | 4 | a0001c0001t0024g0026a0001c0001t0024g0027a0001c0001t0042g0025others(1): Show | 4 | HG01361.hp2 HG02559.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+931C>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23012994 | ||||||
chr7:23013114
|
T | C | 1 | a0001c0002t0005g0024 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-29+811A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23013114 | ||||||
chr7:23013196
|
C | A | 1 | a0001c0001t0043g0028 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-29+729G>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23013196 | ||||||
chr7:23013267
|
G | A | 1 | a0001c0002t0045g0036 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-29+658C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23013267 | ||||||
chr7:23013412
|
T | C | 1 | a0007c0009t0074g0344 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-29+513A>G | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23013412 | ||||||
chr7:23013472
|
G | A | 1 | a0001c0001t0076g0345 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-29+453C>T | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23013472 | ||||||
chr7:23013635
|
G | T | 1 | a0001c0002t0045g0036 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-29+290C>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23013635 | ||||||
chr7:23013645
|
G | T | 2 | a0001c0002t0105g0035a0001c0002t0106g0034 | 2 | NA19077.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.-29+280C>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23013645 | ||||||
chr7:23013693
|
G | GC | 346 | a0001c0001t0002g0063a0001c0001t0002g0064a0001c0001t0002g0066others(343): Show | 385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.-29+231dupG | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23013693 | ||||||
chr7:23013756
|
C | T | 2 | a0001c0001t0036g0031a0001c0001t0036g0032 | 2 | HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-29+169G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23013756 | ||||||
chr7:23013823
|
C | T | 1 | a0001c0002t0005g0030 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-29+102G>A | HYCC1 | ENSG00000122591.13 | transcript | ENST00000432176.7 | protein_coding | 1/10 | chr7 | 23013823 |