Item | Value |
---|---|
geneid | 7273 |
ensemblid | ENSG00000155657.29 |
hgncid | 12403 |
symbol | TTN |
name | titin |
refseq_nuc | NM_133379.5 |
refseq_prot | NP_596870.2 |
ensembl_nuc | ENST00000360870.10 |
ensembl_prot | ENSP00000354117.4 |
mane_status | MANE Plus Clinical |
chr | chr2 |
start | 178744405 |
end | 178807423 |
strand | - |
ver | v1.2 |
region | chr2:178744405-178807423 |
region5000 | chr2:178739405-178812423 |
regionname0 | TTN_chr2_178744405_178807423 |
regionname5000 | TTN_chr2_178739405_178812423 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 5604 | 78 | 11 | 17 | 30 | 4 | 15 | 25 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0002 | 0/0 | 5604 | 67 | 8 | 9 | 43 | 0 | 7 | 30 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0003 | 0/0 | 5604 | 28 | 0 | 0 | 26 | 0 | 2 | 24 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0004 | 0/0 | 5604 | 23 | 10 | 9 | 0 | 1 | 3 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0005 | 0/0 | 5604 | 21 | 0 | 12 | 9 | 0 | 0 | 7 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0006 | 0/0 | 5604 | 15 | 1 | 8 | 0 | 0 | 6 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0007 | 0/0 | 5604 | 12 | 0 | 0 | 12 | 0 | 0 | 10 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0008 | 0/0 | 5604 | 7 | 0 | 1 | 6 | 0 | 0 | 5 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0009 | 0/0 | 5604 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0010 | 0/0 | 5604 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0011 | 0/0 | 5604 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0012 | 0/0 | 5604 | 4 | 0 | 0 | 4 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0013 | 0/0 | 5604 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0014 | 0/0 | 5604 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0015 | 0/0 | 5604 | 3 | 0 | 2 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0016 | 0/0 | 5604 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0017 | 0/0 | 5604 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0018 | 0/0 | 5604 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0019 | 0/0 | 5604 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0020 | 0/0 | 5604 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0021 | 0/0 | 5604 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0022 | 0/0 | 5604 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0023 | 0/0 | 5604 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0024 | 0/0 | 5604 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0025 | 0/0 | 5604 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0026 | 0/0 | 5604 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0027 | 0/0 | 5604 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0028 | 0/0 | 5604 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0029 | 0/0 | 5604 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0030 | 1/0 | 5604 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0031 | 0/0 | 5604 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0032 | 0/0 | 5604 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0033 | 0/0 | 5604 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0034 | 0/0 | 5604 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0035 | 0/0 | 5604 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0036 | 0/0 | 5604 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0037 | 0/0 | 5604 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0038 | 0/0 | 5604 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0039 | 0/0 | 5604 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0040 | 0/0 | 5604 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0041 | 0/0 | 5604 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0042 | 0/0 | 5604 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0043 | 0/0 | 5604 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0044 | 0/0 | 5604 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0045 | 0/0 | 5604 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0046 | 0/0 | 5604 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0047 | 0/0 | 5604 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0048 | 0/0 | 5604 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0049 | 0/0 | 5604 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0050 | 0/0 | 5604 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0051 | 0/0 | 5604 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0052 | 0/0 | 5604 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0053 | 0/0 | 5604 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0054 | 0/0 | 5604 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0055 | 0/0 | 5604 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0056 | 0/0 | 5604 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0057 | 0/0 | 5604 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0058 | 0/0 | 5604 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0059 | 0/0 | 5604 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0060 | 0/0 | 5604 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0061 | 0/0 | 5604 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0062 | 0/0 | 5604 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0063 | 0/0 | 5604 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0064 | 0/0 | 5604 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0065 | 0/0 | 5604 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0066 | 0/0 | 5604 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0067 | 0/0 | 5604 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0068 | 0/0 | 5604 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0069 | 0/0 | 5604 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0070 | 0/0 | 5604 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0071 | 0/0 | 5604 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0072 | 0/0 | 5604 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0073 | 0/0 | 5604 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0074 | 0/0 | 5582 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5577): Show |
chr2 | 178739405 | 178812423 |
a0075 | 0/0 | 5604 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0076 | 0/0 | 5604 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0077 | 0/0 | 5604 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0078 | 0/0 | 5604 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0079 | 0/0 | 5604 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0080 | 0/0 | 5604 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0081 | 0/0 | 5604 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0082 | 0/0 | 5604 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0083 | 0/0 | 5604 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
a0084 | 0/0 | 5604 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTN_chr2_178739405_178812423 | TTN | MTTQA others(5599): Show |
chr2 | 178739405 | 178812423 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002 | 0/0 | 16812 | 36 | 5 | 10 | 11 | 4 | 6 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0001c0003 | 0/0 | 16812 | 32 | 4 | 4 | 17 | 0 | 7 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0001c0015 | 0/1 | 16812 | 4 | 1 | 2 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0001c0044 | 0/0 | 16812 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0001c0061 | 0/0 | 16812 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0001c0068 | 0/0 | 16812 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0001c0069 | 0/0 | 16812 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0001c0076 | 0/0 | 16812 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0001c0077 | 0/0 | 16812 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0002c0001 | 0/0 | 16812 | 65 | 8 | 9 | 41 | 0 | 7 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0002c0087 | 0/0 | 16812 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0002c0089 | 0/0 | 16812 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0003c0004 | 0/0 | 16812 | 26 | 0 | 0 | 24 | 0 | 2 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0003c0041 | 0/0 | 16812 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0003c0047 | 0/0 | 16812 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0004c0006 | 0/0 | 16812 | 17 | 4 | 9 | 0 | 1 | 3 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0004c0011 | 0/0 | 16812 | 6 | 6 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0005c0005 | 0/0 | 16812 | 21 | 0 | 12 | 9 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0006c0007 | 0/0 | 16812 | 14 | 1 | 8 | 0 | 0 | 5 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0006c0056 | 0/0 | 16812 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0007c0008 | 0/0 | 16812 | 11 | 0 | 0 | 11 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0007c0079 | 0/0 | 16812 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0008c0009 | 0/0 | 16812 | 7 | 0 | 1 | 6 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0009c0013 | 0/0 | 16812 | 5 | 5 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0009c0022 | 0/0 | 16812 | 2 | 2 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0010c0010 | 0/0 | 16812 | 7 | 7 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0011c0012 | 0/0 | 16812 | 5 | 5 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0012c0018 | 0/0 | 16812 | 3 | 0 | 0 | 3 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0012c0055 | 0/0 | 16812 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0013c0014 | 0/0 | 16812 | 4 | 4 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0014c0017 | 0/0 | 16812 | 3 | 3 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0014c0049 | 0/0 | 16812 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0015c0033 | 0/0 | 16812 | 2 | 0 | 2 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0015c0100 | 0/0 | 16812 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0016c0016 | 0/0 | 16812 | 3 | 3 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0017c0019 | 0/0 | 16812 | 3 | 3 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0018c0027 | 0/0 | 16812 | 2 | 0 | 0 | 2 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0019c0023 | 0/0 | 16812 | 2 | 0 | 2 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0020c0025 | 0/0 | 16812 | 2 | 2 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0021c0029 | 0/0 | 16812 | 2 | 2 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0022c0032 | 0/0 | 16812 | 2 | 2 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0023c0020 | 0/0 | 16812 | 2 | 2 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0024c0030 | 0/0 | 16812 | 2 | 2 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0025c0021 | 0/0 | 16812 | 2 | 2 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0026c0024 | 0/0 | 16812 | 2 | 0 | 0 | 2 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0027c0031 | 0/0 | 16812 | 2 | 0 | 0 | 2 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0028c0026 | 0/0 | 16812 | 2 | 0 | 0 | 2 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0029c0028 | 0/0 | 16812 | 2 | 0 | 0 | 2 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0030c0051 | 1/0 | 16812 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0031c0073 | 0/0 | 16812 | 1 | 0 | 0 | 0 | 1 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0032c0080 | 0/0 | 16812 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0033c0074 | 0/0 | 16812 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0034c0103 | 0/0 | 16812 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0035c0040 | 0/0 | 16812 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0036c0037 | 0/0 | 16812 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0037c0066 | 0/0 | 16812 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0038c0038 | 0/0 | 16812 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0039c0048 | 0/0 | 16812 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0040c0075 | 0/0 | 16812 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0041c0042 | 0/0 | 16812 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0042c0059 | 0/0 | 16812 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0043c0054 | 0/0 | 16812 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0044c0082 | 0/0 | 16812 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0045c0062 | 0/0 | 16812 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0046c0091 | 0/0 | 16812 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0047c0065 | 0/0 | 16812 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0048c0094 | 0/0 | 16812 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0049c0052 | 0/0 | 16812 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0050c0053 | 0/0 | 16812 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0051c0078 | 0/0 | 16812 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0052c0102 | 0/0 | 16812 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0053c0098 | 0/0 | 16812 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0054c0046 | 0/0 | 16812 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0055c0084 | 0/0 | 16812 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0056c0036 | 0/0 | 16812 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0057c0095 | 0/0 | 16812 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0058c0099 | 0/0 | 16812 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0059c0039 | 0/0 | 16812 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0060c0045 | 0/0 | 16812 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0061c0097 | 0/0 | 16812 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0062c0071 | 0/0 | 16812 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0063c0070 | 0/0 | 16812 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0064c0035 | 0/0 | 16812 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0065c0101 | 0/0 | 16812 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0066c0058 | 0/0 | 16812 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0067c0060 | 0/0 | 16812 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0068c0067 | 0/0 | 16812 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0069c0057 | 0/0 | 16812 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0070c0086 | 0/0 | 16812 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0071c0093 | 0/0 | 16812 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0072c0081 | 0/0 | 16812 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0073c0090 | 0/0 | 16812 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0074c0085 | 0/0 | 16746 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16741): Show |
chr2 | 178739405 | 178812423 | ||
a0075c0034 | 0/0 | 16812 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0076c0092 | 0/0 | 16812 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0077c0063 | 0/0 | 16812 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0078c0083 | 0/0 | 16812 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0079c0088 | 0/0 | 16812 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0080c0043 | 0/0 | 16812 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0081c0096 | 0/0 | 16812 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0082c0072 | 0/0 | 16812 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0083c0050 | 0/0 | 16812 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 | ||
a0084c0064 | 0/0 | 16812 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | ATGAC others(16807): Show |
chr2 | 178739405 | 178812423 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001 | 0/0 | 18220 | 28 | 4 | 7 | 8 | 4 | 5 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0001c0002t0002 | 0/0 | 18220 | 6 | 1 | 3 | 1 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0001c0002t0004 | 0/0 | 18220 | 2 | 0 | 0 | 2 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0001c0003t0001 | 0/0 | 18220 | 9 | 3 | 3 | 2 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0001c0003t0004 | 0/0 | 18220 | 22 | 0 | 1 | 15 | 0 | 6 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0001c0003t0021 | 0/0 | 18220 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0001c0015t0001 | 0/1 | 18220 | 3 | 0 | 2 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0001c0015t0008 | 0/0 | 18220 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0001c0044t0004 | 0/0 | 18220 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0001c0061t0004 | 0/0 | 18220 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0001c0068t0008 | 0/0 | 18220 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0001c0069t0001 | 0/0 | 18220 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0001c0076t0001 | 0/0 | 18220 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0001c0077t0001 | 0/0 | 18220 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0002c0001t0001 | 0/0 | 18220 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0002c0001t0002 | 0/0 | 18220 | 62 | 6 | 9 | 40 | 0 | 7 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0002c0001t0012 | 0/0 | 18220 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0002c0001t0018 | 0/0 | 18220 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0002c0087t0002 | 0/0 | 18220 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0002c0089t0002 | 0/0 | 18220 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0003c0004t0001 | 0/0 | 18220 | 24 | 0 | 0 | 22 | 0 | 2 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0003c0004t0002 | 0/0 | 18220 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0003c0004t0004 | 0/0 | 18220 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0003c0041t0001 | 0/0 | 18220 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0003c0047t0001 | 0/0 | 18220 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0004c0006t0001 | 0/0 | 18220 | 17 | 4 | 9 | 0 | 1 | 3 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0004c0011t0001 | 0/0 | 18220 | 6 | 6 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0005c0005t0003 | 0/0 | 18220 | 21 | 0 | 12 | 9 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0006c0007t0005 | 0/0 | 18220 | 13 | 0 | 8 | 0 | 0 | 5 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0006c0007t0015 | 0/0 | 18220 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0006c0056t0005 | 0/0 | 18220 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0007c0008t0003 | 0/0 | 18220 | 11 | 0 | 0 | 11 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0007c0079t0003 | 0/0 | 18220 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0008c0009t0001 | 0/0 | 18220 | 7 | 0 | 1 | 6 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0009c0013t0006 | 0/0 | 18220 | 5 | 5 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0009c0022t0006 | 0/0 | 18220 | 2 | 2 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0010c0010t0001 | 0/0 | 18220 | 5 | 5 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0010c0010t0013 | 0/0 | 18220 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0010c0010t0020 | 0/0 | 18220 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0011c0012t0001 | 0/0 | 18220 | 5 | 5 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0012c0018t0005 | 0/0 | 18220 | 3 | 0 | 0 | 3 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0012c0055t0005 | 0/0 | 18220 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0013c0014t0001 | 0/0 | 18220 | 4 | 4 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0014c0017t0007 | 0/0 | 18220 | 3 | 3 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0014c0049t0007 | 0/0 | 18220 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0015c0033t0002 | 0/0 | 18220 | 2 | 0 | 2 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0015c0100t0002 | 0/0 | 18220 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0016c0016t0001 | 0/0 | 18220 | 3 | 3 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0017c0019t0001 | 0/0 | 18220 | 3 | 3 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0018c0027t0003 | 0/0 | 18220 | 2 | 0 | 0 | 2 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0019c0023t0001 | 0/0 | 18220 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0019c0023t0002 | 0/0 | 18220 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0020c0025t0001 | 0/0 | 18220 | 2 | 2 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0021c0029t0010 | 0/0 | 18220 | 2 | 2 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0022c0032t0002 | 0/0 | 18220 | 2 | 2 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0023c0020t0001 | 0/0 | 18220 | 2 | 2 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0024c0030t0001 | 0/0 | 18220 | 2 | 2 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0025c0021t0001 | 0/0 | 18220 | 2 | 2 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0026c0024t0001 | 0/0 | 18220 | 2 | 0 | 0 | 2 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0027c0031t0003 | 0/0 | 18220 | 2 | 0 | 0 | 2 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0028c0026t0003 | 0/0 | 18220 | 2 | 0 | 0 | 2 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0029c0028t0004 | 0/0 | 18220 | 2 | 0 | 0 | 2 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0030c0051t0001 | 1/0 | 18220 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0031c0073t0001 | 0/0 | 18220 | 1 | 0 | 0 | 0 | 1 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0032c0080t0003 | 0/0 | 18220 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0033c0074t0001 | 0/0 | 18220 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0034c0103t0002 | 0/0 | 18220 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0035c0040t0001 | 0/0 | 18220 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0036c0037t0001 | 0/0 | 18220 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0037c0066t0001 | 0/0 | 18220 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0038c0038t0001 | 0/0 | 18220 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0039c0048t0001 | 0/0 | 18220 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0040c0075t0001 | 0/0 | 18220 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0041c0042t0003 | 0/0 | 18220 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0042c0059t0001 | 0/0 | 18220 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0043c0054t0005 | 0/0 | 18220 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0044c0082t0002 | 0/0 | 18220 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0045c0062t0003 | 0/0 | 18220 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0046c0091t0011 | 0/0 | 18220 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0047c0065t0004 | 0/0 | 18220 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0048c0094t0002 | 0/0 | 18220 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0049c0052t0009 | 0/0 | 18220 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0050c0053t0001 | 0/0 | 18220 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0051c0078t0001 | 0/0 | 18220 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0052c0102t0002 | 0/0 | 18220 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0053c0098t0002 | 0/0 | 18220 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0054c0046t0001 | 0/0 | 18220 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0055c0084t0002 | 0/0 | 18220 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0056c0036t0016 | 0/0 | 18220 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0057c0095t0009 | 0/0 | 18220 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0058c0099t0002 | 0/0 | 18220 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0059c0039t0001 | 0/0 | 18220 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0060c0045t0004 | 0/0 | 18220 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0061c0097t0017 | 0/0 | 18548 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18543): Show |
chr2 | 178739405 | 178812423 |
a0062c0071t0001 | 0/0 | 18220 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0063c0070t0008 | 0/0 | 18220 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0064c0035t0014 | 0/0 | 18220 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0065c0101t0002 | 0/0 | 18220 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0066c0058t0011 | 0/0 | 18220 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0067c0060t0001 | 0/0 | 18220 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0068c0067t0001 | 0/0 | 18220 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0069c0057t0005 | 0/0 | 18220 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0070c0086t0002 | 0/0 | 18220 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0071c0093t0004 | 0/0 | 18220 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0072c0081t0003 | 0/0 | 18220 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0073c0090t0002 | 0/0 | 18220 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0074c0085t0002 | 0/0 | 18154 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18149): Show |
chr2 | 178739405 | 178812423 |
a0075c0034t0002 | 0/0 | 18220 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0076c0092t0003 | 0/0 | 18220 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0077c0063t0004 | 0/0 | 18220 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0078c0083t0003 | 0/0 | 18220 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0079c0088t0002 | 0/0 | 18220 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0080c0043t0003 | 0/0 | 18220 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0081c0096t0001 | 0/0 | 18220 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0082c0072t0001 | 0/0 | 18220 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0083c0050t0019 | 0/0 | 18220 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
a0084c0064t0005 | 0/0 | 18220 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | GAGCA others(18215): Show |
chr2 | 178739405 | 178812423 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001g0005 | 0/0 | 4 | 0 | 0 | 0 | 1 | 3 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0002t0001g0028 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0002t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0002t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0002t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0002t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0002t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0002t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0002t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0002t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0002t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0002t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0002t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0002t0004g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0003t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0003t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0003t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0003t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0003t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0003t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0003t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0003t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0003t0004g0002 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0003t0004g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0003t0004g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0003t0004g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0003t0004g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0003t0004g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0003t0004g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0003t0004g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0003t0004g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0003t0004g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0003t0004g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0003t0004g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0003t0021g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0015t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0015t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0015t0001g0145 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0015t0008g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0044t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0061t0004g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0068t0008g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0069t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0076t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0001c0077t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0002c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0002c0001t0002g0001 | 0/0 | 11 | 0 | 2 | 9 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0002c0001t0002g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0002c0001t0002g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0002c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0002c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0002c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0002c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0002c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0002c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0002c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0002c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0002c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0002c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0002c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0002c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0002c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0002c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0002c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0002c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0002c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0002c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0002c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0002c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0002c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0002c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0002c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0002c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0002c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0002c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0002c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0002c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0002c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0002c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0002c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0002c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0002c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0002c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0002c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0002c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0002c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0002c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0002c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0002c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0002c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0002c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0002c0001t0012g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0002c0001t0018g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0002c0087t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0002c0089t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0003c0004t0001g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0003c0004t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0003c0004t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0003c0004t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0003c0004t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0003c0004t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0003c0004t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0003c0004t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0003c0004t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0003c0004t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0003c0004t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0003c0004t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0003c0004t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0003c0004t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0003c0004t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0003c0004t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0003c0004t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0003c0004t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0003c0004t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0003c0041t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0003c0047t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0004c0006t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0004c0006t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0004c0006t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0004c0006t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0004c0006t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0004c0006t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0004c0006t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0004c0006t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0004c0006t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0004c0006t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0004c0006t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0004c0006t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0004c0006t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0004c0006t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0004c0011t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0004c0011t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0004c0011t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0004c0011t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0004c0011t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0005c0005t0003g0010 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0005c0005t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0005c0005t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0005c0005t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0005c0005t0003g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0005c0005t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0005c0005t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0005c0005t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0005c0005t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0005c0005t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0005c0005t0003g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0005c0005t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0005c0005t0003g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0005c0005t0003g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0005c0005t0003g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0005c0005t0003g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0005c0005t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0005c0005t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0005c0005t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0006c0007t0005g0003 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0006c0007t0005g0030 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0006c0007t0005g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0006c0007t0005g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0006c0007t0005g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0006c0007t0005g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0006c0007t0005g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0006c0007t0015g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0006c0056t0005g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0007c0008t0003g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0007c0008t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0007c0008t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0007c0008t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0007c0008t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0007c0008t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0007c0008t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0007c0008t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0007c0008t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0007c0008t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0007c0079t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0008c0009t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0008c0009t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0008c0009t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0008c0009t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0009c0013t0006g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0009c0013t0006g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0009c0013t0006g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0009c0013t0006g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0009c0022t0006g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0010c0010t0001g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0010c0010t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0010c0010t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0010c0010t0013g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0010c0010t0020g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0011c0012t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0011c0012t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0012c0018t0005g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0012c0018t0005g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0012c0018t0005g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0012c0055t0005g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0013c0014t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0013c0014t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0013c0014t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0013c0014t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0014c0017t0007g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0014c0017t0007g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0014c0017t0007g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0014c0049t0007g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0015c0033t0002g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0015c0100t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0016c0016t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0016c0016t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0017c0019t0001g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0018c0027t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0018c0027t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0019c0023t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0019c0023t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0020c0025t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0020c0025t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0021c0029t0010g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0021c0029t0010g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0022c0032t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0022c0032t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0023c0020t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0024c0030t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0024c0030t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0025c0021t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0025c0021t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0026c0024t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0026c0024t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0027c0031t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0027c0031t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0028c0026t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0028c0026t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0029c0028t0004g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0030c0051t0001g0122 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0031c0073t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0032c0080t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0033c0074t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0034c0103t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0035c0040t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0036c0037t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0037c0066t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0038c0038t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0039c0048t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0040c0075t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0041c0042t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0042c0059t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0043c0054t0005g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0044c0082t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0045c0062t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0046c0091t0011g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0047c0065t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0048c0094t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0049c0052t0009g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0050c0053t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0051c0078t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0052c0102t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0053c0098t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0054c0046t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0055c0084t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0056c0036t0016g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0057c0095t0009g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0058c0099t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0059c0039t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0060c0045t0004g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0061c0097t0017g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0062c0071t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0063c0070t0008g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0064c0035t0014g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0065c0101t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0066c0058t0011g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0067c0060t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0068c0067t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0069c0057t0005g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0070c0086t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0071c0093t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0072c0081t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0073c0090t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0074c0085t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0075c0034t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0076c0092t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0077c0063t0004g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0078c0083t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0079c0088t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0080c0043t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0081c0096t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0082c0072t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0083c0050t0019g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
a0084c0064t0005g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0004 | c0006 | t0001 | g0136 | EUR | GBR | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG00099 | hp2 | a0001 | c0002 | t0001 | g0005 | EUR | GBR | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG00140 | hp1 | a0001 | c0002 | t0001 | g0175 | EUR | GBR | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG00140 | hp2 | a0031 | c0073 | t0001 | g0137 | EUR | GBR | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG00408 | hp1 | a0002 | c0001 | t0002 | g0085 | EAS | CHS | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG00408 | hp2 | a0001 | c0003 | t0004 | g0002 | EAS | CHS | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG00423 | hp1 | a0001 | c0002 | t0001 | g0191 | EAS | CHS | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG00423 | hp2 | a0002 | c0001 | t0002 | g0020 | EAS | CHS | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG00438 | hp1 | a0003 | c0004 | t0001 | g0276 | EAS | CHS | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG00438 | hp2 | a0018 | c0027 | t0003 | g0241 | EAS | CHS | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG00544 | hp1 | a0002 | c0089 | t0002 | g0083 | EAS | CHS | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG00544 | hp2 | a0012 | c0055 | t0005 | g0252 | EAS | CHS | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG00558 | hp1 | a0008 | c0009 | t0001 | g0012 | EAS | CHS | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG00558 | hp2 | a0032 | c0080 | t0003 | g0153 | EAS | CHS | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG00597 | hp1 | a0005 | c0005 | t0003 | g0201 | EAS | CHS | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG00597 | hp2 | a0002 | c0001 | t0002 | g0001 | EAS | CHS | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG00609 | hp1 | a0002 | c0001 | t0002 | g0081 | EAS | CHS | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG00609 | hp2 | a0018 | c0027 | t0003 | g0240 | EAS | CHS | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG00621 | hp1 | a0002 | c0001 | t0018 | g0078 | EAS | CHS | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG00621 | hp2 | a0001 | c0002 | t0001 | g0185 | EAS | CHS | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG00639 | hp1 | a0001 | c0002 | t0002 | g0183 | AMR | PUR | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG00639 | hp2 | a0001 | c0003 | t0001 | g0149 | AMR | PUR | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG00642 | hp1 | a0001 | c0003 | t0004 | g0281 | AMR | PUR | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG00642 | hp2 | a0006 | c0007 | t0005 | g0003 | AMR | PUR | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG00673 | hp1 | a0007 | c0008 | t0003 | g0106 | EAS | CHS | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG00673 | hp2 | a0002 | c0001 | t0002 | g0054 | EAS | CHS | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG00733 | hp1 | a0033 | c0074 | t0001 | g0134 | AMR | PUR | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG00733 | hp2 | a0002 | c0001 | t0002 | g0001 | AMR | PUR | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG00735 | hp1 | a0034 | c0103 | t0002 | g0117 | AMR | PUR | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG00735 | hp2 | a0001 | c0002 | t0001 | g0028 | AMR | PUR | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG00738 | hp1 | a0004 | c0006 | t0001 | g0045 | AMR | PUR | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG00738 | hp2 | a0004 | c0006 | t0001 | g0022 | AMR | PUR | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG00741 | hp1 | a0015 | c0033 | t0002 | g0019 | AMR | PUR | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG00741 | hp2 | a0004 | c0006 | t0001 | g0131 | AMR | PUR | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01071 | hp1 | a0035 | c0040 | t0001 | g0177 | AMR | PUR | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01071 | hp2 | a0004 | c0006 | t0001 | g0021 | AMR | PUR | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01074 | hp1 | a0004 | c0006 | t0001 | g0021 | AMR | PUR | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01074 | hp2 | a0001 | c0076 | t0001 | g0180 | AMR | PUR | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01081 | hp1 | a0001 | c0002 | t0001 | g0178 | AMR | PUR | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01081 | hp2 | a0002 | c0001 | t0002 | g0056 | AMR | PUR | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01099 | hp1 | a0015 | c0033 | t0002 | g0019 | AMR | PUR | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01099 | hp2 | a0005 | c0005 | t0003 | g0010 | AMR | PUR | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01106 | hp1 | a0036 | c0037 | t0001 | g0169 | AMR | PUR | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01106 | hp2 | a0001 | c0015 | t0001 | g0128 | AMR | PUR | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01167 | hp1 | a0001 | c0002 | t0001 | g0197 | AMR | PUR | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01167 | hp2 | a0019 | c0023 | t0001 | g0170 | AMR | PUR | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01168 | hp1 | a0037 | c0066 | t0001 | g0158 | AMR | PUR | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01168 | hp2 | a0005 | c0005 | t0003 | g0202 | AMR | PUR | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01169 | hp1 | a0001 | c0002 | t0001 | g0176 | AMR | PUR | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01169 | hp2 | a0005 | c0005 | t0003 | g0222 | AMR | PUR | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01175 | hp1 | a0004 | c0006 | t0001 | g0120 | AMR | PUR | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01175 | hp2 | a0001 | c0002 | t0002 | g0184 | AMR | PUR | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01192 | hp1 | a0001 | c0002 | t0001 | g0198 | AMR | PUR | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01192 | hp2 | a0008 | c0009 | t0001 | g0274 | AMR | PUR | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01243 | hp1 | a0038 | c0038 | t0001 | g0172 | AMR | PUR | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01243 | hp2 | a0004 | c0006 | t0001 | g0159 | AMR | PUR | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01255 | hp1 | a0004 | c0006 | t0001 | g0135 | AMR | CLM | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01255 | hp2 | a0039 | c0048 | t0001 | g0256 | AMR | CLM | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01256 | hp1 | a0001 | c0002 | t0001 | g0174 | AMR | CLM | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01256 | hp2 | a0002 | c0001 | t0002 | g0052 | AMR | CLM | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01257 | hp1 | a0006 | c0007 | t0005 | g0003 | AMR | CLM | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01257 | hp2 | a0002 | c0001 | t0002 | g0093 | AMR | CLM | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01261 | hp1 | a0040 | c0075 | t0001 | g0147 | AMR | CLM | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01261 | hp2 | a0005 | c0005 | t0003 | g0219 | AMR | CLM | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01346 | hp1 | a0002 | c0001 | t0002 | g0001 | AMR | CLM | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01346 | hp2 | a0006 | c0007 | t0005 | g0003 | AMR | CLM | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0179 | AMR | CLM | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01358 | hp2 | a0041 | c0042 | t0003 | g0209 | AMR | CLM | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01361 | hp1 | a0001 | c0003 | t0001 | g0152 | AMR | CLM | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01361 | hp2 | a0042 | c0059 | t0001 | g0245 | AMR | CLM | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01433 | hp1 | a0004 | c0006 | t0001 | g0022 | AMR | CLM | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01433 | hp2 | a0005 | c0005 | t0003 | g0211 | AMR | CLM | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01496 | hp1 | a0001 | c0015 | t0001 | g0125 | AMR | CLM | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01496 | hp2 | a0006 | c0007 | t0005 | g0003 | AMR | CLM | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01517 | hp1 | a0001 | c0002 | t0001 | g0196 | EUR | IBS | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01517 | hp2 | a0001 | c0002 | t0001 | g0028 | EUR | IBS | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01884 | hp1 | a0004 | c0006 | t0001 | g0133 | AFR | ACB | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01884 | hp2 | a0002 | c0001 | t0002 | g0099 | AFR | ACB | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01891 | hp1 | a0001 | c0002 | t0001 | g0163 | AFR | ACB | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01891 | hp2 | a0002 | c0001 | t0002 | g0006 | AFR | ACB | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01928 | hp1 | a0005 | c0005 | t0003 | g0224 | AMR | PEL | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01928 | hp2 | a0043 | c0054 | t0005 | g0230 | AMR | PEL | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01943 | hp1 | a0005 | c0005 | t0003 | g0225 | AMR | PEL | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01943 | hp2 | a0044 | c0082 | t0002 | g0109 | AMR | PEL | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01952 | hp1 | a0005 | c0005 | t0003 | g0242 | AMR | PEL | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01952 | hp2 | a0006 | c0007 | t0005 | g0003 | AMR | PEL | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01975 | hp1 | a0005 | c0005 | t0003 | g0221 | AMR | PEL | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01975 | hp2 | a0002 | c0001 | t0002 | g0104 | AMR | PEL | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01978 | hp1 | a0002 | c0001 | t0002 | g0094 | AMR | PEL | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01978 | hp2 | a0001 | c0003 | t0001 | g0150 | AMR | PEL | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01981 | hp1 | a0005 | c0005 | t0003 | g0223 | AMR | PEL | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG01981 | hp2 | a0001 | c0002 | t0002 | g0199 | AMR | PEL | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02004 | hp1 | a0006 | c0007 | t0005 | g0239 | AMR | PEL | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02004 | hp2 | a0005 | c0005 | t0003 | g0226 | AMR | PEL | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02015 | hp1 | a0002 | c0001 | t0002 | g0066 | EAS | KHV | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02015 | hp2 | a0012 | c0018 | t0005 | g0253 | EAS | KHV | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02027 | hp1 | a0002 | c0001 | t0002 | g0074 | EAS | KHV | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02027 | hp2 | a0045 | c0062 | t0003 | g0284 | EAS | KHV | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0195 | EAS | KHV | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02040 | hp2 | a0012 | c0018 | t0005 | g0254 | EAS | KHV | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02055 | hp1 | a0046 | c0091 | t0011 | g0053 | AFR | ACB | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02055 | hp2 | a0004 | c0011 | t0001 | g0146 | AFR | ACB | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02080 | hp1 | a0047 | c0065 | t0004 | g0287 | EAS | KHV | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02080 | hp2 | a0048 | c0094 | t0002 | g0100 | EAS | KHV | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02129 | hp1 | a0001 | c0002 | t0001 | g0190 | EAS | KHV | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02129 | hp2 | a0002 | c0001 | t0002 | g0017 | EAS | KHV | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02145 | hp1 | a0009 | c0022 | t0006 | g0025 | AFR | ACB | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02145 | hp2 | a0004 | c0006 | t0001 | g0024 | AFR | ACB | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02155 | hp1 | a0002 | c0001 | t0002 | g0070 | EAS | CDX | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02155 | hp2 | a0012 | c0018 | t0005 | g0255 | EAS | CDX | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02165 | hp1 | a0002 | c0001 | t0002 | g0020 | EAS | CDX | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02165 | hp2 | a0003 | c0004 | t0001 | g0041 | EAS | CDX | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02257 | hp1 | a0050 | c0053 | t0001 | g0238 | AFR | ACB | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02257 | hp2 | a0016 | c0016 | t0001 | g0014 | AFR | ACB | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02258 | hp1 | a0021 | c0029 | t0010 | g0141 | AFR | ACB | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02258 | hp2 | a0051 | c0078 | t0001 | g0247 | AFR | ACB | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02273 | hp1 | a0002 | c0001 | t0002 | g0092 | AMR | PEL | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02273 | hp2 | a0006 | c0007 | t0005 | g0003 | AMR | PEL | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02280 | hp1 | a0022 | c0032 | t0002 | g0076 | AFR | ACB | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02280 | hp2 | a0020 | c0025 | t0001 | g0166 | AFR | ACB | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02293 | hp1 | a0006 | c0007 | t0005 | g0030 | AMR | PEL | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02293 | hp2 | a0002 | c0001 | t0002 | g0112 | AMR | PEL | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02300 | hp1 | a0005 | c0005 | t0003 | g0218 | AMR | PEL | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02300 | hp2 | a0019 | c0023 | t0002 | g0189 | AMR | PEL | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02451 | hp1 | a0023 | c0020 | t0001 | g0026 | AFR | ACB | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02451 | hp2 | a0013 | c0014 | t0001 | g0208 | AFR | ACB | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02523 | hp1 | a0002 | c0001 | t0002 | g0073 | EAS | KHV | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02523 | hp2 | a0005 | c0005 | t0003 | g0210 | EAS | KHV | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02602 | hp1 | a0001 | c0002 | t0001 | g0005 | SAS | PJL | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02602 | hp2 | a0002 | c0001 | t0002 | g0048 | SAS | PJL | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02615 | hp1 | a0016 | c0016 | t0001 | g0042 | AFR | GWD | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02615 | hp2 | a0052 | c0102 | t0002 | g0114 | AFR | GWD | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02622 | hp1 | a0001 | c0003 | t0001 | g0143 | AFR | GWD | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02622 | hp2 | a0053 | c0098 | t0002 | g0113 | AFR | GWD | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02630 | hp1 | a0010 | c0010 | t0001 | g0246 | AFR | GWD | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02630 | hp2 | a0004 | c0011 | t0001 | g0124 | AFR | GWD | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02647 | hp1 | a0001 | c0002 | t0002 | g0164 | AFR | GWD | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02647 | hp2 | a0002 | c0001 | t0012 | g0036 | AFR | GWD | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02683 | hp1 | a0001 | c0002 | t0002 | g0182 | SAS | PJL | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02683 | hp2 | a0054 | c0046 | t0001 | g0157 | SAS | PJL | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02698 | hp1 | a0001 | c0003 | t0004 | g0292 | SAS | PJL | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02698 | hp2 | a0055 | c0084 | t0002 | g0072 | SAS | PJL | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02717 | hp1 | a0056 | c0036 | t0016 | g0300 | AFR | GWD | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02717 | hp2 | a0001 | c0068 | t0008 | g0126 | AFR | GWD | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02723 | hp1 | a0057 | c0095 | t0009 | g0299 | AFR | GWD | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02723 | hp2 | a0058 | c0099 | t0002 | g0115 | AFR | GWD | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02735 | hp1 | a0004 | c0006 | t0001 | g0129 | SAS | PJL | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02735 | hp2 | a0059 | c0039 | t0001 | g0188 | SAS | PJL | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02738 | hp1 | a0060 | c0045 | t0004 | g0280 | SAS | PJL | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02738 | hp2 | a0061 | c0097 | t0017 | g0203 | SAS | PJL | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02809 | hp1 | a0010 | c0010 | t0001 | g0011 | AFR | GWD | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02809 | hp2 | a0062 | c0071 | t0001 | g0140 | AFR | GWD | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02818 | hp1 | a0002 | c0001 | t0002 | g0006 | AFR | GWD | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02818 | hp2 | a0011 | c0012 | t0001 | g0008 | AFR | GWD | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02895 | hp1 | a0009 | c0013 | t0006 | g0298 | AFR | GWD | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02895 | hp2 | a0010 | c0010 | t0001 | g0011 | AFR | GWD | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02896 | hp1 | a0009 | c0013 | t0006 | g0035 | AFR | GWD | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02896 | hp2 | a0063 | c0070 | t0008 | g0121 | AFR | GWD | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02897 | hp1 | a0009 | c0013 | t0006 | g0035 | AFR | GWD | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02897 | hp2 | a0010 | c0010 | t0001 | g0011 | AFR | GWD | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02922 | hp1 | a0013 | c0014 | t0001 | g0207 | AFR | ESN | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02922 | hp2 | a0001 | c0015 | t0008 | g0127 | AFR | ESN | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02965 | hp1 | a0021 | c0029 | t0010 | g0047 | AFR | ESN | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02965 | hp2 | a0024 | c0030 | t0001 | g0232 | AFR | ESN | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02970 | hp1 | a0017 | c0019 | t0001 | g0009 | AFR | ESN | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02970 | hp2 | a0064 | c0035 | t0014 | g0227 | AFR | ESN | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02976 | hp1 | a0002 | c0001 | t0002 | g0098 | AFR | ESN | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02976 | hp2 | a0004 | c0006 | t0001 | g0024 | AFR | ESN | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG03017 | hp1 | a0004 | c0006 | t0001 | g0130 | SAS | PJL | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG03017 | hp2 | a0002 | c0001 | t0002 | g0096 | SAS | PJL | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG03041 | hp1 | a0006 | c0007 | t0015 | g0236 | AFR | GWD | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG03041 | hp2 | a0025 | c0021 | t0001 | g0168 | AFR | GWD | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG03098 | hp1 | a0065 | c0101 | t0002 | g0116 | AFR | MSL | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG03098 | hp2 | a0024 | c0030 | t0001 | g0231 | AFR | MSL | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG03130 | hp1 | a0011 | c0012 | t0001 | g0008 | AFR | ESN | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG03130 | hp2 | a0014 | c0017 | t0007 | g0037 | AFR | ESN | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG03139 | hp1 | a0002 | c0001 | t0001 | g0080 | AFR | ESN | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG03139 | hp2 | a0014 | c0017 | t0007 | g0038 | AFR | ESN | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG03195 | hp1 | a0011 | c0012 | t0001 | g0027 | AFR | ESN | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG03195 | hp2 | a0017 | c0019 | t0001 | g0009 | AFR | ESN | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG03209 | hp1 | a0001 | c0002 | t0001 | g0161 | AFR | MSL | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG03209 | hp2 | a0009 | c0013 | t0006 | g0296 | AFR | MSL | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG03239 | hp1 | a0001 | c0003 | t0001 | g0046 | SAS | PJL | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG03239 | hp2 | a0003 | c0004 | t0001 | g0262 | SAS | PJL | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG03453 | hp1 | a0004 | c0011 | t0001 | g0023 | AFR | MSL | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG03453 | hp2 | a0001 | c0003 | t0001 | g0144 | AFR | MSL | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG03490 | hp1 | a0006 | c0007 | t0005 | g0030 | SAS | PJL | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG03490 | hp2 | a0001 | c0003 | t0004 | g0018 | SAS | PJL | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG03492 | hp1 | a0001 | c0003 | t0004 | g0018 | SAS | PJL | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0173 | SAS | PJL | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG03516 | hp1 | a0001 | c0003 | t0001 | g0142 | AFR | ESN | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG03516 | hp2 | a0066 | c0058 | t0011 | g0204 | AFR | ESN | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG03540 | hp1 | a0010 | c0010 | t0013 | g0251 | AFR | GWD | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG03540 | hp2 | a0067 | c0060 | t0001 | g0301 | AFR | GWD | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG03579 | hp1 | a0068 | c0067 | t0001 | g0043 | AFR | MSL | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG03579 | hp2 | a0011 | c0012 | t0001 | g0008 | AFR | MSL | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG03669 | hp1 | a0006 | c0007 | t0005 | g0248 | SAS | PJL | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG03669 | hp2 | a0002 | c0001 | t0002 | g0105 | SAS | PJL | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG03688 | hp1 | a0001 | c0069 | t0001 | g0132 | SAS | STU | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG03688 | hp2 | a0001 | c0002 | t0001 | g0005 | SAS | STU | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG03710 | hp1 | a0006 | c0007 | t0005 | g0244 | SAS | PJL | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG03710 | hp2 | a0001 | c0003 | t0004 | g0279 | SAS | PJL | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG03831 | hp1 | a0002 | c0001 | t0002 | g0095 | SAS | BEB | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG03831 | hp2 | a0001 | c0061 | t0004 | g0288 | SAS | BEB | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG03927 | hp1 | a0006 | c0007 | t0005 | g0237 | SAS | BEB | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG03927 | hp2 | a0002 | c0001 | t0002 | g0119 | SAS | BEB | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG04115 | hp1 | a0001 | c0002 | t0001 | g0171 | SAS | STU | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG04115 | hp2 | a0004 | c0006 | t0001 | g0160 | SAS | STU | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG04184 | hp1 | a0001 | c0003 | t0004 | g0295 | SAS | BEB | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG04184 | hp2 | a0006 | c0056 | t0005 | g0233 | SAS | BEB | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG04199 | hp1 | a0006 | c0007 | t0005 | g0234 | SAS | STU | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG04199 | hp2 | a0002 | c0001 | t0002 | g0067 | SAS | STU | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG04204 | hp1 | a0001 | c0003 | t0004 | g0294 | SAS | STU | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG04204 | hp2 | a0002 | c0001 | t0002 | g0118 | SAS | STU | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG04228 | hp1 | a0003 | c0004 | t0001 | g0263 | SAS | STU | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG04228 | hp2 | a0069 | c0057 | t0005 | g0235 | SAS | STU | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18522 | hp1 | a0011 | c0012 | t0001 | g0027 | AFR | YRI | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18522 | hp2 | a0001 | c0003 | t0021 | g0302 | AFR | YRI | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18612 | hp1 | a0007 | c0008 | t0003 | g0015 | EAS | CHB | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18612 | hp2 | a0015 | c0100 | t0002 | g0044 | EAS | CHB | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18906 | hp1 | a0017 | c0019 | t0001 | g0009 | AFR | YRI | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18906 | hp2 | a0014 | c0049 | t0007 | g0040 | AFR | YRI | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18943 | hp1 | a0003 | c0004 | t0001 | g0004 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18943 | hp2 | a0005 | c0005 | t0003 | g0214 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18945 | hp1 | a0002 | c0001 | t0002 | g0001 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18945 | hp2 | a0001 | c0003 | t0004 | g0013 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18946 | hp1 | a0003 | c0004 | t0001 | g0269 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18946 | hp2 | a0070 | c0086 | t0002 | g0102 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18948 | hp1 | a0001 | c0044 | t0004 | g0286 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18948 | hp2 | a0003 | c0004 | t0001 | g0033 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18949 | hp1 | a0071 | c0093 | t0004 | g0110 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18949 | hp2 | a0003 | c0004 | t0002 | g0277 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18950 | hp1 | a0026 | c0024 | t0001 | g0186 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18950 | hp2 | a0002 | c0001 | t0002 | g0007 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18951 | hp1 | a0001 | c0003 | t0004 | g0002 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18951 | hp2 | a0002 | c0001 | t0002 | g0082 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18954 | hp1 | a0005 | c0005 | t0003 | g0217 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18954 | hp2 | a0072 | c0081 | t0003 | g0065 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18956 | hp1 | a0008 | c0009 | t0001 | g0012 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18956 | hp2 | a0073 | c0090 | t0002 | g0090 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18957 | hp1 | a0002 | c0001 | t0002 | g0101 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18957 | hp2 | a0001 | c0003 | t0004 | g0002 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18960 | hp1 | a0002 | c0001 | t0002 | g0001 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18960 | hp2 | a0001 | c0003 | t0004 | g0002 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18963 | hp1 | a0001 | c0003 | t0004 | g0283 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18963 | hp2 | a0002 | c0001 | t0002 | g0001 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18964 | hp1 | a0003 | c0004 | t0001 | g0273 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18964 | hp2 | a0074 | c0085 | t0002 | g0050 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18965 | hp1 | a0003 | c0004 | t0001 | g0259 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18965 | hp2 | a0002 | c0001 | t0002 | g0007 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18966 | hp1 | a0007 | c0008 | t0003 | g0057 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18966 | hp2 | a0075 | c0034 | t0002 | g0049 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18967 | hp1 | a0003 | c0004 | t0001 | g0004 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18967 | hp2 | a0002 | c0001 | t0002 | g0156 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18968 | hp1 | a0003 | c0004 | t0001 | g0267 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18968 | hp2 | a0001 | c0003 | t0004 | g0013 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18970 | hp1 | a0002 | c0001 | t0002 | g0001 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18970 | hp2 | a0001 | c0003 | t0004 | g0293 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18971 | hp1 | a0003 | c0004 | t0001 | g0272 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18971 | hp2 | a0076 | c0092 | t0003 | g0111 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18974 | hp1 | a0005 | c0005 | t0003 | g0215 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18974 | hp2 | a0077 | c0063 | t0004 | g0282 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18975 | hp1 | a0008 | c0009 | t0001 | g0278 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18975 | hp2 | a0002 | c0001 | t0002 | g0084 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18977 | hp1 | a0007 | c0008 | t0003 | g0108 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18977 | hp2 | a0003 | c0047 | t0001 | g0266 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18978 | hp1 | a0003 | c0004 | t0001 | g0268 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18978 | hp2 | a0001 | c0003 | t0004 | g0002 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18980 | hp1 | a0003 | c0004 | t0001 | g0033 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18980 | hp2 | a0027 | c0031 | t0003 | g0060 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18981 | hp1 | a0001 | c0002 | t0001 | g0228 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18981 | hp2 | a0002 | c0001 | t0002 | g0017 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18984 | hp1 | a0003 | c0004 | t0001 | g0032 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18984 | hp2 | a0007 | c0008 | t0003 | g0064 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18986 | hp1 | a0003 | c0004 | t0001 | g0258 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18986 | hp2 | a0007 | c0008 | t0003 | g0063 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18987 | hp1 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18987 | hp2 | a0002 | c0001 | t0002 | g0001 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18988 | hp1 | a0028 | c0026 | t0003 | g0213 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18988 | hp2 | a0002 | c0001 | t0002 | g0091 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18991 | hp1 | a0003 | c0004 | t0001 | g0004 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18991 | hp2 | a0002 | c0001 | t0002 | g0001 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18992 | hp1 | a0001 | c0003 | t0004 | g0289 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18992 | hp2 | a0002 | c0087 | t0002 | g0079 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18995 | hp1 | a0002 | c0001 | t0002 | g0086 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18995 | hp2 | a0005 | c0005 | t0003 | g0010 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18998 | hp1 | a0008 | c0009 | t0001 | g0012 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18998 | hp2 | a0005 | c0005 | t0003 | g0010 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19000 | hp1 | a0002 | c0001 | t0002 | g0155 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19000 | hp2 | a0005 | c0005 | t0003 | g0220 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19002 | hp1 | a0078 | c0083 | t0003 | g0089 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19002 | hp2 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19004 | hp1 | a0007 | c0008 | t0003 | g0059 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19004 | hp2 | a0001 | c0003 | t0004 | g0285 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19005 | hp1 | a0029 | c0028 | t0004 | g0034 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19005 | hp2 | a0002 | c0001 | t0002 | g0007 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19006 | hp1 | a0079 | c0088 | t0002 | g0087 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19006 | hp2 | a0005 | c0005 | t0003 | g0216 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19007 | hp1 | a0002 | c0001 | t0002 | g0001 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19007 | hp2 | a0028 | c0026 | t0003 | g0212 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19010 | hp1 | a0001 | c0077 | t0001 | g0181 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19010 | hp2 | a0002 | c0001 | t0002 | g0051 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19011 | hp1 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19011 | hp2 | a0003 | c0004 | t0001 | g0004 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19030 | hp1 | a0025 | c0021 | t0001 | g0167 | AFR | LWK | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19030 | hp2 | a0009 | c0022 | t0006 | g0025 | AFR | LWK | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19043 | hp1 | a0010 | c0010 | t0001 | g0250 | AFR | LWK | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19043 | hp2 | a0004 | c0011 | t0001 | g0023 | AFR | LWK | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19054 | hp1 | a0008 | c0009 | t0001 | g0031 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19054 | hp2 | a0080 | c0043 | t0003 | g0243 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19055 | hp1 | a0081 | c0096 | t0001 | g0261 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19055 | hp2 | a0007 | c0079 | t0003 | g0055 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19058 | hp1 | a0026 | c0024 | t0001 | g0187 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19058 | hp2 | a0003 | c0004 | t0001 | g0264 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19060 | hp1 | a0003 | c0041 | t0001 | g0275 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19060 | hp2 | a0007 | c0008 | t0003 | g0015 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19063 | hp1 | a0002 | c0001 | t0002 | g0069 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19063 | hp2 | a0003 | c0004 | t0001 | g0032 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19064 | hp1 | a0001 | c0003 | t0001 | g0291 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19064 | hp2 | a0001 | c0002 | t0004 | g0193 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19065 | hp1 | a0003 | c0004 | t0001 | g0004 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19065 | hp2 | a0002 | c0001 | t0002 | g0068 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19070 | hp1 | a0007 | c0008 | t0003 | g0061 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19070 | hp2 | a0001 | c0003 | t0004 | g0013 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19074 | hp1 | a0001 | c0003 | t0004 | g0002 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19074 | hp2 | a0002 | c0001 | t0002 | g0016 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19077 | hp1 | a0008 | c0009 | t0001 | g0031 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19077 | hp2 | a0002 | c0001 | t0002 | g0071 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19080 | hp1 | a0002 | c0001 | t0002 | g0016 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19080 | hp2 | a0003 | c0004 | t0004 | g0271 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19081 | hp1 | a0002 | c0001 | t0002 | g0088 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19081 | hp2 | a0082 | c0072 | t0001 | g0260 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19082 | hp1 | a0027 | c0031 | t0003 | g0058 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19082 | hp2 | a0001 | c0003 | t0004 | g0002 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19084 | hp1 | a0007 | c0008 | t0003 | g0062 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19084 | hp2 | a0001 | c0003 | t0004 | g0002 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19085 | hp1 | a0003 | c0004 | t0001 | g0004 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19085 | hp2 | a0002 | c0001 | t0002 | g0103 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19086 | hp1 | a0001 | c0002 | t0002 | g0194 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19086 | hp2 | a0002 | c0001 | t0002 | g0001 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19088 | hp1 | a0002 | c0001 | t0002 | g0107 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19088 | hp2 | a0003 | c0004 | t0001 | g0270 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19090 | hp1 | a0007 | c0008 | t0003 | g0154 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19090 | hp2 | a0029 | c0028 | t0004 | g0034 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19091 | hp1 | a0001 | c0002 | t0004 | g0192 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19091 | hp2 | a0001 | c0003 | t0001 | g0290 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19240 | hp1 | a0013 | c0014 | t0001 | g0205 | AFR | YRI | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA19240 | hp2 | a0002 | c0001 | t0002 | g0006 | AFR | YRI | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA20129 | hp1 | a0022 | c0032 | t0002 | g0075 | AFR | ASW | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA20129 | hp2 | a0001 | c0002 | t0001 | g0162 | AFR | ASW | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA20905 | hp1 | a0084 | c0064 | t0005 | g0151 | SAS | GIH | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0005 | SAS | GIH | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02109 | hp1 | a0020 | c0025 | t0001 | g0165 | AFR | ACB | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02109 | hp2 | a0049 | c0052 | t0009 | g0257 | AFR | ACB | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02486 | hp1 | a0016 | c0016 | t0001 | g0014 | AFR | ACB | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02486 | hp2 | a0002 | c0001 | t0002 | g0097 | AFR | ACB | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02559 | hp1 | a0014 | c0017 | t0007 | g0039 | AFR | ACB | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG02559 | hp2 | a0023 | c0020 | t0001 | g0026 | AFR | ACB | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG03471 | hp1 | a0001 | c0002 | t0001 | g0148 | AFR | MSL | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG03471 | hp2 | a0004 | c0011 | t0001 | g0138 | AFR | MSL | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG06807 | hp1 | a0010 | c0010 | t0020 | g0249 | AFR | USA | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
HG06807 | hp2 | a0004 | c0011 | t0001 | g0139 | AFR | USA | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18955 | hp1 | a0002 | c0001 | t0002 | g0077 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA18955 | hp2 | a0003 | c0004 | t0001 | g0265 | EAS | JPT | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA20300 | hp1 | a0083 | c0050 | t0019 | g0123 | AFR | USA | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA20300 | hp2 | a0009 | c0013 | t0006 | g0297 | AFR | USA | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA21309 | hp1 | a0004 | c0006 | t0001 | g0200 | AFR | LWK | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
NA21309 | hp2 | a0013 | c0014 | t0001 | g0206 | AFR | LWK | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
homoSapiens | chm13v2 | a0001 | c0015 | t0001 | g0145 | REF | REF | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
homoSapiens | grch38p0 | a0030 | c0051 | t0001 | g0122 | REF | REF | TTN_chr2_178739405_178812423 | TTN | chr2 | 178739405 | 178812423 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:178745968 | C | T | 6 | a0009 a0014 a0049 others(3): Show |
15 | HG02109.hp2 HG02145.hp1 HG02559.hp1 others(12): Show |
missense_variant | MODERATE | c.16432G>A | p.Val5478Met | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 16657/18220 | 16432/16815 | 5478/5604 | chr2 | 178745968 | |||
chr2:178746240 | C | T | 1 | a0039 | 1 | HG01255.hp2 | missense_variant | MODERATE | c.16160G>A | p.Cys5387Tyr | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 16385/18220 | 16160/16815 | 5387/5604 | chr2 | 178746240 | |||
chr2:178746976 | C | T | 1 | a0065 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.15424G>A | p.Gly5142Ser | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 15649/18220 | 15424/16815 | 5142/5604 | chr2 | 178746976 | |||
chr2:178746984 | C | A | 12 | a0005 a0007 a0018 others(9): Show |
46 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(43): Show |
missense_variant | MODERATE | c.15416G>T | p.Arg5139Met | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 15641/18220 | 15416/16815 | 5139/5604 | chr2 | 178746984 | |||
chr2:178747087 | GCTCTAGA others(59): Show |
G | 1 | a0074 | 1 | NA18964.hp2 | conservative_inframe_deletion | MODERATE | c.15247_15312delAGAT others(62): Show |
p.Arg5083_Glu5104del | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 15537/18220 | 15247/16815 | 5083/5604 | chr2 | 178747087 | |||
chr2:178747519 | G | A | 1 | a0072 | 1 | NA18954.hp2 | missense_variant | MODERATE | c.14881C>T | p.Arg4961Cys | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 15106/18220 | 14881/16815 | 4961/5604 | chr2 | 178747519 | |||
chr2:178747656 | C | T | 1 | a0033 | 1 | HG00733.hp1 | missense_variant | MODERATE | c.14744G>A | p.Arg4915His | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 14969/18220 | 14744/16815 | 4915/5604 | chr2 | 178747656 | |||
chr2:178747908 | C | T | 1 | a0061 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.14492G>A | p.Cys4831Tyr | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 14717/18220 | 14492/16815 | 4831/5604 | chr2 | 178747908 | |||
chr2:178748073 | A | G | 1 | a0084 | 1 | NA20905.hp1 | missense_variant | MODERATE | c.14327T>C | p.Leu4776Ser | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 14552/18220 | 14327/16815 | 4776/5604 | chr2 | 178748073 | |||
chr2:178748322 | A | G | 1 | a0031 | 1 | HG00140.hp2 | missense_variant | MODERATE | c.14078T>C | p.Ile4693Thr | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 14303/18220 | 14078/16815 | 4693/5604 | chr2 | 178748322 | |||
chr2:178748420 | G | C | 6 | a0009 a0014 a0049 others(3): Show |
15 | HG02109.hp2 HG02145.hp1 HG02559.hp1 others(12): Show |
missense_variant | MODERATE | c.13980C>G | p.His4660Gln | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 14205/18220 | 13980/16815 | 4660/5604 | chr2 | 178748420 | |||
chr2:178748464 | T | C | 1 | a0040 | 1 | HG01261.hp1 | missense_variant | MODERATE | c.13936A>G | p.Lys4646Glu | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 14161/18220 | 13936/16815 | 4646/5604 | chr2 | 178748464 | |||
chr2:178748537 | C | T | 3 | a0018 a0078 a0080 |
4 | HG00438.hp2 HG00609.hp2 NA19002.hp1 others(1): Show |
missense_variant | MODERATE | c.13863G>A | p.Met4621Ile | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 14088/18220 | 13863/16815 | 4621/5604 | chr2 | 178748537 | |||
chr2:178748541 | T | G | 1 | a0012 | 4 | HG00544.hp2 HG02015.hp2 HG02040.hp2 others(1): Show |
missense_variant | MODERATE | c.13859A>C | p.Gln4620Pro | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 14084/18220 | 13859/16815 | 4620/5604 | chr2 | 178748541 | |||
chr2:178748601 | T | G | 1 | a0070 | 1 | NA18946.hp2 | missense_variant | MODERATE | c.13799A>C | p.Glu4600Ala | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 14024/18220 | 13799/16815 | 4600/5604 | chr2 | 178748601 | |||
chr2:178748767 | C | T | 1 | a0017 | 3 | HG02970.hp1 HG03195.hp2 NA18906.hp1 |
missense_variant | MODERATE | c.13633G>A | p.Ala4545Thr | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 13858/18220 | 13633/16815 | 4545/5604 | chr2 | 178748767 | |||
chr2:178748786 | T | G | 1 | a0026 | 2 | NA18950.hp1 NA19058.hp1 |
missense_variant | MODERATE | c.13614A>C | p.Gln4538His | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 13839/18220 | 13614/16815 | 4538/5604 | chr2 | 178748786 | |||
chr2:178748839 | T | C | 1 | a0080 | 1 | NA19054.hp2 | missense_variant | MODERATE | c.13561A>G | p.Thr4521Ala | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 13786/18220 | 13561/16815 | 4521/5604 | chr2 | 178748839 | |||
chr2:178748922 | T | G | 1 | a0009 | 7 | HG02145.hp1 HG02895.hp1 HG02896.hp1 others(4): Show |
missense_variant | MODERATE | c.13478A>C | p.Lys4493Thr | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 13703/18220 | 13478/16815 | 4493/5604 | chr2 | 178748922 | |||
chr2:178749053 | T | C | 1 | a0023 | 2 | HG02451.hp1 HG02559.hp2 |
missense_variant | MODERATE | c.13347A>G | p.Ile4449Met | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 13572/18220 | 13347/16815 | 4449/5604 | chr2 | 178749053 | |||
chr2:178749235 | C | T | 1 | a0014 | 4 | HG02559.hp1 HG03130.hp2 HG03139.hp2 others(1): Show |
missense_variant | MODERATE | c.13165G>A | p.Val4389Ile | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 13390/18220 | 13165/16815 | 4389/5604 | chr2 | 178749235 | |||
chr2:178749355 | G | T | 1 | a0025 | 2 | HG03041.hp2 NA19030.hp1 |
missense_variant | MODERATE | c.13045C>A | p.Pro4349Thr | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 13270/18220 | 13045/16815 | 4349/5604 | chr2 | 178749355 | |||
chr2:178749414 | G | C | 1 | a0038 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.12986C>G | p.Ser4329Cys | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 13211/18220 | 12986/16815 | 4329/5604 | chr2 | 178749414 | |||
chr2:178749837 | G | C | 1 | a0069 | 1 | HG04228.hp2 | missense_variant | MODERATE | c.12563C>G | p.Pro4188Arg | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 12788/18220 | 12563/16815 | 4188/5604 | chr2 | 178749837 | |||
chr2:178750759 | C | T | 1 | a0027 | 2 | NA18980.hp2 NA19082.hp1 |
missense_variant | MODERATE | c.11641G>A | p.Glu3881Lys | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 11866/18220 | 11641/16815 | 3881/5604 | chr2 | 178750759 | |||
chr2:178750927 | C | A | 1 | a0079 | 1 | NA19006.hp1 | missense_variant | MODERATE | c.11473G>T | p.Gly3825Cys | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 11698/18220 | 11473/16815 | 3825/5604 | chr2 | 178750927 | |||
chr2:178750981 | T | C | 1 | a0047 | 1 | HG02080.hp1 | missense_variant | MODERATE | c.11419A>G | p.Arg3807Gly | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 11644/18220 | 11419/16815 | 3807/5604 | chr2 | 178750981 | |||
chr2:178751146 | A | T | 1 | a0068 | 1 | HG03579.hp1 | missense_variant | MODERATE | c.11254T>A | p.Ser3752Thr | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 11479/18220 | 11254/16815 | 3752/5604 | chr2 | 178751146 | |||
chr2:178751160 | T | C | 48 | a0001 a0002 a0003 others(45): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
missense_variant | MODERATE | c.11240A>G | p.Asp3747Gly | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 11465/18220 | 11240/16815 | 3747/5604 | chr2 | 178751160 | |||
chr2:178751204 | C | G | 79 | a0001 a0002 a0003 others(76): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
missense_variant | MODERATE | c.11196G>C | p.Leu3732Phe | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 11421/18220 | 11196/16815 | 3732/5604 | chr2 | 178751204 | |||
chr2:178751232 | G | A | 1 | a0059 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.11168C>T | p.Thr3723Met | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 11393/18220 | 11168/16815 | 3723/5604 | chr2 | 178751232 | |||
chr2:178751394 | T | C | 1 | a0021 | 2 | HG02258.hp1 HG02965.hp1 |
missense_variant | MODERATE | c.11006A>G | p.Asp3669Gly | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 11231/18220 | 11006/16815 | 3669/5604 | chr2 | 178751394 | |||
chr2:178751557 | G | A | 2 | a0081 a0082 |
2 | NA19055.hp1 NA19081.hp2 |
missense_variant | MODERATE | c.10843C>T | p.Arg3615Trp | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 11068/18220 | 10843/16815 | 3615/5604 | chr2 | 178751557 | |||
chr2:178751752 | G | A | 1 | a0034 | 1 | HG00735.hp1 | missense_variant | MODERATE | c.10648C>T | p.Arg3550Trp | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 10873/18220 | 10648/16815 | 3550/5604 | chr2 | 178751752 | |||
chr2:178751754 | C | T | 1 | a0037 | 1 | HG01168.hp1 | missense_variant | MODERATE | c.10646G>A | p.Arg3549His | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 10871/18220 | 10646/16815 | 3549/5604 | chr2 | 178751754 | |||
chr2:178751806 | T | A | 1 | a0029 | 2 | NA19005.hp1 NA19090.hp2 |
missense_variant | MODERATE | c.10594A>T | p.Thr3532Ser | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 10819/18220 | 10594/16815 | 3532/5604 | chr2 | 178751806 | |||
chr2:178759031 | C | T | 61 | a0001 a0002 a0003 others(58): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
missense_variant | MODERATE | c.10256G>A | p.Ser3419Asn | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/46 | 10481/18220 | 10256/16815 | 3419/5604 | chr2 | 178759031 | |||
chr2:178759124 | C | T | 1 | a0075 | 1 | NA18966.hp2 | missense_variant | MODERATE | c.10163G>A | p.Arg3388Gln | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/46 | 10388/18220 | 10163/16815 | 3388/5604 | chr2 | 178759124 | |||
chr2:178764191 | C | T | 2 | a0041 a0077 |
2 | HG01358.hp2 NA18974.hp2 |
missense_variant | MODERATE | c.10100G>A | p.Arg3367Gln | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/46 | 10325/18220 | 10100/16815 | 3367/5604 | chr2 | 178764191 | |||
chr2:178764203 | C | T | 1 | a0066 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.10088G>A | p.Arg3363His | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/46 | 10313/18220 | 10088/16815 | 3363/5604 | chr2 | 178764203 | |||
chr2:178764734 | C | T | 59 | a0001 a0002 a0003 others(56): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
missense_variant | MODERATE | c.9781G>A | p.Val3261Met | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 42/46 | 10006/18220 | 9781/16815 | 3261/5604 | chr2 | 178764734 | |||
chr2:178764745 | C | T | 1 | a0043 | 1 | HG01928.hp2 | missense_variant | MODERATE | c.9770G>A | p.Arg3257His | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 42/46 | 9995/18220 | 9770/16815 | 3257/5604 | chr2 | 178764745 | |||
chr2:178767769 | T | C | 7 | a0006 a0012 a0024 others(4): Show |
25 | HG00544.hp2 HG00642.hp2 HG01257.hp1 others(22): Show |
missense_variant | MODERATE | c.9461A>G | p.Lys3154Arg | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 40/46 | 9686/18220 | 9461/16815 | 3154/5604 | chr2 | 178767769 | |||
chr2:178767871 | C | T | 1 | a0055 | 1 | HG02698.hp2 | missense_variant | MODERATE | c.9359G>A | p.Arg3120Gln | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 40/46 | 9584/18220 | 9359/16815 | 3120/5604 | chr2 | 178767871 | |||
chr2:178767892 | C | T | 2 | a0028 a0045 |
3 | HG02027.hp2 NA18988.hp1 NA19007.hp2 |
missense_variant | MODERATE | c.9338G>A | p.Arg3113His | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 40/46 | 9563/18220 | 9338/16815 | 3113/5604 | chr2 | 178767892 | |||
chr2:178768110 | A | G | 1 | a0032 | 1 | HG00558.hp2 | missense_variant | MODERATE | c.9209T>C | p.Leu3070Pro | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 39/46 | 9434/18220 | 9209/16815 | 3070/5604 | chr2 | 178768110 | |||
chr2:178768759 | T | A | 1 | a0049 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.9077A>T | p.Asn3026Ile | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 38/46 | 9302/18220 | 9077/16815 | 3026/5604 | chr2 | 178768759 | |||
chr2:178768898 | C | T | 1 | a0064 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.8938G>A | p.Ala2980Thr | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 38/46 | 9163/18220 | 8938/16815 | 2980/5604 | chr2 | 178768898 | |||
chr2:178770209 | C | T | 11 | a0005 a0007 a0018 others(8): Show |
45 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(42): Show |
missense_variant | MODERATE | c.8492G>A | p.Ser2831Asn | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 36/46 | 8717/18220 | 8492/16815 | 2831/5604 | chr2 | 178770209 | |||
chr2:178770234 | C | A | 1 | a0019 | 2 | HG01167.hp2 HG02300.hp2 |
missense_variant | MODERATE | c.8467G>T | p.Val2823Phe | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 36/46 | 8692/18220 | 8467/16815 | 2823/5604 | chr2 | 178770234 | |||
chr2:178771258 | G | A | 1 | a0026 | 2 | NA18950.hp1 NA19058.hp1 |
missense_variant | MODERATE | c.8069C>T | p.Thr2690Ile | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 34/46 | 8294/18220 | 8069/16815 | 2690/5604 | chr2 | 178771258 | |||
chr2:178771393 | T | C | 1 | a0051 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.7934A>G | p.Asn2645Ser | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 34/46 | 8159/18220 | 7934/16815 | 2645/5604 | chr2 | 178771393 | |||
chr2:178773134 | C | G | 9 | a0005 a0007 a0018 others(6): Show |
43 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(40): Show |
missense_variant | MODERATE | c.7830G>C | p.Met2610Ile | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 33/46 | 8055/18220 | 7830/16815 | 2610/5604 | chr2 | 178773134 | |||
chr2:178773224 | A | C | 1 | a0050 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.7740T>G | p.Ile2580Met | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 33/46 | 7965/18220 | 7740/16815 | 2580/5604 | chr2 | 178773224 | |||
chr2:178773714 | T | C | 1 | a0035 | 1 | HG01071.hp1 | missense_variant | MODERATE | c.7342A>G | p.Ile2448Val | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 32/46 | 7567/18220 | 7342/16815 | 2448/5604 | chr2 | 178773714 | |||
chr2:178773994 | C | T | 7 | a0006 a0012 a0024 others(4): Show |
25 | HG00544.hp2 HG00642.hp2 HG01257.hp1 others(22): Show |
missense_variant | MODERATE | c.7174G>A | p.Gly2392Ser | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 31/46 | 7399/18220 | 7174/16815 | 2392/5604 | chr2 | 178773994 | |||
chr2:178774107 | C | T | 1 | a0042 | 1 | HG01361.hp2 | missense_variant | MODERATE | c.7061G>A | p.Arg2354His | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 31/46 | 7286/18220 | 7061/16815 | 2354/5604 | chr2 | 178774107 | |||
chr2:178774984 | C | A | 2 | a0046 a0066 |
2 | HG02055.hp1 HG03516.hp2 |
missense_variant | MODERATE | c.6727G>T | p.Asp2243Tyr | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 29/46 | 6952/18220 | 6727/16815 | 2243/5604 | chr2 | 178774984 | |||
chr2:178775026 | G | A | 1 | a0073 | 1 | NA18956.hp2 | missense_variant | MODERATE | c.6685C>T | p.His2229Tyr | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 29/46 | 6910/18220 | 6685/16815 | 2229/5604 | chr2 | 178775026 | |||
chr2:178775511 | A | G | 1 | a0017 | 3 | HG02970.hp1 HG03195.hp2 NA18906.hp1 |
missense_variant | MODERATE | c.6353T>C | p.Ile2118Thr | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 28/46 | 6578/18220 | 6353/16815 | 2118/5604 | chr2 | 178775511 | |||
chr2:178775871 | C | T | 1 | a0061 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.5993G>A | p.Arg1998His | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 28/46 | 6218/18220 | 5993/16815 | 1998/5604 | chr2 | 178775871 | |||
chr2:178776196 | G | A | 1 | a0063 | 1 | HG02896.hp2 | missense_variant | MODERATE | c.5668C>T | p.Arg1890Cys | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 28/46 | 5893/18220 | 5668/16815 | 1890/5604 | chr2 | 178776196 | |||
chr2:178776633 | G | A | 1 | a0008 | 7 | HG00558.hp1 HG01192.hp2 NA18956.hp1 others(4): Show |
missense_variant | MODERATE | c.5231C>T | p.Pro1744Leu | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 28/46 | 5456/18220 | 5231/16815 | 1744/5604 | chr2 | 178776633 | |||
chr2:178777224 | G | A | 2 | a0020 a0056 |
3 | HG02109.hp1 HG02280.hp2 HG02717.hp1 |
missense_variant | MODERATE | c.4739C>T | p.Thr1580Met | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 27/46 | 4964/18220 | 4739/16815 | 1580/5604 | chr2 | 178777224 | |||
chr2:178777248 | C | T | 9 | a0005 a0007 a0018 others(6): Show |
43 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(40): Show |
missense_variant | MODERATE | c.4715G>A | p.Arg1572Gln | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 27/46 | 4940/18220 | 4715/16815 | 1572/5604 | chr2 | 178777248 | |||
chr2:178777435 | T | C | 2 | a0021 a0062 |
3 | HG02258.hp1 HG02809.hp2 HG02965.hp1 |
missense_variant | MODERATE | c.4630A>G | p.Ile1544Val | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 26/46 | 4855/18220 | 4630/16815 | 1544/5604 | chr2 | 178777435 | |||
chr2:178777856 | A | G | 1 | a0044 | 1 | HG01943.hp2 | missense_variant | MODERATE | c.4328T>C | p.Leu1443Pro | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 25/46 | 4553/18220 | 4328/16815 | 1443/5604 | chr2 | 178777856 | |||
chr2:178777862 | C | G | 1 | a0015 | 3 | HG00741.hp1 HG01099.hp1 NA18612.hp2 |
missense_variant | MODERATE | c.4322G>C | p.Arg1441Pro | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 25/46 | 4547/18220 | 4322/16815 | 1441/5604 | chr2 | 178777862 | |||
chr2:178777938 | G | A | 2 | a0010 a0042 |
8 | HG01361.hp2 HG02630.hp1 HG02809.hp1 others(5): Show |
missense_variant | MODERATE | c.4246C>T | p.Arg1416Cys | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 25/46 | 4471/18220 | 4246/16815 | 1416/5604 | chr2 | 178777938 | |||
chr2:178778883 | C | G | 1 | a0023 | 2 | HG02451.hp1 HG02559.hp2 |
missense_variant | MODERATE | c.4199G>C | p.Ser1400Thr | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 24/46 | 4424/18220 | 4199/16815 | 1400/5604 | chr2 | 178778883 | |||
chr2:178778905 | T | C | 5 | a0010 a0013 a0042 others(2): Show |
14 | HG01361.hp2 HG02055.hp1 HG02451.hp2 others(11): Show |
missense_variant | MODERATE | c.4177A>G | p.Ile1393Val | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 24/46 | 4402/18220 | 4177/16815 | 1393/5604 | chr2 | 178778905 | |||
chr2:178778913 | G | A | 1 | a0067 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.4169C>T | p.Pro1390Leu | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 24/46 | 4394/18220 | 4169/16815 | 1390/5604 | chr2 | 178778913 | |||
chr2:178778922 | A | G | 1 | a0050 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.4160T>C | p.Leu1387Pro | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 24/46 | 4385/18220 | 4160/16815 | 1387/5604 | chr2 | 178778922 | |||
chr2:178779048 | C | T | 1 | a0036 | 1 | HG01106.hp1 | missense_variant | MODERATE | c.4034G>A | p.Gly1345Asp | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 24/46 | 4259/18220 | 4034/16815 | 1345/5604 | chr2 | 178779048 | |||
chr2:178779237 | A | T | 1 | a0058 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.3955T>A | p.Leu1319Ile | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 23/46 | 4180/18220 | 3955/16815 | 1319/5604 | chr2 | 178779237 | |||
chr2:178779308 | G | A | 71 | a0001 a0002 a0004 others(68): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
missense_variant | MODERATE | c.3884C>T | p.Ser1295Leu | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 23/46 | 4109/18220 | 3884/16815 | 1295/5604 | chr2 | 178779308 | |||
chr2:178780061 | G | A | 1 | a0017 | 3 | HG02970.hp1 HG03195.hp2 NA18906.hp1 |
missense_variant | MODERATE | c.3668C>T | p.Ala1223Val | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 22/46 | 3893/18220 | 3668/16815 | 1223/5604 | chr2 | 178780061 | |||
chr2:178780128 | T | C | 31 | a0001 a0004 a0011 others(28): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
missense_variant | MODERATE | c.3601A>G | p.Lys1201Glu | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 22/46 | 3826/18220 | 3601/16815 | 1201/5604 | chr2 | 178780128 | |||
chr2:178781121 | C | T | 1 | a0054 | 1 | HG02683.hp2 | missense_variant&splice_region_variant | MODERATE | c.3523G>A | p.Ala1175Thr | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 21/46 | 3748/18220 | 3523/16815 | 1175/5604 | chr2 | 178781121 | |||
chr2:178781258 | T | C | 2 | a0081 a0082 |
2 | NA19055.hp1 NA19081.hp2 |
missense_variant | MODERATE | c.3386A>G | p.Lys1129Arg | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 21/46 | 3611/18220 | 3386/16815 | 1129/5604 | chr2 | 178781258 | |||
chr2:178782806 | C | T | 1 | a0060 | 1 | HG02738.hp1 | missense_variant&splice_region_variant | MODERATE | c.3100G>A | p.Val1034Met | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 18/46 | 3325/18220 | 3100/16815 | 1034/5604 | chr2 | 178782806 | |||
chr2:178784080 | C | T | 1 | a0016 | 3 | HG02257.hp2 HG02486.hp1 HG02615.hp1 |
missense_variant | MODERATE | c.2765G>A | p.Arg922His | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 16/46 | 2990/18220 | 2765/16815 | 922/5604 | chr2 | 178784080 | |||
chr2:178785681 | G | A | 4 | a0004 a0031 a0033 others(1): Show |
26 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(23): Show |
missense_variant | MODERATE | c.2432C>T | p.Thr811Ile | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 15/46 | 2657/18220 | 2432/16815 | 811/5604 | chr2 | 178785681 | |||
chr2:178785717 | G | A | 1 | a0048 | 1 | HG02080.hp2 | missense_variant | MODERATE | c.2396C>T | p.Thr799Met | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 15/46 | 2621/18220 | 2396/16815 | 799/5604 | chr2 | 178785717 | |||
chr2:178785948 | G | A | 1 | a0024 | 2 | HG02965.hp2 HG03098.hp2 |
missense_variant | MODERATE | c.2270C>T | p.Pro757Leu | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 14/46 | 2495/18220 | 2270/16815 | 757/5604 | chr2 | 178785948 | |||
chr2:178794500 | C | T | 1 | a0053 | 1 | HG02622.hp2 | missense_variant | MODERATE | c.1297G>A | p.Val433Ile | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 8/46 | 1522/18220 | 1297/16815 | 433/5604 | chr2 | 178794500 | |||
chr2:178795088 | C | G | 3 | a0056 a0061 a0064 |
3 | HG02717.hp1 HG02738.hp2 HG02970.hp2 |
missense_variant | MODERATE | c.1079G>C | p.Arg360Thr | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 7/46 | 1304/18220 | 1079/16815 | 360/5604 | chr2 | 178795088 | |||
chr2:178795164 | C | T | 1 | a0009 | 7 | HG02145.hp1 HG02895.hp1 HG02896.hp1 others(4): Show |
missense_variant | MODERATE | c.1003G>A | p.Val335Met | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 7/46 | 1228/18220 | 1003/16815 | 335/5604 | chr2 | 178795164 | |||
chr2:178795185 | G | A | 24 | a0002 a0007 a0015 others(21): Show |
105 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(102): Show |
missense_variant | MODERATE | c.982C>T | p.Arg328Cys | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 7/46 | 1207/18220 | 982/16815 | 328/5604 | chr2 | 178795185 | |||
chr2:178795197 | G | A | 1 | a0057 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.970C>T | p.Pro324Ser | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 7/46 | 1195/18220 | 970/16815 | 324/5604 | chr2 | 178795197 | |||
chr2:178800436 | C | T | 3 | a0011 a0023 a0025 |
9 | HG02451.hp1 HG02559.hp2 HG02818.hp2 others(6): Show |
missense_variant | MODERATE | c.542G>A | p.Ser181Asn | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 4/46 | 767/18220 | 542/16815 | 181/5604 | chr2 | 178800436 | |||
chr2:178800482 | C | A | 1 | a0081 | 1 | NA19055.hp1 | missense_variant | MODERATE | c.496G>T | p.Ala166Ser | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 4/46 | 721/18220 | 496/16815 | 166/5604 | chr2 | 178800482 | |||
chr2:178800631 | C | G | 1 | a0075 | 1 | NA18966.hp2 | missense_variant | MODERATE | c.347G>C | p.Arg116Thr | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 4/46 | 572/18220 | 347/16815 | 116/5604 | chr2 | 178800631 | |||
chr2:178802255 | C | A | 6 | a0015 a0034 a0052 others(3): Show |
8 | HG00735.hp1 HG00741.hp1 HG01099.hp1 others(5): Show |
missense_variant | MODERATE | c.178G>T | p.Asp60Tyr | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 3/46 | 403/18220 | 178/16815 | 60/5604 | chr2 | 178802255 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:178745750 | A | G | 1 | a0014c0049 | 1 | NA18906.hp2 | synonymous_variant | LOW | c.16650T>C | p.Asp5550Asp | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 16875/18220 | 16650/16815 | 5550/5604 | chr2 | 178745750 | |||
chr2:178746176 | A | C | 1 | a0061c0097 | 1 | HG02738.hp2 | synonymous_variant | LOW | c.16224T>G | p.Thr5408Thr | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 16449/18220 | 16224/16815 | 5408/5604 | chr2 | 178746176 | |||
chr2:178746953 | G | A | 10 | a0009c0013 a0009c0022 a0014c0017 others(7): Show |
17 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(14): Show |
synonymous_variant | LOW | c.15447C>T | p.Tyr5149Tyr | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 15672/18220 | 15447/16815 | 5149/5604 | chr2 | 178746953 | |||
chr2:178747124 | C | T | 8 | a0009c0013 a0009c0022 a0014c0017 others(5): Show |
15 | HG02109.hp2 HG02145.hp1 HG02559.hp1 others(12): Show |
synonymous_variant | LOW | c.15276G>A | p.Leu5092Leu | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 15501/18220 | 15276/16815 | 5092/5604 | chr2 | 178747124 | |||
chr2:178747148 | A | G | 8 | a0009c0013 a0009c0022 a0014c0017 others(5): Show |
15 | HG02109.hp2 HG02145.hp1 HG02559.hp1 others(12): Show |
synonymous_variant | LOW | c.15252T>C | p.Tyr5084Tyr | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 15477/18220 | 15252/16815 | 5084/5604 | chr2 | 178747148 | |||
chr2:178747172 | G | T | 1 | a0009c0022 | 2 | HG02145.hp1 NA19030.hp2 |
synonymous_variant | LOW | c.15228C>A | p.Pro5076Pro | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 15453/18220 | 15228/16815 | 5076/5604 | chr2 | 178747172 | |||
chr2:178747580 | C | T | 1 | a0001c0068 | 1 | HG02717.hp2 | synonymous_variant | LOW | c.14820G>A | p.Val4940Val | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 15045/18220 | 14820/16815 | 4940/5604 | chr2 | 178747580 | |||
chr2:178747646 | A | C | 2 | a0006c0056 a0084c0064 |
2 | HG04184.hp2 NA20905.hp1 |
synonymous_variant | LOW | c.14754T>G | p.Pro4918Pro | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 14979/18220 | 14754/16815 | 4918/5604 | chr2 | 178747646 | |||
chr2:178748531 | A | C | 3 | a0014c0017 a0014c0049 a0083c0050 |
5 | HG02559.hp1 HG03130.hp2 HG03139.hp2 others(2): Show |
synonymous_variant | LOW | c.13869T>G | p.Ser4623Ser | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 14094/18220 | 13869/16815 | 4623/5604 | chr2 | 178748531 | |||
chr2:178748768 | G | A | 2 | a0002c0087 a0007c0079 |
2 | NA18992.hp2 NA19055.hp2 |
synonymous_variant | LOW | c.13632C>T | p.Asp4544Asp | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 13857/18220 | 13632/16815 | 4544/5604 | chr2 | 178748768 | |||
chr2:178748792 | G | A | 2 | a0009c0013 a0009c0022 |
7 | HG02145.hp1 HG02895.hp1 HG02896.hp1 others(4): Show |
synonymous_variant | LOW | c.13608C>T | p.Ser4536Ser | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 13833/18220 | 13608/16815 | 4536/5604 | chr2 | 178748792 | |||
chr2:178748924 | G | A | 1 | a0001c0069 | 1 | HG03688.hp1 | synonymous_variant | LOW | c.13476C>T | p.Asp4492Asp | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 13701/18220 | 13476/16815 | 4492/5604 | chr2 | 178748924 | |||
chr2:178750160 | A | G | 1 | a0003c0047 | 1 | NA18977.hp2 | synonymous_variant | LOW | c.12240T>C | p.Asn4080Asn | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 12465/18220 | 12240/16815 | 4080/5604 | chr2 | 178750160 | |||
chr2:178750225 | A | G | 97 | a0001c0002 a0001c0003 a0001c0015 others(94): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
synonymous_variant | LOW | c.12175T>C | p.Leu4059Leu | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 12400/18220 | 12175/16815 | 4059/5604 | chr2 | 178750225 | |||
chr2:178751123 | A | G | 1 | a0012c0055 | 1 | HG00544.hp2 | synonymous_variant | LOW | c.11277T>C | p.Ser3759Ser | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 11502/18220 | 11277/16815 | 3759/5604 | chr2 | 178751123 | |||
chr2:178751267 | T | C | 97 | a0001c0002 a0001c0003 a0001c0015 others(94): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
synonymous_variant | LOW | c.11133A>G | p.Thr3711Thr | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 11358/18220 | 11133/16815 | 3711/5604 | chr2 | 178751267 | |||
chr2:178751483 | G | A | 1 | a0015c0033 | 2 | HG00741.hp1 HG01099.hp1 |
synonymous_variant | LOW | c.10917C>T | p.Gly3639Gly | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 11142/18220 | 10917/16815 | 3639/5604 | chr2 | 178751483 | |||
chr2:178759123 | C | A | 1 | a0002c0089 | 1 | HG00544.hp1 | synonymous_variant | LOW | c.10164G>T | p.Arg3388Arg | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/46 | 10389/18220 | 10164/16815 | 3388/5604 | chr2 | 178759123 | |||
chr2:178764636 | T | C | 96 | a0001c0002 a0001c0003 a0001c0015 others(93): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
synonymous_variant | LOW | c.9879A>G | p.Glu3293Glu | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 42/46 | 10104/18220 | 9879/16815 | 3293/5604 | chr2 | 178764636 | |||
chr2:178766487 | T | C | 22 | a0005c0005 a0006c0007 a0006c0056 others(19): Show |
71 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(68): Show |
synonymous_variant | LOW | c.9597A>G | p.Glu3199Glu | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 41/46 | 9822/18220 | 9597/16815 | 3199/5604 | chr2 | 178766487 | |||
chr2:178768686 | T | C | 1 | a0057c0095 | 1 | HG02723.hp1 | synonymous_variant | LOW | c.9150A>G | p.Thr3050Thr | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 38/46 | 9375/18220 | 9150/16815 | 3050/5604 | chr2 | 178768686 | |||
chr2:178768917 | G | C | 9 | a0006c0007 a0006c0056 a0012c0018 others(6): Show |
25 | HG00544.hp2 HG00642.hp2 HG01257.hp1 others(22): Show |
synonymous_variant | LOW | c.8919C>G | p.Ser2973Ser | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 38/46 | 9144/18220 | 8919/16815 | 2973/5604 | chr2 | 178768917 | |||
chr2:178773511 | G | A | 9 | a0001c0015 a0001c0068 a0001c0069 others(6): Show |
12 | HG01106.hp2 HG01168.hp1 HG01496.hp1 others(9): Show |
synonymous_variant | LOW | c.7545C>T | p.Tyr2515Tyr | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 32/46 | 7770/18220 | 7545/16815 | 2515/5604 | chr2 | 178773511 | |||
chr2:178776476 | A | G | 1 | a0057c0095 | 1 | HG02723.hp1 | synonymous_variant | LOW | c.5388T>C | p.Asp1796Asp | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 28/46 | 5613/18220 | 5388/16815 | 1796/5604 | chr2 | 178776476 | |||
chr2:178776863 | A | G | 1 | a0001c0061 | 1 | HG03831.hp2 | synonymous_variant | LOW | c.5001T>C | p.Tyr1667Tyr | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 28/46 | 5226/18220 | 5001/16815 | 1667/5604 | chr2 | 178776863 | |||
chr2:178777837 | T | C | 2 | a0009c0013 a0009c0022 |
7 | HG02145.hp1 HG02895.hp1 HG02896.hp1 others(4): Show |
synonymous_variant | LOW | c.4347A>G | p.Ser1449Ser | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 25/46 | 4572/18220 | 4347/16815 | 1449/5604 | chr2 | 178777837 | |||
chr2:178779089 | G | A | 4 | a0009c0013 a0009c0022 a0056c0036 others(1): Show |
9 | HG02145.hp1 HG02717.hp1 HG02895.hp1 others(6): Show |
synonymous_variant | LOW | c.3993C>T | p.Ile1331Ile | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 24/46 | 4218/18220 | 3993/16815 | 1331/5604 | chr2 | 178779089 | |||
chr2:178779433 | T | C | 10 | a0005c0005 a0007c0008 a0007c0079 others(7): Show |
43 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(40): Show |
synonymous_variant | LOW | c.3759A>G | p.Arg1253Arg | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 23/46 | 3984/18220 | 3759/16815 | 1253/5604 | chr2 | 178779433 | |||
chr2:178782819 | A | G | 12 | a0001c0044 a0003c0041 a0005c0005 others(9): Show |
45 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(42): Show |
synonymous_variant | LOW | c.3087T>C | p.Tyr1029Tyr | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 18/46 | 3312/18220 | 3087/16815 | 1029/5604 | chr2 | 178782819 | |||
chr2:178782957 | G | A | 1 | a0004c0011 | 6 | HG02055.hp2 HG02630.hp2 HG03453.hp1 others(3): Show |
synonymous_variant | LOW | c.2949C>T | p.Ile983Ile | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 18/46 | 3174/18220 | 2949/16815 | 983/5604 | chr2 | 178782957 | |||
chr2:178783780 | T | G | 4 | a0009c0013 a0009c0022 a0056c0036 others(1): Show |
9 | HG02145.hp1 HG02717.hp1 HG02895.hp1 others(6): Show |
synonymous_variant | LOW | c.2781A>C | p.Thr927Thr | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 17/46 | 3006/18220 | 2781/16815 | 927/5604 | chr2 | 178783780 | |||
chr2:178785974 | C | T | 13 | a0001c0002 a0001c0076 a0001c0077 others(10): Show |
57 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(54): Show |
synonymous_variant | LOW | c.2244G>A | p.Glu748Glu | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 14/46 | 2469/18220 | 2244/16815 | 748/5604 | chr2 | 178785974 | |||
chr2:178785992 | G | T | 1 | a0007c0079 | 1 | NA19055.hp2 | synonymous_variant | LOW | c.2226C>A | p.Ser742Ser | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 14/46 | 2451/18220 | 2226/16815 | 742/5604 | chr2 | 178785992 | |||
chr2:178789375 | T | C | 1 | a0001c0076 | 1 | HG01074.hp2 | synonymous_variant | LOW | c.2061A>G | p.Gln687Gln | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 13/46 | 2286/18220 | 2061/16815 | 687/5604 | chr2 | 178789375 | |||
chr2:178795030 | T | C | 1 | a0061c0097 | 1 | HG02738.hp2 | synonymous_variant | LOW | c.1137A>G | p.Arg379Arg | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 7/46 | 1362/18220 | 1137/16815 | 379/5604 | chr2 | 178795030 | |||
chr2:178795165 | G | A | 2 | a0001c0077 a0051c0078 |
2 | HG02258.hp2 NA19010.hp1 |
synonymous_variant | LOW | c.1002C>T | p.Thr334Thr | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 7/46 | 1227/18220 | 1002/16815 | 334/5604 | chr2 | 178795165 | |||
chr2:178800552 | G | A | 1 | a0061c0097 | 1 | HG02738.hp2 | synonymous_variant | LOW | c.426C>T | p.Ala142Ala | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 4/46 | 651/18220 | 426/16815 | 142/5604 | chr2 | 178800552 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:178744419 | C | T | 1 | a0006c0007t0015 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1166G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 1166 | chr2 | 178744419 | ||||||
chr2:178744448 | C | T | 1 | a0061c0097t0017 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1137G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 1137 | chr2 | 178744448 | ||||||
chr2:178744517 | T | TAAAGAGT others(321): Show |
1 | a0061c0097t0017 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1067_*1068insTTTT others(324): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 1067 | chr2 | 178744517 | ||||||
chr2:178744518 | A | G | 25 | a0001c0002t0002 a0002c0001t0002 a0002c0001t0012 others(22): Show |
93 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*1067T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 1067 | chr2 | 178744518 | ||||||
chr2:178744580 | G | A | 1 | a0021c0029t0010 | 2 | HG02258.hp1 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1005C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 1005 | chr2 | 178744580 | ||||||
chr2:178744918 | T | C | 1 | a0002c0001t0018 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*667A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 667 | chr2 | 178744918 | ||||||
chr2:178744973 | C | T | 1 | a0056c0036t0016 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*612G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 612 | chr2 | 178744973 | ||||||
chr2:178744979 | C | T | 8 | a0009c0013t0006 a0009c0022t0006 a0014c0017t0007 others(5): Show |
15 | HG02109.hp2 HG02145.hp1 HG02559.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*606G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 606 | chr2 | 178744979 | ||||||
chr2:178745074 | T | C | 5 | a0014c0017t0007 a0014c0049t0007 a0046c0091t0011 others(2): Show |
7 | HG02055.hp1 HG02559.hp1 HG03130.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*511A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 511 | chr2 | 178745074 | ||||||
chr2:178745234 | T | C | 3 | a0001c0015t0008 a0001c0068t0008 a0063c0070t0008 |
3 | HG02717.hp2 HG02896.hp2 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*351A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 351 | chr2 | 178745234 | ||||||
chr2:178745251 | A | C | 13 | a0005c0005t0003 a0007c0008t0003 a0007c0079t0003 others(10): Show |
46 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*334T>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 334 | chr2 | 178745251 | ||||||
chr2:178745259 | G | A | 1 | a0001c0003t0021 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*326C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 326 | chr2 | 178745259 | ||||||
chr2:178745282 | T | G | 13 | a0005c0005t0003 a0007c0008t0003 a0007c0079t0003 others(10): Show |
46 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*303A>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 303 | chr2 | 178745282 | ||||||
chr2:178745297 | G | A | 1 | a0010c0010t0020 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*288C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 288 | chr2 | 178745297 | ||||||
chr2:178745436 | A | T | 8 | a0006c0007t0005 a0006c0007t0015 a0006c0056t0005 others(5): Show |
22 | HG00544.hp2 HG00642.hp2 HG01257.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*149T>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 149 | chr2 | 178745436 | ||||||
chr2:178745445 | T | A | 10 | a0001c0002t0004 a0001c0003t0004 a0001c0044t0004 others(7): Show |
33 | HG00408.hp2 HG00642.hp1 HG02080.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*140A>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 140 | chr2 | 178745445 | ||||||
chr2:178745514 | C | T | 3 | a0049c0052t0009 a0057c0095t0009 a0064c0035t0014 |
3 | HG02109.hp2 HG02723.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*71G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 71 | chr2 | 178745514 | ||||||
chr2:178745529 | A | T | 1 | a0010c0010t0013 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*56T>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 46/46 | 56 | chr2 | 178745529 | ||||||
chr2:178807273 | G | A | 1 | a0001c0003t0021 | 1 | NA18522.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-75C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 1/46 | chr2 | 178807273 | |||||||
chr2:178807306 | C | T | 3 | a0002c0001t0012 a0014c0017t0007 a0014c0049t0007 |
5 | HG02559.hp1 HG02647.hp2 HG03130.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-108G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 1/46 | 2664 | chr2 | 178807306 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:178752043 | GA | G | 245 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(242): Show |
305 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(302): Show |
splice_region_variant&intron_variant | LOW | c.10361-5delT | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 45/45 | chr2 | 178752043 | |||||||
chr2:178752043 | GAA | G | 11 | a0001c0002t0001g0190 a0001c0015t0001g0125 a0001c0015t0001g0128 others(8): Show |
11 | HG01106.hp2 HG01168.hp1 HG01496.hp1 others(8): Show |
splice_region_variant&intron_variant | LOW | c.10361-6_10361-5del others(2): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 45/45 | chr2 | 178752043 | |||||||
chr2:178752045 | A | G | 1 | a0002c0001t0002g0107 | 1 | NA19088.hp1 | splice_region_variant&intron_variant | LOW | c.10361-6T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 45/45 | chr2 | 178752045 | |||||||
chr2:178752053 | A | AC | 3 | a0014c0017t0007g0037 a0014c0017t0007g0038 a0014c0017t0007g0039 |
3 | HG02559.hp1 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.10361-15_10361-14i others(3): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 45/45 | chr2 | 178752053 | |||||||
chr2:178752264 | T | C | 2 | a0046c0091t0011g0053 a0066c0058t0011g0204 |
2 | HG02055.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.10361-225A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 45/45 | chr2 | 178752264 | |||||||
chr2:178752334 | G | T | 1 | a0003c0004t0001g0263 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.10361-295C>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 45/45 | chr2 | 178752334 | |||||||
chr2:178752529 | G | A | 1 | a0004c0006t0001g0136 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.10361-490C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 45/45 | chr2 | 178752529 | |||||||
chr2:178752643 | T | C | 43 | a0005c0005t0003g0010 a0005c0005t0003g0201 a0005c0005t0003g0202 others(40): Show |
46 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.10360+481A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 45/45 | chr2 | 178752643 | |||||||
chr2:178752698 | A | G | 15 | a0006c0007t0005g0003 a0006c0007t0005g0030 a0006c0007t0005g0234 others(12): Show |
21 | HG00544.hp2 HG00642.hp2 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.10360+426T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 45/45 | chr2 | 178752698 | |||||||
chr2:178752785 | G | A | 1 | a0041c0042t0003g0209 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.10360+339C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 45/45 | chr2 | 178752785 | |||||||
chr2:178752807 | A | G | 3 | a0009c0013t0006g0035 a0009c0013t0006g0296 a0009c0013t0006g0297 |
4 | HG02896.hp1 HG02897.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.10360+317T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 45/45 | chr2 | 178752807 | |||||||
chr2:178752840 | C | T | 299 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(296): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.10360+284G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 45/45 | chr2 | 178752840 | |||||||
chr2:178752911 | A | G | 3 | a0005c0005t0003g0211 a0005c0005t0003g0242 a0041c0042t0003g0209 |
3 | HG01358.hp2 HG01433.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.10360+213T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 45/45 | chr2 | 178752911 | |||||||
chr2:178752929 | A | G | 1 | a0002c0001t0002g0097 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.10360+195T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 45/45 | chr2 | 178752929 | |||||||
chr2:178753015 | A | G | 5 | a0001c0002t0001g0185 a0001c0002t0001g0190 a0001c0002t0001g0191 others(2): Show |
5 | HG00423.hp1 HG00621.hp2 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.10360+109T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 45/45 | chr2 | 178753015 | |||||||
chr2:178753292 | T | A | 230 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(227): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.10304-112A>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178753292 | |||||||
chr2:178753396 | T | G | 19 | a0005c0005t0003g0010 a0005c0005t0003g0201 a0005c0005t0003g0202 others(16): Show |
21 | HG00597.hp1 HG01099.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.10304-216A>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178753396 | |||||||
chr2:178753550 | C | T | 6 | a0010c0010t0001g0011 a0010c0010t0001g0246 a0010c0010t0001g0250 others(3): Show |
8 | HG01361.hp2 HG02630.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.10304-370G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178753550 | |||||||
chr2:178753564 | C | T | 5 | a0003c0004t0001g0004 a0003c0004t0001g0267 a0003c0004t0001g0270 others(2): Show |
10 | NA18943.hp1 NA18967.hp1 NA18968.hp1 others(7): Show |
intron_variant | MODIFIER | c.10304-384G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178753564 | |||||||
chr2:178753735 | C | T | 136 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(133): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.10304-555G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178753735 | |||||||
chr2:178753777 | C | T | 1 | a0061c0097t0017g0203 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.10304-597G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178753777 | |||||||
chr2:178754063 | G | A | 299 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(296): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.10304-883C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178754063 | |||||||
chr2:178754448 | C | G | 2 | a0022c0032t0002g0075 a0022c0032t0002g0076 |
2 | HG02280.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.10304-1268G>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178754448 | |||||||
chr2:178754458 | T | C | 1 | a0026c0024t0001g0187 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.10304-1278A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178754458 | |||||||
chr2:178754670 | G | C | 293 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(290): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.10304-1490C>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178754670 | |||||||
chr2:178754673 | T | C | 63 | a0005c0005t0003g0010 a0005c0005t0003g0201 a0005c0005t0003g0202 others(60): Show |
72 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.10304-1493A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178754673 | |||||||
chr2:178754714 | G | T | 1 | a0003c0004t0001g0262 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.10304-1534C>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178754714 | |||||||
chr2:178754858 | T | C | 1 | a0049c0052t0009g0257 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.10304-1678A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178754858 | |||||||
chr2:178755111 | T | C | 2 | a0049c0052t0009g0257 a0057c0095t0009g0299 |
2 | HG02109.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.10304-1931A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178755111 | |||||||
chr2:178755226 | T | TTC | 7 | a0004c0006t0001g0021 a0004c0006t0001g0022 a0004c0006t0001g0130 others(4): Show |
9 | HG00140.hp2 HG00733.hp1 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.10304-2047_10304-2 others(8): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178755226 | |||||||
chr2:178755228 | G | T | 7 | a0004c0006t0001g0021 a0004c0006t0001g0022 a0004c0006t0001g0130 others(4): Show |
9 | HG00140.hp2 HG00733.hp1 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.10304-2048C>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178755228 | |||||||
chr2:178755231 | C | A | 71 | a0001c0002t0002g0182 a0001c0002t0002g0183 a0001c0002t0002g0184 others(68): Show |
87 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.10304-2051G>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178755231 | |||||||
chr2:178755358 | A | G | 5 | a0001c0002t0001g0148 a0004c0011t0001g0023 a0004c0011t0001g0124 others(2): Show |
6 | HG02055.hp2 HG02630.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.10304-2178T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178755358 | |||||||
chr2:178755490 | C | T | 1 | a0001c0003t0004g0289 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.10304-2310G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178755490 | |||||||
chr2:178755504 | C | T | 1 | a0050c0053t0001g0238 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.10304-2324G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178755504 | |||||||
chr2:178755531 | G | A | 1 | a0002c0001t0002g0056 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.10304-2351C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178755531 | |||||||
chr2:178755538 | C | T | 2 | a0003c0004t0001g0258 a0003c0004t0001g0259 |
2 | NA18965.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.10304-2358G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178755538 | |||||||
chr2:178755729 | T | C | 293 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(290): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.10304-2549A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178755729 | |||||||
chr2:178755761 | T | C | 1 | a0001c0002t0002g0194 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.10304-2581A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178755761 | |||||||
chr2:178755826 | C | A | 1 | a0057c0095t0009g0299 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.10304-2646G>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178755826 | |||||||
chr2:178755984 | A | G | 1 | a0064c0035t0014g0227 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.10304-2804T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178755984 | |||||||
chr2:178755996 | C | T | 1 | a0001c0002t0002g0164 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.10304-2816G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178755996 | |||||||
chr2:178756177 | C | T | 1 | a0054c0046t0001g0157 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.10303+2807G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178756177 | |||||||
chr2:178756224 | C | T | 230 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(227): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.10303+2760G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178756224 | |||||||
chr2:178756499 | C | T | 1 | a0035c0040t0001g0177 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.10303+2485G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178756499 | |||||||
chr2:178756545 | C | T | 11 | a0001c0002t0004g0192 a0001c0002t0004g0193 a0001c0003t0004g0002 others(8): Show |
22 | HG00408.hp2 HG03490.hp2 HG03492.hp1 others(19): Show |
intron_variant | MODIFIER | c.10303+2439G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178756545 | |||||||
chr2:178756622 | T | G | 2 | a0013c0014t0001g0205 a0013c0014t0001g0206 |
2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.10303+2362A>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178756622 | |||||||
chr2:178756626 | G | A | 4 | a0014c0017t0007g0037 a0014c0017t0007g0038 a0014c0017t0007g0039 others(1): Show |
4 | HG02559.hp1 HG03130.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.10303+2358C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178756626 | |||||||
chr2:178756750 | T | C | 1 | a0083c0050t0019g0123 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.10303+2234A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178756750 | |||||||
chr2:178757137 | G | A | 63 | a0005c0005t0003g0010 a0005c0005t0003g0201 a0005c0005t0003g0202 others(60): Show |
72 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.10303+1847C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757137 | |||||||
chr2:178757146 | A | ATGCTTTA others(53): Show |
2 | a0002c0001t0002g0052 a0002c0001t0002g0095 |
2 | HG01256.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.10303+1837_10303+1 others(66): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757146 | |||||||
chr2:178757146 | A | ATGCTTTA others(259): Show |
2 | a0001c0002t0001g0176 a0001c0002t0001g0197 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.10303+1837_10303+1 others(272): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757146 | |||||||
chr2:178757146 | A | ATGCTTTA others(203): Show |
1 | a0004c0006t0001g0130 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.10303+1837_10303+1 others(216): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757146 | |||||||
chr2:178757146 | A | ATGCTTTA others(263): Show |
1 | a0004c0006t0001g0045 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.10303+1837_10303+1 others(276): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757146 | |||||||
chr2:178757146 | A | ATGCTTTA others(53): Show |
5 | a0001c0002t0002g0199 a0002c0001t0002g0074 a0002c0001t0002g0081 others(2): Show |
5 | HG00609.hp1 HG01981.hp2 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.10303+1837_10303+1 others(66): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757146 | |||||||
chr2:178757146 | A | ATGCTTTA others(233): Show |
10 | a0004c0006t0001g0021 a0004c0006t0001g0022 a0004c0006t0001g0131 others(7): Show |
12 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(9): Show |
intron_variant | MODIFIER | c.10303+1837_10303+1 others(246): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757146 | |||||||
chr2:178757146 | A | ATGCTTTA others(263): Show |
1 | a0004c0006t0001g0200 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.10303+1837_10303+1 others(276): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757146 | |||||||
chr2:178757146 | A | ATGCTTTA others(83): Show |
9 | a0001c0002t0002g0183 a0002c0001t0002g0086 a0002c0001t0002g0088 others(6): Show |
9 | HG00639.hp1 HG01257.hp2 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.10303+1837_10303+1 others(96): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757146 | |||||||
chr2:178757146 | A | ATGCTTTA others(143): Show |
1 | a0003c0004t0001g0269 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.10303+1837_10303+1 others(156): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757146 | |||||||
chr2:178757146 | A | ATGCTTTA others(113): Show |
5 | a0009c0013t0006g0035 a0009c0013t0006g0296 a0009c0013t0006g0297 others(2): Show |
6 | HG02895.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.10303+1837_10303+1 others(126): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757146 | |||||||
chr2:178757146 | A | ATGCTTTA others(143): Show |
2 | a0001c0003t0001g0152 a0084c0064t0005g0151 |
2 | HG01361.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.10303+1837_10303+1 others(156): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757146 | |||||||
chr2:178757146 | A | ATGCTTTA others(203): Show |
1 | a0003c0004t0001g0033 | 2 | NA18948.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.10303+1837_10303+1 others(216): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757146 | |||||||
chr2:178757146 | A | ATGCTTTA others(173): Show |
6 | a0001c0003t0001g0150 a0001c0015t0008g0127 a0004c0006t0001g0129 others(3): Show |
6 | HG01167.hp2 HG01978.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.10303+1837_10303+1 others(186): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757146 | |||||||
chr2:178757146 | A | ATGCTTTA others(203): Show |
14 | a0001c0002t0004g0193 a0001c0003t0001g0046 a0001c0003t0001g0143 others(11): Show |
16 | HG00639.hp2 HG01496.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.10303+1837_10303+1 others(216): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757146 | |||||||
chr2:178757146 | A | ATGCTTTA others(233): Show |
52 | a0001c0002t0001g0028 a0001c0002t0001g0179 a0001c0002t0001g0196 others(49): Show |
75 | HG00408.hp2 HG00558.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.10303+1837_10303+1 others(246): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757146 | |||||||
chr2:178757146 | A | ATGCTTTA others(263): Show |
30 | a0001c0002t0001g0005 a0001c0002t0001g0029 a0001c0002t0001g0148 others(27): Show |
37 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.10303+1837_10303+1 others(276): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757146 | |||||||
chr2:178757146 | A | ATGCTTTA others(293): Show |
9 | a0001c0002t0001g0163 a0001c0002t0001g0174 a0001c0002t0001g0190 others(6): Show |
9 | HG01071.hp1 HG01243.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.10303+1837_10303+1 others(306): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757146 | |||||||
chr2:178757146 | A | ATGCTTTA others(323): Show |
3 | a0001c0002t0001g0162 a0001c0077t0001g0181 a0059c0039t0001g0188 |
3 | HG02735.hp2 NA19010.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.10303+1837_10303+1 others(336): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757146 | |||||||
chr2:178757146 | A | ATGCTTTA others(289): Show |
1 | a0001c0015t0001g0128 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.10303+1837_10303+1 others(302): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757146 | |||||||
chr2:178757146 | A | ATGCTTTA others(259): Show |
1 | a0003c0004t0001g0041 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.10303+1837_10303+1 others(272): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757146 | |||||||
chr2:178757146 | A | ATGCTTTA others(229): Show |
1 | a0001c0002t0001g0171 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.10303+1837_10303+1 others(242): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757146 | |||||||
chr2:178757146 | A | ATGCTTTA others(259): Show |
1 | a0003c0047t0001g0266 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.10303+1837_10303+1 others(272): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757146 | |||||||
chr2:178757148 | G | GCTTTAAG others(23): Show |
1 | a0057c0095t0009g0299 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.10303+1835_10303+1 others(36): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757148 | |||||||
chr2:178757148 | G | GCTTTAAG others(23): Show |
2 | a0002c0001t0002g0052 a0002c0001t0002g0095 |
2 | HG01256.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.10303+1806_10303+1 others(36): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757148 | |||||||
chr2:178757148 | G | GCTTTAAG others(53): Show |
3 | a0014c0017t0007g0037 a0014c0017t0007g0038 a0014c0017t0007g0039 |
3 | HG02559.hp1 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.10303+1776_10303+1 others(66): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757148 | |||||||
chr2:178757148 | G | GCTTTAAG others(173): Show |
1 | a0006c0056t0005g0233 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.10303+1835_10303+1 others(186): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757148 | |||||||
chr2:178757148 | G | GCTTTAAG others(113): Show |
4 | a0006c0007t0005g0244 a0006c0007t0005g0248 a0012c0018t0005g0253 others(1): Show |
4 | HG02015.hp2 HG02155.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.10303+1835_10303+1 others(126): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757148 | |||||||
chr2:178757148 | G | GCTTTAAG others(143): Show |
9 | a0006c0007t0005g0003 a0006c0007t0005g0030 a0006c0007t0005g0234 others(6): Show |
15 | HG00544.hp2 HG00642.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.10303+1835_10303+1 others(156): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757148 | |||||||
chr2:178757148 | G | GCTTTAAG others(173): Show |
2 | a0024c0030t0001g0232 a0069c0057t0005g0235 |
2 | HG02965.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.10303+1835_10303+1 others(186): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757148 | |||||||
chr2:178757148 | G | GCTTTAAG others(203): Show |
2 | a0006c0007t0005g0237 a0050c0053t0001g0238 |
2 | HG02257.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.10303+1835_10303+1 others(216): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757148 | |||||||
chr2:178757148 | G | GCTTTAAG others(499): Show |
1 | a0005c0005t0003g0225 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.10303+1835_10303+1 others(512): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757148 | |||||||
chr2:178757148 | G | GCTTTAAG others(53): Show |
1 | a0001c0002t0002g0182 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.10303+1835_10303+1 others(66): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757148 | |||||||
chr2:178757148 | G | GCTTTAAG others(83): Show |
48 | a0001c0002t0002g0184 a0002c0001t0001g0080 a0002c0001t0002g0001 others(45): Show |
66 | HG00408.hp1 HG00423.hp2 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.10303+1835_10303+1 others(96): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757148 | |||||||
chr2:178757148 | G | GCTTTAAG others(113): Show |
9 | a0002c0001t0002g0082 a0002c0001t0002g0084 a0002c0001t0002g0105 others(6): Show |
11 | HG00544.hp1 HG02622.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.10303+1835_10303+1 others(126): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757148 | |||||||
chr2:178757148 | G | GCTTTAAG others(143): Show |
1 | a0056c0036t0016g0300 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.10303+1835_10303+1 others(156): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757148 | |||||||
chr2:178757148 | G | GCTTTAAG others(113): Show |
6 | a0002c0001t0002g0077 a0002c0001t0002g0101 a0002c0001t0002g0155 others(3): Show |
6 | HG00735.hp1 HG02280.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.10303+1835_10303+1 others(126): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757148 | |||||||
chr2:178757148 | G | GCTTTAAG others(143): Show |
3 | a0010c0010t0001g0246 a0010c0010t0001g0250 a0013c0014t0001g0208 |
3 | HG02451.hp2 HG02630.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.10303+1835_10303+1 others(156): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757148 | |||||||
chr2:178757148 | G | GCTTTAAG others(173): Show |
1 | a0064c0035t0014g0227 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.10303+1835_10303+1 others(186): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757148 | |||||||
chr2:178757148 | G | GCTTTAAG others(143): Show |
2 | a0009c0022t0006g0025 a0042c0059t0001g0245 |
3 | HG01361.hp2 HG02145.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.10303+1835_10303+1 others(156): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757148 | |||||||
chr2:178757148 | GCTTTAAG others(23): Show |
G | 1 | a0049c0052t0009g0257 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.10303+1806_10303+1 others(36): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757148 | |||||||
chr2:178757157 | A | ACAGTAAG others(559): Show |
1 | a0005c0005t0003g0220 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.10303+1826_10303+1 others(572): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757157 | |||||||
chr2:178757157 | A | ACAGTAAG others(499): Show |
3 | a0005c0005t0003g0221 a0007c0008t0003g0064 a0028c0026t0003g0212 |
3 | HG01975.hp1 NA18984.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.10303+1826_10303+1 others(512): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757157 | |||||||
chr2:178757157 | A | ACAGTAAG others(529): Show |
1 | a0005c0005t0003g0224 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.10303+1826_10303+1 others(542): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757157 | |||||||
chr2:178757157 | A | ACAGTAAG others(439): Show |
1 | a0005c0005t0003g0226 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.10303+1826_10303+1 others(452): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757157 | |||||||
chr2:178757157 | A | ACAGTAAG others(499): Show |
1 | a0005c0005t0003g0223 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.10303+1826_10303+1 others(512): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757157 | |||||||
chr2:178757157 | A | ACAGTAAG others(499): Show |
1 | a0007c0008t0003g0015 | 2 | NA18612.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.10303+1826_10303+1 others(512): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757157 | |||||||
chr2:178757157 | A | ACAGTAAG others(469): Show |
3 | a0005c0005t0003g0010 a0007c0008t0003g0063 a0007c0008t0003g0108 |
5 | HG01099.hp2 NA18977.hp1 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.10303+1826_10303+1 others(482): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757157 | |||||||
chr2:178757157 | A | ACAGTAAG others(499): Show |
1 | a0007c0008t0003g0154 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.10303+1826_10303+1 others(512): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757157 | |||||||
chr2:178757157 | A | ACAGTAAG others(495): Show |
1 | a0080c0043t0003g0243 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.10303+1826_10303+1 others(508): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757157 | |||||||
chr2:178757157 | A | ACAGTAAG others(439): Show |
2 | a0005c0005t0003g0202 a0005c0005t0003g0222 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.10303+1826_10303+1 others(452): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757157 | |||||||
chr2:178757157 | A | ACAGTAAG others(405): Show |
1 | a0027c0031t0003g0058 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.10303+1826_10303+1 others(418): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757157 | |||||||
chr2:178757157 | A | ACAGTAAG others(469): Show |
2 | a0007c0008t0003g0062 a0045c0062t0003g0284 |
2 | HG02027.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.10303+1826_10303+1 others(482): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757157 | |||||||
chr2:178757157 | A | ACAGTAAG others(495): Show |
1 | a0078c0083t0003g0089 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.10303+1826_10303+1 others(508): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757157 | |||||||
chr2:178757157 | A | ACAGTAAG others(439): Show |
2 | a0007c0008t0003g0057 a0032c0080t0003g0153 |
2 | HG00558.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.10303+1826_10303+1 others(452): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757157 | |||||||
chr2:178757157 | A | ACAGTAAG others(465): Show |
1 | a0018c0027t0003g0240 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.10303+1826_10303+1 others(478): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757157 | |||||||
chr2:178757157 | A | ACAGTAAG others(409): Show |
2 | a0007c0008t0003g0061 a0027c0031t0003g0060 |
2 | NA18980.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.10303+1826_10303+1 others(422): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757157 | |||||||
chr2:178757157 | A | ACAGTAAG others(409): Show |
1 | a0018c0027t0003g0241 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.10303+1826_10303+1 others(422): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757157 | |||||||
chr2:178757157 | A | ACAGTAAG others(499): Show |
1 | a0005c0005t0003g0201 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.10303+1826_10303+1 others(512): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757157 | |||||||
chr2:178757157 | A | ACAGTAAG others(469): Show |
1 | a0005c0005t0003g0214 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.10303+1826_10303+1 others(482): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757157 | |||||||
chr2:178757157 | A | ACAGTAAG others(499): Show |
1 | a0005c0005t0003g0211 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.10303+1826_10303+1 others(512): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757157 | |||||||
chr2:178757157 | A | ACAGTAAG others(379): Show |
1 | a0007c0008t0003g0059 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.10303+1826_10303+1 others(392): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757157 | |||||||
chr2:178757157 | A | ACAGTAAG others(379): Show |
1 | a0028c0026t0003g0213 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.10303+1826_10303+1 others(392): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757157 | |||||||
chr2:178757157 | A | ACAGTAAG others(435): Show |
1 | a0041c0042t0003g0209 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.10303+1826_10303+1 others(448): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757157 | |||||||
chr2:178757157 | A | ACAGTAAG others(431): Show |
1 | a0005c0005t0003g0210 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.10303+1826_10303+1 others(444): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757157 | |||||||
chr2:178757162 | A | AAGTAATA others(19): Show |
1 | a0017c0019t0001g0009 | 3 | HG02970.hp1 HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.10303+1821_10303+1 others(32): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757162 | |||||||
chr2:178757171 | T | C | 1 | a0057c0095t0009g0299 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.10303+1813A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757171 | |||||||
chr2:178757174 | A | ACTTACTT others(143): Show |
1 | a0012c0018t0005g0254 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.10303+1809_10303+1 others(156): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757174 | |||||||
chr2:178757178 | A | G | 138 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(135): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.10303+1806T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757178 | |||||||
chr2:178757187 | A | ACAGTAAG others(469): Show |
1 | a0005c0005t0003g0218 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.10303+1796_10303+1 others(482): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757187 | |||||||
chr2:178757187 | A | ACAGTAAG others(503): Show |
1 | a0005c0005t0003g0216 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.10303+1796_10303+1 others(516): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757187 | |||||||
chr2:178757187 | A | ACAGTAAG others(559): Show |
1 | a0005c0005t0003g0242 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.10303+1796_10303+1 others(572): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757187 | |||||||
chr2:178757187 | A | ACAGTAAG others(555): Show |
1 | a0005c0005t0003g0217 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.10303+1796_10303+1 others(568): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757187 | |||||||
chr2:178757187 | A | ACAGTAAG others(439): Show |
2 | a0005c0005t0003g0219 a0072c0081t0003g0065 |
2 | HG01261.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.10303+1796_10303+1 others(452): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757187 | |||||||
chr2:178757187 | A | ACAGTAAG others(469): Show |
1 | a0007c0008t0003g0106 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.10303+1796_10303+1 others(482): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757187 | |||||||
chr2:178757187 | A | ACAGTAAG others(349): Show |
1 | a0007c0079t0003g0055 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.10303+1796_10303+1 others(362): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757187 | |||||||
chr2:178757187 | A | ACAGTAAG others(293): Show |
1 | a0076c0092t0003g0111 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.10303+1796_10303+1 others(306): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757187 | |||||||
chr2:178757192 | A | AAGTAATA others(49): Show |
1 | a0014c0049t0007g0040 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.10303+1791_10303+1 others(62): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757192 | |||||||
chr2:178757201 | T | C | 1 | a0057c0095t0009g0299 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.10303+1783A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757201 | |||||||
chr2:178757208 | A | G | 110 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(107): Show |
140 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.10303+1776T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757208 | |||||||
chr2:178757217 | A | ACAGTAAG others(533): Show |
1 | a0005c0005t0003g0215 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.10303+1766_10303+1 others(546): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757217 | |||||||
chr2:178757217 | A | ACAGTAAG others(323): Show |
1 | a0061c0097t0017g0203 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.10303+1766_10303+1 others(336): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757217 | |||||||
chr2:178757395 | T | C | 1 | a0061c0097t0017g0203 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.10303+1589A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757395 | |||||||
chr2:178757398 | C | T | 1 | a0003c0004t0002g0277 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.10303+1586G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757398 | |||||||
chr2:178757407 | T | C | 1 | a0061c0097t0017g0203 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.10303+1577A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757407 | |||||||
chr2:178757477 | A | C | 1 | a0056c0036t0016g0300 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.10303+1507T>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757477 | |||||||
chr2:178757511 | ATCAAAG | A | 5 | a0009c0013t0006g0035 a0009c0013t0006g0296 a0009c0013t0006g0297 others(2): Show |
7 | HG02145.hp1 HG02895.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.10303+1467_10303+1 others(12): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757511 | |||||||
chr2:178757612 | C | T | 1 | a0001c0003t0001g0144 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.10303+1372G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757612 | |||||||
chr2:178757842 | G | C | 1 | a0014c0049t0007g0040 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.10303+1142C>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178757842 | |||||||
chr2:178758046 | C | A | 1 | a0001c0003t0001g0144 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.10303+938G>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178758046 | |||||||
chr2:178758078 | A | G | 43 | a0005c0005t0003g0010 a0005c0005t0003g0201 a0005c0005t0003g0202 others(40): Show |
46 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.10303+906T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178758078 | |||||||
chr2:178758099 | G | T | 1 | a0061c0097t0017g0203 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.10303+885C>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178758099 | |||||||
chr2:178758123 | C | T | 8 | a0002c0001t0002g0052 a0002c0001t0002g0092 a0002c0001t0002g0093 others(5): Show |
8 | HG01256.hp2 HG01257.hp2 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.10303+861G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178758123 | |||||||
chr2:178758281 | A | G | 293 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(290): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.10303+703T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178758281 | |||||||
chr2:178758298 | A | G | 1 | a0002c0001t0002g0074 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.10303+686T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178758298 | |||||||
chr2:178758415 | A | G | 64 | a0005c0005t0003g0010 a0005c0005t0003g0201 a0005c0005t0003g0202 others(61): Show |
73 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.10303+569T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178758415 | |||||||
chr2:178758444 | A | G | 1 | a0003c0004t0001g0041 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.10303+540T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178758444 | |||||||
chr2:178758610 | C | T | 1 | a0027c0031t0003g0058 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.10303+374G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178758610 | |||||||
chr2:178758850 | G | T | 63 | a0005c0005t0003g0010 a0005c0005t0003g0201 a0005c0005t0003g0202 others(60): Show |
72 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.10303+134C>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178758850 | |||||||
chr2:178758941 | C | A | 1 | a0001c0003t0004g0289 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.10303+43G>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 44/45 | chr2 | 178758941 | |||||||
chr2:178759212 | T | C | 298 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(295): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.10115-40A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178759212 | |||||||
chr2:178759598 | T | C | 19 | a0006c0007t0005g0003 a0006c0007t0005g0030 a0006c0007t0005g0234 others(16): Show |
25 | HG00544.hp2 HG00642.hp2 HG01257.hp1 others(22): Show |
intron_variant | MODIFIER | c.10115-426A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178759598 | |||||||
chr2:178759677 | C | T | 3 | a0008c0009t0001g0012 a0008c0009t0001g0031 a0008c0009t0001g0278 |
6 | HG00558.hp1 NA18956.hp1 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.10115-505G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178759677 | |||||||
chr2:178759715 | A | T | 1 | a0001c0003t0001g0149 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.10115-543T>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178759715 | |||||||
chr2:178759778 | A | C | 1 | a0069c0057t0005g0235 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.10115-606T>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178759778 | |||||||
chr2:178759807 | A | G | 1 | a0056c0036t0016g0300 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.10115-635T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178759807 | |||||||
chr2:178760002 | C | T | 12 | a0010c0010t0001g0011 a0010c0010t0001g0246 a0010c0010t0001g0250 others(9): Show |
14 | HG01361.hp2 HG02055.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.10115-830G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178760002 | |||||||
chr2:178760061 | A | T | 63 | a0005c0005t0003g0010 a0005c0005t0003g0201 a0005c0005t0003g0202 others(60): Show |
72 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.10115-889T>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178760061 | |||||||
chr2:178760151 | C | A | 1 | a0002c0001t0002g0069 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.10115-979G>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178760151 | |||||||
chr2:178760201 | A | T | 1 | a0049c0052t0009g0257 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.10115-1029T>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178760201 | |||||||
chr2:178760273 | T | C | 2 | a0049c0052t0009g0257 a0057c0095t0009g0299 |
2 | HG02109.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.10115-1101A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178760273 | |||||||
chr2:178760314 | G | A | 1 | a0002c0001t0002g0085 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.10115-1142C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178760314 | |||||||
chr2:178760414 | C | A | 1 | a0074c0085t0002g0050 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.10115-1242G>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178760414 | |||||||
chr2:178760460 | G | T | 1 | a0001c0002t0001g0173 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.10115-1288C>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178760460 | |||||||
chr2:178760462 | G | T | 1 | a0061c0097t0017g0203 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.10115-1290C>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178760462 | |||||||
chr2:178760520 | A | G | 1 | a0017c0019t0001g0009 | 3 | HG02970.hp1 HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.10115-1348T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178760520 | |||||||
chr2:178760660 | T | A | 3 | a0014c0017t0007g0037 a0014c0017t0007g0038 a0014c0017t0007g0039 |
3 | HG02559.hp1 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.10115-1488A>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178760660 | |||||||
chr2:178760848 | G | GGT | 85 | a0001c0002t0001g0161 a0001c0002t0001g0162 a0001c0002t0001g0163 others(82): Show |
102 | HG00408.hp1 HG00423.hp2 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.10115-1678_10115-1 others(8): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178760848 | |||||||
chr2:178760848 | G | GGTGT | 4 | a0002c0001t0002g0082 a0002c0001t0002g0084 a0002c0089t0002g0083 others(1): Show |
4 | HG00544.hp1 HG02970.hp2 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.10115-1680_10115-1 others(10): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178760848 | |||||||
chr2:178760848 | G | GGTGTGTG others(1): Show |
6 | a0010c0010t0001g0011 a0010c0010t0001g0246 a0010c0010t0001g0250 others(3): Show |
8 | HG01361.hp2 HG02630.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.10115-1684_10115-1 others(14): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178760848 | |||||||
chr2:178760848 | G | GGTGTGTG others(9): Show |
2 | a0013c0014t0001g0207 a0013c0014t0001g0208 |
2 | HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.10115-1692_10115-1 others(22): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178760848 | |||||||
chr2:178760848 | GGT | G | 117 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(114): Show |
142 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.10115-1678_10115-1 others(8): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178760848 | |||||||
chr2:178760848 | GGTGT | G | 62 | a0003c0004t0001g0004 a0004c0006t0001g0136 a0005c0005t0003g0010 others(59): Show |
71 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.10115-1680_10115-1 others(10): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178760848 | |||||||
chr2:178761112 | G | A | 12 | a0010c0010t0001g0011 a0010c0010t0001g0246 a0010c0010t0001g0250 others(9): Show |
14 | HG01361.hp2 HG02055.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.10115-1940C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178761112 | |||||||
chr2:178761142 | T | C | 2 | a0016c0016t0001g0014 a0016c0016t0001g0042 |
3 | HG02257.hp2 HG02486.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.10115-1970A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178761142 | |||||||
chr2:178761154 | C | CT | 19 | a0006c0007t0005g0003 a0006c0007t0005g0030 a0006c0007t0005g0234 others(16): Show |
25 | HG00544.hp2 HG00642.hp2 HG01257.hp1 others(22): Show |
intron_variant | MODIFIER | c.10115-1983dupA | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178761154 | |||||||
chr2:178761265 | C | T | 2 | a0049c0052t0009g0257 a0057c0095t0009g0299 |
2 | HG02109.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.10115-2093G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178761265 | |||||||
chr2:178761290 | C | T | 65 | a0005c0005t0003g0010 a0005c0005t0003g0201 a0005c0005t0003g0202 others(62): Show |
74 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.10115-2118G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178761290 | |||||||
chr2:178761353 | T | A | 40 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(37): Show |
49 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(46): Show |
intron_variant | MODIFIER | c.10115-2181A>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178761353 | |||||||
chr2:178761631 | G | A | 1 | a0005c0005t0003g0226 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.10115-2459C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178761631 | |||||||
chr2:178761665 | G | T | 1 | a0038c0038t0001g0172 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.10115-2493C>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178761665 | |||||||
chr2:178761670 | T | C | 2 | a0001c0002t0001g0176 a0001c0002t0001g0197 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.10115-2498A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178761670 | |||||||
chr2:178761754 | A | C | 1 | a0002c0001t0002g0073 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.10114+2423T>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178761754 | |||||||
chr2:178761832 | T | C | 292 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(289): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.10114+2345A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178761832 | |||||||
chr2:178761880 | G | C | 292 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(289): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.10114+2297C>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178761880 | |||||||
chr2:178761892 | C | T | 1 | a0006c0007t0005g0244 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.10114+2285G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178761892 | |||||||
chr2:178762074 | A | G | 292 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(289): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.10114+2103T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178762074 | |||||||
chr2:178762213 | T | C | 293 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(290): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.10114+1964A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178762213 | |||||||
chr2:178762428 | C | T | 6 | a0010c0010t0001g0011 a0010c0010t0001g0246 a0010c0010t0001g0250 others(3): Show |
8 | HG01361.hp2 HG02630.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.10114+1749G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178762428 | |||||||
chr2:178762449 | G | C | 19 | a0006c0007t0005g0003 a0006c0007t0005g0030 a0006c0007t0005g0234 others(16): Show |
25 | HG00544.hp2 HG00642.hp2 HG01257.hp1 others(22): Show |
intron_variant | MODIFIER | c.10114+1728C>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178762449 | |||||||
chr2:178762513 | C | G | 1 | a0002c0001t0002g0118 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.10114+1664G>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178762513 | |||||||
chr2:178762638 | A | G | 292 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(289): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.10114+1539T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178762638 | |||||||
chr2:178762847 | A | G | 5 | a0011c0012t0001g0008 a0011c0012t0001g0027 a0023c0020t0001g0026 others(2): Show |
9 | HG02451.hp1 HG02559.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.10114+1330T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178762847 | |||||||
chr2:178762852 | C | T | 1 | a0010c0010t0001g0246 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.10114+1325G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178762852 | |||||||
chr2:178762875 | C | T | 4 | a0014c0017t0007g0037 a0014c0017t0007g0038 a0014c0017t0007g0039 others(1): Show |
4 | HG02559.hp1 HG03130.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.10114+1302G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178762875 | |||||||
chr2:178762995 | T | A | 6 | a0009c0013t0006g0035 a0009c0013t0006g0296 a0009c0013t0006g0297 others(3): Show |
8 | HG02145.hp1 HG02895.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.10114+1182A>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178762995 | |||||||
chr2:178763363 | C | T | 1 | a0009c0022t0006g0025 | 2 | HG02145.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.10114+814G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178763363 | |||||||
chr2:178763476 | C | T | 1 | a0014c0017t0007g0038 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.10114+701G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178763476 | |||||||
chr2:178763504 | T | C | 19 | a0006c0007t0005g0003 a0006c0007t0005g0030 a0006c0007t0005g0234 others(16): Show |
25 | HG00544.hp2 HG00642.hp2 HG01257.hp1 others(22): Show |
intron_variant | MODIFIER | c.10114+673A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178763504 | |||||||
chr2:178763513 | C | T | 7 | a0009c0013t0006g0035 a0009c0013t0006g0296 a0009c0013t0006g0297 others(4): Show |
9 | HG02145.hp1 HG02809.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.10114+664G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178763513 | |||||||
chr2:178763610 | T | C | 273 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(270): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.10114+567A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178763610 | |||||||
chr2:178763625 | C | A | 19 | a0006c0007t0005g0003 a0006c0007t0005g0030 a0006c0007t0005g0234 others(16): Show |
25 | HG00544.hp2 HG00642.hp2 HG01257.hp1 others(22): Show |
intron_variant | MODIFIER | c.10114+552G>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178763625 | |||||||
chr2:178763635 | G | A | 219 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(216): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.10114+542C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178763635 | |||||||
chr2:178763642 | G | T | 200 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(197): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.10114+535C>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178763642 | |||||||
chr2:178763790 | G | A | 73 | a0001c0002t0002g0182 a0001c0002t0002g0183 a0001c0002t0002g0184 others(70): Show |
91 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.10114+387C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178763790 | |||||||
chr2:178763932 | T | G | 1 | a0003c0004t0001g0263 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.10114+245A>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178763932 | |||||||
chr2:178763934 | A | AT | 270 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(267): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.10114+242dupA | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178763934 | |||||||
chr2:178763953 | G | C | 137 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(134): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.10114+224C>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178763953 | |||||||
chr2:178764013 | T | C | 1 | a0004c0006t0001g0024 | 2 | HG02145.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.10114+164A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 43/45 | chr2 | 178764013 | |||||||
chr2:178764378 | T | C | 1 | a0002c0001t0002g0007 | 3 | NA18950.hp2 NA18965.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.9989-76A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 42/45 | chr2 | 178764378 | |||||||
chr2:178764866 | C | T | 1 | a0002c0001t0002g0067 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.9704-55G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 41/45 | chr2 | 178764866 | |||||||
chr2:178765091 | T | G | 1 | a0016c0016t0001g0042 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.9704-280A>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 41/45 | chr2 | 178765091 | |||||||
chr2:178765095 | G | C | 1 | a0016c0016t0001g0042 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.9704-284C>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 41/45 | chr2 | 178765095 | |||||||
chr2:178765148 | C | T | 1 | a0075c0034t0002g0049 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.9704-337G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 41/45 | chr2 | 178765148 | |||||||
chr2:178765285 | A | G | 1 | a0002c0001t0002g0086 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.9704-474T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 41/45 | chr2 | 178765285 | |||||||
chr2:178765517 | C | G | 1 | a0001c0002t0002g0199 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.9704-706G>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 41/45 | chr2 | 178765517 | |||||||
chr2:178765529 | A | T | 19 | a0006c0007t0005g0003 a0006c0007t0005g0030 a0006c0007t0005g0234 others(16): Show |
25 | HG00544.hp2 HG00642.hp2 HG01257.hp1 others(22): Show |
intron_variant | MODIFIER | c.9704-718T>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 41/45 | chr2 | 178765529 | |||||||
chr2:178765574 | G | T | 1 | a0003c0004t0001g0276 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.9704-763C>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 41/45 | chr2 | 178765574 | |||||||
chr2:178765580 | T | C | 1 | a0007c0008t0003g0061 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.9704-769A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 41/45 | chr2 | 178765580 | |||||||
chr2:178765601 | C | T | 4 | a0001c0002t0001g0185 a0001c0002t0001g0190 a0001c0002t0001g0191 others(1): Show |
4 | HG00423.hp1 HG00621.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.9703+780G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 41/45 | chr2 | 178765601 | |||||||
chr2:178765808 | C | T | 1 | a0004c0006t0001g0024 | 2 | HG02145.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.9703+573G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 41/45 | chr2 | 178765808 | |||||||
chr2:178765896 | C | G | 1 | a0056c0036t0016g0300 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.9703+485G>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 41/45 | chr2 | 178765896 | |||||||
chr2:178765980 | A | T | 1 | a0061c0097t0017g0203 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.9703+401T>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 41/45 | chr2 | 178765980 | |||||||
chr2:178766635 | A | C | 63 | a0001c0002t0001g0171 a0002c0001t0002g0092 a0002c0001t0002g0093 others(60): Show |
68 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.9472-23T>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 40/45 | chr2 | 178766635 | |||||||
chr2:178766637 | AC | A | 19 | a0006c0007t0005g0003 a0006c0007t0005g0030 a0006c0007t0005g0234 others(16): Show |
25 | HG00544.hp2 HG00642.hp2 HG01257.hp1 others(22): Show |
intron_variant | MODIFIER | c.9472-26delG | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 40/45 | chr2 | 178766637 | |||||||
chr2:178766656 | C | T | 1 | a0002c0001t0002g0085 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.9472-44G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 40/45 | chr2 | 178766656 | |||||||
chr2:178766829 | C | T | 1 | a0028c0026t0003g0212 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.9472-217G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 40/45 | chr2 | 178766829 | |||||||
chr2:178766961 | C | T | 1 | a0006c0007t0005g0244 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.9472-349G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 40/45 | chr2 | 178766961 | |||||||
chr2:178767124 | C | A | 43 | a0005c0005t0003g0010 a0005c0005t0003g0201 a0005c0005t0003g0202 others(40): Show |
46 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.9472-512G>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 40/45 | chr2 | 178767124 | |||||||
chr2:178767269 | G | C | 1 | a0049c0052t0009g0257 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.9471+490C>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 40/45 | chr2 | 178767269 | |||||||
chr2:178767305 | C | T | 1 | a0020c0025t0001g0165 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.9471+454G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 40/45 | chr2 | 178767305 | |||||||
chr2:178767309 | T | A | 1 | a0014c0017t0007g0039 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.9471+450A>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 40/45 | chr2 | 178767309 | |||||||
chr2:178767406 | A | G | 219 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(216): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.9471+353T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 40/45 | chr2 | 178767406 | |||||||
chr2:178767410 | C | G | 1 | a0014c0017t0007g0037 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.9471+349G>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 40/45 | chr2 | 178767410 | |||||||
chr2:178767955 | G | A | 1 | a0057c0095t0009g0299 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.9306-31C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 39/45 | chr2 | 178767955 | |||||||
chr2:178767983 | T | C | 136 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(133): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.9305+31A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 39/45 | chr2 | 178767983 | |||||||
chr2:178768244 | T | C | 4 | a0005c0005t0003g0210 a0005c0005t0003g0211 a0005c0005t0003g0242 others(1): Show |
4 | HG01358.hp2 HG01433.hp2 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.9164-89A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 38/45 | chr2 | 178768244 | |||||||
chr2:178768286 | T | A | 1 | a0037c0066t0001g0158 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.9164-131A>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 38/45 | chr2 | 178768286 | |||||||
chr2:178768363 | A | G | 42 | a0005c0005t0003g0010 a0005c0005t0003g0201 a0005c0005t0003g0202 others(39): Show |
45 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.9164-208T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 38/45 | chr2 | 178768363 | |||||||
chr2:178768445 | T | G | 1 | a0049c0052t0009g0257 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.9163+228A>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 38/45 | chr2 | 178768445 | |||||||
chr2:178768460 | T | C | 19 | a0006c0007t0005g0003 a0006c0007t0005g0030 a0006c0007t0005g0234 others(16): Show |
25 | HG00544.hp2 HG00642.hp2 HG01257.hp1 others(22): Show |
intron_variant | MODIFIER | c.9163+213A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 38/45 | chr2 | 178768460 | |||||||
chr2:178768550 | C | T | 19 | a0006c0007t0005g0003 a0006c0007t0005g0030 a0006c0007t0005g0234 others(16): Show |
25 | HG00544.hp2 HG00642.hp2 HG01257.hp1 others(22): Show |
intron_variant | MODIFIER | c.9163+123G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 38/45 | chr2 | 178768550 | |||||||
chr2:178768571 | G | T | 154 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(151): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.9163+102C>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 38/45 | chr2 | 178768571 | |||||||
chr2:178768617 | T | C | 2 | a0002c0001t0001g0080 a0002c0001t0002g0006 |
4 | HG01891.hp2 HG02818.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.9163+56A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 38/45 | chr2 | 178768617 | |||||||
chr2:178769089 | A | G | 1 | a0005c0005t0003g0214 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.8903-156T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 37/45 | chr2 | 178769089 | |||||||
chr2:178769293 | G | A | 1 | a0049c0052t0009g0257 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.8903-360C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 37/45 | chr2 | 178769293 | |||||||
chr2:178769341 | C | A | 9 | a0007c0008t0003g0015 a0007c0008t0003g0062 a0007c0008t0003g0063 others(6): Show |
10 | HG00558.hp2 HG00673.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.8902+338G>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 37/45 | chr2 | 178769341 | |||||||
chr2:178769443 | T | G | 1 | a0061c0097t0017g0203 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.8902+236A>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 37/45 | chr2 | 178769443 | |||||||
chr2:178769581 | T | A | 1 | a0049c0052t0009g0257 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.8902+98A>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 37/45 | chr2 | 178769581 | |||||||
chr2:178769649 | GTA | G | 298 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(295): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.8902+28_8902+29del others(2): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 37/45 | chr2 | 178769649 | |||||||
chr2:178769663 | A | T | 6 | a0002c0001t0002g0068 a0002c0001t0002g0071 a0002c0001t0002g0082 others(3): Show |
6 | HG00544.hp1 HG03540.hp2 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.8902+16T>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 37/45 | chr2 | 178769663 | |||||||
chr2:178769665 | A | T | 81 | a0001c0002t0002g0182 a0001c0002t0002g0183 a0001c0002t0002g0184 others(78): Show |
100 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.8902+14T>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 37/45 | chr2 | 178769665 | |||||||
chr2:178771062 | A | T | 284 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(281): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.8116+149T>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 34/45 | chr2 | 178771062 | |||||||
chr2:178771123 | T | C | 42 | a0005c0005t0003g0010 a0005c0005t0003g0201 a0005c0005t0003g0202 others(39): Show |
45 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.8116+88A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 34/45 | chr2 | 178771123 | |||||||
chr2:178771155 | C | T | 293 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(290): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.8116+56G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 34/45 | chr2 | 178771155 | |||||||
chr2:178771192 | C | T | 4 | a0001c0002t0002g0183 a0001c0002t0002g0184 a0019c0023t0001g0170 others(1): Show |
4 | HG00639.hp1 HG01167.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.8116+19G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 34/45 | chr2 | 178771192 | |||||||
chr2:178771530 | T | A | 42 | a0005c0005t0003g0010 a0005c0005t0003g0201 a0005c0005t0003g0202 others(39): Show |
45 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.7856-59A>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 33/45 | chr2 | 178771530 | |||||||
chr2:178771546 | T | C | 1 | a0017c0019t0001g0009 | 3 | HG02970.hp1 HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.7856-75A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 33/45 | chr2 | 178771546 | |||||||
chr2:178771857 | A | T | 4 | a0001c0002t0002g0183 a0001c0002t0002g0184 a0019c0023t0001g0170 others(1): Show |
4 | HG00639.hp1 HG01167.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.7856-386T>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 33/45 | chr2 | 178771857 | |||||||
chr2:178771881 | C | G | 1 | a0013c0014t0001g0207 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.7856-410G>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 33/45 | chr2 | 178771881 | |||||||
chr2:178771911 | A | G | 1 | a0064c0035t0014g0227 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.7856-440T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 33/45 | chr2 | 178771911 | |||||||
chr2:178771933 | G | A | 2 | a0001c0003t0004g0285 a0001c0044t0004g0286 |
2 | NA18948.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.7856-462C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 33/45 | chr2 | 178771933 | |||||||
chr2:178771941 | T | C | 42 | a0005c0005t0003g0010 a0005c0005t0003g0201 a0005c0005t0003g0202 others(39): Show |
45 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.7856-470A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 33/45 | chr2 | 178771941 | |||||||
chr2:178772256 | C | T | 20 | a0006c0007t0005g0003 a0006c0007t0005g0030 a0006c0007t0005g0234 others(17): Show |
26 | HG00544.hp2 HG00642.hp2 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.7856-785G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 33/45 | chr2 | 178772256 | |||||||
chr2:178772524 | C | T | 1 | a0061c0097t0017g0203 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.7855+585G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 33/45 | chr2 | 178772524 | |||||||
chr2:178772539 | A | G | 260 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(257): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.7855+570T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 33/45 | chr2 | 178772539 | |||||||
chr2:178772874 | A | G | 1 | a0057c0095t0009g0299 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.7855+235T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 33/45 | chr2 | 178772874 | |||||||
chr2:178773029 | G | A | 1 | a0002c0001t0002g0081 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.7855+80C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 33/45 | chr2 | 178773029 | |||||||
chr2:178773078 | C | T | 1 | a0014c0049t0007g0040 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.7855+31G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 33/45 | chr2 | 178773078 | |||||||
chr2:178773445 | G | C | 1 | a0003c0004t0001g0270 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.7594+17C>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 32/45 | chr2 | 178773445 | |||||||
chr2:178774181 | A | G | 1 | a0006c0007t0005g0244 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.7057+26T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 30/45 | chr2 | 178774181 | |||||||
chr2:178774570 | C | T | 251 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(248): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.6791-97G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 29/45 | chr2 | 178774570 | |||||||
chr2:178774675 | A | G | 1 | a0017c0019t0001g0009 | 3 | HG02970.hp1 HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.6791-202T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 29/45 | chr2 | 178774675 | |||||||
chr2:178774771 | C | G | 259 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(256): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.6790+150G>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 29/45 | chr2 | 178774771 | |||||||
chr2:178774797 | T | G | 1 | a0002c0001t0002g0099 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.6790+124A>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 29/45 | chr2 | 178774797 | |||||||
chr2:178777075 | A | G | 1 | a0061c0097t0017g0203 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.4815-26T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 27/45 | chr2 | 178777075 | |||||||
chr2:178777698 | G | A | 257 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(254): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
splice_region_variant&intron_variant | LOW | c.4480+6C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 25/45 | chr2 | 178777698 | |||||||
chr2:178778035 | C | T | 1 | a0009c0013t0006g0035 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4209-60G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 24/45 | chr2 | 178778035 | |||||||
chr2:178778068 | T | C | 1 | a0001c0002t0001g0178 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.4209-93A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 24/45 | chr2 | 178778068 | |||||||
chr2:178778098 | G | A | 3 | a0002c0001t0002g0082 a0002c0001t0002g0084 a0002c0089t0002g0083 |
3 | HG00544.hp1 NA18951.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.4209-123C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 24/45 | chr2 | 178778098 | |||||||
chr2:178778155 | T | C | 15 | a0006c0007t0005g0003 a0006c0007t0005g0030 a0006c0007t0005g0234 others(12): Show |
21 | HG00544.hp2 HG00642.hp2 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.4209-180A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 24/45 | chr2 | 178778155 | |||||||
chr2:178778198 | T | C | 299 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(296): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.4209-223A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 24/45 | chr2 | 178778198 | |||||||
chr2:178778367 | T | C | 19 | a0006c0007t0005g0003 a0006c0007t0005g0030 a0006c0007t0005g0234 others(16): Show |
25 | HG00544.hp2 HG00642.hp2 HG01257.hp1 others(22): Show |
intron_variant | MODIFIER | c.4209-392A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 24/45 | chr2 | 178778367 | |||||||
chr2:178778560 | A | G | 1 | a0001c0002t0001g0198 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.4208+314T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 24/45 | chr2 | 178778560 | |||||||
chr2:178778818 | T | C | 12 | a0010c0010t0001g0011 a0010c0010t0001g0246 a0010c0010t0001g0250 others(9): Show |
14 | HG01361.hp2 HG02055.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.4208+56A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 24/45 | chr2 | 178778818 | |||||||
chr2:178778848 | A | G | 1 | a0002c0001t0002g0070 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.4208+26T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 24/45 | chr2 | 178778848 | |||||||
chr2:178779135 | G | C | 1 | a0002c0001t0002g0112 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.3964-17C>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 23/45 | chr2 | 178779135 | |||||||
chr2:178779159 | A | G | 258 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(255): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.3964-41T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 23/45 | chr2 | 178779159 | |||||||
chr2:178779207 | A | G | 258 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(255): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.3963+22T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 23/45 | chr2 | 178779207 | |||||||
chr2:178779577 | G | A | 259 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(256): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.3730-115C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 22/45 | chr2 | 178779577 | |||||||
chr2:178779700 | C | T | 8 | a0010c0010t0001g0011 a0010c0010t0001g0246 a0010c0010t0001g0250 others(5): Show |
10 | HG01361.hp2 HG02451.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.3730-238G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 22/45 | chr2 | 178779700 | |||||||
chr2:178779728 | A | C | 1 | a0017c0019t0001g0009 | 3 | HG02970.hp1 HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3730-266T>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 22/45 | chr2 | 178779728 | |||||||
chr2:178780241 | C | T | 1 | a0009c0013t0006g0296 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3524-36G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 21/45 | chr2 | 178780241 | |||||||
chr2:178780379 | A | T | 258 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(255): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.3524-174T>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 21/45 | chr2 | 178780379 | |||||||
chr2:178780402 | A | G | 1 | a0052c0102t0002g0114 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3524-197T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 21/45 | chr2 | 178780402 | |||||||
chr2:178780457 | C | T | 3 | a0002c0001t0002g0016 a0002c0001t0002g0068 a0002c0001t0002g0069 |
4 | NA19063.hp1 NA19065.hp2 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.3524-252G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 21/45 | chr2 | 178780457 | |||||||
chr2:178780558 | C | G | 40 | a0005c0005t0003g0010 a0005c0005t0003g0201 a0005c0005t0003g0202 others(37): Show |
43 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.3524-353G>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 21/45 | chr2 | 178780558 | |||||||
chr2:178780562 | G | C | 6 | a0010c0010t0001g0011 a0010c0010t0001g0246 a0010c0010t0001g0250 others(3): Show |
8 | HG01361.hp2 HG02630.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.3524-357C>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 21/45 | chr2 | 178780562 | |||||||
chr2:178780850 | C | T | 197 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(194): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.3523+271G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 21/45 | chr2 | 178780850 | |||||||
chr2:178781004 | C | A | 40 | a0005c0005t0003g0010 a0005c0005t0003g0201 a0005c0005t0003g0202 others(37): Show |
43 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.3523+117G>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 21/45 | chr2 | 178781004 | |||||||
chr2:178781383 | C | T | 1 | a0057c0095t0009g0299 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3381-120G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 20/45 | chr2 | 178781383 | |||||||
chr2:178781485 | T | G | 1 | a0002c0001t0002g0105 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3381-222A>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 20/45 | chr2 | 178781485 | |||||||
chr2:178781538 | A | T | 4 | a0024c0030t0001g0231 a0024c0030t0001g0232 a0050c0053t0001g0238 others(1): Show |
4 | HG02257.hp1 HG02965.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.3381-275T>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 20/45 | chr2 | 178781538 | |||||||
chr2:178781583 | A | AT | 40 | a0005c0005t0003g0010 a0005c0005t0003g0201 a0005c0005t0003g0202 others(37): Show |
43 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.3381-321dupA | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 20/45 | chr2 | 178781583 | |||||||
chr2:178781607 | G | A | 258 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(255): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.3381-344C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 20/45 | chr2 | 178781607 | |||||||
chr2:178781756 | C | T | 1 | a0047c0065t0004g0287 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.3380+456G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 20/45 | chr2 | 178781756 | |||||||
chr2:178781803 | T | G | 258 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(255): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.3380+409A>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 20/45 | chr2 | 178781803 | |||||||
chr2:178781905 | A | AGT | 137 | a0001c0002t0001g0148 a0001c0003t0001g0046 a0001c0003t0001g0143 others(134): Show |
164 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.3380+305_3380+306d others(4): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 20/45 | chr2 | 178781905 | |||||||
chr2:178781905 | A | AGTGT | 59 | a0001c0003t0001g0142 a0002c0001t0001g0080 a0002c0001t0002g0001 others(56): Show |
75 | HG00544.hp1 HG00597.hp2 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.3380+303_3380+306d others(6): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 20/45 | chr2 | 178781905 | |||||||
chr2:178781905 | A | AGTGTGT | 3 | a0002c0001t0002g0048 a0002c0001t0002g0067 a0002c0001t0002g0092 |
3 | HG02273.hp1 HG02602.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.3380+301_3380+306d others(8): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 20/45 | chr2 | 178781905 | |||||||
chr2:178781905 | AGT | A | 51 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(48): Show |
62 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.3380+305_3380+306d others(4): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 20/45 | chr2 | 178781905 | |||||||
chr2:178781905 | AGTGT | A | 35 | a0003c0004t0001g0004 a0003c0004t0001g0032 a0003c0004t0001g0033 others(32): Show |
47 | HG00438.hp1 HG00558.hp1 HG01192.hp2 others(44): Show |
intron_variant | MODIFIER | c.3380+303_3380+306d others(6): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 20/45 | chr2 | 178781905 | |||||||
chr2:178781911 | T | C | 1 | a0001c0002t0001g0229 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.3380+301A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 20/45 | chr2 | 178781911 | |||||||
chr2:178781931 | G | T | 1 | a0002c0001t0002g0066 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.3380+281C>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 20/45 | chr2 | 178781931 | |||||||
chr2:178783096 | C | T | 41 | a0003c0004t0001g0004 a0003c0004t0001g0032 a0003c0004t0001g0033 others(38): Show |
53 | HG00438.hp1 HG00558.hp1 HG01192.hp2 others(50): Show |
intron_variant | MODIFIER | c.2842-32G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 17/45 | chr2 | 178783096 | |||||||
chr2:178783097 | G | A | 8 | a0002c0001t0002g0052 a0002c0001t0002g0092 a0002c0001t0002g0093 others(5): Show |
8 | HG01256.hp2 HG01257.hp2 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.2842-33C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 17/45 | chr2 | 178783097 | |||||||
chr2:178783175 | G | T | 40 | a0003c0004t0001g0004 a0003c0004t0001g0032 a0003c0004t0001g0033 others(37): Show |
52 | HG00438.hp1 HG00558.hp1 HG01192.hp2 others(49): Show |
intron_variant | MODIFIER | c.2842-111C>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 17/45 | chr2 | 178783175 | |||||||
chr2:178783235 | ATATAT | A | 66 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(63): Show |
83 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.2842-176_2842-172d others(7): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 17/45 | chr2 | 178783235 | |||||||
chr2:178783391 | G | A | 1 | a0001c0003t0004g0292 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2842-327C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 17/45 | chr2 | 178783391 | |||||||
chr2:178783458 | C | T | 1 | a0061c0097t0017g0203 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2841+262G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 17/45 | chr2 | 178783458 | |||||||
chr2:178783522 | A | G | 29 | a0003c0004t0001g0004 a0003c0004t0001g0032 a0003c0004t0001g0033 others(26): Show |
39 | HG00438.hp1 HG00558.hp1 HG01192.hp2 others(36): Show |
intron_variant | MODIFIER | c.2841+198T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 17/45 | chr2 | 178783522 | |||||||
chr2:178783585 | G | A | 5 | a0002c0001t0002g0056 a0002c0001t0002g0097 a0002c0001t0002g0098 others(2): Show |
5 | HG01081.hp2 HG01884.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2841+135C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 17/45 | chr2 | 178783585 | |||||||
chr2:178784622 | G | A | 47 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(44): Show |
56 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.2494-271C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 15/45 | chr2 | 178784622 | |||||||
chr2:178784647 | C | T | 7 | a0009c0013t0006g0035 a0009c0013t0006g0296 a0009c0013t0006g0297 others(4): Show |
9 | HG02145.hp1 HG02717.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.2494-296G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 15/45 | chr2 | 178784647 | |||||||
chr2:178784734 | G | A | 4 | a0001c0003t0001g0149 a0001c0003t0001g0150 a0001c0003t0001g0152 others(1): Show |
4 | HG00639.hp2 HG01361.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.2494-383C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 15/45 | chr2 | 178784734 | |||||||
chr2:178784788 | C | G | 1 | a0002c0001t0002g0056 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2494-437G>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 15/45 | chr2 | 178784788 | |||||||
chr2:178784843 | A | G | 2 | a0016c0016t0001g0014 a0016c0016t0001g0042 |
3 | HG02257.hp2 HG02486.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.2494-492T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 15/45 | chr2 | 178784843 | |||||||
chr2:178784987 | G | A | 1 | a0001c0002t0001g0198 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2493+633C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 15/45 | chr2 | 178784987 | |||||||
chr2:178785023 | C | A | 134 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(131): Show |
163 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.2493+597G>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 15/45 | chr2 | 178785023 | |||||||
chr2:178785144 | G | A | 47 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(44): Show |
56 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.2493+476C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 15/45 | chr2 | 178785144 | |||||||
chr2:178785185 | T | C | 1 | a0061c0097t0017g0203 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2493+435A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 15/45 | chr2 | 178785185 | |||||||
chr2:178785198 | GA | G | 85 | a0002c0001t0001g0080 a0002c0001t0002g0001 a0002c0001t0002g0006 others(82): Show |
104 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.2493+421delT | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 15/45 | chr2 | 178785198 | |||||||
chr2:178785280 | T | A | 6 | a0010c0010t0001g0011 a0010c0010t0001g0246 a0010c0010t0001g0250 others(3): Show |
8 | HG01361.hp2 HG02630.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.2493+340A>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 15/45 | chr2 | 178785280 | |||||||
chr2:178785344 | G | A | 1 | a0001c0002t0001g0179 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2493+276C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 15/45 | chr2 | 178785344 | |||||||
chr2:178785501 | C | T | 1 | a0017c0019t0001g0009 | 3 | HG02970.hp1 HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2493+119G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 15/45 | chr2 | 178785501 | |||||||
chr2:178785507 | C | A | 2 | a0001c0002t0002g0182 a0001c0002t0002g0199 |
2 | HG01981.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.2493+113G>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 15/45 | chr2 | 178785507 | |||||||
chr2:178786227 | G | A | 77 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(74): Show |
89 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.2077-86C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 13/45 | chr2 | 178786227 | |||||||
chr2:178786397 | C | T | 1 | a0056c0036t0016g0300 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2077-256G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 13/45 | chr2 | 178786397 | |||||||
chr2:178786523 | T | C | 14 | a0004c0006t0001g0021 a0004c0006t0001g0022 a0004c0006t0001g0045 others(11): Show |
16 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.2077-382A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 13/45 | chr2 | 178786523 | |||||||
chr2:178786528 | G | T | 2 | a0016c0016t0001g0014 a0016c0016t0001g0042 |
3 | HG02257.hp2 HG02486.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.2077-387C>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 13/45 | chr2 | 178786528 | |||||||
chr2:178786529 | A | T | 2 | a0016c0016t0001g0014 a0016c0016t0001g0042 |
3 | HG02257.hp2 HG02486.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.2077-388T>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 13/45 | chr2 | 178786529 | |||||||
chr2:178786646 | A | T | 1 | a0061c0097t0017g0203 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2077-505T>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 13/45 | chr2 | 178786646 | |||||||
chr2:178786665 | A | C | 1 | a0064c0035t0014g0227 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2077-524T>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 13/45 | chr2 | 178786665 | |||||||
chr2:178787019 | C | T | 4 | a0014c0017t0007g0037 a0014c0017t0007g0038 a0014c0017t0007g0039 others(1): Show |
4 | HG02559.hp1 HG03130.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2077-878G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 13/45 | chr2 | 178787019 | |||||||
chr2:178787091 | AAAGT | A | 18 | a0006c0007t0005g0003 a0006c0007t0005g0030 a0006c0007t0005g0234 others(15): Show |
24 | HG00544.hp2 HG00642.hp2 HG01257.hp1 others(21): Show |
intron_variant | MODIFIER | c.2077-954_2077-951d others(6): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 13/45 | chr2 | 178787091 | |||||||
chr2:178787320 | C | T | 47 | a0003c0004t0001g0004 a0003c0004t0001g0032 a0003c0004t0001g0033 others(44): Show |
63 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.2077-1179G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 13/45 | chr2 | 178787320 | |||||||
chr2:178787467 | A | G | 1 | a0057c0095t0009g0299 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2077-1326T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 13/45 | chr2 | 178787467 | |||||||
chr2:178787517 | A | C | 1 | a0061c0097t0017g0203 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2077-1376T>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 13/45 | chr2 | 178787517 | |||||||
chr2:178787712 | T | C | 87 | a0003c0004t0001g0004 a0003c0004t0001g0032 a0003c0004t0001g0033 others(84): Show |
107 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.2077-1571A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 13/45 | chr2 | 178787712 | |||||||
chr2:178787734 | A | G | 61 | a0003c0004t0001g0004 a0003c0004t0001g0032 a0003c0004t0001g0033 others(58): Show |
79 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.2077-1593T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 13/45 | chr2 | 178787734 | |||||||
chr2:178787786 | T | C | 61 | a0003c0004t0001g0004 a0003c0004t0001g0032 a0003c0004t0001g0033 others(58): Show |
79 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.2076+1574A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 13/45 | chr2 | 178787786 | |||||||
chr2:178787962 | G | A | 1 | a0004c0006t0001g0024 | 2 | HG02145.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2076+1398C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 13/45 | chr2 | 178787962 | |||||||
chr2:178787964 | G | C | 29 | a0003c0004t0001g0004 a0003c0004t0001g0032 a0003c0004t0001g0033 others(26): Show |
39 | HG00438.hp1 HG00558.hp1 HG01192.hp2 others(36): Show |
intron_variant | MODIFIER | c.2076+1396C>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 13/45 | chr2 | 178787964 | |||||||
chr2:178788075 | A | G | 232 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(229): Show |
284 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(281): Show |
intron_variant | MODIFIER | c.2076+1285T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 13/45 | chr2 | 178788075 | |||||||
chr2:178788180 | T | C | 8 | a0009c0013t0006g0035 a0009c0013t0006g0296 a0009c0013t0006g0297 others(5): Show |
10 | HG02145.hp1 HG02717.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.2076+1180A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 13/45 | chr2 | 178788180 | |||||||
chr2:178788238 | G | C | 3 | a0002c0001t0002g0101 a0002c0001t0002g0103 a0070c0086t0002g0102 |
3 | NA18946.hp2 NA18957.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.2076+1122C>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 13/45 | chr2 | 178788238 | |||||||
chr2:178788528 | T | G | 1 | a0051c0078t0001g0247 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2076+832A>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 13/45 | chr2 | 178788528 | |||||||
chr2:178788841 | T | C | 1 | a0067c0060t0001g0301 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2076+519A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 13/45 | chr2 | 178788841 | |||||||
chr2:178789586 | A | G | 15 | a0006c0007t0005g0003 a0006c0007t0005g0030 a0006c0007t0005g0234 others(12): Show |
21 | HG00544.hp2 HG00642.hp2 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.1939-89T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 12/45 | chr2 | 178789586 | |||||||
chr2:178789863 | G | A | 2 | a0046c0091t0011g0053 a0066c0058t0011g0204 |
2 | HG02055.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1938+115C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 12/45 | chr2 | 178789863 | |||||||
chr2:178789968 | C | G | 1 | a0061c0097t0017g0203 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1938+10G>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 12/45 | chr2 | 178789968 | |||||||
chr2:178790319 | G | GA | 43 | a0003c0004t0001g0004 a0003c0004t0001g0032 a0003c0004t0001g0033 others(40): Show |
55 | HG00438.hp1 HG00558.hp1 HG01192.hp2 others(52): Show |
intron_variant | MODIFIER | c.1801-205dupT | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 11/45 | chr2 | 178790319 | |||||||
chr2:178790468 | C | T | 14 | a0001c0003t0001g0290 a0001c0003t0001g0291 a0001c0003t0004g0002 others(11): Show |
24 | HG00408.hp2 HG02027.hp2 HG02080.hp1 others(21): Show |
intron_variant | MODIFIER | c.1800+240G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 11/45 | chr2 | 178790468 | |||||||
chr2:178790897 | T | C | 18 | a0005c0005t0003g0010 a0005c0005t0003g0201 a0005c0005t0003g0202 others(15): Show |
20 | HG00597.hp1 HG01099.hp2 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.1663-52A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 10/45 | chr2 | 178790897 | |||||||
chr2:178790916 | C | T | 6 | a0013c0014t0001g0207 a0013c0014t0001g0208 a0014c0017t0007g0037 others(3): Show |
6 | HG02451.hp2 HG02559.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1663-71G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 10/45 | chr2 | 178790916 | |||||||
chr2:178790942 | T | C | 1 | a0001c0077t0001g0181 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1663-97A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 10/45 | chr2 | 178790942 | |||||||
chr2:178791385 | G | A | 1 | a0002c0001t0002g0103 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1663-540C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 10/45 | chr2 | 178791385 | |||||||
chr2:178791388 | C | T | 1 | a0006c0056t0005g0233 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1663-543G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 10/45 | chr2 | 178791388 | |||||||
chr2:178791415 | A | C | 1 | a0061c0097t0017g0203 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1663-570T>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 10/45 | chr2 | 178791415 | |||||||
chr2:178791506 | C | T | 1 | a0004c0006t0001g0131 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1662+566G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 10/45 | chr2 | 178791506 | |||||||
chr2:178791663 | A | ATG | 40 | a0001c0003t0004g0285 a0001c0015t0001g0125 a0003c0004t0001g0004 others(37): Show |
52 | HG00438.hp1 HG00558.hp1 HG01192.hp2 others(49): Show |
intron_variant | MODIFIER | c.1662+407_1662+408d others(4): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 10/45 | chr2 | 178791663 | |||||||
chr2:178791663 | A | ATGTG | 26 | a0006c0007t0005g0003 a0006c0007t0005g0030 a0006c0007t0005g0234 others(23): Show |
34 | HG00642.hp2 HG01257.hp1 HG01346.hp2 others(31): Show |
intron_variant | MODIFIER | c.1662+405_1662+408d others(6): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 10/45 | chr2 | 178791663 | |||||||
chr2:178791663 | A | ATGTGTG | 35 | a0005c0005t0003g0010 a0005c0005t0003g0202 a0005c0005t0003g0210 others(32): Show |
43 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.1662+403_1662+408d others(8): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 10/45 | chr2 | 178791663 | |||||||
chr2:178791663 | A | ATGTGTGT others(1): Show |
39 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(36): Show |
44 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.1662+401_1662+408d others(10): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 10/45 | chr2 | 178791663 | |||||||
chr2:178791663 | A | ATGTGTGT others(3): Show |
7 | a0001c0002t0001g0161 a0001c0002t0001g0162 a0001c0002t0001g0163 others(4): Show |
7 | HG00621.hp2 HG00639.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.1662+399_1662+408d others(12): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 10/45 | chr2 | 178791663 | |||||||
chr2:178791755 | G | A | 126 | a0002c0001t0001g0080 a0002c0001t0002g0001 a0002c0001t0002g0006 others(123): Show |
157 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.1662+317C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 10/45 | chr2 | 178791755 | |||||||
chr2:178791765 | A | G | 1 | a0064c0035t0014g0227 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1662+307T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 10/45 | chr2 | 178791765 | |||||||
chr2:178791952 | T | C | 12 | a0010c0010t0001g0011 a0010c0010t0001g0246 a0010c0010t0001g0250 others(9): Show |
14 | HG01361.hp2 HG02055.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1662+120A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 10/45 | chr2 | 178791952 | |||||||
chr2:178792030 | T | C | 2 | a0003c0004t0001g0264 a0003c0004t0001g0276 |
2 | HG00438.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.1662+42A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 10/45 | chr2 | 178792030 | |||||||
chr2:178792201 | C | T | 2 | a0002c0001t0002g0054 a0074c0085t0002g0050 |
2 | HG00673.hp2 NA18964.hp2 |
splice_region_variant&intron_variant | LOW | c.1537-4G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 9/45 | chr2 | 178792201 | |||||||
chr2:178792238 | C | A | 6 | a0009c0013t0006g0035 a0009c0013t0006g0296 a0009c0013t0006g0297 others(3): Show |
8 | HG02145.hp1 HG02895.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1537-41G>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 9/45 | chr2 | 178792238 | |||||||
chr2:178792250 | A | C | 2 | a0015c0033t0002g0019 a0015c0100t0002g0044 |
3 | HG00741.hp1 HG01099.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.1537-53T>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 9/45 | chr2 | 178792250 | |||||||
chr2:178792266 | A | C | 1 | a0004c0006t0001g0130 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1537-69T>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 9/45 | chr2 | 178792266 | |||||||
chr2:178792368 | C | T | 1 | a0056c0036t0016g0300 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1537-171G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 9/45 | chr2 | 178792368 | |||||||
chr2:178792527 | G | A | 7 | a0003c0004t0001g0272 a0003c0004t0001g0273 a0003c0004t0002g0277 others(4): Show |
10 | HG00558.hp1 HG01192.hp2 NA18949.hp2 others(7): Show |
intron_variant | MODIFIER | c.1537-330C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 9/45 | chr2 | 178792527 | |||||||
chr2:178792561 | T | C | 1 | a0003c0004t0001g0276 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1537-364A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 9/45 | chr2 | 178792561 | |||||||
chr2:178792704 | G | T | 2 | a0024c0030t0001g0231 a0024c0030t0001g0232 |
2 | HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1537-507C>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 9/45 | chr2 | 178792704 | |||||||
chr2:178792737 | T | G | 43 | a0003c0004t0001g0004 a0003c0004t0001g0032 a0003c0004t0001g0033 others(40): Show |
55 | HG00438.hp1 HG00558.hp1 HG01192.hp2 others(52): Show |
intron_variant | MODIFIER | c.1537-540A>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 9/45 | chr2 | 178792737 | |||||||
chr2:178792778 | C | T | 2 | a0046c0091t0011g0053 a0066c0058t0011g0204 |
2 | HG02055.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1537-581G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 9/45 | chr2 | 178792778 | |||||||
chr2:178792784 | C | T | 5 | a0009c0013t0006g0035 a0009c0013t0006g0296 a0009c0013t0006g0297 others(2): Show |
7 | HG02145.hp1 HG02895.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1537-587G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 9/45 | chr2 | 178792784 | |||||||
chr2:178792848 | G | C | 4 | a0001c0003t0001g0142 a0001c0003t0001g0143 a0001c0003t0001g0144 others(1): Show |
4 | HG02622.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1536+556C>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 9/45 | chr2 | 178792848 | |||||||
chr2:178792895 | C | T | 1 | a0057c0095t0009g0299 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1536+509G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 9/45 | chr2 | 178792895 | |||||||
chr2:178792903 | A | G | 1 | a0043c0054t0005g0230 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1536+501T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 9/45 | chr2 | 178792903 | |||||||
chr2:178792938 | G | T | 3 | a0014c0017t0007g0037 a0014c0017t0007g0038 a0014c0017t0007g0039 |
3 | HG02559.hp1 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1536+466C>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 9/45 | chr2 | 178792938 | |||||||
chr2:178793020 | T | C | 6 | a0004c0006t0001g0024 a0004c0011t0001g0023 a0004c0011t0001g0124 others(3): Show |
8 | HG02055.hp2 HG02145.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1536+384A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 9/45 | chr2 | 178793020 | |||||||
chr2:178793051 | C | T | 3 | a0001c0003t0004g0283 a0045c0062t0003g0284 a0077c0063t0004g0282 |
3 | HG02027.hp2 NA18963.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.1536+353G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 9/45 | chr2 | 178793051 | |||||||
chr2:178793173 | C | T | 1 | a0001c0002t0002g0182 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1536+231G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 9/45 | chr2 | 178793173 | |||||||
chr2:178793200 | T | C | 1 | a0001c0003t0004g0293 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1536+204A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 9/45 | chr2 | 178793200 | |||||||
chr2:178793275 | A | G | 1 | a0061c0097t0017g0203 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1536+129T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 9/45 | chr2 | 178793275 | |||||||
chr2:178793694 | C | T | 1 | a0004c0006t0001g0129 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1399-153G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 8/45 | chr2 | 178793694 | |||||||
chr2:178794006 | T | C | 1 | a0051c0078t0001g0247 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1398+393A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 8/45 | chr2 | 178794006 | |||||||
chr2:178794048 | A | G | 6 | a0013c0014t0001g0207 a0013c0014t0001g0208 a0014c0017t0007g0037 others(3): Show |
6 | HG02451.hp2 HG02559.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1398+351T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 8/45 | chr2 | 178794048 | |||||||
chr2:178794161 | A | ATATAGCC others(15): Show |
29 | a0003c0004t0001g0004 a0003c0004t0001g0032 a0003c0004t0001g0033 others(26): Show |
39 | HG00438.hp1 HG00558.hp1 HG01192.hp2 others(36): Show |
intron_variant | MODIFIER | c.1398+216_1398+237d others(24): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 8/45 | chr2 | 178794161 | |||||||
chr2:178794370 | C | T | 1 | a0002c0001t0002g0048 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1398+29G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 8/45 | chr2 | 178794370 | |||||||
chr2:178794383 | G | A | 1 | a0061c0097t0017g0203 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1398+16C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 8/45 | chr2 | 178794383 | |||||||
chr2:178794391 | G | A | 5 | a0009c0013t0006g0035 a0009c0013t0006g0296 a0009c0013t0006g0297 others(2): Show |
7 | HG02145.hp1 HG02895.hp1 HG02896.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.1398+8C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 8/45 | chr2 | 178794391 | |||||||
chr2:178794607 | A | C | 43 | a0003c0004t0001g0004 a0003c0004t0001g0032 a0003c0004t0001g0033 others(40): Show |
55 | HG00438.hp1 HG00558.hp1 HG01192.hp2 others(52): Show |
intron_variant | MODIFIER | c.1246-56T>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 7/45 | chr2 | 178794607 | |||||||
chr2:178795303 | T | C | 45 | a0003c0004t0001g0004 a0003c0004t0001g0032 a0003c0004t0001g0033 others(42): Show |
57 | HG00438.hp1 HG00558.hp1 HG01192.hp2 others(54): Show |
intron_variant | MODIFIER | c.915-51A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 6/45 | chr2 | 178795303 | |||||||
chr2:178795375 | C | T | 45 | a0003c0004t0001g0004 a0003c0004t0001g0032 a0003c0004t0001g0033 others(42): Show |
57 | HG00438.hp1 HG00558.hp1 HG01192.hp2 others(54): Show |
intron_variant | MODIFIER | c.915-123G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 6/45 | chr2 | 178795375 | |||||||
chr2:178795452 | T | C | 29 | a0003c0004t0001g0004 a0003c0004t0001g0032 a0003c0004t0001g0033 others(26): Show |
39 | HG00438.hp1 HG00558.hp1 HG01192.hp2 others(36): Show |
intron_variant | MODIFIER | c.915-200A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 6/45 | chr2 | 178795452 | |||||||
chr2:178795510 | C | T | 1 | a0061c0097t0017g0203 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.915-258G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 6/45 | chr2 | 178795510 | |||||||
chr2:178795515 | TA | T | 54 | a0002c0001t0002g0051 a0002c0001t0002g0052 a0003c0004t0001g0004 others(51): Show |
69 | HG00438.hp1 HG00558.hp1 HG01192.hp2 others(66): Show |
intron_variant | MODIFIER | c.915-264delT | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 6/45 | chr2 | 178795515 | |||||||
chr2:178795551 | T | C | 1 | a0017c0019t0001g0009 | 3 | HG02970.hp1 HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.915-299A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 6/45 | chr2 | 178795551 | |||||||
chr2:178795672 | G | C | 1 | a0002c0001t0002g0104 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.915-420C>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 6/45 | chr2 | 178795672 | |||||||
chr2:178795723 | AT | A | 30 | a0002c0001t0002g0105 a0003c0041t0001g0275 a0005c0005t0003g0010 others(27): Show |
32 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.915-472delA | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 6/45 | chr2 | 178795723 | |||||||
chr2:178795797 | G | A | 49 | a0003c0004t0001g0004 a0003c0004t0001g0032 a0003c0004t0001g0033 others(46): Show |
63 | HG00438.hp1 HG00558.hp1 HG01192.hp2 others(60): Show |
intron_variant | MODIFIER | c.915-545C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 6/45 | chr2 | 178795797 | |||||||
chr2:178795799 | G | C | 2 | a0016c0016t0001g0014 a0016c0016t0001g0042 |
3 | HG02257.hp2 HG02486.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.915-547C>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 6/45 | chr2 | 178795799 | |||||||
chr2:178796078 | G | A | 1 | a0007c0008t0003g0106 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.915-826C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 6/45 | chr2 | 178796078 | |||||||
chr2:178796200 | A | T | 1 | a0057c0095t0009g0299 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.915-948T>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 6/45 | chr2 | 178796200 | |||||||
chr2:178796227 | A | T | 25 | a0005c0005t0003g0010 a0005c0005t0003g0201 a0005c0005t0003g0202 others(22): Show |
27 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.915-975T>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 6/45 | chr2 | 178796227 | |||||||
chr2:178796840 | T | C | 1 | a0002c0001t0002g0107 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.915-1588A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 6/45 | chr2 | 178796840 | |||||||
chr2:178797126 | T | C | 43 | a0003c0004t0001g0004 a0003c0004t0001g0032 a0003c0004t0001g0033 others(40): Show |
55 | HG00438.hp1 HG00558.hp1 HG01192.hp2 others(52): Show |
intron_variant | MODIFIER | c.915-1874A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 6/45 | chr2 | 178797126 | |||||||
chr2:178797242 | A | AT | 25 | a0005c0005t0003g0010 a0005c0005t0003g0201 a0005c0005t0003g0202 others(22): Show |
27 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.915-1991dupA | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 6/45 | chr2 | 178797242 | |||||||
chr2:178797245 | T | A | 2 | a0013c0014t0001g0207 a0013c0014t0001g0208 |
2 | HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.915-1993A>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 6/45 | chr2 | 178797245 | |||||||
chr2:178797376 | TTCA | T | 10 | a0001c0003t0001g0046 a0001c0015t0001g0125 a0001c0015t0001g0128 others(7): Show |
10 | HG01106.hp2 HG01168.hp1 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.914+2108_914+2110d others(5): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 6/45 | chr2 | 178797376 | |||||||
chr2:178797379 | A | G | 3 | a0001c0002t0002g0194 a0001c0002t0004g0193 a0001c0077t0001g0181 |
3 | NA19010.hp1 NA19064.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.914+2108T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 6/45 | chr2 | 178797379 | |||||||
chr2:178797380 | CAT | C | 33 | a0001c0003t0001g0142 a0001c0003t0001g0143 a0001c0003t0001g0144 others(30): Show |
44 | HG00408.hp2 HG00639.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.914+2105_914+2106d others(4): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 6/45 | chr2 | 178797380 | |||||||
chr2:178797382 | T | C | 10 | a0001c0003t0001g0046 a0001c0015t0001g0125 a0001c0015t0001g0128 others(7): Show |
10 | HG01106.hp2 HG01168.hp1 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.914+2105A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 6/45 | chr2 | 178797382 | |||||||
chr2:178797438 | CT | C | 16 | a0005c0005t0003g0010 a0005c0005t0003g0201 a0005c0005t0003g0202 others(13): Show |
18 | HG00597.hp1 HG01099.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.914+2048delA | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 6/45 | chr2 | 178797438 | |||||||
chr2:178797548 | A | G | 1 | a0004c0006t0001g0045 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.914+1939T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 6/45 | chr2 | 178797548 | |||||||
chr2:178797653 | T | G | 1 | a0061c0097t0017g0203 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.914+1834A>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 6/45 | chr2 | 178797653 | |||||||
chr2:178797693 | T | C | 1 | a0004c0011t0001g0146 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.914+1794A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 6/45 | chr2 | 178797693 | |||||||
chr2:178797740 | T | G | 1 | a0061c0097t0017g0203 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.914+1747A>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 6/45 | chr2 | 178797740 | |||||||
chr2:178797817 | T | A | 1 | a0051c0078t0001g0247 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.914+1670A>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 6/45 | chr2 | 178797817 | |||||||
chr2:178798049 | A | C | 1 | a0061c0097t0017g0203 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.914+1438T>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 6/45 | chr2 | 178798049 | |||||||
chr2:178798120 | T | C | 1 | a0007c0008t0003g0108 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.914+1367A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 6/45 | chr2 | 178798120 | |||||||
chr2:178798176 | A | T | 1 | a0001c0077t0001g0181 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.914+1311T>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 6/45 | chr2 | 178798176 | |||||||
chr2:178798213 | A | T | 1 | a0001c0002t0001g0161 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.914+1274T>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 6/45 | chr2 | 178798213 | |||||||
chr2:178798310 | C | T | 1 | a0004c0011t0001g0124 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.914+1177G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 6/45 | chr2 | 178798310 | |||||||
chr2:178798473 | T | G | 18 | a0003c0004t0001g0004 a0003c0004t0001g0032 a0003c0004t0001g0033 others(15): Show |
28 | HG00558.hp1 HG01192.hp2 NA18943.hp1 others(25): Show |
intron_variant | MODIFIER | c.914+1014A>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 6/45 | chr2 | 178798473 | |||||||
chr2:178798497 | C | T | 1 | a0061c0097t0017g0203 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.914+990G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 6/45 | chr2 | 178798497 | |||||||
chr2:178798528 | G | A | 29 | a0003c0004t0001g0004 a0003c0004t0001g0032 a0003c0004t0001g0033 others(26): Show |
39 | HG00438.hp1 HG00558.hp1 HG01192.hp2 others(36): Show |
intron_variant | MODIFIER | c.914+959C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 6/45 | chr2 | 178798528 | |||||||
chr2:178799089 | C | G | 3 | a0001c0002t0001g0029 a0001c0002t0001g0228 a0001c0002t0001g0229 |
4 | NA18981.hp1 NA18987.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.914+398G>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 6/45 | chr2 | 178799089 | |||||||
chr2:178799254 | A | G | 5 | a0009c0013t0006g0035 a0009c0013t0006g0296 a0009c0013t0006g0297 others(2): Show |
7 | HG02145.hp1 HG02895.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.914+233T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 6/45 | chr2 | 178799254 | |||||||
chr2:178799323 | A | G | 13 | a0001c0002t0001g0028 a0001c0002t0001g0171 a0001c0002t0001g0173 others(10): Show |
14 | HG00140.hp1 HG00735.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.914+164T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 6/45 | chr2 | 178799323 | |||||||
chr2:178799366 | C | A | 1 | a0011c0012t0001g0008 | 3 | HG02818.hp2 HG03130.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.914+121G>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 6/45 | chr2 | 178799366 | |||||||
chr2:178799390 | G | A | 1 | a0006c0007t0005g0239 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.914+97C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 6/45 | chr2 | 178799390 | |||||||
chr2:178799795 | G | T | 1 | a0074c0085t0002g0050 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.669+30C>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 5/45 | chr2 | 178799795 | |||||||
chr2:178799822 | T | C | 1 | a0080c0043t0003g0243 | 1 | NA19054.hp2 | splice_region_variant&intron_variant | LOW | c.669+3A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 5/45 | chr2 | 178799822 | |||||||
chr2:178800028 | T | C | 1 | a0040c0075t0001g0147 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.584-118A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 4/45 | chr2 | 178800028 | |||||||
chr2:178800113 | T | C | 299 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(296): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.584-203A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 4/45 | chr2 | 178800113 | |||||||
chr2:178800237 | A | G | 1 | a0001c0002t0001g0148 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.583+158T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 4/45 | chr2 | 178800237 | |||||||
chr2:178800321 | G | A | 1 | a0057c0095t0009g0299 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.583+74C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 4/45 | chr2 | 178800321 | |||||||
chr2:178800722 | G | A | 1 | a0044c0082t0002g0109 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.296-40C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 3/45 | chr2 | 178800722 | |||||||
chr2:178800947 | T | G | 1 | a0001c0002t0001g0148 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.296-265A>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 3/45 | chr2 | 178800947 | |||||||
chr2:178800977 | T | G | 3 | a0013c0014t0001g0207 a0013c0014t0001g0208 a0014c0049t0007g0040 |
3 | HG02451.hp2 HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.296-295A>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 3/45 | chr2 | 178800977 | |||||||
chr2:178801096 | C | T | 86 | a0002c0001t0001g0080 a0002c0001t0002g0001 a0002c0001t0002g0006 others(83): Show |
105 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.296-414G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 3/45 | chr2 | 178801096 | |||||||
chr2:178801286 | G | A | 47 | a0003c0004t0001g0004 a0003c0004t0001g0032 a0003c0004t0001g0033 others(44): Show |
61 | HG00438.hp1 HG00558.hp1 HG01192.hp2 others(58): Show |
intron_variant | MODIFIER | c.296-604C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 3/45 | chr2 | 178801286 | |||||||
chr2:178801439 | T | C | 29 | a0003c0004t0001g0004 a0003c0004t0001g0032 a0003c0004t0001g0033 others(26): Show |
39 | HG00438.hp1 HG00558.hp1 HG01192.hp2 others(36): Show |
intron_variant | MODIFIER | c.295+699A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 3/45 | chr2 | 178801439 | |||||||
chr2:178801465 | T | C | 3 | a0002c0001t0002g0007 a0071c0093t0004g0110 a0076c0092t0003g0111 |
5 | NA18949.hp1 NA18950.hp2 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.295+673A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 3/45 | chr2 | 178801465 | |||||||
chr2:178801504 | A | T | 1 | a0002c0001t0002g0048 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.295+634T>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 3/45 | chr2 | 178801504 | |||||||
chr2:178801517 | C | T | 6 | a0001c0002t0001g0161 a0001c0002t0001g0162 a0001c0002t0001g0163 others(3): Show |
6 | HG01891.hp1 HG02109.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.295+621G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 3/45 | chr2 | 178801517 | |||||||
chr2:178801519 | T | A | 25 | a0005c0005t0003g0010 a0005c0005t0003g0201 a0005c0005t0003g0202 others(22): Show |
27 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.295+619A>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 3/45 | chr2 | 178801519 | |||||||
chr2:178801524 | C | T | 33 | a0003c0004t0001g0004 a0003c0004t0001g0032 a0003c0004t0001g0033 others(30): Show |
43 | HG00438.hp1 HG00558.hp1 HG01192.hp2 others(40): Show |
intron_variant | MODIFIER | c.295+614G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 3/45 | chr2 | 178801524 | |||||||
chr2:178801635 | T | C | 1 | a0002c0001t0002g0112 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.295+503A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 3/45 | chr2 | 178801635 | |||||||
chr2:178801638 | GT | G | 35 | a0003c0004t0001g0004 a0003c0004t0001g0032 a0003c0004t0001g0033 others(32): Show |
45 | HG00438.hp1 HG00558.hp1 HG01192.hp2 others(42): Show |
intron_variant | MODIFIER | c.295+499delA | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 3/45 | chr2 | 178801638 | |||||||
chr2:178801698 | G | A | 25 | a0005c0005t0003g0010 a0005c0005t0003g0201 a0005c0005t0003g0202 others(22): Show |
27 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.295+440C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 3/45 | chr2 | 178801698 | |||||||
chr2:178802103 | G | A | 4 | a0001c0003t0001g0149 a0001c0003t0001g0150 a0001c0003t0001g0152 others(1): Show |
4 | HG00639.hp2 HG01361.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.295+35C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 3/45 | chr2 | 178802103 | |||||||
chr2:178802363 | C | T | 233 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(230): Show |
286 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(283): Show |
intron_variant | MODIFIER | c.92-22G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 2/45 | chr2 | 178802363 | |||||||
chr2:178802434 | G | A | 6 | a0010c0010t0001g0011 a0010c0010t0001g0246 a0010c0010t0001g0250 others(3): Show |
8 | HG01361.hp2 HG02630.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.92-93C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 2/45 | chr2 | 178802434 | |||||||
chr2:178802505 | A | C | 5 | a0003c0004t0001g0041 a0003c0004t0001g0258 a0003c0004t0001g0259 others(2): Show |
5 | HG02165.hp2 NA18965.hp1 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.92-164T>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 2/45 | chr2 | 178802505 | |||||||
chr2:178802612 | T | C | 1 | a0061c0097t0017g0203 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.92-271A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 2/45 | chr2 | 178802612 | |||||||
chr2:178802888 | A | G | 4 | a0001c0003t0004g0279 a0001c0003t0004g0281 a0001c0003t0004g0294 others(1): Show |
4 | HG00642.hp1 HG02738.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-547T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 2/45 | chr2 | 178802888 | |||||||
chr2:178803079 | C | T | 48 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(45): Show |
57 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.92-738G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 2/45 | chr2 | 178803079 | |||||||
chr2:178803144 | G | A | 4 | a0010c0010t0001g0011 a0010c0010t0001g0250 a0010c0010t0013g0251 others(1): Show |
6 | HG02809.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.92-803C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 2/45 | chr2 | 178803144 | |||||||
chr2:178803213 | G | A | 1 | a0034c0103t0002g0117 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.92-872C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 2/45 | chr2 | 178803213 | |||||||
chr2:178803214 | C | A | 1 | a0034c0103t0002g0117 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.92-873G>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 2/45 | chr2 | 178803214 | |||||||
chr2:178803324 | C | T | 1 | a0063c0070t0008g0121 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.92-983G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 2/45 | chr2 | 178803324 | |||||||
chr2:178803395 | CTGAG | C | 6 | a0009c0013t0006g0035 a0009c0013t0006g0296 a0009c0013t0006g0297 others(3): Show |
8 | HG02145.hp1 HG02723.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.92-1058_92-1055del others(4): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 2/45 | chr2 | 178803395 | |||||||
chr2:178803414 | T | C | 1 | a0056c0036t0016g0300 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.92-1073A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 2/45 | chr2 | 178803414 | |||||||
chr2:178803464 | T | C | 1 | a0002c0001t0002g0020 | 2 | HG00423.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.91+1088A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 2/45 | chr2 | 178803464 | |||||||
chr2:178803525 | T | C | 1 | a0006c0007t0005g0248 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.91+1027A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 2/45 | chr2 | 178803525 | |||||||
chr2:178803612 | A | G | 1 | a0004c0006t0001g0120 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.91+940T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 2/45 | chr2 | 178803612 | |||||||
chr2:178803624 | T | C | 2 | a0002c0001t0002g0118 a0002c0001t0002g0119 |
2 | HG03927.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.91+928A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 2/45 | chr2 | 178803624 | |||||||
chr2:178803651 | A | T | 1 | a0061c0097t0017g0203 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.91+901T>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 2/45 | chr2 | 178803651 | |||||||
chr2:178803767 | T | C | 1 | a0006c0007t0005g0244 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.91+785A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 2/45 | chr2 | 178803767 | |||||||
chr2:178804123 | G | A | 47 | a0003c0004t0001g0004 a0003c0004t0001g0032 a0003c0004t0001g0033 others(44): Show |
61 | HG00438.hp1 HG00558.hp1 HG01192.hp2 others(58): Show |
intron_variant | MODIFIER | c.91+429C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 2/45 | chr2 | 178804123 | |||||||
chr2:178804445 | C | T | 1 | a0061c0097t0017g0203 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.91+107G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 2/45 | chr2 | 178804445 | |||||||
chr2:178804497 | T | C | 6 | a0009c0013t0006g0035 a0009c0013t0006g0296 a0009c0013t0006g0297 others(3): Show |
8 | HG02145.hp1 HG02723.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.91+55A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 2/45 | chr2 | 178804497 | |||||||
chr2:178804500 | CTGGAG | C | 33 | a0003c0004t0001g0004 a0003c0004t0001g0032 a0003c0004t0001g0033 others(30): Show |
43 | HG00438.hp1 HG00558.hp1 HG01192.hp2 others(40): Show |
intron_variant | MODIFIER | c.91+47_91+51delCTCC others(1): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 2/45 | chr2 | 178804500 | |||||||
chr2:178804851 | T | C | 1 | a0051c0078t0001g0247 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-13-196A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 1/45 | chr2 | 178804851 | |||||||
chr2:178805114 | G | A | 38 | a0003c0004t0001g0004 a0003c0004t0001g0032 a0003c0004t0001g0033 others(35): Show |
49 | HG00438.hp1 HG00558.hp1 HG01192.hp2 others(46): Show |
intron_variant | MODIFIER | c.-13-459C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 1/45 | chr2 | 178805114 | |||||||
chr2:178805204 | C | T | 87 | a0001c0003t0004g0018 a0002c0001t0001g0080 a0002c0001t0002g0001 others(84): Show |
107 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.-13-549G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 1/45 | chr2 | 178805204 | |||||||
chr2:178805343 | C | CA | 36 | a0001c0002t0001g0029 a0001c0002t0001g0228 a0001c0002t0001g0229 others(33): Show |
42 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.-13-689dupT | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 1/45 | chr2 | 178805343 | |||||||
chr2:178805343 | C | CAA | 9 | a0006c0007t0005g0030 a0006c0007t0005g0248 a0010c0010t0001g0011 others(6): Show |
12 | HG02040.hp2 HG02155.hp2 HG02293.hp1 others(9): Show |
intron_variant | MODIFIER | c.-13-690_-13-689dup others(2): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 1/45 | chr2 | 178805343 | |||||||
chr2:178805343 | C | CAAAAAA | 5 | a0009c0013t0006g0035 a0009c0013t0006g0296 a0009c0013t0006g0297 others(2): Show |
6 | HG02723.hp1 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13-694_-13-689dup others(6): Show |
TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 1/45 | chr2 | 178805343 | |||||||
chr2:178805343 | CA | C | 55 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0161 others(52): Show |
65 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.-13-689delT | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 1/45 | chr2 | 178805343 | |||||||
chr2:178805360 | A | T | 1 | a0068c0067t0001g0043 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-13-705T>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 1/45 | chr2 | 178805360 | |||||||
chr2:178805361 | A | T | 1 | a0016c0016t0001g0042 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-13-706T>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 1/45 | chr2 | 178805361 | |||||||
chr2:178805365 | T | A | 4 | a0012c0018t0005g0253 a0012c0018t0005g0254 a0012c0018t0005g0255 others(1): Show |
4 | HG00544.hp2 HG02015.hp2 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13-710A>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 1/45 | chr2 | 178805365 | |||||||
chr2:178805533 | C | T | 39 | a0002c0001t0012g0036 a0003c0004t0001g0004 a0003c0004t0001g0032 others(36): Show |
50 | HG00438.hp1 HG00558.hp1 HG01192.hp2 others(47): Show |
intron_variant | MODIFIER | c.-13-878G>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 1/45 | chr2 | 178805533 | |||||||
chr2:178805549 | G | A | 146 | a0001c0002t0001g0005 a0001c0002t0001g0028 a0001c0002t0001g0029 others(143): Show |
178 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.-13-894C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 1/45 | chr2 | 178805549 | |||||||
chr2:178805577 | C | A | 27 | a0003c0004t0001g0004 a0003c0004t0001g0032 a0003c0004t0001g0033 others(24): Show |
37 | HG00438.hp1 HG00558.hp1 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.-13-922G>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 1/45 | chr2 | 178805577 | |||||||
chr2:178805633 | G | A | 39 | a0002c0001t0012g0036 a0003c0004t0001g0004 a0003c0004t0001g0032 others(36): Show |
50 | HG00438.hp1 HG00558.hp1 HG01192.hp2 others(47): Show |
intron_variant | MODIFIER | c.-13-978C>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 1/45 | chr2 | 178805633 | |||||||
chr2:178805912 | A | G | 1 | a0057c0095t0009g0299 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-13-1257T>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 1/45 | chr2 | 178805912 | |||||||
chr2:178805956 | T | C | 20 | a0001c0003t0001g0290 a0001c0003t0001g0291 a0001c0003t0004g0002 others(17): Show |
30 | HG00408.hp2 HG00642.hp1 HG02027.hp2 others(27): Show |
intron_variant | MODIFIER | c.-14+1256A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 1/45 | chr2 | 178805956 | |||||||
chr2:178806070 | T | C | 1 | a0057c0095t0009g0299 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-14+1142A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 1/45 | chr2 | 178806070 | |||||||
chr2:178806101 | T | G | 5 | a0009c0013t0006g0035 a0009c0013t0006g0296 a0009c0013t0006g0297 others(2): Show |
6 | HG02723.hp1 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14+1111A>C | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 1/45 | chr2 | 178806101 | |||||||
chr2:178806596 | C | A | 1 | a0056c0036t0016g0300 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-14+616G>T | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 1/45 | chr2 | 178806596 | |||||||
chr2:178806635 | T | C | 1 | a0067c0060t0001g0301 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-14+577A>G | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 1/45 | chr2 | 178806635 | |||||||
chr2:178806901 | G | T | 1 | a0003c0004t0001g0041 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-14+311C>A | TTN | ENSG00000155657.29 | transcript | ENST00000360870.10 | protein_coding | 1/45 | chr2 | 178806901 |