Item | Value |
---|---|
geneid | 6900 |
ensemblid | ENSG00000184144.12 |
hgncid | 2172 |
symbol | CNTN2 |
name | contactin 2 |
refseq_nuc | NM_005076.5 |
refseq_prot | NP_005067.1 |
ensembl_nuc | ENST00000331830.7 |
ensembl_prot | ENSP00000330633.4 |
mane_status | MANE Select |
chr | chr1 |
start | 205043212 |
end | 205078289 |
strand | + |
ver | v1.2 |
region | chr1:205043212-205078289 |
region5000 | chr1:205038212-205083289 |
regionname0 | CNTN2_chr1_205043212_205078289 |
regionname5000 | CNTN2_chr1_205038212_205083289 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1040 | 153 | 68 | 34 | 26 | 8 | 15 | 20 | CNTN2_chr1_205038212_205083289 | CNTN2 | MGTAT others(1035): Show |
chr1 | 205038212 | 205083289 |
a0002 | 0/0 | 1040 | 106 | 6 | 19 | 67 | 4 | 10 | 54 | CNTN2_chr1_205038212_205083289 | CNTN2 | MGTAT others(1035): Show |
chr1 | 205038212 | 205083289 |
a0003 | 0/0 | 1040 | 80 | 3 | 15 | 55 | 0 | 7 | 43 | CNTN2_chr1_205038212_205083289 | CNTN2 | MGTAT others(1035): Show |
chr1 | 205038212 | 205083289 |
a0004 | 0/0 | 1040 | 18 | 5 | 2 | 3 | 2 | 6 | 2 | CNTN2_chr1_205038212_205083289 | CNTN2 | MGTAT others(1035): Show |
chr1 | 205038212 | 205083289 |
a0005 | 0/0 | 1040 | 10 | 9 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | MGTAT others(1035): Show |
chr1 | 205038212 | 205083289 |
a0006 | 0/0 | 1040 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | MGTAT others(1035): Show |
chr1 | 205038212 | 205083289 |
a0007 | 0/0 | 1040 | 2 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | MGTAT others(1035): Show |
chr1 | 205038212 | 205083289 |
a0008 | 0/0 | 1040 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | MGTAT others(1035): Show |
chr1 | 205038212 | 205083289 |
a0009 | 0/0 | 1040 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | MGTAT others(1035): Show |
chr1 | 205038212 | 205083289 |
a0010 | 0/0 | 1040 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | MGTAT others(1035): Show |
chr1 | 205038212 | 205083289 |
a0011 | 0/0 | 1040 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | MGTAT others(1035): Show |
chr1 | 205038212 | 205083289 |
a0012 | 0/0 | 1040 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | MGTAT others(1035): Show |
chr1 | 205038212 | 205083289 |
a0013 | 0/0 | 1040 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | MGTAT others(1035): Show |
chr1 | 205038212 | 205083289 |
a0014 | 0/0 | 1040 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | MGTAT others(1035): Show |
chr1 | 205038212 | 205083289 |
a0015 | 0/0 | 1040 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CNTN2_chr1_205038212_205083289 | CNTN2 | MGTAT others(1035): Show |
chr1 | 205038212 | 205083289 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 3120 | 119 | 56 | 28 | 16 | 6 | 11 | CNTN2_chr1_205038212_205083289 | CNTN2 | ATGGG others(3115): Show |
chr1 | 205038212 | 205083289 | ||
a0001c0004 | 0/0 | 3120 | 24 | 2 | 6 | 10 | 2 | 4 | CNTN2_chr1_205038212_205083289 | CNTN2 | ATGGG others(3115): Show |
chr1 | 205038212 | 205083289 | ||
a0001c0008 | 0/0 | 3120 | 7 | 7 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ATGGG others(3115): Show |
chr1 | 205038212 | 205083289 | ||
a0001c0012 | 0/0 | 3120 | 3 | 3 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ATGGG others(3115): Show |
chr1 | 205038212 | 205083289 | ||
a0002c0002 | 0/0 | 3120 | 93 | 6 | 17 | 58 | 4 | 8 | CNTN2_chr1_205038212_205083289 | CNTN2 | ATGGG others(3115): Show |
chr1 | 205038212 | 205083289 | ||
a0002c0006 | 0/0 | 3120 | 11 | 0 | 2 | 9 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ATGGG others(3115): Show |
chr1 | 205038212 | 205083289 | ||
a0002c0015 | 0/0 | 3120 | 2 | 0 | 0 | 0 | 0 | 2 | CNTN2_chr1_205038212_205083289 | CNTN2 | ATGGG others(3115): Show |
chr1 | 205038212 | 205083289 | ||
a0003c0003 | 0/0 | 3120 | 68 | 0 | 11 | 51 | 0 | 6 | CNTN2_chr1_205038212_205083289 | CNTN2 | ATGGG others(3115): Show |
chr1 | 205038212 | 205083289 | ||
a0003c0009 | 0/0 | 3120 | 4 | 0 | 0 | 4 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ATGGG others(3115): Show |
chr1 | 205038212 | 205083289 | ||
a0003c0010 | 0/0 | 3120 | 3 | 0 | 3 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ATGGG others(3115): Show |
chr1 | 205038212 | 205083289 | ||
a0003c0013 | 0/0 | 3120 | 3 | 2 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ATGGG others(3115): Show |
chr1 | 205038212 | 205083289 | ||
a0003c0016 | 0/0 | 3120 | 2 | 1 | 0 | 0 | 0 | 1 | CNTN2_chr1_205038212_205083289 | CNTN2 | ATGGG others(3115): Show |
chr1 | 205038212 | 205083289 | ||
a0004c0005 | 0/0 | 3120 | 17 | 5 | 2 | 3 | 2 | 5 | CNTN2_chr1_205038212_205083289 | CNTN2 | ATGGG others(3115): Show |
chr1 | 205038212 | 205083289 | ||
a0004c0019 | 0/0 | 3120 | 1 | 0 | 0 | 0 | 0 | 1 | CNTN2_chr1_205038212_205083289 | CNTN2 | ATGGG others(3115): Show |
chr1 | 205038212 | 205083289 | ||
a0005c0007 | 0/0 | 3120 | 10 | 9 | 0 | 0 | 1 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ATGGG others(3115): Show |
chr1 | 205038212 | 205083289 | ||
a0006c0011 | 0/0 | 3120 | 3 | 0 | 3 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ATGGG others(3115): Show |
chr1 | 205038212 | 205083289 | ||
a0007c0014 | 0/0 | 3120 | 2 | 1 | 0 | 0 | 1 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ATGGG others(3115): Show |
chr1 | 205038212 | 205083289 | ||
a0008c0021 | 0/0 | 3120 | 1 | 0 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ATGGG others(3115): Show |
chr1 | 205038212 | 205083289 | ||
a0009c0023 | 0/0 | 3120 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ATGGG others(3115): Show |
chr1 | 205038212 | 205083289 | ||
a0010c0018 | 0/0 | 3120 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ATGGG others(3115): Show |
chr1 | 205038212 | 205083289 | ||
a0011c0017 | 0/0 | 3120 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ATGGG others(3115): Show |
chr1 | 205038212 | 205083289 | ||
a0012c0020 | 0/0 | 3120 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ATGGG others(3115): Show |
chr1 | 205038212 | 205083289 | ||
a0013c0024 | 0/0 | 3120 | 1 | 0 | 0 | 0 | 0 | 1 | CNTN2_chr1_205038212_205083289 | CNTN2 | ATGGG others(3115): Show |
chr1 | 205038212 | 205083289 | ||
a0014c0025 | 0/0 | 3120 | 1 | 0 | 0 | 0 | 0 | 1 | CNTN2_chr1_205038212_205083289 | CNTN2 | ATGGG others(3115): Show |
chr1 | 205038212 | 205083289 | ||
a0015c0022 | 0/0 | 3120 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ATGGG others(3115): Show |
chr1 | 205038212 | 205083289 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/0 | 7916 | 3 | 2 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0001c0001t0003 | 0/1 | 7916 | 38 | 7 | 15 | 5 | 5 | 5 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0001c0001t0004 | 0/0 | 7916 | 39 | 25 | 5 | 9 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0001c0001t0007 | 1/0 | 7916 | 11 | 0 | 3 | 0 | 1 | 6 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0001c0001t0010 | 0/0 | 7916 | 7 | 7 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0001c0001t0011 | 0/0 | 7916 | 6 | 4 | 2 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0001c0001t0012 | 0/0 | 7916 | 5 | 5 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0001c0001t0018 | 0/0 | 7916 | 2 | 0 | 2 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0001c0001t0021 | 0/0 | 7916 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0001c0001t0022 | 0/0 | 7916 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0001c0001t0023 | 0/0 | 7916 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0001c0001t0024 | 0/0 | 7916 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0001c0001t0025 | 0/0 | 7916 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0001c0001t0028 | 0/0 | 7916 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0001c0001t0033 | 0/0 | 7916 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0001c0001t0034 | 0/0 | 7916 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0001c0004t0001 | 0/0 | 7916 | 11 | 0 | 5 | 2 | 2 | 2 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0001c0004t0005 | 0/0 | 7916 | 2 | 2 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0001c0004t0008 | 0/0 | 7916 | 8 | 0 | 1 | 5 | 0 | 2 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0001c0004t0019 | 0/0 | 7916 | 2 | 0 | 0 | 2 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0001c0004t0035 | 0/0 | 7916 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0001c0008t0005 | 0/0 | 7916 | 7 | 7 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0001c0012t0003 | 0/0 | 7916 | 3 | 3 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0002c0002t0002 | 0/0 | 7916 | 65 | 4 | 9 | 50 | 0 | 2 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0002c0002t0006 | 0/0 | 7916 | 16 | 1 | 7 | 0 | 4 | 4 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0002c0002t0017 | 0/0 | 7916 | 3 | 0 | 0 | 3 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0002c0002t0029 | 0/0 | 7916 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0002c0002t0030 | 0/0 | 7916 | 1 | 0 | 0 | 0 | 0 | 1 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0002c0002t0031 | 0/0 | 7916 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0002c0002t0032 | 0/0 | 7916 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0002c0002t0036 | 0/0 | 7916 | 1 | 0 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0002c0002t0037 | 0/0 | 7916 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0002c0002t0038 | 0/0 | 7916 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0002c0002t0039 | 0/0 | 7916 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0002c0002t0043 | 0/0 | 7916 | 1 | 0 | 0 | 0 | 0 | 1 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0002c0006t0001 | 0/0 | 7916 | 6 | 0 | 0 | 6 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0002c0006t0008 | 0/0 | 7916 | 2 | 0 | 0 | 2 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0002c0006t0016 | 0/0 | 7916 | 3 | 0 | 2 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0002c0015t0002 | 0/0 | 7916 | 2 | 0 | 0 | 0 | 0 | 2 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0003c0003t0001 | 0/0 | 7916 | 62 | 0 | 11 | 45 | 0 | 6 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0003c0003t0002 | 0/0 | 7916 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0003c0003t0020 | 0/0 | 7915 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7910): Show |
chr1 | 205038212 | 205083289 |
a0003c0003t0027 | 0/0 | 7916 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0003c0003t0040 | 0/0 | 7916 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0003c0003t0041 | 0/0 | 7916 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0003c0003t0042 | 0/0 | 7916 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0003c0009t0013 | 0/0 | 7915 | 4 | 0 | 0 | 4 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7910): Show |
chr1 | 205038212 | 205083289 |
a0003c0010t0002 | 0/0 | 7916 | 1 | 0 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0003c0010t0003 | 0/0 | 7916 | 2 | 0 | 2 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0003c0013t0014 | 0/0 | 7914 | 3 | 2 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7909): Show |
chr1 | 205038212 | 205083289 |
a0003c0016t0002 | 0/0 | 7916 | 1 | 0 | 0 | 0 | 0 | 1 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0003c0016t0004 | 0/0 | 7916 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0004c0005t0005 | 0/0 | 7916 | 14 | 5 | 2 | 2 | 1 | 4 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0004c0005t0044 | 0/0 | 7916 | 1 | 0 | 0 | 0 | 0 | 1 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0004c0005t0045 | 0/0 | 7916 | 1 | 0 | 0 | 0 | 1 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0004c0005t0046 | 0/0 | 7916 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0004c0019t0005 | 0/0 | 7916 | 1 | 0 | 0 | 0 | 0 | 1 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0005c0007t0009 | 0/0 | 7916 | 10 | 9 | 0 | 0 | 1 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0006c0011t0015 | 0/0 | 7913 | 3 | 0 | 3 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7908): Show |
chr1 | 205038212 | 205083289 |
a0007c0014t0005 | 0/0 | 7916 | 2 | 1 | 0 | 0 | 1 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0008c0021t0026 | 0/0 | 7916 | 1 | 0 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0009c0023t0007 | 0/0 | 7916 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0010c0018t0005 | 0/0 | 7916 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0011c0017t0005 | 0/0 | 7916 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0012c0020t0014 | 0/0 | 7914 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7909): Show |
chr1 | 205038212 | 205083289 |
a0013c0024t0005 | 0/0 | 7916 | 1 | 0 | 0 | 0 | 0 | 1 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0014c0025t0007 | 0/0 | 7916 | 1 | 0 | 0 | 0 | 0 | 1 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
a0015c0022t0008 | 0/0 | 7916 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | ACACA others(7911): Show |
chr1 | 205038212 | 205083289 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0003g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0003g0013 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0003g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0003g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0003g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0003g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0003g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0003g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0003g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0003g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0003g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0003g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0003g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0003g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0003g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0003g0285 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0003g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0003g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0004g0009 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0004g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0004g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0004g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0004g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0004g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0004g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0004g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0004g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0004g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0004g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0004g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0004g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0004g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0004g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0004g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0004g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0004g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0004g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0007g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0007g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0007g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0007g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0007g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0007g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0007g0226 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0007g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0007g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0007g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0010g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0010g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0010g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0010g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0010g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0010g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0011g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0011g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0011g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0011g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0011g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0012g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0012g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0012g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0012g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0018g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0018g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0021g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0022g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0023g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0024g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0025g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0028g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0033g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0001t0034g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0004t0001g0037 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0004t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0004t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0004t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0004t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0004t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0004t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0004t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0004t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0004t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0004t0005g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0004t0005g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0004t0008g0006 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0004t0008g0017 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0004t0008g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0004t0008g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0004t0019g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0004t0019g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0004t0035g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0008t0005g0003 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0008t0005g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0008t0005g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0012t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0012t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0001c0012t0003g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0004 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0019 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0006g0002 | 0/0 | 10 | 0 | 7 | 0 | 2 | 1 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0006g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0006g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0006g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0006g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0006g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0006g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0017g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0017g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0029g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0030g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0031g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0032g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0036g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0037g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0038g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0039g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0002t0043g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0006t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0006t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0006t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0006t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0006t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0006t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0006t0008g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0006t0008g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0006t0016g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0006t0016g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0006t0016g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0015t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0002c0015t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0003t0001g0001 | 0/0 | 15 | 0 | 6 | 9 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0003t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0003t0001g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0003t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0003t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0003t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0003t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0003t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0003t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0003t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0003t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0003t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0003t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0003t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0003t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0003t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0003t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0003t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0003t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0003t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0003t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0003t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0003t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0003t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0003t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0003t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0003t0020g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0003t0027g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0003t0040g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0003t0041g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0003t0042g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0009t0013g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0010t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0010t0003g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0010t0003g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0013t0014g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0013t0014g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0016t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0003c0016t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0004c0005t0005g0011 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0004c0005t0005g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0004c0005t0005g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0004c0005t0005g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0004c0005t0005g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0004c0005t0005g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0004c0005t0005g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0004c0005t0005g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0004c0005t0005g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0004c0005t0005g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0004c0005t0005g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0004c0005t0005g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0004c0005t0005g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0004c0005t0044g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0004c0005t0045g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0004c0005t0046g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0004c0019t0005g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0005c0007t0009g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0005c0007t0009g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0005c0007t0009g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0005c0007t0009g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0005c0007t0009g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0005c0007t0009g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0005c0007t0009g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0005c0007t0009g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0005c0007t0009g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0006c0011t0015g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0006c0011t0015g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0006c0011t0015g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0007c0014t0005g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0007c0014t0005g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0008c0021t0026g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0009c0023t0007g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0010c0018t0005g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0011c0017t0005g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0012c0020t0014g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0013c0024t0005g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0014c0025t0007g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
a0015c0022t0008g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0282 | EUR | GBR | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG00099 | hp2 | a0004 | c0005 | t0005 | g0011 | EUR | GBR | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG00140 | hp1 | a0001 | c0001 | t0007 | g0229 | EUR | GBR | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG00140 | hp2 | a0002 | c0002 | t0006 | g0212 | EUR | GBR | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG00280 | hp1 | a0001 | c0004 | t0001 | g0289 | EUR | FIN | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG00280 | hp2 | a0004 | c0005 | t0045 | g0011 | EUR | FIN | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG00323 | hp1 | a0001 | c0001 | t0003 | g0271 | EUR | FIN | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG00323 | hp2 | a0007 | c0014 | t0005 | g0291 | EUR | FIN | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG00408 | hp1 | a0003 | c0003 | t0001 | g0154 | EAS | CHS | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG00408 | hp2 | a0003 | c0003 | t0001 | g0117 | EAS | CHS | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG00544 | hp1 | a0001 | c0001 | t0022 | g0126 | EAS | CHS | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG00544 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | CHS | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG00558 | hp1 | a0001 | c0004 | t0008 | g0215 | EAS | CHS | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG00558 | hp2 | a0002 | c0002 | t0002 | g0018 | EAS | CHS | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG00597 | hp1 | a0003 | c0003 | t0001 | g0184 | EAS | CHS | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG00597 | hp2 | a0003 | c0003 | t0001 | g0043 | EAS | CHS | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG00609 | hp1 | a0003 | c0003 | t0001 | g0185 | EAS | CHS | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG00609 | hp2 | a0002 | c0002 | t0002 | g0140 | EAS | CHS | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG00621 | hp1 | a0002 | c0006 | t0001 | g0075 | EAS | CHS | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG00621 | hp2 | a0003 | c0003 | t0001 | g0113 | EAS | CHS | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG00639 | hp1 | a0001 | c0001 | t0007 | g0195 | AMR | PUR | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG00639 | hp2 | a0001 | c0001 | t0003 | g0284 | AMR | PUR | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0273 | AMR | PUR | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG00733 | hp2 | a0002 | c0002 | t0006 | g0002 | AMR | PUR | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG00735 | hp1 | a0006 | c0011 | t0015 | g0160 | AMR | PUR | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG00735 | hp2 | a0002 | c0002 | t0006 | g0002 | AMR | PUR | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG00738 | hp1 | a0002 | c0002 | t0002 | g0004 | AMR | PUR | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG00738 | hp2 | a0001 | c0004 | t0008 | g0017 | AMR | PUR | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG00741 | hp1 | a0001 | c0001 | t0007 | g0228 | AMR | PUR | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG00741 | hp2 | a0001 | c0001 | t0007 | g0210 | AMR | PUR | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01069 | hp1 | a0008 | c0021 | t0026 | g0262 | AMR | PUR | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01069 | hp2 | a0001 | c0001 | t0004 | g0014 | AMR | PUR | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01070 | hp1 | a0001 | c0004 | t0001 | g0281 | AMR | PUR | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01070 | hp2 | a0002 | c0002 | t0006 | g0002 | AMR | PUR | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01071 | hp1 | a0001 | c0001 | t0004 | g0014 | AMR | PUR | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01071 | hp2 | a0002 | c0002 | t0006 | g0002 | AMR | PUR | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01081 | hp1 | a0003 | c0003 | t0001 | g0001 | AMR | PUR | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01081 | hp2 | a0002 | c0002 | t0036 | g0089 | AMR | PUR | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0138 | AMR | PUR | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01106 | hp1 | a0001 | c0001 | t0003 | g0288 | AMR | PUR | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01106 | hp2 | a0002 | c0002 | t0006 | g0002 | AMR | PUR | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01109 | hp1 | a0001 | c0001 | t0011 | g0071 | AMR | PUR | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01109 | hp2 | a0001 | c0001 | t0011 | g0260 | AMR | PUR | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01167 | hp1 | a0006 | c0011 | t0015 | g0161 | AMR | PUR | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01167 | hp2 | a0002 | c0002 | t0006 | g0002 | AMR | PUR | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01168 | hp2 | a0003 | c0003 | t0001 | g0001 | AMR | PUR | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01169 | hp1 | a0006 | c0011 | t0015 | g0162 | AMR | PUR | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0276 | AMR | PUR | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01175 | hp1 | a0003 | c0003 | t0001 | g0078 | AMR | PUR | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01175 | hp2 | a0004 | c0005 | t0005 | g0144 | AMR | PUR | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01192 | hp1 | a0003 | c0013 | t0014 | g0129 | AMR | PUR | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01192 | hp2 | a0001 | c0001 | t0018 | g0263 | AMR | PUR | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01243 | hp1 | a0003 | c0010 | t0002 | g0180 | AMR | PUR | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01243 | hp2 | a0001 | c0001 | t0004 | g0009 | AMR | PUR | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01255 | hp1 | a0003 | c0003 | t0001 | g0001 | AMR | CLM | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01255 | hp2 | a0003 | c0010 | t0003 | g0175 | AMR | CLM | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0038 | AMR | CLM | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01256 | hp2 | a0001 | c0001 | t0003 | g0261 | AMR | CLM | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01257 | hp1 | a0002 | c0006 | t0016 | g0238 | AMR | CLM | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01257 | hp2 | a0002 | c0002 | t0006 | g0002 | AMR | CLM | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01258 | hp1 | a0002 | c0006 | t0016 | g0240 | AMR | CLM | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01258 | hp2 | a0001 | c0001 | t0003 | g0038 | AMR | CLM | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01261 | hp1 | a0003 | c0003 | t0001 | g0022 | AMR | CLM | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01261 | hp2 | a0004 | c0005 | t0005 | g0143 | AMR | CLM | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01346 | hp1 | a0001 | c0001 | t0003 | g0278 | AMR | CLM | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01346 | hp2 | a0003 | c0003 | t0001 | g0186 | AMR | CLM | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01358 | hp1 | a0002 | c0002 | t0002 | g0004 | AMR | CLM | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01358 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | CLM | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01433 | hp1 | a0001 | c0001 | t0018 | g0277 | AMR | CLM | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01433 | hp2 | a0003 | c0010 | t0003 | g0118 | AMR | CLM | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01496 | hp1 | a0001 | c0004 | t0001 | g0085 | AMR | CLM | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01496 | hp2 | a0001 | c0001 | t0004 | g0066 | AMR | CLM | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01515 | hp1 | a0005 | c0007 | t0009 | g0072 | EUR | IBS | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01515 | hp2 | a0002 | c0002 | t0006 | g0213 | EUR | IBS | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01517 | hp1 | a0002 | c0002 | t0006 | g0002 | EUR | IBS | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0274 | EUR | IBS | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01884 | hp1 | a0005 | c0007 | t0009 | g0149 | AFR | ACB | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01884 | hp2 | a0001 | c0001 | t0024 | g0151 | AFR | ACB | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01891 | hp1 | a0001 | c0012 | t0003 | g0194 | AFR | ACB | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01891 | hp2 | a0002 | c0002 | t0002 | g0059 | AFR | ACB | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01928 | hp1 | a0001 | c0001 | t0003 | g0051 | AMR | PEL | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01928 | hp2 | a0003 | c0003 | t0001 | g0181 | AMR | PEL | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01943 | hp1 | a0002 | c0002 | t0002 | g0019 | AMR | PEL | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01943 | hp2 | a0003 | c0003 | t0001 | g0178 | AMR | PEL | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01975 | hp1 | a0002 | c0002 | t0002 | g0103 | AMR | PEL | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01975 | hp2 | a0003 | c0003 | t0001 | g0001 | AMR | PEL | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01978 | hp1 | a0001 | c0004 | t0001 | g0084 | AMR | PEL | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01978 | hp2 | a0002 | c0002 | t0002 | g0076 | AMR | PEL | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01981 | hp1 | a0001 | c0004 | t0001 | g0208 | AMR | PEL | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01981 | hp2 | a0002 | c0002 | t0002 | g0235 | AMR | PEL | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01993 | hp1 | a0003 | c0003 | t0001 | g0001 | AMR | PEL | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01993 | hp2 | a0001 | c0001 | t0004 | g0106 | AMR | PEL | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02004 | hp1 | a0002 | c0002 | t0002 | g0104 | AMR | PEL | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02004 | hp2 | a0001 | c0001 | t0003 | g0190 | AMR | PEL | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02027 | hp1 | a0001 | c0001 | t0004 | g0133 | EAS | KHV | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02027 | hp2 | a0003 | c0003 | t0001 | g0010 | EAS | KHV | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02040 | hp1 | a0002 | c0002 | t0002 | g0054 | EAS | KHV | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02040 | hp2 | a0004 | c0005 | t0005 | g0011 | EAS | KHV | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02055 | hp1 | a0001 | c0012 | t0003 | g0047 | AFR | ACB | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02055 | hp2 | a0001 | c0001 | t0012 | g0026 | AFR | ACB | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02071 | hp1 | a0003 | c0003 | t0001 | g0119 | EAS | KHV | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02071 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | KHV | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02080 | hp1 | a0003 | c0003 | t0001 | g0022 | EAS | KHV | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02080 | hp2 | a0001 | c0004 | t0035 | g0216 | EAS | KHV | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02083 | hp1 | a0002 | c0006 | t0001 | g0098 | EAS | KHV | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02083 | hp2 | a0002 | c0002 | t0002 | g0188 | EAS | KHV | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02132 | hp1 | a0002 | c0002 | t0002 | g0058 | EAS | KHV | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02132 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | KHV | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02145 | hp1 | a0001 | c0001 | t0004 | g0033 | AFR | ACB | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02145 | hp2 | a0001 | c0001 | t0011 | g0081 | AFR | ACB | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02155 | hp1 | a0001 | c0004 | t0019 | g0130 | EAS | CDX | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02155 | hp2 | a0002 | c0002 | t0002 | g0099 | EAS | CDX | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02165 | hp1 | a0002 | c0002 | t0002 | g0259 | EAS | CDX | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02165 | hp2 | a0002 | c0002 | t0002 | g0234 | EAS | CDX | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02257 | hp1 | a0001 | c0001 | t0010 | g0267 | AFR | ACB | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02257 | hp2 | a0001 | c0001 | t0011 | g0016 | AFR | ACB | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02258 | hp1 | a0001 | c0001 | t0004 | g0077 | AFR | ACB | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02258 | hp2 | a0001 | c0001 | t0010 | g0068 | AFR | ACB | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02273 | hp1 | a0002 | c0002 | t0002 | g0236 | AMR | PEL | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02273 | hp2 | a0003 | c0003 | t0001 | g0001 | AMR | PEL | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02280 | hp1 | a0001 | c0001 | t0004 | g0107 | AFR | ACB | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0029 | AFR | ACB | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0283 | AMR | PEL | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02300 | hp2 | a0001 | c0004 | t0001 | g0037 | AMR | PEL | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02451 | hp1 | a0001 | c0001 | t0004 | g0080 | AFR | ACB | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02451 | hp2 | a0005 | c0007 | t0009 | g0148 | AFR | ACB | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02572 | hp1 | a0001 | c0001 | t0004 | g0298 | AFR | GWD | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02572 | hp2 | a0001 | c0008 | t0005 | g0003 | AFR | GWD | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02602 | hp1 | a0001 | c0001 | t0007 | g0137 | SAS | PJL | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02602 | hp2 | a0004 | c0019 | t0005 | g0232 | SAS | PJL | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02615 | hp1 | a0004 | c0005 | t0005 | g0245 | AFR | GWD | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02615 | hp2 | a0003 | c0016 | t0004 | g0201 | AFR | GWD | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02622 | hp1 | a0001 | c0008 | t0005 | g0003 | AFR | GWD | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02622 | hp2 | a0001 | c0001 | t0010 | g0015 | AFR | GWD | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02630 | hp1 | a0001 | c0001 | t0004 | g0033 | AFR | GWD | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0204 | AFR | GWD | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02647 | hp1 | a0010 | c0018 | t0005 | g0252 | AFR | GWD | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02647 | hp2 | a0001 | c0001 | t0011 | g0016 | AFR | GWD | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02717 | hp1 | a0001 | c0008 | t0005 | g0003 | AFR | GWD | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02717 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | GWD | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02723 | hp1 | a0001 | c0001 | t0004 | g0203 | AFR | GWD | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02723 | hp2 | a0001 | c0001 | t0004 | g0109 | AFR | GWD | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02735 | hp1 | a0001 | c0004 | t0008 | g0006 | SAS | PJL | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02735 | hp2 | a0001 | c0001 | t0007 | g0230 | SAS | PJL | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02738 | hp1 | a0002 | c0002 | t0030 | g0192 | SAS | PJL | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02738 | hp2 | a0001 | c0001 | t0003 | g0280 | SAS | PJL | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02809 | hp1 | a0001 | c0001 | t0033 | g0045 | AFR | GWD | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02809 | hp2 | a0001 | c0001 | t0004 | g0110 | AFR | GWD | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02818 | hp1 | a0001 | c0001 | t0012 | g0026 | AFR | GWD | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02818 | hp2 | a0011 | c0017 | t0005 | g0253 | AFR | GWD | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02895 | hp1 | a0001 | c0008 | t0005 | g0266 | AFR | GWD | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02895 | hp2 | a0003 | c0013 | t0014 | g0039 | AFR | GWD | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02896 | hp1 | a0001 | c0008 | t0005 | g0069 | AFR | GWD | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02896 | hp2 | a0001 | c0001 | t0010 | g0015 | AFR | GWD | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02897 | hp1 | a0001 | c0001 | t0010 | g0064 | AFR | GWD | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02897 | hp2 | a0003 | c0013 | t0014 | g0039 | AFR | GWD | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02922 | hp1 | a0005 | c0007 | t0009 | g0249 | AFR | ESN | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02922 | hp2 | a0001 | c0001 | t0012 | g0295 | AFR | ESN | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02965 | hp1 | a0001 | c0008 | t0005 | g0003 | AFR | ESN | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02965 | hp2 | a0001 | c0001 | t0004 | g0070 | AFR | ESN | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02970 | hp1 | a0001 | c0001 | t0004 | g0247 | AFR | ESN | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02970 | hp2 | a0005 | c0007 | t0009 | g0023 | AFR | ESN | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02976 | hp1 | a0004 | c0005 | t0005 | g0132 | AFR | ESN | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02976 | hp2 | a0002 | c0002 | t0032 | g0056 | AFR | ESN | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0013 | SAS | PJL | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG03017 | hp2 | a0002 | c0002 | t0043 | g0156 | SAS | PJL | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG03041 | hp1 | a0004 | c0005 | t0005 | g0302 | AFR | GWD | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG03041 | hp2 | a0002 | c0002 | t0002 | g0101 | AFR | GWD | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0248 | AFR | MSL | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG03098 | hp2 | a0001 | c0004 | t0005 | g0296 | AFR | MSL | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG03130 | hp1 | a0001 | c0001 | t0004 | g0205 | AFR | ESN | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG03130 | hp2 | a0001 | c0001 | t0004 | g0145 | AFR | ESN | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG03139 | hp1 | a0001 | c0001 | t0034 | g0301 | AFR | ESN | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG03139 | hp2 | a0005 | c0007 | t0009 | g0251 | AFR | ESN | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG03195 | hp1 | a0001 | c0001 | t0012 | g0193 | AFR | ESN | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG03195 | hp2 | a0004 | c0005 | t0005 | g0239 | AFR | ESN | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG03209 | hp1 | a0001 | c0001 | t0010 | g0046 | AFR | MSL | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG03209 | hp2 | a0001 | c0008 | t0005 | g0003 | AFR | MSL | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG03225 | hp1 | a0001 | c0001 | t0021 | g0294 | AFR | MSL | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG03225 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | MSL | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG03239 | hp1 | a0004 | c0005 | t0005 | g0237 | SAS | PJL | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG03239 | hp2 | a0001 | c0001 | t0007 | g0224 | SAS | PJL | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG03453 | hp1 | a0001 | c0001 | t0004 | g0146 | AFR | MSL | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG03453 | hp2 | a0012 | c0020 | t0014 | g0102 | AFR | MSL | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG03486 | hp1 | a0001 | c0001 | t0004 | g0246 | AFR | MSL | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG03486 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | MSL | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0013 | SAS | PJL | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG03491 | hp2 | a0002 | c0002 | t0002 | g0004 | SAS | PJL | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0013 | SAS | PJL | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG03492 | hp2 | a0003 | c0003 | t0001 | g0123 | SAS | PJL | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0029 | AFR | ESN | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG03516 | hp2 | a0001 | c0001 | t0004 | g0250 | AFR | ESN | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0299 | AFR | GWD | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG03540 | hp2 | a0005 | c0007 | t0009 | g0040 | AFR | GWD | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0153 | AFR | MSL | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG03579 | hp2 | a0001 | c0001 | t0010 | g0065 | AFR | MSL | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG03654 | hp1 | a0001 | c0004 | t0001 | g0279 | SAS | PJL | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG03654 | hp2 | a0004 | c0005 | t0005 | g0241 | SAS | PJL | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG03669 | hp1 | a0003 | c0003 | t0001 | g0073 | SAS | PJL | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG03669 | hp2 | a0002 | c0002 | t0006 | g0209 | SAS | PJL | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG03688 | hp1 | a0001 | c0001 | t0007 | g0139 | SAS | STU | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG03688 | hp2 | a0001 | c0004 | t0001 | g0265 | SAS | STU | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG03704 | hp1 | a0002 | c0002 | t0006 | g0214 | SAS | PJL | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG03704 | hp2 | a0001 | c0001 | t0007 | g0031 | SAS | PJL | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0300 | SAS | BEB | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG03831 | hp2 | a0002 | c0002 | t0006 | g0127 | SAS | BEB | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG03834 | hp1 | a0004 | c0005 | t0044 | g0233 | SAS | BEB | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG03834 | hp2 | a0003 | c0003 | t0001 | g0048 | SAS | BEB | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG03927 | hp1 | a0002 | c0002 | t0002 | g0050 | SAS | BEB | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG03927 | hp2 | a0001 | c0004 | t0008 | g0017 | SAS | BEB | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG04115 | hp1 | a0003 | c0016 | t0002 | g0243 | SAS | STU | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG04115 | hp2 | a0004 | c0005 | t0005 | g0242 | SAS | STU | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG04184 | hp1 | a0004 | c0005 | t0005 | g0142 | SAS | BEB | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG04184 | hp2 | a0003 | c0003 | t0001 | g0042 | SAS | BEB | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG04199 | hp1 | a0002 | c0015 | t0002 | g0115 | SAS | STU | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG04199 | hp2 | a0013 | c0024 | t0005 | g0141 | SAS | STU | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG04204 | hp1 | a0003 | c0003 | t0001 | g0136 | SAS | STU | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG04204 | hp2 | a0002 | c0015 | t0002 | g0114 | SAS | STU | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG04228 | hp1 | a0014 | c0025 | t0007 | g0225 | SAS | STU | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG04228 | hp2 | a0002 | c0002 | t0006 | g0002 | SAS | STU | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18522 | hp1 | a0001 | c0001 | t0004 | g0152 | AFR | YRI | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18522 | hp2 | a0002 | c0002 | t0002 | g0268 | AFR | YRI | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18612 | hp1 | a0003 | c0003 | t0042 | g0010 | EAS | CHB | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18612 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | CHB | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18747 | hp1 | a0003 | c0003 | t0001 | g0158 | EAS | CHB | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18747 | hp2 | a0002 | c0002 | t0002 | g0105 | EAS | CHB | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18906 | hp1 | a0001 | c0001 | t0004 | g0206 | AFR | YRI | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18906 | hp2 | a0001 | c0001 | t0004 | g0257 | AFR | YRI | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18941 | hp1 | a0002 | c0002 | t0002 | g0027 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18941 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18942 | hp1 | a0002 | c0002 | t0037 | g0191 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18942 | hp2 | a0003 | c0003 | t0001 | g0183 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18943 | hp1 | a0001 | c0004 | t0019 | g0218 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18943 | hp2 | a0002 | c0002 | t0002 | g0231 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18944 | hp1 | a0002 | c0002 | t0002 | g0086 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18944 | hp2 | a0003 | c0003 | t0001 | g0170 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18948 | hp1 | a0003 | c0009 | t0013 | g0005 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18948 | hp2 | a0004 | c0005 | t0005 | g0034 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18950 | hp1 | a0002 | c0002 | t0017 | g0021 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18950 | hp2 | a0003 | c0003 | t0002 | g0122 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18951 | hp1 | a0003 | c0003 | t0001 | g0121 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18951 | hp2 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18952 | hp1 | a0001 | c0001 | t0004 | g0030 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18952 | hp2 | a0002 | c0002 | t0002 | g0097 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18954 | hp1 | a0003 | c0003 | t0001 | g0157 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18954 | hp2 | a0001 | c0001 | t0004 | g0134 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18957 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18957 | hp2 | a0002 | c0002 | t0002 | g0032 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18959 | hp1 | a0002 | c0002 | t0017 | g0021 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18959 | hp2 | a0003 | c0003 | t0001 | g0111 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18961 | hp1 | a0003 | c0003 | t0001 | g0159 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18961 | hp2 | a0002 | c0002 | t0002 | g0256 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18962 | hp1 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18962 | hp2 | a0015 | c0022 | t0008 | g0219 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18963 | hp1 | a0002 | c0002 | t0002 | g0198 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18963 | hp2 | a0002 | c0002 | t0002 | g0200 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18964 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18964 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18966 | hp1 | a0002 | c0006 | t0008 | g0167 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18967 | hp1 | a0001 | c0001 | t0003 | g0292 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18967 | hp2 | a0002 | c0006 | t0016 | g0067 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18969 | hp1 | a0002 | c0002 | t0017 | g0100 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18969 | hp2 | a0003 | c0003 | t0001 | g0169 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18972 | hp1 | a0001 | c0001 | t0004 | g0220 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18972 | hp2 | a0002 | c0006 | t0001 | g0093 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18974 | hp1 | a0003 | c0003 | t0001 | g0024 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18974 | hp2 | a0002 | c0002 | t0031 | g0091 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18975 | hp1 | a0003 | c0003 | t0001 | g0189 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18975 | hp2 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18979 | hp1 | a0002 | c0002 | t0038 | g0128 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18979 | hp2 | a0003 | c0003 | t0001 | g0025 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18980 | hp1 | a0001 | c0004 | t0008 | g0131 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18980 | hp2 | a0002 | c0002 | t0002 | g0090 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18981 | hp1 | a0002 | c0006 | t0001 | g0088 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18981 | hp2 | a0002 | c0002 | t0002 | g0062 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18982 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18982 | hp2 | a0003 | c0003 | t0001 | g0176 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18983 | hp2 | a0002 | c0002 | t0002 | g0057 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18984 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18984 | hp2 | a0001 | c0001 | t0004 | g0223 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18988 | hp1 | a0003 | c0003 | t0001 | g0165 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18988 | hp2 | a0002 | c0002 | t0002 | g0258 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18990 | hp1 | a0001 | c0004 | t0001 | g0275 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18990 | hp2 | a0003 | c0003 | t0001 | g0166 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18992 | hp1 | a0002 | c0002 | t0002 | g0155 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18992 | hp2 | a0003 | c0003 | t0001 | g0112 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18993 | hp1 | a0002 | c0006 | t0001 | g0094 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18993 | hp2 | a0003 | c0003 | t0001 | g0010 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18994 | hp1 | a0002 | c0002 | t0002 | g0199 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18994 | hp2 | a0002 | c0006 | t0008 | g0187 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18995 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA18995 | hp2 | a0002 | c0002 | t0002 | g0027 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19000 | hp1 | a0003 | c0003 | t0001 | g0120 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19000 | hp2 | a0002 | c0002 | t0002 | g0087 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19002 | hp1 | a0003 | c0009 | t0013 | g0005 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19002 | hp2 | a0003 | c0003 | t0001 | g0164 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19003 | hp1 | a0002 | c0002 | t0002 | g0044 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19003 | hp2 | a0001 | c0004 | t0008 | g0006 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19005 | hp1 | a0003 | c0003 | t0041 | g0001 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19005 | hp2 | a0001 | c0001 | t0004 | g0030 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19007 | hp1 | a0001 | c0004 | t0008 | g0006 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19007 | hp2 | a0003 | c0009 | t0013 | g0005 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19009 | hp1 | a0002 | c0002 | t0002 | g0060 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19009 | hp2 | a0002 | c0002 | t0002 | g0061 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19011 | hp1 | a0001 | c0001 | t0025 | g0083 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19011 | hp2 | a0002 | c0002 | t0002 | g0053 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19012 | hp1 | a0002 | c0002 | t0002 | g0052 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19012 | hp2 | a0001 | c0004 | t0008 | g0006 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19030 | hp1 | a0001 | c0001 | t0003 | g0125 | AFR | LWK | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19030 | hp2 | a0001 | c0001 | t0004 | g0063 | AFR | LWK | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19043 | hp1 | a0001 | c0001 | t0012 | g0049 | AFR | LWK | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | LWK | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19054 | hp1 | a0003 | c0003 | t0001 | g0171 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19054 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19056 | hp1 | a0002 | c0002 | t0002 | g0124 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19056 | hp2 | a0003 | c0003 | t0001 | g0179 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19059 | hp1 | a0003 | c0003 | t0001 | g0024 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19059 | hp2 | a0002 | c0002 | t0002 | g0092 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19063 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19063 | hp2 | a0001 | c0004 | t0001 | g0217 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19064 | hp1 | a0002 | c0002 | t0039 | g0032 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19064 | hp2 | a0003 | c0003 | t0001 | g0174 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19065 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19065 | hp2 | a0001 | c0001 | t0004 | g0221 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19066 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19066 | hp2 | a0003 | c0009 | t0013 | g0005 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19068 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19068 | hp2 | a0002 | c0002 | t0029 | g0163 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19070 | hp1 | a0003 | c0003 | t0001 | g0255 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19070 | hp2 | a0002 | c0002 | t0002 | g0079 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19074 | hp1 | a0003 | c0003 | t0001 | g0182 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19074 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19076 | hp1 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19076 | hp2 | a0003 | c0003 | t0001 | g0025 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19079 | hp1 | a0001 | c0001 | t0004 | g0222 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19079 | hp2 | a0004 | c0005 | t0046 | g0034 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19080 | hp1 | a0003 | c0003 | t0020 | g0207 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19080 | hp2 | a0002 | c0002 | t0002 | g0096 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19082 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19082 | hp2 | a0002 | c0002 | t0002 | g0074 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19083 | hp1 | a0003 | c0003 | t0040 | g0172 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19083 | hp2 | a0001 | c0001 | t0004 | g0135 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19084 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19084 | hp2 | a0002 | c0002 | t0002 | g0197 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19085 | hp1 | a0002 | c0006 | t0001 | g0095 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19085 | hp2 | a0003 | c0003 | t0027 | g0254 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19088 | hp1 | a0002 | c0002 | t0002 | g0168 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19088 | hp2 | a0003 | c0003 | t0001 | g0173 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19091 | hp1 | a0003 | c0003 | t0001 | g0177 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19091 | hp2 | a0002 | c0002 | t0002 | g0196 | EAS | JPT | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19240 | hp1 | a0001 | c0001 | t0028 | g0202 | AFR | YRI | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA19240 | hp2 | a0001 | c0001 | t0011 | g0082 | AFR | YRI | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA20129 | hp1 | a0005 | c0007 | t0009 | g0041 | AFR | ASW | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA20129 | hp2 | a0004 | c0005 | t0005 | g0244 | AFR | ASW | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA20752 | hp1 | a0002 | c0002 | t0006 | g0002 | EUR | TSI | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA20752 | hp2 | a0001 | c0001 | t0003 | g0286 | EUR | TSI | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA20805 | hp1 | a0001 | c0004 | t0001 | g0037 | EUR | TSI | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA20805 | hp2 | a0001 | c0001 | t0003 | g0264 | EUR | TSI | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA20905 | hp1 | a0001 | c0001 | t0007 | g0031 | SAS | GIH | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA20905 | hp2 | a0003 | c0003 | t0001 | g0227 | SAS | GIH | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0270 | AMR | CLM | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG01123 | hp2 | a0002 | c0002 | t0002 | g0293 | AMR | CLM | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02109 | hp1 | a0001 | c0001 | t0004 | g0108 | AFR | ACB | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0287 | AFR | ACB | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02486 | hp1 | a0001 | c0001 | t0023 | g0272 | AFR | ACB | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG02486 | hp2 | a0009 | c0023 | t0007 | g0116 | AFR | ACB | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG03471 | hp1 | a0005 | c0007 | t0009 | g0023 | AFR | MSL | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG03471 | hp2 | a0001 | c0012 | t0003 | g0290 | AFR | MSL | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG06807 | hp1 | a0002 | c0002 | t0002 | g0055 | AFR | USA | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
HG06807 | hp2 | a0002 | c0002 | t0006 | g0211 | AFR | USA | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA20300 | hp1 | a0005 | c0007 | t0009 | g0147 | AFR | USA | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0269 | AFR | USA | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA21309 | hp1 | a0001 | c0004 | t0005 | g0297 | AFR | LWK | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
NA21309 | hp2 | a0007 | c0014 | t0005 | g0150 | AFR | LWK | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0285 | REF | REF | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
homoSapiens | grch38p0 | a0001 | c0001 | t0007 | g0226 | REF | REF | CNTN2_chr1_205038212_205083289 | CNTN2 | chr1 | 205038212 | 205083289 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:205058028 | G | A | 2 | a0010 a0011 |
2 | HG02647.hp1 HG02818.hp2 |
missense_variant | MODERATE | c.178G>A | p.Ala60Thr | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 3/23 | 447/7916 | 178/3123 | 60/1040 | chr1 | 205058028 | |||
chr1:205058058 | A | G | 1 | a0014 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.208A>G | p.Thr70Ala | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 3/23 | 477/7916 | 208/3123 | 70/1040 | chr1 | 205058058 | |||
chr1:205058609 | G | A | 5 | a0003 a0004 a0006 others(2): Show |
103 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(100): Show |
missense_variant | MODERATE | c.433G>A | p.Ala145Thr | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 5/23 | 702/7916 | 433/3123 | 145/1040 | chr1 | 205058609 | |||
chr1:205059101 | C | T | 1 | a0009 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.505C>T | p.Leu169Phe | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 6/23 | 774/7916 | 505/3123 | 169/1040 | chr1 | 205059101 | |||
chr1:205061988 | C | T | 7 | a0002 a0003 a0004 others(4): Show |
219 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(216): Show |
missense_variant | MODERATE | c.1097C>T | p.Pro366Leu | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 9/23 | 1366/7916 | 1097/3123 | 366/1040 | chr1 | 205061988 | |||
chr1:205062443 | C | T | 1 | a0013 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.1114C>T | p.Arg372Trp | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 10/23 | 1383/7916 | 1114/3123 | 372/1040 | chr1 | 205062443 | |||
chr1:205064390 | C | G | 2 | a0005 a0012 |
11 | HG01515.hp1 HG01884.hp1 HG02451.hp2 others(8): Show |
missense_variant | MODERATE | c.1309C>G | p.Leu437Val | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 11/23 | 1578/7916 | 1309/3123 | 437/1040 | chr1 | 205064390 | |||
chr1:205064642 | G | A | 1 | a0008 | 1 | HG01069.hp1 | missense_variant | MODERATE | c.1411G>A | p.Gly471Ser | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 12/23 | 1680/7916 | 1411/3123 | 471/1040 | chr1 | 205064642 | |||
chr1:205066599 | A | G | 1 | a0006 | 3 | HG00735.hp1 HG01167.hp1 HG01169.hp1 |
missense_variant&splice_region_variant | MODERATE | c.1975A>G | p.Asn659Asp | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 15/23 | 2244/7916 | 1975/3123 | 659/1040 | chr1 | 205066599 | |||
chr1:205067182 | T | C | 1 | a0015 | 1 | NA18962.hp2 | missense_variant | MODERATE | c.2057T>C | p.Ile686Thr | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 16/23 | 2326/7916 | 2057/3123 | 686/1040 | chr1 | 205067182 | |||
chr1:205073712 | G | A | 4 | a0004 a0007 a0011 others(1): Show |
22 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(19): Show |
missense_variant | MODERATE | c.3070G>A | p.Val1024Ile | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 3339/7916 | 3070/3123 | 1024/1040 | chr1 | 205073712 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:205058262 | C | T | 5 | a0003c0009 a0003c0013 a0003c0016 others(2): Show |
27 | HG00099.hp2 HG00280.hp2 HG01175.hp2 others(24): Show |
synonymous_variant | LOW | c.297C>T | p.Asn99Asn | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 4/23 | 566/7916 | 297/3123 | 99/1040 | chr1 | 205058262 | |||
chr1:205058662 | A | C | 3 | a0003c0016 a0004c0005 a0013c0024 |
20 | HG00099.hp2 HG00280.hp2 HG01175.hp2 others(17): Show |
splice_region_variant&synonymous_variant | LOW | c.486A>C | p.Pro162Pro | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 5/23 | 755/7916 | 486/3123 | 162/1040 | chr1 | 205058662 | |||
chr1:205064747 | C | A | 2 | a0010c0018 a0011c0017 |
2 | HG02647.hp1 HG02818.hp2 |
synonymous_variant | LOW | c.1516C>A | p.Arg506Arg | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 12/23 | 1785/7916 | 1516/3123 | 506/1040 | chr1 | 205064747 | |||
chr1:205066520 | C | T | 1 | a0001c0012 | 3 | HG01891.hp1 HG02055.hp1 HG03471.hp2 |
synonymous_variant | LOW | c.1896C>T | p.Phe632Phe | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 15/23 | 2165/7916 | 1896/3123 | 632/1040 | chr1 | 205066520 | |||
chr1:205072030 | C | T | 12 | a0001c0004 a0001c0008 a0002c0006 others(9): Show |
138 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(135): Show |
synonymous_variant | LOW | c.2628C>T | p.Ser876Ser | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 20/23 | 2897/7916 | 2628/3123 | 876/1040 | chr1 | 205072030 | |||
chr1:205073109 | C | T | 2 | a0003c0013 a0012c0020 |
4 | HG01192.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
synonymous_variant | LOW | c.2886C>T | p.His962His | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 22/23 | 3155/7916 | 2886/3123 | 962/1040 | chr1 | 205073109 | |||
chr1:205073145 | T | G | 1 | a0001c0008 | 7 | HG02572.hp2 HG02622.hp1 HG02717.hp1 others(4): Show |
synonymous_variant | LOW | c.2922T>G | p.Pro974Pro | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 22/23 | 3191/7916 | 2922/3123 | 974/1040 | chr1 | 205073145 | |||
chr1:205073187 | G | A | 1 | a0002c0015 | 2 | HG04199.hp1 HG04204.hp2 |
synonymous_variant | LOW | c.2964G>A | p.Gly988Gly | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 22/23 | 3233/7916 | 2964/3123 | 988/1040 | chr1 | 205073187 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:205053103 | CT | C | 2 | a0003c0003t0020 a0003c0009t0013 |
5 | NA18948.hp1 NA19002.hp1 NA19007.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-80delT | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 2/23 | 80 | INFO_REALIGN_3_PRIME | chr1 | 205053103 | |||||
chr1:205073790 | G | A | 2 | a0003c0013t0014 a0012c0020t0014 |
4 | HG01192.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*25G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 25 | chr1 | 205073790 | ||||||
chr1:205073800 | G | A | 2 | a0001c0001t0012 a0001c0001t0021 |
6 | HG02055.hp2 HG02818.hp1 HG02922.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*35G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 35 | chr1 | 205073800 | ||||||
chr1:205073811 | C | T | 14 | a0001c0004t0005 a0001c0008t0005 a0002c0002t0006 others(11): Show |
59 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*46C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 46 | chr1 | 205073811 | ||||||
chr1:205073976 | G | A | 1 | a0001c0001t0022 | 1 | HG00544.hp1 | 3_prime_UTR_variant | MODIFIER | c.*211G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 211 | chr1 | 205073976 | ||||||
chr1:205074054 | A | C | 1 | a0003c0009t0013 | 4 | NA18948.hp1 NA19002.hp1 NA19007.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*289A>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 289 | chr1 | 205074054 | ||||||
chr1:205074122 | G | C | 11 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0018 others(8): Show |
58 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*357G>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 357 | chr1 | 205074122 | ||||||
chr1:205074135 | G | A | 1 | a0001c0001t0023 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*370G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 370 | chr1 | 205074135 | ||||||
chr1:205074294 | G | A | 1 | a0003c0003t0027 | 1 | NA19085.hp2 | 3_prime_UTR_variant | MODIFIER | c.*529G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 529 | chr1 | 205074294 | ||||||
chr1:205074313 | T | C | 2 | a0001c0001t0028 a0005c0007t0009 |
11 | HG01515.hp1 HG01884.hp1 HG02451.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*548T>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 548 | chr1 | 205074313 | ||||||
chr1:205074444 | G | A | 1 | a0002c0002t0029 | 1 | NA19068.hp2 | 3_prime_UTR_variant | MODIFIER | c.*679G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 679 | chr1 | 205074444 | ||||||
chr1:205074560 | G | A | 2 | a0003c0013t0014 a0012c0020t0014 |
4 | HG01192.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*795G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 795 | chr1 | 205074560 | ||||||
chr1:205074578 | G | A | 1 | a0002c0002t0030 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*813G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 813 | chr1 | 205074578 | ||||||
chr1:205074603 | G | A | 1 | a0002c0002t0031 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*838G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 838 | chr1 | 205074603 | ||||||
chr1:205074683 | T | C | 1 | a0002c0002t0032 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*918T>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 918 | chr1 | 205074683 | ||||||
chr1:205074726 | C | A | 1 | a0001c0001t0033 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*961C>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 961 | chr1 | 205074726 | ||||||
chr1:205074731 | A | G | 1 | a0008c0021t0026 | 1 | HG01069.hp1 | 3_prime_UTR_variant | MODIFIER | c.*966A>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 966 | chr1 | 205074731 | ||||||
chr1:205075125 | G | A | 1 | a0001c0004t0019 | 2 | HG02155.hp1 NA18943.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1360G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 1360 | chr1 | 205075125 | ||||||
chr1:205075211 | A | G | 41 | a0001c0001t0002 a0001c0001t0018 a0001c0001t0028 others(38): Show |
235 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(232): Show |
3_prime_UTR_variant | MODIFIER | c.*1446A>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 1446 | chr1 | 205075211 | ||||||
chr1:205075226 | G | A | 58 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0011 others(55): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(308): Show |
3_prime_UTR_variant | MODIFIER | c.*1461G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 1461 | chr1 | 205075226 | ||||||
chr1:205075251 | G | A | 1 | a0001c0004t0035 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1486G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 1486 | chr1 | 205075251 | ||||||
chr1:205075288 | C | A | 65 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(62): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(363): Show |
3_prime_UTR_variant | MODIFIER | c.*1523C>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 1523 | chr1 | 205075288 | ||||||
chr1:205075374 | A | G | 14 | a0001c0001t0028 a0001c0004t0005 a0001c0008t0005 others(11): Show |
47 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*1609A>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 1609 | chr1 | 205075374 | ||||||
chr1:205075403 | T | A | 1 | a0004c0005t0044 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1638T>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 1638 | chr1 | 205075403 | ||||||
chr1:205075476 | C | T | 1 | a0001c0001t0010 | 7 | HG02257.hp1 HG02258.hp2 HG02622.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1711C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 1711 | chr1 | 205075476 | ||||||
chr1:205075629 | A | G | 13 | a0001c0001t0028 a0001c0004t0005 a0001c0008t0005 others(10): Show |
43 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*1864A>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 1864 | chr1 | 205075629 | ||||||
chr1:205075714 | T | C | 17 | a0001c0001t0002 a0002c0002t0002 a0002c0002t0006 others(14): Show |
101 | HG00140.hp2 HG00544.hp2 HG00558.hp2 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*1949T>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 1949 | chr1 | 205075714 | ||||||
chr1:205075738 | G | C | 58 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0011 others(55): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(308): Show |
3_prime_UTR_variant | MODIFIER | c.*1973G>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 1973 | chr1 | 205075738 | ||||||
chr1:205075740 | A | G | 1 | a0003c0003t0042 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1975A>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 1975 | chr1 | 205075740 | ||||||
chr1:205075741 | A | C | 1 | a0003c0003t0042 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1976A>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 1976 | chr1 | 205075741 | ||||||
chr1:205075798 | G | A | 1 | a0001c0001t0011 | 6 | HG01109.hp1 HG01109.hp2 HG02145.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2033G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 2033 | chr1 | 205075798 | ||||||
chr1:205075959 | G | A | 46 | a0001c0001t0002 a0001c0001t0018 a0001c0001t0028 others(43): Show |
251 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(248): Show |
3_prime_UTR_variant | MODIFIER | c.*2194G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 2194 | chr1 | 205075959 | ||||||
chr1:205076128 | G | C | 1 | a0002c0002t0036 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2363G>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 2363 | chr1 | 205076128 | ||||||
chr1:205076212 | G | A | 13 | a0001c0001t0028 a0001c0004t0005 a0001c0008t0005 others(10): Show |
43 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*2447G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 2447 | chr1 | 205076212 | ||||||
chr1:205076440 | T | C | 1 | a0001c0001t0024 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2675T>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 2675 | chr1 | 205076440 | ||||||
chr1:205076442 | G | C | 1 | a0004c0005t0045 | 1 | HG00280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2677G>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 2677 | chr1 | 205076442 | ||||||
chr1:205076455 | A | C | 1 | a0003c0009t0013 | 4 | NA18948.hp1 NA19002.hp1 NA19007.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2690A>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 2690 | chr1 | 205076455 | ||||||
chr1:205076478 | T | A | 1 | a0002c0002t0037 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2713T>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 2713 | chr1 | 205076478 | ||||||
chr1:205076894 | T | G | 1 | a0003c0003t0040 | 1 | NA19083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3129T>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 3129 | chr1 | 205076894 | ||||||
chr1:205077340 | T | G | 1 | a0003c0009t0013 | 4 | NA18948.hp1 NA19002.hp1 NA19007.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3575T>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 3575 | chr1 | 205077340 | ||||||
chr1:205077376 | T | C | 1 | a0003c0003t0041 | 1 | NA19005.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3611T>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 3611 | chr1 | 205077376 | ||||||
chr1:205077415 | T | C | 1 | a0002c0002t0017 | 3 | NA18950.hp1 NA18959.hp1 NA18969.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3650T>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 3650 | chr1 | 205077415 | ||||||
chr1:205077562 | TTC | T | 2 | a0003c0013t0014 a0012c0020t0014 |
4 | HG01192.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3799_*3800delCT | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 3799 | INFO_REALIGN_3_PRIME | chr1 | 205077562 | |||||
chr1:205077599 | C | A | 2 | a0001c0001t0010 a0001c0001t0034 |
8 | HG02257.hp1 HG02258.hp2 HG02622.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3834C>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 3834 | chr1 | 205077599 | ||||||
chr1:205077610 | C | T | 1 | a0002c0006t0016 | 3 | HG01257.hp1 HG01258.hp1 NA18967.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3845C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 3845 | chr1 | 205077610 | ||||||
chr1:205077696 | T | C | 1 | a0001c0001t0025 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3931T>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 3931 | chr1 | 205077696 | ||||||
chr1:205077766 | T | C | 17 | a0001c0001t0002 a0002c0002t0002 a0002c0002t0006 others(14): Show |
101 | HG00140.hp2 HG00544.hp2 HG00558.hp2 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*4001T>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 4001 | chr1 | 205077766 | ||||||
chr1:205077808 | G | A | 1 | a0002c0002t0038 | 1 | NA18979.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4043G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 4043 | chr1 | 205077808 | ||||||
chr1:205077911 | CCTA | C | 1 | a0006c0011t0015 | 3 | HG00735.hp1 HG01167.hp1 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4149_*4151delACT | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 4149 | INFO_REALIGN_3_PRIME | chr1 | 205077911 | |||||
chr1:205078014 | G | A | 2 | a0001c0001t0010 a0001c0001t0034 |
8 | HG02257.hp1 HG02258.hp2 HG02622.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4249G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 4249 | chr1 | 205078014 | ||||||
chr1:205078052 | C | T | 1 | a0004c0005t0046 | 1 | NA19079.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4287C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 4287 | chr1 | 205078052 | ||||||
chr1:205078137 | A | C | 1 | a0002c0002t0043 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4372A>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 4372 | chr1 | 205078137 | ||||||
chr1:205078193 | C | A | 1 | a0001c0001t0021 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4428C>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 4428 | chr1 | 205078193 | ||||||
chr1:205078217 | C | T | 1 | a0002c0002t0039 | 1 | NA19064.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4452C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 23/23 | 4452 | chr1 | 205078217 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:205043585 | T | G | 2 | a0005c0007t0009g0040 a0005c0007t0009g0041 |
2 | HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-87+191T>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205043585 | |||||||
chr1:205043609 | T | C | 80 | a0001c0001t0003g0051 a0001c0001t0004g0009 a0001c0001t0004g0014 others(77): Show |
95 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.-87+215T>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205043609 | |||||||
chr1:205043842 | G | C | 1 | a0001c0001t0004g0110 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-87+448G>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205043842 | |||||||
chr1:205043950 | G | T | 1 | a0004c0005t0005g0302 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-87+556G>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205043950 | |||||||
chr1:205043956 | G | T | 96 | a0001c0001t0002g0299 a0001c0001t0003g0012 a0001c0001t0003g0013 others(93): Show |
118 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.-87+562G>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205043956 | |||||||
chr1:205044092 | T | C | 3 | a0003c0003t0001g0111 a0003c0003t0001g0112 a0003c0003t0001g0113 |
3 | HG00621.hp2 NA18959.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.-87+698T>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205044092 | |||||||
chr1:205044414 | G | A | 2 | a0002c0015t0002g0114 a0002c0015t0002g0115 |
2 | HG04199.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-87+1020G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205044414 | |||||||
chr1:205044458 | T | TG | 60 | a0001c0001t0002g0138 a0001c0001t0003g0125 a0001c0001t0003g0261 others(57): Show |
62 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.-87+1075dupG | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 205044458 | ||||||
chr1:205044458 | TG | T | 14 | a0001c0001t0002g0299 a0001c0001t0003g0300 a0001c0001t0004g0009 others(11): Show |
19 | HG00544.hp2 HG01243.hp2 HG02071.hp2 others(16): Show |
intron_variant | MODIFIER | c.-87+1075delG | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 205044458 | ||||||
chr1:205044495 | G | A | 1 | a0009c0023t0007g0116 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-87+1101G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205044495 | |||||||
chr1:205044618 | C | T | 2 | a0004c0005t0005g0034 a0004c0005t0046g0034 |
2 | NA18948.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.-87+1224C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205044618 | |||||||
chr1:205044634 | T | C | 75 | a0001c0001t0003g0190 a0001c0001t0007g0195 a0001c0001t0012g0026 others(72): Show |
95 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.-87+1240T>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205044634 | |||||||
chr1:205044686 | C | T | 2 | a0004c0005t0005g0034 a0004c0005t0046g0034 |
2 | NA18948.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.-87+1292C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205044686 | |||||||
chr1:205044743 | G | A | 82 | a0001c0001t0003g0028 a0001c0001t0003g0029 a0001c0001t0003g0125 others(79): Show |
108 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.-87+1349G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205044743 | |||||||
chr1:205044792 | C | T | 4 | a0001c0008t0005g0069 a0001c0012t0003g0047 a0010c0018t0005g0252 others(1): Show |
4 | HG02055.hp1 HG02647.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-87+1398C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205044792 | |||||||
chr1:205045121 | G | A | 1 | a0003c0003t0001g0154 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-87+1727G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205045121 | |||||||
chr1:205045144 | C | G | 17 | a0001c0001t0002g0248 a0001c0001t0004g0033 a0001c0001t0004g0145 others(14): Show |
19 | HG01884.hp1 HG01884.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.-87+1750C>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205045144 | |||||||
chr1:205045151 | C | G | 17 | a0001c0001t0002g0248 a0001c0001t0004g0033 a0001c0001t0004g0145 others(14): Show |
19 | HG01884.hp1 HG01884.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.-87+1757C>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205045151 | |||||||
chr1:205045187 | T | G | 1 | a0001c0001t0003g0269 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-87+1793T>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205045187 | |||||||
chr1:205045293 | G | A | 1 | a0002c0002t0002g0155 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-87+1899G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205045293 | |||||||
chr1:205045397 | C | T | 14 | a0001c0001t0004g0077 a0001c0001t0004g0106 a0001c0001t0004g0107 others(11): Show |
15 | HG01993.hp2 HG02109.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.-87+2003C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205045397 | |||||||
chr1:205045411 | T | C | 241 | a0001c0001t0002g0248 a0001c0001t0002g0299 a0001c0001t0003g0012 others(238): Show |
307 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.-87+2017T>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205045411 | |||||||
chr1:205045488 | C | A | 85 | a0001c0001t0002g0248 a0001c0001t0003g0190 a0001c0001t0004g0033 others(82): Show |
112 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.-87+2094C>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205045488 | |||||||
chr1:205045528 | C | T | 1 | a0001c0001t0004g0110 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-87+2134C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205045528 | |||||||
chr1:205045653 | T | C | 1 | a0001c0001t0004g0203 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-87+2259T>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205045653 | |||||||
chr1:205045674 | A | G | 42 | a0002c0002t0002g0007 a0002c0002t0002g0027 a0002c0002t0002g0032 others(39): Show |
47 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.-87+2280A>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205045674 | |||||||
chr1:205045688 | G | A | 1 | a0002c0002t0043g0156 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-87+2294G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205045688 | |||||||
chr1:205045802 | T | C | 254 | a0001c0001t0002g0248 a0001c0001t0002g0299 a0001c0001t0003g0012 others(251): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.-87+2408T>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205045802 | |||||||
chr1:205045865 | T | A | 1 | a0001c0012t0003g0194 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-87+2471T>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205045865 | |||||||
chr1:205045961 | G | T | 1 | a0001c0001t0004g0110 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-87+2567G>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205045961 | |||||||
chr1:205046156 | T | C | 223 | a0001c0001t0002g0248 a0001c0001t0002g0299 a0001c0001t0003g0012 others(220): Show |
272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.-87+2762T>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205046156 | |||||||
chr1:205046300 | T | C | 25 | a0001c0001t0004g0009 a0001c0001t0004g0014 a0001c0001t0004g0030 others(22): Show |
31 | HG01069.hp2 HG01071.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.-87+2906T>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205046300 | |||||||
chr1:205046346 | G | T | 1 | a0001c0001t0003g0013 | 3 | HG03017.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-87+2952G>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205046346 | |||||||
chr1:205046571 | C | T | 220 | a0001c0001t0002g0248 a0001c0001t0002g0299 a0001c0001t0003g0012 others(217): Show |
269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.-87+3177C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205046571 | |||||||
chr1:205046589 | C | T | 49 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0028 others(46): Show |
59 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.-87+3195C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205046589 | |||||||
chr1:205046671 | A | T | 220 | a0001c0001t0002g0248 a0001c0001t0002g0299 a0001c0001t0003g0012 others(217): Show |
269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.-87+3277A>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205046671 | |||||||
chr1:205046696 | G | A | 103 | a0002c0002t0002g0007 a0002c0002t0002g0027 a0002c0002t0002g0032 others(100): Show |
126 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.-87+3302G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205046696 | |||||||
chr1:205046707 | C | T | 1 | a0001c0001t0003g0292 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-87+3313C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205046707 | |||||||
chr1:205046792 | C | T | 120 | a0001c0001t0002g0248 a0001c0001t0002g0299 a0001c0001t0003g0012 others(117): Show |
147 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.-87+3398C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205046792 | |||||||
chr1:205046890 | G | T | 10 | a0001c0001t0011g0260 a0001c0001t0034g0301 a0001c0004t0001g0217 others(7): Show |
13 | HG00558.hp1 HG01109.hp2 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.-87+3496G>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205046890 | |||||||
chr1:205046930 | C | T | 5 | a0001c0004t0005g0296 a0001c0004t0005g0297 a0001c0008t0005g0003 others(2): Show |
9 | HG02572.hp2 HG02622.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-87+3536C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205046930 | |||||||
chr1:205046962 | CAA | C | 2 | a0003c0003t0020g0207 a0003c0009t0013g0005 |
5 | NA18948.hp1 NA19002.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.-87+3570_-87+3571d others(4): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 205046962 | ||||||
chr1:205046965 | A | C | 2 | a0003c0003t0020g0207 a0003c0009t0013g0005 |
5 | NA18948.hp1 NA19002.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.-87+3571A>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205046965 | |||||||
chr1:205046966 | G | T | 2 | a0003c0003t0020g0207 a0003c0009t0013g0005 |
5 | NA18948.hp1 NA19002.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.-87+3572G>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205046966 | |||||||
chr1:205046991 | G | A | 3 | a0001c0001t0003g0051 a0001c0001t0003g0261 a0001c0001t0003g0269 |
3 | HG01256.hp2 HG01928.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-87+3597G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205046991 | |||||||
chr1:205046999 | C | T | 1 | a0002c0002t0002g0293 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-87+3605C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205046999 | |||||||
chr1:205047007 | A | G | 1 | a0004c0005t0005g0132 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-87+3613A>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205047007 | |||||||
chr1:205047088 | G | C | 1 | a0002c0002t0002g0231 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-87+3694G>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205047088 | |||||||
chr1:205047137 | C | CA | 2 | a0001c0001t0004g0009 a0001c0001t0004g0063 |
4 | HG01243.hp2 HG02717.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-87+3744dupA | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 205047137 | ||||||
chr1:205047234 | C | T | 1 | a0007c0014t0005g0291 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-87+3840C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205047234 | |||||||
chr1:205047298 | A | G | 12 | a0001c0001t0011g0260 a0001c0001t0034g0301 a0001c0004t0001g0217 others(9): Show |
18 | HG00558.hp1 HG01109.hp2 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.-87+3904A>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205047298 | |||||||
chr1:205047431 | G | A | 10 | a0001c0001t0011g0260 a0001c0001t0034g0301 a0001c0004t0001g0217 others(7): Show |
13 | HG00558.hp1 HG01109.hp2 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.-87+4037G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205047431 | |||||||
chr1:205047570 | A | C | 50 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0028 others(47): Show |
60 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.-87+4176A>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205047570 | |||||||
chr1:205047645 | G | A | 1 | a0003c0003t0001g0073 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-87+4251G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205047645 | |||||||
chr1:205047654 | G | C | 1 | a0001c0001t0004g0246 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-87+4260G>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205047654 | |||||||
chr1:205047750 | G | C | 3 | a0002c0002t0002g0086 a0002c0002t0002g0198 a0002c0002t0002g0256 |
3 | NA18944.hp1 NA18961.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.-87+4356G>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205047750 | |||||||
chr1:205047788 | A | C | 1 | a0002c0002t0002g0105 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-87+4394A>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205047788 | |||||||
chr1:205048046 | A | G | 5 | a0001c0001t0010g0015 a0001c0001t0010g0046 a0001c0001t0010g0064 others(2): Show |
6 | HG02258.hp2 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-87+4652A>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205048046 | |||||||
chr1:205048075 | A | G | 12 | a0001c0001t0011g0260 a0001c0001t0034g0301 a0001c0004t0001g0217 others(9): Show |
18 | HG00558.hp1 HG01109.hp2 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.-87+4681A>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205048075 | |||||||
chr1:205048211 | G | C | 1 | a0003c0003t0001g0157 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-87+4817G>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205048211 | |||||||
chr1:205048300 | C | T | 10 | a0001c0001t0011g0260 a0001c0001t0034g0301 a0001c0004t0001g0217 others(7): Show |
13 | HG00558.hp1 HG01109.hp2 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.-86-4800C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205048300 | |||||||
chr1:205048303 | G | A | 1 | a0001c0001t0003g0190 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-86-4797G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205048303 | |||||||
chr1:205048325 | TGTC | T | 3 | a0002c0002t0002g0076 a0002c0002t0002g0103 a0002c0002t0002g0104 |
3 | HG01975.hp1 HG01978.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.-86-4772_-86-4770d others(5): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 205048325 | ||||||
chr1:205048346 | T | C | 1 | a0003c0003t0001g0042 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-86-4754T>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205048346 | |||||||
chr1:205048360 | C | T | 10 | a0001c0001t0011g0260 a0001c0001t0034g0301 a0001c0004t0001g0217 others(7): Show |
13 | HG00558.hp1 HG01109.hp2 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.-86-4740C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205048360 | |||||||
chr1:205048411 | A | G | 10 | a0001c0001t0011g0260 a0001c0001t0034g0301 a0001c0004t0001g0217 others(7): Show |
13 | HG00558.hp1 HG01109.hp2 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.-86-4689A>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205048411 | |||||||
chr1:205048527 | C | A | 2 | a0003c0003t0020g0207 a0003c0009t0013g0005 |
5 | NA18948.hp1 NA19002.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.-86-4573C>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205048527 | |||||||
chr1:205048554 | C | T | 1 | a0003c0013t0014g0129 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-86-4546C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205048554 | |||||||
chr1:205048633 | A | G | 2 | a0003c0003t0020g0207 a0003c0009t0013g0005 |
5 | NA18948.hp1 NA19002.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.-86-4467A>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205048633 | |||||||
chr1:205048726 | T | C | 7 | a0001c0001t0003g0270 a0001c0001t0003g0271 a0001c0001t0003g0273 others(4): Show |
7 | HG00323.hp1 HG00323.hp2 HG00733.hp1 others(4): Show |
intron_variant | MODIFIER | c.-86-4374T>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205048726 | |||||||
chr1:205048737 | G | A | 3 | a0003c0003t0001g0117 a0003c0003t0020g0207 a0003c0009t0013g0005 |
6 | HG00408.hp2 NA18948.hp1 NA19002.hp1 others(3): Show |
intron_variant | MODIFIER | c.-86-4363G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205048737 | |||||||
chr1:205048740 | C | T | 2 | a0003c0003t0020g0207 a0003c0009t0013g0005 |
5 | NA18948.hp1 NA19002.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.-86-4360C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205048740 | |||||||
chr1:205048827 | G | A | 1 | a0003c0003t0001g0158 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-86-4273G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205048827 | |||||||
chr1:205048834 | G | A | 12 | a0001c0001t0011g0260 a0001c0001t0034g0301 a0001c0004t0001g0217 others(9): Show |
18 | HG00558.hp1 HG01109.hp2 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.-86-4266G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205048834 | |||||||
chr1:205048910 | C | CGT | 5 | a0001c0001t0003g0269 a0001c0001t0003g0270 a0001c0001t0004g0298 others(2): Show |
5 | HG01123.hp1 HG02145.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-86-4141_-86-4140d others(4): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 205048910 | ||||||
chr1:205048910 | C | CGTGT | 3 | a0001c0001t0004g0110 a0001c0001t0004g0203 a0001c0001t0007g0224 |
3 | HG02723.hp1 HG02809.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.-86-4143_-86-4140d others(6): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 205048910 | ||||||
chr1:205048910 | CGT | C | 52 | a0001c0001t0002g0248 a0001c0001t0003g0012 a0001c0001t0003g0013 others(49): Show |
59 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.-86-4141_-86-4140d others(4): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 205048910 | ||||||
chr1:205048910 | CGTGT | C | 38 | a0001c0001t0003g0038 a0001c0001t0003g0273 a0001c0001t0003g0274 others(35): Show |
53 | HG00140.hp2 HG00733.hp1 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.-86-4143_-86-4140d others(6): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 205048910 | ||||||
chr1:205048910 | CGTGTGT | C | 53 | a0001c0001t0003g0287 a0001c0001t0003g0288 a0001c0001t0012g0193 others(50): Show |
67 | HG00280.hp1 HG00558.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.-86-4145_-86-4140d others(8): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 205048910 | ||||||
chr1:205048910 | CGTGTGTG others(1): Show |
C | 26 | a0001c0001t0004g0014 a0001c0001t0004g0135 a0001c0001t0004g0222 others(23): Show |
33 | HG01069.hp2 HG01071.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.-86-4147_-86-4140d others(10): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 205048910 | ||||||
chr1:205048910 | CGTGTGTG others(3): Show |
C | 75 | a0001c0004t0005g0296 a0001c0004t0005g0297 a0002c0002t0002g0007 others(72): Show |
97 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.-86-4149_-86-4140d others(12): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 205048910 | ||||||
chr1:205048910 | CGTGTGTG others(5): Show |
C | 14 | a0001c0012t0003g0194 a0002c0002t0002g0155 a0003c0016t0004g0201 others(11): Show |
15 | HG00099.hp2 HG00280.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.-86-4151_-86-4140d others(14): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 205048910 | ||||||
chr1:205048910 | CGTGTGTG others(7): Show |
C | 1 | a0003c0003t0001g0123 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-86-4153_-86-4140d others(16): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 205048910 | ||||||
chr1:205048910 | CGTGTGTG others(9): Show |
C | 1 | a0001c0001t0002g0299 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-86-4155_-86-4140d others(18): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 205048910 | ||||||
chr1:205048949 | GTGTGTGT others(4): Show |
G | 1 | a0003c0003t0001g0159 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-86-4149_-86-4139d others(13): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 205048949 | ||||||
chr1:205049132 | C | T | 5 | a0001c0004t0005g0296 a0001c0004t0005g0297 a0001c0008t0005g0003 others(2): Show |
9 | HG02572.hp2 HG02622.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-86-3968C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205049132 | |||||||
chr1:205049133 | G | A | 112 | a0001c0001t0011g0260 a0001c0001t0034g0301 a0001c0004t0001g0217 others(109): Show |
138 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.-86-3967G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205049133 | |||||||
chr1:205049162 | C | T | 9 | a0002c0002t0002g0008 a0002c0002t0002g0044 a0002c0002t0002g0052 others(6): Show |
11 | NA18942.hp1 NA18962.hp1 NA18964.hp2 others(8): Show |
intron_variant | MODIFIER | c.-86-3938C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205049162 | |||||||
chr1:205049186 | A | G | 10 | a0001c0001t0011g0260 a0001c0001t0034g0301 a0001c0004t0001g0217 others(7): Show |
13 | HG00558.hp1 HG01109.hp2 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.-86-3914A>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205049186 | |||||||
chr1:205049280 | C | CAA | 14 | a0002c0002t0002g0027 a0002c0002t0002g0079 a0002c0002t0002g0124 others(11): Show |
15 | HG01257.hp1 HG01981.hp2 HG02165.hp2 others(12): Show |
intron_variant | MODIFIER | c.-86-3820_-86-3819i others(4): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205049280 | |||||||
chr1:205049280 | CGA | C | 44 | a0003c0003t0001g0001 a0003c0003t0001g0010 a0003c0003t0001g0022 others(41): Show |
61 | HG00408.hp1 HG00408.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.-86-3819_-86-3818d others(4): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205049280 | |||||||
chr1:205049280 | CGACA | C | 7 | a0002c0002t0002g0199 a0002c0002t0002g0200 a0003c0003t0001g0043 others(4): Show |
7 | HG00597.hp1 HG00597.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-86-3819_-86-3816d others(6): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205049280 | |||||||
chr1:205049280 | CGACACAC others(5): Show |
C | 1 | a0002c0002t0002g0259 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-86-3819_-86-3808d others(14): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205049280 | |||||||
chr1:205049280 | CGACACAC others(11): Show |
C | 10 | a0001c0001t0011g0260 a0001c0001t0034g0301 a0001c0004t0001g0217 others(7): Show |
13 | HG00558.hp1 HG01109.hp2 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.-86-3819_-86-3802d others(20): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205049280 | |||||||
chr1:205049281 | G | A | 30 | a0002c0002t0002g0007 a0002c0002t0002g0032 a0002c0002t0002g0140 others(27): Show |
34 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.-86-3819G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205049281 | |||||||
chr1:205049281 | G | C | 16 | a0002c0002t0002g0027 a0002c0002t0002g0079 a0002c0002t0002g0124 others(13): Show |
17 | HG01257.hp1 HG01981.hp2 HG02165.hp2 others(14): Show |
intron_variant | MODIFIER | c.-86-3819G>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205049281 | |||||||
chr1:205049281 | G | GAC | 36 | a0001c0001t0004g0080 a0001c0001t0007g0137 a0001c0001t0007g0229 others(33): Show |
39 | HG00140.hp1 HG00280.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.-86-3775_-86-3774d others(4): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 205049281 | ||||||
chr1:205049281 | G | GACAC | 15 | a0001c0001t0003g0028 a0001c0001t0003g0029 a0001c0001t0003g0190 others(12): Show |
19 | HG00738.hp1 HG01081.hp2 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.-86-3777_-86-3774d others(6): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 205049281 | ||||||
chr1:205049281 | G | GACACACA others(1): Show |
3 | a0001c0004t0001g0085 a0005c0007t0009g0040 a0005c0007t0009g0041 |
3 | HG01496.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-86-3781_-86-3774d others(10): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 205049281 | ||||||
chr1:205049281 | GAC | G | 44 | a0001c0001t0003g0012 a0001c0001t0003g0035 a0001c0001t0003g0036 others(41): Show |
60 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.-86-3775_-86-3774d others(4): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 205049281 | ||||||
chr1:205049281 | GACAC | G | 35 | a0001c0001t0003g0270 a0001c0001t0003g0287 a0001c0001t0004g0009 others(32): Show |
39 | HG01123.hp1 HG01243.hp2 HG01891.hp1 others(36): Show |
intron_variant | MODIFIER | c.-86-3777_-86-3774d others(6): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 205049281 | ||||||
chr1:205049281 | GACACAC | G | 15 | a0001c0001t0002g0299 a0001c0001t0003g0264 a0001c0001t0003g0278 others(12): Show |
16 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.-86-3779_-86-3774d others(8): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 205049281 | ||||||
chr1:205049281 | GACACACA others(3): Show |
G | 1 | a0001c0004t0005g0297 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-86-3783_-86-3774d others(12): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 205049281 | ||||||
chr1:205049281 | GACACACA others(5): Show |
G | 9 | a0001c0001t0010g0015 a0001c0001t0010g0046 a0001c0001t0010g0064 others(6): Show |
13 | HG02258.hp2 HG02572.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-86-3785_-86-3774d others(14): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 205049281 | ||||||
chr1:205049283 | C | A | 44 | a0003c0003t0001g0001 a0003c0003t0001g0010 a0003c0003t0001g0022 others(41): Show |
61 | HG00408.hp1 HG00408.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.-86-3817C>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205049283 | |||||||
chr1:205049285 | C | A | 7 | a0002c0002t0002g0199 a0002c0002t0002g0200 a0003c0003t0001g0043 others(4): Show |
7 | HG00597.hp1 HG00597.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-86-3815C>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205049285 | |||||||
chr1:205049287 | C | A | 1 | a0003c0003t0001g0185 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-86-3813C>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205049287 | |||||||
chr1:205049289 | C | A | 1 | a0011c0017t0005g0253 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-86-3811C>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205049289 | |||||||
chr1:205049293 | C | A | 1 | a0002c0002t0002g0259 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-86-3807C>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205049293 | |||||||
chr1:205049298 | A | C | 1 | a0001c0001t0025g0083 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-86-3802A>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205049298 | |||||||
chr1:205049299 | C | A | 10 | a0001c0001t0011g0260 a0001c0001t0034g0301 a0001c0004t0001g0217 others(7): Show |
13 | HG00558.hp1 HG01109.hp2 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.-86-3801C>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205049299 | |||||||
chr1:205049446 | A | AACAG | 113 | a0001c0001t0011g0260 a0001c0001t0034g0301 a0001c0004t0001g0217 others(110): Show |
142 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.-86-3652_-86-3649d others(6): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 205049446 | ||||||
chr1:205049492 | G | A | 4 | a0001c0001t0002g0299 a0001c0001t0021g0294 a0003c0013t0014g0039 others(1): Show |
5 | HG01192.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-86-3608G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205049492 | |||||||
chr1:205049494 | G | A | 51 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0028 others(48): Show |
62 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.-86-3606G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205049494 | |||||||
chr1:205049570 | T | C | 113 | a0001c0001t0011g0260 a0001c0001t0034g0301 a0001c0004t0001g0217 others(110): Show |
142 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.-86-3530T>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205049570 | |||||||
chr1:205049681 | C | T | 1 | a0001c0008t0005g0266 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-86-3419C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205049681 | |||||||
chr1:205049685 | C | T | 1 | a0003c0003t0001g0183 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-86-3415C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205049685 | |||||||
chr1:205049707 | A | G | 113 | a0001c0001t0011g0260 a0001c0001t0034g0301 a0001c0004t0001g0217 others(110): Show |
142 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.-86-3393A>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205049707 | |||||||
chr1:205049738 | T | C | 1 | a0002c0002t0002g0090 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-86-3362T>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205049738 | |||||||
chr1:205049773 | G | A | 1 | a0002c0002t0002g0293 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-86-3327G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205049773 | |||||||
chr1:205049969 | A | T | 2 | a0001c0001t0004g0014 a0001c0001t0033g0045 |
3 | HG01069.hp2 HG01071.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-86-3131A>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205049969 | |||||||
chr1:205049971 | C | T | 113 | a0001c0001t0011g0260 a0001c0001t0034g0301 a0001c0004t0001g0217 others(110): Show |
142 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.-86-3129C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205049971 | |||||||
chr1:205049989 | G | C | 1 | a0004c0005t0005g0244 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-86-3111G>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205049989 | |||||||
chr1:205050022 | CT | C | 111 | a0001c0001t0011g0260 a0001c0001t0034g0301 a0001c0004t0001g0217 others(108): Show |
137 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.-86-3077delT | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205050022 | |||||||
chr1:205050026 | G | C | 111 | a0001c0001t0011g0260 a0001c0001t0034g0301 a0001c0004t0001g0217 others(108): Show |
137 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.-86-3074G>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205050026 | |||||||
chr1:205050051 | T | C | 113 | a0001c0001t0011g0260 a0001c0001t0034g0301 a0001c0004t0001g0217 others(110): Show |
142 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.-86-3049T>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205050051 | |||||||
chr1:205050098 | C | A | 103 | a0002c0002t0002g0007 a0002c0002t0002g0027 a0002c0002t0002g0032 others(100): Show |
129 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.-86-3002C>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205050098 | |||||||
chr1:205050174 | G | A | 2 | a0003c0003t0020g0207 a0003c0009t0013g0005 |
5 | NA18948.hp1 NA19002.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.-86-2926G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205050174 | |||||||
chr1:205050252 | G | T | 103 | a0002c0002t0002g0007 a0002c0002t0002g0027 a0002c0002t0002g0032 others(100): Show |
129 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.-86-2848G>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205050252 | |||||||
chr1:205050276 | TGAGTGTG others(47): Show |
T | 1 | a0002c0002t0002g0050 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-86-2819_-86-2766d others(56): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 205050276 | ||||||
chr1:205050278 | A | AGT | 55 | a0001c0001t0007g0139 a0001c0001t0007g0210 a0001c0001t0007g0230 others(52): Show |
59 | HG00140.hp2 HG00280.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.-86-2784_-86-2783d others(4): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 205050278 | ||||||
chr1:205050278 | A | AGTGT | 34 | a0001c0001t0004g0066 a0001c0001t0007g0137 a0001c0001t0007g0224 others(31): Show |
43 | HG00408.hp1 HG00558.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.-86-2786_-86-2783d others(6): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 205050278 | ||||||
chr1:205050278 | A | AGTGTGT | 16 | a0001c0001t0002g0138 a0001c0004t0008g0017 a0002c0002t0002g0058 others(13): Show |
17 | HG00408.hp2 HG00738.hp2 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.-86-2788_-86-2783d others(8): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 205050278 | ||||||
chr1:205050278 | A | AGTGTGTG others(1): Show |
34 | a0001c0004t0008g0006 a0002c0002t0002g0101 a0002c0002t0006g0002 others(31): Show |
46 | HG00597.hp1 HG00597.hp2 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.-86-2790_-86-2783d others(10): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 205050278 | ||||||
chr1:205050278 | A | AGTGTGTG others(3): Show |
6 | a0002c0006t0008g0167 a0003c0003t0001g0111 a0003c0003t0001g0113 others(3): Show |
6 | HG00621.hp2 HG01928.hp2 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.-86-2792_-86-2783d others(12): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 205050278 | ||||||
chr1:205050278 | AGT | A | 37 | a0001c0001t0002g0248 a0001c0001t0002g0299 a0001c0001t0004g0033 others(34): Show |
40 | HG01884.hp1 HG01993.hp2 HG02109.hp1 others(37): Show |
intron_variant | MODIFIER | c.-86-2784_-86-2783d others(4): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 205050278 | ||||||
chr1:205050278 | AGTGT | A | 25 | a0001c0001t0003g0282 a0001c0001t0003g0288 a0001c0001t0004g0009 others(22): Show |
36 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.-86-2786_-86-2783d others(6): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 205050278 | ||||||
chr1:205050278 | AGTGTGT | A | 51 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0035 others(48): Show |
62 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.-86-2788_-86-2783d others(8): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 205050278 | ||||||
chr1:205050278 | AGTGTGTG others(1): Show |
A | 6 | a0001c0001t0003g0028 a0001c0001t0003g0029 a0001c0001t0003g0125 others(3): Show |
8 | HG01192.hp2 HG01884.hp2 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.-86-2790_-86-2783d others(10): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 205050278 | ||||||
chr1:205050321 | G | C | 1 | a0001c0001t0004g0110 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-86-2779G>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205050321 | |||||||
chr1:205050360 | A | C | 113 | a0001c0001t0011g0260 a0001c0001t0034g0301 a0001c0004t0001g0217 others(110): Show |
142 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.-86-2740A>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205050360 | |||||||
chr1:205050363 | G | A | 1 | a0002c0002t0002g0293 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-86-2737G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205050363 | |||||||
chr1:205050386 | G | C | 2 | a0003c0003t0020g0207 a0003c0009t0013g0005 |
5 | NA18948.hp1 NA19002.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.-86-2714G>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205050386 | |||||||
chr1:205050431 | T | G | 113 | a0001c0001t0011g0260 a0001c0001t0034g0301 a0001c0004t0001g0217 others(110): Show |
142 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.-86-2669T>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205050431 | |||||||
chr1:205050443 | G | A | 101 | a0002c0002t0002g0007 a0002c0002t0002g0027 a0002c0002t0002g0032 others(98): Show |
124 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.-86-2657G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205050443 | |||||||
chr1:205050556 | G | A | 1 | a0005c0007t0009g0249 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-86-2544G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205050556 | |||||||
chr1:205050626 | A | AT | 174 | a0001c0001t0002g0248 a0001c0001t0002g0299 a0001c0001t0004g0009 others(171): Show |
212 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.-86-2465dupT | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 205050626 | ||||||
chr1:205050626 | A | ATT | 5 | a0001c0008t0005g0003 a0001c0008t0005g0069 a0001c0008t0005g0266 others(2): Show |
9 | HG02572.hp2 HG02615.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-86-2466_-86-2465d others(4): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr1 | 205050626 | ||||||
chr1:205050676 | T | C | 1 | a0003c0003t0001g0169 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-86-2424T>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205050676 | |||||||
chr1:205050777 | C | T | 2 | a0010c0018t0005g0252 a0011c0017t0005g0253 |
2 | HG02647.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-86-2323C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205050777 | |||||||
chr1:205050782 | C | A | 5 | a0001c0004t0005g0296 a0001c0004t0005g0297 a0001c0008t0005g0003 others(2): Show |
9 | HG02572.hp2 HG02622.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-86-2318C>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205050782 | |||||||
chr1:205050855 | G | A | 101 | a0002c0002t0002g0007 a0002c0002t0002g0027 a0002c0002t0002g0032 others(98): Show |
124 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.-86-2245G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205050855 | |||||||
chr1:205050915 | G | A | 7 | a0005c0007t0009g0023 a0005c0007t0009g0072 a0005c0007t0009g0147 others(4): Show |
8 | HG01515.hp1 HG01884.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-86-2185G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205050915 | |||||||
chr1:205050932 | G | T | 113 | a0001c0001t0011g0260 a0001c0001t0034g0301 a0001c0004t0001g0217 others(110): Show |
142 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.-86-2168G>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205050932 | |||||||
chr1:205050936 | G | T | 5 | a0002c0002t0002g0198 a0003c0003t0001g0166 a0003c0003t0001g0182 others(2): Show |
5 | NA18950.hp2 NA18963.hp1 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.-86-2164G>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205050936 | |||||||
chr1:205050968 | A | T | 111 | a0001c0001t0011g0260 a0001c0001t0034g0301 a0001c0004t0001g0217 others(108): Show |
137 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.-86-2132A>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205050968 | |||||||
chr1:205050997 | T | C | 113 | a0001c0001t0011g0260 a0001c0001t0034g0301 a0001c0004t0001g0217 others(110): Show |
142 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.-86-2103T>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205050997 | |||||||
chr1:205051109 | G | A | 2 | a0003c0003t0020g0207 a0003c0009t0013g0005 |
5 | NA18948.hp1 NA19002.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.-86-1991G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205051109 | |||||||
chr1:205051129 | C | G | 2 | a0002c0002t0017g0021 a0002c0002t0017g0100 |
3 | NA18950.hp1 NA18959.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.-86-1971C>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205051129 | |||||||
chr1:205051165 | T | C | 1 | a0002c0002t0002g0058 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-86-1935T>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205051165 | |||||||
chr1:205051314 | A | G | 1 | a0001c0001t0003g0284 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-86-1786A>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205051314 | |||||||
chr1:205051323 | G | A | 113 | a0001c0001t0011g0260 a0001c0001t0034g0301 a0001c0004t0001g0217 others(110): Show |
142 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.-86-1777G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205051323 | |||||||
chr1:205051438 | G | A | 113 | a0001c0001t0011g0260 a0001c0001t0034g0301 a0001c0004t0001g0217 others(110): Show |
142 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.-86-1662G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205051438 | |||||||
chr1:205051448 | G | A | 2 | a0003c0003t0020g0207 a0003c0009t0013g0005 |
5 | NA18948.hp1 NA19002.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.-86-1652G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205051448 | |||||||
chr1:205051486 | G | A | 2 | a0003c0003t0020g0207 a0003c0009t0013g0005 |
5 | NA18948.hp1 NA19002.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.-86-1614G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205051486 | |||||||
chr1:205051509 | G | C | 1 | a0001c0001t0010g0068 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-86-1591G>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205051509 | |||||||
chr1:205051560 | C | G | 179 | a0001c0001t0002g0248 a0001c0001t0002g0299 a0001c0001t0004g0009 others(176): Show |
221 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.-86-1540C>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205051560 | |||||||
chr1:205051575 | G | A | 10 | a0001c0001t0011g0260 a0001c0001t0034g0301 a0001c0004t0001g0217 others(7): Show |
13 | HG00558.hp1 HG01109.hp2 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.-86-1525G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205051575 | |||||||
chr1:205051650 | G | A | 113 | a0001c0001t0011g0260 a0001c0001t0034g0301 a0001c0004t0001g0217 others(110): Show |
142 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.-86-1450G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205051650 | |||||||
chr1:205051677 | G | A | 179 | a0001c0001t0002g0248 a0001c0001t0002g0299 a0001c0001t0004g0009 others(176): Show |
221 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.-86-1423G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205051677 | |||||||
chr1:205051769 | T | G | 66 | a0001c0001t0002g0248 a0001c0001t0002g0299 a0001c0001t0004g0009 others(63): Show |
79 | HG01069.hp2 HG01071.hp1 HG01109.hp1 others(76): Show |
intron_variant | MODIFIER | c.-86-1331T>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205051769 | |||||||
chr1:205051809 | T | G | 2 | a0003c0003t0020g0207 a0003c0009t0013g0005 |
5 | NA18948.hp1 NA19002.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.-86-1291T>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205051809 | |||||||
chr1:205051882 | G | C | 2 | a0002c0002t0002g0092 a0002c0002t0031g0091 |
2 | NA18974.hp2 NA19059.hp2 |
intron_variant | MODIFIER | c.-86-1218G>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205051882 | |||||||
chr1:205052020 | G | A | 2 | a0003c0003t0001g0111 a0003c0003t0001g0112 |
2 | NA18959.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.-86-1080G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205052020 | |||||||
chr1:205052151 | G | A | 113 | a0001c0001t0011g0260 a0001c0001t0034g0301 a0001c0004t0001g0217 others(110): Show |
142 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.-86-949G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205052151 | |||||||
chr1:205052326 | C | T | 113 | a0001c0001t0011g0260 a0001c0001t0034g0301 a0001c0004t0001g0217 others(110): Show |
142 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.-86-774C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205052326 | |||||||
chr1:205052353 | A | G | 113 | a0001c0001t0011g0260 a0001c0001t0034g0301 a0001c0004t0001g0217 others(110): Show |
142 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.-86-747A>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205052353 | |||||||
chr1:205052541 | A | G | 67 | a0001c0001t0002g0248 a0001c0001t0002g0299 a0001c0001t0004g0009 others(64): Show |
80 | HG01069.hp2 HG01071.hp1 HG01109.hp1 others(77): Show |
intron_variant | MODIFIER | c.-86-559A>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205052541 | |||||||
chr1:205052741 | A | G | 2 | a0003c0003t0020g0207 a0003c0009t0013g0005 |
5 | NA18948.hp1 NA19002.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.-86-359A>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205052741 | |||||||
chr1:205052821 | G | A | 1 | a0007c0014t0005g0291 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-86-279G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205052821 | |||||||
chr1:205052827 | A | G | 2 | a0003c0003t0001g0111 a0003c0003t0001g0112 |
2 | NA18959.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.-86-273A>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205052827 | |||||||
chr1:205052838 | G | A | 3 | a0001c0001t0003g0028 a0001c0001t0003g0125 a0001c0001t0003g0190 |
4 | HG02004.hp2 HG03486.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.-86-262G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205052838 | |||||||
chr1:205052876 | A | C | 1 | a0001c0001t0003g0283 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-86-224A>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205052876 | |||||||
chr1:205052948 | A | T | 1 | a0003c0013t0014g0039 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-86-152A>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205052948 | |||||||
chr1:205052966 | C | T | 44 | a0002c0002t0002g0007 a0002c0002t0002g0027 a0002c0002t0002g0032 others(41): Show |
49 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.-86-134C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205052966 | |||||||
chr1:205053063 | C | G | 46 | a0002c0002t0002g0007 a0002c0002t0002g0027 a0002c0002t0002g0032 others(43): Show |
51 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.-86-37C>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205053063 | |||||||
chr1:205053079 | C | G | 61 | a0001c0001t0002g0248 a0001c0001t0004g0009 a0001c0001t0004g0014 others(58): Show |
70 | HG01069.hp2 HG01071.hp1 HG01109.hp1 others(67): Show |
intron_variant | MODIFIER | c.-86-21C>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 1/22 | chr1 | 205053079 | |||||||
chr1:205053657 | C | A | 1 | a0012c0020t0014g0102 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.70+402C>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 2/22 | chr1 | 205053657 | |||||||
chr1:205053663 | T | C | 1 | a0001c0001t0004g0204 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.70+408T>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 2/22 | chr1 | 205053663 | |||||||
chr1:205053679 | C | T | 2 | a0003c0003t0020g0207 a0003c0009t0013g0005 |
5 | NA18948.hp1 NA19002.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.70+424C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 2/22 | chr1 | 205053679 | |||||||
chr1:205053786 | G | A | 2 | a0003c0003t0020g0207 a0003c0009t0013g0005 |
5 | NA18948.hp1 NA19002.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.70+531G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 2/22 | chr1 | 205053786 | |||||||
chr1:205053849 | A | G | 172 | a0001c0001t0007g0210 a0001c0001t0011g0260 a0001c0001t0034g0301 others(169): Show |
220 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.70+594A>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 2/22 | chr1 | 205053849 | |||||||
chr1:205053886 | G | A | 173 | a0001c0001t0002g0248 a0001c0001t0002g0299 a0001c0001t0003g0012 others(170): Show |
205 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.70+631G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 2/22 | chr1 | 205053886 | |||||||
chr1:205053893 | C | T | 3 | a0002c0002t0002g0055 a0002c0002t0002g0059 a0002c0002t0032g0056 |
3 | HG01891.hp2 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.70+638C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 2/22 | chr1 | 205053893 | |||||||
chr1:205053895 | G | C | 2 | a0003c0003t0020g0207 a0003c0009t0013g0005 |
5 | NA18948.hp1 NA19002.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.70+640G>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 2/22 | chr1 | 205053895 | |||||||
chr1:205053900 | TCTC | T | 61 | a0001c0001t0007g0210 a0001c0004t0008g0017 a0002c0002t0002g0004 others(58): Show |
80 | HG00140.hp2 HG00558.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.70+650_70+652delTC others(1): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr1 | 205053900 | ||||||
chr1:205054034 | C | T | 1 | a0002c0006t0016g0067 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.70+779C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 2/22 | chr1 | 205054034 | |||||||
chr1:205054035 | G | A | 1 | a0002c0002t0002g0074 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.70+780G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 2/22 | chr1 | 205054035 | |||||||
chr1:205054188 | T | C | 128 | a0001c0001t0007g0210 a0001c0001t0011g0260 a0001c0001t0034g0301 others(125): Show |
171 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.70+933T>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 2/22 | chr1 | 205054188 | |||||||
chr1:205054221 | C | T | 48 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0028 others(45): Show |
58 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.70+966C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 2/22 | chr1 | 205054221 | |||||||
chr1:205054256 | G | A | 2 | a0003c0003t0020g0207 a0003c0009t0013g0005 |
5 | NA18948.hp1 NA19002.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.70+1001G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 2/22 | chr1 | 205054256 | |||||||
chr1:205054330 | C | G | 2 | a0003c0013t0014g0039 a0003c0013t0014g0129 |
3 | HG01192.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.70+1075C>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 2/22 | chr1 | 205054330 | |||||||
chr1:205054416 | C | A | 1 | a0005c0007t0009g0072 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.70+1161C>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 2/22 | chr1 | 205054416 | |||||||
chr1:205054590 | G | C | 1 | a0004c0005t0005g0244 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.70+1335G>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 2/22 | chr1 | 205054590 | |||||||
chr1:205054636 | T | C | 299 | a0001c0001t0002g0138 a0001c0001t0002g0248 a0001c0001t0002g0299 others(296): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(368): Show |
intron_variant | MODIFIER | c.70+1381T>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 2/22 | chr1 | 205054636 | |||||||
chr1:205054884 | C | T | 289 | a0001c0001t0002g0248 a0001c0001t0002g0299 a0001c0001t0003g0012 others(286): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(357): Show |
intron_variant | MODIFIER | c.70+1629C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 2/22 | chr1 | 205054884 | |||||||
chr1:205055038 | G | A | 2 | a0003c0013t0014g0039 a0003c0013t0014g0129 |
3 | HG01192.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.70+1783G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 2/22 | chr1 | 205055038 | |||||||
chr1:205055045 | A | G | 2 | a0003c0013t0014g0039 a0003c0013t0014g0129 |
3 | HG01192.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.70+1790A>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 2/22 | chr1 | 205055045 | |||||||
chr1:205055174 | C | T | 44 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0028 others(41): Show |
54 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.70+1919C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 2/22 | chr1 | 205055174 | |||||||
chr1:205055301 | G | A | 1 | a0001c0001t0003g0284 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.70+2046G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 2/22 | chr1 | 205055301 | |||||||
chr1:205055445 | C | T | 189 | a0001c0001t0002g0248 a0001c0001t0002g0299 a0001c0001t0004g0009 others(186): Show |
233 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.70+2190C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 2/22 | chr1 | 205055445 | |||||||
chr1:205055671 | G | C | 2 | a0003c0003t0020g0207 a0003c0009t0013g0005 |
5 | NA18948.hp1 NA19002.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.71-2250G>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 2/22 | chr1 | 205055671 | |||||||
chr1:205055729 | C | T | 88 | a0001c0001t0002g0248 a0001c0001t0002g0299 a0001c0001t0003g0012 others(85): Show |
104 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.71-2192C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 2/22 | chr1 | 205055729 | |||||||
chr1:205055739 | C | T | 1 | a0002c0002t0002g0086 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.71-2182C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 2/22 | chr1 | 205055739 | |||||||
chr1:205055884 | G | A | 1 | a0004c0005t0005g0237 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.71-2037G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 2/22 | chr1 | 205055884 | |||||||
chr1:205056078 | G | A | 1 | a0002c0002t0002g0076 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.71-1843G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 2/22 | chr1 | 205056078 | |||||||
chr1:205056111 | T | C | 1 | a0004c0005t0005g0237 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.71-1810T>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 2/22 | chr1 | 205056111 | |||||||
chr1:205056146 | G | C | 56 | a0003c0003t0001g0001 a0003c0003t0001g0010 a0003c0003t0001g0022 others(53): Show |
74 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.71-1775G>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 2/22 | chr1 | 205056146 | |||||||
chr1:205056159 | G | T | 2 | a0003c0003t0001g0136 a0003c0003t0001g0227 |
2 | HG04204.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.71-1762G>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 2/22 | chr1 | 205056159 | |||||||
chr1:205056201 | C | T | 1 | a0002c0015t0002g0114 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.71-1720C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 2/22 | chr1 | 205056201 | |||||||
chr1:205056236 | G | C | 1 | a0001c0001t0007g0210 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.71-1685G>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 2/22 | chr1 | 205056236 | |||||||
chr1:205056259 | C | A | 48 | a0001c0001t0002g0248 a0001c0001t0004g0014 a0001c0001t0004g0030 others(45): Show |
53 | HG01069.hp2 HG01071.hp1 HG01515.hp1 others(50): Show |
intron_variant | MODIFIER | c.71-1662C>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 2/22 | chr1 | 205056259 | |||||||
chr1:205056259 | C | T | 3 | a0001c0001t0003g0264 a0001c0001t0003g0278 a0001c0001t0003g0282 |
3 | HG00099.hp1 HG01346.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.71-1662C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 2/22 | chr1 | 205056259 | |||||||
chr1:205056325 | G | A | 10 | a0001c0001t0004g0070 a0001c0001t0004g0077 a0001c0001t0004g0106 others(7): Show |
10 | HG01993.hp2 HG02109.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.71-1596G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 2/22 | chr1 | 205056325 | |||||||
chr1:205056367 | GC | G | 19 | a0003c0016t0002g0243 a0003c0016t0004g0201 a0004c0005t0005g0011 others(16): Show |
20 | HG00099.hp2 HG00280.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.71-1552delC | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr1 | 205056367 | ||||||
chr1:205056732 | A | G | 1 | a0003c0009t0013g0005 | 4 | NA18948.hp1 NA19002.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-1189A>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 2/22 | chr1 | 205056732 | |||||||
chr1:205057124 | G | A | 1 | a0003c0003t0001g0136 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.71-797G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 2/22 | chr1 | 205057124 | |||||||
chr1:205057326 | T | C | 10 | a0001c0001t0011g0260 a0001c0001t0034g0301 a0001c0004t0001g0217 others(7): Show |
13 | HG00558.hp1 HG01109.hp2 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.71-595T>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 2/22 | chr1 | 205057326 | |||||||
chr1:205057546 | G | A | 1 | a0001c0004t0035g0216 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.71-375G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 2/22 | chr1 | 205057546 | |||||||
chr1:205057741 | C | T | 1 | a0001c0001t0004g0246 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.71-180C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 2/22 | chr1 | 205057741 | |||||||
chr1:205058368 | G | A | 5 | a0001c0001t0011g0016 a0001c0001t0011g0071 a0001c0001t0011g0081 others(2): Show |
6 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.391+12G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 4/22 | chr1 | 205058368 | |||||||
chr1:205058428 | A | G | 1 | a0003c0003t0020g0207 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.391+72A>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 4/22 | chr1 | 205058428 | |||||||
chr1:205058433 | G | T | 80 | a0003c0003t0001g0001 a0003c0003t0001g0010 a0003c0003t0001g0022 others(77): Show |
103 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.391+77G>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 4/22 | chr1 | 205058433 | |||||||
chr1:205058451 | C | A | 1 | a0004c0019t0005g0232 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.391+95C>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 4/22 | chr1 | 205058451 | |||||||
chr1:205058756 | G | A | 5 | a0001c0004t0005g0296 a0001c0004t0005g0297 a0001c0008t0005g0003 others(2): Show |
9 | HG02572.hp2 HG02622.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.487+93G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 5/22 | chr1 | 205058756 | |||||||
chr1:205059018 | G | A | 1 | a0001c0001t0007g0137 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.488-66G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 5/22 | chr1 | 205059018 | |||||||
chr1:205059024 | A | AC | 58 | a0003c0003t0001g0001 a0003c0003t0001g0010 a0003c0003t0001g0022 others(55): Show |
76 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.488-57dupC | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr1 | 205059024 | ||||||
chr1:205059311 | G | T | 22 | a0003c0009t0013g0005 a0003c0013t0014g0039 a0003c0013t0014g0129 others(19): Show |
27 | HG00099.hp2 HG00280.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.697+18G>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 6/22 | chr1 | 205059311 | |||||||
chr1:205059396 | C | T | 1 | a0002c0002t0017g0100 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.697+103C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 6/22 | chr1 | 205059396 | |||||||
chr1:205059453 | C | G | 85 | a0001c0004t0008g0017 a0002c0002t0002g0004 a0002c0002t0002g0007 others(82): Show |
108 | HG00140.hp2 HG00544.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.698-130C>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 6/22 | chr1 | 205059453 | |||||||
chr1:205059534 | C | G | 1 | a0002c0002t0037g0191 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.698-49C>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 6/22 | chr1 | 205059534 | |||||||
chr1:205059695 | A | AG | 58 | a0003c0003t0001g0001 a0003c0003t0001g0010 a0003c0003t0001g0022 others(55): Show |
76 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.797+16dupG | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr1 | 205059695 | ||||||
chr1:205059755 | CAG | C | 48 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0028 others(45): Show |
58 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.797+76_797+77delAG | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr1 | 205059755 | ||||||
chr1:205059787 | C | T | 50 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0028 others(47): Show |
60 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.797+105C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 7/22 | chr1 | 205059787 | |||||||
chr1:205059846 | C | A | 80 | a0003c0003t0001g0001 a0003c0003t0001g0010 a0003c0003t0001g0022 others(77): Show |
103 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.797+164C>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 7/22 | chr1 | 205059846 | |||||||
chr1:205060174 | G | A | 1 | a0001c0001t0010g0068 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.797+492G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 7/22 | chr1 | 205060174 | |||||||
chr1:205060450 | C | A | 1 | a0002c0002t0002g0101 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.797+768C>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 7/22 | chr1 | 205060450 | |||||||
chr1:205060531 | G | A | 1 | a0002c0002t0002g0060 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.798-714G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 7/22 | chr1 | 205060531 | |||||||
chr1:205060585 | G | A | 6 | a0001c0001t0010g0015 a0001c0001t0010g0046 a0001c0001t0010g0064 others(3): Show |
7 | HG02257.hp1 HG02258.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.798-660G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 7/22 | chr1 | 205060585 | |||||||
chr1:205060710 | C | T | 1 | a0002c0002t0002g0099 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.798-535C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 7/22 | chr1 | 205060710 | |||||||
chr1:205060711 | G | A | 1 | a0004c0005t0005g0244 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.798-534G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 7/22 | chr1 | 205060711 | |||||||
chr1:205060715 | C | CA | 6 | a0001c0001t0002g0299 a0002c0002t0002g0044 a0002c0002t0002g0074 others(3): Show |
6 | HG03540.hp1 NA18972.hp2 NA18988.hp2 others(3): Show |
intron_variant | MODIFIER | c.798-511dupA | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr1 | 205060715 | ||||||
chr1:205060715 | CA | C | 135 | a0001c0001t0002g0248 a0001c0001t0004g0014 a0001c0001t0004g0030 others(132): Show |
168 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.798-511delA | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr1 | 205060715 | ||||||
chr1:205060726 | A | G | 39 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0035 others(36): Show |
47 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.798-519A>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 7/22 | chr1 | 205060726 | |||||||
chr1:205060730 | A | G | 80 | a0003c0003t0001g0001 a0003c0003t0001g0010 a0003c0003t0001g0022 others(77): Show |
103 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.798-515A>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 7/22 | chr1 | 205060730 | |||||||
chr1:205060941 | C | A | 1 | a0003c0009t0013g0005 | 4 | NA18948.hp1 NA19002.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.798-304C>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 7/22 | chr1 | 205060941 | |||||||
chr1:205060943 | G | A | 80 | a0003c0003t0001g0001 a0003c0003t0001g0010 a0003c0003t0001g0022 others(77): Show |
103 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.798-302G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 7/22 | chr1 | 205060943 | |||||||
chr1:205060948 | G | A | 1 | a0002c0002t0006g0211 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.798-297G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 7/22 | chr1 | 205060948 | |||||||
chr1:205060993 | G | A | 83 | a0001c0001t0002g0248 a0001c0001t0004g0033 a0001c0001t0004g0145 others(80): Show |
107 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.798-252G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 7/22 | chr1 | 205060993 | |||||||
chr1:205061062 | C | T | 2 | a0003c0013t0014g0039 a0003c0013t0014g0129 |
3 | HG01192.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.798-183C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 7/22 | chr1 | 205061062 | |||||||
chr1:205061158 | C | T | 2 | a0002c0002t0002g0199 a0002c0002t0002g0200 |
2 | NA18963.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.798-87C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 7/22 | chr1 | 205061158 | |||||||
chr1:205061459 | C | T | 19 | a0003c0016t0002g0243 a0003c0016t0004g0201 a0004c0005t0005g0011 others(16): Show |
20 | HG00099.hp2 HG00280.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.973+39C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 8/22 | chr1 | 205061459 | |||||||
chr1:205061541 | G | A | 1 | a0002c0006t0001g0093 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.973+121G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 8/22 | chr1 | 205061541 | |||||||
chr1:205061667 | C | T | 1 | a0003c0003t0001g0181 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.974-198C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 8/22 | chr1 | 205061667 | |||||||
chr1:205061689 | C | T | 77 | a0002c0002t0002g0004 a0002c0002t0002g0007 a0002c0002t0002g0008 others(74): Show |
90 | HG00544.hp2 HG00558.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.974-176C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 8/22 | chr1 | 205061689 | |||||||
chr1:205061734 | C | T | 85 | a0002c0002t0002g0004 a0002c0002t0002g0007 a0002c0002t0002g0008 others(82): Show |
107 | HG00140.hp2 HG00544.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.974-131C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 8/22 | chr1 | 205061734 | |||||||
chr1:205062075 | CTT | C | 4 | a0002c0002t0002g0018 a0002c0002t0002g0092 a0002c0002t0002g0096 others(1): Show |
5 | HG00558.hp2 NA18974.hp2 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1110+75_1110+76del others(2): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 9/22 | chr1 | 205062075 | |||||||
chr1:205062296 | A | G | 1 | a0003c0009t0013g0005 | 4 | NA18948.hp1 NA19002.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.1111-144A>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 9/22 | chr1 | 205062296 | |||||||
chr1:205062616 | G | A | 85 | a0002c0002t0002g0004 a0002c0002t0002g0007 a0002c0002t0002g0008 others(82): Show |
107 | HG00140.hp2 HG00544.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.1240+47G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 10/22 | chr1 | 205062616 | |||||||
chr1:205062641 | G | A | 85 | a0002c0002t0002g0004 a0002c0002t0002g0007 a0002c0002t0002g0008 others(82): Show |
107 | HG00140.hp2 HG00544.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.1240+72G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 10/22 | chr1 | 205062641 | |||||||
chr1:205062664 | T | A | 1 | a0004c0005t0005g0302 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1240+95T>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 10/22 | chr1 | 205062664 | |||||||
chr1:205063085 | C | T | 1 | a0001c0001t0011g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1240+516C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 10/22 | chr1 | 205063085 | |||||||
chr1:205063123 | C | T | 3 | a0002c0002t0002g0044 a0002c0002t0002g0060 a0002c0002t0002g0062 |
3 | NA18981.hp2 NA19003.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1240+554C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 10/22 | chr1 | 205063123 | |||||||
chr1:205063315 | G | C | 1 | a0003c0003t0001g0171 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1240+746G>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 10/22 | chr1 | 205063315 | |||||||
chr1:205063323 | A | G | 5 | a0001c0001t0011g0016 a0001c0001t0011g0071 a0001c0001t0011g0081 others(2): Show |
6 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1240+754A>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 10/22 | chr1 | 205063323 | |||||||
chr1:205063371 | T | C | 2 | a0002c0015t0002g0114 a0002c0015t0002g0115 |
2 | HG04199.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1240+802T>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 10/22 | chr1 | 205063371 | |||||||
chr1:205063504 | G | A | 1 | a0002c0002t0002g0231 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1241-818G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 10/22 | chr1 | 205063504 | |||||||
chr1:205063629 | TA | T | 9 | a0001c0001t0003g0264 a0001c0001t0003g0274 a0001c0001t0010g0064 others(6): Show |
9 | HG01517.hp2 HG02895.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.1241-680delA | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr1 | 205063629 | ||||||
chr1:205063646 | GAAGA | G | 2 | a0003c0013t0014g0039 a0003c0013t0014g0129 |
3 | HG01192.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1241-669_1241-666d others(6): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr1 | 205063646 | ||||||
chr1:205063665 | A | AAAAG | 10 | a0001c0001t0004g0246 a0001c0001t0007g0228 a0001c0001t0034g0301 others(7): Show |
14 | HG00558.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.1241-633_1241-630d others(6): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr1 | 205063665 | ||||||
chr1:205063665 | AAAAG | A | 187 | a0001c0001t0002g0299 a0001c0001t0010g0015 a0001c0001t0010g0046 others(184): Show |
238 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.1241-633_1241-630d others(6): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr1 | 205063665 | ||||||
chr1:205063713 | G | A | 1 | a0004c0005t0005g0142 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1241-609G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 10/22 | chr1 | 205063713 | |||||||
chr1:205063878 | G | A | 4 | a0001c0001t0003g0287 a0001c0012t0003g0047 a0001c0012t0003g0194 others(1): Show |
4 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.1241-444G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 10/22 | chr1 | 205063878 | |||||||
chr1:205063908 | G | A | 1 | a0003c0013t0014g0039 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1241-414G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 10/22 | chr1 | 205063908 | |||||||
chr1:205063910 | A | G | 2 | a0001c0001t0018g0263 a0001c0001t0018g0277 |
2 | HG01192.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.1241-412A>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 10/22 | chr1 | 205063910 | |||||||
chr1:205063978 | G | A | 18 | a0003c0016t0004g0201 a0004c0005t0005g0011 a0004c0005t0005g0034 others(15): Show |
19 | HG00099.hp2 HG00280.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.1241-344G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 10/22 | chr1 | 205063978 | |||||||
chr1:205063983 | G | A | 10 | a0001c0001t0034g0301 a0001c0004t0001g0217 a0001c0004t0008g0006 others(7): Show |
14 | HG00558.hp1 HG00738.hp2 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.1241-339G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 10/22 | chr1 | 205063983 | |||||||
chr1:205064126 | AG | A | 186 | a0001c0001t0002g0299 a0001c0001t0034g0301 a0001c0004t0001g0217 others(183): Show |
236 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.1241-189delG | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr1 | 205064126 | ||||||
chr1:205064128 | G | C | 50 | a0001c0001t0002g0248 a0001c0001t0004g0014 a0001c0001t0004g0030 others(47): Show |
59 | HG01069.hp2 HG01071.hp1 HG01993.hp2 others(56): Show |
intron_variant | MODIFIER | c.1241-194G>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 10/22 | chr1 | 205064128 | |||||||
chr1:205064129 | G | C | 2 | a0002c0006t0016g0238 a0002c0006t0016g0240 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1241-193G>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 10/22 | chr1 | 205064129 | |||||||
chr1:205064155 | G | A | 197 | a0001c0001t0002g0299 a0001c0001t0004g0030 a0001c0001t0004g0133 others(194): Show |
249 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.1241-167G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 10/22 | chr1 | 205064155 | |||||||
chr1:205064174 | G | T | 1 | a0001c0001t0011g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1241-148G>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 10/22 | chr1 | 205064174 | |||||||
chr1:205064185 | A | C | 1 | a0001c0001t0004g0246 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1241-137A>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 10/22 | chr1 | 205064185 | |||||||
chr1:205064246 | T | C | 174 | a0001c0001t0002g0299 a0002c0002t0002g0004 a0002c0002t0002g0007 others(171): Show |
220 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.1241-76T>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 10/22 | chr1 | 205064246 | |||||||
chr1:205064258 | G | T | 2 | a0001c0004t0005g0296 a0001c0004t0005g0297 |
2 | HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1241-64G>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 10/22 | chr1 | 205064258 | |||||||
chr1:205064522 | A | G | 18 | a0001c0001t0004g0014 a0001c0001t0004g0030 a0001c0001t0004g0133 others(15): Show |
21 | HG01069.hp2 HG01071.hp1 HG02027.hp1 others(18): Show |
intron_variant | MODIFIER | c.1391+50A>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 11/22 | chr1 | 205064522 | |||||||
chr1:205064833 | T | C | 2 | a0001c0004t0019g0130 a0001c0004t0019g0218 |
2 | HG02155.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.1519+83T>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 12/22 | chr1 | 205064833 | |||||||
chr1:205064952 | G | A | 1 | a0002c0002t0006g0212 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1520-135G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 12/22 | chr1 | 205064952 | |||||||
chr1:205065306 | G | T | 57 | a0002c0006t0001g0095 a0003c0003t0001g0001 a0003c0003t0001g0010 others(54): Show |
75 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.1695+44G>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 13/22 | chr1 | 205065306 | |||||||
chr1:205065316 | G | A | 1 | a0003c0009t0013g0005 | 4 | NA18948.hp1 NA19002.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.1695+54G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 13/22 | chr1 | 205065316 | |||||||
chr1:205065317 | G | T | 1 | a0001c0004t0001g0281 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1695+55G>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 13/22 | chr1 | 205065317 | |||||||
chr1:205065360 | A | G | 142 | a0002c0002t0002g0004 a0002c0002t0002g0007 a0002c0002t0002g0008 others(139): Show |
182 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.1695+98A>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 13/22 | chr1 | 205065360 | |||||||
chr1:205065421 | T | C | 10 | a0005c0007t0009g0023 a0005c0007t0009g0040 a0005c0007t0009g0041 others(7): Show |
11 | HG01515.hp1 HG01884.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1695+159T>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 13/22 | chr1 | 205065421 | |||||||
chr1:205065424 | C | T | 57 | a0002c0006t0001g0095 a0003c0003t0001g0001 a0003c0003t0001g0010 others(54): Show |
75 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.1695+162C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 13/22 | chr1 | 205065424 | |||||||
chr1:205065505 | C | T | 34 | a0001c0001t0002g0248 a0001c0001t0004g0014 a0001c0001t0004g0030 others(31): Show |
39 | HG01069.hp2 HG01071.hp1 HG02027.hp1 others(36): Show |
intron_variant | MODIFIER | c.1695+243C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 13/22 | chr1 | 205065505 | |||||||
chr1:205065595 | C | T | 156 | a0001c0001t0002g0299 a0002c0002t0002g0004 a0002c0002t0002g0007 others(153): Show |
201 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.1696-194C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 13/22 | chr1 | 205065595 | |||||||
chr1:205065629 | G | A | 1 | a0002c0002t0002g0199 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1696-160G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 13/22 | chr1 | 205065629 | |||||||
chr1:205065724 | A | ATGGCCTG others(24): Show |
47 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0028 others(44): Show |
57 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.1696-62_1696-32dup others(31): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr1 | 205065724 | ||||||
chr1:205066301 | C | A | 6 | a0001c0001t0010g0015 a0001c0001t0010g0046 a0001c0001t0010g0064 others(3): Show |
7 | HG02257.hp1 HG02258.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1817-140C>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 14/22 | chr1 | 205066301 | |||||||
chr1:205066327 | A | G | 156 | a0001c0001t0002g0299 a0001c0001t0003g0012 a0001c0001t0003g0013 others(153): Show |
195 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.1817-114A>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 14/22 | chr1 | 205066327 | |||||||
chr1:205066330 | C | G | 7 | a0004c0005t0005g0142 a0004c0005t0005g0237 a0004c0005t0005g0241 others(4): Show |
7 | HG03239.hp1 HG03654.hp2 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.1817-111C>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 14/22 | chr1 | 205066330 | |||||||
chr1:205066804 | G | A | 5 | a0003c0003t0001g0119 a0003c0003t0001g0154 a0003c0003t0001g0171 others(2): Show |
5 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(2): Show |
intron_variant | MODIFIER | c.1975+205G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 15/22 | chr1 | 205066804 | |||||||
chr1:205066817 | G | A | 1 | a0001c0001t0007g0224 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1975+218G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 15/22 | chr1 | 205066817 | |||||||
chr1:205066827 | T | A | 3 | a0001c0008t0005g0003 a0001c0008t0005g0069 a0001c0008t0005g0266 |
7 | HG02572.hp2 HG02622.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1975+228T>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 15/22 | chr1 | 205066827 | |||||||
chr1:205066862 | G | A | 1 | a0002c0002t0002g0076 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1976-239G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 15/22 | chr1 | 205066862 | |||||||
chr1:205066877 | A | G | 1 | a0003c0009t0013g0005 | 4 | NA18948.hp1 NA19002.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.1976-224A>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 15/22 | chr1 | 205066877 | |||||||
chr1:205066912 | T | TG | 88 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0028 others(85): Show |
111 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1976-188dupG | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr1 | 205066912 | ||||||
chr1:205067284 | C | G | 4 | a0003c0009t0013g0005 a0003c0013t0014g0039 a0003c0013t0014g0129 others(1): Show |
8 | HG01192.hp1 HG02895.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.2125+34C>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 16/22 | chr1 | 205067284 | |||||||
chr1:205067333 | A | G | 3 | a0003c0013t0014g0039 a0003c0013t0014g0129 a0012c0020t0014g0102 |
4 | HG01192.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2125+83A>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 16/22 | chr1 | 205067333 | |||||||
chr1:205067411 | A | G | 1 | a0002c0002t0002g0140 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2125+161A>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 16/22 | chr1 | 205067411 | |||||||
chr1:205067476 | C | A | 1 | a0001c0001t0003g0271 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2125+226C>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 16/22 | chr1 | 205067476 | |||||||
chr1:205067555 | T | C | 10 | a0001c0001t0034g0301 a0001c0004t0001g0217 a0001c0004t0008g0006 others(7): Show |
14 | HG00558.hp1 HG00738.hp2 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.2125+305T>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 16/22 | chr1 | 205067555 | |||||||
chr1:205067617 | G | T | 1 | a0003c0009t0013g0005 | 4 | NA18948.hp1 NA19002.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.2125+367G>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 16/22 | chr1 | 205067617 | |||||||
chr1:205067698 | A | G | 236 | a0001c0001t0002g0248 a0001c0001t0002g0299 a0001c0001t0003g0012 others(233): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.2125+448A>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 16/22 | chr1 | 205067698 | |||||||
chr1:205067729 | C | A | 1 | a0003c0003t0001g0024 | 2 | NA18974.hp1 NA19059.hp1 |
intron_variant | MODIFIER | c.2125+479C>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 16/22 | chr1 | 205067729 | |||||||
chr1:205067793 | G | A | 1 | a0003c0009t0013g0005 | 4 | NA18948.hp1 NA19002.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.2125+543G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 16/22 | chr1 | 205067793 | |||||||
chr1:205067890 | T | C | 1 | a0003c0009t0013g0005 | 4 | NA18948.hp1 NA19002.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.2125+640T>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 16/22 | chr1 | 205067890 | |||||||
chr1:205067927 | C | CA | 18 | a0001c0001t0007g0137 a0001c0004t0005g0296 a0004c0005t0005g0011 others(15): Show |
19 | HG00099.hp2 HG00280.hp2 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.2125+705dupA | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr1 | 205067927 | ||||||
chr1:205067927 | CA | C | 23 | a0001c0001t0004g0066 a0001c0001t0004g0204 a0001c0001t0007g0195 others(20): Show |
24 | HG00639.hp1 HG01433.hp2 HG01496.hp2 others(21): Show |
intron_variant | MODIFIER | c.2125+705delA | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr1 | 205067927 | ||||||
chr1:205067927 | CAA | C | 135 | a0001c0001t0002g0248 a0001c0001t0004g0033 a0001c0001t0004g0080 others(132): Show |
180 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.2125+704_2125+705d others(4): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr1 | 205067927 | ||||||
chr1:205067927 | CAAA | C | 40 | a0001c0001t0004g0014 a0001c0001t0004g0030 a0001c0001t0004g0070 others(37): Show |
43 | HG01069.hp2 HG01071.hp1 HG01169.hp1 others(40): Show |
intron_variant | MODIFIER | c.2125+703_2125+705d others(5): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr1 | 205067927 | ||||||
chr1:205067927 | CAAAAAAA | C | 49 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0028 others(46): Show |
59 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.2125+699_2125+705d others(9): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr1 | 205067927 | ||||||
chr1:205067927 | CAAAAAAA others(7): Show |
C | 3 | a0003c0013t0014g0039 a0003c0013t0014g0129 a0012c0020t0014g0102 |
4 | HG01192.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2125+692_2125+705d others(16): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr1 | 205067927 | ||||||
chr1:205067952 | A | G | 1 | a0001c0001t0002g0248 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2125+702A>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 16/22 | chr1 | 205067952 | |||||||
chr1:205068065 | G | C | 15 | a0004c0005t0005g0011 a0004c0005t0005g0034 a0004c0005t0005g0132 others(12): Show |
16 | HG00099.hp2 HG00280.hp2 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.2125+815G>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 16/22 | chr1 | 205068065 | |||||||
chr1:205068071 | AT | A | 1 | a0003c0009t0013g0005 | 4 | NA18948.hp1 NA19002.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.2125+823delT | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr1 | 205068071 | ||||||
chr1:205068105 | C | T | 1 | a0004c0005t0005g0245 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2125+855C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 16/22 | chr1 | 205068105 | |||||||
chr1:205068130 | A | G | 1 | a0003c0009t0013g0005 | 4 | NA18948.hp1 NA19002.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.2125+880A>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 16/22 | chr1 | 205068130 | |||||||
chr1:205068226 | G | A | 86 | a0001c0001t0002g0248 a0001c0001t0002g0299 a0002c0002t0002g0004 others(83): Show |
108 | HG00140.hp2 HG00544.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.2125+976G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 16/22 | chr1 | 205068226 | |||||||
chr1:205068264 | G | A | 1 | a0003c0009t0013g0005 | 4 | NA18948.hp1 NA19002.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.2125+1014G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 16/22 | chr1 | 205068264 | |||||||
chr1:205068533 | T | C | 1 | a0001c0001t0004g0070 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2126-958T>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 16/22 | chr1 | 205068533 | |||||||
chr1:205068548 | T | G | 81 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0028 others(78): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.2126-943T>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 16/22 | chr1 | 205068548 | |||||||
chr1:205068735 | C | A | 5 | a0003c0003t0001g0024 a0003c0003t0001g0159 a0003c0003t0001g0169 others(2): Show |
6 | NA18961.hp1 NA18969.hp2 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.2126-756C>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 16/22 | chr1 | 205068735 | |||||||
chr1:205068833 | C | T | 1 | a0001c0001t0003g0271 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2126-658C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 16/22 | chr1 | 205068833 | |||||||
chr1:205069005 | TTTTG | T | 11 | a0001c0001t0007g0031 a0001c0001t0007g0195 a0001c0001t0007g0229 others(8): Show |
12 | HG00140.hp1 HG00639.hp1 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.2126-449_2126-446d others(6): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr1 | 205069005 | ||||||
chr1:205069005 | TTTTGTTT others(1): Show |
T | 207 | a0001c0001t0002g0138 a0001c0001t0002g0248 a0001c0001t0002g0299 others(204): Show |
261 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(258): Show |
intron_variant | MODIFIER | c.2126-453_2126-446d others(10): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr1 | 205069005 | ||||||
chr1:205069005 | TTTTGTTT others(5): Show |
T | 40 | a0001c0001t0004g0080 a0001c0001t0004g0204 a0001c0001t0004g0206 others(37): Show |
48 | HG00099.hp2 HG00280.hp2 HG01175.hp2 others(45): Show |
intron_variant | MODIFIER | c.2126-457_2126-446d others(14): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr1 | 205069005 | ||||||
chr1:205069005 | TTTTGTTT others(9): Show |
T | 46 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0028 others(43): Show |
56 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.2126-461_2126-446d others(18): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr1 | 205069005 | ||||||
chr1:205069090 | G | A | 3 | a0003c0013t0014g0039 a0003c0013t0014g0129 a0012c0020t0014g0102 |
4 | HG01192.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2126-401G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 16/22 | chr1 | 205069090 | |||||||
chr1:205069092 | G | A | 1 | a0003c0009t0013g0005 | 4 | NA18948.hp1 NA19002.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.2126-399G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 16/22 | chr1 | 205069092 | |||||||
chr1:205069236 | T | C | 3 | a0003c0013t0014g0039 a0003c0013t0014g0129 a0012c0020t0014g0102 |
4 | HG01192.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2126-255T>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 16/22 | chr1 | 205069236 | |||||||
chr1:205069391 | G | A | 2 | a0001c0001t0011g0071 a0001c0001t0011g0082 |
2 | HG01109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2126-100G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 16/22 | chr1 | 205069391 | |||||||
chr1:205069603 | C | T | 173 | a0001c0001t0002g0138 a0001c0001t0002g0248 a0001c0001t0002g0299 others(170): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.2196+42C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 17/22 | chr1 | 205069603 | |||||||
chr1:205069676 | C | G | 1 | a0004c0005t0005g0132 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2196+115C>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 17/22 | chr1 | 205069676 | |||||||
chr1:205069681 | C | G | 10 | a0001c0001t0004g0070 a0001c0001t0004g0077 a0001c0001t0004g0106 others(7): Show |
10 | HG01993.hp2 HG02109.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.2196+120C>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 17/22 | chr1 | 205069681 | |||||||
chr1:205069751 | A | G | 2 | a0002c0002t0002g0103 a0002c0002t0002g0104 |
2 | HG01975.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.2197-76A>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 17/22 | chr1 | 205069751 | |||||||
chr1:205070081 | C | A | 41 | a0001c0001t0034g0301 a0001c0004t0001g0217 a0001c0004t0005g0296 others(38): Show |
50 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.2431+20C>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 18/22 | chr1 | 205070081 | |||||||
chr1:205070160 | T | C | 26 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0038 others(23): Show |
31 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.2431+99T>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 18/22 | chr1 | 205070160 | |||||||
chr1:205070167 | A | C | 84 | a0001c0001t0002g0138 a0001c0001t0002g0248 a0001c0001t0002g0299 others(81): Show |
107 | HG00140.hp2 HG00544.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.2431+106A>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 18/22 | chr1 | 205070167 | |||||||
chr1:205070362 | G | A | 1 | a0004c0005t0005g0142 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2432-64G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 18/22 | chr1 | 205070362 | |||||||
chr1:205070633 | G | A | 3 | a0001c0001t0004g0033 a0001c0001t0004g0145 a0001c0001t0004g0146 |
4 | HG02145.hp1 HG02630.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2544+95G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 19/22 | chr1 | 205070633 | |||||||
chr1:205070825 | G | A | 1 | a0001c0001t0034g0301 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2544+287G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 19/22 | chr1 | 205070825 | |||||||
chr1:205070857 | A | G | 1 | a0001c0001t0003g0269 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2544+319A>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 19/22 | chr1 | 205070857 | |||||||
chr1:205070939 | T | C | 4 | a0001c0001t0003g0287 a0001c0012t0003g0047 a0001c0012t0003g0194 others(1): Show |
4 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.2544+401T>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 19/22 | chr1 | 205070939 | |||||||
chr1:205070995 | C | CA | 78 | a0001c0001t0003g0012 a0001c0001t0003g0038 a0001c0001t0003g0271 others(75): Show |
100 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.2544+474dupA | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr1 | 205070995 | ||||||
chr1:205070995 | CA | C | 5 | a0001c0008t0005g0266 a0003c0013t0014g0039 a0003c0013t0014g0129 others(2): Show |
6 | HG01192.hp1 HG02647.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2544+474delA | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr1 | 205070995 | ||||||
chr1:205071090 | T | C | 13 | a0001c0004t0001g0217 a0001c0004t0008g0006 a0001c0004t0008g0017 others(10): Show |
17 | HG00558.hp1 HG00738.hp2 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.2544+552T>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 19/22 | chr1 | 205071090 | |||||||
chr1:205071100 | A | G | 293 | a0001c0001t0002g0138 a0001c0001t0002g0248 a0001c0001t0002g0299 others(290): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(362): Show |
intron_variant | MODIFIER | c.2544+562A>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 19/22 | chr1 | 205071100 | |||||||
chr1:205071193 | A | G | 1 | a0002c0002t0002g0061 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2544+655A>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 19/22 | chr1 | 205071193 | |||||||
chr1:205071219 | T | C | 1 | a0002c0006t0001g0095 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2544+681T>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 19/22 | chr1 | 205071219 | |||||||
chr1:205071431 | C | T | 2 | a0003c0003t0001g0166 a0003c0003t0001g0182 |
2 | NA18990.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.2545-516C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 19/22 | chr1 | 205071431 | |||||||
chr1:205071598 | A | G | 236 | a0001c0001t0002g0138 a0001c0001t0002g0248 a0001c0001t0002g0299 others(233): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.2545-349A>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 19/22 | chr1 | 205071598 | |||||||
chr1:205071707 | A | G | 236 | a0001c0001t0002g0138 a0001c0001t0002g0248 a0001c0001t0002g0299 others(233): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.2545-240A>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 19/22 | chr1 | 205071707 | |||||||
chr1:205071806 | T | C | 5 | a0001c0001t0011g0016 a0001c0001t0011g0071 a0001c0001t0011g0081 others(2): Show |
6 | HG01109.hp1 HG01109.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.2545-141T>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 19/22 | chr1 | 205071806 | |||||||
chr1:205071815 | C | G | 88 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0028 others(85): Show |
110 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.2545-132C>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 19/22 | chr1 | 205071815 | |||||||
chr1:205071852 | C | T | 2 | a0002c0006t0016g0238 a0002c0006t0016g0240 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2545-95C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 19/22 | chr1 | 205071852 | |||||||
chr1:205071887 | G | A | 43 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0028 others(40): Show |
52 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.2545-60G>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 19/22 | chr1 | 205071887 | |||||||
chr1:205071935 | C | T | 1 | a0001c0001t0007g0137 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2545-12C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 19/22 | chr1 | 205071935 | |||||||
chr1:205072264 | C | G | 1 | a0015c0022t0008g0219 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2731+131C>G | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 20/22 | chr1 | 205072264 | |||||||
chr1:205072337 | T | C | 48 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0028 others(45): Show |
58 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.2732-146T>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 20/22 | chr1 | 205072337 | |||||||
chr1:205072352 | C | T | 67 | a0001c0004t0001g0037 a0001c0004t0001g0084 a0001c0004t0001g0085 others(64): Show |
86 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.2732-131C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 20/22 | chr1 | 205072352 | |||||||
chr1:205072359 | A | ATGGG | 236 | a0001c0001t0002g0138 a0001c0001t0002g0248 a0001c0001t0002g0299 others(233): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.2732-122_2732-121i others(6): Show |
CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr1 | 205072359 | ||||||
chr1:205072414 | T | C | 89 | a0001c0001t0002g0138 a0001c0001t0002g0248 a0001c0001t0002g0299 others(86): Show |
114 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.2732-69T>C | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 20/22 | chr1 | 205072414 | |||||||
chr1:205072824 | C | T | 64 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0028 others(61): Show |
82 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.2844+229C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 21/22 | chr1 | 205072824 | |||||||
chr1:205072914 | C | A | 26 | a0001c0004t0005g0296 a0001c0004t0005g0297 a0001c0008t0005g0003 others(23): Show |
31 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.2845-154C>A | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 21/22 | chr1 | 205072914 | |||||||
chr1:205072987 | C | T | 8 | a0002c0002t0006g0002 a0002c0002t0006g0127 a0002c0002t0006g0209 others(5): Show |
17 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.2845-81C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 21/22 | chr1 | 205072987 | |||||||
chr1:205073455 | C | T | 78 | a0001c0001t0002g0138 a0001c0001t0002g0248 a0001c0001t0002g0299 others(75): Show |
100 | HG00140.hp2 HG00544.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.3014-201C>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 22/22 | chr1 | 205073455 | |||||||
chr1:205073630 | G | T | 2 | a0001c0004t0001g0217 a0003c0003t0001g0174 |
2 | NA19063.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.3014-26G>T | CNTN2 | ENSG00000184144.12 | transcript | ENST00000331830.7 | protein_coding | 22/22 | chr1 | 205073630 |