Item | Value |
---|---|
geneid | 122046 |
ensemblid | ENSG00000175664.10 |
hgncid | 28622 |
symbol | TEX26 |
name | testis expressed 26 |
refseq_nuc | NM_152325.3 |
refseq_prot | NP_689538.1 |
ensembl_nuc | ENST00000380473.8 |
ensembl_prot | ENSP00000369840.3 |
mane_status | MANE Select |
chr | chr13 |
start | 30932656 |
end | 30975500 |
strand | + |
ver | v1.2 |
region | chr13:30932656-30975500 |
region5000 | chr13:30927656-30980500 |
regionname0 | TEX26_chr13_30932656_30975500 |
regionname5000 | TEX26_chr13_30927656_30980500 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 289 | 410 | 92 | 74 | 181 | 16 | 45 | 141 | TEX26_chr13_30927656_30980500 | TEX26 | MEQPG others(284): Show |
chr13 | 30927656 | 30980500 |
a0002 | 0/0 | 289 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | MEQPG others(284): Show |
chr13 | 30927656 | 30980500 |
a0003 | 0/0 | 289 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | MEQPG others(284): Show |
chr13 | 30927656 | 30980500 |
a0004 | 0/0 | 123 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TEX26_chr13_30927656_30980500 | TEX26 | MEQPG others(118): Show |
chr13 | 30927656 | 30980500 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 867 | 410 | 92 | 74 | 181 | 16 | 45 | TEX26_chr13_30927656_30980500 | TEX26 | ATGGA others(862): Show |
chr13 | 30927656 | 30980500 | ||
a0002c0002 | 0/0 | 867 | 2 | 2 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | ATGGA others(862): Show |
chr13 | 30927656 | 30980500 | ||
a0003c0004 | 0/0 | 867 | 1 | 0 | 0 | 0 | 0 | 1 | TEX26_chr13_30927656_30980500 | TEX26 | ATGGA others(862): Show |
chr13 | 30927656 | 30980500 | ||
a0004c0003 | 0/0 | 371 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | ATGGA others(366): Show |
chr13 | 30927656 | 30980500 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1523 | 402 | 86 | 72 | 181 | 16 | 45 | TEX26_chr13_30927656_30980500 | TEX26 | GGCTC others(1518): Show |
chr13 | 30927656 | 30980500 |
a0001c0001t0002 | 0/0 | 1523 | 5 | 4 | 1 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | GGCTC others(1518): Show |
chr13 | 30927656 | 30980500 |
a0001c0001t0003 | 0/0 | 1523 | 1 | 0 | 1 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | GGCTC others(1518): Show |
chr13 | 30927656 | 30980500 |
a0001c0001t0005 | 0/0 | 1523 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | GGCTC others(1518): Show |
chr13 | 30927656 | 30980500 |
a0001c0001t0006 | 0/0 | 1523 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | GGCTC others(1518): Show |
chr13 | 30927656 | 30980500 |
a0002c0002t0001 | 0/0 | 1523 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | GGCTC others(1518): Show |
chr13 | 30927656 | 30980500 |
a0002c0002t0004 | 0/0 | 1523 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | GGCTC others(1518): Show |
chr13 | 30927656 | 30980500 |
a0003c0004t0001 | 0/0 | 1523 | 1 | 0 | 0 | 0 | 0 | 1 | TEX26_chr13_30927656_30980500 | TEX26 | GGCTC others(1518): Show |
chr13 | 30927656 | 30980500 |
a0004c0003t0001 | 0/0 | 1027 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | GGCTC others(1022): Show |
chr13 | 30927656 | 30980500 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0002 | 0/0 | 6 | 0 | 5 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0005 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0009 | 0/0 | 4 | 0 | 1 | 1 | 2 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0012 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0049 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0052 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0154 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0302 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0002g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0005g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0001c0001t0006g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0002c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0002c0002t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0003c0004t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
a0004c0003t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0207 | EUR | GBR | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0285 | EUR | GBR | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | GBR | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0222 | EUR | GBR | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | FIN | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0241 | EUR | FIN | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0308 | EUR | FIN | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | FIN | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | CHS | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | CHS | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | CHS | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | CHS | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0301 | AMR | PUR | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0238 | AMR | PUR | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0316 | AMR | PUR | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0312 | AMR | PUR | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0322 | AMR | PUR | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | CLM | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | CLM | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0317 | AMR | CLM | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0291 | EUR | IBS | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0036 | EUR | IBS | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | IBS | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | ACB | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | ACB | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PEL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0306 | AMR | PEL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | KHV | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | KHV | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | ACB | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | KHV | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PEL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | CDX | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | CDX | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | ACB | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | ACB | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | ACB | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0318 | AMR | PEL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02451 | hp1 | a0002 | c0002 | t0001 | g0055 | AFR | ACB | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | GWD | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02717 | hp2 | a0001 | c0001 | t0005 | g0259 | AFR | GWD | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0280 | SAS | PJL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | GWD | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02886 | hp1 | a0002 | c0002 | t0004 | g0056 | AFR | GWD | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0147 | AFR | ESN | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ESN | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ESN | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | ESN | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0323 | AFR | ESN | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | ESN | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0146 | AFR | MSL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | MSL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0085 | AFR | ESN | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | ESN | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | ESN | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | MSL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | MSL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | MSL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | MSL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | MSL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | MSL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0321 | AFR | MSL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | MSL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | ESN | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | MSL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | MSL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0298 | SAS | PJL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG03688 | hp1 | a0003 | c0004 | t0001 | g0134 | SAS | STU | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | STU | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | PJL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | BEB | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | BEB | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | BEB | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | BEB | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | BEB | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | BEB | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | BEB | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0284 | SAS | STU | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | STU | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | BEB | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | BEB | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | STU | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | STU | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | STU | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | STU | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | STU | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | STU | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | YRI | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | YRI | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CHB | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | CHB | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHB | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | YRI | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | YRI | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19012 | hp1 | a0004 | c0003 | t0001 | g0224 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19043 | hp1 | a0001 | c0001 | t0006 | g0255 | AFR | LWK | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | LWK | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | YRI | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | YRI | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | ASW | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | ASW | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0202 | EUR | TSI | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0125 | EUR | TSI | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0221 | EUR | TSI | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0199 | EUR | TSI | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | GIH | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | GIH | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | ACB | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | MSL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | MSL | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | USA | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | USA | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | USA | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | USA | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | LWK | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | LWK | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0302 | REF | REF | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0154 | REF | REF | TEX26_chr13_30927656_30980500 | TEX26 | chr13 | 30927656 | 30980500 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:30939778 | G | A | 1 | a0002 | 2 | HG02451.hp1 HG02886.hp1 |
missense_variant&splice_region_variant | MODERATE | c.146G>A | p.Arg49His | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/7 | 206/1523 | 146/870 | 49/289 | chr13 | 30939778 | |||
chr13:30952779 | C | T | 1 | a0003 | 1 | HG03688.hp1 | missense_variant | MODERATE | c.266C>T | p.Thr89Ile | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/7 | 326/1523 | 266/870 | 89/289 | chr13 | 30952779 | |||
chr13:30954877 | TAAGTACT others(14670): Show |
T | 1 | a0004 | 1 | NA19012.hp1 | exon_loss_variant | HIGH | c.313-1991_808+512de others(1): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr13 | 30954877 | ||||||
chr13:30956984 | C | T | 1 | a0001 | 1 | NA19063.hp2 | stop_gained | HIGH | c.424C>T | p.Gln142* | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/7 | 484/1523 | 424/870 | 142/289 | chr13 | 30956984 | |||
chr13:30966298 | C | G | 1 | a0001 | 1 | NA18968.hp2 | missense_variant | MODERATE | c.546C>G | p.Phe182Leu | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 5/7 | 606/1523 | 546/870 | 182/289 | chr13 | 30966298 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:30956911 | G | A | 1 | a0001c0001 | 1 | HG03017.hp2 | synonymous_variant | LOW | c.351G>A | p.Thr117Thr | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/7 | 411/1523 | 351/870 | 117/289 | chr13 | 30956911 | |||
chr13:30956947 | G | T | 1 | a0001c0001 | 1 | NA18981.hp1 | synonymous_variant | LOW | c.387G>T | p.Pro129Pro | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/7 | 447/1523 | 387/870 | 129/289 | chr13 | 30956947 | |||
chr13:30968895 | G | A | 1 | a0001c0001 | 1 | HG03017.hp1 | synonymous_variant | LOW | c.657G>A | p.Val219Val | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/7 | 717/1523 | 657/870 | 219/289 | chr13 | 30968895 | |||
chr13:30968958 | C | T | 2 | a0001c0001 a0002c0002 |
88 | HG00099.hp2 HG00423.hp2 HG00609.hp2 others(85): Show |
synonymous_variant | LOW | c.720C>T | p.Tyr240Tyr | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/7 | 780/1523 | 720/870 | 240/289 | chr13 | 30968958 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:30932696 | C | G | 1 | a0001c0001t0006 | 1 | NA19043.hp1 | 5_prime_UTR_variant | MODIFIER | c.-20C>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/7 | 20 | chr13 | 30932696 | ||||||
chr13:30975119 | C | A | 1 | a0001c0001t0003 | 1 | HG01070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*212C>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 7/7 | 212 | chr13 | 30975119 | ||||||
chr13:30975276 | C | T | 2 | a0001c0001t0002 a0001c0001t0005 |
6 | HG01106.hp1 HG02717.hp2 HG02818.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*369C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 7/7 | 369 | chr13 | 30975276 | ||||||
chr13:30975386 | G | T | 1 | a0002c0002t0004 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*479G>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 7/7 | 479 | chr13 | 30975386 | ||||||
chr13:30975393 | A | T | 1 | a0001c0001t0005 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*486A>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 7/7 | 486 | chr13 | 30975393 | ||||||
chr13:30975437 | A | C | 1 | a0001c0001t0005 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*530A>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 7/7 | 530 | chr13 | 30975437 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:30932827 | G | C | 1 | a0001c0001t0001g0054 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.61+51G>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30932827 | |||||||
chr13:30932898 | C | T | 1 | a0001c0001t0001g0323 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.61+122C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30932898 | |||||||
chr13:30932913 | CG | C | 4 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0002c0002t0001g0055 others(1): Show |
4 | HG02451.hp1 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+141delG | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 30932913 | ||||||
chr13:30932938 | C | G | 1 | a0001c0001t0001g0322 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.61+162C>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30932938 | |||||||
chr13:30932939 | C | A | 4 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0002c0002t0001g0055 others(1): Show |
4 | HG02451.hp1 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+163C>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30932939 | |||||||
chr13:30932971 | A | T | 4 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0002c0002t0001g0055 others(1): Show |
4 | HG02451.hp1 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+195A>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30932971 | |||||||
chr13:30933044 | G | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG02717.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.61+268G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30933044 | |||||||
chr13:30933147 | C | A | 4 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0002c0002t0001g0055 others(1): Show |
4 | HG02451.hp1 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+371C>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30933147 | |||||||
chr13:30933156 | G | T | 4 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0002c0002t0001g0055 others(1): Show |
4 | HG02451.hp1 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+380G>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30933156 | |||||||
chr13:30933193 | G | T | 3 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 |
3 | HG02258.hp1 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.61+417G>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30933193 | |||||||
chr13:30933196 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.61+420G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30933196 | |||||||
chr13:30933199 | A | G | 4 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0002c0002t0001g0055 others(1): Show |
4 | HG02451.hp1 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+423A>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30933199 | |||||||
chr13:30933217 | G | C | 4 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0002c0002t0001g0055 others(1): Show |
4 | HG02451.hp1 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+441G>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30933217 | |||||||
chr13:30933295 | C | A | 1 | a0001c0001t0001g0060 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.61+519C>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30933295 | |||||||
chr13:30933499 | G | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0317 a0001c0001t0001g0318 |
5 | HG01256.hp2 HG01257.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+723G>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30933499 | |||||||
chr13:30933590 | G | T | 59 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(56): Show |
89 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.61+814G>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30933590 | |||||||
chr13:30933615 | A | G | 1 | a0001c0001t0001g0308 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.61+839A>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30933615 | |||||||
chr13:30933649 | A | G | 1 | a0001c0001t0001g0271 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.61+873A>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30933649 | |||||||
chr13:30933665 | ATACT | A | 88 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0020 others(85): Show |
106 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.61+892_61+895delCT others(2): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 30933665 | ||||||
chr13:30933694 | A | G | 2 | a0001c0001t0001g0315 a0001c0001t0001g0316 |
2 | HG01070.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.61+918A>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30933694 | |||||||
chr13:30933705 | C | A | 4 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0002c0002t0001g0055 others(1): Show |
4 | HG02451.hp1 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+929C>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30933705 | |||||||
chr13:30933709 | A | G | 7 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0266 others(4): Show |
7 | HG01891.hp2 HG02055.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.61+933A>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30933709 | |||||||
chr13:30933765 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.61+989G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30933765 | |||||||
chr13:30933768 | A | T | 1 | a0001c0001t0001g0263 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.61+992A>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30933768 | |||||||
chr13:30933783 | G | T | 1 | a0001c0001t0001g0262 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.61+1007G>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30933783 | |||||||
chr13:30933949 | A | G | 1 | a0001c0001t0001g0261 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.61+1173A>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30933949 | |||||||
chr13:30934123 | G | A | 2 | a0001c0001t0001g0032 a0001c0001t0001g0132 |
3 | HG01884.hp2 HG02818.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.61+1347G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30934123 | |||||||
chr13:30934214 | C | G | 1 | a0001c0001t0001g0314 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.61+1438C>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30934214 | |||||||
chr13:30934220 | C | T | 3 | a0001c0001t0001g0258 a0001c0001t0001g0260 a0001c0001t0005g0259 |
3 | HG01891.hp1 HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.61+1444C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30934220 | |||||||
chr13:30934247 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.61+1471C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30934247 | |||||||
chr13:30934273 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.61+1497C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30934273 | |||||||
chr13:30934287 | T | C | 8 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0319 others(5): Show |
8 | HG02258.hp1 HG02451.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.61+1511T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30934287 | |||||||
chr13:30934302 | G | C | 4 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0002c0002t0001g0055 others(1): Show |
4 | HG02451.hp1 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+1526G>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30934302 | |||||||
chr13:30934347 | G | C | 8 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0319 others(5): Show |
8 | HG02258.hp1 HG02451.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.61+1571G>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30934347 | |||||||
chr13:30934377 | T | C | 4 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0002c0002t0001g0055 others(1): Show |
4 | HG02451.hp1 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+1601T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30934377 | |||||||
chr13:30934429 | G | A | 3 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 |
3 | HG02258.hp1 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.61+1653G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30934429 | |||||||
chr13:30934437 | A | T | 2 | a0001c0001t0001g0256 a0001c0001t0006g0255 |
2 | HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.61+1661A>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30934437 | |||||||
chr13:30934479 | C | T | 5 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 others(2): Show |
5 | HG00741.hp1 HG01099.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.61+1703C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30934479 | |||||||
chr13:30934484 | A | G | 1 | a0001c0001t0001g0323 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.61+1708A>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30934484 | |||||||
chr13:30934559 | T | A | 1 | a0001c0001t0001g0133 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.61+1783T>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30934559 | |||||||
chr13:30934587 | A | G | 141 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(138): Show |
171 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(168): Show |
intron_variant | MODIFIER | c.61+1811A>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30934587 | |||||||
chr13:30934675 | G | A | 1 | a0003c0004t0001g0134 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.61+1899G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30934675 | |||||||
chr13:30934700 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.61+1924G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30934700 | |||||||
chr13:30934744 | G | A | 5 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0323 others(2): Show |
5 | HG02451.hp1 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.61+1968G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30934744 | |||||||
chr13:30934753 | G | A | 77 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(74): Show |
111 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.61+1977G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30934753 | |||||||
chr13:30934823 | A | T | 1 | a0001c0001t0001g0310 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.61+2047A>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30934823 | |||||||
chr13:30934844 | C | T | 1 | a0001c0001t0001g0323 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.61+2068C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30934844 | |||||||
chr13:30934933 | A | T | 135 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(132): Show |
165 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.61+2157A>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30934933 | |||||||
chr13:30934961 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.61+2185C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30934961 | |||||||
chr13:30935020 | C | T | 78 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(75): Show |
106 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.61+2244C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30935020 | |||||||
chr13:30935047 | AC | A | 4 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0002c0002t0001g0055 others(1): Show |
4 | HG02451.hp1 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+2274delC | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 30935047 | ||||||
chr13:30935073 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.61+2297C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30935073 | |||||||
chr13:30935249 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.61+2473G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30935249 | |||||||
chr13:30935304 | T | C | 8 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0319 others(5): Show |
8 | HG02258.hp1 HG02451.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.61+2528T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30935304 | |||||||
chr13:30935426 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.61+2650C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30935426 | |||||||
chr13:30935474 | ACAG | A | 4 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0002c0002t0001g0055 others(1): Show |
4 | HG02451.hp1 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+2703_61+2705del others(3): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 30935474 | ||||||
chr13:30935492 | A | T | 1 | a0001c0001t0001g0253 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.61+2716A>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30935492 | |||||||
chr13:30935521 | C | T | 6 | a0001c0001t0001g0031 a0001c0001t0001g0057 a0001c0001t0001g0058 others(3): Show |
7 | HG01346.hp1 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.61+2745C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30935521 | |||||||
chr13:30935522 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.61+2746G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30935522 | |||||||
chr13:30935533 | G | A | 4 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0002c0002t0001g0055 others(1): Show |
4 | HG02451.hp1 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+2757G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30935533 | |||||||
chr13:30935566 | G | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | NA18954.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.61+2790G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30935566 | |||||||
chr13:30935607 | G | A | 101 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(98): Show |
124 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.61+2831G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30935607 | |||||||
chr13:30935623 | G | T | 1 | a0001c0001t0001g0252 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.61+2847G>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30935623 | |||||||
chr13:30935689 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.61+2913C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30935689 | |||||||
chr13:30935732 | C | A | 4 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0002c0002t0001g0055 others(1): Show |
4 | HG02451.hp1 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.61+2956C>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30935732 | |||||||
chr13:30935733 | G | A | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(157): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.61+2957G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30935733 | |||||||
chr13:30935803 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.61+3027C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30935803 | |||||||
chr13:30936029 | G | A | 309 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(306): Show |
400 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(397): Show |
intron_variant | MODIFIER | c.61+3253G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30936029 | |||||||
chr13:30936084 | G | A | 3 | a0001c0001t0001g0258 a0001c0001t0001g0260 a0001c0001t0005g0259 |
3 | HG01891.hp1 HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.61+3308G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30936084 | |||||||
chr13:30936092 | A | C | 6 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0150 others(3): Show |
6 | HG02451.hp1 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.61+3316A>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30936092 | |||||||
chr13:30936117 | G | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0165 |
3 | HG02683.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.61+3341G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30936117 | |||||||
chr13:30936496 | C | T | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG02717.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.62-3198C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30936496 | |||||||
chr13:30936551 | A | G | 6 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0150 others(3): Show |
6 | HG02451.hp1 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.62-3143A>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30936551 | |||||||
chr13:30936561 | A | C | 4 | a0001c0001t0001g0034 a0001c0001t0002g0035 a0001c0001t0002g0146 others(1): Show |
6 | HG01106.hp1 HG02818.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.62-3133A>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30936561 | |||||||
chr13:30936569 | C | A | 2 | a0001c0001t0001g0256 a0001c0001t0006g0255 |
2 | HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.62-3125C>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30936569 | |||||||
chr13:30936937 | T | C | 3 | a0001c0001t0001g0038 a0001c0001t0001g0166 a0001c0001t0001g0262 |
4 | NA18944.hp2 NA18948.hp2 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.62-2757T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30936937 | |||||||
chr13:30937032 | A | T | 4 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0002c0002t0001g0055 others(1): Show |
4 | HG02451.hp1 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.62-2662A>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30937032 | |||||||
chr13:30937109 | G | T | 2 | a0001c0001t0001g0269 a0001c0001t0001g0270 |
2 | HG03139.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.62-2585G>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30937109 | |||||||
chr13:30937159 | C | T | 1 | a0001c0001t0001g0309 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.62-2535C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30937159 | |||||||
chr13:30937223 | G | T | 61 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(58): Show |
91 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.62-2471G>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30937223 | |||||||
chr13:30937229 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.62-2465C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30937229 | |||||||
chr13:30937274 | G | A | 1 | a0001c0001t0001g0315 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.62-2420G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30937274 | |||||||
chr13:30937466 | T | A | 3 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 |
3 | HG02258.hp1 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.62-2228T>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30937466 | |||||||
chr13:30937518 | TA | T | 135 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(132): Show |
165 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.62-2175delA | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30937518 | |||||||
chr13:30937530 | G | C | 4 | a0001c0001t0001g0034 a0001c0001t0002g0035 a0001c0001t0002g0146 others(1): Show |
6 | HG01106.hp1 HG02818.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.62-2164G>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30937530 | |||||||
chr13:30937544 | T | C | 1 | a0001c0001t0001g0273 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.62-2150T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30937544 | |||||||
chr13:30937655 | G | A | 3 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 |
3 | HG02258.hp1 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.62-2039G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30937655 | |||||||
chr13:30937694 | A | C | 1 | a0001c0001t0001g0123 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.62-2000A>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30937694 | |||||||
chr13:30937699 | C | T | 33 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0011 others(30): Show |
44 | HG00099.hp1 HG00621.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.62-1995C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30937699 | |||||||
chr13:30937700 | T | G | 1 | a0001c0001t0001g0070 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.62-1994T>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30937700 | |||||||
chr13:30937704 | A | G | 2 | a0001c0001t0001g0041 a0001c0001t0001g0196 |
3 | HG01192.hp2 HG02004.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.62-1990A>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30937704 | |||||||
chr13:30937812 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.62-1882A>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30937812 | |||||||
chr13:30937854 | G | A | 4 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(1): Show |
4 | HG01175.hp2 HG02615.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-1840G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30937854 | |||||||
chr13:30938017 | T | C | 68 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(65): Show |
95 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.62-1677T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30938017 | |||||||
chr13:30938267 | A | G | 141 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(138): Show |
171 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.62-1427A>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30938267 | |||||||
chr13:30938349 | T | C | 138 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(135): Show |
168 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.62-1345T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30938349 | |||||||
chr13:30938498 | G | A | 28 | a0001c0001t0001g0013 a0001c0001t0001g0032 a0001c0001t0001g0043 others(25): Show |
34 | HG00280.hp2 HG00323.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.62-1196G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30938498 | |||||||
chr13:30938505 | C | A | 4 | a0001c0001t0001g0046 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
5 | HG01243.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.62-1189C>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30938505 | |||||||
chr13:30938517 | A | G | 32 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0027 others(29): Show |
42 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.62-1177A>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30938517 | |||||||
chr13:30938537 | C | T | 1 | a0003c0004t0001g0134 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.62-1157C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30938537 | |||||||
chr13:30938658 | T | C | 2 | a0001c0001t0001g0047 a0001c0001t0001g0274 |
3 | NA18951.hp2 NA18985.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.62-1036T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30938658 | |||||||
chr13:30938789 | T | G | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG02451.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.62-905T>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30938789 | |||||||
chr13:30938916 | C | T | 2 | a0001c0001t0001g0025 a0001c0001t0001g0026 |
4 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-778C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30938916 | |||||||
chr13:30939007 | C | T | 1 | a0003c0004t0001g0134 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.62-687C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30939007 | |||||||
chr13:30939008 | G | A | 135 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(132): Show |
165 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.62-686G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30939008 | |||||||
chr13:30939072 | C | G | 1 | a0001c0001t0001g0099 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.62-622C>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30939072 | |||||||
chr13:30939094 | T | C | 1 | a0001c0001t0001g0167 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.62-600T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30939094 | |||||||
chr13:30939213 | G | A | 1 | a0001c0001t0001g0323 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.62-481G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30939213 | |||||||
chr13:30939232 | C | T | 61 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(58): Show |
91 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.62-462C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30939232 | |||||||
chr13:30939263 | G | A | 4 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 others(1): Show |
4 | HG00741.hp1 HG01099.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.62-431G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30939263 | |||||||
chr13:30939288 | A | G | 148 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(145): Show |
178 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.62-406A>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30939288 | |||||||
chr13:30939320 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.62-374G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30939320 | |||||||
chr13:30939380 | G | T | 16 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0135 others(13): Show |
19 | HG01106.hp1 HG01175.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.62-314G>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30939380 | |||||||
chr13:30939485 | T | C | 136 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(133): Show |
166 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.62-209T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30939485 | |||||||
chr13:30939538 | T | C | 1 | a0001c0001t0001g0058 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.62-156T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30939538 | |||||||
chr13:30939662 | C | T | 19 | a0001c0001t0001g0024 a0001c0001t0001g0068 a0001c0001t0001g0069 others(16): Show |
20 | HG00609.hp1 HG02027.hp1 HG02056.hp2 others(17): Show |
intron_variant | MODIFIER | c.62-32C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 1/6 | chr13 | 30939662 | |||||||
chr13:30939794 | T | A | 148 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(145): Show |
178 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.146+16T>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30939794 | |||||||
chr13:30940097 | A | G | 3 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 |
3 | HG02258.hp1 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.146+319A>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30940097 | |||||||
chr13:30940234 | A | C | 1 | a0001c0001t0001g0186 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.146+456A>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30940234 | |||||||
chr13:30940242 | A | G | 1 | a0001c0001t0001g0308 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.146+464A>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30940242 | |||||||
chr13:30940322 | C | CT | 18 | a0001c0001t0001g0018 a0001c0001t0001g0053 a0001c0001t0001g0143 others(15): Show |
21 | HG00735.hp1 HG01978.hp1 HG02027.hp2 others(18): Show |
intron_variant | MODIFIER | c.146+573dupT | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 30940322 | ||||||
chr13:30940322 | C | CTTTTT | 6 | a0001c0001t0001g0020 a0001c0001t0001g0071 a0001c0001t0001g0072 others(3): Show |
7 | HG01256.hp1 HG01258.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.146+569_146+573dup others(5): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 30940322 | ||||||
chr13:30940322 | C | CTTTTTT | 20 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(17): Show |
25 | HG00140.hp2 HG01081.hp1 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.146+568_146+573dup others(6): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 30940322 | ||||||
chr13:30940322 | C | CTTTTTTT | 29 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0025 others(26): Show |
37 | HG00558.hp2 HG00609.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.146+567_146+573dup others(7): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 30940322 | ||||||
chr13:30940322 | C | CTTTTTTT others(1): Show |
31 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0024 others(28): Show |
40 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.146+566_146+573dup others(8): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 30940322 | ||||||
chr13:30940322 | C | CTTTTTTT others(2): Show |
24 | a0001c0001t0001g0013 a0001c0001t0001g0029 a0001c0001t0001g0030 others(21): Show |
29 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(26): Show |
intron_variant | MODIFIER | c.146+565_146+573dup others(9): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 30940322 | ||||||
chr13:30940322 | C | CTTTTTTT others(3): Show |
12 | a0001c0001t0001g0045 a0001c0001t0001g0086 a0001c0001t0001g0098 others(9): Show |
13 | HG00544.hp2 HG00621.hp2 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.146+564_146+573dup others(10): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 30940322 | ||||||
chr13:30940322 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0254 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.146+563_146+573dup others(11): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 30940322 | ||||||
chr13:30940322 | CT | C | 15 | a0001c0001t0001g0034 a0001c0001t0001g0135 a0001c0001t0001g0136 others(12): Show |
17 | HG00735.hp2 HG01106.hp1 HG02148.hp1 others(14): Show |
intron_variant | MODIFIER | c.146+573delT | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 30940322 | ||||||
chr13:30940322 | CTT | C | 12 | a0001c0001t0001g0036 a0001c0001t0001g0165 a0001c0001t0001g0184 others(9): Show |
13 | HG00558.hp1 HG00621.hp1 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.146+572_146+573del others(2): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 30940322 | ||||||
chr13:30940322 | CTTT | C | 59 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(56): Show |
86 | HG00099.hp1 HG00280.hp1 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.146+571_146+573del others(3): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 30940322 | ||||||
chr13:30940322 | CTTTTTTT others(2): Show |
C | 12 | a0001c0001t0001g0046 a0001c0001t0001g0057 a0001c0001t0001g0058 others(9): Show |
13 | HG01243.hp1 HG02451.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.146+565_146+573del others(9): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 30940322 | ||||||
chr13:30940322 | CTTTTTTT others(4): Show |
C | 3 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0003c0004t0001g0134 |
3 | HG02717.hp1 HG03688.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.146+563_146+573del others(11): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 30940322 | ||||||
chr13:30940366 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.146+588C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30940366 | |||||||
chr13:30940373 | G | A | 1 | a0001c0001t0001g0109 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.146+595G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30940373 | |||||||
chr13:30940387 | G | T | 1 | a0001c0001t0001g0213 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.146+609G>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30940387 | |||||||
chr13:30940420 | G | A | 1 | a0001c0001t0001g0298 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.146+642G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30940420 | |||||||
chr13:30940483 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.146+705G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30940483 | |||||||
chr13:30940536 | T | C | 1 | a0001c0001t0001g0241 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.146+758T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30940536 | |||||||
chr13:30940596 | G | A | 1 | a0001c0001t0001g0309 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.146+818G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30940596 | |||||||
chr13:30940794 | C | T | 61 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(58): Show |
91 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.146+1016C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30940794 | |||||||
chr13:30940831 | G | T | 28 | a0001c0001t0001g0013 a0001c0001t0001g0032 a0001c0001t0001g0043 others(25): Show |
34 | HG00280.hp2 HG00323.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.146+1053G>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30940831 | |||||||
chr13:30940832 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.146+1054G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30940832 | |||||||
chr13:30940838 | A | G | 147 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(144): Show |
177 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.146+1060A>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30940838 | |||||||
chr13:30940860 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.146+1082C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30940860 | |||||||
chr13:30940904 | C | T | 4 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0002c0002t0001g0055 others(1): Show |
4 | HG02451.hp1 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.146+1126C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30940904 | |||||||
chr13:30940974 | C | G | 275 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(272): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.146+1196C>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30940974 | |||||||
chr13:30940994 | G | A | 65 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(62): Show |
95 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.146+1216G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30940994 | |||||||
chr13:30941164 | G | A | 107 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(104): Show |
130 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.146+1386G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30941164 | |||||||
chr13:30941205 | T | G | 6 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0319 others(3): Show |
6 | HG02258.hp1 HG02717.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.146+1427T>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30941205 | |||||||
chr13:30941325 | T | C | 4 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0002c0002t0001g0055 others(1): Show |
4 | HG02451.hp1 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.146+1547T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30941325 | |||||||
chr13:30941417 | C | A | 1 | a0001c0001t0001g0104 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.146+1639C>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30941417 | |||||||
chr13:30941426 | T | A | 101 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(98): Show |
124 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.146+1648T>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30941426 | |||||||
chr13:30941475 | G | A | 6 | a0001c0001t0001g0046 a0001c0001t0001g0247 a0001c0001t0001g0248 others(3): Show |
7 | HG01243.hp1 HG02559.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.146+1697G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30941475 | |||||||
chr13:30941507 | C | A | 3 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 |
3 | HG02258.hp1 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.146+1729C>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30941507 | |||||||
chr13:30941523 | A | T | 1 | a0001c0001t0001g0323 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.146+1745A>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30941523 | |||||||
chr13:30941526 | G | A | 112 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(109): Show |
135 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.146+1748G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30941526 | |||||||
chr13:30941537 | G | T | 1 | a0001c0001t0001g0061 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.146+1759G>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30941537 | |||||||
chr13:30941545 | G | C | 3 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0001g0314 |
3 | HG00438.hp1 NA18957.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.146+1767G>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30941545 | |||||||
chr13:30941559 | T | C | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG02717.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.146+1781T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30941559 | |||||||
chr13:30941617 | A | G | 1 | a0001c0001t0001g0211 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.146+1839A>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30941617 | |||||||
chr13:30941663 | T | C | 1 | a0003c0004t0001g0134 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.146+1885T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30941663 | |||||||
chr13:30941739 | T | C | 1 | a0001c0001t0001g0323 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.146+1961T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30941739 | |||||||
chr13:30941813 | A | G | 3 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 |
3 | HG02258.hp1 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.146+2035A>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30941813 | |||||||
chr13:30941918 | G | A | 1 | a0001c0001t0001g0278 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.146+2140G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30941918 | |||||||
chr13:30942050 | C | A | 1 | a0003c0004t0001g0134 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.146+2272C>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30942050 | |||||||
chr13:30942115 | T | C | 1 | a0003c0004t0001g0134 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.146+2337T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30942115 | |||||||
chr13:30942273 | G | A | 101 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(98): Show |
124 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.146+2495G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30942273 | |||||||
chr13:30942288 | G | A | 1 | a0001c0001t0001g0323 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.146+2510G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30942288 | |||||||
chr13:30942309 | ATTTGTAT others(3): Show |
A | 1 | a0001c0001t0001g0150 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.146+2534_146+2543d others(12): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 30942309 | ||||||
chr13:30942434 | C | G | 2 | a0001c0001t0001g0256 a0001c0001t0006g0255 |
2 | HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.146+2656C>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30942434 | |||||||
chr13:30942503 | A | G | 1 | a0001c0001t0001g0210 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.146+2725A>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30942503 | |||||||
chr13:30942718 | G | A | 1 | a0003c0004t0001g0134 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.146+2940G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30942718 | |||||||
chr13:30942779 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.146+3001G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30942779 | |||||||
chr13:30942894 | T | TTGTAGTA others(100): Show |
1 | a0001c0001t0001g0150 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.146+3129_146+3130i others(109): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 30942894 | ||||||
chr13:30943266 | C | T | 2 | a0001c0001t0001g0209 a0001c0001t0001g0213 |
2 | HG03834.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.146+3488C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30943266 | |||||||
chr13:30943267 | G | A | 101 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(98): Show |
124 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.146+3489G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30943267 | |||||||
chr13:30943409 | A | G | 1 | a0001c0001t0001g0183 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.146+3631A>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30943409 | |||||||
chr13:30943475 | G | T | 1 | a0001c0001t0001g0307 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.146+3697G>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30943475 | |||||||
chr13:30943479 | G | A | 101 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(98): Show |
124 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.146+3701G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30943479 | |||||||
chr13:30943528 | C | G | 1 | a0001c0001t0001g0182 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.146+3750C>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30943528 | |||||||
chr13:30943622 | T | A | 1 | a0001c0001t0001g0054 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.146+3844T>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30943622 | |||||||
chr13:30943674 | T | C | 2 | a0001c0001t0001g0170 a0001c0001t0001g0185 |
2 | HG03654.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.146+3896T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30943674 | |||||||
chr13:30943703 | A | T | 111 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(108): Show |
134 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.146+3925A>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30943703 | |||||||
chr13:30943747 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.146+3969C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30943747 | |||||||
chr13:30943833 | A | G | 4 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0002c0002t0001g0055 others(1): Show |
4 | HG02451.hp1 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.146+4055A>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30943833 | |||||||
chr13:30943952 | G | A | 1 | a0003c0004t0001g0134 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.146+4174G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30943952 | |||||||
chr13:30944030 | G | A | 2 | a0001c0001t0001g0197 a0001c0001t0001g0198 |
2 | NA18993.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.146+4252G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30944030 | |||||||
chr13:30944107 | T | A | 1 | a0003c0004t0001g0134 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.146+4329T>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30944107 | |||||||
chr13:30944259 | T | C | 1 | a0003c0004t0001g0134 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.146+4481T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30944259 | |||||||
chr13:30944295 | G | T | 1 | a0001c0001t0001g0208 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.146+4517G>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30944295 | |||||||
chr13:30944303 | G | A | 3 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 |
3 | HG02258.hp1 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.146+4525G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30944303 | |||||||
chr13:30944438 | A | G | 1 | a0001c0001t0001g0321 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.146+4660A>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30944438 | |||||||
chr13:30944458 | G | A | 108 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(105): Show |
131 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.146+4680G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30944458 | |||||||
chr13:30944535 | G | C | 1 | a0001c0001t0002g0085 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.146+4757G>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30944535 | |||||||
chr13:30944667 | C | T | 109 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(106): Show |
132 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.146+4889C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30944667 | |||||||
chr13:30944715 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.146+4937G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30944715 | |||||||
chr13:30944769 | A | G | 309 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(306): Show |
400 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(397): Show |
intron_variant | MODIFIER | c.146+4991A>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30944769 | |||||||
chr13:30945255 | A | C | 1 | a0003c0004t0001g0134 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.146+5477A>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30945255 | |||||||
chr13:30945471 | G | T | 4 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(1): Show |
4 | HG01175.hp2 HG02615.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.146+5693G>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30945471 | |||||||
chr13:30945652 | C | T | 68 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(65): Show |
95 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.146+5874C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30945652 | |||||||
chr13:30945750 | G | A | 3 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 |
3 | HG02258.hp1 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.146+5972G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30945750 | |||||||
chr13:30945883 | A | G | 111 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(108): Show |
134 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.146+6105A>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30945883 | |||||||
chr13:30946036 | C | T | 1 | a0001c0001t0001g0263 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.146+6258C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30946036 | |||||||
chr13:30946081 | A | T | 78 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(75): Show |
106 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.146+6303A>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30946081 | |||||||
chr13:30946100 | T | C | 8 | a0001c0001t0001g0036 a0001c0001t0001g0187 a0001c0001t0001g0188 others(5): Show |
9 | HG00639.hp2 HG00735.hp2 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.146+6322T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30946100 | |||||||
chr13:30946128 | C | T | 78 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(75): Show |
106 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.146+6350C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30946128 | |||||||
chr13:30946155 | T | A | 2 | a0001c0001t0001g0048 a0001c0001t0001g0279 |
3 | NA18981.hp2 NA18999.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.146+6377T>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30946155 | |||||||
chr13:30946261 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.147-6399G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30946261 | |||||||
chr13:30946309 | A | T | 9 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0135 others(6): Show |
12 | HG00099.hp1 HG01081.hp2 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.147-6351A>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30946309 | |||||||
chr13:30946327 | A | C | 1 | a0001c0001t0001g0315 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.147-6333A>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30946327 | |||||||
chr13:30946368 | A | T | 78 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(75): Show |
106 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.147-6292A>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30946368 | |||||||
chr13:30946369 | T | C | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG02451.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.147-6291T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30946369 | |||||||
chr13:30946391 | G | A | 1 | a0001c0001t0001g0323 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.147-6269G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30946391 | |||||||
chr13:30946850 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.147-5810G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30946850 | |||||||
chr13:30946940 | C | A | 1 | a0001c0001t0001g0059 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.147-5720C>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30946940 | |||||||
chr13:30947122 | A | C | 17 | a0001c0001t0001g0013 a0001c0001t0001g0043 a0001c0001t0001g0044 others(14): Show |
22 | HG00280.hp2 HG00323.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.147-5538A>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30947122 | |||||||
chr13:30947141 | A | C | 1 | a0003c0004t0001g0134 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.147-5519A>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30947141 | |||||||
chr13:30947166 | T | C | 3 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 |
3 | HG02258.hp1 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.147-5494T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30947166 | |||||||
chr13:30947308 | A | T | 4 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0002c0002t0001g0055 others(1): Show |
4 | HG02451.hp1 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.147-5352A>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30947308 | |||||||
chr13:30947323 | T | C | 6 | a0001c0001t0001g0002 a0001c0001t0001g0041 a0001c0001t0001g0164 others(3): Show |
12 | HG00597.hp1 HG01192.hp2 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.147-5337T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30947323 | |||||||
chr13:30947346 | A | C | 1 | a0001c0001t0001g0052 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.147-5314A>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30947346 | |||||||
chr13:30947512 | G | A | 85 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0020 others(82): Show |
103 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.147-5148G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30947512 | |||||||
chr13:30947586 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.147-5074G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30947586 | |||||||
chr13:30947586 | G | C | 4 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0002c0002t0001g0055 others(1): Show |
4 | HG02451.hp1 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.147-5074G>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30947586 | |||||||
chr13:30947603 | GA | G | 2 | a0001c0001t0001g0032 a0001c0001t0001g0132 |
3 | HG01884.hp2 HG02818.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.147-5053delA | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 30947603 | ||||||
chr13:30947637 | G | A | 4 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(1): Show |
4 | NA18959.hp2 NA18984.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.147-5023G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30947637 | |||||||
chr13:30947798 | C | T | 17 | a0001c0001t0001g0013 a0001c0001t0001g0043 a0001c0001t0001g0044 others(14): Show |
22 | HG00280.hp2 HG00323.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.147-4862C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30947798 | |||||||
chr13:30947802 | A | G | 1 | a0001c0001t0001g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.147-4858A>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30947802 | |||||||
chr13:30947819 | G | A | 36 | a0001c0001t0001g0021 a0001c0001t0001g0024 a0001c0001t0001g0031 others(33): Show |
39 | HG00140.hp2 HG00609.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.147-4841G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30947819 | |||||||
chr13:30947870 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.147-4790G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30947870 | |||||||
chr13:30947919 | G | A | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.147-4741G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30947919 | |||||||
chr13:30947985 | C | T | 1 | a0001c0001t0001g0206 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.147-4675C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30947985 | |||||||
chr13:30948003 | C | G | 2 | a0001c0001t0001g0004 a0001c0001t0001g0205 |
7 | NA18941.hp1 NA18944.hp1 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.147-4657C>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30948003 | |||||||
chr13:30948088 | T | C | 4 | a0001c0001t0001g0034 a0001c0001t0002g0035 a0001c0001t0002g0146 others(1): Show |
6 | HG01106.hp1 HG02818.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.147-4572T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30948088 | |||||||
chr13:30948189 | G | A | 14 | a0001c0001t0001g0036 a0001c0001t0001g0058 a0001c0001t0001g0187 others(11): Show |
15 | HG00639.hp2 HG00735.hp2 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.147-4471G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30948189 | |||||||
chr13:30948202 | G | A | 3 | a0001c0001t0001g0223 a0001c0001t0001g0225 a0004c0003t0001g0224 |
3 | HG02056.hp1 HG02165.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.147-4458G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30948202 | |||||||
chr13:30948222 | C | T | 101 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(98): Show |
124 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.147-4438C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30948222 | |||||||
chr13:30948510 | ATG | A | 8 | a0001c0001t0001g0034 a0001c0001t0001g0135 a0001c0001t0001g0136 others(5): Show |
10 | HG01106.hp1 HG01175.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.147-4146_147-4145d others(4): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 30948510 | ||||||
chr13:30948524 | C | T | 1 | a0001c0001t0001g0308 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.147-4136C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30948524 | |||||||
chr13:30948533 | C | G | 1 | a0001c0001t0001g0297 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.147-4127C>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30948533 | |||||||
chr13:30948908 | A | G | 4 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(1): Show |
4 | HG01175.hp2 HG02615.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.147-3752A>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30948908 | |||||||
chr13:30948976 | A | G | 8 | a0001c0001t0001g0033 a0001c0001t0001g0139 a0001c0001t0001g0140 others(5): Show |
9 | HG02145.hp2 HG02280.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.147-3684A>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30948976 | |||||||
chr13:30948996 | G | A | 1 | a0001c0001t0001g0101 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.147-3664G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30948996 | |||||||
chr13:30949012 | G | T | 3 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 |
3 | HG02258.hp1 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.147-3648G>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30949012 | |||||||
chr13:30949073 | C | T | 1 | a0003c0004t0001g0134 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.147-3587C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30949073 | |||||||
chr13:30949192 | C | T | 2 | a0001c0001t0001g0256 a0001c0001t0006g0255 |
2 | HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.147-3468C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30949192 | |||||||
chr13:30949529 | A | G | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG02717.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.147-3131A>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30949529 | |||||||
chr13:30950040 | A | C | 1 | a0001c0001t0001g0296 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.147-2620A>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30950040 | |||||||
chr13:30950141 | C | T | 3 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 |
3 | HG02258.hp1 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.147-2519C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30950141 | |||||||
chr13:30950148 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.147-2512G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30950148 | |||||||
chr13:30950298 | C | T | 61 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(58): Show |
91 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.147-2362C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30950298 | |||||||
chr13:30950353 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.147-2307C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30950353 | |||||||
chr13:30950447 | C | T | 4 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0181 others(1): Show |
10 | NA18953.hp1 NA18959.hp1 NA18989.hp1 others(7): Show |
intron_variant | MODIFIER | c.147-2213C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30950447 | |||||||
chr13:30950488 | C | T | 109 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(106): Show |
132 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.147-2172C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30950488 | |||||||
chr13:30950526 | A | G | 1 | a0001c0001t0001g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.147-2134A>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30950526 | |||||||
chr13:30950528 | G | A | 4 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0250 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.147-2132G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30950528 | |||||||
chr13:30950656 | T | C | 1 | a0003c0004t0001g0134 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.147-2004T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30950656 | |||||||
chr13:30950668 | G | A | 1 | a0003c0004t0001g0134 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.147-1992G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30950668 | |||||||
chr13:30950708 | AC | A | 4 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0250 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.147-1949delC | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 30950708 | ||||||
chr13:30950831 | G | A | 1 | a0001c0001t0001g0199 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.147-1829G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30950831 | |||||||
chr13:30950841 | C | T | 1 | a0001c0001t0001g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.147-1819C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30950841 | |||||||
chr13:30950955 | C | T | 3 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0119 |
3 | HG02155.hp1 NA18612.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.147-1705C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30950955 | |||||||
chr13:30950998 | G | C | 5 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 others(2): Show |
5 | HG00741.hp1 HG01099.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.147-1662G>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30950998 | |||||||
chr13:30951037 | T | C | 28 | a0001c0001t0001g0013 a0001c0001t0001g0032 a0001c0001t0001g0043 others(25): Show |
34 | HG00280.hp2 HG00323.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.147-1623T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30951037 | |||||||
chr13:30951086 | C | T | 1 | a0001c0001t0005g0259 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.147-1574C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30951086 | |||||||
chr13:30951089 | C | T | 1 | a0003c0004t0001g0134 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.147-1571C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30951089 | |||||||
chr13:30951182 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.147-1478C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30951182 | |||||||
chr13:30951302 | G | C | 1 | a0001c0001t0001g0217 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.147-1358G>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30951302 | |||||||
chr13:30951349 | C | T | 5 | a0001c0001t0001g0045 a0001c0001t0001g0239 a0001c0001t0001g0240 others(2): Show |
6 | HG00738.hp2 HG01255.hp2 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.147-1311C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30951349 | |||||||
chr13:30951355 | CA | C | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(193): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.147-1289delA | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 30951355 | ||||||
chr13:30951453 | T | G | 1 | a0003c0004t0001g0134 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.147-1207T>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30951453 | |||||||
chr13:30951881 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.147-779C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30951881 | |||||||
chr13:30951907 | A | C | 1 | a0001c0001t0001g0225 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.147-753A>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30951907 | |||||||
chr13:30951945 | C | CT | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(206): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.147-702dupT | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 30951945 | ||||||
chr13:30951945 | C | CTT | 109 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(106): Show |
134 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.147-703_147-702dup others(2): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 30951945 | ||||||
chr13:30952001 | A | AT | 9 | a0001c0001t0001g0150 a0001c0001t0001g0153 a0001c0001t0001g0157 others(6): Show |
9 | HG02055.hp1 HG02559.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.147-616dupT | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 30952001 | ||||||
chr13:30952001 | A | ATTTTTTT others(3): Show |
1 | a0001c0001t0001g0273 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.147-625_147-616dup others(10): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 30952001 | ||||||
chr13:30952001 | AT | A | 14 | a0001c0001t0001g0017 a0001c0001t0001g0051 a0001c0001t0001g0053 others(11): Show |
18 | HG00639.hp1 HG01175.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.147-616delT | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 30952001 | ||||||
chr13:30952001 | ATT | A | 20 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0050 others(17): Show |
26 | HG00423.hp2 HG00438.hp1 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.147-617_147-616del others(2): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 30952001 | ||||||
chr13:30952001 | ATTT | A | 13 | a0001c0001t0001g0015 a0001c0001t0001g0034 a0001c0001t0001g0067 others(10): Show |
17 | HG00099.hp2 HG00544.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.147-618_147-616del others(3): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 30952001 | ||||||
chr13:30952001 | ATTTT | A | 17 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0014 others(14): Show |
27 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.147-619_147-616del others(4): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 30952001 | ||||||
chr13:30952001 | ATTTTT | A | 6 | a0001c0001t0001g0049 a0001c0001t0001g0064 a0001c0001t0001g0280 others(3): Show |
7 | HG01975.hp2 HG02451.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.147-620_147-616del others(5): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 30952001 | ||||||
chr13:30952001 | ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0001g0152 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.147-626_147-616del others(11): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 30952001 | ||||||
chr13:30952001 | ATTTTTTT others(6): Show |
A | 1 | a0001c0001t0001g0155 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.147-628_147-616del others(13): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 30952001 | ||||||
chr13:30952001 | ATTTTTTT others(8): Show |
A | 3 | a0001c0001t0001g0258 a0001c0001t0001g0260 a0001c0001t0005g0259 |
3 | HG01891.hp1 HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.147-630_147-616del others(15): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 30952001 | ||||||
chr13:30952001 | ATTTTTTT others(9): Show |
A | 1 | a0001c0001t0001g0149 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.147-631_147-616del others(16): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 30952001 | ||||||
chr13:30952001 | ATTTTTTT others(10): Show |
A | 1 | a0001c0001t0001g0148 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.147-632_147-616del others(17): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 30952001 | ||||||
chr13:30952001 | ATTTTTTT others(11): Show |
A | 9 | a0001c0001t0001g0033 a0001c0001t0001g0139 a0001c0001t0001g0140 others(6): Show |
10 | HG02145.hp2 HG02280.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.147-633_147-616del others(18): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 30952001 | ||||||
chr13:30952001 | ATTTTTTT others(12): Show |
A | 40 | a0001c0001t0001g0013 a0001c0001t0001g0043 a0001c0001t0001g0044 others(37): Show |
46 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.147-634_147-616del others(19): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 30952001 | ||||||
chr13:30952001 | ATTTTTTT others(13): Show |
A | 71 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(68): Show |
100 | HG00280.hp1 HG00597.hp1 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.147-635_147-616del others(20): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 30952001 | ||||||
chr13:30952001 | ATTTTTTT others(14): Show |
A | 5 | a0001c0001t0001g0028 a0001c0001t0001g0048 a0001c0001t0001g0167 others(2): Show |
7 | HG00558.hp1 HG00597.hp2 NA18981.hp2 others(4): Show |
intron_variant | MODIFIER | c.147-636_147-616del others(21): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 30952001 | ||||||
chr13:30952001 | ATTTTTTT others(15): Show |
A | 17 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(14): Show |
24 | HG01106.hp2 HG01934.hp1 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.147-637_147-616del others(22): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 30952001 | ||||||
chr13:30952001 | ATTTTTTT others(16): Show |
A | 80 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0020 others(77): Show |
95 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.147-638_147-616del others(23): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 30952001 | ||||||
chr13:30952001 | ATTTTTTT others(17): Show |
A | 3 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0110 |
3 | HG01258.hp1 HG02630.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.147-639_147-616del others(24): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 30952001 | ||||||
chr13:30952001 | ATTTTTTT others(21): Show |
A | 1 | a0001c0001t0001g0151 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.147-643_147-616del others(28): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 30952001 | ||||||
chr13:30952056 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.147-604T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30952056 | |||||||
chr13:30952159 | G | A | 1 | a0003c0004t0001g0134 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.147-501G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30952159 | |||||||
chr13:30952213 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.147-447G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30952213 | |||||||
chr13:30952348 | A | G | 3 | a0001c0001t0001g0052 a0001c0001t0001g0291 a0001c0001t0001g0294 |
4 | HG00639.hp1 HG01257.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.147-312A>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30952348 | |||||||
chr13:30952386 | A | T | 1 | a0001c0001t0001g0202 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.147-274A>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30952386 | |||||||
chr13:30952396 | T | C | 101 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(98): Show |
124 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.147-264T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30952396 | |||||||
chr13:30952554 | A | G | 1 | a0001c0001t0001g0321 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.147-106A>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | chr13 | 30952554 | |||||||
chr13:30952648 | G | GT | 6 | a0001c0001t0001g0036 a0001c0001t0001g0191 a0001c0001t0001g0192 others(3): Show |
7 | HG00639.hp2 HG00735.hp2 HG01515.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.147-5dupT | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 30952648 | ||||||
chr13:30953088 | C | A | 5 | a0001c0001t0001g0019 a0001c0001t0001g0226 a0001c0001t0001g0232 others(2): Show |
7 | HG01256.hp2 HG01257.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.312+263C>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30953088 | |||||||
chr13:30953152 | C | A | 3 | a0001c0001t0001g0200 a0001c0001t0001g0209 a0001c0001t0001g0213 |
3 | HG03834.hp1 HG04199.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.312+327C>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30953152 | |||||||
chr13:30953204 | G | A | 2 | a0001c0001t0001g0250 a0001c0001t0001g0251 |
2 | HG02559.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.312+379G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30953204 | |||||||
chr13:30953204 | G | T | 1 | a0001c0001t0001g0214 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.312+379G>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30953204 | |||||||
chr13:30953237 | G | A | 1 | a0001c0001t0001g0310 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.312+412G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30953237 | |||||||
chr13:30953407 | G | A | 1 | a0001c0001t0001g0086 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.312+582G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30953407 | |||||||
chr13:30953529 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.312+704G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30953529 | |||||||
chr13:30953784 | T | C | 1 | a0001c0001t0001g0068 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.312+959T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30953784 | |||||||
chr13:30953890 | A | C | 4 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0002c0002t0001g0055 others(1): Show |
4 | HG02451.hp1 HG02630.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.312+1065A>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30953890 | |||||||
chr13:30953897 | A | G | 118 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(115): Show |
142 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.312+1072A>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30953897 | |||||||
chr13:30953908 | G | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0074 a0001c0001t0001g0125 |
4 | HG01346.hp1 HG02486.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.312+1083G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30953908 | |||||||
chr13:30953921 | T | C | 2 | a0001c0001t0001g0025 a0001c0001t0001g0026 |
4 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.312+1096T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30953921 | |||||||
chr13:30953930 | G | T | 1 | a0001c0001t0001g0320 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.312+1105G>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30953930 | |||||||
chr13:30954149 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.312+1324G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30954149 | |||||||
chr13:30954153 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.312+1328T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30954153 | |||||||
chr13:30954255 | A | T | 2 | a0001c0001t0001g0151 a0001c0001t0001g0297 |
2 | NA19064.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.312+1430A>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30954255 | |||||||
chr13:30954257 | T | A | 1 | a0003c0004t0001g0134 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.312+1432T>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30954257 | |||||||
chr13:30954277 | T | TAC | 5 | a0001c0001t0001g0046 a0001c0001t0001g0057 a0001c0001t0001g0247 others(2): Show |
6 | HG01243.hp1 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.312+1494_312+1495d others(4): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr13 | 30954277 | ||||||
chr13:30954277 | TAC | T | 10 | a0001c0001t0001g0058 a0001c0001t0001g0091 a0001c0001t0001g0118 others(7): Show |
10 | HG01884.hp1 HG02056.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.312+1494_312+1495d others(4): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr13 | 30954277 | ||||||
chr13:30954277 | TACAC | T | 87 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(84): Show |
103 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.312+1492_312+1495d others(6): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr13 | 30954277 | ||||||
chr13:30954277 | TACACAC | T | 100 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(97): Show |
136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.312+1490_312+1495d others(8): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr13 | 30954277 | ||||||
chr13:30954277 | TACACACA others(1): Show |
T | 92 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(89): Show |
124 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.312+1488_312+1495d others(10): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr13 | 30954277 | ||||||
chr13:30954277 | TACACACA others(3): Show |
T | 11 | a0001c0001t0001g0005 a0001c0001t0001g0043 a0001c0001t0001g0049 others(8): Show |
12 | HG00735.hp1 HG01167.hp1 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.312+1486_312+1495d others(12): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr13 | 30954277 | ||||||
chr13:30954277 | TACACACA others(5): Show |
T | 6 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0258 others(3): Show |
6 | HG00323.hp1 HG01891.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.312+1484_312+1495d others(14): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr13 | 30954277 | ||||||
chr13:30954277 | TACACACA others(7): Show |
T | 3 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 |
3 | HG02258.hp1 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.312+1482_312+1495d others(16): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr13 | 30954277 | ||||||
chr13:30954344 | G | C | 1 | a0001c0001t0001g0191 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.312+1519G>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30954344 | |||||||
chr13:30954368 | C | T | 139 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(136): Show |
169 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.312+1543C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30954368 | |||||||
chr13:30954371 | T | TA | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(155): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.312+1551dupA | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr13 | 30954371 | ||||||
chr13:30954480 | G | A | 107 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(104): Show |
131 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.312+1655G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30954480 | |||||||
chr13:30954543 | C | T | 4 | a0001c0001t0001g0052 a0001c0001t0001g0291 a0001c0001t0001g0294 others(1): Show |
5 | HG00639.hp1 HG01175.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.312+1718C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30954543 | |||||||
chr13:30954544 | G | A | 1 | a0001c0001t0001g0280 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.312+1719G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30954544 | |||||||
chr13:30954579 | C | T | 8 | a0001c0001t0001g0033 a0001c0001t0001g0139 a0001c0001t0001g0140 others(5): Show |
9 | HG02145.hp2 HG02280.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.312+1754C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30954579 | |||||||
chr13:30954618 | C | G | 3 | a0001c0001t0001g0258 a0001c0001t0001g0260 a0001c0001t0005g0259 |
3 | HG01891.hp1 HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.312+1793C>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30954618 | |||||||
chr13:30954721 | G | T | 3 | a0001c0001t0001g0070 a0001c0001t0001g0108 a0001c0001t0001g0113 |
3 | HG02083.hp1 NA19054.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.312+1896G>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30954721 | |||||||
chr13:30954794 | TTACAATA others(14): Show |
T | 1 | a0001c0001t0001g0082 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.312+1988_312+2008d others(23): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr13 | 30954794 | ||||||
chr13:30954895 | C | G | 11 | a0001c0001t0001g0033 a0001c0001t0001g0139 a0001c0001t0001g0140 others(8): Show |
12 | HG02145.hp2 HG02258.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.313-1978C>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30954895 | |||||||
chr13:30954931 | C | T | 222 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(219): Show |
277 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.313-1942C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30954931 | |||||||
chr13:30955010 | C | T | 1 | a0001c0001t0001g0194 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.313-1863C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30955010 | |||||||
chr13:30955063 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.313-1810C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30955063 | |||||||
chr13:30955080 | T | C | 1 | a0003c0004t0001g0134 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.313-1793T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30955080 | |||||||
chr13:30955112 | G | GGAA | 232 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(229): Show |
284 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.313-1754_313-1752d others(5): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr13 | 30955112 | ||||||
chr13:30955181 | A | T | 2 | a0001c0001t0001g0191 a0001c0001t0001g0228 |
2 | HG00639.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.313-1692A>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30955181 | |||||||
chr13:30955188 | C | A | 1 | a0001c0001t0001g0011 | 3 | HG01081.hp2 HG01358.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.313-1685C>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30955188 | |||||||
chr13:30955194 | A | C | 1 | a0001c0001t0001g0014 | 3 | NA18969.hp2 NA19002.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.313-1679A>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30955194 | |||||||
chr13:30955360 | T | C | 57 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0022 others(54): Show |
67 | HG00280.hp2 HG00323.hp2 HG00738.hp2 others(64): Show |
intron_variant | MODIFIER | c.313-1513T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30955360 | |||||||
chr13:30955394 | C | T | 15 | a0001c0001t0001g0013 a0001c0001t0001g0044 a0001c0001t0001g0045 others(12): Show |
19 | HG00280.hp2 HG00323.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.313-1479C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30955394 | |||||||
chr13:30955579 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.313-1294G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30955579 | |||||||
chr13:30955648 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.313-1225T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30955648 | |||||||
chr13:30955677 | T | G | 316 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(313): Show |
407 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(404): Show |
intron_variant | MODIFIER | c.313-1196T>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30955677 | |||||||
chr13:30955767 | T | A | 7 | a0001c0001t0001g0237 a0001c0001t0001g0242 a0001c0001t0001g0264 others(4): Show |
7 | HG01891.hp2 HG02257.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.313-1106T>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30955767 | |||||||
chr13:30955796 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.313-1077G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30955796 | |||||||
chr13:30955825 | C | T | 3 | a0001c0001t0001g0166 a0001c0001t0001g0236 a0001c0001t0001g0262 |
3 | HG03704.hp2 NA18961.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.313-1048C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30955825 | |||||||
chr13:30956044 | T | C | 12 | a0001c0001t0001g0132 a0001c0001t0001g0135 a0001c0001t0001g0137 others(9): Show |
12 | HG01175.hp2 HG01884.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.313-829T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30956044 | |||||||
chr13:30956107 | T | G | 1 | a0001c0001t0001g0038 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.313-766T>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30956107 | |||||||
chr13:30956108 | G | C | 1 | a0001c0001t0001g0038 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.313-765G>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30956108 | |||||||
chr13:30956109 | C | A | 1 | a0001c0001t0001g0038 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.313-764C>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30956109 | |||||||
chr13:30956120 | T | C | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG02451.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.313-753T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30956120 | |||||||
chr13:30956143 | A | C | 82 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(79): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.313-730A>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30956143 | |||||||
chr13:30956160 | C | T | 6 | a0001c0001t0001g0036 a0001c0001t0001g0191 a0001c0001t0001g0193 others(3): Show |
7 | HG00639.hp2 HG00735.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.313-713C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30956160 | |||||||
chr13:30956223 | T | A | 8 | a0001c0001t0001g0033 a0001c0001t0001g0139 a0001c0001t0001g0140 others(5): Show |
9 | HG02145.hp2 HG02280.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.313-650T>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30956223 | |||||||
chr13:30956308 | T | C | 1 | a0001c0001t0001g0013 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.313-565T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30956308 | |||||||
chr13:30956350 | A | C | 1 | a0001c0001t0001g0286 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.313-523A>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30956350 | |||||||
chr13:30956364 | C | T | 5 | a0001c0001t0002g0035 a0001c0001t0002g0085 a0001c0001t0002g0146 others(2): Show |
6 | HG01106.hp1 HG02717.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.313-509C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30956364 | |||||||
chr13:30956376 | T | C | 2 | a0001c0001t0001g0037 a0001c0001t0001g0165 |
3 | HG02683.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.313-497T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30956376 | |||||||
chr13:30956385 | T | C | 2 | a0001c0001t0001g0005 a0001c0001t0001g0301 |
2 | HG00735.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.313-488T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30956385 | |||||||
chr13:30956416 | T | G | 1 | a0001c0001t0001g0150 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.313-457T>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30956416 | |||||||
chr13:30956777 | G | C | 2 | a0001c0001t0001g0258 a0001c0001t0001g0260 |
2 | HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.313-96G>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30956777 | |||||||
chr13:30956866 | T | C | 13 | a0001c0001t0001g0033 a0001c0001t0001g0057 a0001c0001t0001g0139 others(10): Show |
14 | HG02145.hp2 HG02280.hp2 HG02451.hp2 others(11): Show |
splice_region_variant&intron_variant | LOW | c.313-7T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30956866 | |||||||
chr13:30956872 | G | A | 80 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(77): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(99): Show |
splice_acceptor_variant&intron_variant | HIGH | c.313-1G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 3/6 | chr13 | 30956872 | |||||||
chr13:30957038 | T | G | 2 | a0001c0001t0001g0082 a0001c0001t0001g0190 |
2 | HG02109.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.469+9T>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30957038 | |||||||
chr13:30957058 | T | C | 319 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(316): Show |
410 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(407): Show |
intron_variant | MODIFIER | c.469+29T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30957058 | |||||||
chr13:30957123 | G | T | 1 | a0001c0001t0001g0057 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.469+94G>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30957123 | |||||||
chr13:30957293 | G | A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0075 |
2 | HG03017.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.469+264G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30957293 | |||||||
chr13:30957345 | A | G | 20 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0082 others(17): Show |
22 | HG01175.hp2 HG01884.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.469+316A>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30957345 | |||||||
chr13:30957447 | C | G | 2 | a0001c0001t0001g0258 a0001c0001t0001g0260 |
2 | HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.469+418C>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30957447 | |||||||
chr13:30957672 | G | A | 87 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(84): Show |
111 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.469+643G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30957672 | |||||||
chr13:30957680 | G | T | 2 | a0001c0001t0002g0085 a0001c0001t0005g0259 |
2 | HG02717.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.469+651G>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30957680 | |||||||
chr13:30957864 | C | G | 8 | a0001c0001t0001g0150 a0001c0001t0001g0258 a0001c0001t0001g0260 others(5): Show |
9 | HG01106.hp1 HG01891.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.469+835C>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30957864 | |||||||
chr13:30957987 | T | C | 3 | a0001c0001t0002g0035 a0001c0001t0002g0146 a0001c0001t0002g0147 |
4 | HG01106.hp1 HG02818.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.469+958T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30957987 | |||||||
chr13:30958237 | C | T | 2 | a0001c0001t0001g0005 a0001c0001t0001g0301 |
2 | HG00735.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.469+1208C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30958237 | |||||||
chr13:30958255 | A | G | 5 | a0001c0001t0001g0109 a0001c0001t0001g0112 a0001c0001t0001g0118 others(2): Show |
5 | HG00609.hp2 NA18981.hp1 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.469+1226A>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30958255 | |||||||
chr13:30958348 | G | A | 309 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(306): Show |
400 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(397): Show |
intron_variant | MODIFIER | c.469+1319G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30958348 | |||||||
chr13:30958395 | C | T | 2 | a0001c0001t0002g0085 a0001c0001t0005g0259 |
2 | HG02717.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.469+1366C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30958395 | |||||||
chr13:30958603 | A | G | 2 | a0001c0001t0001g0166 a0001c0001t0001g0262 |
2 | NA18961.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.469+1574A>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30958603 | |||||||
chr13:30958628 | G | A | 1 | a0001c0001t0001g0006 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.469+1599G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30958628 | |||||||
chr13:30958808 | G | C | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG02451.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.469+1779G>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30958808 | |||||||
chr13:30958842 | A | G | 8 | a0001c0001t0001g0045 a0001c0001t0001g0235 a0001c0001t0001g0239 others(5): Show |
9 | HG00738.hp2 HG01123.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.469+1813A>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30958842 | |||||||
chr13:30958863 | T | C | 1 | a0001c0001t0001g0203 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.469+1834T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30958863 | |||||||
chr13:30959028 | A | G | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(273): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.469+1999A>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30959028 | |||||||
chr13:30959451 | T | A | 33 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0022 others(30): Show |
39 | HG00280.hp2 HG00323.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.469+2422T>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30959451 | |||||||
chr13:30959569 | G | A | 146 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(143): Show |
203 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.469+2540G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30959569 | |||||||
chr13:30959603 | CTCTTA | C | 41 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0033 others(38): Show |
45 | HG01106.hp1 HG01175.hp2 HG01884.hp1 others(42): Show |
intron_variant | MODIFIER | c.469+2576_469+2580d others(7): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr13 | 30959603 | ||||||
chr13:30959638 | C | T | 3 | a0001c0001t0002g0035 a0001c0001t0002g0146 a0001c0001t0002g0147 |
4 | HG01106.hp1 HG02818.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.469+2609C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30959638 | |||||||
chr13:30959714 | A | G | 1 | a0001c0001t0001g0153 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.469+2685A>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30959714 | |||||||
chr13:30959731 | C | T | 1 | a0001c0001t0001g0023 | 2 | HG02886.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.469+2702C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30959731 | |||||||
chr13:30960111 | C | T | 2 | a0001c0001t0001g0257 a0001c0001t0001g0265 |
2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.469+3082C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30960111 | |||||||
chr13:30960299 | G | T | 1 | a0001c0001t0001g0029 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.469+3270G>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30960299 | |||||||
chr13:30960493 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.469+3464C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30960493 | |||||||
chr13:30960533 | C | A | 2 | a0001c0001t0001g0047 a0001c0001t0001g0274 |
3 | NA18951.hp2 NA18985.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.469+3504C>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30960533 | |||||||
chr13:30960602 | T | C | 5 | a0001c0001t0002g0035 a0001c0001t0002g0085 a0001c0001t0002g0146 others(2): Show |
6 | HG01106.hp1 HG02717.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.469+3573T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30960602 | |||||||
chr13:30960825 | C | T | 146 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(143): Show |
203 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.469+3796C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30960825 | |||||||
chr13:30960863 | T | C | 8 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0082 others(5): Show |
10 | HG02109.hp1 HG02559.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.469+3834T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30960863 | |||||||
chr13:30960876 | T | G | 1 | a0001c0001t0001g0243 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.469+3847T>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30960876 | |||||||
chr13:30960918 | C | T | 2 | a0001c0001t0001g0021 a0001c0001t0001g0123 |
2 | NA18612.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.469+3889C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30960918 | |||||||
chr13:30960945 | A | G | 1 | a0001c0001t0001g0003 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.469+3916A>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30960945 | |||||||
chr13:30961179 | C | T | 13 | a0001c0001t0001g0033 a0001c0001t0001g0057 a0001c0001t0001g0139 others(10): Show |
14 | HG02145.hp2 HG02280.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.469+4150C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30961179 | |||||||
chr13:30961300 | G | T | 64 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(61): Show |
83 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.469+4271G>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30961300 | |||||||
chr13:30961541 | TA | T | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(273): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.469+4519delA | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr13 | 30961541 | ||||||
chr13:30961627 | T | C | 146 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(143): Show |
203 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.470-4595T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30961627 | |||||||
chr13:30961754 | G | A | 33 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0022 others(30): Show |
39 | HG00280.hp2 HG00323.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.470-4468G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30961754 | |||||||
chr13:30961861 | T | G | 1 | a0001c0001t0001g0161 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.470-4361T>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30961861 | |||||||
chr13:30962189 | T | C | 1 | a0001c0001t0002g0146 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.470-4033T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30962189 | |||||||
chr13:30962204 | T | A | 41 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0033 others(38): Show |
45 | HG01106.hp1 HG01175.hp2 HG01884.hp1 others(42): Show |
intron_variant | MODIFIER | c.470-4018T>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30962204 | |||||||
chr13:30962360 | G | A | 19 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0082 others(16): Show |
21 | HG01175.hp2 HG01884.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.470-3862G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30962360 | |||||||
chr13:30962391 | G | C | 2 | a0001c0001t0001g0258 a0001c0001t0001g0260 |
2 | HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.470-3831G>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30962391 | |||||||
chr13:30962433 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.470-3789G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30962433 | |||||||
chr13:30962488 | C | T | 3 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 |
3 | HG02258.hp1 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.470-3734C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30962488 | |||||||
chr13:30962567 | G | A | 1 | a0001c0001t0001g0271 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.470-3655G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30962567 | |||||||
chr13:30962624 | C | T | 1 | a0001c0001t0001g0006 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.470-3598C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30962624 | |||||||
chr13:30962829 | GT | G | 150 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(147): Show |
209 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.470-3382delT | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr13 | 30962829 | ||||||
chr13:30962829 | GTT | G | 40 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0033 others(37): Show |
44 | HG01106.hp1 HG01175.hp2 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.470-3383_470-3382d others(4): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr13 | 30962829 | ||||||
chr13:30962836 | T | G | 8 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(5): Show |
8 | HG03831.hp1 HG04115.hp2 HG04228.hp1 others(5): Show |
intron_variant | MODIFIER | c.470-3386T>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30962836 | |||||||
chr13:30962840 | T | G | 1 | a0001c0001t0001g0054 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.470-3382T>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30962840 | |||||||
chr13:30962989 | A | AT | 4 | a0001c0001t0001g0014 a0001c0001t0001g0119 a0001c0001t0001g0211 others(1): Show |
6 | HG01169.hp1 NA18969.hp1 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.470-3221dupT | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr13 | 30962989 | ||||||
chr13:30962989 | A | ATT | 19 | a0001c0001t0001g0033 a0001c0001t0001g0057 a0001c0001t0001g0139 others(16): Show |
20 | HG01891.hp1 HG02145.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.470-3222_470-3221d others(4): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr13 | 30962989 | ||||||
chr13:30962989 | A | ATTT | 22 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0082 others(19): Show |
25 | HG01106.hp1 HG01175.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.470-3223_470-3221d others(5): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr13 | 30962989 | ||||||
chr13:30963073 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.470-3149C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30963073 | |||||||
chr13:30963080 | G | A | 40 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0022 others(37): Show |
46 | HG00280.hp2 HG00323.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.470-3142G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30963080 | |||||||
chr13:30963156 | T | C | 13 | a0001c0001t0001g0033 a0001c0001t0001g0057 a0001c0001t0001g0139 others(10): Show |
14 | HG02145.hp2 HG02280.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.470-3066T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30963156 | |||||||
chr13:30963304 | G | C | 40 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0022 others(37): Show |
46 | HG00280.hp2 HG00323.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.470-2918G>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30963304 | |||||||
chr13:30963365 | T | C | 81 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0022 others(78): Show |
91 | HG00280.hp2 HG00323.hp2 HG00738.hp2 others(88): Show |
intron_variant | MODIFIER | c.470-2857T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30963365 | |||||||
chr13:30963582 | C | T | 2 | a0001c0001t0001g0287 a0001c0001t0001g0292 |
2 | HG02015.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.470-2640C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30963582 | |||||||
chr13:30963586 | A | T | 8 | a0001c0001t0001g0150 a0001c0001t0001g0258 a0001c0001t0001g0260 others(5): Show |
9 | HG01106.hp1 HG01891.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.470-2636A>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30963586 | |||||||
chr13:30963677 | A | G | 4 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0082 others(1): Show |
6 | HG02109.hp1 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.470-2545A>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30963677 | |||||||
chr13:30963725 | G | T | 41 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0033 others(38): Show |
45 | HG01106.hp1 HG01175.hp2 HG01884.hp1 others(42): Show |
intron_variant | MODIFIER | c.470-2497G>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30963725 | |||||||
chr13:30963918 | T | A | 1 | a0001c0001t0001g0282 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.470-2304T>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30963918 | |||||||
chr13:30963925 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.470-2297C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30963925 | |||||||
chr13:30964008 | C | A | 1 | a0001c0001t0001g0114 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.470-2214C>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30964008 | |||||||
chr13:30964192 | G | A | 2 | a0001c0001t0001g0078 a0001c0001t0001g0142 |
2 | HG01081.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.470-2030G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30964192 | |||||||
chr13:30964259 | C | T | 2 | a0001c0001t0001g0118 a0001c0001t0001g0124 |
2 | NA18981.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.470-1963C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30964259 | |||||||
chr13:30964269 | G | A | 40 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0022 others(37): Show |
46 | HG00280.hp2 HG00323.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.470-1953G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30964269 | |||||||
chr13:30964335 | G | A | 6 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0041 others(3): Show |
12 | HG02004.hp1 HG02071.hp1 NA18953.hp1 others(9): Show |
intron_variant | MODIFIER | c.470-1887G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30964335 | |||||||
chr13:30964341 | T | C | 6 | a0001c0001t0001g0150 a0001c0001t0002g0035 a0001c0001t0002g0085 others(3): Show |
7 | HG01106.hp1 HG02717.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.470-1881T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30964341 | |||||||
chr13:30964407 | C | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0189 |
3 | HG02109.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.470-1815C>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30964407 | |||||||
chr13:30964502 | T | C | 6 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0071 others(3): Show |
7 | HG01256.hp1 HG01258.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.470-1720T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30964502 | |||||||
chr13:30964731 | A | G | 2 | a0001c0001t0001g0258 a0001c0001t0001g0260 |
2 | HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.470-1491A>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30964731 | |||||||
chr13:30964781 | C | G | 20 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0082 others(17): Show |
22 | HG01175.hp2 HG01884.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.470-1441C>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30964781 | |||||||
chr13:30964796 | G | C | 5 | a0001c0001t0001g0109 a0001c0001t0001g0112 a0001c0001t0001g0118 others(2): Show |
5 | HG00609.hp2 NA18981.hp1 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.470-1426G>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30964796 | |||||||
chr13:30964970 | G | A | 3 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 |
3 | HG01175.hp2 HG02615.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.470-1252G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30964970 | |||||||
chr13:30965020 | C | G | 1 | a0001c0001t0001g0004 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.470-1202C>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30965020 | |||||||
chr13:30965130 | T | C | 235 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(232): Show |
304 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(301): Show |
intron_variant | MODIFIER | c.470-1092T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30965130 | |||||||
chr13:30965183 | G | C | 3 | a0001c0001t0002g0035 a0001c0001t0002g0146 a0001c0001t0002g0147 |
4 | HG01106.hp1 HG02818.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.470-1039G>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30965183 | |||||||
chr13:30965195 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.470-1027G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30965195 | |||||||
chr13:30965279 | A | G | 1 | a0001c0001t0001g0244 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.470-943A>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30965279 | |||||||
chr13:30965668 | A | T | 7 | a0001c0001t0001g0032 a0001c0001t0001g0046 a0001c0001t0001g0062 others(4): Show |
9 | HG01243.hp1 HG01243.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.470-554A>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30965668 | |||||||
chr13:30965972 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.470-250A>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30965972 | |||||||
chr13:30966066 | G | C | 1 | a0001c0001t0001g0062 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.470-156G>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30966066 | |||||||
chr13:30966181 | A | G | 6 | a0001c0001t0001g0150 a0001c0001t0002g0035 a0001c0001t0002g0085 others(3): Show |
7 | HG01106.hp1 HG02717.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.470-41A>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30966181 | |||||||
chr13:30966216 | C | T | 7 | a0001c0001t0001g0237 a0001c0001t0001g0242 a0001c0001t0001g0264 others(4): Show |
7 | HG01891.hp2 HG02257.hp2 HG02615.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.470-6C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 4/6 | chr13 | 30966216 | |||||||
chr13:30966432 | C | CT | 78 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(75): Show |
97 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.646+56dupT | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr13 | 30966432 | ||||||
chr13:30966432 | C | CTT | 13 | a0001c0001t0001g0003 a0001c0001t0001g0033 a0001c0001t0001g0042 others(10): Show |
14 | HG01169.hp2 HG02145.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.646+55_646+56dupTT | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr13 | 30966432 | ||||||
chr13:30966432 | C | CTTT | 10 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0135 others(7): Show |
12 | HG01884.hp1 HG02451.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.646+54_646+56dupTT others(1): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr13 | 30966432 | ||||||
chr13:30966432 | C | CTTTT | 14 | a0001c0001t0001g0082 a0001c0001t0001g0132 a0001c0001t0001g0137 others(11): Show |
14 | HG01175.hp2 HG02055.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.646+53_646+56dupTT others(2): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr13 | 30966432 | ||||||
chr13:30966432 | CT | C | 15 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0044 others(12): Show |
16 | HG01069.hp2 HG01255.hp2 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.646+56delT | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr13 | 30966432 | ||||||
chr13:30966432 | CTTT | C | 82 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(79): Show |
113 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.646+54_646+56delTT others(1): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr13 | 30966432 | ||||||
chr13:30966432 | CTTTT | C | 70 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(67): Show |
92 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.646+53_646+56delTT others(2): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr13 | 30966432 | ||||||
chr13:30966432 | CTTTTTTT others(6): Show |
C | 6 | a0001c0001t0001g0150 a0001c0001t0002g0035 a0001c0001t0002g0085 others(3): Show |
7 | HG01106.hp1 HG02717.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.646+44_646+56delTT others(11): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr13 | 30966432 | ||||||
chr13:30966437 | T | C | 2 | a0001c0001t0001g0014 a0001c0001t0001g0104 |
4 | HG01934.hp1 NA18969.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.646+39T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 5/6 | chr13 | 30966437 | |||||||
chr13:30966459 | C | T | 7 | a0001c0001t0001g0036 a0001c0001t0001g0158 a0001c0001t0001g0191 others(4): Show |
8 | HG00639.hp2 HG00735.hp2 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.646+61C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 5/6 | chr13 | 30966459 | |||||||
chr13:30966477 | G | T | 7 | a0001c0001t0001g0032 a0001c0001t0001g0046 a0001c0001t0001g0062 others(4): Show |
9 | HG01243.hp1 HG01243.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.646+79G>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 5/6 | chr13 | 30966477 | |||||||
chr13:30966516 | A | C | 41 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0033 others(38): Show |
45 | HG01106.hp1 HG01175.hp2 HG01884.hp1 others(42): Show |
intron_variant | MODIFIER | c.646+118A>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 5/6 | chr13 | 30966516 | |||||||
chr13:30966562 | C | T | 42 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0033 others(39): Show |
46 | HG01106.hp1 HG01175.hp2 HG01884.hp1 others(43): Show |
intron_variant | MODIFIER | c.646+164C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 5/6 | chr13 | 30966562 | |||||||
chr13:30966743 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.646+345C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 5/6 | chr13 | 30966743 | |||||||
chr13:30966881 | C | T | 20 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0082 others(17): Show |
22 | HG01175.hp2 HG01884.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.646+483C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 5/6 | chr13 | 30966881 | |||||||
chr13:30966882 | G | A | 2 | a0001c0001t0001g0061 a0001c0001t0001g0063 |
2 | HG03710.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.646+484G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 5/6 | chr13 | 30966882 | |||||||
chr13:30966903 | C | T | 1 | a0001c0001t0001g0086 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.646+505C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 5/6 | chr13 | 30966903 | |||||||
chr13:30967035 | C | T | 6 | a0001c0001t0001g0150 a0001c0001t0002g0035 a0001c0001t0002g0085 others(3): Show |
7 | HG01106.hp1 HG02717.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.646+637C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 5/6 | chr13 | 30967035 | |||||||
chr13:30967129 | G | T | 1 | a0001c0001t0001g0059 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.646+731G>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 5/6 | chr13 | 30967129 | |||||||
chr13:30967186 | G | A | 3 | a0001c0001t0001g0013 a0001c0001t0001g0044 a0001c0001t0001g0241 |
5 | HG00280.hp2 HG00323.hp2 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.646+788G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 5/6 | chr13 | 30967186 | |||||||
chr13:30967265 | T | G | 1 | a0001c0001t0001g0086 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.646+867T>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 5/6 | chr13 | 30967265 | |||||||
chr13:30967267 | C | T | 8 | a0001c0001t0001g0039 a0001c0001t0001g0094 a0001c0001t0001g0106 others(5): Show |
9 | HG02071.hp2 NA18939.hp1 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.646+869C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 5/6 | chr13 | 30967267 | |||||||
chr13:30967305 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.646+907C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 5/6 | chr13 | 30967305 | |||||||
chr13:30967314 | A | G | 15 | a0001c0001t0001g0008 a0001c0001t0001g0043 a0001c0001t0001g0059 others(12): Show |
16 | HG00423.hp2 HG01192.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.646+916A>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 5/6 | chr13 | 30967314 | |||||||
chr13:30967352 | C | T | 2 | a0001c0001t0001g0013 a0001c0001t0003g0238 |
2 | HG01070.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.646+954C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 5/6 | chr13 | 30967352 | |||||||
chr13:30967373 | T | C | 232 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(229): Show |
301 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(298): Show |
intron_variant | MODIFIER | c.646+975T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 5/6 | chr13 | 30967373 | |||||||
chr13:30967374 | G | A | 5 | a0001c0001t0001g0264 a0001c0001t0001g0266 a0001c0001t0001g0268 others(2): Show |
5 | HG01891.hp2 HG02257.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.646+976G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 5/6 | chr13 | 30967374 | |||||||
chr13:30967406 | G | T | 1 | a0001c0001t0001g0321 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.646+1008G>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 5/6 | chr13 | 30967406 | |||||||
chr13:30967412 | T | C | 233 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(230): Show |
302 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(299): Show |
intron_variant | MODIFIER | c.646+1014T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 5/6 | chr13 | 30967412 | |||||||
chr13:30967420 | C | T | 18 | a0001c0001t0001g0012 a0001c0001t0001g0042 a0001c0001t0001g0068 others(15): Show |
21 | HG00140.hp2 HG00642.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.646+1022C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 5/6 | chr13 | 30967420 | |||||||
chr13:30967475 | G | T | 1 | a0001c0001t0001g0323 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.646+1077G>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 5/6 | chr13 | 30967475 | |||||||
chr13:30967520 | C | T | 226 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(223): Show |
293 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(290): Show |
intron_variant | MODIFIER | c.646+1122C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 5/6 | chr13 | 30967520 | |||||||
chr13:30967709 | G | T | 13 | a0001c0001t0001g0033 a0001c0001t0001g0057 a0001c0001t0001g0139 others(10): Show |
14 | HG02145.hp2 HG02280.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.647-1176G>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 5/6 | chr13 | 30967709 | |||||||
chr13:30967760 | T | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0189 |
3 | HG02109.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.647-1125T>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 5/6 | chr13 | 30967760 | |||||||
chr13:30967895 | G | A | 81 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0022 others(78): Show |
91 | HG00280.hp2 HG00323.hp2 HG00738.hp2 others(88): Show |
intron_variant | MODIFIER | c.647-990G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 5/6 | chr13 | 30967895 | |||||||
chr13:30967995 | C | T | 33 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0022 others(30): Show |
39 | HG00280.hp2 HG00323.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.647-890C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 5/6 | chr13 | 30967995 | |||||||
chr13:30968118 | A | C | 1 | a0001c0001t0001g0288 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.647-767A>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 5/6 | chr13 | 30968118 | |||||||
chr13:30968136 | A | C | 147 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(144): Show |
204 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.647-749A>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 5/6 | chr13 | 30968136 | |||||||
chr13:30968327 | T | TA | 3 | a0001c0001t0001g0001 a0001c0001t0001g0115 a0001c0001t0001g0198 |
3 | HG02155.hp1 HG02155.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.647-555dupA | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr13 | 30968327 | ||||||
chr13:30968360 | G | T | 41 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0033 others(38): Show |
45 | HG01106.hp1 HG01175.hp2 HG01884.hp1 others(42): Show |
intron_variant | MODIFIER | c.647-525G>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 5/6 | chr13 | 30968360 | |||||||
chr13:30968362 | A | T | 1 | a0001c0001t0001g0030 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.647-523A>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 5/6 | chr13 | 30968362 | |||||||
chr13:30968375 | T | C | 2 | a0001c0001t0001g0258 a0001c0001t0001g0260 |
2 | HG01891.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.647-510T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 5/6 | chr13 | 30968375 | |||||||
chr13:30968414 | A | T | 13 | a0001c0001t0001g0033 a0001c0001t0001g0057 a0001c0001t0001g0139 others(10): Show |
14 | HG02145.hp2 HG02280.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.647-471A>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 5/6 | chr13 | 30968414 | |||||||
chr13:30968580 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.647-305G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 5/6 | chr13 | 30968580 | |||||||
chr13:30968660 | G | A | 33 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0022 others(30): Show |
39 | HG00280.hp2 HG00323.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.647-225G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 5/6 | chr13 | 30968660 | |||||||
chr13:30968684 | G | T | 2 | a0001c0001t0002g0085 a0001c0001t0005g0259 |
2 | HG02717.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.647-201G>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 5/6 | chr13 | 30968684 | |||||||
chr13:30969104 | T | C | 1 | a0001c0001t0001g0043 | 2 | NA18988.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.808+58T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30969104 | |||||||
chr13:30969166 | C | CA | 118 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(115): Show |
158 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.808+134dupA | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr13 | 30969166 | ||||||
chr13:30969385 | C | T | 4 | a0001c0001t0001g0174 a0001c0001t0001g0177 a0001c0001t0001g0182 others(1): Show |
4 | HG00738.hp1 HG00741.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.808+339C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30969385 | |||||||
chr13:30969394 | G | T | 1 | a0001c0001t0001g0172 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.808+348G>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30969394 | |||||||
chr13:30969435 | T | C | 20 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0082 others(17): Show |
22 | HG01175.hp2 HG01884.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.808+389T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30969435 | |||||||
chr13:30969579 | C | T | 2 | a0001c0001t0001g0099 a0001c0001t0001g0207 |
2 | HG00099.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.808+533C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30969579 | |||||||
chr13:30969590 | C | A | 12 | a0001c0001t0001g0132 a0001c0001t0001g0135 a0001c0001t0001g0137 others(9): Show |
12 | HG01175.hp2 HG01884.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.808+544C>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30969590 | |||||||
chr13:30969606 | GA | G | 3 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0249 |
3 | HG01243.hp1 HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.808+561delA | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30969606 | |||||||
chr13:30969646 | G | A | 7 | a0001c0001t0001g0032 a0001c0001t0001g0046 a0001c0001t0001g0062 others(4): Show |
9 | HG01243.hp1 HG01243.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.808+600G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30969646 | |||||||
chr13:30969861 | TA | T | 41 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0033 others(38): Show |
45 | HG01106.hp1 HG01175.hp2 HG01884.hp1 others(42): Show |
intron_variant | MODIFIER | c.808+817delA | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr13 | 30969861 | ||||||
chr13:30969922 | C | T | 234 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(231): Show |
303 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.808+876C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30969922 | |||||||
chr13:30970036 | G | C | 12 | a0001c0001t0001g0132 a0001c0001t0001g0135 a0001c0001t0001g0137 others(9): Show |
12 | HG01175.hp2 HG01884.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.808+990G>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30970036 | |||||||
chr13:30970101 | G | T | 40 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0022 others(37): Show |
46 | HG00280.hp2 HG00323.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.808+1055G>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30970101 | |||||||
chr13:30970112 | C | T | 8 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0082 others(5): Show |
10 | HG02109.hp1 HG02559.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.808+1066C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30970112 | |||||||
chr13:30970131 | C | T | 13 | a0001c0001t0001g0033 a0001c0001t0001g0057 a0001c0001t0001g0139 others(10): Show |
14 | HG02145.hp2 HG02280.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.808+1085C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30970131 | |||||||
chr13:30970154 | G | A | 2 | a0001c0001t0001g0287 a0001c0001t0001g0292 |
2 | HG02015.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.808+1108G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30970154 | |||||||
chr13:30970168 | AGT | A | 10 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0095 others(7): Show |
10 | HG00642.hp1 HG01361.hp2 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.808+1166_808+1167d others(4): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr13 | 30970168 | ||||||
chr13:30970168 | AGTGT | A | 34 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0031 others(31): Show |
39 | HG00140.hp2 HG00741.hp1 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.808+1164_808+1167d others(6): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr13 | 30970168 | ||||||
chr13:30970168 | AGTGTGT | A | 71 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(68): Show |
85 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.808+1162_808+1167d others(8): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr13 | 30970168 | ||||||
chr13:30970168 | AGTGTGTG others(1): Show |
A | 38 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0022 others(35): Show |
41 | HG00280.hp2 HG00323.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.808+1160_808+1167d others(10): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr13 | 30970168 | ||||||
chr13:30970168 | AGTGTGTG others(3): Show |
A | 7 | a0001c0001t0001g0020 a0001c0001t0001g0057 a0001c0001t0001g0200 others(4): Show |
7 | HG00099.hp1 HG01255.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.808+1158_808+1167d others(12): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr13 | 30970168 | ||||||
chr13:30970168 | AGTGTGTG others(5): Show |
A | 4 | a0001c0001t0001g0022 a0001c0001t0001g0168 a0001c0001t0001g0209 others(1): Show |
4 | HG03239.hp1 HG03834.hp1 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.808+1156_808+1167d others(14): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr13 | 30970168 | ||||||
chr13:30970168 | AGTGTGTG others(7): Show |
A | 10 | a0001c0001t0001g0150 a0001c0001t0001g0237 a0001c0001t0001g0242 others(7): Show |
10 | HG01891.hp2 HG02257.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.808+1154_808+1167d others(16): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr13 | 30970168 | ||||||
chr13:30970168 | AGTGTGTG others(9): Show |
A | 16 | a0001c0001t0001g0032 a0001c0001t0001g0037 a0001c0001t0001g0046 others(13): Show |
21 | HG01069.hp1 HG01106.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.808+1152_808+1167d others(18): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr13 | 30970168 | ||||||
chr13:30970168 | AGTGTGTG others(11): Show |
A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(127): Show |
182 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.808+1150_808+1167d others(20): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr13 | 30970168 | ||||||
chr13:30970168 | AGTGTGTG others(13): Show |
A | 7 | a0001c0001t0001g0017 a0001c0001t0001g0036 a0001c0001t0001g0191 others(4): Show |
8 | HG00639.hp2 HG00735.hp2 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.808+1148_808+1167d others(22): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr13 | 30970168 | ||||||
chr13:30970168 | AGTGTGTG others(15): Show |
A | 2 | a0001c0001t0001g0029 a0001c0001t0001g0292 |
2 | HG02015.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.808+1146_808+1167d others(24): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr13 | 30970168 | ||||||
chr13:30970178 | T | A | 1 | a0001c0001t0001g0130 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.808+1132T>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30970178 | |||||||
chr13:30970544 | G | A | 5 | a0001c0001t0001g0036 a0001c0001t0001g0191 a0001c0001t0001g0193 others(2): Show |
6 | HG00639.hp2 HG00735.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.808+1498G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30970544 | |||||||
chr13:30970624 | G | A | 41 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0033 others(38): Show |
45 | HG01106.hp1 HG01175.hp2 HG01884.hp1 others(42): Show |
intron_variant | MODIFIER | c.808+1578G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30970624 | |||||||
chr13:30970732 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.808+1686G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30970732 | |||||||
chr13:30970949 | C | A | 1 | a0001c0001t0001g0206 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.808+1903C>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30970949 | |||||||
chr13:30971282 | T | C | 3 | a0001c0001t0001g0140 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | HG02145.hp2 HG02976.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.808+2236T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30971282 | |||||||
chr13:30971529 | C | T | 1 | a0004c0003t0001g0224 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.808+2483C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30971529 | |||||||
chr13:30971624 | T | G | 1 | a0001c0001t0001g0312 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.808+2578T>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30971624 | |||||||
chr13:30971729 | G | A | 8 | a0001c0001t0001g0033 a0001c0001t0001g0139 a0001c0001t0001g0140 others(5): Show |
9 | HG02145.hp2 HG02280.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.808+2683G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30971729 | |||||||
chr13:30971807 | T | C | 13 | a0001c0001t0001g0013 a0001c0001t0001g0044 a0001c0001t0001g0045 others(10): Show |
17 | HG00280.hp2 HG00323.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.808+2761T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30971807 | |||||||
chr13:30971844 | G | T | 1 | a0001c0001t0001g0064 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.808+2798G>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30971844 | |||||||
chr13:30971851 | T | C | 33 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0022 others(30): Show |
39 | HG00280.hp2 HG00323.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.808+2805T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30971851 | |||||||
chr13:30971956 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.809-2890T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30971956 | |||||||
chr13:30971999 | A | C | 69 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(66): Show |
88 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.809-2847A>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30971999 | |||||||
chr13:30972113 | T | G | 1 | a0001c0001t0001g0239 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.809-2733T>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30972113 | |||||||
chr13:30972358 | AT | A | 6 | a0001c0001t0001g0150 a0001c0001t0002g0035 a0001c0001t0002g0085 others(3): Show |
7 | HG01106.hp1 HG02717.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.809-2486delT | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr13 | 30972358 | ||||||
chr13:30972412 | C | A | 6 | a0001c0001t0001g0150 a0001c0001t0002g0035 a0001c0001t0002g0085 others(3): Show |
7 | HG01106.hp1 HG02717.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.809-2434C>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30972412 | |||||||
chr13:30972436 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.809-2410G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30972436 | |||||||
chr13:30972445 | A | AT | 8 | a0001c0001t0001g0150 a0001c0001t0001g0258 a0001c0001t0001g0260 others(5): Show |
9 | HG01106.hp1 HG01891.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.809-2394dupT | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr13 | 30972445 | ||||||
chr13:30972445 | A | G | 1 | a0001c0001t0001g0187 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.809-2401A>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30972445 | |||||||
chr13:30972687 | C | T | 19 | a0001c0001t0001g0082 a0001c0001t0001g0132 a0001c0001t0001g0135 others(16): Show |
19 | HG01175.hp2 HG01243.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.809-2159C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30972687 | |||||||
chr13:30972696 | G | A | 2 | a0001c0001t0001g0320 a0001c0001t0001g0321 |
2 | HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.809-2150G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30972696 | |||||||
chr13:30972749 | C | T | 6 | a0001c0001t0001g0032 a0001c0001t0001g0046 a0001c0001t0001g0062 others(3): Show |
8 | HG01243.hp2 HG01884.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.809-2097C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30972749 | |||||||
chr13:30972966 | G | C | 1 | a0001c0001t0001g0198 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.809-1880G>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30972966 | |||||||
chr13:30972998 | A | C | 42 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0033 others(39): Show |
46 | HG01106.hp1 HG01175.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.809-1848A>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30972998 | |||||||
chr13:30973078 | C | T | 8 | a0001c0001t0001g0045 a0001c0001t0001g0235 a0001c0001t0001g0239 others(5): Show |
9 | HG00738.hp2 HG01123.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.809-1768C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30973078 | |||||||
chr13:30973144 | C | T | 82 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Show |
92 | HG00280.hp2 HG00323.hp2 HG00738.hp2 others(89): Show |
intron_variant | MODIFIER | c.809-1702C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30973144 | |||||||
chr13:30973176 | C | T | 6 | a0001c0001t0001g0032 a0001c0001t0001g0046 a0001c0001t0001g0062 others(3): Show |
8 | HG01243.hp2 HG01884.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.809-1670C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30973176 | |||||||
chr13:30973250 | C | T | 144 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(141): Show |
201 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.809-1596C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30973250 | |||||||
chr13:30973318 | C | T | 1 | a0001c0001t0001g0290 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.809-1528C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30973318 | |||||||
chr13:30973480 | A | C | 3 | a0001c0001t0002g0035 a0001c0001t0002g0146 a0001c0001t0002g0147 |
4 | HG01106.hp1 HG02818.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.809-1366A>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30973480 | |||||||
chr13:30973500 | T | C | 1 | a0001c0001t0001g0287 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.809-1346T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30973500 | |||||||
chr13:30973580 | A | G | 1 | a0001c0001t0001g0265 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.809-1266A>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30973580 | |||||||
chr13:30973612 | A | G | 42 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0033 others(39): Show |
46 | HG01106.hp1 HG01175.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.809-1234A>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30973612 | |||||||
chr13:30973718 | A | G | 6 | a0001c0001t0001g0032 a0001c0001t0001g0046 a0001c0001t0001g0062 others(3): Show |
8 | HG01243.hp2 HG01884.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.809-1128A>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30973718 | |||||||
chr13:30973829 | C | T | 1 | a0001c0001t0001g0311 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.809-1017C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30973829 | |||||||
chr13:30973848 | T | G | 1 | a0001c0001t0001g0227 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.809-998T>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30973848 | |||||||
chr13:30973999 | T | C | 1 | a0001c0001t0001g0271 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.809-847T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30973999 | |||||||
chr13:30974075 | C | T | 1 | a0001c0001t0001g0322 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.809-771C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30974075 | |||||||
chr13:30974119 | T | TA | 8 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0171 others(5): Show |
10 | HG01070.hp1 HG02293.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.809-714dupA | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr13 | 30974119 | ||||||
chr13:30974119 | T | TAA | 5 | a0001c0001t0001g0032 a0001c0001t0001g0077 a0001c0001t0001g0190 others(2): Show |
6 | HG01884.hp2 HG02723.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.809-715_809-714dup others(2): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr13 | 30974119 | ||||||
chr13:30974119 | T | TAAA | 18 | a0001c0001t0001g0029 a0001c0001t0001g0046 a0001c0001t0001g0062 others(15): Show |
20 | HG00423.hp1 HG00621.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.809-716_809-714dup others(3): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr13 | 30974119 | ||||||
chr13:30974119 | T | TAAAAAA | 6 | a0001c0001t0001g0237 a0001c0001t0001g0242 a0001c0001t0001g0264 others(3): Show |
6 | HG01891.hp2 HG02257.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.809-719_809-714dup others(6): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr13 | 30974119 | ||||||
chr13:30974129 | A | ATATATAT others(6): Show |
1 | a0001c0001t0005g0259 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.809-717_809-716ins others(13): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30974129 | |||||||
chr13:30974131 | A | AAAAAAAA others(5): Show |
4 | a0001c0001t0001g0155 a0001c0001t0001g0159 a0001c0001t0001g0160 others(1): Show |
4 | HG01884.hp1 HG02559.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.809-714_809-713ins others(12): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr13 | 30974131 | ||||||
chr13:30974131 | A | AAAAAAAA others(3): Show |
9 | a0001c0001t0001g0078 a0001c0001t0001g0132 a0001c0001t0001g0135 others(6): Show |
9 | HG01081.hp1 HG01175.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.809-714_809-713ins others(10): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr13 | 30974131 | ||||||
chr13:30974131 | A | AAAAAAAA others(5): Show |
1 | a0001c0001t0001g0162 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.809-714_809-713ins others(12): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr13 | 30974131 | ||||||
chr13:30974131 | A | AAAAAAAT | 13 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0022 others(10): Show |
19 | HG00280.hp2 HG00323.hp2 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.809-714_809-713ins others(7): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr13 | 30974131 | ||||||
chr13:30974131 | A | AAAAAAAT others(4): Show |
2 | a0001c0001t0001g0201 a0001c0001t0001g0317 |
2 | HG01496.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.809-714_809-713ins others(11): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr13 | 30974131 | ||||||
chr13:30974131 | A | AAAAAAAT others(6): Show |
2 | a0001c0001t0001g0271 a0001c0001t0001g0316 |
2 | HG01070.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.809-714_809-713ins others(13): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr13 | 30974131 | ||||||
chr13:30974131 | A | AAAAAATA others(3): Show |
3 | a0001c0001t0001g0058 a0001c0001t0001g0079 a0001c0001t0001g0083 |
3 | HG02257.hp1 HG02486.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.809-714_809-713ins others(10): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr13 | 30974131 | ||||||
chr13:30974131 | A | AAAAAATA others(9): Show |
1 | a0001c0001t0001g0319 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.809-714_809-713ins others(16): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr13 | 30974131 | ||||||
chr13:30974131 | A | AAAAAATA others(21): Show |
1 | a0001c0001t0001g0222 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.809-714_809-713ins others(28): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr13 | 30974131 | ||||||
chr13:30974131 | A | AAAAATAT | 13 | a0001c0001t0001g0045 a0001c0001t0001g0103 a0001c0001t0001g0105 others(10): Show |
14 | HG00738.hp2 HG01123.hp1 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.809-714_809-713ins others(7): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr13 | 30974131 | ||||||
chr13:30974131 | A | AAAAATAT others(2): Show |
32 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0043 others(29): Show |
41 | HG00099.hp2 HG00423.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.809-714_809-713ins others(9): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr13 | 30974131 | ||||||
chr13:30974131 | A | AAAAATAT others(4): Show |
6 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0059 others(3): Show |
10 | HG01081.hp2 HG01256.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.809-714_809-713ins others(11): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr13 | 30974131 | ||||||
chr13:30974131 | A | AAAAATAT others(6): Show |
2 | a0001c0001t0001g0034 a0001c0001t0001g0189 |
3 | HG02109.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.809-714_809-713ins others(13): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr13 | 30974131 | ||||||
chr13:30974131 | A | AAAAATAT others(8): Show |
7 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0001g0049 others(4): Show |
13 | HG00735.hp1 HG01167.hp1 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.809-714_809-713ins others(15): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr13 | 30974131 | ||||||
chr13:30974131 | A | AAAAATAT others(12): Show |
2 | a0001c0001t0001g0114 a0001c0001t0001g0278 |
2 | NA18612.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.809-714_809-713ins others(19): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr13 | 30974131 | ||||||
chr13:30974131 | A | AAAAATAT others(14): Show |
4 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0092 others(1): Show |
4 | NA18954.hp1 NA18961.hp2 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.809-714_809-713ins others(21): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr13 | 30974131 | ||||||
chr13:30974131 | A | AAAAT | 8 | a0001c0001t0001g0033 a0001c0001t0001g0139 a0001c0001t0001g0140 others(5): Show |
9 | HG02145.hp2 HG02280.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.809-714_809-713ins others(4): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr13 | 30974131 | ||||||
chr13:30974131 | A | AAAATATA others(3): Show |
4 | a0001c0001t0001g0023 a0001c0001t0001g0037 a0001c0001t0001g0165 others(1): Show |
6 | HG02683.hp1 HG02886.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.809-714_809-713ins others(10): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr13 | 30974131 | ||||||
chr13:30974131 | A | AAAATATA others(7): Show |
1 | a0001c0001t0001g0320 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.809-714_809-713ins others(14): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr13 | 30974131 | ||||||
chr13:30974131 | A | AAAATATA others(11): Show |
1 | a0001c0001t0001g0216 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.809-714_809-713ins others(18): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr13 | 30974131 | ||||||
chr13:30974131 | A | AAAATATA others(13): Show |
1 | a0001c0001t0001g0228 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.809-714_809-713ins others(20): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr13 | 30974131 | ||||||
chr13:30974131 | A | AAAATATA others(15): Show |
2 | a0001c0001t0001g0227 a0001c0001t0001g0253 |
2 | HG02280.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.809-714_809-713ins others(22): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr13 | 30974131 | ||||||
chr13:30974131 | A | AAAATATA others(23): Show |
1 | a0001c0001t0001g0229 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.809-714_809-713ins others(30): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr13 | 30974131 | ||||||
chr13:30974131 | A | AAAATATA others(27): Show |
1 | a0001c0001t0001g0012 | 3 | HG03491.hp1 HG03492.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.809-714_809-713ins others(34): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr13 | 30974131 | ||||||
chr13:30974131 | A | AAAATATA others(31): Show |
2 | a0001c0001t0001g0210 a0001c0001t0001g0230 |
2 | HG04204.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.809-714_809-713ins others(38): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr13 | 30974131 | ||||||
chr13:30974131 | A | AAAT | 42 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(39): Show |
72 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.809-714_809-713ins others(3): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr13 | 30974131 | ||||||
chr13:30974131 | A | AAATAT | 5 | a0001c0001t0001g0014 a0001c0001t0001g0057 a0001c0001t0001g0119 others(2): Show |
7 | HG03688.hp1 NA18969.hp1 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.809-714_809-713ins others(5): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr13 | 30974131 | ||||||
chr13:30974131 | A | AAATATAT others(6): Show |
1 | a0001c0001t0001g0289 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.809-714_809-713ins others(13): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr13 | 30974131 | ||||||
chr13:30974131 | A | AAATATAT others(18): Show |
1 | a0001c0001t0001g0232 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.809-714_809-713ins others(25): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr13 | 30974131 | ||||||
chr13:30974131 | A | AAATATAT others(22): Show |
1 | a0001c0001t0001g0042 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.809-714_809-713ins others(29): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr13 | 30974131 | ||||||
chr13:30974131 | A | AAATATAT others(36): Show |
1 | a0001c0001t0001g0226 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.809-714_809-713ins others(43): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr13 | 30974131 | ||||||
chr13:30974131 | A | AAT | 8 | a0001c0001t0001g0074 a0001c0001t0001g0081 a0001c0001t0001g0089 others(5): Show |
8 | HG00609.hp1 HG01515.hp1 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.809-691_809-690dup others(2): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr13 | 30974131 | ||||||
chr13:30974131 | A | AT | 3 | a0001c0001t0001g0086 a0001c0001t0001g0177 a0001c0001t0001g0221 |
3 | HG00738.hp1 NA18966.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.809-715_809-714ins others(1): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30974131 | |||||||
chr13:30974131 | A | ATATATAT others(10): Show |
1 | a0001c0001t0002g0085 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.809-715_809-714ins others(17): Show |
TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30974131 | |||||||
chr13:30974131 | A | T | 1 | a0001c0001t0005g0259 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.809-715A>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30974131 | |||||||
chr13:30974133 | T | A | 34 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0032 others(31): Show |
40 | HG00099.hp1 HG01070.hp1 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.809-713T>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30974133 | |||||||
chr13:30974135 | T | A | 7 | a0001c0001t0001g0032 a0001c0001t0001g0046 a0001c0001t0001g0062 others(4): Show |
9 | HG01070.hp1 HG01243.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.809-711T>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30974135 | |||||||
chr13:30974137 | T | A | 2 | a0001c0001t0001g0032 a0001c0001t0001g0077 |
3 | HG01884.hp2 HG02818.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.809-709T>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30974137 | |||||||
chr13:30974143 | T | C | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
4 | NA18939.hp2 NA18953.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.809-703T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30974143 | |||||||
chr13:30974239 | G | T | 140 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(137): Show |
197 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.809-607G>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30974239 | |||||||
chr13:30974312 | A | G | 21 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0082 others(18): Show |
23 | HG01175.hp2 HG01243.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.809-534A>G | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30974312 | |||||||
chr13:30974312 | A | T | 1 | a0001c0001t0001g0149 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.809-534A>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30974312 | |||||||
chr13:30974481 | G | A | 7 | a0001c0001t0001g0237 a0001c0001t0001g0242 a0001c0001t0001g0264 others(4): Show |
7 | HG01891.hp2 HG02257.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.809-365G>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30974481 | |||||||
chr13:30974551 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.809-295T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30974551 | |||||||
chr13:30974566 | C | A | 52 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0026 others(49): Show |
59 | HG00140.hp2 HG00642.hp1 HG01070.hp2 others(56): Show |
intron_variant | MODIFIER | c.809-280C>A | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30974566 | |||||||
chr13:30974636 | C | T | 2 | a0001c0001t0001g0226 a0001c0001t0001g0232 |
2 | NA18994.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.809-210C>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30974636 | |||||||
chr13:30974707 | G | T | 1 | a0001c0001t0001g0075 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.809-139G>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30974707 | |||||||
chr13:30974733 | A | T | 1 | a0001c0001t0001g0219 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.809-113A>T | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30974733 | |||||||
chr13:30974815 | T | C | 1 | a0001c0001t0001g0225 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.809-31T>C | TEX26 | ENSG00000175664.10 | transcript | ENST00000380473.8 | protein_coding | 6/6 | chr13 | 30974815 |