Item | Value |
---|---|
geneid | 147409 |
ensemblid | ENSG00000175065.12 |
hgncid | 21307 |
symbol | DSG4 |
name | desmoglein 4 |
refseq_nuc | NM_177986.5 |
refseq_prot | NP_817123.1 |
ensembl_nuc | ENST00000308128.9 |
ensembl_prot | ENSP00000311859.4 |
mane_status | MANE Select |
chr | chr18 |
start | 31376777 |
end | 31414909 |
strand | + |
ver | v1.2 |
region | chr18:31376777-31414909 |
region5000 | chr18:31371777-31419909 |
regionname0 | DSG4_chr18_31376777_31414909 |
regionname5000 | DSG4_chr18_31371777_31419909 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 1040 | 302 | 64 | 47 | 149 | 9 | 32 | 116 | DSG4_chr18_31371777_31419909 | DSG4 | MDWLF others(1035): Show |
chr18 | 31371777 | 31419909 |
a0002 | 0/0 | 1040 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | MDWLF others(1035): Show |
chr18 | 31371777 | 31419909 |
a0003 | 1/0 | 1040 | 4 | 0 | 2 | 0 | 0 | 1 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | MDWLF others(1035): Show |
chr18 | 31371777 | 31419909 |
a0004 | 0/0 | 1040 | 4 | 0 | 0 | 0 | 0 | 4 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | MDWLF others(1035): Show |
chr18 | 31371777 | 31419909 |
a0005 | 0/0 | 1040 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | MDWLF others(1035): Show |
chr18 | 31371777 | 31419909 |
a0006 | 0/0 | 1040 | 3 | 2 | 0 | 0 | 0 | 1 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | MDWLF others(1035): Show |
chr18 | 31371777 | 31419909 |
a0007 | 0/0 | 1040 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | DSG4_chr18_31371777_31419909 | DSG4 | MDWLF others(1035): Show |
chr18 | 31371777 | 31419909 |
a0008 | 0/0 | 1040 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | MDWLF others(1035): Show |
chr18 | 31371777 | 31419909 |
a0009 | 0/0 | 1040 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | MDWLF others(1035): Show |
chr18 | 31371777 | 31419909 |
a0010 | 0/0 | 1040 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | MDWLF others(1035): Show |
chr18 | 31371777 | 31419909 |
a0011 | 0/0 | 1040 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | MDWLF others(1035): Show |
chr18 | 31371777 | 31419909 |
a0012 | 0/0 | 1040 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | MDWLF others(1035): Show |
chr18 | 31371777 | 31419909 |
a0013 | 0/0 | 1040 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | MDWLF others(1035): Show |
chr18 | 31371777 | 31419909 |
a0014 | 0/0 | 1040 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | MDWLF others(1035): Show |
chr18 | 31371777 | 31419909 |
a0015 | 0/0 | 1053 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | MDWLF others(1048): Show |
chr18 | 31371777 | 31419909 |
a0016 | 0/0 | 1040 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | MDWLF others(1035): Show |
chr18 | 31371777 | 31419909 |
a0017 | 0/0 | 1040 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | MDWLF others(1035): Show |
chr18 | 31371777 | 31419909 |
a0018 | 0/0 | 1040 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | MDWLF others(1035): Show |
chr18 | 31371777 | 31419909 |
a0019 | 0/0 | 1040 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | MDWLF others(1035): Show |
chr18 | 31371777 | 31419909 |
a0020 | 0/0 | 1040 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | MDWLF others(1035): Show |
chr18 | 31371777 | 31419909 |
a0021 | 0/0 | 1040 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | MDWLF others(1035): Show |
chr18 | 31371777 | 31419909 |
a0022 | 0/0 | 1040 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DSG4_chr18_31371777_31419909 | DSG4 | MDWLF others(1035): Show |
chr18 | 31371777 | 31419909 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 3120 | 96 | 11 | 18 | 59 | 3 | 5 | DSG4_chr18_31371777_31419909 | DSG4 | ATGGA others(3115): Show |
chr18 | 31371777 | 31419909 | ||
a0001c0002 | 0/0 | 3120 | 52 | 6 | 9 | 30 | 1 | 6 | DSG4_chr18_31371777_31419909 | DSG4 | ATGGA others(3115): Show |
chr18 | 31371777 | 31419909 | ||
a0001c0003 | 0/0 | 3120 | 34 | 6 | 9 | 15 | 0 | 4 | DSG4_chr18_31371777_31419909 | DSG4 | ATGGA others(3115): Show |
chr18 | 31371777 | 31419909 | ||
a0001c0004 | 0/0 | 3120 | 30 | 5 | 1 | 21 | 1 | 2 | DSG4_chr18_31371777_31419909 | DSG4 | ATGGA others(3115): Show |
chr18 | 31371777 | 31419909 | ||
a0001c0005 | 0/0 | 3120 | 17 | 7 | 0 | 10 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | ATGGA others(3115): Show |
chr18 | 31371777 | 31419909 | ||
a0001c0006 | 0/0 | 3120 | 17 | 2 | 5 | 1 | 0 | 9 | DSG4_chr18_31371777_31419909 | DSG4 | ATGGA others(3115): Show |
chr18 | 31371777 | 31419909 | ||
a0001c0007 | 0/1 | 3120 | 15 | 4 | 4 | 2 | 2 | 2 | DSG4_chr18_31371777_31419909 | DSG4 | ATGGA others(3115): Show |
chr18 | 31371777 | 31419909 | ||
a0001c0008 | 0/0 | 3120 | 11 | 1 | 0 | 6 | 2 | 2 | DSG4_chr18_31371777_31419909 | DSG4 | ATGGA others(3115): Show |
chr18 | 31371777 | 31419909 | ||
a0001c0009 | 0/0 | 3120 | 7 | 7 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | ATGGA others(3115): Show |
chr18 | 31371777 | 31419909 | ||
a0001c0013 | 0/0 | 3120 | 4 | 2 | 0 | 2 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | ATGGA others(3115): Show |
chr18 | 31371777 | 31419909 | ||
a0001c0015 | 0/0 | 3120 | 3 | 0 | 0 | 3 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | ATGGA others(3115): Show |
chr18 | 31371777 | 31419909 | ||
a0001c0016 | 0/0 | 3120 | 3 | 1 | 0 | 0 | 0 | 2 | DSG4_chr18_31371777_31419909 | DSG4 | ATGGA others(3115): Show |
chr18 | 31371777 | 31419909 | ||
a0001c0018 | 0/0 | 3120 | 2 | 2 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | ATGGA others(3115): Show |
chr18 | 31371777 | 31419909 | ||
a0001c0019 | 0/0 | 3120 | 2 | 2 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | ATGGA others(3115): Show |
chr18 | 31371777 | 31419909 | ||
a0001c0025 | 0/0 | 3120 | 2 | 2 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | ATGGA others(3115): Show |
chr18 | 31371777 | 31419909 | ||
a0001c0026 | 0/0 | 3120 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | ATGGA others(3115): Show |
chr18 | 31371777 | 31419909 | ||
a0001c0027 | 0/0 | 3120 | 1 | 0 | 1 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | ATGGA others(3115): Show |
chr18 | 31371777 | 31419909 | ||
a0001c0030 | 0/0 | 3120 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | ATGGA others(3115): Show |
chr18 | 31371777 | 31419909 | ||
a0001c0032 | 0/0 | 3120 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | ATGGA others(3115): Show |
chr18 | 31371777 | 31419909 | ||
a0001c0039 | 0/0 | 3120 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | ATGGA others(3115): Show |
chr18 | 31371777 | 31419909 | ||
a0001c0040 | 0/0 | 3120 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | ATGGA others(3115): Show |
chr18 | 31371777 | 31419909 | ||
a0001c0045 | 0/0 | 3120 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | ATGGA others(3115): Show |
chr18 | 31371777 | 31419909 | ||
a0002c0010 | 0/0 | 3120 | 5 | 5 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | ATGGA others(3115): Show |
chr18 | 31371777 | 31419909 | ||
a0002c0036 | 0/0 | 3120 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | ATGGA others(3115): Show |
chr18 | 31371777 | 31419909 | ||
a0003c0011 | 1/0 | 3120 | 4 | 0 | 2 | 0 | 0 | 1 | DSG4_chr18_31371777_31419909 | DSG4 | ATGGA others(3115): Show |
chr18 | 31371777 | 31419909 | ||
a0004c0012 | 0/0 | 3120 | 4 | 0 | 0 | 0 | 0 | 4 | DSG4_chr18_31371777_31419909 | DSG4 | ATGGA others(3115): Show |
chr18 | 31371777 | 31419909 | ||
a0005c0023 | 0/0 | 3120 | 2 | 2 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | ATGGA others(3115): Show |
chr18 | 31371777 | 31419909 | ||
a0005c0043 | 0/0 | 3120 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | ATGGA others(3115): Show |
chr18 | 31371777 | 31419909 | ||
a0006c0017 | 0/0 | 3120 | 3 | 2 | 0 | 0 | 0 | 1 | DSG4_chr18_31371777_31419909 | DSG4 | ATGGA others(3115): Show |
chr18 | 31371777 | 31419909 | ||
a0007c0014 | 0/0 | 3120 | 3 | 0 | 0 | 3 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | ATGGA others(3115): Show |
chr18 | 31371777 | 31419909 | ||
a0008c0024 | 0/0 | 3120 | 2 | 2 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | ATGGA others(3115): Show |
chr18 | 31371777 | 31419909 | ||
a0009c0021 | 0/0 | 3120 | 2 | 2 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | ATGGA others(3115): Show |
chr18 | 31371777 | 31419909 | ||
a0010c0020 | 0/0 | 3120 | 2 | 2 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | ATGGA others(3115): Show |
chr18 | 31371777 | 31419909 | ||
a0011c0022 | 0/0 | 3120 | 2 | 2 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | ATGGA others(3115): Show |
chr18 | 31371777 | 31419909 | ||
a0012c0035 | 0/0 | 3120 | 1 | 0 | 0 | 0 | 1 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | ATGGA others(3115): Show |
chr18 | 31371777 | 31419909 | ||
a0013c0044 | 0/0 | 3120 | 1 | 0 | 1 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | ATGGA others(3115): Show |
chr18 | 31371777 | 31419909 | ||
a0014c0038 | 0/0 | 3120 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | ATGGA others(3115): Show |
chr18 | 31371777 | 31419909 | ||
a0015c0031 | 0/0 | 3159 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | ATGGA others(3154): Show |
chr18 | 31371777 | 31419909 | ||
a0016c0042 | 0/0 | 3120 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | ATGGA others(3115): Show |
chr18 | 31371777 | 31419909 | ||
a0017c0041 | 0/0 | 3120 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | ATGGA others(3115): Show |
chr18 | 31371777 | 31419909 | ||
a0018c0028 | 0/0 | 3120 | 1 | 0 | 0 | 0 | 0 | 1 | DSG4_chr18_31371777_31419909 | DSG4 | ATGGA others(3115): Show |
chr18 | 31371777 | 31419909 | ||
a0019c0033 | 0/0 | 3120 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | ATGGA others(3115): Show |
chr18 | 31371777 | 31419909 | ||
a0020c0037 | 0/0 | 3120 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | ATGGA others(3115): Show |
chr18 | 31371777 | 31419909 | ||
a0021c0034 | 0/0 | 3120 | 1 | 0 | 0 | 0 | 0 | 1 | DSG4_chr18_31371777_31419909 | DSG4 | ATGGA others(3115): Show |
chr18 | 31371777 | 31419909 | ||
a0022c0029 | 0/0 | 3120 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | ATGGA others(3115): Show |
chr18 | 31371777 | 31419909 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4568 | 92 | 10 | 16 | 58 | 3 | 5 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4563): Show |
chr18 | 31371777 | 31419909 |
a0001c0001t0002 | 0/0 | 4572 | 2 | 0 | 2 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4567): Show |
chr18 | 31371777 | 31419909 |
a0001c0001t0011 | 0/0 | 4568 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4563): Show |
chr18 | 31371777 | 31419909 |
a0001c0001t0014 | 0/0 | 4568 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4563): Show |
chr18 | 31371777 | 31419909 |
a0001c0002t0002 | 0/0 | 4572 | 10 | 2 | 1 | 7 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4567): Show |
chr18 | 31371777 | 31419909 |
a0001c0002t0004 | 0/0 | 4572 | 37 | 3 | 6 | 22 | 1 | 5 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4567): Show |
chr18 | 31371777 | 31419909 |
a0001c0002t0007 | 0/0 | 4572 | 2 | 0 | 2 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4567): Show |
chr18 | 31371777 | 31419909 |
a0001c0002t0015 | 0/0 | 4572 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4567): Show |
chr18 | 31371777 | 31419909 |
a0001c0002t0016 | 0/0 | 4572 | 1 | 0 | 0 | 0 | 0 | 1 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4567): Show |
chr18 | 31371777 | 31419909 |
a0001c0002t0018 | 0/0 | 4572 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4567): Show |
chr18 | 31371777 | 31419909 |
a0001c0003t0003 | 0/0 | 4572 | 32 | 4 | 9 | 15 | 0 | 4 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4567): Show |
chr18 | 31371777 | 31419909 |
a0001c0003t0005 | 0/0 | 4572 | 2 | 2 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4567): Show |
chr18 | 31371777 | 31419909 |
a0001c0004t0002 | 0/0 | 4572 | 25 | 3 | 1 | 18 | 1 | 2 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4567): Show |
chr18 | 31371777 | 31419909 |
a0001c0004t0004 | 0/0 | 4572 | 5 | 2 | 0 | 3 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4567): Show |
chr18 | 31371777 | 31419909 |
a0001c0005t0002 | 0/0 | 4572 | 11 | 4 | 0 | 7 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4567): Show |
chr18 | 31371777 | 31419909 |
a0001c0005t0004 | 0/0 | 4572 | 2 | 2 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4567): Show |
chr18 | 31371777 | 31419909 |
a0001c0005t0009 | 0/0 | 4572 | 2 | 0 | 0 | 2 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | CATCA others(4567): Show |
chr18 | 31371777 | 31419909 |
a0001c0005t0017 | 0/0 | 4572 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4567): Show |
chr18 | 31371777 | 31419909 |
a0001c0005t0019 | 0/0 | 4572 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | CATCA others(4567): Show |
chr18 | 31371777 | 31419909 |
a0001c0006t0001 | 0/0 | 4568 | 17 | 2 | 5 | 1 | 0 | 9 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4563): Show |
chr18 | 31371777 | 31419909 |
a0001c0007t0003 | 0/1 | 4572 | 15 | 4 | 4 | 2 | 2 | 2 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4567): Show |
chr18 | 31371777 | 31419909 |
a0001c0008t0002 | 0/0 | 4572 | 7 | 1 | 0 | 6 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4567): Show |
chr18 | 31371777 | 31419909 |
a0001c0008t0004 | 0/0 | 4572 | 4 | 0 | 0 | 0 | 2 | 2 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4567): Show |
chr18 | 31371777 | 31419909 |
a0001c0009t0003 | 0/0 | 4572 | 2 | 2 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4567): Show |
chr18 | 31371777 | 31419909 |
a0001c0009t0005 | 0/0 | 4572 | 3 | 3 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4567): Show |
chr18 | 31371777 | 31419909 |
a0001c0009t0008 | 0/0 | 4572 | 2 | 2 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4567): Show |
chr18 | 31371777 | 31419909 |
a0001c0013t0001 | 0/0 | 4568 | 4 | 2 | 0 | 2 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4563): Show |
chr18 | 31371777 | 31419909 |
a0001c0015t0001 | 0/0 | 4568 | 3 | 0 | 0 | 3 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4563): Show |
chr18 | 31371777 | 31419909 |
a0001c0016t0001 | 0/0 | 4568 | 3 | 1 | 0 | 0 | 0 | 2 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4563): Show |
chr18 | 31371777 | 31419909 |
a0001c0018t0004 | 0/0 | 4572 | 2 | 2 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4567): Show |
chr18 | 31371777 | 31419909 |
a0001c0019t0003 | 0/0 | 4572 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4567): Show |
chr18 | 31371777 | 31419909 |
a0001c0019t0005 | 0/0 | 4572 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4567): Show |
chr18 | 31371777 | 31419909 |
a0001c0025t0003 | 0/0 | 4572 | 2 | 2 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4567): Show |
chr18 | 31371777 | 31419909 |
a0001c0026t0002 | 0/0 | 4572 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4567): Show |
chr18 | 31371777 | 31419909 |
a0001c0027t0004 | 0/0 | 4572 | 1 | 0 | 1 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4567): Show |
chr18 | 31371777 | 31419909 |
a0001c0030t0002 | 0/0 | 4572 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4567): Show |
chr18 | 31371777 | 31419909 |
a0001c0032t0003 | 0/0 | 4572 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4567): Show |
chr18 | 31371777 | 31419909 |
a0001c0039t0003 | 0/0 | 4572 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4567): Show |
chr18 | 31371777 | 31419909 |
a0001c0040t0004 | 0/0 | 4572 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4567): Show |
chr18 | 31371777 | 31419909 |
a0001c0045t0003 | 0/0 | 4572 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4567): Show |
chr18 | 31371777 | 31419909 |
a0002c0010t0002 | 0/0 | 4572 | 5 | 5 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4567): Show |
chr18 | 31371777 | 31419909 |
a0002c0036t0002 | 0/0 | 4572 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4567): Show |
chr18 | 31371777 | 31419909 |
a0003c0011t0003 | 1/0 | 4572 | 4 | 0 | 2 | 0 | 0 | 1 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4567): Show |
chr18 | 31371777 | 31419909 |
a0004c0012t0001 | 0/0 | 4568 | 4 | 0 | 0 | 0 | 0 | 4 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4563): Show |
chr18 | 31371777 | 31419909 |
a0005c0023t0002 | 0/0 | 4572 | 2 | 2 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4567): Show |
chr18 | 31371777 | 31419909 |
a0005c0043t0003 | 0/0 | 4572 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4567): Show |
chr18 | 31371777 | 31419909 |
a0006c0017t0002 | 0/0 | 4572 | 2 | 2 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4567): Show |
chr18 | 31371777 | 31419909 |
a0006c0017t0004 | 0/0 | 4572 | 1 | 0 | 0 | 0 | 0 | 1 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4567): Show |
chr18 | 31371777 | 31419909 |
a0007c0014t0003 | 0/0 | 4572 | 3 | 0 | 0 | 3 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4567): Show |
chr18 | 31371777 | 31419909 |
a0008c0024t0006 | 0/0 | 4573 | 2 | 2 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4568): Show |
chr18 | 31371777 | 31419909 |
a0009c0021t0010 | 0/0 | 4573 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4568): Show |
chr18 | 31371777 | 31419909 |
a0009c0021t0012 | 0/0 | 4573 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4568): Show |
chr18 | 31371777 | 31419909 |
a0010c0020t0006 | 0/0 | 4573 | 2 | 2 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4568): Show |
chr18 | 31371777 | 31419909 |
a0011c0022t0006 | 0/0 | 4573 | 2 | 2 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4568): Show |
chr18 | 31371777 | 31419909 |
a0012c0035t0003 | 0/0 | 4572 | 1 | 0 | 0 | 0 | 1 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4567): Show |
chr18 | 31371777 | 31419909 |
a0013c0044t0002 | 0/0 | 4572 | 1 | 0 | 1 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4567): Show |
chr18 | 31371777 | 31419909 |
a0014c0038t0004 | 0/0 | 4572 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4567): Show |
chr18 | 31371777 | 31419909 |
a0015c0031t0013 | 0/0 | 4611 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4606): Show |
chr18 | 31371777 | 31419909 |
a0016c0042t0003 | 0/0 | 4572 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4567): Show |
chr18 | 31371777 | 31419909 |
a0017c0041t0002 | 0/0 | 4572 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4567): Show |
chr18 | 31371777 | 31419909 |
a0018c0028t0003 | 0/0 | 4572 | 1 | 0 | 0 | 0 | 0 | 1 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4567): Show |
chr18 | 31371777 | 31419909 |
a0019c0033t0004 | 0/0 | 4572 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4567): Show |
chr18 | 31371777 | 31419909 |
a0020c0037t0003 | 0/0 | 4572 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4567): Show |
chr18 | 31371777 | 31419909 |
a0021c0034t0003 | 0/0 | 4572 | 1 | 0 | 0 | 0 | 0 | 1 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4567): Show |
chr18 | 31371777 | 31419909 |
a0022c0029t0001 | 0/0 | 4568 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | CACCA others(4563): Show |
chr18 | 31371777 | 31419909 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 30 | 4 | 6 | 17 | 1 | 2 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0001t0001g0002 | 0/0 | 9 | 0 | 4 | 5 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0001t0001g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0001t0002g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0001t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0001t0011g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0001t0014g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0002t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0002t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0002t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0002t0004g0003 | 0/0 | 11 | 1 | 1 | 7 | 0 | 2 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0002t0004g0017 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0002t0004g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0002t0004g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0002t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0002t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0002t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0002t0004g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0002t0004g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0002t0004g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0002t0004g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0002t0004g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0002t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0002t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0002t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0002t0004g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0002t0004g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0002t0004g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0002t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0002t0004g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0002t0004g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0002t0004g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0002t0004g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0002t0007g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0002t0015g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0002t0016g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0002t0018g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0003t0003g0005 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0003t0003g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0003t0003g0014 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0003t0003g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0003t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0003t0003g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0003t0003g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0003t0003g0041 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0003t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0003t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0003t0003g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0003t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0003t0003g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0003t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0003t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0003t0003g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0003t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0003t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0003t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0003t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0003t0005g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0003t0005g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0004t0002g0004 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0004t0002g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0004t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0004t0002g0038 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0004t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0004t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0004t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0004t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0004t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0004t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0004t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0004t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0004t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0004t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0004t0004g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0004t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0004t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0004t0004g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0005t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0005t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0005t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0005t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0005t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0005t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0005t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0005t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0005t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0005t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0005t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0005t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0005t0009g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0005t0017g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0005t0019g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0006t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0006t0001g0028 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0006t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0006t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0006t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0006t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0006t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0006t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0006t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0006t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0006t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0006t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0006t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0006t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0006t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0007t0003g0006 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0007t0003g0008 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0007t0003g0013 | 0/1 | 3 | 0 | 0 | 0 | 1 | 1 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0007t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0007t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0007t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0007t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0007t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0007t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0007t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0008t0002g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0008t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0008t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0008t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0008t0004g0006 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0008t0004g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0009t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0009t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0009t0005g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0009t0008g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0013t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0013t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0013t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0013t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0015t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0015t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0016t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0016t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0016t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0018t0004g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0019t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0019t0005g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0025t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0025t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0026t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0027t0004g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0030t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0032t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0039t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0040t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0001c0045t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0002c0010t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0002c0010t0002g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0002c0010t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0002c0036t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0003c0011t0003g0026 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0003c0011t0003g0086 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0003c0011t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0004c0012t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0004c0012t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0004c0012t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0005c0023t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0005c0023t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0005c0043t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0006c0017t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0006c0017t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0006c0017t0004g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0007c0014t0003g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0007c0014t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0008c0024t0006g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0009c0021t0010g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0009c0021t0012g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0010c0020t0006g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0011c0022t0006g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0011c0022t0006g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0012c0035t0003g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0013c0044t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0014c0038t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0015c0031t0013g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0016c0042t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0017c0041t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0018c0028t0003g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0019c0033t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0020c0037t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0021c0034t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
a0022c0029t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0004 | t0002 | g0038 | EUR | GBR | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG00099 | hp2 | a0001 | c0008 | t0004 | g0006 | EUR | GBR | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG00140 | hp1 | a0001 | c0007 | t0003 | g0013 | EUR | GBR | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG00140 | hp2 | a0001 | c0008 | t0004 | g0006 | EUR | GBR | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0132 | EUR | FIN | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG00323 | hp2 | a0012 | c0035 | t0003 | g0008 | EUR | FIN | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG00408 | hp1 | a0001 | c0002 | t0004 | g0003 | EAS | CHS | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG00423 | hp1 | a0001 | c0004 | t0002 | g0167 | EAS | CHS | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG00438 | hp1 | a0001 | c0002 | t0002 | g0143 | EAS | CHS | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG00544 | hp1 | a0001 | c0002 | t0004 | g0018 | EAS | CHS | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG00558 | hp2 | a0001 | c0004 | t0002 | g0004 | EAS | CHS | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG00609 | hp2 | a0001 | c0003 | t0003 | g0010 | EAS | CHS | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG00639 | hp2 | a0001 | c0002 | t0004 | g0147 | AMR | PUR | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG00735 | hp1 | a0001 | c0003 | t0003 | g0041 | AMR | PUR | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG00735 | hp2 | a0001 | c0007 | t0003 | g0074 | AMR | PUR | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG00738 | hp1 | a0001 | c0002 | t0004 | g0196 | AMR | PUR | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG01070 | hp2 | a0003 | c0011 | t0003 | g0026 | AMR | PUR | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG01071 | hp1 | a0001 | c0002 | t0002 | g0109 | AMR | PUR | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG01081 | hp1 | a0001 | c0003 | t0003 | g0040 | AMR | PUR | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG01099 | hp1 | a0001 | c0003 | t0003 | g0005 | AMR | PUR | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG01099 | hp2 | a0001 | c0002 | t0004 | g0139 | AMR | PUR | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG01109 | hp2 | a0001 | c0004 | t0002 | g0159 | AMR | PUR | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG01167 | hp1 | a0001 | c0002 | t0007 | g0027 | AMR | PUR | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG01169 | hp1 | a0001 | c0002 | t0007 | g0027 | AMR | PUR | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG01169 | hp2 | a0001 | c0006 | t0001 | g0028 | AMR | PUR | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG01175 | hp1 | a0013 | c0044 | t0002 | g0154 | AMR | PUR | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG01175 | hp2 | a0001 | c0006 | t0001 | g0172 | AMR | PUR | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG01192 | hp1 | a0001 | c0006 | t0001 | g0097 | AMR | PUR | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG01192 | hp2 | a0003 | c0011 | t0003 | g0087 | AMR | PUR | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG01255 | hp2 | a0001 | c0007 | t0003 | g0008 | AMR | CLM | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG01256 | hp1 | a0001 | c0002 | t0004 | g0003 | AMR | CLM | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG01258 | hp1 | a0001 | c0002 | t0004 | g0018 | AMR | CLM | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG01258 | hp2 | a0001 | c0003 | t0003 | g0207 | AMR | CLM | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG01361 | hp1 | a0001 | c0006 | t0001 | g0171 | AMR | CLM | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG01361 | hp2 | a0001 | c0007 | t0003 | g0008 | AMR | CLM | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG01433 | hp2 | a0001 | c0003 | t0003 | g0040 | AMR | CLM | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG01496 | hp1 | a0001 | c0006 | t0001 | g0163 | AMR | CLM | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG01496 | hp2 | a0001 | c0003 | t0003 | g0029 | AMR | CLM | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG01515 | hp1 | a0001 | c0007 | t0003 | g0006 | EUR | IBS | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG01884 | hp1 | a0001 | c0018 | t0004 | g0002 | AFR | ACB | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG01884 | hp2 | a0001 | c0009 | t0005 | g0012 | AFR | ACB | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG01891 | hp1 | a0005 | c0043 | t0003 | g0169 | AFR | ACB | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG01891 | hp2 | a0001 | c0039 | t0003 | g0064 | AFR | ACB | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG01943 | hp1 | a0001 | c0007 | t0003 | g0006 | AMR | PEL | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG01943 | hp2 | a0001 | c0003 | t0003 | g0129 | AMR | PEL | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG01975 | hp2 | a0001 | c0003 | t0003 | g0029 | AMR | PEL | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG01981 | hp1 | a0001 | c0003 | t0003 | g0212 | AMR | PEL | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02027 | hp2 | a0001 | c0013 | t0001 | g0079 | EAS | KHV | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02040 | hp1 | a0001 | c0005 | t0002 | g0007 | EAS | KHV | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02040 | hp2 | a0001 | c0005 | t0019 | g0007 | EAS | KHV | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02056 | hp1 | a0001 | c0003 | t0003 | g0209 | EAS | KHV | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02056 | hp2 | a0014 | c0038 | t0004 | g0071 | EAS | KHV | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02074 | hp1 | a0001 | c0007 | t0003 | g0062 | EAS | KHV | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02074 | hp2 | a0001 | c0002 | t0004 | g0121 | EAS | KHV | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02083 | hp1 | a0001 | c0002 | t0004 | g0003 | EAS | KHV | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02083 | hp2 | a0001 | c0008 | t0002 | g0023 | EAS | KHV | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02129 | hp1 | a0001 | c0007 | t0003 | g0073 | EAS | KHV | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02129 | hp2 | a0001 | c0003 | t0003 | g0014 | EAS | KHV | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02132 | hp1 | a0001 | c0002 | t0004 | g0188 | EAS | KHV | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02132 | hp2 | a0001 | c0002 | t0002 | g0120 | EAS | KHV | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02145 | hp2 | a0001 | c0007 | t0003 | g0067 | AFR | ACB | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | CDX | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02165 | hp1 | a0001 | c0004 | t0002 | g0016 | EAS | CDX | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CDX | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02257 | hp1 | a0005 | c0023 | t0002 | g0170 | AFR | ACB | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02257 | hp2 | a0008 | c0024 | t0006 | g0039 | AFR | ACB | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02258 | hp1 | a0001 | c0007 | t0003 | g0008 | AFR | ACB | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02258 | hp2 | a0001 | c0009 | t0005 | g0012 | AFR | ACB | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02280 | hp1 | a0006 | c0017 | t0002 | g0099 | AFR | ACB | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02300 | hp1 | a0001 | c0027 | t0004 | g0003 | AMR | PEL | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02451 | hp1 | a0001 | c0009 | t0008 | g0019 | AFR | ACB | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02451 | hp2 | a0001 | c0019 | t0003 | g0125 | AFR | ACB | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02572 | hp1 | a0001 | c0004 | t0004 | g0161 | AFR | GWD | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02572 | hp2 | a0001 | c0026 | t0002 | g0146 | AFR | GWD | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02602 | hp1 | a0003 | c0011 | t0003 | g0026 | SAS | PJL | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02602 | hp2 | a0001 | c0006 | t0001 | g0166 | SAS | PJL | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02615 | hp1 | a0001 | c0009 | t0003 | g0048 | AFR | GWD | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02615 | hp2 | a0001 | c0019 | t0005 | g0134 | AFR | GWD | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02622 | hp1 | a0001 | c0018 | t0004 | g0002 | AFR | GWD | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02622 | hp2 | a0002 | c0010 | t0002 | g0024 | AFR | GWD | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02630 | hp1 | a0001 | c0004 | t0004 | g0168 | AFR | GWD | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02630 | hp2 | a0001 | c0002 | t0002 | g0091 | AFR | GWD | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02647 | hp1 | a0001 | c0003 | t0003 | g0213 | AFR | GWD | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02647 | hp2 | a0001 | c0002 | t0018 | g0044 | AFR | GWD | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02683 | hp1 | a0001 | c0007 | t0003 | g0013 | SAS | PJL | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02683 | hp2 | a0001 | c0006 | t0001 | g0156 | SAS | PJL | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02698 | hp1 | a0001 | c0003 | t0003 | g0203 | SAS | PJL | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02723 | hp1 | a0016 | c0042 | t0003 | g0047 | AFR | GWD | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02723 | hp2 | a0006 | c0017 | t0002 | g0100 | AFR | GWD | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02735 | hp1 | a0001 | c0006 | t0001 | g0028 | SAS | PJL | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02735 | hp2 | a0001 | c0003 | t0003 | g0211 | SAS | PJL | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02738 | hp1 | a0001 | c0003 | t0003 | g0041 | SAS | PJL | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02738 | hp2 | a0001 | c0004 | t0002 | g0151 | SAS | PJL | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02809 | hp1 | a0009 | c0021 | t0012 | g0055 | AFR | GWD | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02809 | hp2 | a0001 | c0007 | t0003 | g0022 | AFR | GWD | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02818 | hp1 | a0001 | c0002 | t0004 | g0126 | AFR | GWD | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02818 | hp2 | a0001 | c0013 | t0001 | g0075 | AFR | GWD | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02886 | hp1 | a0001 | c0016 | t0001 | g0063 | AFR | GWD | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02886 | hp2 | a0002 | c0010 | t0002 | g0025 | AFR | GWD | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02895 | hp1 | a0017 | c0041 | t0002 | g0060 | AFR | GWD | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02895 | hp2 | a0002 | c0010 | t0002 | g0025 | AFR | GWD | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02922 | hp1 | a0001 | c0009 | t0008 | g0019 | AFR | ESN | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02965 | hp1 | a0001 | c0005 | t0002 | g0061 | AFR | ESN | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02965 | hp2 | a0001 | c0005 | t0002 | g0088 | AFR | ESN | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02970 | hp1 | a0001 | c0006 | t0001 | g0165 | AFR | ESN | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02970 | hp2 | a0001 | c0003 | t0005 | g0202 | AFR | ESN | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02976 | hp1 | a0010 | c0020 | t0006 | g0020 | AFR | ESN | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02976 | hp2 | a0001 | c0003 | t0003 | g0033 | AFR | ESN | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG03017 | hp1 | a0018 | c0028 | t0003 | g0192 | SAS | PJL | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG03017 | hp2 | a0001 | c0004 | t0002 | g0038 | SAS | PJL | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG03041 | hp1 | a0001 | c0008 | t0002 | g0084 | AFR | GWD | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG03041 | hp2 | a0011 | c0022 | t0006 | g0059 | AFR | GWD | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG03098 | hp2 | a0001 | c0005 | t0002 | g0085 | AFR | MSL | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG03130 | hp1 | a0008 | c0024 | t0006 | g0039 | AFR | ESN | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG03130 | hp2 | a0019 | c0033 | t0004 | g0197 | AFR | ESN | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG03139 | hp1 | a0001 | c0001 | t0011 | g0001 | AFR | ESN | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG03139 | hp2 | a0001 | c0025 | t0003 | g0217 | AFR | ESN | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG03195 | hp1 | a0001 | c0025 | t0003 | g0218 | AFR | ESN | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG03195 | hp2 | a0001 | c0002 | t0004 | g0104 | AFR | ESN | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG03209 | hp1 | a0001 | c0005 | t0004 | g0049 | AFR | MSL | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG03209 | hp2 | a0001 | c0045 | t0003 | g0164 | AFR | MSL | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG03225 | hp1 | a0001 | c0005 | t0004 | g0051 | AFR | MSL | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG03225 | hp2 | a0001 | c0009 | t0005 | g0012 | AFR | MSL | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG03453 | hp1 | a0001 | c0003 | t0003 | g0108 | AFR | MSL | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG03453 | hp2 | a0001 | c0005 | t0017 | g0050 | AFR | MSL | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG03486 | hp1 | a0001 | c0002 | t0002 | g0176 | AFR | MSL | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG03486 | hp2 | a0001 | c0006 | t0001 | g0094 | AFR | MSL | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG03490 | hp1 | a0006 | c0017 | t0004 | g0101 | SAS | PJL | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG03490 | hp2 | a0001 | c0006 | t0001 | g0036 | SAS | PJL | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG03491 | hp1 | a0004 | c0012 | t0001 | g0021 | SAS | PJL | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG03491 | hp2 | a0001 | c0006 | t0001 | g0175 | SAS | PJL | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG03492 | hp1 | a0001 | c0006 | t0001 | g0036 | SAS | PJL | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG03492 | hp2 | a0004 | c0012 | t0001 | g0021 | SAS | PJL | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG03516 | hp2 | a0010 | c0020 | t0006 | g0020 | AFR | ESN | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG03540 | hp1 | a0009 | c0021 | t0010 | g0056 | AFR | GWD | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG03540 | hp2 | a0020 | c0037 | t0003 | g0022 | AFR | GWD | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG03654 | hp1 | a0001 | c0006 | t0001 | g0152 | SAS | PJL | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG03654 | hp2 | a0001 | c0002 | t0004 | g0003 | SAS | PJL | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG03669 | hp1 | a0001 | c0006 | t0001 | g0160 | SAS | PJL | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG03688 | hp1 | a0021 | c0034 | t0003 | g0070 | SAS | STU | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG03688 | hp2 | a0001 | c0008 | t0004 | g0068 | SAS | STU | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG03710 | hp1 | a0004 | c0012 | t0001 | g0065 | SAS | PJL | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG03710 | hp2 | a0001 | c0002 | t0004 | g0190 | SAS | PJL | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG03834 | hp1 | a0001 | c0016 | t0001 | g0072 | SAS | BEB | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG03927 | hp1 | a0001 | c0008 | t0004 | g0006 | SAS | BEB | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG03927 | hp2 | a0001 | c0002 | t0004 | g0017 | SAS | BEB | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG03942 | hp1 | a0001 | c0016 | t0001 | g0045 | SAS | BEB | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG03942 | hp2 | a0004 | c0012 | t0001 | g0199 | SAS | BEB | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG04115 | hp2 | a0001 | c0002 | t0004 | g0003 | SAS | STU | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG04184 | hp1 | a0001 | c0002 | t0016 | g0194 | SAS | BEB | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG04184 | hp2 | a0001 | c0002 | t0004 | g0193 | SAS | BEB | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG04204 | hp1 | a0001 | c0006 | t0001 | g0098 | SAS | STU | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG04204 | hp2 | a0001 | c0003 | t0003 | g0014 | SAS | STU | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | STU | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG04228 | hp2 | a0001 | c0007 | t0003 | g0083 | SAS | STU | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18522 | hp1 | a0001 | c0004 | t0002 | g0096 | AFR | YRI | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18522 | hp2 | a0002 | c0010 | t0002 | g0052 | AFR | YRI | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18612 | hp1 | a0001 | c0003 | t0003 | g0010 | EAS | CHB | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18612 | hp2 | a0001 | c0015 | t0001 | g0035 | EAS | CHB | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18747 | hp1 | a0001 | c0013 | t0001 | g0082 | EAS | CHB | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18747 | hp2 | a0001 | c0002 | t0002 | g0195 | EAS | CHB | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18906 | hp1 | a0002 | c0036 | t0002 | g0053 | AFR | YRI | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18940 | hp2 | a0001 | c0004 | t0002 | g0037 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18942 | hp1 | a0001 | c0008 | t0002 | g0023 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18942 | hp2 | a0001 | c0004 | t0002 | g0004 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18944 | hp1 | a0001 | c0008 | t0002 | g0011 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18944 | hp2 | a0001 | c0004 | t0002 | g0016 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18947 | hp2 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18948 | hp1 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18952 | hp1 | a0001 | c0004 | t0002 | g0113 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18954 | hp1 | a0001 | c0002 | t0004 | g0017 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18956 | hp2 | a0001 | c0004 | t0002 | g0004 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18957 | hp1 | a0001 | c0002 | t0002 | g0145 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18959 | hp1 | a0001 | c0004 | t0002 | g0157 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18959 | hp2 | a0001 | c0004 | t0004 | g0173 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18962 | hp2 | a0001 | c0002 | t0004 | g0178 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18964 | hp1 | a0001 | c0008 | t0002 | g0066 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18965 | hp1 | a0001 | c0005 | t0002 | g0007 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18965 | hp2 | a0001 | c0002 | t0002 | g0144 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18966 | hp1 | a0001 | c0005 | t0009 | g0007 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18966 | hp2 | a0001 | c0003 | t0003 | g0014 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18967 | hp2 | a0001 | c0008 | t0002 | g0011 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18968 | hp2 | a0001 | c0004 | t0004 | g0004 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18970 | hp2 | a0001 | c0003 | t0003 | g0215 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18971 | hp1 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18971 | hp2 | a0001 | c0004 | t0002 | g0153 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18972 | hp2 | a0001 | c0002 | t0004 | g0184 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18975 | hp1 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18977 | hp1 | a0001 | c0008 | t0002 | g0011 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18978 | hp1 | a0001 | c0002 | t0004 | g0187 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18979 | hp1 | a0007 | c0014 | t0003 | g0210 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18981 | hp1 | a0001 | c0002 | t0004 | g0183 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18985 | hp1 | a0022 | c0029 | t0001 | g0002 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18985 | hp2 | a0001 | c0004 | t0002 | g0177 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18987 | hp2 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18990 | hp1 | a0001 | c0002 | t0004 | g0185 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18990 | hp2 | a0001 | c0001 | t0014 | g0138 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18991 | hp2 | a0001 | c0003 | t0003 | g0205 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18993 | hp2 | a0001 | c0004 | t0002 | g0004 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18995 | hp1 | a0001 | c0015 | t0001 | g0035 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18995 | hp2 | a0001 | c0004 | t0002 | g0037 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA18999 | hp2 | a0001 | c0005 | t0002 | g0078 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19000 | hp1 | a0001 | c0003 | t0003 | g0216 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19000 | hp2 | a0001 | c0002 | t0004 | g0189 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19002 | hp1 | a0001 | c0004 | t0002 | g0016 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19003 | hp2 | a0001 | c0003 | t0003 | g0010 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19005 | hp1 | a0001 | c0005 | t0009 | g0007 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19005 | hp2 | a0001 | c0002 | t0015 | g0191 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19009 | hp2 | a0001 | c0002 | t0002 | g0219 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19010 | hp1 | a0001 | c0015 | t0001 | g0150 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19010 | hp2 | a0001 | c0005 | t0002 | g0080 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19012 | hp1 | a0001 | c0004 | t0002 | g0004 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19012 | hp2 | a0001 | c0003 | t0003 | g0208 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19030 | hp1 | a0001 | c0004 | t0002 | g0095 | AFR | LWK | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19030 | hp2 | a0001 | c0003 | t0005 | g0201 | AFR | LWK | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19043 | hp1 | a0001 | c0009 | t0003 | g0057 | AFR | LWK | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19043 | hp2 | a0001 | c0005 | t0002 | g0089 | AFR | LWK | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19054 | hp2 | a0001 | c0003 | t0003 | g0005 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19056 | hp2 | a0007 | c0014 | t0003 | g0005 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19057 | hp1 | a0007 | c0014 | t0003 | g0005 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19057 | hp2 | a0001 | c0002 | t0002 | g0128 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19060 | hp2 | a0001 | c0005 | t0002 | g0081 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19062 | hp1 | a0001 | c0003 | t0003 | g0005 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19063 | hp2 | a0001 | c0002 | t0004 | g0017 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19066 | hp1 | a0001 | c0004 | t0004 | g0004 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19068 | hp2 | a0001 | c0002 | t0004 | g0043 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19072 | hp1 | a0001 | c0005 | t0002 | g0077 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19072 | hp2 | a0001 | c0004 | t0002 | g0004 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19076 | hp1 | a0001 | c0004 | t0002 | g0004 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19076 | hp2 | a0001 | c0006 | t0001 | g0009 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19079 | hp1 | a0001 | c0003 | t0003 | g0032 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19079 | hp2 | a0001 | c0002 | t0004 | g0182 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19081 | hp2 | a0001 | c0002 | t0004 | g0043 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19083 | hp2 | a0001 | c0004 | t0002 | g0004 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19086 | hp2 | a0001 | c0005 | t0002 | g0076 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19088 | hp1 | a0001 | c0003 | t0003 | g0010 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19089 | hp2 | a0001 | c0002 | t0004 | g0180 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19091 | hp2 | a0001 | c0003 | t0003 | g0005 | EAS | JPT | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19240 | hp1 | a0001 | c0013 | t0001 | g0046 | AFR | YRI | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA19240 | hp2 | a0001 | c0030 | t0002 | g0200 | AFR | YRI | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ASW | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ASW | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA20752 | hp1 | a0001 | c0002 | t0004 | g0186 | EUR | TSI | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0118 | EUR | TSI | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG01123 | hp2 | a0001 | c0002 | t0004 | g0181 | AMR | CLM | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02109 | hp1 | a0001 | c0002 | t0004 | g0003 | AFR | ACB | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02109 | hp2 | a0015 | c0031 | t0013 | g0090 | AFR | ACB | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02559 | hp1 | a0001 | c0040 | t0004 | g0054 | AFR | ACB | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG02559 | hp2 | a0001 | c0032 | t0003 | g0032 | AFR | ACB | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG03471 | hp1 | a0005 | c0023 | t0002 | g0162 | AFR | MSL | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG03471 | hp2 | a0001 | c0007 | t0003 | g0069 | AFR | MSL | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | USA | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
HG06807 | hp2 | a0011 | c0022 | t0006 | g0058 | AFR | USA | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA20300 | hp1 | a0002 | c0010 | t0002 | g0024 | AFR | USA | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA21309 | hp1 | a0001 | c0004 | t0002 | g0174 | AFR | LWK | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
NA21309 | hp2 | a0001 | c0003 | t0003 | g0033 | AFR | LWK | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
homoSapiens | chm13v2 | a0001 | c0007 | t0003 | g0013 | REF | REF | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
homoSapiens | grch38p0 | a0003 | c0011 | t0003 | g0086 | REF | REF | DSG4_chr18_31371777_31419909 | DSG4 | chr18 | 31371777 | 31419909 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:31388386 | C | T | 1 | a0006 | 3 | HG02280.hp1 HG02723.hp2 HG03490.hp1 |
missense_variant | MODERATE | c.236C>T | p.Ser79Leu | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 4/16 | 371/4572 | 236/3123 | 79/1040 | chr18 | 31388386 | |||
chr18:31388884 | G | A | 1 | a0021 | 1 | HG03688.hp1 | missense_variant | MODERATE | c.383G>A | p.Arg128Gln | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 5/16 | 518/4572 | 383/3123 | 128/1040 | chr18 | 31388884 | |||
chr18:31388961 | G | A | 1 | a0010 | 2 | HG02976.hp1 HG03516.hp2 |
missense_variant | MODERATE | c.460G>A | p.Ala154Thr | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 5/16 | 595/4572 | 460/3123 | 154/1040 | chr18 | 31388961 | |||
chr18:31391108 | G | A | 1 | a0012 | 1 | HG00323.hp2 | missense_variant | MODERATE | c.715G>A | p.Gly239Ser | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 7/16 | 850/4572 | 715/3123 | 239/1040 | chr18 | 31391108 | |||
chr18:31392315 | A | G | 1 | a0019 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.980A>G | p.Asn327Ser | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/16 | 1115/4572 | 980/3123 | 327/1040 | chr18 | 31392315 | |||
chr18:31399464 | G | A | 1 | a0006 | 3 | HG02280.hp1 HG02723.hp2 HG03490.hp1 |
missense_variant | MODERATE | c.1198G>A | p.Gly400Arg | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 9/16 | 1333/4572 | 1198/3123 | 400/1040 | chr18 | 31399464 | |||
chr18:31400919 | T | C | 1 | a0005 | 3 | HG01891.hp1 HG02257.hp1 HG03471.hp1 |
missense_variant | MODERATE | c.1316T>C | p.Ile439Thr | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 10/16 | 1451/4572 | 1316/3123 | 439/1040 | chr18 | 31400919 | |||
chr18:31403602 | T | C | 1 | a0002 | 6 | HG02622.hp2 HG02886.hp2 HG02895.hp2 others(3): Show |
missense_variant | MODERATE | c.1604T>C | p.Ile535Thr | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 11/16 | 1739/4572 | 1604/3123 | 535/1040 | chr18 | 31403602 | |||
chr18:31406095 | C | A | 1 | a0018 | 1 | HG03017.hp1 | missense_variant | MODERATE | c.1655C>A | p.Thr552Lys | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 12/16 | 1790/4572 | 1655/3123 | 552/1040 | chr18 | 31406095 | |||
chr18:31406210 | T | A | 1 | a0020 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.1770T>A | p.Asp590Glu | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 12/16 | 1905/4572 | 1770/3123 | 590/1040 | chr18 | 31406210 | |||
chr18:31406370 | A | C | 21 | a0001 a0002 a0004 others(18): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
missense_variant | MODERATE | c.1930A>C | p.Ile644Leu | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 12/16 | 2065/4572 | 1930/3123 | 644/1040 | chr18 | 31406370 | |||
chr18:31409523 | C | T | 1 | a0017 | 1 | HG02895.hp1 | missense_variant | MODERATE | c.2005C>T | p.Pro669Ser | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 13/16 | 2140/4572 | 2005/3123 | 669/1040 | chr18 | 31409523 | |||
chr18:31409775 | G | A | 1 | a0022 | 1 | NA18985.hp1 | missense_variant | MODERATE | c.2104G>A | p.Ala702Thr | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 14/16 | 2239/4572 | 2104/3123 | 702/1040 | chr18 | 31409775 | |||
chr18:31411303 | G | A | 1 | a0014 | 1 | HG02056.hp2 | missense_variant | MODERATE | c.2210G>A | p.Gly737Asp | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 15/16 | 2345/4572 | 2210/3123 | 737/1040 | chr18 | 31411303 | |||
chr18:31411386 | A | ACCTCAGG others(32): Show |
1 | a0015 | 1 | HG02109.hp2 | conservative_inframe_insertion | MODERATE | c.2295_2296insTCAGGG others(33): Show |
p.Thr765_Leu766insSe others(37): Show |
DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 15/16 | 2431/4572 | 2296/3123 | 766/1040 | INFO_REALIGN_3_PRIME | chr18 | 31411386 | ||
chr18:31411386 | A | G | 3 | a0008 a0010 a0011 |
6 | HG02257.hp2 HG02976.hp1 HG03041.hp2 others(3): Show |
missense_variant | MODERATE | c.2293A>G | p.Thr765Ala | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 15/16 | 2428/4572 | 2293/3123 | 765/1040 | chr18 | 31411386 | |||
chr18:31412838 | C | T | 1 | a0015 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.2366C>T | p.Ala789Val | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 16/16 | 2501/4572 | 2366/3123 | 789/1040 | chr18 | 31412838 | |||
chr18:31412859 | G | T | 1 | a0016 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.2387G>T | p.Gly796Val | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 16/16 | 2522/4572 | 2387/3123 | 796/1040 | chr18 | 31412859 | |||
chr18:31413110 | T | A | 1 | a0008 | 2 | HG02257.hp2 HG03130.hp1 |
missense_variant | MODERATE | c.2638T>A | p.Ser880Thr | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 16/16 | 2773/4572 | 2638/3123 | 880/1040 | chr18 | 31413110 | |||
chr18:31413268 | T | G | 1 | a0004 | 4 | HG03491.hp1 HG03492.hp2 HG03710.hp1 others(1): Show |
missense_variant | MODERATE | c.2796T>G | p.Asn932Lys | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 16/16 | 2931/4572 | 2796/3123 | 932/1040 | chr18 | 31413268 | |||
chr18:31413492 | T | C | 1 | a0013 | 1 | HG01175.hp1 | missense_variant | MODERATE | c.3020T>C | p.Met1007Thr | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 16/16 | 3155/4572 | 3020/3123 | 1007/1040 | chr18 | 31413492 | |||
chr18:31413495 | G | A | 1 | a0009 | 2 | HG02809.hp1 HG03540.hp1 |
missense_variant | MODERATE | c.3023G>A | p.Ser1008Asn | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 16/16 | 3158/4572 | 3023/3123 | 1008/1040 | chr18 | 31413495 | |||
chr18:31413541 | G | A | 4 | a0008 a0009 a0010 others(1): Show |
8 | HG02257.hp2 HG02809.hp1 HG02976.hp1 others(5): Show |
missense_variant | MODERATE | c.3069G>A | p.Met1023Ile | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 16/16 | 3204/4572 | 3069/3123 | 1023/1040 | chr18 | 31413541 | |||
chr18:31413576 | T | C | 1 | a0007 | 3 | NA18979.hp1 NA19056.hp2 NA19057.hp1 |
missense_variant | MODERATE | c.3104T>C | p.Ile1035Thr | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 16/16 | 3239/4572 | 3104/3123 | 1035/1040 | chr18 | 31413576 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:31376932 | A | G | 1 | a0001c0025 | 2 | HG03139.hp2 HG03195.hp1 |
synonymous_variant | LOW | c.21A>G | p.Arg7Arg | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/16 | 156/4572 | 21/3123 | 7/1040 | chr18 | 31376932 | |||
chr18:31376941 | C | T | 7 | a0001c0004 a0001c0006 a0001c0045 others(4): Show |
54 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(51): Show |
synonymous_variant | LOW | c.30C>T | p.Cys10Cys | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/16 | 165/4572 | 30/3123 | 10/1040 | chr18 | 31376941 | |||
chr18:31388408 | G | A | 24 | a0001c0001 a0001c0002 a0001c0003 others(21): Show |
259 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(256): Show |
synonymous_variant | LOW | c.258G>A | p.Arg86Arg | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 4/16 | 393/4572 | 258/3123 | 86/1040 | chr18 | 31388408 | |||
chr18:31388996 | C | T | 32 | a0001c0001 a0001c0002 a0001c0003 others(29): Show |
295 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(292): Show |
synonymous_variant | LOW | c.495C>T | p.Ser165Ser | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 5/16 | 630/4572 | 495/3123 | 165/1040 | chr18 | 31388996 | |||
chr18:31392190 | G | A | 2 | a0001c0025 a0001c0026 |
3 | HG02572.hp2 HG03139.hp2 HG03195.hp1 |
synonymous_variant | LOW | c.855G>A | p.Ser285Ser | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/16 | 990/4572 | 855/3123 | 285/1040 | chr18 | 31392190 | |||
chr18:31399394 | T | C | 1 | a0001c0027 | 1 | HG02300.hp1 | synonymous_variant | LOW | c.1128T>C | p.Val376Val | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 9/16 | 1263/4572 | 1128/3123 | 376/1040 | chr18 | 31399394 | |||
chr18:31403537 | C | T | 4 | a0001c0018 a0001c0019 a0001c0032 others(1): Show |
6 | HG01884.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
synonymous_variant | LOW | c.1539C>T | p.Ile513Ile | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 11/16 | 1674/4572 | 1539/3123 | 513/1040 | chr18 | 31403537 | |||
chr18:31406172 | T | C | 2 | a0002c0036 a0017c0041 |
2 | HG02895.hp1 NA18906.hp1 |
synonymous_variant | LOW | c.1732T>C | p.Leu578Leu | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 12/16 | 1867/4572 | 1732/3123 | 578/1040 | chr18 | 31406172 | |||
chr18:31409522 | T | C | 1 | a0017c0041 | 1 | HG02895.hp1 | synonymous_variant | LOW | c.2004T>C | p.Ala668Ala | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 13/16 | 2139/4572 | 2004/3123 | 668/1040 | chr18 | 31409522 | |||
chr18:31412863 | A | C | 3 | a0001c0032 a0001c0039 a0001c0045 |
3 | HG01891.hp2 HG02559.hp2 HG03209.hp2 |
synonymous_variant | LOW | c.2391A>C | p.Arg797Arg | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 16/16 | 2526/4572 | 2391/3123 | 797/1040 | chr18 | 31412863 | |||
chr18:31412914 | C | T | 1 | a0001c0030 | 1 | NA19240.hp2 | synonymous_variant | LOW | c.2442C>T | p.Pro814Pro | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 16/16 | 2577/4572 | 2442/3123 | 814/1040 | chr18 | 31412914 | |||
chr18:31413061 | A | C | 1 | a0001c0015 | 3 | NA18612.hp2 NA18995.hp1 NA19010.hp1 |
synonymous_variant | LOW | c.2589A>C | p.Pro863Pro | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 16/16 | 2724/4572 | 2589/3123 | 863/1040 | chr18 | 31413061 | |||
chr18:31413220 | A | G | 7 | a0001c0001 a0001c0006 a0001c0013 others(4): Show |
128 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(125): Show |
synonymous_variant | LOW | c.2748A>G | p.Pro916Pro | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 16/16 | 2883/4572 | 2748/3123 | 916/1040 | chr18 | 31413220 | |||
chr18:31413538 | C | A | 28 | a0001c0001 a0001c0002 a0001c0004 others(25): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(264): Show |
synonymous_variant | LOW | c.3066C>A | p.Pro1022Pro | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 16/16 | 3201/4572 | 3066/3123 | 1022/1040 | chr18 | 31413538 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:31376779 | C | T | 2 | a0001c0005t0009 a0001c0005t0019 |
3 | HG02040.hp2 NA18966.hp1 NA19005.hp1 |
5_prime_UTR_variant | MODIFIER | c.-133C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/16 | 133 | chr18 | 31376779 | ||||||
chr18:31376835 | G | A | 1 | a0009c0021t0010 | 1 | HG03540.hp1 | 5_prime_UTR_variant | MODIFIER | c.-77G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/16 | 77 | chr18 | 31376835 | ||||||
chr18:31376869 | A | C | 1 | a0001c0002t0018 | 1 | HG02647.hp2 | 5_prime_UTR_variant | MODIFIER | c.-43A>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/16 | 43 | chr18 | 31376869 | ||||||
chr18:31413626 | C | T | 14 | a0001c0002t0004 a0001c0002t0015 a0001c0002t0016 others(11): Show |
59 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*31C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 16/16 | 31 | chr18 | 31413626 | ||||||
chr18:31413666 | A | G | 3 | a0008c0024t0006 a0010c0020t0006 a0011c0022t0006 |
6 | HG02257.hp2 HG02976.hp1 HG03041.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*71A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 16/16 | 71 | chr18 | 31413666 | ||||||
chr18:31413721 | G | A | 3 | a0008c0024t0006 a0010c0020t0006 a0011c0022t0006 |
6 | HG02257.hp2 HG02976.hp1 HG03041.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*126G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 16/16 | 126 | chr18 | 31413721 | ||||||
chr18:31413724 | A | G | 1 | a0001c0005t0019 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*129A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 16/16 | 129 | chr18 | 31413724 | ||||||
chr18:31413735 | A | G | 1 | a0001c0009t0008 | 2 | HG02451.hp1 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*140A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 16/16 | 140 | chr18 | 31413735 | ||||||
chr18:31413783 | T | A | 1 | a0001c0001t0011 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*188T>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 16/16 | 188 | chr18 | 31413783 | ||||||
chr18:31413933 | C | T | 1 | a0001c0005t0017 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*338C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 16/16 | 338 | chr18 | 31413933 | ||||||
chr18:31414049 | A | T | 1 | a0001c0001t0014 | 1 | NA18990.hp2 | 3_prime_UTR_variant | MODIFIER | c.*454A>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 16/16 | 454 | chr18 | 31414049 | ||||||
chr18:31414080 | G | T | 3 | a0008c0024t0006 a0010c0020t0006 a0011c0022t0006 |
6 | HG02257.hp2 HG02976.hp1 HG03041.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*485G>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 16/16 | 485 | chr18 | 31414080 | ||||||
chr18:31414127 | T | A | 1 | a0001c0002t0007 | 2 | HG01167.hp1 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*532T>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 16/16 | 532 | chr18 | 31414127 | ||||||
chr18:31414243 | A | G | 1 | a0015c0031t0013 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*648A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 16/16 | 648 | chr18 | 31414243 | ||||||
chr18:31414286 | G | A | 3 | a0001c0003t0005 a0001c0009t0005 a0001c0019t0005 |
6 | HG01884.hp2 HG02258.hp2 HG02615.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*691G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 16/16 | 691 | chr18 | 31414286 | ||||||
chr18:31414287 | C | CA | 5 | a0008c0024t0006 a0009c0021t0010 a0009c0021t0012 others(2): Show |
8 | HG02257.hp2 HG02809.hp1 HG02976.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*701dupA | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 16/16 | 702 | INFO_REALIGN_3_PRIME | chr18 | 31414287 | |||||
chr18:31414474 | A | C | 1 | a0001c0002t0016 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*879A>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 16/16 | 879 | chr18 | 31414474 | ||||||
chr18:31414529 | G | A | 1 | a0015c0031t0013 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*934G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 16/16 | 934 | chr18 | 31414529 | ||||||
chr18:31414598 | C | G | 1 | a0001c0002t0015 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1003C>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 16/16 | 1003 | chr18 | 31414598 | ||||||
chr18:31414623 | A | T | 1 | a0001c0002t0007 | 2 | HG01167.hp1 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1028A>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 16/16 | 1028 | chr18 | 31414623 | ||||||
chr18:31414758 | C | A | 1 | a0015c0031t0013 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1163C>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 16/16 | 1163 | chr18 | 31414758 | ||||||
chr18:31414789 | T | A | 45 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0011 others(42): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(265): Show |
3_prime_UTR_variant | MODIFIER | c.*1194T>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 16/16 | 1194 | chr18 | 31414789 | ||||||
chr18:31414868 | GAAAT | G | 9 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0014 others(6): Show |
126 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*1277_*1280delTAAA | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 16/16 | 1277 | INFO_REALIGN_3_PRIME | chr18 | 31414868 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:31377079 | C | G | 2 | a0001c0002t0002g0219 a0001c0002t0004g0043 |
3 | NA19009.hp2 NA19068.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.48+120C>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31377079 | |||||||
chr18:31377109 | A | T | 25 | a0001c0001t0001g0042 a0001c0001t0001g0204 a0001c0001t0001g0206 others(22): Show |
35 | HG00609.hp2 HG00735.hp1 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.48+150A>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31377109 | |||||||
chr18:31377118 | C | T | 2 | a0001c0025t0003g0217 a0001c0025t0003g0218 |
2 | HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.48+159C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31377118 | |||||||
chr18:31377353 | T | A | 1 | a0001c0008t0002g0011 | 3 | NA18944.hp1 NA18967.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.48+394T>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31377353 | |||||||
chr18:31377419 | T | C | 26 | a0001c0001t0001g0042 a0001c0001t0001g0204 a0001c0001t0001g0206 others(23): Show |
36 | HG00609.hp2 HG00735.hp1 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.48+460T>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31377419 | |||||||
chr18:31377434 | A | G | 1 | a0004c0012t0001g0199 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.48+475A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31377434 | |||||||
chr18:31377560 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.48+601A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31377560 | |||||||
chr18:31377762 | G | A | 26 | a0001c0001t0001g0042 a0001c0001t0001g0204 a0001c0001t0001g0206 others(23): Show |
36 | HG00609.hp2 HG00735.hp1 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.48+803G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31377762 | |||||||
chr18:31377848 | C | G | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(138): Show |
220 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.48+889C>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31377848 | |||||||
chr18:31377899 | T | C | 25 | a0001c0001t0001g0042 a0001c0001t0001g0204 a0001c0001t0001g0206 others(22): Show |
35 | HG00609.hp2 HG00735.hp1 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.48+940T>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31377899 | |||||||
chr18:31377937 | C | A | 1 | a0001c0002t0002g0091 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.48+978C>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31377937 | |||||||
chr18:31377960 | G | A | 25 | a0001c0001t0001g0042 a0001c0001t0001g0204 a0001c0001t0001g0206 others(22): Show |
35 | HG00609.hp2 HG00735.hp1 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.48+1001G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31377960 | |||||||
chr18:31378125 | G | A | 1 | a0001c0016t0001g0045 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.48+1166G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31378125 | |||||||
chr18:31378139 | C | T | 1 | a0015c0031t0013g0090 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.48+1180C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31378139 | |||||||
chr18:31378212 | C | T | 2 | a0001c0005t0002g0088 a0001c0005t0002g0089 |
2 | HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.48+1253C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31378212 | |||||||
chr18:31378336 | C | A | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | HG02280.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.48+1377C>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31378336 | |||||||
chr18:31378356 | T | A | 1 | a0001c0002t0018g0044 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.48+1397T>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31378356 | |||||||
chr18:31378407 | G | C | 3 | a0001c0009t0005g0012 a0001c0009t0008g0019 a0001c0013t0001g0046 |
6 | HG01884.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.48+1448G>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31378407 | |||||||
chr18:31378542 | A | T | 1 | a0001c0002t0007g0027 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.48+1583A>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31378542 | |||||||
chr18:31378723 | C | G | 1 | a0019c0033t0004g0197 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.48+1764C>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31378723 | |||||||
chr18:31378744 | G | A | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(228): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.48+1785G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31378744 | |||||||
chr18:31378822 | A | G | 1 | a0001c0005t0002g0085 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.48+1863A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31378822 | |||||||
chr18:31378899 | C | A | 1 | a0019c0033t0004g0197 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.48+1940C>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31378899 | |||||||
chr18:31379018 | C | T | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(166): Show |
259 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.48+2059C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31379018 | |||||||
chr18:31379202 | C | T | 1 | a0001c0008t0002g0084 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.48+2243C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31379202 | |||||||
chr18:31379363 | T | C | 3 | a0001c0004t0002g0095 a0001c0004t0002g0096 a0001c0006t0001g0094 |
3 | HG03486.hp2 NA18522.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.48+2404T>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31379363 | |||||||
chr18:31379440 | A | T | 2 | a0002c0010t0002g0024 a0002c0010t0002g0025 |
4 | HG02622.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.48+2481A>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31379440 | |||||||
chr18:31379825 | C | G | 1 | a0001c0007t0003g0083 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.48+2866C>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31379825 | |||||||
chr18:31379872 | G | A | 3 | a0001c0006t0001g0028 a0001c0006t0001g0097 a0001c0006t0001g0098 |
4 | HG01169.hp2 HG01192.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.48+2913G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31379872 | |||||||
chr18:31379904 | A | G | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(134): Show |
216 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.48+2945A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31379904 | |||||||
chr18:31379961 | C | T | 1 | a0001c0002t0018g0044 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.48+3002C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31379961 | |||||||
chr18:31379981 | A | G | 1 | a0001c0002t0007g0027 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.48+3022A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31379981 | |||||||
chr18:31380160 | A | T | 1 | a0001c0002t0007g0027 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.48+3201A>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31380160 | |||||||
chr18:31380313 | C | T | 26 | a0001c0001t0001g0179 a0001c0001t0002g0018 a0001c0002t0002g0195 others(23): Show |
40 | HG00408.hp1 HG00544.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.48+3354C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31380313 | |||||||
chr18:31380354 | A | T | 11 | a0001c0005t0002g0007 a0001c0005t0002g0076 a0001c0005t0002g0077 others(8): Show |
13 | HG02027.hp2 HG02040.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.48+3395A>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31380354 | |||||||
chr18:31380447 | G | A | 17 | a0001c0005t0002g0007 a0001c0005t0002g0076 a0001c0005t0002g0077 others(14): Show |
19 | HG02027.hp2 HG02040.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.48+3488G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31380447 | |||||||
chr18:31380654 | G | A | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(201): Show |
302 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(299): Show |
intron_variant | MODIFIER | c.48+3695G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31380654 | |||||||
chr18:31380659 | A | G | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(164): Show |
256 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(253): Show |
intron_variant | MODIFIER | c.48+3700A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31380659 | |||||||
chr18:31380691 | G | A | 3 | a0001c0009t0005g0012 a0001c0009t0008g0019 a0001c0013t0001g0046 |
6 | HG01884.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.48+3732G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31380691 | |||||||
chr18:31380737 | C | T | 1 | a0010c0020t0006g0020 | 2 | HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.48+3778C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31380737 | |||||||
chr18:31380838 | A | G | 1 | a0001c0005t0002g0085 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.48+3879A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31380838 | |||||||
chr18:31380839 | A | G | 1 | a0001c0004t0002g0177 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.48+3880A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31380839 | |||||||
chr18:31380899 | A | G | 25 | a0001c0001t0001g0042 a0001c0001t0001g0204 a0001c0001t0001g0206 others(22): Show |
35 | HG00609.hp2 HG00735.hp1 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.48+3940A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31380899 | |||||||
chr18:31381284 | A | G | 3 | a0001c0007t0003g0073 a0001c0007t0003g0074 a0001c0016t0001g0072 |
3 | HG00735.hp2 HG02129.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.49-3852A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31381284 | |||||||
chr18:31381304 | G | A | 1 | a0001c0002t0004g0178 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.49-3832G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31381304 | |||||||
chr18:31381382 | T | TA | 24 | a0001c0001t0001g0042 a0001c0001t0001g0204 a0001c0001t0001g0206 others(21): Show |
34 | HG00609.hp2 HG00735.hp1 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.49-3743dupA | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 31381382 | ||||||
chr18:31381451 | T | C | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(202): Show |
303 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(300): Show |
intron_variant | MODIFIER | c.49-3685T>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31381451 | |||||||
chr18:31381523 | C | T | 1 | a0001c0004t0002g0177 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.49-3613C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31381523 | |||||||
chr18:31381592 | C | T | 1 | a0001c0002t0002g0176 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.49-3544C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31381592 | |||||||
chr18:31381614 | C | T | 6 | a0001c0005t0002g0085 a0001c0005t0004g0049 a0001c0005t0004g0051 others(3): Show |
6 | HG02615.hp1 HG02723.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.49-3522C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31381614 | |||||||
chr18:31381686 | G | A | 1 | a0001c0013t0001g0075 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.49-3450G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31381686 | |||||||
chr18:31381792 | T | C | 1 | a0001c0002t0018g0044 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.49-3344T>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31381792 | |||||||
chr18:31381817 | C | T | 1 | a0001c0005t0002g0061 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.49-3319C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31381817 | |||||||
chr18:31381827 | A | AT | 44 | a0001c0001t0001g0155 a0001c0001t0001g0158 a0001c0002t0004g0196 others(41): Show |
60 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.49-3294dupT | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 31381827 | ||||||
chr18:31381827 | AT | A | 6 | a0001c0001t0001g0179 a0001c0040t0004g0054 a0002c0010t0002g0024 others(3): Show |
8 | HG02559.hp1 HG02622.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.49-3294delT | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 31381827 | ||||||
chr18:31381905 | G | A | 1 | a0001c0004t0002g0151 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.49-3231G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31381905 | |||||||
chr18:31381972 | T | A | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(134): Show |
216 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.49-3164T>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31381972 | |||||||
chr18:31381974 | G | T | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(167): Show |
261 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(258): Show |
intron_variant | MODIFIER | c.49-3162G>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31381974 | |||||||
chr18:31381995 | T | A | 1 | a0010c0020t0006g0020 | 2 | HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.49-3141T>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31381995 | |||||||
chr18:31382245 | T | G | 1 | a0001c0002t0002g0176 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.49-2891T>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31382245 | |||||||
chr18:31382247 | G | C | 1 | a0015c0031t0013g0090 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.49-2889G>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31382247 | |||||||
chr18:31382267 | A | G | 139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(136): Show |
217 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.49-2869A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31382267 | |||||||
chr18:31382757 | A | G | 2 | a0001c0015t0001g0035 a0001c0015t0001g0150 |
3 | NA18612.hp2 NA18995.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.49-2379A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31382757 | |||||||
chr18:31382818 | A | T | 1 | a0001c0001t0001g0149 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.49-2318A>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31382818 | |||||||
chr18:31383080 | A | G | 5 | a0001c0040t0004g0054 a0002c0010t0002g0024 a0002c0010t0002g0025 others(2): Show |
7 | HG02559.hp1 HG02622.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.49-2056A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31383080 | |||||||
chr18:31383087 | A | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(164): Show |
256 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(253): Show |
intron_variant | MODIFIER | c.49-2049A>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31383087 | |||||||
chr18:31383177 | C | A | 1 | a0001c0001t0001g0149 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.49-1959C>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31383177 | |||||||
chr18:31383204 | G | A | 1 | a0001c0002t0007g0027 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.49-1932G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31383204 | |||||||
chr18:31383253 | G | A | 3 | a0001c0009t0005g0012 a0001c0009t0008g0019 a0001c0013t0001g0046 |
6 | HG01884.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.49-1883G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31383253 | |||||||
chr18:31383310 | C | T | 1 | a0019c0033t0004g0197 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.49-1826C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31383310 | |||||||
chr18:31383402 | G | C | 2 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
2 | NA18994.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.49-1734G>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31383402 | |||||||
chr18:31383419 | C | A | 2 | a0001c0002t0002g0091 a0001c0002t0004g0104 |
2 | HG02630.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.49-1717C>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31383419 | |||||||
chr18:31383533 | A | T | 1 | a0001c0002t0002g0195 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.49-1603A>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31383533 | |||||||
chr18:31383708 | C | A | 1 | a0015c0031t0013g0090 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.49-1428C>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31383708 | |||||||
chr18:31383875 | C | A | 5 | a0001c0004t0002g0004 a0001c0004t0002g0037 a0001c0004t0002g0153 others(2): Show |
14 | HG00558.hp2 NA18940.hp2 NA18942.hp2 others(11): Show |
intron_variant | MODIFIER | c.49-1261C>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31383875 | |||||||
chr18:31383983 | G | A | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(167): Show |
261 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(258): Show |
intron_variant | MODIFIER | c.49-1153G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31383983 | |||||||
chr18:31384063 | T | G | 1 | a0001c0002t0007g0027 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.49-1073T>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31384063 | |||||||
chr18:31384072 | C | G | 1 | a0001c0004t0002g0151 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.49-1064C>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31384072 | |||||||
chr18:31384328 | G | GA | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(201): Show |
302 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(299): Show |
intron_variant | MODIFIER | c.49-803dupA | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr18 | 31384328 | ||||||
chr18:31384445 | T | C | 2 | a0001c0025t0003g0217 a0001c0025t0003g0218 |
2 | HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.49-691T>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31384445 | |||||||
chr18:31384657 | A | G | 1 | a0001c0001t0001g0148 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.49-479A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31384657 | |||||||
chr18:31384671 | G | A | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(134): Show |
216 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.49-465G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31384671 | |||||||
chr18:31384705 | G | A | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(201): Show |
302 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(299): Show |
intron_variant | MODIFIER | c.49-431G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31384705 | |||||||
chr18:31384716 | A | T | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(164): Show |
256 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(253): Show |
intron_variant | MODIFIER | c.49-420A>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31384716 | |||||||
chr18:31384800 | T | C | 25 | a0001c0001t0001g0042 a0001c0001t0001g0204 a0001c0001t0001g0206 others(22): Show |
35 | HG00609.hp2 HG00735.hp1 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.49-336T>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31384800 | |||||||
chr18:31384897 | T | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(164): Show |
256 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(253): Show |
intron_variant | MODIFIER | c.49-239T>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31384897 | |||||||
chr18:31384945 | T | C | 1 | a0013c0044t0002g0154 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.49-191T>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 1/15 | chr18 | 31384945 | |||||||
chr18:31385509 | C | A | 1 | a0001c0001t0001g0155 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.84+338C>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 2/15 | chr18 | 31385509 | |||||||
chr18:31385937 | G | T | 2 | a0001c0006t0001g0036 a0001c0006t0001g0152 |
3 | HG03490.hp2 HG03492.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.85-751G>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 2/15 | chr18 | 31385937 | |||||||
chr18:31385938 | T | A | 2 | a0001c0006t0001g0036 a0001c0006t0001g0152 |
3 | HG03490.hp2 HG03492.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.85-750T>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 2/15 | chr18 | 31385938 | |||||||
chr18:31385958 | G | T | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(166): Show |
259 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.85-730G>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 2/15 | chr18 | 31385958 | |||||||
chr18:31386024 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.85-664G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 2/15 | chr18 | 31386024 | |||||||
chr18:31386073 | A | C | 29 | a0001c0005t0002g0007 a0001c0005t0002g0061 a0001c0005t0002g0076 others(26): Show |
34 | HG01884.hp2 HG02027.hp2 HG02040.hp1 others(31): Show |
intron_variant | MODIFIER | c.85-615A>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 2/15 | chr18 | 31386073 | |||||||
chr18:31386127 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.85-561T>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 2/15 | chr18 | 31386127 | |||||||
chr18:31386195 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.85-493G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 2/15 | chr18 | 31386195 | |||||||
chr18:31386291 | T | C | 1 | a0001c0008t0002g0084 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.85-397T>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 2/15 | chr18 | 31386291 | |||||||
chr18:31386321 | T | A | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(166): Show |
259 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.85-367T>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 2/15 | chr18 | 31386321 | |||||||
chr18:31386331 | C | G | 1 | a0001c0013t0001g0075 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.85-357C>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 2/15 | chr18 | 31386331 | |||||||
chr18:31386513 | C | T | 1 | a0001c0013t0001g0082 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.85-175C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 2/15 | chr18 | 31386513 | |||||||
chr18:31386524 | C | T | 1 | a0001c0002t0007g0027 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.85-164C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 2/15 | chr18 | 31386524 | |||||||
chr18:31386555 | G | C | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(166): Show |
259 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.85-133G>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 2/15 | chr18 | 31386555 | |||||||
chr18:31386842 | G | A | 1 | a0001c0006t0001g0156 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.216+23G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 3/15 | chr18 | 31386842 | |||||||
chr18:31387062 | C | G | 1 | a0001c0002t0004g0147 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.216+243C>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 3/15 | chr18 | 31387062 | |||||||
chr18:31387075 | A | G | 1 | a0001c0003t0003g0215 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.216+256A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 3/15 | chr18 | 31387075 | |||||||
chr18:31387112 | A | G | 1 | a0019c0033t0004g0197 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.216+293A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 3/15 | chr18 | 31387112 | |||||||
chr18:31387447 | G | T | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(166): Show |
259 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.216+628G>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 3/15 | chr18 | 31387447 | |||||||
chr18:31387520 | C | T | 3 | a0006c0017t0002g0099 a0006c0017t0002g0100 a0006c0017t0004g0101 |
3 | HG02280.hp1 HG02723.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.216+701C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 3/15 | chr18 | 31387520 | |||||||
chr18:31387552 | T | C | 1 | a0004c0012t0001g0199 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.216+733T>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 3/15 | chr18 | 31387552 | |||||||
chr18:31387650 | G | C | 1 | a0001c0001t0001g0107 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.217-717G>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 3/15 | chr18 | 31387650 | |||||||
chr18:31387651 | G | A | 1 | a0001c0005t0002g0076 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.217-716G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 3/15 | chr18 | 31387651 | |||||||
chr18:31387715 | TA | T | 3 | a0001c0002t0007g0027 a0001c0026t0002g0146 a0015c0031t0013g0090 |
4 | HG01167.hp1 HG01169.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.217-646delA | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr18 | 31387715 | ||||||
chr18:31387766 | G | C | 1 | a0019c0033t0004g0197 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.217-601G>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 3/15 | chr18 | 31387766 | |||||||
chr18:31387817 | C | G | 1 | a0001c0026t0002g0146 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.217-550C>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 3/15 | chr18 | 31387817 | |||||||
chr18:31387831 | G | A | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(202): Show |
303 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(300): Show |
intron_variant | MODIFIER | c.217-536G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 3/15 | chr18 | 31387831 | |||||||
chr18:31388037 | G | T | 3 | a0001c0002t0002g0143 a0001c0002t0002g0144 a0001c0002t0002g0145 |
3 | HG00438.hp1 NA18957.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.217-330G>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 3/15 | chr18 | 31388037 | |||||||
chr18:31388127 | G | A | 11 | a0001c0005t0002g0007 a0001c0005t0002g0076 a0001c0005t0002g0077 others(8): Show |
13 | HG02027.hp2 HG02040.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.217-240G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 3/15 | chr18 | 31388127 | |||||||
chr18:31388156 | C | T | 1 | a0014c0038t0004g0071 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.217-211C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 3/15 | chr18 | 31388156 | |||||||
chr18:31388233 | C | T | 3 | a0001c0009t0005g0012 a0001c0009t0008g0019 a0001c0013t0001g0046 |
6 | HG01884.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.217-134C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 3/15 | chr18 | 31388233 | |||||||
chr18:31388783 | T | A | 1 | a0004c0012t0001g0021 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.373-91T>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 4/15 | chr18 | 31388783 | |||||||
chr18:31388841 | G | A | 1 | a0001c0005t0002g0085 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.373-33G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 4/15 | chr18 | 31388841 | |||||||
chr18:31389045 | C | T | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(163): Show |
255 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.517+27C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 5/15 | chr18 | 31389045 | |||||||
chr18:31389053 | C | T | 1 | a0001c0040t0004g0054 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.517+35C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 5/15 | chr18 | 31389053 | |||||||
chr18:31389054 | A | G | 1 | a0001c0006t0001g0152 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.517+36A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 5/15 | chr18 | 31389054 | |||||||
chr18:31389055 | T | G | 29 | a0001c0005t0002g0007 a0001c0005t0002g0061 a0001c0005t0002g0076 others(26): Show |
34 | HG01884.hp2 HG02027.hp2 HG02040.hp1 others(31): Show |
intron_variant | MODIFIER | c.517+37T>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 5/15 | chr18 | 31389055 | |||||||
chr18:31389081 | T | C | 29 | a0001c0005t0002g0007 a0001c0005t0002g0061 a0001c0005t0002g0076 others(26): Show |
34 | HG01884.hp2 HG02027.hp2 HG02040.hp1 others(31): Show |
intron_variant | MODIFIER | c.517+63T>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 5/15 | chr18 | 31389081 | |||||||
chr18:31389235 | C | T | 1 | a0001c0002t0007g0027 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.517+217C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 5/15 | chr18 | 31389235 | |||||||
chr18:31389472 | T | C | 3 | a0001c0025t0003g0217 a0001c0025t0003g0218 a0001c0026t0002g0146 |
3 | HG02572.hp2 HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.517+454T>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 5/15 | chr18 | 31389472 | |||||||
chr18:31389568 | T | C | 3 | a0001c0009t0005g0012 a0001c0009t0008g0019 a0001c0013t0001g0046 |
6 | HG01884.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.517+550T>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 5/15 | chr18 | 31389568 | |||||||
chr18:31389573 | C | A | 1 | a0016c0042t0003g0047 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.517+555C>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 5/15 | chr18 | 31389573 | |||||||
chr18:31389646 | C | T | 1 | a0001c0002t0007g0027 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.517+628C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 5/15 | chr18 | 31389646 | |||||||
chr18:31389671 | G | A | 1 | a0001c0030t0002g0200 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.517+653G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 5/15 | chr18 | 31389671 | |||||||
chr18:31389705 | T | A | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(145): Show |
229 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.517+687T>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 5/15 | chr18 | 31389705 | |||||||
chr18:31389828 | G | A | 2 | a0002c0010t0002g0024 a0002c0010t0002g0025 |
4 | HG02622.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.517+810G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 5/15 | chr18 | 31389828 | |||||||
chr18:31389893 | G | A | 1 | a0001c0007t0003g0062 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.518-763G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 5/15 | chr18 | 31389893 | |||||||
chr18:31390184 | G | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(157): Show |
249 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(246): Show |
intron_variant | MODIFIER | c.518-472G>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 5/15 | chr18 | 31390184 | |||||||
chr18:31390193 | T | C | 5 | a0001c0040t0004g0054 a0002c0010t0002g0024 a0002c0010t0002g0025 others(2): Show |
7 | HG02559.hp1 HG02622.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.518-463T>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 5/15 | chr18 | 31390193 | |||||||
chr18:31390288 | AT | A | 4 | a0001c0007t0003g0022 a0001c0016t0001g0063 a0001c0039t0003g0064 others(1): Show |
4 | HG01891.hp2 HG02809.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.518-363delT | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr18 | 31390288 | ||||||
chr18:31390468 | T | C | 3 | a0006c0017t0002g0099 a0006c0017t0002g0100 a0006c0017t0004g0101 |
3 | HG02280.hp1 HG02723.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.518-188T>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 5/15 | chr18 | 31390468 | |||||||
chr18:31390562 | G | A | 9 | a0001c0005t0002g0061 a0001c0005t0002g0088 a0001c0005t0002g0089 others(6): Show |
9 | HG02809.hp1 HG02895.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.518-94G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 5/15 | chr18 | 31390562 | |||||||
chr18:31390628 | C | T | 1 | a0001c0006t0001g0175 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.518-28C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 5/15 | chr18 | 31390628 | |||||||
chr18:31390910 | T | A | 1 | a0001c0003t0003g0108 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.684+88T>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 6/15 | chr18 | 31390910 | |||||||
chr18:31390970 | A | T | 1 | a0001c0002t0004g0104 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.685-108A>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 6/15 | chr18 | 31390970 | |||||||
chr18:31390994 | G | C | 1 | a0001c0002t0002g0109 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.685-84G>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 6/15 | chr18 | 31390994 | |||||||
chr18:31391019 | G | A | 29 | a0001c0005t0002g0007 a0001c0005t0002g0061 a0001c0005t0002g0076 others(26): Show |
32 | HG02027.hp2 HG02040.hp1 HG02040.hp2 others(29): Show |
intron_variant | MODIFIER | c.685-59G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 6/15 | chr18 | 31391019 | |||||||
chr18:31391056 | G | A | 1 | a0001c0005t0002g0085 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.685-22G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 6/15 | chr18 | 31391056 | |||||||
chr18:31391454 | T | C | 1 | a0001c0002t0004g0180 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.819+242T>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 7/15 | chr18 | 31391454 | |||||||
chr18:31391521 | G | A | 2 | a0001c0007t0003g0006 a0001c0008t0004g0006 |
5 | HG00099.hp2 HG00140.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.819+309G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 7/15 | chr18 | 31391521 | |||||||
chr18:31391587 | A | G | 30 | a0001c0005t0002g0007 a0001c0005t0002g0061 a0001c0005t0002g0076 others(27): Show |
33 | HG02027.hp2 HG02040.hp1 HG02040.hp2 others(30): Show |
intron_variant | MODIFIER | c.819+375A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 7/15 | chr18 | 31391587 | |||||||
chr18:31391603 | A | G | 2 | a0001c0001t0001g0042 a0001c0001t0001g0214 |
3 | NA18946.hp2 NA19064.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.819+391A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 7/15 | chr18 | 31391603 | |||||||
chr18:31391659 | G | A | 2 | a0001c0007t0003g0073 a0001c0016t0001g0072 |
2 | HG02129.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.819+447G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 7/15 | chr18 | 31391659 | |||||||
chr18:31391663 | T | TAA | 5 | a0001c0040t0004g0054 a0002c0010t0002g0024 a0002c0010t0002g0025 others(2): Show |
7 | HG02559.hp1 HG02622.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.819+461_819+462dup others(2): Show |
DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr18 | 31391663 | ||||||
chr18:31391676 | AAAAAAAC others(5): Show |
A | 3 | a0001c0025t0003g0217 a0001c0025t0003g0218 a0001c0026t0002g0146 |
3 | HG02572.hp2 HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.820-471_820-460del others(12): Show |
DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr18 | 31391676 | ||||||
chr18:31391770 | G | A | 2 | a0001c0003t0005g0201 a0001c0003t0005g0202 |
2 | HG02970.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.820-385G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 7/15 | chr18 | 31391770 | |||||||
chr18:31391899 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.820-256A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 7/15 | chr18 | 31391899 | |||||||
chr18:31391945 | C | T | 1 | a0001c0002t0016g0194 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.820-210C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 7/15 | chr18 | 31391945 | |||||||
chr18:31392040 | G | T | 1 | a0001c0002t0004g0193 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.820-115G>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 7/15 | chr18 | 31392040 | |||||||
chr18:31392400 | A | C | 24 | a0001c0001t0001g0179 a0001c0001t0002g0018 a0001c0002t0002g0195 others(21): Show |
38 | HG00408.hp1 HG00544.hp1 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.1005+60A>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31392400 | |||||||
chr18:31392470 | G | A | 2 | a0001c0001t0001g0110 a0001c0006t0001g0094 |
2 | HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1005+130G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31392470 | |||||||
chr18:31392624 | T | C | 2 | a0009c0021t0010g0056 a0009c0021t0012g0055 |
2 | HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1005+284T>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31392624 | |||||||
chr18:31392651 | T | C | 1 | a0001c0003t0003g0203 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1005+311T>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31392651 | |||||||
chr18:31392724 | T | A | 3 | a0006c0017t0002g0099 a0006c0017t0002g0100 a0006c0017t0004g0101 |
3 | HG02280.hp1 HG02723.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.1005+384T>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31392724 | |||||||
chr18:31392818 | T | C | 6 | a0001c0005t0002g0061 a0001c0009t0003g0057 a0009c0021t0010g0056 others(3): Show |
6 | HG02809.hp1 HG02965.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1005+478T>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31392818 | |||||||
chr18:31392863 | G | T | 2 | a0009c0021t0010g0056 a0009c0021t0012g0055 |
2 | HG02809.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1005+523G>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31392863 | |||||||
chr18:31392874 | C | T | 11 | a0001c0005t0002g0007 a0001c0005t0002g0076 a0001c0005t0002g0077 others(8): Show |
13 | HG02027.hp2 HG02040.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.1005+534C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31392874 | |||||||
chr18:31392956 | A | T | 1 | a0001c0002t0007g0027 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1005+616A>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31392956 | |||||||
chr18:31392960 | T | G | 1 | a0001c0009t0003g0048 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1005+620T>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31392960 | |||||||
chr18:31393153 | T | TAACA | 3 | a0001c0009t0005g0012 a0001c0009t0008g0019 a0001c0013t0001g0046 |
6 | HG01884.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1005+815_1005+818d others(6): Show |
DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr18 | 31393153 | ||||||
chr18:31393314 | G | A | 1 | a0001c0008t0002g0084 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1005+974G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31393314 | |||||||
chr18:31393377 | C | T | 1 | a0001c0003t0003g0213 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1005+1037C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31393377 | |||||||
chr18:31393632 | C | A | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG01261.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.1005+1292C>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31393632 | |||||||
chr18:31393742 | C | G | 1 | a0001c0002t0004g0181 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1005+1402C>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31393742 | |||||||
chr18:31393743 | C | T | 2 | a0001c0005t0002g0088 a0001c0005t0002g0089 |
2 | HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1005+1403C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31393743 | |||||||
chr18:31393763 | G | A | 2 | a0001c0004t0002g0113 a0001c0004t0002g0157 |
2 | NA18952.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.1005+1423G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31393763 | |||||||
chr18:31393904 | AT | A | 5 | a0001c0005t0002g0085 a0001c0005t0004g0049 a0001c0005t0004g0051 others(2): Show |
5 | HG02615.hp1 HG03098.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1005+1565delT | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31393904 | |||||||
chr18:31394015 | C | T | 2 | a0001c0002t0004g0181 a0001c0002t0004g0196 |
2 | HG00738.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.1005+1675C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31394015 | |||||||
chr18:31394026 | A | C | 1 | a0001c0025t0003g0218 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1005+1686A>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31394026 | |||||||
chr18:31394092 | A | G | 1 | a0001c0002t0018g0044 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1005+1752A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31394092 | |||||||
chr18:31394102 | A | G | 2 | a0001c0006t0001g0036 a0001c0006t0001g0152 |
3 | HG03490.hp2 HG03492.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1005+1762A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31394102 | |||||||
chr18:31394186 | A | C | 1 | a0001c0004t0002g0096 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1005+1846A>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31394186 | |||||||
chr18:31394289 | T | A | 1 | a0001c0001t0001g0114 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1005+1949T>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31394289 | |||||||
chr18:31394349 | G | A | 3 | a0006c0017t0002g0099 a0006c0017t0002g0100 a0006c0017t0004g0101 |
3 | HG02280.hp1 HG02723.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.1005+2009G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31394349 | |||||||
chr18:31394447 | CAT | C | 3 | a0001c0009t0005g0012 a0001c0009t0008g0019 a0001c0013t0001g0046 |
6 | HG01884.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1005+2108_1005+210 others(6): Show |
DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31394447 | |||||||
chr18:31394463 | A | G | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(202): Show |
303 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(300): Show |
intron_variant | MODIFIER | c.1005+2123A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31394463 | |||||||
chr18:31394491 | C | T | 3 | a0001c0009t0005g0012 a0001c0009t0008g0019 a0001c0013t0001g0046 |
6 | HG01884.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1005+2151C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31394491 | |||||||
chr18:31394502 | G | A | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(132): Show |
214 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.1005+2162G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31394502 | |||||||
chr18:31394575 | A | G | 6 | a0001c0025t0003g0217 a0001c0025t0003g0218 a0001c0026t0002g0146 others(3): Show |
6 | HG02280.hp1 HG02572.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1005+2235A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31394575 | |||||||
chr18:31394680 | GAA | G | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(220): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.1005+2354_1005+235 others(6): Show |
DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr18 | 31394680 | ||||||
chr18:31394789 | T | C | 1 | a0001c0002t0002g0195 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1005+2449T>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31394789 | |||||||
chr18:31394886 | T | C | 1 | a0001c0002t0007g0027 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1005+2546T>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31394886 | |||||||
chr18:31394910 | A | G | 1 | a0010c0020t0006g0020 | 2 | HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1005+2570A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31394910 | |||||||
chr18:31394972 | A | G | 2 | a0001c0005t0004g0049 a0001c0005t0004g0051 |
2 | HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1005+2632A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31394972 | |||||||
chr18:31395088 | A | G | 1 | a0001c0001t0001g0141 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1005+2748A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31395088 | |||||||
chr18:31395169 | A | G | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(187): Show |
285 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(282): Show |
intron_variant | MODIFIER | c.1005+2829A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31395169 | |||||||
chr18:31395233 | T | C | 3 | a0006c0017t0002g0099 a0006c0017t0002g0100 a0006c0017t0004g0101 |
3 | HG02280.hp1 HG02723.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.1005+2893T>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31395233 | |||||||
chr18:31395271 | TA | T | 34 | a0001c0001t0001g0034 a0001c0001t0001g0140 a0001c0001t0002g0018 others(31): Show |
54 | HG00408.hp1 HG00544.hp1 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.1005+2945delA | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr18 | 31395271 | ||||||
chr18:31395295 | A | G | 2 | a0001c0003t0003g0211 a0001c0003t0003g0212 |
2 | HG01981.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1005+2955A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31395295 | |||||||
chr18:31395321 | A | C | 1 | a0001c0001t0001g0137 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1005+2981A>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31395321 | |||||||
chr18:31395388 | C | T | 1 | a0001c0004t0002g0174 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1005+3048C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31395388 | |||||||
chr18:31395515 | A | C | 1 | a0001c0002t0007g0027 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1005+3175A>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31395515 | |||||||
chr18:31395560 | CCT | C | 25 | a0001c0005t0002g0007 a0001c0005t0002g0061 a0001c0005t0002g0076 others(22): Show |
27 | HG02027.hp2 HG02040.hp1 HG02040.hp2 others(24): Show |
intron_variant | MODIFIER | c.1005+3224_1005+322 others(6): Show |
DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr18 | 31395560 | ||||||
chr18:31395626 | C | T | 1 | a0001c0001t0001g0015 | 3 | HG02165.hp2 NA19003.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.1005+3286C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31395626 | |||||||
chr18:31395745 | A | G | 1 | a0010c0020t0006g0020 | 2 | HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1005+3405A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31395745 | |||||||
chr18:31395827 | C | T | 2 | a0011c0022t0006g0058 a0011c0022t0006g0059 |
2 | HG03041.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1006-3445C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31395827 | |||||||
chr18:31395839 | G | A | 1 | a0010c0020t0006g0020 | 2 | HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1006-3433G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31395839 | |||||||
chr18:31396057 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1006-3215G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31396057 | |||||||
chr18:31396120 | AGT | A | 6 | a0001c0005t0002g0085 a0001c0005t0004g0049 a0001c0005t0004g0051 others(3): Show |
6 | HG02615.hp1 HG02723.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1006-3143_1006-314 others(6): Show |
DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr18 | 31396120 | ||||||
chr18:31396182 | G | T | 1 | a0018c0028t0003g0192 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1006-3090G>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31396182 | |||||||
chr18:31396210 | A | G | 1 | a0001c0003t0003g0213 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1006-3062A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31396210 | |||||||
chr18:31396303 | T | C | 1 | a0001c0008t0002g0084 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1006-2969T>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31396303 | |||||||
chr18:31396333 | C | T | 3 | a0006c0017t0002g0099 a0006c0017t0002g0100 a0006c0017t0004g0101 |
3 | HG02280.hp1 HG02723.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.1006-2939C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31396333 | |||||||
chr18:31396334 | G | A | 3 | a0001c0009t0005g0012 a0001c0009t0008g0019 a0001c0013t0001g0046 |
6 | HG01884.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1006-2938G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31396334 | |||||||
chr18:31396354 | C | CT | 75 | a0001c0001t0001g0002 a0001c0001t0001g0093 a0001c0001t0001g0105 others(72): Show |
91 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.1006-2891dupT | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr18 | 31396354 | ||||||
chr18:31396354 | CT | C | 27 | a0001c0001t0001g0102 a0001c0001t0001g0204 a0001c0004t0002g0038 others(24): Show |
33 | HG00099.hp1 HG01109.hp2 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.1006-2891delT | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr18 | 31396354 | ||||||
chr18:31396467 | G | A | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(157): Show |
249 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(246): Show |
intron_variant | MODIFIER | c.1006-2805G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31396467 | |||||||
chr18:31396478 | C | A | 2 | a0001c0007t0003g0013 a0001c0007t0003g0067 |
3 | HG00140.hp1 HG02145.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.1006-2794C>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31396478 | |||||||
chr18:31396608 | A | G | 3 | a0001c0025t0003g0217 a0001c0025t0003g0218 a0001c0026t0002g0146 |
3 | HG02572.hp2 HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1006-2664A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31396608 | |||||||
chr18:31396806 | C | T | 1 | a0001c0002t0007g0027 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1006-2466C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31396806 | |||||||
chr18:31396854 | G | A | 4 | a0002c0010t0002g0024 a0002c0010t0002g0025 a0002c0010t0002g0052 others(1): Show |
6 | HG02622.hp2 HG02886.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1006-2418G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31396854 | |||||||
chr18:31396919 | C | T | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(157): Show |
249 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(246): Show |
intron_variant | MODIFIER | c.1006-2353C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31396919 | |||||||
chr18:31396943 | G | A | 1 | a0001c0002t0007g0027 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1006-2329G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31396943 | |||||||
chr18:31397033 | A | AT | 4 | a0001c0001t0001g0031 a0001c0001t0001g0136 a0001c0001t0001g0142 others(1): Show |
5 | HG00639.hp1 HG00741.hp1 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.1006-2237dupT | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr18 | 31397033 | ||||||
chr18:31397165 | G | T | 201 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(198): Show |
299 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(296): Show |
intron_variant | MODIFIER | c.1006-2107G>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31397165 | |||||||
chr18:31397175 | T | G | 1 | a0001c0003t0003g0213 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1006-2097T>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31397175 | |||||||
chr18:31397214 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1006-2058A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31397214 | |||||||
chr18:31397402 | C | G | 1 | a0001c0002t0007g0027 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1006-1870C>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31397402 | |||||||
chr18:31397488 | C | A | 1 | a0010c0020t0006g0020 | 2 | HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1006-1784C>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31397488 | |||||||
chr18:31397519 | C | T | 1 | a0001c0002t0002g0109 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1006-1753C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31397519 | |||||||
chr18:31397620 | G | A | 1 | a0001c0004t0002g0159 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1006-1652G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31397620 | |||||||
chr18:31397636 | A | G | 1 | a0006c0017t0002g0100 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1006-1636A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31397636 | |||||||
chr18:31397716 | A | T | 1 | a0001c0002t0007g0027 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1006-1556A>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31397716 | |||||||
chr18:31397769 | G | A | 3 | a0001c0002t0004g0178 a0001c0002t0004g0184 a0001c0002t0004g0185 |
3 | NA18962.hp2 NA18972.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1006-1503G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31397769 | |||||||
chr18:31397799 | G | T | 1 | a0001c0002t0007g0027 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1006-1473G>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31397799 | |||||||
chr18:31397811 | A | G | 1 | a0001c0002t0007g0027 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1006-1461A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31397811 | |||||||
chr18:31397895 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1006-1377C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31397895 | |||||||
chr18:31397949 | T | C | 1 | a0001c0002t0007g0027 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1006-1323T>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31397949 | |||||||
chr18:31397957 | G | A | 1 | a0002c0036t0002g0053 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1006-1315G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31397957 | |||||||
chr18:31397966 | G | A | 1 | a0001c0002t0007g0027 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1006-1306G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31397966 | |||||||
chr18:31397971 | G | A | 4 | a0002c0010t0002g0024 a0002c0010t0002g0025 a0002c0010t0002g0052 others(1): Show |
6 | HG02622.hp2 HG02886.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1006-1301G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31397971 | |||||||
chr18:31398022 | G | A | 3 | a0001c0008t0002g0011 a0001c0008t0002g0023 a0014c0038t0004g0071 |
6 | HG02056.hp2 HG02083.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.1006-1250G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31398022 | |||||||
chr18:31398026 | CA | C | 161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(158): Show |
253 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.1006-1223delA | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr18 | 31398026 | ||||||
chr18:31398026 | CAA | C | 12 | a0001c0002t0007g0027 a0001c0005t0002g0085 a0001c0005t0004g0049 others(9): Show |
16 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1006-1224_1006-122 others(6): Show |
DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr18 | 31398026 | ||||||
chr18:31398052 | T | G | 1 | a0002c0010t0002g0024 | 2 | HG02622.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1006-1220T>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31398052 | |||||||
chr18:31398198 | G | A | 1 | a0002c0010t0002g0052 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1006-1074G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31398198 | |||||||
chr18:31398308 | G | A | 3 | a0001c0004t0002g0096 a0001c0005t0002g0088 a0001c0005t0002g0089 |
3 | HG02965.hp2 NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1006-964G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31398308 | |||||||
chr18:31398349 | C | T | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(157): Show |
249 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(246): Show |
intron_variant | MODIFIER | c.1006-923C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31398349 | |||||||
chr18:31398582 | A | G | 3 | a0001c0001t0001g0179 a0001c0002t0004g0180 a0001c0002t0004g0182 |
3 | NA18957.hp2 NA19079.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.1006-690A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31398582 | |||||||
chr18:31398604 | T | C | 23 | a0001c0001t0001g0042 a0001c0001t0001g0204 a0001c0001t0001g0206 others(20): Show |
33 | HG00609.hp2 HG00735.hp1 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.1006-668T>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31398604 | |||||||
chr18:31398728 | C | T | 5 | a0001c0001t0001g0031 a0001c0001t0001g0105 a0001c0001t0001g0136 others(2): Show |
6 | HG00639.hp1 HG00741.hp1 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.1006-544C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31398728 | |||||||
chr18:31398963 | A | C | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(159): Show |
252 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(249): Show |
intron_variant | MODIFIER | c.1006-309A>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31398963 | |||||||
chr18:31398963 | A | T | 2 | a0001c0002t0018g0044 a0019c0033t0004g0197 |
2 | HG02647.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1006-309A>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31398963 | |||||||
chr18:31399048 | C | T | 6 | a0001c0025t0003g0217 a0001c0025t0003g0218 a0001c0026t0002g0146 others(3): Show |
6 | HG02280.hp1 HG02572.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1006-224C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31399048 | |||||||
chr18:31399105 | T | C | 3 | a0001c0002t0018g0044 a0015c0031t0013g0090 a0019c0033t0004g0197 |
3 | HG02109.hp2 HG02647.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1006-167T>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 8/15 | chr18 | 31399105 | |||||||
chr18:31399628 | C | T | 2 | a0001c0004t0002g0113 a0001c0004t0002g0157 |
2 | NA18952.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.1277+85C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 9/15 | chr18 | 31399628 | |||||||
chr18:31399876 | G | C | 1 | a0001c0001t0001g0118 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1277+333G>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 9/15 | chr18 | 31399876 | |||||||
chr18:31399884 | T | A | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(201): Show |
302 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(299): Show |
intron_variant | MODIFIER | c.1277+341T>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 9/15 | chr18 | 31399884 | |||||||
chr18:31400298 | T | A | 1 | a0001c0002t0007g0027 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1278-583T>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 9/15 | chr18 | 31400298 | |||||||
chr18:31400432 | T | A | 1 | a0001c0002t0007g0027 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1278-449T>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 9/15 | chr18 | 31400432 | |||||||
chr18:31400451 | T | C | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(229): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.1278-430T>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 9/15 | chr18 | 31400451 | |||||||
chr18:31400452 | C | A | 1 | a0010c0020t0006g0020 | 2 | HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1278-429C>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 9/15 | chr18 | 31400452 | |||||||
chr18:31400484 | T | C | 1 | a0001c0001t0001g0119 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1278-397T>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 9/15 | chr18 | 31400484 | |||||||
chr18:31400511 | C | CA | 3 | a0001c0009t0005g0012 a0001c0009t0008g0019 a0001c0013t0001g0046 |
6 | HG01884.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1278-362dupA | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr18 | 31400511 | ||||||
chr18:31400513 | A | G | 1 | a0001c0002t0007g0027 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1278-368A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 9/15 | chr18 | 31400513 | |||||||
chr18:31400623 | ACT | A | 4 | a0002c0010t0002g0024 a0002c0010t0002g0025 a0002c0010t0002g0052 others(1): Show |
6 | HG02622.hp2 HG02886.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1278-256_1278-255d others(4): Show |
DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr18 | 31400623 | ||||||
chr18:31400649 | C | A | 5 | a0001c0003t0003g0040 a0001c0003t0003g0041 a0001c0003t0003g0203 others(2): Show |
7 | HG00735.hp1 HG01081.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.1278-232C>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 9/15 | chr18 | 31400649 | |||||||
chr18:31400701 | T | A | 3 | a0001c0002t0002g0120 a0001c0002t0004g0121 a0001c0003t0003g0014 |
5 | HG02074.hp2 HG02129.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.1278-180T>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 9/15 | chr18 | 31400701 | |||||||
chr18:31400740 | G | A | 1 | a0001c0002t0007g0027 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1278-141G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 9/15 | chr18 | 31400740 | |||||||
chr18:31400779 | T | A | 1 | a0016c0042t0003g0047 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1278-102T>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 9/15 | chr18 | 31400779 | |||||||
chr18:31400794 | A | T | 1 | a0001c0002t0015g0191 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1278-87A>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 9/15 | chr18 | 31400794 | |||||||
chr18:31400858 | C | T | 4 | a0001c0001t0001g0030 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
5 | HG02155.hp1 HG04228.hp1 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.1278-23C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 9/15 | chr18 | 31400858 | |||||||
chr18:31400868 | T | C | 1 | a0015c0031t0013g0090 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1278-13T>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 9/15 | chr18 | 31400868 | |||||||
chr18:31401068 | T | C | 1 | a0001c0005t0002g0076 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1417+48T>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 10/15 | chr18 | 31401068 | |||||||
chr18:31401145 | G | A | 4 | a0001c0008t0004g0068 a0004c0012t0001g0021 a0004c0012t0001g0065 others(1): Show |
5 | HG03491.hp1 HG03492.hp2 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.1417+125G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 10/15 | chr18 | 31401145 | |||||||
chr18:31401176 | C | T | 1 | a0010c0020t0006g0020 | 2 | HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1417+156C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 10/15 | chr18 | 31401176 | |||||||
chr18:31401322 | T | C | 1 | a0001c0004t0002g0038 | 2 | HG00099.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1417+302T>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 10/15 | chr18 | 31401322 | |||||||
chr18:31401551 | T | A | 4 | a0002c0010t0002g0024 a0002c0010t0002g0025 a0002c0010t0002g0052 others(1): Show |
6 | HG02622.hp2 HG02886.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1417+531T>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 10/15 | chr18 | 31401551 | |||||||
chr18:31401588 | A | C | 1 | a0001c0002t0004g0188 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1417+568A>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 10/15 | chr18 | 31401588 | |||||||
chr18:31401591 | C | T | 4 | a0001c0002t0007g0027 a0001c0002t0018g0044 a0015c0031t0013g0090 others(1): Show |
5 | HG01167.hp1 HG01169.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1417+571C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 10/15 | chr18 | 31401591 | |||||||
chr18:31401881 | A | G | 161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(158): Show |
250 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.1417+861A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 10/15 | chr18 | 31401881 | |||||||
chr18:31402048 | C | T | 12 | a0001c0004t0002g0004 a0001c0004t0002g0016 a0001c0004t0002g0037 others(9): Show |
24 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.1417+1028C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 10/15 | chr18 | 31402048 | |||||||
chr18:31402100 | ATAAT | A | 3 | a0006c0017t0002g0099 a0006c0017t0002g0100 a0006c0017t0004g0101 |
3 | HG02280.hp1 HG02723.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.1417+1083_1417+108 others(8): Show |
DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr18 | 31402100 | ||||||
chr18:31402260 | A | G | 2 | a0001c0003t0003g0033 a0001c0003t0003g0108 |
3 | HG02976.hp2 HG03453.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1418-1156A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 10/15 | chr18 | 31402260 | |||||||
chr18:31402289 | C | G | 1 | a0001c0003t0003g0207 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1418-1127C>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 10/15 | chr18 | 31402289 | |||||||
chr18:31402425 | C | T | 3 | a0001c0025t0003g0217 a0001c0025t0003g0218 a0001c0026t0002g0146 |
3 | HG02572.hp2 HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1418-991C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 10/15 | chr18 | 31402425 | |||||||
chr18:31402473 | G | C | 10 | a0001c0005t0002g0007 a0001c0005t0002g0076 a0001c0005t0002g0077 others(7): Show |
12 | HG02027.hp2 HG02040.hp1 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.1418-943G>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 10/15 | chr18 | 31402473 | |||||||
chr18:31402493 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1418-923T>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 10/15 | chr18 | 31402493 | |||||||
chr18:31402620 | G | T | 1 | a0001c0002t0007g0027 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1418-796G>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 10/15 | chr18 | 31402620 | |||||||
chr18:31402707 | C | CA | 161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(158): Show |
250 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.1418-701dupA | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr18 | 31402707 | ||||||
chr18:31402719 | C | T | 2 | a0001c0001t0001g0106 a0001c0005t0002g0061 |
2 | HG00544.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1418-697C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 10/15 | chr18 | 31402719 | |||||||
chr18:31402781 | C | A | 1 | a0001c0002t0007g0027 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1418-635C>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 10/15 | chr18 | 31402781 | |||||||
chr18:31402817 | C | T | 4 | a0001c0004t0002g0096 a0001c0005t0002g0088 a0001c0005t0002g0089 others(1): Show |
4 | HG02895.hp1 HG02965.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1418-599C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 10/15 | chr18 | 31402817 | |||||||
chr18:31402852 | T | G | 1 | a0001c0001t0001g0130 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1418-564T>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 10/15 | chr18 | 31402852 | |||||||
chr18:31403037 | T | C | 2 | a0001c0001t0001g0140 a0001c0001t0014g0138 |
2 | NA18972.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.1418-379T>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 10/15 | chr18 | 31403037 | |||||||
chr18:31403084 | G | A | 33 | a0001c0004t0002g0096 a0001c0005t0002g0007 a0001c0005t0002g0061 others(30): Show |
41 | HG01884.hp2 HG02027.hp2 HG02040.hp1 others(38): Show |
intron_variant | MODIFIER | c.1418-332G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 10/15 | chr18 | 31403084 | |||||||
chr18:31403148 | G | T | 1 | a0015c0031t0013g0090 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1418-268G>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 10/15 | chr18 | 31403148 | |||||||
chr18:31403166 | G | A | 1 | a0001c0001t0014g0138 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1418-250G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 10/15 | chr18 | 31403166 | |||||||
chr18:31403314 | G | A | 2 | a0001c0001t0001g0009 a0001c0006t0001g0009 |
4 | NA18977.hp2 NA19002.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.1418-102G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 10/15 | chr18 | 31403314 | |||||||
chr18:31403400 | A | G | 1 | a0001c0001t0001g0158 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1418-16A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 10/15 | chr18 | 31403400 | |||||||
chr18:31403711 | T | G | 1 | a0001c0001t0001g0122 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1636+77T>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 11/15 | chr18 | 31403711 | |||||||
chr18:31403746 | T | C | 10 | a0001c0005t0002g0007 a0001c0005t0002g0076 a0001c0005t0002g0077 others(7): Show |
12 | HG02027.hp2 HG02040.hp1 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.1636+112T>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 11/15 | chr18 | 31403746 | |||||||
chr18:31403833 | T | C | 2 | a0001c0001t0001g0155 a0001c0001t0001g0158 |
2 | NA18960.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.1636+199T>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 11/15 | chr18 | 31403833 | |||||||
chr18:31404296 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1636+662G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 11/15 | chr18 | 31404296 | |||||||
chr18:31404451 | T | C | 1 | a0001c0005t0017g0050 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1636+817T>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 11/15 | chr18 | 31404451 | |||||||
chr18:31404588 | G | GC | 4 | a0001c0002t0007g0027 a0001c0004t0004g0161 a0001c0004t0004g0168 others(1): Show |
5 | HG01167.hp1 HG01169.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1636+954_1636+955i others(3): Show |
DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 11/15 | chr18 | 31404588 | |||||||
chr18:31405034 | C | A | 1 | a0001c0001t0001g0123 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1637-1043C>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 11/15 | chr18 | 31405034 | |||||||
chr18:31405059 | G | A | 4 | a0002c0010t0002g0024 a0002c0010t0002g0025 a0002c0010t0002g0052 others(1): Show |
6 | HG02622.hp2 HG02886.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1637-1018G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 11/15 | chr18 | 31405059 | |||||||
chr18:31405413 | G | A | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(169): Show |
266 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.1637-664G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 11/15 | chr18 | 31405413 | |||||||
chr18:31405432 | T | C | 1 | a0001c0001t0001g0124 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1637-645T>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 11/15 | chr18 | 31405432 | |||||||
chr18:31405595 | T | C | 1 | a0001c0002t0004g0187 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1637-482T>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 11/15 | chr18 | 31405595 | |||||||
chr18:31405630 | T | A | 12 | a0001c0002t0002g0120 a0001c0002t0002g0219 a0001c0005t0002g0007 others(9): Show |
14 | HG02027.hp2 HG02040.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.1637-447T>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 11/15 | chr18 | 31405630 | |||||||
chr18:31405631 | C | G | 6 | a0002c0010t0002g0024 a0002c0010t0002g0025 a0002c0010t0002g0052 others(3): Show |
8 | HG02622.hp2 HG02886.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1637-446C>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 11/15 | chr18 | 31405631 | |||||||
chr18:31405896 | GAAT | G | 27 | a0001c0001t0001g0042 a0001c0001t0001g0204 a0001c0001t0001g0214 others(24): Show |
41 | HG00609.hp2 HG00735.hp1 HG01099.hp1 others(38): Show |
intron_variant | MODIFIER | c.1637-163_1637-161d others(5): Show |
DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr18 | 31405896 | ||||||
chr18:31405931 | A | T | 6 | a0002c0010t0002g0024 a0002c0010t0002g0025 a0002c0010t0002g0052 others(3): Show |
8 | HG02622.hp2 HG02886.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1637-146A>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 11/15 | chr18 | 31405931 | |||||||
chr18:31406007 | G | A | 1 | a0001c0002t0004g0188 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1637-70G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 11/15 | chr18 | 31406007 | |||||||
chr18:31406025 | T | C | 4 | a0001c0005t0002g0085 a0001c0019t0003g0125 a0001c0025t0003g0217 others(1): Show |
4 | HG02451.hp2 HG03098.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1637-52T>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 11/15 | chr18 | 31406025 | |||||||
chr18:31406436 | G | A | 1 | a0001c0009t0003g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1933+63G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 12/15 | chr18 | 31406436 | |||||||
chr18:31406473 | G | C | 1 | a0018c0028t0003g0192 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1933+100G>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 12/15 | chr18 | 31406473 | |||||||
chr18:31406597 | T | A | 1 | a0019c0033t0004g0197 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1933+224T>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 12/15 | chr18 | 31406597 | |||||||
chr18:31406762 | AT | A | 29 | a0001c0002t0002g0120 a0001c0002t0002g0143 a0001c0002t0002g0144 others(26): Show |
31 | HG00438.hp1 HG01891.hp1 HG02040.hp1 others(28): Show |
intron_variant | MODIFIER | c.1933+399delT | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 31406762 | ||||||
chr18:31406809 | G | A | 1 | a0001c0002t0004g0180 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1933+436G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 12/15 | chr18 | 31406809 | |||||||
chr18:31406863 | T | C | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(199): Show |
300 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(297): Show |
intron_variant | MODIFIER | c.1933+490T>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 12/15 | chr18 | 31406863 | |||||||
chr18:31406864 | G | A | 15 | a0001c0004t0002g0096 a0001c0005t0002g0061 a0001c0005t0002g0088 others(12): Show |
15 | HG01891.hp1 HG02451.hp2 HG02809.hp1 others(12): Show |
intron_variant | MODIFIER | c.1933+491G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 12/15 | chr18 | 31406864 | |||||||
chr18:31406903 | G | A | 37 | a0001c0002t0002g0120 a0001c0002t0002g0143 a0001c0002t0002g0144 others(34): Show |
42 | HG00438.hp1 HG01167.hp1 HG01169.hp1 others(39): Show |
intron_variant | MODIFIER | c.1933+530G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 12/15 | chr18 | 31406903 | |||||||
chr18:31406913 | G | A | 1 | a0001c0001t0001g0148 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1933+540G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 12/15 | chr18 | 31406913 | |||||||
chr18:31406935 | G | A | 4 | a0001c0002t0002g0091 a0001c0002t0004g0126 a0001c0002t0018g0044 others(1): Show |
5 | HG02451.hp1 HG02630.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1933+562G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 12/15 | chr18 | 31406935 | |||||||
chr18:31406966 | C | T | 7 | a0001c0005t0002g0085 a0001c0026t0002g0146 a0002c0010t0002g0024 others(4): Show |
9 | HG02280.hp1 HG02572.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1933+593C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 12/15 | chr18 | 31406966 | |||||||
chr18:31407060 | G | C | 1 | a0001c0008t0002g0066 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1933+687G>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 12/15 | chr18 | 31407060 | |||||||
chr18:31407146 | A | G | 1 | a0001c0003t0003g0212 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1933+773A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 12/15 | chr18 | 31407146 | |||||||
chr18:31407229 | G | A | 1 | a0010c0020t0006g0020 | 2 | HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1933+856G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 12/15 | chr18 | 31407229 | |||||||
chr18:31407469 | GT | G | 26 | a0001c0001t0001g0042 a0001c0001t0001g0214 a0001c0003t0003g0005 others(23): Show |
42 | HG00609.hp2 HG00735.hp1 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.1933+1103delT | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr18 | 31407469 | ||||||
chr18:31407471 | T | C | 26 | a0001c0001t0001g0042 a0001c0001t0001g0214 a0001c0003t0003g0005 others(23): Show |
42 | HG00609.hp2 HG00735.hp1 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.1933+1098T>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 12/15 | chr18 | 31407471 | |||||||
chr18:31407482 | T | A | 47 | a0001c0001t0001g0042 a0001c0001t0001g0214 a0001c0002t0002g0176 others(44): Show |
75 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.1933+1109T>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 12/15 | chr18 | 31407482 | |||||||
chr18:31407528 | T | C | 4 | a0001c0002t0004g0017 a0001c0002t0004g0183 a0001c0002t0004g0189 others(1): Show |
6 | HG03927.hp2 NA18954.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.1933+1155T>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 12/15 | chr18 | 31407528 | |||||||
chr18:31407733 | G | A | 1 | a0011c0022t0006g0059 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1933+1360G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 12/15 | chr18 | 31407733 | |||||||
chr18:31407741 | C | T | 1 | a0001c0001t0001g0127 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1933+1368C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 12/15 | chr18 | 31407741 | |||||||
chr18:31407770 | G | A | 4 | a0001c0002t0002g0091 a0001c0002t0004g0126 a0001c0002t0018g0044 others(1): Show |
5 | HG02451.hp1 HG02630.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1933+1397G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 12/15 | chr18 | 31407770 | |||||||
chr18:31407776 | A | G | 1 | a0015c0031t0013g0090 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1933+1403A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 12/15 | chr18 | 31407776 | |||||||
chr18:31407962 | A | G | 27 | a0001c0002t0002g0120 a0001c0002t0002g0143 a0001c0002t0002g0144 others(24): Show |
29 | HG00438.hp1 HG01891.hp1 HG02040.hp1 others(26): Show |
intron_variant | MODIFIER | c.1934-1490A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 12/15 | chr18 | 31407962 | |||||||
chr18:31407989 | G | A | 1 | a0001c0002t0002g0128 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1934-1463G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 12/15 | chr18 | 31407989 | |||||||
chr18:31408192 | G | A | 1 | a0001c0002t0004g0139 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1934-1260G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 12/15 | chr18 | 31408192 | |||||||
chr18:31408249 | T | C | 1 | a0001c0002t0007g0027 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1934-1203T>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 12/15 | chr18 | 31408249 | |||||||
chr18:31408271 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1934-1181C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 12/15 | chr18 | 31408271 | |||||||
chr18:31408505 | A | C | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(73): Show |
124 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.1934-947A>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 12/15 | chr18 | 31408505 | |||||||
chr18:31408761 | C | T | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(199): Show |
300 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(297): Show |
intron_variant | MODIFIER | c.1934-691C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 12/15 | chr18 | 31408761 | |||||||
chr18:31408827 | A | G | 2 | a0001c0001t0001g0135 a0001c0016t0001g0045 |
2 | HG03942.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1934-625A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 12/15 | chr18 | 31408827 | |||||||
chr18:31408953 | A | G | 4 | a0001c0001t0001g0110 a0001c0006t0001g0094 a0001c0006t0001g0165 others(1): Show |
4 | HG02970.hp1 HG03486.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1934-499A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 12/15 | chr18 | 31408953 | |||||||
chr18:31409026 | G | C | 1 | a0001c0001t0001g0030 | 2 | NA18960.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.1934-426G>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 12/15 | chr18 | 31409026 | |||||||
chr18:31409032 | A | G | 1 | a0015c0031t0013g0090 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1934-420A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 12/15 | chr18 | 31409032 | |||||||
chr18:31409202 | G | A | 11 | a0001c0004t0002g0096 a0001c0005t0002g0088 a0001c0005t0002g0089 others(8): Show |
11 | HG01891.hp1 HG02451.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.1934-250G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 12/15 | chr18 | 31409202 | |||||||
chr18:31409221 | G | A | 1 | a0001c0002t0007g0027 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1934-231G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 12/15 | chr18 | 31409221 | |||||||
chr18:31409253 | A | G | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(74): Show |
125 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.1934-199A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 12/15 | chr18 | 31409253 | |||||||
chr18:31409269 | C | T | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(200): Show |
301 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(298): Show |
intron_variant | MODIFIER | c.1934-183C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 12/15 | chr18 | 31409269 | |||||||
chr18:31409303 | C | T | 1 | a0001c0005t0002g0080 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1934-149C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 12/15 | chr18 | 31409303 | |||||||
chr18:31409304 | C | T | 1 | a0001c0001t0001g0114 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1934-148C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 12/15 | chr18 | 31409304 | |||||||
chr18:31409711 | C | T | 51 | a0001c0001t0001g0042 a0001c0001t0001g0214 a0001c0002t0002g0091 others(48): Show |
80 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.2074-34C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 13/15 | chr18 | 31409711 | |||||||
chr18:31409844 | T | C | 2 | a0001c0001t0001g0122 a0001c0001t0001g0141 |
2 | HG00438.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.2137+36T>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 14/15 | chr18 | 31409844 | |||||||
chr18:31409965 | T | G | 1 | a0002c0036t0002g0053 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2137+157T>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 14/15 | chr18 | 31409965 | |||||||
chr18:31410021 | C | T | 1 | a0001c0002t0004g0043 | 2 | NA19068.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.2137+213C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 14/15 | chr18 | 31410021 | |||||||
chr18:31410165 | A | G | 1 | a0021c0034t0003g0070 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2137+357A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 14/15 | chr18 | 31410165 | |||||||
chr18:31410243 | C | T | 1 | a0001c0008t0002g0084 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2137+435C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 14/15 | chr18 | 31410243 | |||||||
chr18:31410349 | AATAC | A | 23 | a0001c0002t0002g0176 a0001c0004t0002g0004 a0001c0004t0002g0016 others(20): Show |
35 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.2137+549_2137+552d others(6): Show |
DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr18 | 31410349 | ||||||
chr18:31410358 | A | T | 13 | a0001c0005t0002g0061 a0001c0005t0017g0050 a0001c0008t0002g0084 others(10): Show |
13 | HG01891.hp1 HG02451.hp2 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.2137+550A>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 14/15 | chr18 | 31410358 | |||||||
chr18:31410398 | T | C | 1 | a0001c0004t0002g0153 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2137+590T>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 14/15 | chr18 | 31410398 | |||||||
chr18:31410444 | T | C | 2 | a0001c0005t0002g0061 a0017c0041t0002g0060 |
2 | HG02895.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.2137+636T>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 14/15 | chr18 | 31410444 | |||||||
chr18:31410457 | C | T | 4 | a0001c0002t0002g0091 a0001c0002t0004g0126 a0001c0002t0018g0044 others(1): Show |
5 | HG02451.hp1 HG02630.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2137+649C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 14/15 | chr18 | 31410457 | |||||||
chr18:31410486 | C | CACAGAGT others(7): Show |
14 | a0001c0002t0007g0027 a0001c0005t0002g0061 a0001c0005t0017g0050 others(11): Show |
15 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.2137+680_2137+681i others(16): Show |
DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr18 | 31410486 | ||||||
chr18:31410616 | C | A | 1 | a0001c0005t0002g0078 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2138-615C>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 14/15 | chr18 | 31410616 | |||||||
chr18:31410644 | C | T | 1 | a0003c0011t0003g0087 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2138-587C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 14/15 | chr18 | 31410644 | |||||||
chr18:31410727 | C | T | 4 | a0001c0001t0001g0042 a0001c0001t0001g0214 a0001c0003t0003g0010 others(1): Show |
8 | HG00609.hp2 HG02056.hp1 NA18612.hp1 others(5): Show |
intron_variant | MODIFIER | c.2138-504C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 14/15 | chr18 | 31410727 | |||||||
chr18:31410865 | C | A | 1 | a0001c0004t0002g0151 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2138-366C>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 14/15 | chr18 | 31410865 | |||||||
chr18:31410935 | G | C | 7 | a0001c0005t0002g0085 a0001c0026t0002g0146 a0002c0010t0002g0024 others(4): Show |
9 | HG02280.hp1 HG02572.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.2138-296G>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 14/15 | chr18 | 31410935 | |||||||
chr18:31411038 | G | A | 1 | a0001c0002t0016g0194 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2138-193G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 14/15 | chr18 | 31411038 | |||||||
chr18:31411078 | G | T | 7 | a0001c0001t0001g0030 a0001c0001t0001g0103 a0001c0001t0001g0130 others(4): Show |
8 | HG02027.hp2 HG02155.hp1 HG03942.hp1 others(5): Show |
intron_variant | MODIFIER | c.2138-153G>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 14/15 | chr18 | 31411078 | |||||||
chr18:31411098 | T | G | 61 | a0001c0001t0001g0206 a0001c0001t0002g0018 a0001c0002t0002g0120 others(58): Show |
78 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.2138-133T>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 14/15 | chr18 | 31411098 | |||||||
chr18:31411112 | T | C | 1 | a0015c0031t0013g0090 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2138-119T>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 14/15 | chr18 | 31411112 | |||||||
chr18:31411542 | T | C | 60 | a0001c0001t0002g0018 a0001c0002t0002g0120 a0001c0002t0002g0143 others(57): Show |
77 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.2355+94T>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 15/15 | chr18 | 31411542 | |||||||
chr18:31411785 | G | GA | 9 | a0001c0009t0003g0057 a0001c0019t0003g0125 a0001c0025t0003g0217 others(6): Show |
9 | HG01891.hp1 HG02109.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2355+343dupA | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | 31411785 | ||||||
chr18:31412008 | C | T | 1 | a0001c0006t0001g0172 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2355+560C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 15/15 | chr18 | 31412008 | |||||||
chr18:31412058 | A | C | 1 | a0001c0002t0004g0190 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2355+610A>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 15/15 | chr18 | 31412058 | |||||||
chr18:31412095 | T | C | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(170): Show |
258 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.2355+647T>C | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 15/15 | chr18 | 31412095 | |||||||
chr18:31412098 | C | T | 4 | a0001c0002t0002g0128 a0001c0008t0002g0011 a0001c0008t0002g0023 others(1): Show |
7 | HG02083.hp2 HG03041.hp1 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.2355+650C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 15/15 | chr18 | 31412098 | |||||||
chr18:31412149 | C | T | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(174): Show |
264 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.2356-679C>T | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 15/15 | chr18 | 31412149 | |||||||
chr18:31412236 | G | A | 1 | a0001c0003t0003g0205 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2356-592G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 15/15 | chr18 | 31412236 | |||||||
chr18:31412540 | G | A | 1 | a0009c0021t0012g0055 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2356-288G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 15/15 | chr18 | 31412540 | |||||||
chr18:31412659 | A | G | 1 | a0015c0031t0013g0090 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2356-169A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 15/15 | chr18 | 31412659 | |||||||
chr18:31412679 | A | G | 2 | a0001c0002t0004g0126 a0001c0002t0018g0044 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.2356-149A>G | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 15/15 | chr18 | 31412679 | |||||||
chr18:31412728 | G | A | 1 | a0017c0041t0002g0060 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2356-100G>A | DSG4 | ENSG00000175065.12 | transcript | ENST00000308128.9 | protein_coding | 15/15 | chr18 | 31412728 |