Item | Value |
---|---|
geneid | 127 |
ensemblid | ENSG00000198099.10 |
hgncid | 252 |
symbol | ADH4 |
name | alcohol dehydrogenase 4 (class II), pi polypeptide |
refseq_nuc | NM_000670.5 |
refseq_prot | NP_000661.2 |
ensembl_nuc | ENST00000265512.12 |
ensembl_prot | ENSP00000265512.7 |
mane_status | MANE Select |
chr | chr4 |
start | 99123658 |
end | 99144297 |
strand | - |
ver | v1.2 |
region | chr4:99123658-99144297 |
region5000 | chr4:99118658-99149297 |
regionname0 | ADH4_chr4_99123658_99144297 |
regionname5000 | ADH4_chr4_99118658_99149297 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 380 | 292 | 77 | 53 | 129 | 10 | 23 | 101 | ADH4_chr4_99118658_99149297 | ADH4 | MGTKG others(375): Show |
chr4 | 99118658 | 99149297 |
a0002 | 1/1 | 380 | 35 | 10 | 18 | 0 | 4 | 1 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | MGTKG others(375): Show |
chr4 | 99118658 | 99149297 |
a0003 | 0/0 | 380 | 4 | 0 | 0 | 4 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | MGTKG others(375): Show |
chr4 | 99118658 | 99149297 |
a0004 | 0/0 | 380 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | MGTKG others(375): Show |
chr4 | 99118658 | 99149297 |
a0005 | 0/0 | 380 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | MGTKG others(375): Show |
chr4 | 99118658 | 99149297 |
a0006 | 0/0 | 380 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | MGTKG others(375): Show |
chr4 | 99118658 | 99149297 |
a0007 | 0/0 | 380 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | MGTKG others(375): Show |
chr4 | 99118658 | 99149297 |
a0008 | 0/0 | 380 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | MGTKG others(375): Show |
chr4 | 99118658 | 99149297 |
a0009 | 0/0 | 380 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADH4_chr4_99118658_99149297 | ADH4 | MGTKG others(375): Show |
chr4 | 99118658 | 99149297 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1140 | 291 | 77 | 53 | 128 | 10 | 23 | ADH4_chr4_99118658_99149297 | ADH4 | ATGGG others(1135): Show |
chr4 | 99118658 | 99149297 | ||
a0001c0007 | 0/0 | 1140 | 1 | 0 | 0 | 1 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | ATGGG others(1135): Show |
chr4 | 99118658 | 99149297 | ||
a0002c0002 | 0/1 | 1140 | 27 | 4 | 17 | 0 | 4 | 1 | ADH4_chr4_99118658_99149297 | ADH4 | ATGGG others(1135): Show |
chr4 | 99118658 | 99149297 | ||
a0002c0003 | 1/0 | 1140 | 8 | 6 | 1 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | ATGGG others(1135): Show |
chr4 | 99118658 | 99149297 | ||
a0003c0004 | 0/0 | 1140 | 4 | 0 | 0 | 4 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | ATGGG others(1135): Show |
chr4 | 99118658 | 99149297 | ||
a0004c0005 | 0/0 | 1140 | 2 | 2 | 0 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | ATGGG others(1135): Show |
chr4 | 99118658 | 99149297 | ||
a0005c0008 | 0/0 | 1140 | 1 | 0 | 1 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | ATGGG others(1135): Show |
chr4 | 99118658 | 99149297 | ||
a0006c0010 | 0/0 | 1140 | 1 | 1 | 0 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | ATGGG others(1135): Show |
chr4 | 99118658 | 99149297 | ||
a0007c0006 | 0/0 | 1140 | 1 | 0 | 0 | 0 | 0 | 1 | ADH4_chr4_99118658_99149297 | ADH4 | ATGGG others(1135): Show |
chr4 | 99118658 | 99149297 | ||
a0008c0011 | 0/0 | 1140 | 1 | 0 | 0 | 0 | 0 | 1 | ADH4_chr4_99118658_99149297 | ADH4 | ATGGG others(1135): Show |
chr4 | 99118658 | 99149297 | ||
a0009c0009 | 0/0 | 1140 | 1 | 0 | 0 | 1 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | ATGGG others(1135): Show |
chr4 | 99118658 | 99149297 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2002 | 274 | 61 | 52 | 128 | 10 | 23 | ADH4_chr4_99118658_99149297 | ADH4 | ACGGA others(1997): Show |
chr4 | 99118658 | 99149297 |
a0001c0001t0003 | 0/0 | 2002 | 14 | 14 | 0 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | ACGGA others(1997): Show |
chr4 | 99118658 | 99149297 |
a0001c0001t0004 | 0/0 | 2002 | 1 | 1 | 0 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | ACGGA others(1997): Show |
chr4 | 99118658 | 99149297 |
a0001c0001t0005 | 0/0 | 2002 | 1 | 1 | 0 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | ACGGA others(1997): Show |
chr4 | 99118658 | 99149297 |
a0001c0001t0006 | 0/0 | 2002 | 1 | 0 | 1 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | ACGGA others(1997): Show |
chr4 | 99118658 | 99149297 |
a0001c0007t0001 | 0/0 | 2002 | 1 | 0 | 0 | 1 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | ACGGA others(1997): Show |
chr4 | 99118658 | 99149297 |
a0002c0002t0002 | 0/1 | 2002 | 27 | 4 | 17 | 0 | 4 | 1 | ADH4_chr4_99118658_99149297 | ADH4 | ACGGA others(1997): Show |
chr4 | 99118658 | 99149297 |
a0002c0003t0002 | 1/0 | 2002 | 1 | 0 | 0 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | ACGGA others(1997): Show |
chr4 | 99118658 | 99149297 |
a0002c0003t0003 | 0/0 | 2002 | 7 | 6 | 1 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | ACGGA others(1997): Show |
chr4 | 99118658 | 99149297 |
a0003c0004t0001 | 0/0 | 2002 | 4 | 0 | 0 | 4 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | ACGGA others(1997): Show |
chr4 | 99118658 | 99149297 |
a0004c0005t0001 | 0/0 | 2002 | 2 | 2 | 0 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | ACGGA others(1997): Show |
chr4 | 99118658 | 99149297 |
a0005c0008t0001 | 0/0 | 2002 | 1 | 0 | 1 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | ACGGA others(1997): Show |
chr4 | 99118658 | 99149297 |
a0006c0010t0003 | 0/0 | 2002 | 1 | 1 | 0 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | ACGGA others(1997): Show |
chr4 | 99118658 | 99149297 |
a0007c0006t0001 | 0/0 | 2002 | 1 | 0 | 0 | 0 | 0 | 1 | ADH4_chr4_99118658_99149297 | ADH4 | ACGGA others(1997): Show |
chr4 | 99118658 | 99149297 |
a0008c0011t0001 | 0/0 | 2002 | 1 | 0 | 0 | 0 | 0 | 1 | ADH4_chr4_99118658_99149297 | ADH4 | ACGGA others(1997): Show |
chr4 | 99118658 | 99149297 |
a0009c0009t0001 | 0/0 | 2002 | 1 | 0 | 0 | 1 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | ACGGA others(1997): Show |
chr4 | 99118658 | 99149297 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 48 | 1 | 15 | 29 | 1 | 2 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0002 | 0/0 | 38 | 0 | 0 | 38 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0003 | 0/0 | 24 | 1 | 8 | 9 | 0 | 6 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0004 | 0/0 | 23 | 1 | 9 | 4 | 4 | 5 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0005 | 0/0 | 21 | 15 | 6 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0006 | 0/0 | 20 | 0 | 1 | 14 | 2 | 3 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0009 | 0/0 | 7 | 1 | 3 | 0 | 2 | 1 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0011 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0014 | 0/0 | 4 | 1 | 2 | 0 | 0 | 1 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0018 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0020 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0003g0008 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0003g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0003g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0003g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0004g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0005g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0001t0006g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0001c0007t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0002c0002t0002g0007 | 0/0 | 11 | 2 | 9 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0002c0002t0002g0010 | 0/0 | 6 | 0 | 3 | 0 | 2 | 1 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0002c0002t0002g0037 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0002c0002t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0002c0002t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0002c0002t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0002c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0002c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0002c0002t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0002c0002t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0002c0002t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0002c0002t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0002c0003t0002g0060 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0002c0003t0003g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0002c0003t0003g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0002c0003t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0003c0004t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0004c0005t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0005c0008t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0006c0010t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0007c0006t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0008c0011t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
a0009c0009t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | GBR | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0091 | EUR | FIN | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | CHS | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG00733 | hp2 | a0005 | c0008 | t0001 | g0082 | AMR | PUR | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG00741 | hp1 | a0002 | c0002 | t0002 | g0010 | AMR | PUR | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG00741 | hp2 | a0002 | c0002 | t0002 | g0007 | AMR | PUR | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01069 | hp1 | a0002 | c0002 | t0002 | g0007 | AMR | PUR | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01074 | hp2 | a0002 | c0002 | t0002 | g0007 | AMR | PUR | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01081 | hp2 | a0002 | c0002 | t0002 | g0007 | AMR | PUR | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01106 | hp1 | a0002 | c0002 | t0002 | g0040 | AMR | PUR | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01243 | hp2 | a0001 | c0001 | t0006 | g0052 | AMR | PUR | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01256 | hp2 | a0002 | c0002 | t0002 | g0007 | AMR | CLM | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01258 | hp1 | a0002 | c0002 | t0002 | g0007 | AMR | CLM | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01261 | hp1 | a0002 | c0002 | t0002 | g0010 | AMR | CLM | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01346 | hp1 | a0002 | c0002 | t0002 | g0044 | AMR | CLM | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01358 | hp2 | a0002 | c0002 | t0002 | g0007 | AMR | CLM | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01361 | hp1 | a0002 | c0002 | t0002 | g0039 | AMR | CLM | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01361 | hp2 | a0002 | c0002 | t0002 | g0045 | AMR | CLM | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01496 | hp2 | a0002 | c0002 | t0002 | g0010 | AMR | CLM | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01515 | hp1 | a0002 | c0002 | t0002 | g0041 | EUR | IBS | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01516 | hp2 | a0002 | c0002 | t0002 | g0042 | EUR | IBS | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01517 | hp1 | a0002 | c0002 | t0002 | g0010 | EUR | IBS | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02027 | hp1 | a0003 | c0004 | t0001 | g0015 | EAS | KHV | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02071 | hp2 | a0001 | c0007 | t0001 | g0081 | EAS | KHV | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02083 | hp2 | a0003 | c0004 | t0001 | g0015 | EAS | KHV | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02132 | hp2 | a0003 | c0004 | t0001 | g0015 | EAS | KHV | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02135 | hp2 | a0003 | c0004 | t0001 | g0015 | EAS | KHV | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02148 | hp2 | a0002 | c0002 | t0002 | g0007 | AMR | PEL | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02257 | hp1 | a0006 | c0010 | t0003 | g0058 | AFR | ACB | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02258 | hp2 | a0002 | c0003 | t0003 | g0013 | AFR | ACB | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0057 | AFR | ACB | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02293 | hp1 | a0002 | c0003 | t0003 | g0059 | AMR | PEL | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02300 | hp1 | a0002 | c0002 | t0002 | g0007 | AMR | PEL | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02451 | hp1 | a0002 | c0003 | t0003 | g0013 | AFR | ACB | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02602 | hp1 | a0002 | c0002 | t0002 | g0010 | SAS | PJL | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02602 | hp2 | a0007 | c0006 | t0001 | g0095 | SAS | PJL | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02615 | hp2 | a0002 | c0002 | t0002 | g0007 | AFR | GWD | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02622 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | GWD | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02622 | hp2 | a0002 | c0002 | t0002 | g0096 | AFR | GWD | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02630 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | GWD | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02647 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02723 | hp2 | a0002 | c0003 | t0003 | g0021 | AFR | GWD | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02818 | hp2 | a0001 | c0001 | t0005 | g0092 | AFR | GWD | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0022 | AFR | ESN | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ESN | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02970 | hp2 | a0002 | c0003 | t0003 | g0013 | AFR | ESN | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG03209 | hp1 | a0004 | c0005 | t0001 | g0027 | AFR | MSL | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG03225 | hp1 | a0001 | c0001 | t0003 | g0022 | AFR | MSL | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | MSL | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG03486 | hp2 | a0002 | c0003 | t0003 | g0013 | AFR | MSL | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | MSL | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG03688 | hp2 | a0008 | c0011 | t0001 | g0055 | SAS | STU | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | STU | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | YRI | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHB | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | LWK | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | LWK | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | LWK | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19059 | hp1 | a0009 | c0009 | t0001 | g0070 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19059 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | YRI | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ASW | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA20129 | hp2 | a0002 | c0002 | t0002 | g0038 | AFR | ASW | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | TSI | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA20805 | hp2 | a0002 | c0002 | t0002 | g0010 | EUR | TSI | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01123 | hp1 | a0002 | c0002 | t0002 | g0043 | AMR | CLM | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02109 | hp2 | a0001 | c0001 | t0004 | g0094 | AFR | ACB | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | ACB | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02559 | hp1 | a0004 | c0005 | t0001 | g0027 | AFR | ACB | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | ACB | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | MSL | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG06807 | hp1 | a0002 | c0003 | t0003 | g0021 | AFR | USA | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | USA | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA20300 | hp1 | a0002 | c0002 | t0002 | g0007 | AFR | USA | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | USA | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | LWK | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
homoSapiens | chm13v2 | a0002 | c0002 | t0002 | g0037 | REF | REF | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
homoSapiens | grch38p0 | a0002 | c0003 | t0002 | g0060 | REF | REF | ADH4_chr4_99118658_99149297 | ADH4 | chr4 | 99118658 | 99149297 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:99124464 | A | C | 1 | a0001 | 1 | HG02071.hp2 | missense_variant&splice_region_variant | MODERATE | c.1121T>G | p.Val374Gly | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 9/9 | 1196/2002 | 1121/1143 | 374/380 | chr4 | 99124464 | |||
chr4:99124465 | C | T | 8 | a0001 a0003 a0004 others(5): Show |
303 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(300): Show |
missense_variant&splice_region_variant | MODERATE | c.1120G>A | p.Val374Ile | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 9/9 | 1195/2002 | 1120/1143 | 374/380 | chr4 | 99124465 | |||
chr4:99126690 | T | C | 1 | a0005 | 1 | HG00733.hp2 | missense_variant | MODERATE | c.1022A>G | p.Tyr341Cys | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 8/9 | 1097/2002 | 1022/1143 | 341/380 | chr4 | 99126690 | |||
chr4:99127242 | T | G | 1 | a0009 | 1 | NA19059.hp1 | missense_variant | MODERATE | c.946A>C | p.Ile316Leu | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 7/9 | 1021/2002 | 946/1143 | 316/380 | chr4 | 99127242 | |||
chr4:99127257 | G | A | 1 | a0009 | 1 | NA19059.hp1 | missense_variant | MODERATE | c.931C>T | p.Pro311Ser | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 7/9 | 1006/2002 | 931/1143 | 311/380 | chr4 | 99127257 | |||
chr4:99127263 | T | C | 8 | a0001 a0003 a0004 others(5): Show |
303 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(300): Show |
missense_variant | MODERATE | c.925A>G | p.Ile309Val | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 7/9 | 1000/2002 | 925/1143 | 309/380 | chr4 | 99127263 | |||
chr4:99131701 | C | G | 1 | a0007 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.646G>C | p.Gly216Arg | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/9 | 721/2002 | 646/1143 | 216/380 | chr4 | 99131701 | |||
chr4:99136576 | C | A | 1 | a0003 | 4 | HG02027.hp1 HG02083.hp2 HG02132.hp2 others(1): Show |
missense_variant | MODERATE | c.472G>T | p.Val158Leu | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/9 | 547/2002 | 472/1143 | 158/380 | chr4 | 99136576 | |||
chr4:99141555 | G | A | 1 | a0006 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.248C>T | p.Thr83Ile | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 3/9 | 323/2002 | 248/1143 | 83/380 | chr4 | 99141555 | |||
chr4:99141570 | A | G | 1 | a0004 | 2 | HG02559.hp1 HG03209.hp1 |
missense_variant | MODERATE | c.233T>C | p.Ile78Thr | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 3/9 | 308/2002 | 233/1143 | 78/380 | chr4 | 99141570 | |||
chr4:99141640 | C | A | 1 | a0008 | 1 | HG03688.hp2 | missense_variant | MODERATE | c.163G>T | p.Asp55Tyr | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 3/9 | 238/2002 | 163/1143 | 55/380 | chr4 | 99141640 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:99126661 | G | A | 1 | a0002c0002 | 26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
synonymous_variant | LOW | c.1051C>T | p.Leu351Leu | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 8/9 | 1126/2002 | 1051/1143 | 351/380 | chr4 | 99126661 | |||
chr4:99131582 | C | A | 9 | a0001c0001 a0001c0007 a0003c0004 others(6): Show |
303 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(300): Show |
synonymous_variant | LOW | c.765G>T | p.Pro255Pro | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/9 | 840/2002 | 765/1143 | 255/380 | chr4 | 99131582 | |||
chr4:99141668 | A | G | 10 | a0001c0001 a0001c0007 a0002c0002 others(7): Show |
329 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(326): Show |
synonymous_variant | LOW | c.135T>C | p.Ser45Ser | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 3/9 | 210/2002 | 135/1143 | 45/380 | chr4 | 99141668 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:99123671 | T | C | 14 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(11): Show |
310 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(307): Show |
3_prime_UTR_variant | MODIFIER | c.*771A>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 9/9 | 771 | chr4 | 99123671 | ||||||
chr4:99123990 | C | T | 11 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(8): Show |
288 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(285): Show |
3_prime_UTR_variant | MODIFIER | c.*452G>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 9/9 | 452 | chr4 | 99123990 | ||||||
chr4:99124012 | T | C | 1 | a0001c0001t0005 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*430A>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 9/9 | 430 | chr4 | 99124012 | ||||||
chr4:99124257 | A | G | 1 | a0001c0001t0004 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*185T>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 9/9 | 185 | chr4 | 99124257 | ||||||
chr4:99124349 | T | G | 14 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(11): Show |
310 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(307): Show |
3_prime_UTR_variant | MODIFIER | c.*93A>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 9/9 | 93 | chr4 | 99124349 | ||||||
chr4:99124394 | G | A | 1 | a0001c0001t0006 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*48C>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 9/9 | 48 | chr4 | 99124394 | ||||||
chr4:99124423 | T | C | 14 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(11): Show |
310 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(307): Show |
3_prime_UTR_variant | MODIFIER | c.*19A>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 9/9 | 19 | chr4 | 99124423 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:99124496 | A | G | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(82): Show |
310 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(307): Show |
intron_variant | MODIFIER | c.1119-30T>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 8/8 | chr4 | 99124496 | |||||||
chr4:99124565 | T | C | 2 | a0001c0001t0001g0068 a0001c0001t0001g0071 |
2 | HG00544.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.1119-99A>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 8/8 | chr4 | 99124565 | |||||||
chr4:99124689 | C | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(82): Show |
310 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(307): Show |
intron_variant | MODIFIER | c.1119-223G>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 8/8 | chr4 | 99124689 | |||||||
chr4:99124701 | C | T | 1 | a0001c0001t0003g0008 | 7 | HG02486.hp2 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1119-235G>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 8/8 | chr4 | 99124701 | |||||||
chr4:99124702 | G | A | 2 | a0001c0001t0001g0072 a0002c0002t0002g0043 |
2 | HG01123.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.1119-236C>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 8/8 | chr4 | 99124702 | |||||||
chr4:99124823 | T | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(82): Show |
310 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(307): Show |
intron_variant | MODIFIER | c.1119-357A>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 8/8 | chr4 | 99124823 | |||||||
chr4:99124902 | C | A | 1 | a0001c0001t0004g0094 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1119-436G>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 8/8 | chr4 | 99124902 | |||||||
chr4:99124905 | CA | C | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(79): Show |
303 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(300): Show |
intron_variant | MODIFIER | c.1119-440delT | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 8/8 | chr4 | 99124905 | |||||||
chr4:99124940 | G | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(82): Show |
310 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(307): Show |
intron_variant | MODIFIER | c.1119-474C>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 8/8 | chr4 | 99124940 | |||||||
chr4:99124953 | T | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(82): Show |
310 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(307): Show |
intron_variant | MODIFIER | c.1119-487A>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 8/8 | chr4 | 99124953 | |||||||
chr4:99125056 | A | G | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(82): Show |
310 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(307): Show |
intron_variant | MODIFIER | c.1119-590T>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 8/8 | chr4 | 99125056 | |||||||
chr4:99125104 | C | A | 1 | a0009c0009t0001g0070 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.1119-638G>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 8/8 | chr4 | 99125104 | |||||||
chr4:99125105 | A | C | 1 | a0009c0009t0001g0070 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.1119-639T>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 8/8 | chr4 | 99125105 | |||||||
chr4:99125142 | A | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(82): Show |
310 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(307): Show |
intron_variant | MODIFIER | c.1119-676T>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 8/8 | chr4 | 99125142 | |||||||
chr4:99125168 | A | T | 1 | a0009c0009t0001g0070 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.1119-702T>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 8/8 | chr4 | 99125168 | |||||||
chr4:99125183 | G | C | 2 | a0001c0001t0001g0031 a0001c0001t0001g0084 |
3 | HG03139.hp2 HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1119-717C>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 8/8 | chr4 | 99125183 | |||||||
chr4:99125503 | G | C | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.1119-1037C>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 8/8 | chr4 | 99125503 | |||||||
chr4:99125529 | T | C | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.1119-1063A>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 8/8 | chr4 | 99125529 | |||||||
chr4:99125534 | T | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(90): Show |
329 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(326): Show |
intron_variant | MODIFIER | c.1118+1060A>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 8/8 | chr4 | 99125534 | |||||||
chr4:99125616 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1118+978G>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 8/8 | chr4 | 99125616 | |||||||
chr4:99125672 | A | G | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.1118+922T>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 8/8 | chr4 | 99125672 | |||||||
chr4:99125933 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1118+661G>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 8/8 | chr4 | 99125933 | |||||||
chr4:99125942 | T | A | 6 | a0001c0001t0003g0008 a0001c0001t0003g0022 a0001c0001t0003g0023 others(3): Show |
15 | HG02257.hp1 HG02280.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.1118+652A>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 8/8 | chr4 | 99125942 | |||||||
chr4:99125978 | A | T | 1 | a0009c0009t0001g0070 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.1118+616T>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 8/8 | chr4 | 99125978 | |||||||
chr4:99126000 | A | T | 1 | a0009c0009t0001g0070 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.1118+594T>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 8/8 | chr4 | 99126000 | |||||||
chr4:99126001 | T | C | 1 | a0009c0009t0001g0070 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.1118+593A>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 8/8 | chr4 | 99126001 | |||||||
chr4:99126006 | C | A | 1 | a0009c0009t0001g0070 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.1118+588G>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 8/8 | chr4 | 99126006 | |||||||
chr4:99126006 | C | CA | 81 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(78): Show |
302 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(299): Show |
intron_variant | MODIFIER | c.1118+587dupT | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 8/8 | chr4 | 99126006 | |||||||
chr4:99126069 | G | T | 1 | a0009c0009t0001g0070 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.1118+525C>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 8/8 | chr4 | 99126069 | |||||||
chr4:99126222 | G | A | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.1118+372C>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 8/8 | chr4 | 99126222 | |||||||
chr4:99126279 | C | G | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(92): Show |
335 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.1118+315G>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 8/8 | chr4 | 99126279 | |||||||
chr4:99126282 | C | T | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.1118+312G>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 8/8 | chr4 | 99126282 | |||||||
chr4:99126296 | C | CATT | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(92): Show |
335 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.1118+297_1118+298i others(5): Show |
ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 8/8 | chr4 | 99126296 | |||||||
chr4:99126331 | G | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(90): Show |
329 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(326): Show |
intron_variant | MODIFIER | c.1118+263C>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 8/8 | chr4 | 99126331 | |||||||
chr4:99126351 | T | G | 1 | a0009c0009t0001g0070 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.1118+243A>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 8/8 | chr4 | 99126351 | |||||||
chr4:99126467 | A | T | 1 | a0009c0009t0001g0070 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.1118+127T>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 8/8 | chr4 | 99126467 | |||||||
chr4:99126485 | G | T | 1 | a0001c0001t0001g0048 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1118+109C>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 8/8 | chr4 | 99126485 | |||||||
chr4:99126739 | T | A | 6 | a0001c0001t0003g0008 a0001c0001t0003g0022 a0001c0001t0003g0023 others(3): Show |
15 | HG02257.hp1 HG02280.hp2 HG02486.hp2 others(12): Show |
splice_region_variant&intron_variant | LOW | c.980-7A>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 7/8 | chr4 | 99126739 | |||||||
chr4:99126778 | G | A | 19 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(16): Show |
81 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.980-46C>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 7/8 | chr4 | 99126778 | |||||||
chr4:99126787 | T | A | 1 | a0009c0009t0001g0070 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.980-55A>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 7/8 | chr4 | 99126787 | |||||||
chr4:99126788 | A | G | 1 | a0009c0009t0001g0070 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.980-56T>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 7/8 | chr4 | 99126788 | |||||||
chr4:99126940 | A | G | 6 | a0001c0001t0003g0008 a0001c0001t0003g0022 a0001c0001t0003g0023 others(3): Show |
15 | HG02257.hp1 HG02280.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.980-208T>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 7/8 | chr4 | 99126940 | |||||||
chr4:99126953 | A | G | 1 | a0001c0001t0001g0085 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.980-221T>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 7/8 | chr4 | 99126953 | |||||||
chr4:99127060 | C | A | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(90): Show |
329 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(326): Show |
intron_variant | MODIFIER | c.979+149G>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 7/8 | chr4 | 99127060 | |||||||
chr4:99127176 | G | A | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(89): Show |
328 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(325): Show |
intron_variant | MODIFIER | c.979+33C>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 7/8 | chr4 | 99127176 | |||||||
chr4:99127355 | G | A | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(90): Show |
329 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(326): Show |
intron_variant | MODIFIER | c.844-11C>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99127355 | |||||||
chr4:99127358 | T | C | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.844-14A>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99127358 | |||||||
chr4:99127476 | ACAT | A | 3 | a0001c0001t0003g0008 a0001c0001t0003g0023 a0001c0001t0003g0024 |
11 | HG02486.hp2 HG02559.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.844-135_844-133del others(3): Show |
ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99127476 | |||||||
chr4:99127658 | G | A | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.844-314C>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99127658 | |||||||
chr4:99127800 | G | C | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.844-456C>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99127800 | |||||||
chr4:99127831 | C | CA | 13 | a0001c0001t0001g0030 a0001c0001t0001g0064 a0002c0002t0002g0007 others(10): Show |
29 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.844-488dupT | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99127831 | |||||||
chr4:99127848 | A | G | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.844-504T>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99127848 | |||||||
chr4:99127962 | G | T | 1 | a0001c0001t0001g0067 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.844-618C>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99127962 | |||||||
chr4:99127994 | G | A | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(79): Show |
303 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(300): Show |
intron_variant | MODIFIER | c.844-650C>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99127994 | |||||||
chr4:99128003 | C | CTTTT | 9 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(6): Show |
24 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.844-663_844-660dup others(4): Show |
ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99128003 | |||||||
chr4:99128102 | T | G | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.844-758A>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99128102 | |||||||
chr4:99128201 | A | G | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.844-857T>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99128201 | |||||||
chr4:99128239 | A | G | 6 | a0001c0001t0003g0008 a0001c0001t0003g0022 a0001c0001t0003g0023 others(3): Show |
15 | HG02257.hp1 HG02280.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.844-895T>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99128239 | |||||||
chr4:99128363 | G | A | 1 | a0002c0003t0003g0013 | 4 | HG02258.hp2 HG02451.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.844-1019C>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99128363 | |||||||
chr4:99128377 | G | A | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.844-1033C>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99128377 | |||||||
chr4:99128428 | C | T | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.844-1084G>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99128428 | |||||||
chr4:99128811 | C | CT | 81 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(78): Show |
269 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.844-1468dupA | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99128811 | |||||||
chr4:99128817 | T | TA | 12 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0035 others(9): Show |
60 | HG00642.hp1 HG00733.hp2 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.844-1474_844-1473i others(3): Show |
ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99128817 | |||||||
chr4:99128867 | A | G | 5 | a0002c0002t0002g0010 a0002c0002t0002g0038 a0002c0002t0002g0040 others(2): Show |
10 | HG00741.hp1 HG01106.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.844-1523T>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99128867 | |||||||
chr4:99128872 | T | A | 1 | a0001c0001t0001g0032 | 2 | HG02572.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.844-1528A>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99128872 | |||||||
chr4:99129040 | T | A | 1 | a0009c0009t0001g0070 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.844-1696A>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99129040 | |||||||
chr4:99129049 | C | A | 12 | a0001c0001t0001g0091 a0002c0002t0002g0007 a0002c0002t0002g0010 others(9): Show |
27 | HG00323.hp1 HG00741.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.844-1705G>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99129049 | |||||||
chr4:99129168 | A | T | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.844-1824T>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99129168 | |||||||
chr4:99129195 | G | A | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(90): Show |
329 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(326): Show |
intron_variant | MODIFIER | c.844-1851C>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99129195 | |||||||
chr4:99129249 | T | C | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.844-1905A>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99129249 | |||||||
chr4:99129258 | A | G | 1 | a0002c0002t0002g0041 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.844-1914T>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99129258 | |||||||
chr4:99129377 | A | G | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.844-2033T>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99129377 | |||||||
chr4:99129393 | G | A | 7 | a0001c0001t0001g0018 a0001c0001t0001g0033 a0001c0001t0001g0034 others(4): Show |
12 | HG01109.hp2 HG02145.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.844-2049C>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99129393 | |||||||
chr4:99129635 | C | A | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.843+1869G>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99129635 | |||||||
chr4:99129669 | T | G | 1 | a0009c0009t0001g0070 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.843+1835A>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99129669 | |||||||
chr4:99129752 | A | G | 1 | a0001c0001t0003g0008 | 7 | HG02486.hp2 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.843+1752T>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99129752 | |||||||
chr4:99129773 | G | T | 1 | a0009c0009t0001g0070 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.843+1731C>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99129773 | |||||||
chr4:99129823 | C | G | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.843+1681G>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99129823 | |||||||
chr4:99129936 | A | G | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.843+1568T>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99129936 | |||||||
chr4:99130010 | C | A | 19 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0029 others(16): Show |
89 | HG00642.hp1 HG00733.hp2 HG00735.hp2 others(86): Show |
intron_variant | MODIFIER | c.843+1494G>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99130010 | |||||||
chr4:99130040 | T | TCAAAATA others(4): Show |
1 | a0001c0001t0001g0034 | 2 | HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.843+1453_843+1463d others(13): Show |
ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99130040 | |||||||
chr4:99130152 | T | C | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.843+1352A>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99130152 | |||||||
chr4:99130322 | AGGTTATA others(27): Show |
A | 1 | a0001c0001t0001g0073 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.843+1148_843+1181d others(36): Show |
ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99130322 | |||||||
chr4:99130405 | A | T | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.843+1099T>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99130405 | |||||||
chr4:99130543 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.843+961T>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99130543 | |||||||
chr4:99130571 | T | C | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.843+933A>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99130571 | |||||||
chr4:99130582 | A | G | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.843+922T>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99130582 | |||||||
chr4:99130650 | A | G | 1 | a0001c0001t0001g0079 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.843+854T>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99130650 | |||||||
chr4:99130668 | C | T | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(79): Show |
303 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(300): Show |
intron_variant | MODIFIER | c.843+836G>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99130668 | |||||||
chr4:99130708 | A | C | 1 | a0001c0001t0003g0057 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.843+796T>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99130708 | |||||||
chr4:99130726 | T | C | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.843+778A>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99130726 | |||||||
chr4:99130790 | C | T | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.843+714G>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99130790 | |||||||
chr4:99130834 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.843+670T>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99130834 | |||||||
chr4:99130901 | TAAAG | T | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.843+599_843+602del others(4): Show |
ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99130901 | |||||||
chr4:99131189 | C | A | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.843+315G>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99131189 | |||||||
chr4:99131213 | G | A | 5 | a0001c0001t0001g0017 a0001c0001t0001g0028 a0001c0001t0001g0074 others(2): Show |
10 | HG01070.hp2 HG02559.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.843+291C>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99131213 | |||||||
chr4:99131233 | G | A | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.843+271C>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99131233 | |||||||
chr4:99131388 | A | C | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.843+116T>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99131388 | |||||||
chr4:99131404 | G | C | 1 | a0001c0001t0001g0014 | 4 | HG01257.hp1 HG01258.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.843+100C>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99131404 | |||||||
chr4:99131429 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.843+75T>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99131429 | |||||||
chr4:99131503 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG02135.hp1 | splice_donor_variant&intron_variant | HIGH | c.843+1G>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 6/8 | chr4 | 99131503 | |||||||
chr4:99131812 | C | CT | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.583-49dupA | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99131812 | |||||||
chr4:99131836 | G | A | 1 | a0001c0001t0001g0031 | 2 | HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.583-72C>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99131836 | |||||||
chr4:99131874 | G | T | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.583-110C>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99131874 | |||||||
chr4:99131909 | T | A | 2 | a0001c0001t0001g0093 a0001c0001t0004g0094 |
2 | HG02109.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.583-145A>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99131909 | |||||||
chr4:99131940 | T | C | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.583-176A>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99131940 | |||||||
chr4:99132125 | G | A | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.583-361C>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99132125 | |||||||
chr4:99132296 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.583-532C>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99132296 | |||||||
chr4:99132582 | T | C | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(79): Show |
303 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(300): Show |
intron_variant | MODIFIER | c.583-818A>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99132582 | |||||||
chr4:99132631 | T | A | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.583-867A>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99132631 | |||||||
chr4:99132710 | T | C | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.583-946A>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99132710 | |||||||
chr4:99132740 | A | G | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.583-976T>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99132740 | |||||||
chr4:99132743 | A | T | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(79): Show |
303 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(300): Show |
intron_variant | MODIFIER | c.583-979T>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99132743 | |||||||
chr4:99132830 | A | T | 2 | a0002c0003t0003g0013 a0002c0003t0003g0021 |
6 | HG02258.hp2 HG02451.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.583-1066T>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99132830 | |||||||
chr4:99132865 | A | G | 1 | a0001c0001t0001g0028 | 2 | HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.583-1101T>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99132865 | |||||||
chr4:99132917 | C | T | 1 | a0006c0010t0003g0058 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.583-1153G>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99132917 | |||||||
chr4:99132955 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.583-1191T>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99132955 | |||||||
chr4:99132965 | C | T | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.583-1201G>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99132965 | |||||||
chr4:99133041 | A | G | 19 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(16): Show |
83 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.583-1277T>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99133041 | |||||||
chr4:99133046 | G | T | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.583-1282C>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99133046 | |||||||
chr4:99133093 | G | T | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.583-1329C>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99133093 | |||||||
chr4:99133161 | A | G | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.583-1397T>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99133161 | |||||||
chr4:99133572 | G | C | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.583-1808C>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99133572 | |||||||
chr4:99133637 | AT | A | 32 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(29): Show |
105 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.583-1874delA | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99133637 | |||||||
chr4:99133646 | G | A | 1 | a0002c0002t0002g0038 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.583-1882C>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99133646 | |||||||
chr4:99133676 | C | T | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(79): Show |
303 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(300): Show |
intron_variant | MODIFIER | c.583-1912G>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99133676 | |||||||
chr4:99133693 | A | G | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.583-1929T>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99133693 | |||||||
chr4:99133819 | A | G | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.583-2055T>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99133819 | |||||||
chr4:99133860 | G | C | 1 | a0001c0001t0004g0094 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.583-2096C>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99133860 | |||||||
chr4:99133875 | T | C | 1 | a0001c0001t0003g0022 | 2 | HG02965.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.583-2111A>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99133875 | |||||||
chr4:99133928 | G | A | 1 | a0001c0001t0001g0020 | 3 | HG02109.hp1 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.583-2164C>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99133928 | |||||||
chr4:99134005 | A | G | 3 | a0001c0001t0003g0008 a0001c0001t0003g0023 a0001c0001t0003g0024 |
11 | HG02486.hp2 HG02559.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.583-2241T>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99134005 | |||||||
chr4:99134022 | A | G | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.583-2258T>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99134022 | |||||||
chr4:99134044 | G | T | 2 | a0001c0001t0001g0088 a0001c0001t0001g0090 |
2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.583-2280C>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99134044 | |||||||
chr4:99134264 | A | G | 1 | a0003c0004t0001g0015 | 4 | HG02027.hp1 HG02083.hp2 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.582+2202T>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99134264 | |||||||
chr4:99134266 | T | C | 1 | a0001c0001t0001g0025 | 2 | NA18950.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.582+2200A>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99134266 | |||||||
chr4:99134380 | G | A | 1 | a0002c0002t0002g0040 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.582+2086C>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99134380 | |||||||
chr4:99134380 | G | GTATA | 10 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(7): Show |
25 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.582+2082_582+2085d others(6): Show |
ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99134380 | |||||||
chr4:99134397 | C | T | 1 | a0001c0001t0001g0077 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.582+2069G>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99134397 | |||||||
chr4:99134424 | A | G | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.582+2042T>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99134424 | |||||||
chr4:99134588 | G | A | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.582+1878C>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99134588 | |||||||
chr4:99134592 | T | C | 1 | a0001c0001t0001g0083 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.582+1874A>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99134592 | |||||||
chr4:99134604 | T | C | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.582+1862A>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99134604 | |||||||
chr4:99134649 | C | T | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(73): Show |
288 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.582+1817G>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99134649 | |||||||
chr4:99134674 | G | A | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.582+1792C>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99134674 | |||||||
chr4:99134711 | A | G | 19 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(16): Show |
83 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.582+1755T>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99134711 | |||||||
chr4:99134757 | T | C | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.582+1709A>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99134757 | |||||||
chr4:99134909 | G | A | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.582+1557C>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99134909 | |||||||
chr4:99134944 | C | A | 1 | a0002c0003t0003g0021 | 2 | HG02723.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.582+1522G>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99134944 | |||||||
chr4:99135099 | C | T | 1 | a0001c0001t0001g0029 | 2 | NA18970.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.582+1367G>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99135099 | |||||||
chr4:99135388 | C | T | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.582+1078G>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99135388 | |||||||
chr4:99135808 | C | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(90): Show |
329 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(326): Show |
intron_variant | MODIFIER | c.582+658G>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99135808 | |||||||
chr4:99135847 | A | G | 7 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0062 others(4): Show |
45 | HG00408.hp2 HG00609.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.582+619T>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99135847 | |||||||
chr4:99135869 | G | A | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.582+597C>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99135869 | |||||||
chr4:99136081 | G | A | 1 | a0001c0001t0001g0069 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.582+385C>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99136081 | |||||||
chr4:99136093 | T | G | 2 | a0001c0001t0001g0031 a0001c0001t0001g0084 |
3 | HG03139.hp2 HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.582+373A>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 5/8 | chr4 | 99136093 | |||||||
chr4:99136707 | T | TA | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.351-11dupT | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 4/8 | chr4 | 99136707 | |||||||
chr4:99136879 | A | T | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.351-182T>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 4/8 | chr4 | 99136879 | |||||||
chr4:99136925 | C | T | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(92): Show |
335 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.351-228G>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 4/8 | chr4 | 99136925 | |||||||
chr4:99136953 | ATT | A | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.351-258_351-257del others(2): Show |
ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 4/8 | chr4 | 99136953 | |||||||
chr4:99136970 | C | T | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.351-273G>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 4/8 | chr4 | 99136970 | |||||||
chr4:99137043 | G | A | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.351-346C>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 4/8 | chr4 | 99137043 | |||||||
chr4:99137104 | T | C | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.351-407A>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 4/8 | chr4 | 99137104 | |||||||
chr4:99137135 | AT | A | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(79): Show |
303 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(300): Show |
intron_variant | MODIFIER | c.351-439delA | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 4/8 | chr4 | 99137135 | |||||||
chr4:99137136 | T | TTA | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.351-440_351-439ins others(2): Show |
ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 4/8 | chr4 | 99137136 | |||||||
chr4:99137139 | T | A | 14 | a0001c0001t0001g0074 a0001c0001t0001g0085 a0001c0001t0001g0090 others(11): Show |
29 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.351-442A>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 4/8 | chr4 | 99137139 | |||||||
chr4:99137186 | G | A | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.351-489C>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 4/8 | chr4 | 99137186 | |||||||
chr4:99137188 | C | T | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.351-491G>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 4/8 | chr4 | 99137188 | |||||||
chr4:99137288 | C | T | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.351-591G>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 4/8 | chr4 | 99137288 | |||||||
chr4:99137289 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.351-592C>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 4/8 | chr4 | 99137289 | |||||||
chr4:99137348 | G | A | 1 | a0002c0002t0002g0045 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.351-651C>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 4/8 | chr4 | 99137348 | |||||||
chr4:99137376 | T | G | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.351-679A>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 4/8 | chr4 | 99137376 | |||||||
chr4:99137377 | C | T | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.351-680G>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 4/8 | chr4 | 99137377 | |||||||
chr4:99137511 | T | C | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.351-814A>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 4/8 | chr4 | 99137511 | |||||||
chr4:99137546 | C | G | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.351-849G>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 4/8 | chr4 | 99137546 | |||||||
chr4:99137576 | C | T | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.351-879G>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 4/8 | chr4 | 99137576 | |||||||
chr4:99137619 | C | A | 17 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0029 others(14): Show |
87 | HG00642.hp1 HG00733.hp2 HG00735.hp2 others(84): Show |
intron_variant | MODIFIER | c.351-922G>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 4/8 | chr4 | 99137619 | |||||||
chr4:99137621 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.351-924A>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 4/8 | chr4 | 99137621 | |||||||
chr4:99137623 | T | A | 1 | a0001c0001t0001g0076 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.351-926A>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 4/8 | chr4 | 99137623 | |||||||
chr4:99137624 | A | C | 1 | a0001c0001t0001g0076 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.351-927T>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 4/8 | chr4 | 99137624 | |||||||
chr4:99137625 | T | A | 1 | a0001c0001t0001g0076 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.351-928A>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 4/8 | chr4 | 99137625 | |||||||
chr4:99137626 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.351-929A>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 4/8 | chr4 | 99137626 | |||||||
chr4:99137627 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.351-930T>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 4/8 | chr4 | 99137627 | |||||||
chr4:99137630 | T | G | 1 | a0001c0001t0001g0076 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.351-933A>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 4/8 | chr4 | 99137630 | |||||||
chr4:99137631 | C | A | 1 | a0001c0001t0001g0076 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.351-934G>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 4/8 | chr4 | 99137631 | |||||||
chr4:99137633 | T | G | 1 | a0001c0001t0001g0076 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.351-936A>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 4/8 | chr4 | 99137633 | |||||||
chr4:99137634 | A | T | 1 | a0001c0001t0001g0076 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.351-937T>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 4/8 | chr4 | 99137634 | |||||||
chr4:99137635 | A | T | 1 | a0001c0001t0001g0076 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.351-938T>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 4/8 | chr4 | 99137635 | |||||||
chr4:99137733 | T | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(90): Show |
329 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(326): Show |
intron_variant | MODIFIER | c.351-1036A>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 4/8 | chr4 | 99137733 | |||||||
chr4:99137929 | CT | C | 12 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(9): Show |
27 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.350+1131delA | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 4/8 | chr4 | 99137929 | |||||||
chr4:99137988 | T | C | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.350+1073A>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 4/8 | chr4 | 99137988 | |||||||
chr4:99138161 | G | A | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.350+900C>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 4/8 | chr4 | 99138161 | |||||||
chr4:99138250 | T | A | 1 | a0001c0001t0001g0071 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.350+811A>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 4/8 | chr4 | 99138250 | |||||||
chr4:99138417 | G | T | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.350+644C>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 4/8 | chr4 | 99138417 | |||||||
chr4:99138468 | G | T | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.350+593C>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 4/8 | chr4 | 99138468 | |||||||
chr4:99138581 | T | A | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.350+480A>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 4/8 | chr4 | 99138581 | |||||||
chr4:99138656 | G | C | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.350+405C>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 4/8 | chr4 | 99138656 | |||||||
chr4:99138675 | T | A | 3 | a0001c0001t0001g0009 a0001c0001t0001g0063 a0001c0001t0001g0072 |
9 | HG00140.hp2 HG01099.hp2 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.350+386A>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 4/8 | chr4 | 99138675 | |||||||
chr4:99139338 | T | A | 1 | a0001c0001t0001g0086 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.263-190A>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 3/8 | chr4 | 99139338 | |||||||
chr4:99139339 | A | T | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.263-191T>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 3/8 | chr4 | 99139339 | |||||||
chr4:99139362 | C | T | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.263-214G>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 3/8 | chr4 | 99139362 | |||||||
chr4:99139387 | A | G | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.263-239T>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 3/8 | chr4 | 99139387 | |||||||
chr4:99139433 | A | G | 1 | a0001c0001t0001g0012 | 5 | NA18747.hp1 NA18979.hp1 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.263-285T>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 3/8 | chr4 | 99139433 | |||||||
chr4:99139472 | C | T | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.263-324G>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 3/8 | chr4 | 99139472 | |||||||
chr4:99139643 | A | G | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.263-495T>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 3/8 | chr4 | 99139643 | |||||||
chr4:99139685 | G | A | 22 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(19): Show |
84 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.263-537C>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 3/8 | chr4 | 99139685 | |||||||
chr4:99139731 | A | G | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.263-583T>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 3/8 | chr4 | 99139731 | |||||||
chr4:99139748 | C | T | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.263-600G>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 3/8 | chr4 | 99139748 | |||||||
chr4:99139922 | A | G | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.263-774T>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 3/8 | chr4 | 99139922 | |||||||
chr4:99139998 | G | A | 1 | a0001c0001t0003g0057 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.263-850C>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 3/8 | chr4 | 99139998 | |||||||
chr4:99140008 | G | T | 1 | a0001c0001t0003g0023 | 2 | HG02630.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.263-860C>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 3/8 | chr4 | 99140008 | |||||||
chr4:99140053 | G | T | 1 | a0002c0002t0002g0039 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.263-905C>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 3/8 | chr4 | 99140053 | |||||||
chr4:99140094 | G | T | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.263-946C>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 3/8 | chr4 | 99140094 | |||||||
chr4:99140127 | A | G | 4 | a0001c0001t0001g0018 a0001c0001t0001g0088 a0001c0001t0001g0089 others(1): Show |
7 | HG02145.hp2 HG02572.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.263-979T>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 3/8 | chr4 | 99140127 | |||||||
chr4:99140133 | CA | C | 3 | a0001c0001t0003g0008 a0001c0001t0003g0023 a0001c0001t0003g0024 |
11 | HG02486.hp2 HG02559.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.263-986delT | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 3/8 | chr4 | 99140133 | |||||||
chr4:99140152 | A | G | 1 | a0002c0002t0002g0038 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.263-1004T>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 3/8 | chr4 | 99140152 | |||||||
chr4:99140237 | T | C | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.263-1089A>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 3/8 | chr4 | 99140237 | |||||||
chr4:99140250 | T | TAGAAGTT others(27): Show |
1 | a0001c0001t0001g0073 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.263-1103_263-1102i others(36): Show |
ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 3/8 | chr4 | 99140250 | |||||||
chr4:99140376 | G | C | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.262+1165C>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 3/8 | chr4 | 99140376 | |||||||
chr4:99140380 | C | T | 18 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0029 others(15): Show |
88 | HG00642.hp1 HG00733.hp2 HG00735.hp2 others(85): Show |
intron_variant | MODIFIER | c.262+1161G>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 3/8 | chr4 | 99140380 | |||||||
chr4:99140411 | T | C | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.262+1130A>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 3/8 | chr4 | 99140411 | |||||||
chr4:99140438 | A | G | 2 | a0002c0003t0003g0013 a0002c0003t0003g0021 |
6 | HG02258.hp2 HG02451.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.262+1103T>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 3/8 | chr4 | 99140438 | |||||||
chr4:99140528 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.262+1013G>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 3/8 | chr4 | 99140528 | |||||||
chr4:99140541 | T | A | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.262+1000A>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 3/8 | chr4 | 99140541 | |||||||
chr4:99140575 | CA | C | 2 | a0002c0003t0003g0013 a0002c0003t0003g0021 |
6 | HG02258.hp2 HG02451.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.262+965delT | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 3/8 | chr4 | 99140575 | |||||||
chr4:99140633 | C | T | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.262+908G>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 3/8 | chr4 | 99140633 | |||||||
chr4:99140686 | G | A | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.262+855C>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 3/8 | chr4 | 99140686 | |||||||
chr4:99140693 | A | C | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(92): Show |
335 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.262+848T>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 3/8 | chr4 | 99140693 | |||||||
chr4:99140719 | T | G | 1 | a0006c0010t0003g0058 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.262+822A>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 3/8 | chr4 | 99140719 | |||||||
chr4:99140830 | A | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(90): Show |
329 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(326): Show |
intron_variant | MODIFIER | c.262+711T>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 3/8 | chr4 | 99140830 | |||||||
chr4:99140866 | CA | C | 73 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(70): Show |
288 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.262+674delT | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 3/8 | chr4 | 99140866 | |||||||
chr4:99140866 | CAA | C | 7 | a0001c0001t0001g0017 a0001c0001t0001g0028 a0001c0001t0001g0048 others(4): Show |
12 | HG01070.hp2 HG01168.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.262+673_262+674del others(2): Show |
ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 3/8 | chr4 | 99140866 | |||||||
chr4:99140913 | A | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(90): Show |
329 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(326): Show |
intron_variant | MODIFIER | c.262+628T>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 3/8 | chr4 | 99140913 | |||||||
chr4:99141065 | G | A | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.262+476C>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 3/8 | chr4 | 99141065 | |||||||
chr4:99141187 | C | T | 18 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0029 others(15): Show |
88 | HG00642.hp1 HG00733.hp2 HG00735.hp2 others(85): Show |
intron_variant | MODIFIER | c.262+354G>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 3/8 | chr4 | 99141187 | |||||||
chr4:99141279 | A | G | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.262+262T>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 3/8 | chr4 | 99141279 | |||||||
chr4:99141315 | G | A | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.262+226C>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 3/8 | chr4 | 99141315 | |||||||
chr4:99141375 | T | C | 5 | a0001c0001t0001g0017 a0001c0001t0001g0028 a0001c0001t0001g0074 others(2): Show |
10 | HG01070.hp2 HG02559.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.262+166A>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 3/8 | chr4 | 99141375 | |||||||
chr4:99141464 | T | C | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | NA18944.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.262+77A>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 3/8 | chr4 | 99141464 | |||||||
chr4:99141524 | T | G | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.262+17A>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 3/8 | chr4 | 99141524 | |||||||
chr4:99141993 | A | G | 1 | a0001c0001t0001g0016 | 4 | NA18950.hp1 NA18966.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.121-311T>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 2/8 | chr4 | 99141993 | |||||||
chr4:99141996 | C | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(90): Show |
329 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(326): Show |
intron_variant | MODIFIER | c.121-314G>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 2/8 | chr4 | 99141996 | |||||||
chr4:99142026 | A | G | 5 | a0001c0001t0001g0017 a0001c0001t0001g0028 a0001c0001t0001g0074 others(2): Show |
10 | HG01070.hp2 HG02559.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.121-344T>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 2/8 | chr4 | 99142026 | |||||||
chr4:99142053 | A | T | 1 | a0001c0001t0001g0046 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.121-371T>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 2/8 | chr4 | 99142053 | |||||||
chr4:99142083 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.121-401C>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 2/8 | chr4 | 99142083 | |||||||
chr4:99142303 | T | C | 2 | a0001c0001t0003g0023 a0001c0001t0003g0024 |
4 | HG02630.hp2 HG02647.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+376A>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 2/8 | chr4 | 99142303 | |||||||
chr4:99142374 | T | C | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(79): Show |
303 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(300): Show |
intron_variant | MODIFIER | c.120+305A>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 2/8 | chr4 | 99142374 | |||||||
chr4:99142430 | G | C | 6 | a0001c0001t0003g0008 a0001c0001t0003g0022 a0001c0001t0003g0023 others(3): Show |
15 | HG02257.hp1 HG02280.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.120+249C>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 2/8 | chr4 | 99142430 | |||||||
chr4:99143001 | A | G | 1 | a0001c0001t0003g0022 | 2 | HG02965.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.19-221T>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 1/8 | chr4 | 99143001 | |||||||
chr4:99143015 | G | GA | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(79): Show |
303 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(300): Show |
intron_variant | MODIFIER | c.19-236dupT | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 1/8 | chr4 | 99143015 | |||||||
chr4:99143082 | G | A | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.19-302C>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 1/8 | chr4 | 99143082 | |||||||
chr4:99143096 | G | T | 19 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(16): Show |
83 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.19-316C>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 1/8 | chr4 | 99143096 | |||||||
chr4:99143120 | T | C | 1 | a0007c0006t0001g0095 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.19-340A>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 1/8 | chr4 | 99143120 | |||||||
chr4:99143154 | C | G | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(92): Show |
335 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.19-374G>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 1/8 | chr4 | 99143154 | |||||||
chr4:99143163 | T | A | 1 | a0001c0001t0001g0047 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.19-383A>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 1/8 | chr4 | 99143163 | |||||||
chr4:99143164 | A | T | 1 | a0001c0001t0001g0047 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.19-384T>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 1/8 | chr4 | 99143164 | |||||||
chr4:99143175 | A | T | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.19-395T>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 1/8 | chr4 | 99143175 | |||||||
chr4:99143207 | T | A | 1 | a0001c0001t0001g0061 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.19-427A>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 1/8 | chr4 | 99143207 | |||||||
chr4:99143209 | T | G | 1 | a0001c0001t0001g0061 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.19-429A>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 1/8 | chr4 | 99143209 | |||||||
chr4:99143210 | G | A | 1 | a0001c0001t0001g0061 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.19-430C>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 1/8 | chr4 | 99143210 | |||||||
chr4:99143213 | A | C | 1 | a0001c0001t0001g0061 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.19-433T>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 1/8 | chr4 | 99143213 | |||||||
chr4:99143214 | C | G | 1 | a0001c0001t0001g0061 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.19-434G>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 1/8 | chr4 | 99143214 | |||||||
chr4:99143215 | T | A | 1 | a0001c0001t0001g0061 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.19-435A>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 1/8 | chr4 | 99143215 | |||||||
chr4:99143217 | G | C | 6 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0016 others(3): Show |
38 | HG00609.hp2 HG01074.hp1 HG01123.hp2 others(35): Show |
intron_variant | MODIFIER | c.19-437C>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 1/8 | chr4 | 99143217 | |||||||
chr4:99143219 | A | T | 1 | a0001c0001t0001g0061 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.19-439T>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 1/8 | chr4 | 99143219 | |||||||
chr4:99143231 | G | A | 1 | a0001c0001t0001g0061 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.19-451C>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 1/8 | chr4 | 99143231 | |||||||
chr4:99143498 | T | C | 54 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(51): Show |
204 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.18+707A>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 1/8 | chr4 | 99143498 | |||||||
chr4:99143643 | C | G | 2 | a0001c0001t0001g0019 a0001c0001t0001g0046 |
4 | HG02809.hp2 HG02895.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.18+562G>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 1/8 | chr4 | 99143643 | |||||||
chr4:99143705 | TA | T | 11 | a0002c0002t0002g0007 a0002c0002t0002g0010 a0002c0002t0002g0038 others(8): Show |
26 | HG00741.hp1 HG00741.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.18+499delT | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 1/8 | chr4 | 99143705 | |||||||
chr4:99143841 | T | C | 1 | a0002c0002t0002g0096 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.18+364A>G | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 1/8 | chr4 | 99143841 | |||||||
chr4:99143905 | C | T | 1 | a0001c0001t0001g0036 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.18+300G>A | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 1/8 | chr4 | 99143905 | |||||||
chr4:99144053 | C | G | 1 | a0001c0001t0001g0035 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.18+152G>C | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 1/8 | chr4 | 99144053 | |||||||
chr4:99144074 | G | A | 2 | a0001c0001t0001g0097 a0001c0001t0001g0098 |
2 | HG02896.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.18+131C>T | ADH4 | ENSG00000198099.10 | transcript | ENST00000265512.12 | protein_coding | 1/8 | chr4 | 99144074 |