Search by Gene
| Item | Value |
|---|---|
| geneid | 128 |
| ensemblid | ENSG00000197894.12 |
| hgncid | 253 |
| symbol | ADH5 |
| name | alcohol dehydrogenase 5 (class III), chi polypeptide |
| refseq_nuc | NM_000671.4 |
| refseq_prot | NP_000662.3 |
| ensembl_nuc | ENST00000296412.14 |
| ensembl_prot | ENSP00000296412.8 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 99070978 |
| end | 99088788 |
| strand | - |
| ver | v1.2 |
| region | chr4:99070978-99088788 |
| region5000 | chr4:99065978-99093788 |
| regionname0 | ADH5_chr4_99070978_99088788 |
| regionname5000 | ADH5_chr4_99065978_99093788 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 374 | 331 | 82 | 69 | 132 | 14 | 32 | ADH5_chr4_99065978_99093788 | ADH5 | MANEV others(369): Show |
chr4 | 99065978 | 99093788 |
| a0002 | 0/0 | 374 | 4 | 4 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | MANEV others(369): Show |
chr4 | 99065978 | 99093788 |
| a0003 | 0/0 | 374 | 1 | 0 | 1 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | MANEV others(369): Show |
chr4 | 99065978 | 99093788 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1122 | 312 | 68 | 66 | 132 | 13 | 31 | ADH5_chr4_99065978_99093788 | ADH5 | ATGGC others(1117): Show |
chr4 | 99065978 | 99093788 | ||
| a0001c0002 | 0/0 | 1122 | 18 | 14 | 3 | 0 | 1 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | ATGGC others(1117): Show |
chr4 | 99065978 | 99093788 | ||
| a0001c0004 | 0/0 | 1122 | 1 | 0 | 0 | 0 | 0 | 1 | ADH5_chr4_99065978_99093788 | ADH5 | ATGGC others(1117): Show |
chr4 | 99065978 | 99093788 | ||
| a0002c0003 | 0/0 | 1122 | 4 | 4 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | ATGGC others(1117): Show |
chr4 | 99065978 | 99093788 | ||
| a0003c0005 | 0/0 | 1122 | 1 | 0 | 1 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | ATGGC others(1117): Show |
chr4 | 99065978 | 99093788 |
| acthapid | grch38/chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2652 | 273 | 50 | 55 | 131 | 9 | 28 | ADH5_chr4_99065978_99093788 | ADH5 | CTCGC others(2647): Show |
chr4 | 99065978 | 99093788 |
| a0001c0001t0002 | 1/0 | 2652 | 16 | 9 | 5 | 0 | 0 | 1 | ADH5_chr4_99065978_99093788 | ADH5 | CTCGC others(2647): Show |
chr4 | 99065978 | 99093788 |
| a0001c0001t0003 | 0/0 | 2652 | 15 | 4 | 6 | 0 | 4 | 1 | ADH5_chr4_99065978_99093788 | ADH5 | CTCGC others(2647): Show |
chr4 | 99065978 | 99093788 |
| a0001c0001t0007 | 0/0 | 2652 | 2 | 2 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | CTCGC others(2647): Show |
chr4 | 99065978 | 99093788 |
| a0001c0001t0008 | 0/0 | 2652 | 1 | 1 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | CTCGC others(2647): Show |
chr4 | 99065978 | 99093788 |
| a0001c0001t0009 | 0/0 | 2652 | 1 | 1 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | CTCGC others(2647): Show |
chr4 | 99065978 | 99093788 |
| a0001c0001t0010 | 0/1 | 2652 | 1 | 0 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | CTCGC others(2647): Show |
chr4 | 99065978 | 99093788 |
| a0001c0001t0011 | 0/0 | 2652 | 1 | 1 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | CTCGC others(2647): Show |
chr4 | 99065978 | 99093788 |
| a0001c0001t0012 | 0/0 | 2652 | 1 | 0 | 0 | 0 | 0 | 1 | ADH5_chr4_99065978_99093788 | ADH5 | CTCGC others(2647): Show |
chr4 | 99065978 | 99093788 |
| a0001c0001t0013 | 0/0 | 2652 | 1 | 0 | 0 | 1 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | CTCGC others(2647): Show |
chr4 | 99065978 | 99093788 |
| a0001c0002t0004 | 0/0 | 2652 | 14 | 14 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | CTCGC others(2647): Show |
chr4 | 99065978 | 99093788 |
| a0001c0002t0005 | 0/0 | 2652 | 4 | 0 | 3 | 0 | 1 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | CTCGC others(2647): Show |
chr4 | 99065978 | 99093788 |
| a0001c0004t0001 | 0/0 | 2652 | 1 | 0 | 0 | 0 | 0 | 1 | ADH5_chr4_99065978_99093788 | ADH5 | CTCGC others(2647): Show |
chr4 | 99065978 | 99093788 |
| a0002c0003t0006 | 0/0 | 2652 | 4 | 4 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | CTCGC others(2647): Show |
chr4 | 99065978 | 99093788 |
| a0003c0005t0001 | 0/0 | 2652 | 1 | 0 | 1 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | CTCGC others(2647): Show |
chr4 | 99065978 | 99093788 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 37 | 11 | 7 | 16 | 1 | 2 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0002 | 0/0 | 27 | 0 | 2 | 22 | 3 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0003 | 0/0 | 22 | 4 | 8 | 10 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0004 | 0/0 | 21 | 0 | 0 | 19 | 0 | 2 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0005 | 0/0 | 13 | 2 | 1 | 8 | 0 | 2 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0006 | 0/0 | 10 | 0 | 3 | 5 | 0 | 2 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0007 | 0/0 | 6 | 0 | 0 | 3 | 1 | 2 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0008 | 0/0 | 6 | 1 | 1 | 4 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0026 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0040 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0002g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0002g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0002g0071 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0003g0010 | 0/0 | 4 | 1 | 2 | 0 | 0 | 1 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0003g0014 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0003g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0007g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0007g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0008g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0009g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0010g0065 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0011g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0012g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0001t0013g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0002t0004g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0002t0004g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0002t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0002t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0002t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0002t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0002t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0002t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0002t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0002t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0002t0005g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0002t0005g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0002t0005g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0001c0004t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0002c0003t0006g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0002c0003t0006g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0002c0003t0006g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0002c0003t0006g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| a0003c0005t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0097 | EUR | GBR | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0075 | EUR | FIN | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG00323 | hp2 | a0001 | c0002 | t0005 | g0059 | EUR | FIN | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG00741 | hp1 | a0003 | c0005 | t0001 | g0064 | AMR | PUR | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PUR | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0070 | AMR | PUR | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0020 | AMR | PUR | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0048 | AMR | PUR | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01256 | hp2 | a0001 | c0002 | t0005 | g0019 | AMR | CLM | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01258 | hp2 | a0001 | c0002 | t0005 | g0019 | AMR | CLM | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0010 | AMR | CLM | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0063 | AMR | CLM | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0072 | AMR | CLM | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0074 | EUR | IBS | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0084 | EUR | IBS | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0014 | EUR | IBS | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0014 | EUR | IBS | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02132 | hp1 | a0001 | c0001 | t0013 | g0090 | EAS | KHV | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PEL | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02257 | hp2 | a0001 | c0001 | t0008 | g0042 | AFR | ACB | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02258 | hp1 | a0002 | c0003 | t0006 | g0050 | AFR | ACB | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02280 | hp1 | a0001 | c0001 | t0009 | g0043 | AFR | ACB | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02280 | hp2 | a0001 | c0001 | t0011 | g0135 | AFR | ACB | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | PEL | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0020 | AMR | PEL | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02451 | hp1 | a0002 | c0003 | t0006 | g0055 | AFR | ACB | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0010 | SAS | PJL | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0069 | AFR | GWD | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02622 | hp1 | a0001 | c0002 | t0004 | g0054 | AFR | GWD | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0066 | AFR | GWD | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02630 | hp2 | a0001 | c0002 | t0004 | g0018 | AFR | GWD | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02647 | hp2 | a0001 | c0002 | t0004 | g0060 | AFR | GWD | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02717 | hp1 | a0001 | c0002 | t0004 | g0018 | AFR | GWD | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0045 | AFR | GWD | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | GWD | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | GWD | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02922 | hp1 | a0001 | c0002 | t0004 | g0057 | AFR | ESN | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02922 | hp2 | a0001 | c0002 | t0004 | g0009 | AFR | ESN | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02965 | hp1 | a0001 | c0001 | t0007 | g0156 | AFR | ESN | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02970 | hp1 | a0002 | c0003 | t0006 | g0053 | AFR | ESN | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ESN | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0062 | AFR | MSL | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG03225 | hp1 | a0001 | c0002 | t0004 | g0051 | AFR | MSL | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG03225 | hp2 | a0001 | c0001 | t0007 | g0155 | AFR | MSL | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | MSL | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG03486 | hp2 | a0002 | c0003 | t0006 | g0056 | AFR | MSL | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG03490 | hp1 | a0001 | c0004 | t0001 | g0092 | SAS | PJL | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | BEB | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | BEB | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | STU | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0046 | SAS | STU | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG04228 | hp2 | a0001 | c0001 | t0012 | g0078 | SAS | STU | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | YRI | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | YRI | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | CHB | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19030 | hp1 | a0001 | c0002 | t0004 | g0009 | AFR | LWK | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | LWK | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA19240 | hp2 | a0001 | c0002 | t0004 | g0009 | AFR | YRI | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | ASW | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | TSI | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0014 | EUR | TSI | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01123 | hp1 | a0001 | c0002 | t0005 | g0049 | AMR | CLM | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02486 | hp1 | a0001 | c0002 | t0004 | g0009 | AFR | ACB | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02486 | hp2 | a0001 | c0002 | t0004 | g0126 | AFR | ACB | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02559 | hp1 | a0001 | c0002 | t0004 | g0061 | AFR | ACB | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0067 | AFR | ACB | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG03471 | hp2 | a0001 | c0002 | t0004 | g0052 | AFR | MSL | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0044 | AFR | USA | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | USA | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA20300 | hp1 | a0001 | c0002 | t0004 | g0058 | AFR | USA | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0068 | AFR | USA | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | LWK | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0134 | AFR | LWK | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0010 | g0065 | REF | REF | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0071 | REF | REF | ADH5_chr4_99065978_99093788 | ADH5 | chr4 | 99065978 | 99093788 |
| view | chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:99076780 | A | G | 1 | a0002 | 4 | HG02258.hp1 HG02451.hp1 HG02970.hp1 others(1): Show |
missense_variant | MODERATE | c.488T>C | p.Leu163Ser | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 5/9 | 576/2652 | 488/1125 | 163/374 | chr4 | 99076780 | |||
| chr4:99085123 | G | C | 1 | a0003 | 1 | HG00741.hp1 | missense_variant | MODERATE | c.106C>G | p.Arg36Gly | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 2/9 | 194/2652 | 106/1125 | 36/374 | chr4 | 99085123 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:99072682 | A | G | 1 | a0001c0002 | 18 | HG00323.hp2 HG01123.hp1 HG01256.hp2 others(15): Show |
synonymous_variant | LOW | c.991T>C | p.Leu331Leu | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 8/9 | 1079/2652 | 991/1125 | 331/374 | chr4 | 99072682 | |||
| chr4:99076406 | G | A | 1 | a0001c0004 | 1 | HG03490.hp1 | synonymous_variant | LOW | c.711C>T | p.Ala237Ala | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 6/9 | 799/2652 | 711/1125 | 237/374 | chr4 | 99076406 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:99071451 | T | C | 4 | a0001c0001t0003a0001c0002t0004a0001c0002t0005others(1): Show | 37 | HG00323.hp2 HG00741.hp2 HG01069.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*966A>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 9/9 | 966 | chr4 | 99071451 | ||||||
| chr4:99071500 | C | A | 2 | a0001c0002t0004a0001c0002t0005 | 18 | HG00323.hp2 HG01123.hp1 HG01256.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*917G>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 9/9 | 917 | chr4 | 99071500 | ||||||
| chr4:99071501 | G | A | 2 | a0001c0002t0004a0001c0002t0005 | 18 | HG00323.hp2 HG01123.hp1 HG01256.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*916C>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 9/9 | 916 | chr4 | 99071501 | ||||||
| chr4:99071612 | A | G | 1 | a0001c0001t0009 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*805T>C | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 9/9 | 805 | chr4 | 99071612 | ||||||
| chr4:99071642 | A | C | 2 | a0001c0001t0003a0002c0003t0006 | 19 | HG00741.hp2 HG01069.hp1 HG01074.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*775T>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 9/9 | 775 | chr4 | 99071642 | ||||||
| chr4:99071702 | G | A | 1 | a0001c0001t0003 | 15 | HG00741.hp2 HG01069.hp1 HG01074.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*715C>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 9/9 | 715 | chr4 | 99071702 | ||||||
| chr4:99071804 | T | C | 1 | a0001c0001t0011 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*613A>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 9/9 | 613 | chr4 | 99071804 | ||||||
| chr4:99071843 | T | C | 2 | a0001c0002t0004a0001c0002t0005 | 18 | HG00323.hp2 HG01123.hp1 HG01256.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*574A>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 9/9 | 574 | chr4 | 99071843 | ||||||
| chr4:99071924 | C | A | 7 | a0001c0001t0001a0001c0001t0007a0001c0001t0011others(4): Show | 280 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(277): Show |
3_prime_UTR_variant | MODIFIER | c.*493G>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 9/9 | 493 | chr4 | 99071924 | ||||||
| chr4:99072000 | C | T | 1 | a0001c0001t0003 | 15 | HG00741.hp2 HG01069.hp1 HG01074.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*417G>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 9/9 | 417 | chr4 | 99072000 | ||||||
| chr4:99072110 | A | G | 1 | a0001c0001t0008 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*307T>C | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 9/9 | 307 | chr4 | 99072110 | ||||||
| chr4:99072141 | G | A | 1 | a0001c0001t0012 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*276C>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 9/9 | 276 | chr4 | 99072141 | ||||||
| chr4:99072199 | A | G | 4 | a0001c0001t0003a0001c0002t0004a0001c0002t0005others(1): Show | 37 | HG00323.hp2 HG00741.hp2 HG01069.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*218T>C | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 9/9 | 218 | chr4 | 99072199 | ||||||
| chr4:99072225 | A | G | 4 | a0001c0001t0003a0001c0002t0004a0001c0002t0005others(1): Show | 37 | HG00323.hp2 HG00741.hp2 HG01069.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*192T>C | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 9/9 | 192 | chr4 | 99072225 | ||||||
| chr4:99072281 | G | C | 1 | a0001c0001t0013 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*136C>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 9/9 | 136 | chr4 | 99072281 | ||||||
| chr4:99072327 | C | A | 1 | a0001c0002t0005 | 4 | HG00323.hp2 HG01123.hp1 HG01256.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*90G>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 9/9 | 90 | chr4 | 99072327 | ||||||
| chr4:99072347 | C | T | 2 | a0001c0002t0004a0001c0002t0005 | 18 | HG00323.hp2 HG01123.hp1 HG01256.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*70G>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 9/9 | 70 | chr4 | 99072347 | ||||||
| chr4:99088755 | G | A | 1 | a0001c0001t0007 | 2 | HG02965.hp1 HG03225.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-55C>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/9 | chr4 | 99088755 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:99072507 | C | T | 1 | a0001c0001t0001g0089 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1100+66G>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 8/8 | chr4 | 99072507 | |||||||
| chr4:99072510 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1100+63G>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 8/8 | chr4 | 99072510 | |||||||
| chr4:99072535 | C | T | 13 | a0001c0002t0004g0009a0001c0002t0004g0018a0001c0002t0004g0051others(10): Show | 18 | HG00323.hp2 HG01123.hp1 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.1100+38G>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 8/8 | chr4 | 99072535 | |||||||
| chr4:99072718 | G | T | 9 | a0001c0001t0003g0010a0001c0001t0003g0014a0001c0001t0003g0020others(6): Show | 15 | HG00741.hp2 HG01069.hp1 HG01074.hp2 others(12): Show |
splice_region_variant&intron_variant | LOW | c.962-7C>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 7/8 | chr4 | 99072718 | |||||||
| chr4:99072762 | G | T | 4 | a0001c0001t0001g0013a0001c0001t0001g0040a0001c0001t0001g0150others(1): Show | 8 | HG01070.hp2 HG02630.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.962-51C>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 7/8 | chr4 | 99072762 | |||||||
| chr4:99072894 | T | C | 13 | a0001c0002t0004g0009a0001c0002t0004g0018a0001c0002t0004g0051others(10): Show | 18 | HG00323.hp2 HG01123.hp1 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.962-183A>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 7/8 | chr4 | 99072894 | |||||||
| chr4:99072902 | C | T | 13 | a0001c0001t0003g0010a0001c0001t0003g0014a0001c0001t0003g0020others(10): Show | 19 | HG00741.hp2 HG01069.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.962-191G>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 7/8 | chr4 | 99072902 | |||||||
| chr4:99073111 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.962-400C>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 7/8 | chr4 | 99073111 | |||||||
| chr4:99073178 | A | AGTTT | 140 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(137): Show | 317 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(314): Show |
intron_variant | MODIFIER | c.962-471_962-468dup others(4): Show |
ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 7/8 | chr4 | 99073178 | |||||||
| chr4:99073217 | C | T | 2 | a0001c0001t0007g0155a0001c0001t0007g0156 | 2 | HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.962-506G>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 7/8 | chr4 | 99073217 | |||||||
| chr4:99073254 | T | C | 4 | a0001c0001t0001g0025a0001c0001t0001g0105a0001c0001t0001g0110others(1): Show | 5 | HG01257.hp2 HG01258.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.962-543A>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 7/8 | chr4 | 99073254 | |||||||
| chr4:99073304 | G | A | 56 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(53): Show | 96 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.962-593C>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 7/8 | chr4 | 99073304 | |||||||
| chr4:99073414 | G | A | 13 | a0001c0001t0003g0010a0001c0001t0003g0014a0001c0001t0003g0020others(10): Show | 19 | HG00741.hp2 HG01069.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.962-703C>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 7/8 | chr4 | 99073414 | |||||||
| chr4:99073457 | C | T | 13 | a0001c0001t0003g0010a0001c0001t0003g0014a0001c0001t0003g0020others(10): Show | 19 | HG00741.hp2 HG01069.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.962-746G>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 7/8 | chr4 | 99073457 | |||||||
| chr4:99073462 | GCCACCAG others(3): Show |
G | 12 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0041others(9): Show | 14 | HG01109.hp2 HG02109.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.962-761_962-752del others(10): Show |
ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 7/8 | chr4 | 99073462 | |||||||
| chr4:99073471 | C | G | 9 | a0001c0001t0003g0010a0001c0001t0003g0014a0001c0001t0003g0020others(6): Show | 15 | HG00741.hp2 HG01069.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.962-760G>C | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 7/8 | chr4 | 99073471 | |||||||
| chr4:99073521 | C | A | 1 | a0001c0001t0001g0145 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.962-810G>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 7/8 | chr4 | 99073521 | |||||||
| chr4:99073718 | C | T | 1 | a0001c0002t0004g0126 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.962-1007G>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 7/8 | chr4 | 99073718 | |||||||
| chr4:99073851 | G | C | 4 | a0002c0003t0006g0050a0002c0003t0006g0053a0002c0003t0006g0055others(1): Show | 4 | HG02258.hp1 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.961+1063C>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 7/8 | chr4 | 99073851 | |||||||
| chr4:99073987 | T | G | 9 | a0001c0001t0003g0010a0001c0001t0003g0014a0001c0001t0003g0020others(6): Show | 15 | HG00741.hp2 HG01069.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.961+927A>C | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 7/8 | chr4 | 99073987 | |||||||
| chr4:99074152 | G | C | 3 | a0001c0001t0002g0031a0001c0001t0002g0034a0001c0001t0002g0134 | 5 | HG02896.hp2 HG02897.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.961+762C>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 7/8 | chr4 | 99074152 | |||||||
| chr4:99074341 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.961+573C>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 7/8 | chr4 | 99074341 | |||||||
| chr4:99074452 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.961+462C>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 7/8 | chr4 | 99074452 | |||||||
| chr4:99074488 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.961+426A>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 7/8 | chr4 | 99074488 | |||||||
| chr4:99074537 | G | A | 1 | a0001c0001t0008g0042 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.961+377C>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 7/8 | chr4 | 99074537 | |||||||
| chr4:99074552 | G | A | 26 | a0001c0001t0003g0010a0001c0001t0003g0014a0001c0001t0003g0020others(23): Show | 37 | HG00323.hp2 HG00741.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.961+362C>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 7/8 | chr4 | 99074552 | |||||||
| chr4:99074552 | G | T | 1 | a0001c0001t0001g0154 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.961+362C>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 7/8 | chr4 | 99074552 | |||||||
| chr4:99074564 | A | T | 5 | a0001c0002t0004g0009a0001c0002t0004g0051a0001c0002t0004g0054others(2): Show | 8 | HG02486.hp1 HG02559.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.961+350T>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 7/8 | chr4 | 99074564 | |||||||
| chr4:99074614 | T | A | 10 | a0001c0002t0004g0009a0001c0002t0004g0018a0001c0002t0004g0051others(7): Show | 14 | HG02486.hp1 HG02486.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.961+300A>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 7/8 | chr4 | 99074614 | |||||||
| chr4:99074700 | C | CAGG | 140 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(137): Show | 317 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(314): Show |
intron_variant | MODIFIER | c.961+211_961+213dup others(3): Show |
ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 7/8 | chr4 | 99074700 | |||||||
| chr4:99074719 | C | A | 1 | a0001c0001t0001g0116 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.961+195G>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 7/8 | chr4 | 99074719 | |||||||
| chr4:99074721 | C | G | 3 | a0001c0001t0001g0024a0001c0001t0001g0098a0001c0001t0001g0099 | 4 | HG02896.hp1 HG03209.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.961+193G>C | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 7/8 | chr4 | 99074721 | |||||||
| chr4:99074757 | T | A | 1 | a0001c0001t0001g0110 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.961+157A>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 7/8 | chr4 | 99074757 | |||||||
| chr4:99074885 | A | G | 3 | a0001c0001t0002g0031a0001c0001t0002g0034a0001c0001t0002g0134 | 5 | HG02896.hp2 HG02897.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.961+29T>C | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 7/8 | chr4 | 99074885 | |||||||
| chr4:99075101 | GAAC | G | 9 | a0001c0001t0003g0010a0001c0001t0003g0014a0001c0001t0003g0020others(6): Show | 15 | HG00741.hp2 HG01069.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.826-55_826-53delGT others(1): Show |
ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 6/8 | chr4 | 99075101 | |||||||
| chr4:99075135 | A | C | 3 | a0001c0002t0005g0019a0001c0002t0005g0049a0001c0002t0005g0059 | 4 | HG00323.hp2 HG01123.hp1 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.826-86T>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 6/8 | chr4 | 99075135 | |||||||
| chr4:99075205 | A | G | 2 | a0001c0001t0001g0011a0001c0001t0001g0016 | 7 | HG01074.hp1 HG01123.hp2 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.826-156T>C | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 6/8 | chr4 | 99075205 | |||||||
| chr4:99075222 | G | T | 87 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(84): Show | 184 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.826-173C>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 6/8 | chr4 | 99075222 | |||||||
| chr4:99075225 | G | T | 1 | a0001c0001t0001g0096 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.826-176C>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 6/8 | chr4 | 99075225 | |||||||
| chr4:99075225 | GT | G | 119 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(116): Show | 285 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.826-177delA | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 6/8 | chr4 | 99075225 | |||||||
| chr4:99075225 | GTT | G | 23 | a0001c0001t0001g0137a0001c0001t0003g0010a0001c0001t0003g0014others(20): Show | 34 | HG00323.hp2 HG00741.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.826-178_826-177del others(2): Show |
ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 6/8 | chr4 | 99075225 | |||||||
| chr4:99075228 | T | G | 9 | a0001c0001t0003g0010a0001c0001t0003g0014a0001c0001t0003g0020others(6): Show | 15 | HG00741.hp2 HG01069.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.826-179A>C | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 6/8 | chr4 | 99075228 | |||||||
| chr4:99075331 | C | T | 1 | a0001c0002t0004g0057 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.826-282G>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 6/8 | chr4 | 99075331 | |||||||
| chr4:99075336 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.826-287G>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 6/8 | chr4 | 99075336 | |||||||
| chr4:99075475 | G | A | 2 | a0001c0001t0001g0113a0001c0001t0001g0132 | 2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.826-426C>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 6/8 | chr4 | 99075475 | |||||||
| chr4:99075579 | GCTTT | G | 4 | a0002c0003t0006g0050a0002c0003t0006g0053a0002c0003t0006g0055others(1): Show | 4 | HG02258.hp1 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.826-534_826-531del others(4): Show |
ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 6/8 | chr4 | 99075579 | |||||||
| chr4:99075701 | T | C | 17 | a0001c0002t0004g0009a0001c0002t0004g0018a0001c0002t0004g0051others(14): Show | 22 | HG00323.hp2 HG01123.hp1 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.825+591A>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 6/8 | chr4 | 99075701 | |||||||
| chr4:99075911 | G | GTTCA | 9 | a0001c0001t0003g0010a0001c0001t0003g0014a0001c0001t0003g0020others(6): Show | 15 | HG00741.hp2 HG01069.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.825+377_825+380dup others(4): Show |
ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 6/8 | chr4 | 99075911 | |||||||
| chr4:99075924 | C | A | 1 | a0001c0001t0001g0091 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.825+368G>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 6/8 | chr4 | 99075924 | |||||||
| chr4:99076028 | C | G | 9 | a0001c0001t0003g0010a0001c0001t0003g0014a0001c0001t0003g0020others(6): Show | 15 | HG00741.hp2 HG01069.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.825+264G>C | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 6/8 | chr4 | 99076028 | |||||||
| chr4:99076031 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.825+261G>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 6/8 | chr4 | 99076031 | |||||||
| chr4:99076078 | A | C | 4 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(1): Show | 4 | NA18950.hp1 NA18966.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.825+214T>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 6/8 | chr4 | 99076078 | |||||||
| chr4:99076140 | T | C | 1 | a0001c0001t0001g0138 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.825+152A>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 6/8 | chr4 | 99076140 | |||||||
| chr4:99076182 | A | T | 1 | a0001c0001t0001g0110 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.825+110T>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 6/8 | chr4 | 99076182 | |||||||
| chr4:99076183 | T | A | 1 | a0001c0001t0001g0110 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.825+109A>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 6/8 | chr4 | 99076183 | |||||||
| chr4:99076258 | C | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0079 | 4 | HG00639.hp1 HG00733.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.825+34G>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 6/8 | chr4 | 99076258 | |||||||
| chr4:99076278 | A | C | 1 | a0001c0001t0001g0115 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.825+14T>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 6/8 | chr4 | 99076278 | |||||||
| chr4:99076649 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.564+55C>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 5/8 | chr4 | 99076649 | |||||||
| chr4:99077050 | T | C | 4 | a0001c0001t0001g0013a0001c0001t0001g0040a0001c0001t0001g0150others(1): Show | 8 | HG01070.hp2 HG02630.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.345-127A>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 4/8 | chr4 | 99077050 | |||||||
| chr4:99077184 | A | G | 26 | a0001c0001t0003g0010a0001c0001t0003g0014a0001c0001t0003g0020others(23): Show | 37 | HG00323.hp2 HG00741.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.345-261T>C | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 4/8 | chr4 | 99077184 | |||||||
| chr4:99077237 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.345-314C>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 4/8 | chr4 | 99077237 | |||||||
| chr4:99077296 | G | A | 9 | a0001c0001t0003g0010a0001c0001t0003g0014a0001c0001t0003g0020others(6): Show | 15 | HG00741.hp2 HG01069.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.345-373C>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 4/8 | chr4 | 99077296 | |||||||
| chr4:99077308 | G | C | 1 | a0001c0001t0001g0124 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.345-385C>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 4/8 | chr4 | 99077308 | |||||||
| chr4:99077463 | C | A | 1 | a0001c0001t0011g0135 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.345-540G>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 4/8 | chr4 | 99077463 | |||||||
| chr4:99077487 | C | A | 1 | a0001c0001t0001g0035 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.345-564G>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 4/8 | chr4 | 99077487 | |||||||
| chr4:99077500 | T | TA | 17 | a0001c0002t0004g0009a0001c0002t0004g0018a0001c0002t0004g0051others(14): Show | 22 | HG00323.hp2 HG01123.hp1 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.345-578dupT | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 4/8 | chr4 | 99077500 | |||||||
| chr4:99077585 | C | G | 9 | a0001c0001t0003g0010a0001c0001t0003g0014a0001c0001t0003g0020others(6): Show | 15 | HG00741.hp2 HG01069.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.345-662G>C | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 4/8 | chr4 | 99077585 | |||||||
| chr4:99077619 | T | C | 3 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0009g0043 | 3 | HG02280.hp1 HG02723.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.345-696A>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 4/8 | chr4 | 99077619 | |||||||
| chr4:99077638 | A | T | 1 | a0001c0001t0001g0145 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.345-715T>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 4/8 | chr4 | 99077638 | |||||||
| chr4:99077715 | T | A | 9 | a0001c0001t0003g0010a0001c0001t0003g0014a0001c0001t0003g0020others(6): Show | 15 | HG00741.hp2 HG01069.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.345-792A>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 4/8 | chr4 | 99077715 | |||||||
| chr4:99077781 | T | C | 3 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0009g0043 | 3 | HG02280.hp1 HG02723.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.345-858A>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 4/8 | chr4 | 99077781 | |||||||
| chr4:99077851 | C | T | 4 | a0002c0003t0006g0050a0002c0003t0006g0053a0002c0003t0006g0055others(1): Show | 4 | HG02258.hp1 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.345-928G>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 4/8 | chr4 | 99077851 | |||||||
| chr4:99077882 | T | C | 56 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(53): Show | 96 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.345-959A>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 4/8 | chr4 | 99077882 | |||||||
| chr4:99077930 | C | T | 2 | a0001c0001t0003g0062a0001c0001t0003g0067 | 2 | HG02559.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.345-1007G>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 4/8 | chr4 | 99077930 | |||||||
| chr4:99077972 | T | C | 3 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0009g0043 | 3 | HG02280.hp1 HG02723.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.345-1049A>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 4/8 | chr4 | 99077972 | |||||||
| chr4:99077979 | A | G | 9 | a0001c0001t0003g0010a0001c0001t0003g0014a0001c0001t0003g0020others(6): Show | 15 | HG00741.hp2 HG01069.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.345-1056T>C | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 4/8 | chr4 | 99077979 | |||||||
| chr4:99078009 | T | C | 9 | a0001c0001t0003g0010a0001c0001t0003g0014a0001c0001t0003g0020others(6): Show | 15 | HG00741.hp2 HG01069.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.345-1086A>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 4/8 | chr4 | 99078009 | |||||||
| chr4:99078074 | T | C | 22 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(19): Show | 87 | HG00642.hp2 HG00733.hp1 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.345-1151A>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 4/8 | chr4 | 99078074 | |||||||
| chr4:99078444 | G | A | 18 | a0001c0001t0001g0076a0001c0002t0004g0009a0001c0002t0004g0018others(15): Show | 23 | HG00323.hp2 HG01123.hp1 HG01256.hp2 others(20): Show |
intron_variant | MODIFIER | c.345-1521C>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 4/8 | chr4 | 99078444 | |||||||
| chr4:99078505 | G | A | 2 | a0001c0001t0001g0036a0001c0001t0001g0117 | 3 | HG01167.hp1 HG01169.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.345-1582C>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 4/8 | chr4 | 99078505 | |||||||
| chr4:99078697 | C | T | 9 | a0001c0001t0003g0010a0001c0001t0003g0014a0001c0001t0003g0020others(6): Show | 15 | HG00741.hp2 HG01069.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.345-1774G>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 4/8 | chr4 | 99078697 | |||||||
| chr4:99078985 | T | C | 20 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(17): Show | 75 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.345-2062A>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 4/8 | chr4 | 99078985 | |||||||
| chr4:99079025 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.345-2102A>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 4/8 | chr4 | 99079025 | |||||||
| chr4:99079059 | C | G | 12 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0041others(9): Show | 14 | HG01109.hp2 HG02109.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.345-2136G>C | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 4/8 | chr4 | 99079059 | |||||||
| chr4:99079099 | G | A | 1 | a0001c0001t0002g0047 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.345-2176C>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 4/8 | chr4 | 99079099 | |||||||
| chr4:99079107 | T | C | 3 | a0001c0002t0005g0019a0001c0002t0005g0049a0001c0002t0005g0059 | 4 | HG00323.hp2 HG01123.hp1 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.345-2184A>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 4/8 | chr4 | 99079107 | |||||||
| chr4:99079212 | A | C | 1 | a0001c0001t0001g0041 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.344+2153T>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 4/8 | chr4 | 99079212 | |||||||
| chr4:99079367 | GA | G | 147 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(144): Show | 326 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(323): Show |
intron_variant | MODIFIER | c.344+1997delT | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 4/8 | chr4 | 99079367 | |||||||
| chr4:99079390 | G | C | 1 | a0001c0001t0003g0074 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.344+1975C>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 4/8 | chr4 | 99079390 | |||||||
| chr4:99079401 | G | T | 20 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(17): Show | 75 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.344+1964C>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 4/8 | chr4 | 99079401 | |||||||
| chr4:99079461 | G | A | 2 | a0001c0001t0003g0020a0001c0001t0003g0070 | 3 | HG01069.hp1 HG01074.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.344+1904C>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 4/8 | chr4 | 99079461 | |||||||
| chr4:99079543 | G | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0151 | 5 | HG02630.hp1 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.344+1822C>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 4/8 | chr4 | 99079543 | |||||||
| chr4:99079760 | G | C | 6 | a0001c0001t0003g0010a0001c0001t0003g0014a0001c0001t0003g0048others(3): Show | 11 | HG00741.hp2 HG01106.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.344+1605C>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 4/8 | chr4 | 99079760 | |||||||
| chr4:99079887 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.344+1478C>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 4/8 | chr4 | 99079887 | |||||||
| chr4:99079951 | G | A | 11 | a0001c0001t0001g0127a0001c0002t0004g0009a0001c0002t0004g0018others(8): Show | 15 | HG02486.hp1 HG02486.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.344+1414C>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 4/8 | chr4 | 99079951 | |||||||
| chr4:99080096 | T | C | 147 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(144): Show | 326 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(323): Show |
intron_variant | MODIFIER | c.344+1269A>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 4/8 | chr4 | 99080096 | |||||||
| chr4:99080289 | T | G | 12 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0041others(9): Show | 14 | HG01109.hp2 HG02109.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.344+1076A>C | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 4/8 | chr4 | 99080289 | |||||||
| chr4:99080309 | C | A | 3 | a0001c0002t0004g0018a0001c0002t0004g0052a0001c0002t0004g0060 | 4 | HG02630.hp2 HG02647.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.344+1056G>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 4/8 | chr4 | 99080309 | |||||||
| chr4:99080362 | G | T | 5 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0136others(2): Show | 5 | HG00597.hp2 HG02056.hp2 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.344+1003C>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 4/8 | chr4 | 99080362 | |||||||
| chr4:99080387 | G | A | 1 | a0001c0001t0008g0042 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.344+978C>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 4/8 | chr4 | 99080387 | |||||||
| chr4:99080389 | C | T | 9 | a0001c0001t0003g0010a0001c0001t0003g0014a0001c0001t0003g0020others(6): Show | 15 | HG00741.hp2 HG01069.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.344+976G>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 4/8 | chr4 | 99080389 | |||||||
| chr4:99080403 | G | C | 6 | a0001c0002t0004g0009a0001c0002t0004g0051a0001c0002t0004g0054others(3): Show | 9 | HG02486.hp1 HG02559.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.344+962C>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 4/8 | chr4 | 99080403 | |||||||
| chr4:99080416 | T | C | 1 | a0001c0001t0001g0094 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.344+949A>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 4/8 | chr4 | 99080416 | |||||||
| chr4:99080504 | CTTTT | C | 114 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(111): Show | 280 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(277): Show |
intron_variant | MODIFIER | c.344+857_344+860del others(4): Show |
ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 4/8 | chr4 | 99080504 | |||||||
| chr4:99080531 | G | T | 26 | a0001c0001t0003g0010a0001c0001t0003g0014a0001c0001t0003g0020others(23): Show | 37 | HG00323.hp2 HG00741.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.344+834C>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 4/8 | chr4 | 99080531 | |||||||
| chr4:99080781 | T | A | 9 | a0001c0001t0003g0010a0001c0001t0003g0014a0001c0001t0003g0020others(6): Show | 15 | HG00741.hp2 HG01069.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.344+584A>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 4/8 | chr4 | 99080781 | |||||||
| chr4:99080890 | C | T | 3 | a0001c0002t0005g0019a0001c0002t0005g0049a0001c0002t0005g0059 | 4 | HG00323.hp2 HG01123.hp1 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.344+475G>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 4/8 | chr4 | 99080890 | |||||||
| chr4:99080893 | T | C | 1 | a0001c0001t0001g0030 | 2 | NA19001.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.344+472A>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 4/8 | chr4 | 99080893 | |||||||
| chr4:99081160 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.344+205G>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 4/8 | chr4 | 99081160 | |||||||
| chr4:99081221 | C | T | 114 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(111): Show | 280 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(277): Show |
intron_variant | MODIFIER | c.344+144G>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 4/8 | chr4 | 99081221 | |||||||
| chr4:99081493 | AT | A | 9 | a0001c0001t0003g0010a0001c0001t0003g0014a0001c0001t0003g0020others(6): Show | 15 | HG00741.hp2 HG01069.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.257-42delA | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 3/8 | chr4 | 99081493 | |||||||
| chr4:99081616 | A | G | 1 | a0001c0001t0001g0023 | 2 | HG02698.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.257-164T>C | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 3/8 | chr4 | 99081616 | |||||||
| chr4:99081659 | A | G | 1 | a0001c0001t0001g0107 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.257-207T>C | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 3/8 | chr4 | 99081659 | |||||||
| chr4:99082137 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.115-21G>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 2/8 | chr4 | 99082137 | |||||||
| chr4:99082143 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.115-27A>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 2/8 | chr4 | 99082143 | |||||||
| chr4:99082150 | A | T | 17 | a0001c0002t0004g0009a0001c0002t0004g0018a0001c0002t0004g0051others(14): Show | 22 | HG00323.hp2 HG01123.hp1 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.115-34T>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 2/8 | chr4 | 99082150 | |||||||
| chr4:99082182 | A | G | 9 | a0001c0001t0003g0010a0001c0001t0003g0014a0001c0001t0003g0020others(6): Show | 15 | HG00741.hp2 HG01069.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.115-66T>C | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 2/8 | chr4 | 99082182 | |||||||
| chr4:99082207 | A | G | 5 | a0001c0002t0004g0009a0001c0002t0004g0051a0001c0002t0004g0054others(2): Show | 8 | HG02486.hp1 HG02559.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.115-91T>C | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 2/8 | chr4 | 99082207 | |||||||
| chr4:99082424 | C | T | 4 | a0002c0003t0006g0050a0002c0003t0006g0053a0002c0003t0006g0055others(1): Show | 4 | HG02258.hp1 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.115-308G>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 2/8 | chr4 | 99082424 | |||||||
| chr4:99082592 | C | T | 9 | a0001c0001t0003g0010a0001c0001t0003g0014a0001c0001t0003g0020others(6): Show | 15 | HG00741.hp2 HG01069.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.115-476G>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 2/8 | chr4 | 99082592 | |||||||
| chr4:99082596 | G | A | 9 | a0001c0001t0003g0010a0001c0001t0003g0014a0001c0001t0003g0020others(6): Show | 15 | HG00741.hp2 HG01069.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.115-480C>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 2/8 | chr4 | 99082596 | |||||||
| chr4:99082693 | T | G | 12 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0041others(9): Show | 14 | HG01109.hp2 HG02109.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.115-577A>C | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 2/8 | chr4 | 99082693 | |||||||
| chr4:99082763 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.115-647C>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 2/8 | chr4 | 99082763 | |||||||
| chr4:99082835 | C | T | 1 | a0001c0001t0011g0135 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.115-719G>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 2/8 | chr4 | 99082835 | |||||||
| chr4:99082943 | T | C | 2 | a0001c0001t0003g0020a0001c0001t0003g0070 | 3 | HG01069.hp1 HG01074.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.115-827A>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 2/8 | chr4 | 99082943 | |||||||
| chr4:99083036 | T | G | 1 | a0001c0001t0001g0095 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.115-920A>C | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 2/8 | chr4 | 99083036 | |||||||
| chr4:99083075 | C | T | 23 | a0001c0001t0003g0010a0001c0001t0003g0014a0001c0001t0003g0020others(20): Show | 33 | HG00741.hp2 HG01069.hp1 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.115-959G>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 2/8 | chr4 | 99083075 | |||||||
| chr4:99083190 | C | T | 9 | a0001c0001t0003g0010a0001c0001t0003g0014a0001c0001t0003g0020others(6): Show | 15 | HG00741.hp2 HG01069.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.115-1074G>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 2/8 | chr4 | 99083190 | |||||||
| chr4:99083442 | A | G | 1 | a0001c0001t0001g0081 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.115-1326T>C | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 2/8 | chr4 | 99083442 | |||||||
| chr4:99083455 | C | T | 2 | a0001c0001t0002g0066a0001c0001t0002g0068 | 2 | HG02622.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.115-1339G>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 2/8 | chr4 | 99083455 | |||||||
| chr4:99083469 | G | A | 3 | a0001c0002t0005g0019a0001c0002t0005g0049a0001c0002t0005g0059 | 4 | HG00323.hp2 HG01123.hp1 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.115-1353C>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 2/8 | chr4 | 99083469 | |||||||
| chr4:99083500 | C | T | 132 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(129): Show | 304 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(301): Show |
intron_variant | MODIFIER | c.115-1384G>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 2/8 | chr4 | 99083500 | |||||||
| chr4:99083510 | G | C | 1 | a0001c0001t0001g0097 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.115-1394C>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 2/8 | chr4 | 99083510 | |||||||
| chr4:99083548 | C | T | 3 | a0001c0001t0001g0080a0001c0001t0001g0087a0001c0001t0001g0088 | 3 | HG02809.hp2 HG02895.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.115-1432G>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 2/8 | chr4 | 99083548 | |||||||
| chr4:99083554 | C | T | 3 | a0001c0002t0004g0018a0001c0002t0004g0052a0001c0002t0004g0060 | 4 | HG02630.hp2 HG02647.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.115-1438G>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 2/8 | chr4 | 99083554 | |||||||
| chr4:99083600 | C | CA | 11 | a0001c0001t0001g0082a0001c0001t0001g0099a0001c0001t0001g0108others(8): Show | 12 | HG01081.hp1 HG01192.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.115-1485dupT | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 2/8 | chr4 | 99083600 | |||||||
| chr4:99083600 | CA | C | 67 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(64): Show | 155 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.115-1485delT | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 2/8 | chr4 | 99083600 | |||||||
| chr4:99083600 | CAAA | C | 7 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0063others(4): Show | 8 | HG00323.hp2 HG01123.hp1 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.115-1487_115-1485d others(5): Show |
ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 2/8 | chr4 | 99083600 | |||||||
| chr4:99083600 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0118 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.115-1495_115-1485d others(13): Show |
ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 2/8 | chr4 | 99083600 | |||||||
| chr4:99083600 | CAAAAAAA others(8): Show |
C | 22 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(19): Show | 87 | HG00642.hp2 HG00733.hp1 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.115-1499_115-1485d others(17): Show |
ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 2/8 | chr4 | 99083600 | |||||||
| chr4:99083764 | G | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0151 | 5 | HG02630.hp1 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.114+1351C>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 2/8 | chr4 | 99083764 | |||||||
| chr4:99084017 | T | G | 2 | a0001c0001t0001g0028a0001c0001t0001g0083 | 3 | HG02735.hp1 HG03654.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.114+1098A>C | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 2/8 | chr4 | 99084017 | |||||||
| chr4:99084053 | A | G | 17 | a0001c0002t0004g0009a0001c0002t0004g0018a0001c0002t0004g0051others(14): Show | 22 | HG00323.hp2 HG01123.hp1 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.114+1062T>C | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 2/8 | chr4 | 99084053 | |||||||
| chr4:99084167 | C | T | 6 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0046others(3): Show | 6 | HG02257.hp2 HG02280.hp1 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.114+948G>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 2/8 | chr4 | 99084167 | |||||||
| chr4:99084174 | T | C | 1 | a0001c0001t0008g0042 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.114+941A>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 2/8 | chr4 | 99084174 | |||||||
| chr4:99084268 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.114+847A>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 2/8 | chr4 | 99084268 | |||||||
| chr4:99084278 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.114+837T>C | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 2/8 | chr4 | 99084278 | |||||||
| chr4:99084387 | C | T | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 311 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.114+728G>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 2/8 | chr4 | 99084387 | |||||||
| chr4:99084392 | T | C | 17 | a0001c0002t0004g0009a0001c0002t0004g0018a0001c0002t0004g0051others(14): Show | 22 | HG00323.hp2 HG01123.hp1 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.114+723A>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 2/8 | chr4 | 99084392 | |||||||
| chr4:99084706 | C | A | 1 | a0001c0001t0007g0156 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.114+409G>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 2/8 | chr4 | 99084706 | |||||||
| chr4:99084840 | C | A | 17 | a0001c0002t0004g0009a0001c0002t0004g0018a0001c0002t0004g0051others(14): Show | 22 | HG00323.hp2 HG01123.hp1 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.114+275G>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 2/8 | chr4 | 99084840 | |||||||
| chr4:99084959 | G | A | 5 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0046others(2): Show | 5 | HG02280.hp1 HG02293.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.114+156C>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 2/8 | chr4 | 99084959 | |||||||
| chr4:99084977 | G | A | 1 | a0001c0001t0001g0086 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.114+138C>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 2/8 | chr4 | 99084977 | |||||||
| chr4:99085003 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.114+112A>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 2/8 | chr4 | 99085003 | |||||||
| chr4:99085033 | C | T | 10 | a0001c0002t0004g0009a0001c0002t0004g0018a0001c0002t0004g0051others(7): Show | 14 | HG02486.hp1 HG02486.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.114+82G>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 2/8 | chr4 | 99085033 | |||||||
| chr4:99085494 | A | G | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 311 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.13-278T>C | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99085494 | |||||||
| chr4:99085517 | C | T | 1 | a0001c0001t0002g0046 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.13-301G>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99085517 | |||||||
| chr4:99085518 | G | A | 4 | a0002c0003t0006g0050a0002c0003t0006g0053a0002c0003t0006g0055others(1): Show | 4 | HG02258.hp1 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.13-302C>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99085518 | |||||||
| chr4:99085883 | A | T | 7 | a0001c0001t0001g0073a0001c0001t0003g0010a0001c0001t0003g0014others(4): Show | 12 | HG00741.hp2 HG01106.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.13-667T>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99085883 | |||||||
| chr4:99085932 | G | A | 3 | a0001c0001t0001g0029a0001c0001t0001g0100a0001c0001t0001g0101 | 4 | HG03017.hp2 HG03491.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.13-716C>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99085932 | |||||||
| chr4:99085990 | T | C | 1 | a0001c0001t0009g0043 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.13-774A>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99085990 | |||||||
| chr4:99086037 | A | AAAAC | 2 | a0001c0001t0001g0030a0001c0001t0001g0084 | 3 | HG01516.hp1 NA19001.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.13-825_13-822dupGT others(2): Show |
ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99086037 | |||||||
| chr4:99086037 | A | AAAACAAA others(1): Show |
39 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(36): Show | 109 | HG00323.hp2 HG00642.hp2 HG00733.hp1 others(106): Show |
intron_variant | MODIFIER | c.13-829_13-822dupGT others(6): Show |
ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99086037 | |||||||
| chr4:99086037 | A | AAAACAAA others(5): Show |
94 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(91): Show | 196 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.13-833_13-822dupGT others(10): Show |
ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99086037 | |||||||
| chr4:99086037 | A | AAAACAAA others(9): Show |
3 | a0001c0001t0001g0076a0001c0001t0002g0044a0001c0001t0008g0042 | 3 | HG01358.hp1 HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.13-837_13-822dupGT others(14): Show |
ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99086037 | |||||||
| chr4:99086283 | T | TATATC | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 311 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.13-1068_13-1067ins others(5): Show |
ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99086283 | |||||||
| chr4:99086315 | G | C | 5 | a0001c0001t0001g0073a0001c0001t0003g0010a0001c0001t0003g0014others(2): Show | 10 | HG00741.hp2 HG01106.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.13-1099C>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99086315 | |||||||
| chr4:99086359 | A | T | 4 | a0002c0003t0006g0050a0002c0003t0006g0053a0002c0003t0006g0055others(1): Show | 4 | HG02258.hp1 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.13-1143T>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99086359 | |||||||
| chr4:99086377 | A | G | 2 | a0001c0001t0002g0044a0001c0001t0002g0045 | 2 | HG02723.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.13-1161T>C | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99086377 | |||||||
| chr4:99086504 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.13-1288G>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99086504 | |||||||
| chr4:99086587 | G | T | 1 | a0001c0001t0001g0086 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.13-1371C>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99086587 | |||||||
| chr4:99086701 | T | C | 4 | a0002c0003t0006g0050a0002c0003t0006g0053a0002c0003t0006g0055others(1): Show | 4 | HG02258.hp1 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.13-1485A>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99086701 | |||||||
| chr4:99086719 | C | A | 21 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(18): Show | 77 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.13-1503G>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99086719 | |||||||
| chr4:99086769 | T | C | 9 | a0001c0002t0004g0009a0001c0002t0004g0018a0001c0002t0004g0051others(6): Show | 13 | HG02486.hp1 HG02559.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.13-1553A>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99086769 | |||||||
| chr4:99086797 | A | G | 9 | a0001c0002t0004g0009a0001c0002t0004g0018a0001c0002t0004g0051others(6): Show | 13 | HG02486.hp1 HG02559.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.13-1581T>C | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99086797 | |||||||
| chr4:99086800 | G | T | 9 | a0001c0002t0004g0009a0001c0002t0004g0018a0001c0002t0004g0051others(6): Show | 13 | HG02486.hp1 HG02559.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.13-1584C>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99086800 | |||||||
| chr4:99086802 | A | T | 9 | a0001c0002t0004g0009a0001c0002t0004g0018a0001c0002t0004g0051others(6): Show | 13 | HG02486.hp1 HG02559.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.13-1586T>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99086802 | |||||||
| chr4:99086811 | T | G | 9 | a0001c0002t0004g0009a0001c0002t0004g0018a0001c0002t0004g0051others(6): Show | 13 | HG02486.hp1 HG02559.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.13-1595A>C | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99086811 | |||||||
| chr4:99086812 | C | T | 9 | a0001c0002t0004g0009a0001c0002t0004g0018a0001c0002t0004g0051others(6): Show | 13 | HG02486.hp1 HG02559.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.13-1596G>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99086812 | |||||||
| chr4:99086823 | A | C | 9 | a0001c0002t0004g0009a0001c0002t0004g0018a0001c0002t0004g0051others(6): Show | 13 | HG02486.hp1 HG02559.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.13-1607T>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99086823 | |||||||
| chr4:99086828 | T | A | 9 | a0001c0002t0004g0009a0001c0002t0004g0018a0001c0002t0004g0051others(6): Show | 13 | HG02486.hp1 HG02559.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.13-1612A>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99086828 | |||||||
| chr4:99086831 | C | T | 9 | a0001c0002t0004g0009a0001c0002t0004g0018a0001c0002t0004g0051others(6): Show | 13 | HG02486.hp1 HG02559.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.13-1615G>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99086831 | |||||||
| chr4:99086832 | G | C | 9 | a0001c0002t0004g0009a0001c0002t0004g0018a0001c0002t0004g0051others(6): Show | 13 | HG02486.hp1 HG02559.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.13-1616C>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99086832 | |||||||
| chr4:99086853 | C | T | 9 | a0001c0002t0004g0009a0001c0002t0004g0018a0001c0002t0004g0051others(6): Show | 13 | HG02486.hp1 HG02559.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.13-1637G>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99086853 | |||||||
| chr4:99086887 | C | A | 16 | a0001c0002t0004g0009a0001c0002t0004g0018a0001c0002t0004g0051others(13): Show | 21 | HG00323.hp2 HG01123.hp1 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.13-1671G>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99086887 | |||||||
| chr4:99086889 | G | A | 3 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0009g0043 | 3 | HG02280.hp1 HG02723.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.13-1673C>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99086889 | |||||||
| chr4:99086894 | C | T | 3 | a0001c0001t0003g0062a0001c0001t0003g0067a0001c0001t0008g0042 | 3 | HG02257.hp2 HG02559.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.13-1678G>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99086894 | |||||||
| chr4:99086896 | C | T | 16 | a0001c0002t0004g0009a0001c0002t0004g0018a0001c0002t0004g0051others(13): Show | 21 | HG00323.hp2 HG01123.hp1 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.13-1680G>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99086896 | |||||||
| chr4:99086939 | C | CAAAA | 8 | a0001c0002t0004g0009a0001c0002t0004g0018a0001c0002t0004g0054others(5): Show | 12 | HG00323.hp2 HG01123.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.13-1727_13-1724dup others(4): Show |
ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99086939 | |||||||
| chr4:99086939 | C | CAAAAA | 5 | a0001c0002t0004g0060a0001c0002t0004g0061a0001c0002t0005g0019others(2): Show | 6 | HG01256.hp2 HG01258.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.13-1728_13-1724dup others(5): Show |
ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99086939 | |||||||
| chr4:99086939 | CA | C | 16 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0039others(13): Show | 26 | HG01070.hp2 HG01109.hp1 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.13-1724delT | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99086939 | |||||||
| chr4:99086939 | CAA | C | 93 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(90): Show | 249 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.13-1725_13-1724del others(2): Show |
ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99086939 | |||||||
| chr4:99086939 | CAAA | C | 11 | a0001c0001t0001g0022a0001c0001t0001g0033a0001c0001t0001g0086others(8): Show | 13 | HG01168.hp2 HG01256.hp1 HG02129.hp2 others(10): Show |
intron_variant | MODIFIER | c.13-1726_13-1724del others(3): Show |
ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99086939 | |||||||
| chr4:99087039 | A | G | 4 | a0001c0001t0001g0013a0001c0001t0001g0040a0001c0001t0001g0150others(1): Show | 8 | HG01070.hp2 HG02630.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.12+1650T>C | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99087039 | |||||||
| chr4:99087181 | G | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 311 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.12+1508C>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99087181 | |||||||
| chr4:99087238 | C | T | 1 | a0001c0001t0002g0066 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.12+1451G>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99087238 | |||||||
| chr4:99087343 | T | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 311 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.12+1346A>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99087343 | |||||||
| chr4:99087396 | A | AG | 53 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(50): Show | 127 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(124): Show |
intron_variant | MODIFIER | c.12+1292dupC | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99087396 | |||||||
| chr4:99087396 | AG | A | 15 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0152others(12): Show | 20 | HG00323.hp2 HG01123.hp1 HG01256.hp2 others(17): Show |
intron_variant | MODIFIER | c.12+1292delC | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99087396 | |||||||
| chr4:99087427 | T | C | 1 | a0001c0001t0001g0149 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.12+1262A>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99087427 | |||||||
| chr4:99087471 | T | C | 2 | a0001c0001t0002g0046a0001c0001t0002g0047 | 2 | HG02293.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.12+1218A>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99087471 | |||||||
| chr4:99087476 | G | C | 4 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(1): Show | 4 | NA18950.hp1 NA18966.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.12+1213C>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99087476 | |||||||
| chr4:99087593 | A | C | 1 | a0001c0002t0005g0049 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.12+1096T>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99087593 | |||||||
| chr4:99087599 | G | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 311 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.12+1090C>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99087599 | |||||||
| chr4:99087640 | C | T | 1 | a0001c0001t0008g0042 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.12+1049G>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99087640 | |||||||
| chr4:99087797 | C | T | 16 | a0001c0002t0004g0009a0001c0002t0004g0018a0001c0002t0004g0051others(13): Show | 21 | HG00323.hp2 HG01123.hp1 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.12+892G>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99087797 | |||||||
| chr4:99087853 | A | T | 52 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(49): Show | 91 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.12+836T>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99087853 | |||||||
| chr4:99087859 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.12+830A>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99087859 | |||||||
| chr4:99087983 | C | T | 1 | a0001c0001t0003g0048 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.12+706G>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99087983 | |||||||
| chr4:99087984 | T | C | 4 | a0001c0001t0001g0013a0001c0001t0001g0040a0001c0001t0001g0150others(1): Show | 8 | HG01070.hp2 HG02630.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.12+705A>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99087984 | |||||||
| chr4:99088047 | C | A | 2 | a0001c0001t0002g0046a0001c0001t0002g0047 | 2 | HG02293.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.12+642G>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99088047 | |||||||
| chr4:99088200 | G | A | 2 | a0001c0001t0001g0152a0001c0001t0001g0153 | 2 | HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.12+489C>T | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99088200 | |||||||
| chr4:99088439 | C | T | 122 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(119): Show | 290 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.12+250G>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99088439 | |||||||
| chr4:99088445 | C | G | 52 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(49): Show | 91 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.12+244G>C | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99088445 | |||||||
| chr4:99088493 | T | C | 1 | a0001c0001t0001g0154 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.12+196A>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99088493 | |||||||
| chr4:99088587 | G | C | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(113): Show | 284 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(281): Show |
intron_variant | MODIFIER | c.12+102C>G | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99088587 | |||||||
| chr4:99088649 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.12+40G>A | ADH5 | ENSG00000197894.12 | transcript | ENST00000296412.14 | protein_coding | 1/8 | chr4 | 99088649 |