| geneid | 2108 |
|---|---|
| ensemblid | ENSG00000140374.17 |
| hgncid | 3481 |
| symbol | ETFA |
| name | electron transfer flavoprotein subunit alpha |
| refseq_nuc | NM_000126.4 |
| refseq_prot | NP_000117.1 |
| ensembl_nuc | ENST00000557943.6 |
| ensembl_prot | ENSP00000452762.1 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 76215353 |
| end | 76311469 |
| strand | - |
| ver | v1.2 |
| region | chr15:76215353-76311469 |
| region5000 | chr15:76210353-76316469 |
| regionname0 | ETFA_chr15_76215353_76311469 |
| regionname5000 | ETFA_chr15_76210353_76316469 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 333 | 319 | 90 | 58 | 124 | 11 | 34 | 98 | ETFA_chr15_76210353_76316469 | ETFA | copy fasta | chr15 | 76210353 | 76316469 |
| a0002 | 0/0 | 333 | 16 | 0 | 2 | 11 | 1 | 2 | 8 | ETFA_chr15_76210353_76316469 | ETFA | copy fasta | chr15 | 76210353 | 76316469 |
| a0003 | 0/0 | 333 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | copy fasta | chr15 | 76210353 | 76316469 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1002 | 319 | 90 | 58 | 124 | 11 | 34 | ETFA_chr15_76210353_76316469 | ETFA | copy fasta | chr15 | 76210353 | 76316469 |
| c0002 | 0/0 | 1002 | 16 | 0 | 2 | 11 | 1 | 2 | ETFA_chr15_76210353_76316469 | ETFA | copy fasta | chr15 | 76210353 | 76316469 |
| c0003 | 0/0 | 1002 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | copy fasta | chr15 | 76210353 | 76316469 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 1288 | 121 | 11 | 25 | 65 | 5 | 15 | ETFA_chr15_76210353_76316469 | ETFA | copy fasta | chr15 | 76210353 | 76316469 |
| t0002 | 0/1 | 1288 | 111 | 8 | 25 | 57 | 5 | 15 | ETFA_chr15_76210353_76316469 | ETFA | copy fasta | chr15 | 76210353 | 76316469 |
| t0003 | 0/0 | 1288 | 43 | 35 | 5 | 0 | 1 | 2 | ETFA_chr15_76210353_76316469 | ETFA | copy fasta | chr15 | 76210353 | 76316469 |
| t0004 | 0/0 | 1284 | 36 | 17 | 5 | 11 | 1 | 2 | ETFA_chr15_76210353_76316469 | ETFA | copy fasta | chr15 | 76210353 | 76316469 |
| t0005 | 1/0 | 1288 | 9 | 8 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | copy fasta | chr15 | 76210353 | 76316469 |
| t0006 | 0/0 | 1288 | 5 | 5 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | copy fasta | chr15 | 76210353 | 76316469 |
| t0007 | 0/0 | 1288 | 2 | 0 | 0 | 2 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | copy fasta | chr15 | 76210353 | 76316469 |
| t0008 | 0/0 | 1288 | 2 | 0 | 0 | 0 | 0 | 2 | ETFA_chr15_76210353_76316469 | ETFA | copy fasta | chr15 | 76210353 | 76316469 |
| t0009 | 0/0 | 1284 | 2 | 2 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | copy fasta | chr15 | 76210353 | 76316469 |
| t0010 | 0/0 | 1288 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | copy fasta | chr15 | 76210353 | 76316469 |
| t0011 | 0/0 | 1288 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | copy fasta | chr15 | 76210353 | 76316469 |
| t0012 | 0/0 | 1213 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | copy fasta | chr15 | 76210353 | 76316469 |
| t0013 | 0/0 | 1288 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | copy fasta | chr15 | 76210353 | 76316469 |
| t0014 | 0/0 | 1288 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | copy fasta | chr15 | 76210353 | 76316469 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0212 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0263 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1002 | 319 | 90 | 58 | 124 | 11 | 34 | ETFA_chr15_76210353_76316469 | ETFA | copy fasta | chr15 | 76210353 | 76316469 |
| a0002c0002 | 0/0 | 1002 | 16 | 0 | 2 | 11 | 1 | 2 | ETFA_chr15_76210353_76316469 | ETFA | copy fasta | chr15 | 76210353 | 76316469 |
| a0003c0003 | 0/0 | 1002 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | copy fasta | chr15 | 76210353 | 76316469 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2289 | 120 | 11 | 24 | 65 | 5 | 15 | ETFA_chr15_76210353_76316469 | ETFA | copy fasta | chr15 | 76210353 | 76316469 |
| a0001c0001t0002 | 0/1 | 2289 | 110 | 8 | 25 | 56 | 5 | 15 | ETFA_chr15_76210353_76316469 | ETFA | copy fasta | chr15 | 76210353 | 76316469 |
| a0001c0001t0003 | 0/0 | 2289 | 43 | 35 | 5 | 0 | 1 | 2 | ETFA_chr15_76210353_76316469 | ETFA | copy fasta | chr15 | 76210353 | 76316469 |
| a0001c0001t0004 | 0/0 | 2285 | 21 | 17 | 4 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | copy fasta | chr15 | 76210353 | 76316469 |
| a0001c0001t0005 | 1/0 | 2289 | 9 | 8 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | copy fasta | chr15 | 76210353 | 76316469 |
| a0001c0001t0006 | 0/0 | 2289 | 5 | 5 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | copy fasta | chr15 | 76210353 | 76316469 |
| a0001c0001t0007 | 0/0 | 2289 | 2 | 0 | 0 | 2 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | copy fasta | chr15 | 76210353 | 76316469 |
| a0001c0001t0008 | 0/0 | 2289 | 2 | 0 | 0 | 0 | 0 | 2 | ETFA_chr15_76210353_76316469 | ETFA | copy fasta | chr15 | 76210353 | 76316469 |
| a0001c0001t0009 | 0/0 | 2285 | 2 | 2 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | copy fasta | chr15 | 76210353 | 76316469 |
| a0001c0001t0010 | 0/0 | 2289 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | copy fasta | chr15 | 76210353 | 76316469 |
| a0001c0001t0011 | 0/0 | 2289 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | copy fasta | chr15 | 76210353 | 76316469 |
| a0001c0001t0012 | 0/0 | 2214 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | copy fasta | chr15 | 76210353 | 76316469 |
| a0001c0001t0013 | 0/0 | 2289 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | copy fasta | chr15 | 76210353 | 76316469 |
| a0001c0001t0014 | 0/0 | 2289 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | copy fasta | chr15 | 76210353 | 76316469 |
| a0002c0002t0001 | 0/0 | 2289 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | copy fasta | chr15 | 76210353 | 76316469 |
| a0002c0002t0004 | 0/0 | 2285 | 15 | 0 | 1 | 11 | 1 | 2 | ETFA_chr15_76210353_76316469 | ETFA | copy fasta | chr15 | 76210353 | 76316469 |
| a0003c0003t0002 | 0/0 | 2289 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | copy fasta | chr15 | 76210353 | 76316469 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0212 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0003g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0003g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0003g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0003g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0003g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0003g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0003g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0003g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0003g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0003g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0003g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0003g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0003g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0003g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0003g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0003g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0003g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0004g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0004g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0004g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0004g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0004g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0004g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0004g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0004g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0004g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0004g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0004g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0004g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0004g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0004g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0004g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0005g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0005g0263 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0005g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0005g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0005g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0005g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0005g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0005g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0006g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0006g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0006g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0006g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0006g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0007g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0007g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0008g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0008g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0009g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0009g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0010g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0011g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0012g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0013g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0001c0001t0014g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0002c0002t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0002c0002t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0002c0002t0004g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0002c0002t0004g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0002c0002t0004g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0002c0002t0004g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0002c0002t0004g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0002c0002t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0002c0002t0004g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0002c0002t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0002c0002t0004g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0002c0002t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0002c0002t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0002c0002t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0002c0002t0004g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0002c0002t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| a0003c0003t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0144 | EUR | GBR | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0198 | EUR | GBR | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0202 | EUR | GBR | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0299 | EUR | GBR | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0078 | EUR | FIN | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0199 | EUR | FIN | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG00438 | hp2 | a0002 | c0002 | t0004 | g0261 | EAS | CHS | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | CHS | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | CHS | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG00597 | hp2 | a0003 | c0003 | t0002 | g0121 | EAS | CHS | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | CHS | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG00621 | hp2 | a0002 | c0002 | t0004 | g0260 | EAS | CHS | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0213 | AMR | PUR | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | CHS | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0136 | AMR | PUR | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0023 | AMR | PUR | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0149 | AMR | PUR | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0163 | AMR | PUR | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0157 | AMR | PUR | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0211 | AMR | PUR | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0224 | AMR | PUR | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | PUR | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0222 | AMR | PUR | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0022 | AMR | PUR | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0018 | AMR | PUR | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0156 | AMR | PUR | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0231 | AMR | PUR | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0241 | AMR | PUR | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0217 | AMR | PUR | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0313 | AMR | PUR | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0244 | AMR | PUR | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0312 | AMR | PUR | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0252 | AMR | PUR | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0322 | AMR | PUR | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0274 | AMR | CLM | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG01255 | hp2 | a0002 | c0002 | t0004 | g0253 | AMR | CLM | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0138 | AMR | CLM | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0148 | AMR | CLM | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0216 | AMR | CLM | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | CLM | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0316 | AMR | CLM | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0159 | AMR | CLM | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0303 | AMR | CLM | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0323 | AMR | CLM | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0225 | AMR | CLM | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0105 | EUR | IBS | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0315 | EUR | IBS | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0305 | EUR | IBS | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0227 | EUR | IBS | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0318 | AFR | ACB | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0174 | AFR | ACB | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0164 | AFR | ACB | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0112 | AFR | ACB | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0172 | AMR | PEL | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0151 | AMR | PEL | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0181 | AMR | PEL | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0167 | AMR | PEL | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0209 | AMR | PEL | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0215 | AMR | PEL | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | KHV | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02027 | hp2 | a0002 | c0002 | t0004 | g0259 | EAS | KHV | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | KHV | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | KHV | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02055 | hp1 | a0001 | c0001 | t0006 | g0278 | AFR | ACB | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0242 | AFR | ACB | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | KHV | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | KHV | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02080 | hp2 | a0001 | c0001 | t0007 | g0132 | EAS | KHV | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02083 | hp1 | a0001 | c0001 | t0007 | g0133 | EAS | KHV | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | KHV | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | KHV | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0264 | AFR | ACB | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0103 | AFR | ACB | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | CDX | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | CDX | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02257 | hp1 | a0001 | c0001 | t0011 | g0330 | AFR | ACB | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | ACB | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0238 | AFR | ACB | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0019 | AFR | ACB | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0127 | AMR | PEL | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0120 | AMR | PEL | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0114 | AFR | ACB | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0115 | AFR | ACB | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0210 | AMR | PEL | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | ACB | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0327 | AFR | ACB | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0269 | AFR | GWD | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0208 | SAS | PJL | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0028 | SAS | PJL | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0226 | AFR | GWD | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0113 | AFR | GWD | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0277 | AFR | GWD | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0106 | AFR | GWD | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0271 | AFR | GWD | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0017 | AFR | GWD | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0141 | SAS | PJL | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0232 | AFR | GWD | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0207 | AFR | GWD | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0329 | AFR | GWD | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0003 | AFR | GWD | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0214 | SAS | PJL | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0109 | AFR | GWD | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0248 | AFR | GWD | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0107 | AFR | GWD | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0025 | AFR | GWD | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0251 | AFR | GWD | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0266 | AFR | GWD | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0245 | AFR | GWD | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0328 | AFR | GWD | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0265 | AFR | GWD | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0246 | AFR | GWD | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0236 | AFR | ESN | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | ESN | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0235 | AFR | ESN | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | ESN | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0275 | AFR | ESN | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0234 | AFR | ESN | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0015 | SAS | PJL | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0332 | AFR | GWD | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG03041 | hp2 | a0001 | c0001 | t0010 | g0004 | AFR | GWD | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0325 | AFR | MSL | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0279 | AFR | MSL | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0326 | AFR | ESN | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0108 | AFR | ESN | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG03195 | hp1 | a0001 | c0001 | t0009 | g0239 | AFR | ESN | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | ESN | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | MSL | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0243 | AFR | MSL | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0267 | AFR | MSL | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | MSL | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0143 | SAS | PJL | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0206 | AFR | MSL | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0003 | AFR | MSL | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0249 | AFR | MSL | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0125 | SAS | PJL | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG03491 | hp2 | a0001 | c0001 | t0008 | g0165 | SAS | PJL | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG03516 | hp1 | a0001 | c0001 | t0006 | g0280 | AFR | ESN | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0240 | AFR | ESN | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG03540 | hp1 | a0001 | c0001 | t0009 | g0230 | AFR | GWD | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | GWD | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0270 | AFR | MSL | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0333 | AFR | MSL | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0178 | SAS | PJL | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0160 | SAS | PJL | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0314 | SAS | PJL | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0220 | SAS | STU | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | STU | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG03704 | hp1 | a0002 | c0002 | t0004 | g0254 | SAS | PJL | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0140 | SAS | PJL | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0158 | SAS | PJL | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG03710 | hp2 | a0002 | c0002 | t0004 | g0255 | SAS | PJL | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0168 | SAS | BEB | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0155 | SAS | BEB | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0139 | SAS | BEB | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | BEB | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | BEB | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG03942 | hp2 | a0001 | c0001 | t0008 | g0173 | SAS | BEB | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | STU | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | STU | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | STU | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0166 | SAS | STU | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0321 | AFR | YRI | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0237 | AFR | YRI | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18943 | hp2 | a0002 | c0002 | t0004 | g0283 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18946 | hp1 | a0002 | c0002 | t0004 | g0257 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18948 | hp1 | a0002 | c0002 | t0004 | g0228 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18957 | hp1 | a0002 | c0002 | t0004 | g0262 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18972 | hp2 | a0002 | c0002 | t0004 | g0247 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18973 | hp1 | a0001 | c0001 | t0014 | g0302 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18988 | hp2 | a0002 | c0002 | t0004 | g0284 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA19007 | hp1 | a0002 | c0002 | t0004 | g0258 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA19030 | hp1 | a0001 | c0001 | t0012 | g0268 | AFR | LWK | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0087 | AFR | LWK | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0331 | AFR | LWK | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0233 | AFR | LWK | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA19091 | hp2 | a0002 | c0002 | t0004 | g0256 | EAS | JPT | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0201 | AFR | YRI | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | YRI | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA20129 | hp1 | a0001 | c0001 | t0006 | g0281 | AFR | ASW | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0250 | AFR | ASW | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA20752 | hp1 | a0002 | c0002 | t0004 | g0229 | EUR | TSI | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0021 | EUR | TSI | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0146 | SAS | GIH | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | GIH | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0147 | AMR | CLM | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0272 | AMR | CLM | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0273 | AFR | ACB | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0324 | AFR | ACB | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0110 | AFR | ACB | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0218 | AFR | ACB | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | ACB | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG02559 | hp2 | a0001 | c0001 | t0006 | g0282 | AFR | ACB | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | USA | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0111 | AFR | USA | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0223 | AFR | USA | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA20300 | hp2 | a0001 | c0001 | t0013 | g0301 | AFR | USA | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | g0102 | AFR | LWK | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0276 | AFR | LWK | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0212 | REF | REF | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0005 | g0263 | REF | REF | ETFA_chr15_76210353_76316469 | ETFA | chr15 | 76210353 | 76316469 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:76215354
|
A | G | 1 | a0001 | 5 | HG02055.hp1 HG02559.hp2 HG03098.hp2 others(2): Show |
splice_region_variant | LOW | c.*1205T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 12/12 | chr15 | 76215354 | ||||||
| chr15:76286421
|
G | A | 1 | a0002 | 16 | HG00438.hp2 HG00621.hp2 HG01175.hp1 others(13): Show |
missense_variant | MODERATE | c.512C>T | p.Thr171Ile | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 6/12 | 593/2289 | 512/1002 | 171/333 | chr15 | 76286421 | ||
| chr15:76295634
|
C | T | 1 | a0003 | 1 | HG00597.hp2 | missense_variant | MODERATE | c.143G>A | p.Gly48Glu | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 2/12 | 224/2289 | 143/1002 | 48/333 | chr15 | 76295634 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:76215371
|
T | A | 1 | a0001c0001t0007 | 2 | HG02080.hp2 HG02083.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1188A>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 12/12 | 1188 | chr15 | 76215371 | |||||
| chr15:76215497
|
C | G | 4 | a0001c0001t0002a0001c0001t0007a0001c0001t0008others(1): Show | 115 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*1062G>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 12/12 | 1062 | chr15 | 76215497 | |||||
| chr15:76215505
|
T | C | 1 | a0001c0001t0013 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1054A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 12/12 | 1054 | chr15 | 76215505 | |||||
| chr15:76215592
|
C | T | 1 | a0001c0001t0009 | 2 | HG03195.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*967G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 12/12 | 967 | chr15 | 76215592 | |||||
| chr15:76215611
|
C | T | 4 | a0001c0001t0001a0001c0001t0013a0001c0001t0014others(1): Show | 123 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*948G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 12/12 | 948 | chr15 | 76215611 | |||||
| chr15:76215720
|
ACACAGGC others(68): Show |
A | 1 | a0001c0001t0012 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*764_*838delCAGAGA others(69): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 12/12 | 764 | chr15 | 76215720 | |||||
| chr15:76215811
|
G | A | 1 | a0001c0001t0008 | 2 | HG03491.hp2 HG03942.hp2 |
3_prime_UTR_variant | MODIFIER | c.*748C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 12/12 | 748 | chr15 | 76215811 | |||||
| chr15:76216069
|
C | T | 1 | a0001c0001t0012 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*490G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 12/12 | 490 | chr15 | 76216069 | |||||
| chr15:76216224
|
AAAAT | A | 3 | a0001c0001t0004a0001c0001t0009a0002c0002t0004 | 38 | HG00438.hp2 HG00621.hp2 HG01109.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*331_*334delATTT | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 12/12 | 331 | chr15 | 76216224 | |||||
| chr15:76216343
|
T | A | 15 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(12): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
3_prime_UTR_variant | MODIFIER | c.*216A>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 12/12 | 216 | chr15 | 76216343 | |||||
| chr15:76216460
|
C | T | 1 | a0001c0001t0011 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*99G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 12/12 | 99 | chr15 | 76216460 | |||||
| chr15:76216532
|
G | A | 1 | a0001c0001t0014 | 1 | NA18973.hp1 | 3_prime_UTR_variant | MODIFIER | c.*27C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 12/12 | 27 | chr15 | 76216532 | |||||
| chr15:76311459
|
A | G | 1 | a0001c0001t0010 | 1 | HG03041.hp2 | 5_prime_UTR_variant | MODIFIER | c.-71T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/12 | 71 | chr15 | 76311459 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:76216795
|
G | A | 1 | a0001c0001t0012g0268 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.964-198C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76216795 | ||||||
| chr15:76216836
|
T | C | 1 | a0001c0001t0002g0138 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.964-239A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76216836 | ||||||
| chr15:76216840
|
C | CT | 18 | a0001c0001t0001g0031a0001c0001t0001g0057a0001c0001t0001g0059others(15): Show | 19 | HG01167.hp2 HG01243.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.964-244dupA | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76216840 | ||||||
| chr15:76216840
|
C | CTT | 103 | a0001c0001t0001g0321a0001c0001t0002g0117a0001c0001t0002g0118others(100): Show | 103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
intron_variant | MODIFIER | c.964-245_964-244dup others(2): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76216840 | ||||||
| chr15:76216840
|
C | CTTT | 30 | a0001c0001t0002g0002a0001c0001t0002g0054a0001c0001t0002g0116others(27): Show | 31 | HG00544.hp1 HG00621.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.964-246_964-244dup others(3): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76216840 | ||||||
| chr15:76216840
|
C | CTTTT | 35 | a0001c0001t0003g0018a0001c0001t0003g0020a0001c0001t0003g0021others(32): Show | 35 | HG00438.hp2 HG01081.hp2 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.964-247_964-244dup others(4): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76216840 | ||||||
| chr15:76216840
|
C | CTTTTT | 14 | a0001c0001t0003g0015a0001c0001t0003g0023a0001c0001t0003g0112others(11): Show | 14 | HG00621.hp2 HG00735.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.964-248_964-244dup others(5): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76216840 | ||||||
| chr15:76216864
|
G | A | 1 | a0001c0001t0005g0003 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.964-267C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76216864 | ||||||
| chr15:76217097
|
G | A | 3 | a0001c0001t0003g0264a0001c0001t0003g0275a0001c0001t0003g0277 | 3 | HG02145.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.964-500C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76217097 | ||||||
| chr15:76217111
|
A | T | 1 | a0001c0001t0002g0141 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.964-514T>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76217111 | ||||||
| chr15:76217504
|
C | T | 1 | a0001c0001t0003g0276 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.964-907G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76217504 | ||||||
| chr15:76217526
|
A | C | 1 | a0001c0001t0001g0082 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.964-929T>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76217526 | ||||||
| chr15:76217650
|
T | C | 1 | a0001c0001t0011g0330 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.964-1053A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76217650 | ||||||
| chr15:76217695
|
C | A | 5 | a0001c0001t0006g0278a0001c0001t0006g0279a0001c0001t0006g0280others(2): Show | 5 | HG02055.hp1 HG02559.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.964-1098G>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76217695 | ||||||
| chr15:76217732
|
G | A | 324 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(321): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.964-1135C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76217732 | ||||||
| chr15:76217900
|
G | A | 5 | a0001c0001t0006g0278a0001c0001t0006g0279a0001c0001t0006g0280others(2): Show | 5 | HG02055.hp1 HG02559.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.964-1303C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76217900 | ||||||
| chr15:76217963
|
G | A | 114 | a0001c0001t0002g0002a0001c0001t0002g0054a0001c0001t0002g0116others(111): Show | 115 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(112): Show |
intron_variant | MODIFIER | c.964-1366C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76217963 | ||||||
| chr15:76218154
|
T | C | 1 | a0001c0001t0012g0268 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.964-1557A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76218154 | ||||||
| chr15:76218173
|
A | T | 1 | a0001c0001t0001g0049 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.964-1576T>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76218173 | ||||||
| chr15:76218184
|
G | A | 10 | a0001c0001t0003g0324a0001c0001t0003g0325a0001c0001t0003g0326others(7): Show | 10 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.964-1587C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76218184 | ||||||
| chr15:76218241
|
G | A | 325 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(322): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.964-1644C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76218241 | ||||||
| chr15:76218328
|
C | T | 4 | a0001c0001t0006g0279a0001c0001t0006g0280a0001c0001t0006g0281others(1): Show | 4 | HG02559.hp2 HG03098.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.964-1731G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76218328 | ||||||
| chr15:76218353
|
C | T | 2 | a0001c0001t0003g0020a0001c0001t0003g0022 | 2 | HG01081.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.964-1756G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76218353 | ||||||
| chr15:76218355
|
T | C | 325 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(322): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.964-1758A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76218355 | ||||||
| chr15:76218359
|
C | T | 89 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(86): Show | 90 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.964-1762G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76218359 | ||||||
| chr15:76218840
|
C | T | 2 | a0001c0001t0003g0005a0001c0001t0003g0006 | 2 | HG01243.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.964-2243G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76218840 | ||||||
| chr15:76218961
|
C | T | 5 | a0001c0001t0002g0211a0001c0001t0002g0214a0001c0001t0002g0215others(2): Show | 5 | HG01070.hp2 HG01257.hp1 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.964-2364G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76218961 | ||||||
| chr15:76219064
|
A | G | 10 | a0001c0001t0003g0324a0001c0001t0003g0325a0001c0001t0003g0326others(7): Show | 10 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.964-2467T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76219064 | ||||||
| chr15:76219332
|
G | A | 2 | a0001c0001t0003g0328a0001c0001t0003g0329 | 2 | HG02723.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.964-2735C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76219332 | ||||||
| chr15:76219387
|
G | A | 1 | a0001c0001t0001g0053 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.964-2790C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76219387 | ||||||
| chr15:76219446
|
C | G | 2 | a0002c0002t0004g0261a0002c0002t0004g0262 | 2 | HG00438.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.964-2849G>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76219446 | ||||||
| chr15:76219594
|
T | C | 4 | a0001c0001t0003g0106a0001c0001t0003g0107a0001c0001t0003g0108others(1): Show | 4 | HG02630.hp2 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.964-2997A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76219594 | ||||||
| chr15:76219623
|
C | A | 1 | a0001c0001t0001g0322 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.964-3026G>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76219623 | ||||||
| chr15:76219640
|
G | A | 10 | a0001c0001t0003g0324a0001c0001t0003g0325a0001c0001t0003g0326others(7): Show | 10 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.964-3043C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76219640 | ||||||
| chr15:76219686
|
A | G | 320 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(317): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.964-3089T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76219686 | ||||||
| chr15:76219776
|
T | C | 1 | a0001c0001t0011g0330 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.964-3179A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76219776 | ||||||
| chr15:76219794
|
C | CT | 3 | a0001c0001t0003g0264a0001c0001t0003g0275a0001c0001t0003g0277 | 3 | HG02145.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.964-3198dupA | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76219794 | ||||||
| chr15:76219857
|
T | G | 1 | a0001c0001t0006g0278 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.964-3260A>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76219857 | ||||||
| chr15:76219997
|
T | C | 1 | a0001c0001t0011g0330 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.964-3400A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76219997 | ||||||
| chr15:76220016
|
A | G | 13 | a0001c0001t0003g0015a0001c0001t0003g0018a0001c0001t0003g0020others(10): Show | 13 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.964-3419T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76220016 | ||||||
| chr15:76220066
|
C | T | 7 | a0001c0001t0003g0273a0001c0001t0003g0274a0001c0001t0006g0278others(4): Show | 7 | HG01255.hp1 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.964-3469G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76220066 | ||||||
| chr15:76220210
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.964-3613C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76220210 | ||||||
| chr15:76220288
|
G | A | 1 | a0001c0001t0002g0181 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.964-3691C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76220288 | ||||||
| chr15:76220327
|
C | G | 1 | a0001c0001t0001g0316 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.964-3730G>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76220327 | ||||||
| chr15:76220635
|
C | T | 2 | a0002c0002t0004g0229a0002c0002t0004g0254 | 2 | HG03704.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.964-4038G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76220635 | ||||||
| chr15:76220659
|
T | G | 4 | a0001c0001t0002g0212a0001c0001t0002g0217a0001c0001t0002g0224others(1): Show | 4 | HG01074.hp1 HG01167.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.964-4062A>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76220659 | ||||||
| chr15:76220784
|
T | C | 1 | a0001c0001t0002g0205 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.964-4187A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76220784 | ||||||
| chr15:76220787
|
C | T | 3 | a0001c0001t0003g0264a0001c0001t0003g0275a0001c0001t0003g0277 | 3 | HG02145.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.964-4190G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76220787 | ||||||
| chr15:76220899
|
A | G | 121 | a0001c0001t0002g0002a0001c0001t0002g0054a0001c0001t0002g0116others(118): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.964-4302T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76220899 | ||||||
| chr15:76220939
|
C | T | 2 | a0001c0001t0001g0035a0001c0001t0001g0065 | 2 | HG02027.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.964-4342G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76220939 | ||||||
| chr15:76221003
|
G | A | 1 | a0001c0001t0001g0303 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.964-4406C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76221003 | ||||||
| chr15:76221082
|
C | T | 3 | a0001c0001t0003g0264a0001c0001t0003g0275a0001c0001t0003g0277 | 3 | HG02145.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.964-4485G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76221082 | ||||||
| chr15:76221212
|
G | A | 311 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(308): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.964-4615C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76221212 | ||||||
| chr15:76221286
|
A | C | 14 | a0001c0001t0003g0015a0001c0001t0003g0018a0001c0001t0003g0020others(11): Show | 14 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.963+4563T>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76221286 | ||||||
| chr15:76221328
|
G | A | 1 | a0001c0001t0002g0178 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.963+4521C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76221328 | ||||||
| chr15:76221345
|
G | A | 3 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287 | 3 | HG02572.hp1 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.963+4504C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76221345 | ||||||
| chr15:76221540
|
G | A | 1 | a0001c0001t0003g0276 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.963+4309C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76221540 | ||||||
| chr15:76221625
|
A | T | 9 | a0001c0001t0003g0324a0001c0001t0003g0325a0001c0001t0003g0326others(6): Show | 9 | HG02109.hp2 HG02451.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.963+4224T>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76221625 | ||||||
| chr15:76221677
|
T | C | 1 | a0001c0001t0003g0276 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.963+4172A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76221677 | ||||||
| chr15:76222020
|
A | G | 122 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(119): Show | 123 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.963+3829T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76222020 | ||||||
| chr15:76222326
|
AT | A | 132 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(129): Show | 133 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.963+3522delA | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76222326 | ||||||
| chr15:76222523
|
G | A | 1 | a0001c0001t0002g0145 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.963+3326C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76222523 | ||||||
| chr15:76222555
|
T | C | 16 | a0001c0001t0004g0102a0002c0002t0004g0228a0002c0002t0004g0229others(13): Show | 16 | HG00438.hp2 HG00621.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.963+3294A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76222555 | ||||||
| chr15:76222604
|
C | T | 15 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0148others(12): Show | 15 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(12): Show |
intron_variant | MODIFIER | c.963+3245G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76222604 | ||||||
| chr15:76222625
|
G | A | 2 | a0002c0002t0004g0283a0002c0002t0004g0284 | 2 | NA18943.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.963+3224C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76222625 | ||||||
| chr15:76222644
|
G | A | 3 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287 | 3 | HG02572.hp1 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.963+3205C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76222644 | ||||||
| chr15:76222690
|
T | TA | 10 | a0001c0001t0003g0324a0001c0001t0003g0325a0001c0001t0003g0326others(7): Show | 10 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.963+3158dupT | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76222690 | ||||||
| chr15:76222779
|
G | C | 132 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(129): Show | 133 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.963+3070C>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76222779 | ||||||
| chr15:76222838
|
AT | A | 161 | a0001c0001t0002g0002a0001c0001t0002g0054a0001c0001t0002g0116others(158): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.963+3010delA | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76222838 | ||||||
| chr15:76222940
|
A | C | 310 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(307): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.963+2909T>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76222940 | ||||||
| chr15:76223087
|
C | T | 3 | a0001c0001t0003g0264a0001c0001t0003g0275a0001c0001t0003g0277 | 3 | HG02145.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.963+2762G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76223087 | ||||||
| chr15:76223216
|
C | CT | 130 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(127): Show | 132 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.963+2632dupA | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76223216 | ||||||
| chr15:76223216
|
C | CTT | 100 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0001g0057others(97): Show | 100 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(97): Show |
intron_variant | MODIFIER | c.963+2631_963+2632d others(4): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76223216 | ||||||
| chr15:76223216
|
CT | C | 16 | a0001c0001t0003g0015a0001c0001t0003g0018a0001c0001t0003g0020others(13): Show | 16 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.963+2632delA | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76223216 | ||||||
| chr15:76223236
|
G | T | 2 | a0001c0001t0004g0236a0001c0001t0004g0237 | 2 | HG02922.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.963+2613C>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76223236 | ||||||
| chr15:76223237
|
A | T | 2 | a0001c0001t0004g0236a0001c0001t0004g0237 | 2 | HG02922.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.963+2612T>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76223237 | ||||||
| chr15:76223265
|
T | C | 1 | a0001c0001t0002g0205 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.963+2584A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76223265 | ||||||
| chr15:76223363
|
A | G | 13 | a0001c0001t0003g0015a0001c0001t0003g0018a0001c0001t0003g0020others(10): Show | 13 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.963+2486T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76223363 | ||||||
| chr15:76223474
|
C | T | 1 | a0001c0001t0003g0114 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.963+2375G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76223474 | ||||||
| chr15:76223792
|
G | C | 1 | a0001c0001t0001g0031 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.963+2057C>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76223792 | ||||||
| chr15:76223819
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.963+2030C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76223819 | ||||||
| chr15:76224044
|
G | A | 1 | a0001c0001t0001g0046 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.963+1805C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76224044 | ||||||
| chr15:76224391
|
C | T | 1 | a0001c0001t0003g0087 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.963+1458G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76224391 | ||||||
| chr15:76224707
|
G | A | 131 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(128): Show | 132 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.963+1142C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76224707 | ||||||
| chr15:76224826
|
A | G | 311 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(308): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.963+1023T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76224826 | ||||||
| chr15:76224970
|
G | A | 1 | a0001c0001t0002g0209 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.963+879C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76224970 | ||||||
| chr15:76225152
|
C | T | 3 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287 | 3 | HG02572.hp1 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.963+697G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76225152 | ||||||
| chr15:76225363
|
A | G | 1 | a0001c0001t0011g0330 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.963+486T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76225363 | ||||||
| chr15:76225531
|
C | T | 2 | a0001c0001t0003g0328a0001c0001t0003g0329 | 2 | HG02723.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.963+318G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76225531 | ||||||
| chr15:76225535
|
C | T | 1 | a0001c0001t0011g0330 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.963+314G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76225535 | ||||||
| chr15:76225536
|
G | A | 13 | a0001c0001t0003g0015a0001c0001t0003g0018a0001c0001t0003g0020others(10): Show | 13 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.963+313C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76225536 | ||||||
| chr15:76225542
|
G | A | 1 | a0001c0001t0003g0276 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.963+307C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76225542 | ||||||
| chr15:76225553
|
T | C | 26 | a0001c0001t0001g0098a0001c0001t0001g0288a0001c0001t0001g0289others(23): Show | 26 | HG00140.hp2 HG00544.hp2 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.963+296A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76225553 | ||||||
| chr15:76225585
|
G | A | 2 | a0001c0001t0001g0035a0001c0001t0001g0065 | 2 | HG02027.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.963+264C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76225585 | ||||||
| chr15:76225588
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.963+261G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76225588 | ||||||
| chr15:76225589
|
G | A | 2 | a0001c0001t0003g0005a0001c0001t0003g0006 | 2 | HG01243.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.963+260C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76225589 | ||||||
| chr15:76225641
|
T | C | 4 | a0001c0001t0003g0106a0001c0001t0003g0107a0001c0001t0003g0108others(1): Show | 4 | HG02630.hp2 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.963+208A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76225641 | ||||||
| chr15:76225717
|
T | G | 1 | a0001c0001t0001g0323 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.963+132A>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 11/11 | chr15 | 76225717 | ||||||
| chr15:76226005
|
C | CCCTTA | 320 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(317): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.883-77_883-76insTA others(3): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76226005 | ||||||
| chr15:76226029
|
G | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0011 | 2 | HG00733.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.883-100C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76226029 | ||||||
| chr15:76226198
|
A | T | 4 | a0001c0001t0003g0106a0001c0001t0003g0107a0001c0001t0003g0108others(1): Show | 4 | HG02630.hp2 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.883-269T>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76226198 | ||||||
| chr15:76226299
|
T | G | 132 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(129): Show | 133 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.883-370A>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76226299 | ||||||
| chr15:76226424
|
A | G | 2 | a0001c0001t0003g0005a0001c0001t0003g0006 | 2 | HG01243.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.883-495T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76226424 | ||||||
| chr15:76226505
|
A | C | 3 | a0001c0001t0003g0264a0001c0001t0003g0275a0001c0001t0003g0277 | 3 | HG02145.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.883-576T>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76226505 | ||||||
| chr15:76226600
|
C | T | 5 | a0001c0001t0004g0235a0001c0001t0004g0248a0001c0001t0004g0249others(2): Show | 5 | HG02809.hp2 HG02886.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.883-671G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76226600 | ||||||
| chr15:76226608
|
G | A | 5 | a0001c0001t0006g0278a0001c0001t0006g0279a0001c0001t0006g0280others(2): Show | 5 | HG02055.hp1 HG02559.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-679C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76226608 | ||||||
| chr15:76226706
|
G | A | 2 | a0001c0001t0003g0273a0001c0001t0003g0274 | 2 | HG01255.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.883-777C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76226706 | ||||||
| chr15:76226735
|
C | T | 5 | a0001c0001t0003g0110a0001c0001t0003g0111a0001c0001t0003g0112others(2): Show | 5 | HG01891.hp2 HG02486.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.883-806G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76226735 | ||||||
| chr15:76226739
|
C | T | 1 | a0001c0001t0011g0330 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.883-810G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76226739 | ||||||
| chr15:76226793
|
G | A | 131 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(128): Show | 132 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.883-864C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76226793 | ||||||
| chr15:76226795
|
C | T | 131 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(128): Show | 132 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.883-866G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76226795 | ||||||
| chr15:76226865
|
T | C | 324 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(321): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.883-936A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76226865 | ||||||
| chr15:76226892
|
T | G | 4 | a0001c0001t0003g0106a0001c0001t0003g0107a0001c0001t0003g0108others(1): Show | 4 | HG02630.hp2 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.883-963A>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76226892 | ||||||
| chr15:76226896
|
T | A | 1 | a0001c0001t0001g0304 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.883-967A>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76226896 | ||||||
| chr15:76226908
|
C | A | 2 | a0001c0001t0001g0290a0001c0001t0003g0115 | 2 | HG02135.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.883-979G>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76226908 | ||||||
| chr15:76227114
|
C | G | 2 | a0001c0001t0003g0005a0001c0001t0003g0006 | 2 | HG01243.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.883-1185G>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76227114 | ||||||
| chr15:76227140
|
A | G | 7 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(4): Show | 7 | HG00438.hp1 HG00733.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.883-1211T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76227140 | ||||||
| chr15:76227191
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.883-1262G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76227191 | ||||||
| chr15:76227219
|
G | A | 3 | a0001c0001t0002g0217a0001c0001t0002g0224a0001c0001t0002g0225 | 3 | HG01074.hp1 HG01167.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.883-1290C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76227219 | ||||||
| chr15:76227515
|
C | CAAAAAA | 106 | a0001c0001t0002g0002a0001c0001t0002g0054a0001c0001t0002g0116others(103): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.883-1592_883-1587d others(8): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76227515 | ||||||
| chr15:76227515
|
C | CAAAAAAA others(4): Show |
2 | a0001c0001t0001g0030a0001c0001t0001g0031 | 2 | HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.883-1597_883-1587d others(13): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76227515 | ||||||
| chr15:76227515
|
C | CAAAAAAA others(5): Show |
13 | a0001c0001t0001g0010a0001c0001t0001g0303a0001c0001t0001g0312others(10): Show | 13 | HG00733.hp2 HG01168.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.883-1598_883-1587d others(14): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76227515 | ||||||
| chr15:76227515
|
C | CAAAAAAA others(6): Show |
98 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(95): Show | 99 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.883-1599_883-1587d others(15): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76227515 | ||||||
| chr15:76227515
|
C | CAAAAAAA others(7): Show |
61 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(58): Show | 61 | HG00438.hp2 HG00621.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.883-1587_883-1586i others(16): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76227515 | ||||||
| chr15:76227515
|
C | CAAAAAAA others(8): Show |
24 | a0001c0001t0003g0005a0001c0001t0003g0277a0001c0001t0003g0324others(21): Show | 24 | HG01109.hp2 HG01123.hp2 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.883-1587_883-1586i others(17): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76227515 | ||||||
| chr15:76227515
|
C | CAAAAAAA others(9): Show |
7 | a0001c0001t0003g0333a0001c0001t0004g0237a0001c0001t0004g0240others(4): Show | 7 | HG02055.hp1 HG02055.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.883-1587_883-1586i others(18): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76227515 | ||||||
| chr15:76227515
|
C | CAAAAAAA others(10): Show |
1 | a0001c0001t0003g0264 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.883-1587_883-1586i others(19): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76227515 | ||||||
| chr15:76227515
|
C | CAAAAAAA others(24): Show |
4 | a0001c0001t0003g0106a0001c0001t0003g0107a0001c0001t0003g0108others(1): Show | 4 | HG02630.hp2 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.883-1587_883-1586i others(33): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76227515 | ||||||
| chr15:76227609
|
G | T | 2 | a0001c0001t0001g0322a0001c0001t0001g0323 | 2 | HG01243.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.883-1680C>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76227609 | ||||||
| chr15:76227816
|
A | G | 1 | a0001c0001t0002g0128 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.883-1887T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76227816 | ||||||
| chr15:76227830
|
G | T | 1 | a0001c0001t0001g0310 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.883-1901C>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76227830 | ||||||
| chr15:76228023
|
T | G | 10 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0019others(7): Show | 10 | HG02145.hp2 HG02258.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.883-2094A>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76228023 | ||||||
| chr15:76228119
|
G | C | 1 | a0001c0001t0003g0115 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.883-2190C>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76228119 | ||||||
| chr15:76228176
|
A | T | 3 | a0001c0001t0002g0160a0001c0001t0008g0165a0001c0001t0008g0173 | 3 | HG03491.hp2 HG03669.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.883-2247T>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76228176 | ||||||
| chr15:76228243
|
G | A | 1 | a0001c0001t0002g0151 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.883-2314C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76228243 | ||||||
| chr15:76228309
|
T | A | 1 | a0001c0001t0001g0291 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.883-2380A>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76228309 | ||||||
| chr15:76228332
|
G | A | 1 | a0001c0001t0003g0331 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.883-2403C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76228332 | ||||||
| chr15:76228335
|
C | T | 1 | a0001c0001t0004g0272 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.883-2406G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76228335 | ||||||
| chr15:76228501
|
A | C | 7 | a0001c0001t0003g0273a0001c0001t0003g0274a0001c0001t0006g0278others(4): Show | 7 | HG01255.hp1 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.883-2572T>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76228501 | ||||||
| chr15:76228745
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.882+2588A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76228745 | ||||||
| chr15:76228751
|
C | CT | 15 | a0001c0001t0001g0053a0001c0001t0001g0075a0001c0001t0001g0300others(12): Show | 15 | HG01168.hp1 HG01168.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.882+2581dupA | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76228751 | ||||||
| chr15:76228751
|
C | CTT | 106 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(103): Show | 107 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.882+2580_882+2581d others(4): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76228751 | ||||||
| chr15:76228751
|
C | CTTT | 11 | a0001c0001t0001g0009a0001c0001t0001g0039a0001c0001t0001g0043others(8): Show | 11 | HG01106.hp1 HG01175.hp2 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.882+2579_882+2581d others(5): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76228751 | ||||||
| chr15:76228751
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.882+2582G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76228751 | ||||||
| chr15:76228751
|
CT | C | 46 | a0001c0001t0002g0119a0001c0001t0002g0125a0001c0001t0002g0138others(43): Show | 46 | HG00438.hp2 HG00621.hp2 HG01109.hp2 others(43): Show |
intron_variant | MODIFIER | c.882+2581delA | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76228751 | ||||||
| chr15:76228900
|
G | A | 1 | a0001c0001t0006g0278 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.882+2433C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76228900 | ||||||
| chr15:76229047
|
T | C | 1 | a0001c0001t0003g0276 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.882+2286A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76229047 | ||||||
| chr15:76229429
|
G | A | 116 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(113): Show | 117 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.882+1904C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76229429 | ||||||
| chr15:76229457
|
C | T | 116 | a0001c0001t0002g0002a0001c0001t0002g0054a0001c0001t0002g0116others(113): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.882+1876G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76229457 | ||||||
| chr15:76229591
|
T | C | 1 | a0002c0002t0004g0228 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.882+1742A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76229591 | ||||||
| chr15:76229618
|
T | G | 3 | a0001c0001t0001g0321a0001c0001t0001g0322a0001c0001t0001g0323 | 3 | HG01243.hp2 HG01496.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.882+1715A>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76229618 | ||||||
| chr15:76229699
|
G | A | 9 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0019others(6): Show | 9 | HG02145.hp2 HG02258.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.882+1634C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76229699 | ||||||
| chr15:76229747
|
G | A | 1 | a0001c0001t0001g0309 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.882+1586C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76229747 | ||||||
| chr15:76229763
|
A | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(113): Show | 117 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.882+1570T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76229763 | ||||||
| chr15:76229839
|
G | A | 1 | a0001c0001t0008g0165 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.882+1494C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76229839 | ||||||
| chr15:76229865
|
T | C | 5 | a0001c0001t0006g0278a0001c0001t0006g0279a0001c0001t0006g0280others(2): Show | 5 | HG02055.hp1 HG02559.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+1468A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76229865 | ||||||
| chr15:76229875
|
G | A | 1 | a0001c0001t0003g0332 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.882+1458C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76229875 | ||||||
| chr15:76230004
|
C | T | 2 | a0001c0001t0003g0005a0001c0001t0003g0087 | 2 | HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.882+1329G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76230004 | ||||||
| chr15:76230159
|
G | C | 4 | a0001c0001t0003g0106a0001c0001t0003g0107a0001c0001t0003g0108others(1): Show | 4 | HG02630.hp2 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+1174C>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76230159 | ||||||
| chr15:76230218
|
C | CTTT | 27 | a0001c0001t0004g0102a0001c0001t0004g0232a0001c0001t0004g0233others(24): Show | 27 | HG00438.hp2 HG01123.hp2 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.882+1112_882+1114d others(5): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76230218 | ||||||
| chr15:76230218
|
C | CTTTT | 7 | a0001c0001t0004g0231a0001c0001t0004g0238a0001c0001t0004g0242others(4): Show | 7 | HG01109.hp2 HG01175.hp1 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.882+1111_882+1114d others(6): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76230218 | ||||||
| chr15:76230218
|
C | CTTTTTTT others(3): Show |
29 | a0001c0001t0002g0116a0001c0001t0002g0119a0001c0001t0002g0120others(26): Show | 29 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.882+1105_882+1114d others(12): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76230218 | ||||||
| chr15:76230218
|
C | CTTTTTTT others(4): Show |
50 | a0001c0001t0002g0002a0001c0001t0002g0054a0001c0001t0002g0117others(47): Show | 51 | HG00621.hp1 HG00639.hp2 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.882+1104_882+1114d others(13): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76230218 | ||||||
| chr15:76230218
|
C | CTTTTTTT others(5): Show |
34 | a0001c0001t0002g0118a0001c0001t0002g0122a0001c0001t0002g0129others(31): Show | 34 | HG00597.hp2 HG00673.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.882+1103_882+1114d others(14): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76230218 | ||||||
| chr15:76230218
|
C | CTTTTTTT others(6): Show |
9 | a0001c0001t0002g0167a0001c0001t0002g0171a0001c0001t0002g0183others(6): Show | 9 | HG01257.hp1 HG01496.hp2 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.882+1102_882+1114d others(15): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76230218 | ||||||
| chr15:76230218
|
C | CTTTTTTT others(7): Show |
1 | a0001c0001t0001g0321 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.882+1101_882+1114d others(16): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76230218 | ||||||
| chr15:76230218
|
CTTT | C | 12 | a0001c0001t0003g0015a0001c0001t0003g0018a0001c0001t0003g0020others(9): Show | 12 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.882+1112_882+1114d others(5): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76230218 | ||||||
| chr15:76230218
|
CTTTTTTT others(1): Show |
C | 9 | a0001c0001t0003g0324a0001c0001t0003g0325a0001c0001t0003g0326others(6): Show | 9 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.882+1107_882+1114d others(10): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76230218 | ||||||
| chr15:76230218
|
CTTTTTTT others(4): Show |
C | 1 | a0002c0002t0004g0256 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.882+1104_882+1114d others(13): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76230218 | ||||||
| chr15:76230218
|
CTTTTTTT others(10): Show |
C | 115 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(112): Show | 116 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.882+1098_882+1114d others(19): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76230218 | ||||||
| chr15:76230250
|
G | A | 121 | a0001c0001t0002g0002a0001c0001t0002g0054a0001c0001t0002g0116others(118): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.882+1083C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76230250 | ||||||
| chr15:76230265
|
C | T | 57 | a0001c0001t0001g0293a0001c0001t0001g0297a0001c0001t0001g0308others(54): Show | 57 | HG00438.hp2 HG00621.hp2 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.882+1068G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76230265 | ||||||
| chr15:76230284
|
T | G | 10 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0019others(7): Show | 10 | HG02145.hp2 HG02258.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.882+1049A>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76230284 | ||||||
| chr15:76230290
|
G | A | 114 | a0001c0001t0002g0002a0001c0001t0002g0054a0001c0001t0002g0116others(111): Show | 115 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(112): Show |
intron_variant | MODIFIER | c.882+1043C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76230290 | ||||||
| chr15:76230354
|
G | A | 1 | a0001c0001t0002g0128 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.882+979C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76230354 | ||||||
| chr15:76230423
|
T | C | 9 | a0001c0001t0003g0324a0001c0001t0003g0325a0001c0001t0003g0326others(6): Show | 9 | HG02109.hp2 HG02451.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.882+910A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76230423 | ||||||
| chr15:76230514
|
C | CCGCGCCC others(69): Show |
111 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(108): Show | 112 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.882+818_882+819ins others(76): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76230514 | ||||||
| chr15:76230514
|
C | CCGCGCCC others(70): Show |
20 | a0001c0001t0001g0029a0001c0001t0001g0036a0001c0001t0001g0039others(17): Show | 20 | HG00438.hp1 HG01175.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.882+818_882+819ins others(77): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76230514 | ||||||
| chr15:76230514
|
C | CCGCGCCC others(71): Show |
1 | a0001c0001t0003g0087 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.882+818_882+819ins others(78): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76230514 | ||||||
| chr15:76230514
|
C | CCGCGCCC others(75): Show |
3 | a0001c0001t0002g0138a0001c0001t0002g0143a0001c0001t0002g0148 | 3 | HG01256.hp1 HG01256.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.882+818_882+819ins others(82): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76230514 | ||||||
| chr15:76230514
|
C | CCGCGCCC others(76): Show |
76 | a0001c0001t0002g0002a0001c0001t0002g0116a0001c0001t0002g0119others(73): Show | 77 | HG00099.hp1 HG00544.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.882+818_882+819ins others(83): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76230514 | ||||||
| chr15:76230514
|
C | CCGCGCCC others(77): Show |
5 | a0001c0001t0003g0110a0001c0001t0003g0111a0001c0001t0003g0112others(2): Show | 5 | HG01891.hp2 HG02486.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.882+818_882+819ins others(84): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76230514 | ||||||
| chr15:76230514
|
C | CCGCGCCC others(77): Show |
31 | a0001c0001t0002g0054a0001c0001t0002g0117a0001c0001t0002g0118others(28): Show | 31 | HG00597.hp2 HG00621.hp1 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.882+818_882+819ins others(84): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76230514 | ||||||
| chr15:76230514
|
C | CCGCGCCC others(78): Show |
25 | a0001c0001t0003g0015a0001c0001t0003g0021a0001c0001t0003g0022others(22): Show | 25 | HG00438.hp2 HG00735.hp1 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.882+818_882+819ins others(85): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76230514 | ||||||
| chr15:76230514
|
C | CCGCGCCC others(78): Show |
10 | a0001c0001t0002g0145a0001c0001t0002g0198a0001c0001t0002g0202others(7): Show | 10 | HG00099.hp2 HG00140.hp1 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.882+818_882+819ins others(85): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76230514 | ||||||
| chr15:76230514
|
C | CCGCGCCC others(79): Show |
18 | a0001c0001t0003g0018a0001c0001t0003g0020a0001c0001t0004g0102others(15): Show | 18 | HG00621.hp2 HG01106.hp2 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.882+818_882+819ins others(86): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76230514 | ||||||
| chr15:76230514
|
C | CCGCGCCC others(79): Show |
4 | a0001c0001t0002g0199a0001c0001t0002g0208a0001c0001t0006g0279others(1): Show | 4 | HG00280.hp2 HG02602.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+818_882+819ins others(86): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76230514 | ||||||
| chr15:76230514
|
C | CCGCGCCC others(80): Show |
4 | a0001c0001t0004g0237a0001c0001t0004g0240a0001c0001t0004g0242others(1): Show | 4 | HG01123.hp2 HG02055.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.882+818_882+819ins others(87): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76230514 | ||||||
| chr15:76230514
|
C | CCGCGCCC others(81): Show |
3 | a0001c0001t0002g0136a0001c0001t0002g0151a0001c0001t0002g0172 | 3 | HG00733.hp1 HG01928.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.882+818_882+819ins others(88): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76230514 | ||||||
| chr15:76230514
|
C | CCGCGCCC others(82): Show |
2 | a0001c0001t0002g0149a0001c0001t0002g0167 | 2 | HG00735.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.882+818_882+819ins others(89): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76230514 | ||||||
| chr15:76230514
|
C | CCGCGCCC others(83): Show |
3 | a0001c0001t0002g0157a0001c0001t0003g0025a0001c0001t0003g0026 | 3 | HG00741.hp2 HG02886.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.882+818_882+819ins others(90): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76230514 | ||||||
| chr15:76230514
|
C | CCGCGCCC others(84): Show |
1 | a0001c0001t0003g0027 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.882+818_882+819ins others(91): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76230514 | ||||||
| chr15:76230514
|
C | CCGCGCCC others(85): Show |
2 | a0001c0001t0003g0016a0001c0001t0003g0024 | 2 | HG02895.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.882+818_882+819ins others(92): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76230514 | ||||||
| chr15:76230514
|
C | CCGCGCCC others(86): Show |
2 | a0001c0001t0003g0017a0001c0001t0003g0019 | 2 | HG02258.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.882+818_882+819ins others(93): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76230514 | ||||||
| chr15:76230514
|
C | CCGCGCCC others(88): Show |
2 | a0001c0001t0003g0103a0001c0001t0003g0115 | 2 | HG02145.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.882+818_882+819ins others(95): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76230514 | ||||||
| chr15:76230514
|
C | CCGCGCCT others(79): Show |
1 | a0002c0002t0004g0283 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.882+818_882+819ins others(86): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76230514 | ||||||
| chr15:76230601
|
T | C | 325 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(322): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.882+732A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76230601 | ||||||
| chr15:76230641
|
G | T | 10 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0019others(7): Show | 10 | HG02145.hp2 HG02258.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.882+692C>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76230641 | ||||||
| chr15:76230933
|
A | G | 9 | a0001c0001t0003g0324a0001c0001t0003g0325a0001c0001t0003g0326others(6): Show | 9 | HG02109.hp2 HG02451.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.882+400T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76230933 | ||||||
| chr15:76231220
|
C | T | 1 | a0001c0001t0012g0268 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.882+113G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76231220 | ||||||
| chr15:76231279
|
C | A | 9 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0019others(6): Show | 9 | HG02145.hp2 HG02258.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.882+54G>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 10/11 | chr15 | 76231279 | ||||||
| chr15:76231430
|
T | C | 13 | a0001c0001t0003g0015a0001c0001t0003g0018a0001c0001t0003g0020others(10): Show | 13 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.817-32A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76231430 | ||||||
| chr15:76231483
|
T | A | 2 | a0001c0001t0003g0005a0001c0001t0003g0006 | 2 | HG01243.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.817-85A>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76231483 | ||||||
| chr15:76231718
|
T | G | 9 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0019others(6): Show | 9 | HG02145.hp2 HG02258.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-320A>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76231718 | ||||||
| chr15:76231798
|
A | T | 5 | a0001c0001t0006g0278a0001c0001t0006g0279a0001c0001t0006g0280others(2): Show | 5 | HG02055.hp1 HG02559.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.817-400T>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76231798 | ||||||
| chr15:76231943
|
T | G | 1 | a0001c0001t0003g0015 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.817-545A>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76231943 | ||||||
| chr15:76232109
|
C | T | 325 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(322): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.817-711G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76232109 | ||||||
| chr15:76232301
|
G | A | 2 | a0001c0001t0001g0073a0001c0001t0001g0076 | 2 | HG00738.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.817-903C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76232301 | ||||||
| chr15:76232303
|
T | G | 132 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(129): Show | 133 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.817-905A>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76232303 | ||||||
| chr15:76232464
|
C | T | 3 | a0001c0001t0001g0038a0001c0001t0001g0063a0001c0001t0001g0064 | 3 | NA18939.hp1 NA18986.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.817-1066G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76232464 | ||||||
| chr15:76232513
|
T | C | 1 | a0001c0001t0002g0159 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.817-1115A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76232513 | ||||||
| chr15:76232753
|
G | A | 2 | a0001c0001t0001g0074a0001c0001t0001g0077 | 2 | HG00639.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.817-1355C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76232753 | ||||||
| chr15:76232882
|
G | A | 10 | a0001c0001t0003g0324a0001c0001t0003g0325a0001c0001t0003g0326others(7): Show | 10 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.817-1484C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76232882 | ||||||
| chr15:76232917
|
T | C | 7 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(4): Show | 7 | HG00438.hp1 HG00733.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.817-1519A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76232917 | ||||||
| chr15:76232987
|
C | T | 1 | a0001c0001t0011g0330 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.817-1589G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76232987 | ||||||
| chr15:76233033
|
G | C | 1 | a0001c0001t0001g0064 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.817-1635C>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76233033 | ||||||
| chr15:76233085
|
G | A | 131 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(128): Show | 132 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.817-1687C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76233085 | ||||||
| chr15:76233325
|
C | CT | 70 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0040others(67): Show | 70 | HG00438.hp2 HG00735.hp1 HG01081.hp2 others(67): Show |
intron_variant | MODIFIER | c.817-1928dupA | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76233325 | ||||||
| chr15:76233325
|
C | CTT | 114 | a0001c0001t0002g0002a0001c0001t0002g0054a0001c0001t0002g0116others(111): Show | 115 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(112): Show |
intron_variant | MODIFIER | c.817-1929_817-1928d others(4): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76233325 | ||||||
| chr15:76233360
|
C | A | 1 | a0001c0001t0003g0276 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.817-1962G>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76233360 | ||||||
| chr15:76233432
|
C | T | 3 | a0001c0001t0003g0264a0001c0001t0003g0275a0001c0001t0003g0277 | 3 | HG02145.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.817-2034G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76233432 | ||||||
| chr15:76233447
|
G | A | 1 | a0001c0001t0002g0142 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.817-2049C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76233447 | ||||||
| chr15:76233492
|
G | C | 9 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0019others(6): Show | 9 | HG02145.hp2 HG02258.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-2094C>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76233492 | ||||||
| chr15:76233619
|
C | T | 1 | a0001c0001t0013g0301 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.817-2221G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76233619 | ||||||
| chr15:76233949
|
GTAAACA | G | 4 | a0001c0001t0003g0106a0001c0001t0003g0107a0001c0001t0003g0108others(1): Show | 4 | HG02630.hp2 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.817-2557_817-2552d others(8): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76233949 | ||||||
| chr15:76234069
|
C | G | 26 | a0001c0001t0001g0098a0001c0001t0001g0288a0001c0001t0001g0289others(23): Show | 26 | HG00140.hp2 HG00544.hp2 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.817-2671G>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76234069 | ||||||
| chr15:76234566
|
T | C | 325 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(322): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.817-3168A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76234566 | ||||||
| chr15:76234571
|
G | C | 176 | a0001c0001t0002g0002a0001c0001t0002g0054a0001c0001t0002g0116others(173): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.817-3173C>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76234571 | ||||||
| chr15:76234574
|
G | A | 1 | a0002c0002t0001g0252 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.817-3176C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76234574 | ||||||
| chr15:76234744
|
T | C | 10 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0019others(7): Show | 10 | HG02145.hp2 HG02258.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.817-3346A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76234744 | ||||||
| chr15:76234837
|
C | A | 1 | a0001c0001t0003g0005 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.817-3439G>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76234837 | ||||||
| chr15:76234980
|
G | A | 1 | a0001c0001t0010g0004 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.817-3582C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76234980 | ||||||
| chr15:76235145
|
ACTC | A | 3 | a0001c0001t0003g0264a0001c0001t0003g0275a0001c0001t0003g0277 | 3 | HG02145.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.817-3750_817-3748d others(5): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76235145 | ||||||
| chr15:76235289
|
G | A | 131 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(128): Show | 132 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.817-3891C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76235289 | ||||||
| chr15:76235327
|
C | A | 5 | a0001c0001t0002g0175a0001c0001t0002g0184a0001c0001t0002g0185others(2): Show | 5 | NA18939.hp2 NA18960.hp2 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.817-3929G>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76235327 | ||||||
| chr15:76235369
|
A | C | 1 | a0001c0001t0002g0177 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.817-3971T>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76235369 | ||||||
| chr15:76235472
|
T | C | 2 | a0001c0001t0003g0273a0001c0001t0003g0274 | 2 | HG01255.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.817-4074A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76235472 | ||||||
| chr15:76235482
|
G | A | 4 | a0001c0001t0003g0106a0001c0001t0003g0107a0001c0001t0003g0108others(1): Show | 4 | HG02630.hp2 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.817-4084C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76235482 | ||||||
| chr15:76235614
|
G | C | 129 | a0001c0001t0002g0002a0001c0001t0002g0054a0001c0001t0002g0116others(126): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.817-4216C>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76235614 | ||||||
| chr15:76235700
|
A | C | 8 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0195others(5): Show | 8 | HG02080.hp2 HG02083.hp1 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.817-4302T>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76235700 | ||||||
| chr15:76235819
|
A | G | 10 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0019others(7): Show | 10 | HG02145.hp2 HG02258.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.817-4421T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76235819 | ||||||
| chr15:76235894
|
T | C | 1 | a0001c0001t0001g0066 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.817-4496A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76235894 | ||||||
| chr15:76235902
|
A | C | 1 | a0001c0001t0002g0175 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.817-4504T>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76235902 | ||||||
| chr15:76235903
|
C | A | 1 | a0001c0001t0002g0175 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.817-4505G>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76235903 | ||||||
| chr15:76236490
|
C | T | 114 | a0001c0001t0002g0002a0001c0001t0002g0054a0001c0001t0002g0116others(111): Show | 115 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(112): Show |
intron_variant | MODIFIER | c.817-5092G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76236490 | ||||||
| chr15:76236620
|
G | A | 4 | a0001c0001t0003g0106a0001c0001t0003g0107a0001c0001t0003g0108others(1): Show | 4 | HG02630.hp2 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.817-5222C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76236620 | ||||||
| chr15:76236693
|
G | A | 10 | a0001c0001t0003g0324a0001c0001t0003g0325a0001c0001t0003g0326others(7): Show | 10 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.817-5295C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76236693 | ||||||
| chr15:76236707
|
G | C | 5 | a0001c0001t0001g0303a0001c0001t0001g0305a0001c0001t0001g0314others(2): Show | 5 | HG01346.hp2 HG01433.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.817-5309C>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76236707 | ||||||
| chr15:76237126
|
C | T | 1 | a0001c0001t0002g0180 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.817-5728G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76237126 | ||||||
| chr15:76237127
|
G | A | 4 | a0001c0001t0003g0106a0001c0001t0003g0107a0001c0001t0003g0108others(1): Show | 4 | HG02630.hp2 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.817-5729C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76237127 | ||||||
| chr15:76237137
|
CT | C | 5 | a0001c0001t0001g0042a0001c0001t0001g0071a0001c0001t0001g0074others(2): Show | 5 | HG00639.hp1 HG01257.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.817-5740delA | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76237137 | ||||||
| chr15:76237244
|
G | A | 1 | a0001c0001t0002g0140 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.817-5846C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76237244 | ||||||
| chr15:76237382
|
A | G | 325 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(322): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.817-5984T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76237382 | ||||||
| chr15:76237398
|
G | A | 1 | a0001c0001t0002g0166 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.817-6000C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76237398 | ||||||
| chr15:76237480
|
A | G | 3 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287 | 3 | HG02572.hp1 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.817-6082T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76237480 | ||||||
| chr15:76237699
|
A | T | 1 | a0001c0001t0001g0046 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.817-6301T>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76237699 | ||||||
| chr15:76237762
|
G | C | 121 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(118): Show | 122 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.817-6364C>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76237762 | ||||||
| chr15:76237876
|
A | T | 1 | a0001c0001t0003g0103 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.817-6478T>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76237876 | ||||||
| chr15:76237926
|
C | A | 323 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(320): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.817-6528G>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76237926 | ||||||
| chr15:76238027
|
C | T | 1 | a0001c0001t0001g0046 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.817-6629G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76238027 | ||||||
| chr15:76238093
|
A | C | 5 | a0001c0001t0001g0045a0001c0001t0001g0056a0001c0001t0001g0058others(2): Show | 5 | HG01361.hp1 HG01928.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.817-6695T>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76238093 | ||||||
| chr15:76238143
|
G | A | 1 | a0001c0001t0002g0191 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.817-6745C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76238143 | ||||||
| chr15:76238352
|
T | C | 1 | a0001c0001t0001g0045 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.817-6954A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76238352 | ||||||
| chr15:76238390
|
T | C | 1 | a0001c0001t0003g0027 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.817-6992A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76238390 | ||||||
| chr15:76238403
|
A | G | 1 | a0001c0001t0009g0230 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.817-7005T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76238403 | ||||||
| chr15:76238499
|
T | C | 327 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(324): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.817-7101A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76238499 | ||||||
| chr15:76238763
|
A | G | 1 | a0001c0001t0013g0301 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.817-7365T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76238763 | ||||||
| chr15:76239109
|
C | T | 120 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(117): Show | 121 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.817-7711G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76239109 | ||||||
| chr15:76239162
|
T | C | 5 | a0001c0001t0004g0235a0001c0001t0004g0248a0001c0001t0004g0249others(2): Show | 5 | HG02809.hp2 HG02886.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.817-7764A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76239162 | ||||||
| chr15:76239166
|
G | C | 1 | a0001c0001t0003g0276 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.817-7768C>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76239166 | ||||||
| chr15:76239179
|
A | C | 99 | a0001c0001t0002g0002a0001c0001t0002g0054a0001c0001t0002g0116others(96): Show | 100 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.817-7781T>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76239179 | ||||||
| chr15:76239300
|
C | G | 26 | a0001c0001t0001g0098a0001c0001t0001g0288a0001c0001t0001g0289others(23): Show | 26 | HG00140.hp2 HG00544.hp2 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.817-7902G>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76239300 | ||||||
| chr15:76239320
|
G | A | 23 | a0001c0001t0004g0231a0001c0001t0004g0232a0001c0001t0004g0233others(20): Show | 23 | HG01109.hp2 HG01123.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.817-7922C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76239320 | ||||||
| chr15:76239362
|
A | G | 2 | a0001c0001t0003g0328a0001c0001t0003g0329 | 2 | HG02723.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.817-7964T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76239362 | ||||||
| chr15:76239537
|
C | T | 1 | a0001c0001t0002g0172 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.817-8139G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76239537 | ||||||
| chr15:76239755
|
T | C | 1 | a0001c0001t0001g0321 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.817-8357A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76239755 | ||||||
| chr15:76239786
|
TA | T | 19 | a0001c0001t0001g0086a0001c0001t0001g0321a0001c0001t0002g0002others(16): Show | 20 | HG00544.hp1 HG00621.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.817-8389delT | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76239786 | ||||||
| chr15:76239902
|
G | A | 2 | a0001c0001t0003g0005a0001c0001t0003g0006 | 2 | HG01243.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.817-8504C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76239902 | ||||||
| chr15:76240070
|
C | A | 1 | a0001c0001t0001g0105 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.817-8672G>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76240070 | ||||||
| chr15:76240329
|
T | C | 3 | a0001c0001t0002g0147a0001c0001t0002g0148a0001c0001t0002g0220 | 3 | HG01123.hp1 HG01256.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.817-8931A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76240329 | ||||||
| chr15:76240504
|
G | C | 309 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(306): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.817-9106C>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76240504 | ||||||
| chr15:76241324
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.817-9926C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76241324 | ||||||
| chr15:76241576
|
G | A | 115 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(112): Show | 116 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.817-10178C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76241576 | ||||||
| chr15:76241597
|
C | T | 3 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287 | 3 | HG02572.hp1 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.817-10199G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76241597 | ||||||
| chr15:76241607
|
T | C | 3 | a0001c0001t0003g0264a0001c0001t0003g0275a0001c0001t0003g0277 | 3 | HG02145.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.817-10209A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76241607 | ||||||
| chr15:76241645
|
C | CA | 131 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(128): Show | 132 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.817-10248dupT | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76241645 | ||||||
| chr15:76241721
|
G | A | 14 | a0001c0001t0003g0015a0001c0001t0003g0018a0001c0001t0003g0020others(11): Show | 14 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.817-10323C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76241721 | ||||||
| chr15:76241727
|
G | A | 3 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287 | 3 | HG02572.hp1 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.817-10329C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76241727 | ||||||
| chr15:76241774
|
C | T | 2 | a0001c0001t0003g0025a0001c0001t0003g0026 | 2 | HG02886.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.817-10376G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76241774 | ||||||
| chr15:76241780
|
C | T | 1 | a0001c0001t0003g0276 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.817-10382G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76241780 | ||||||
| chr15:76241801
|
C | CA | 42 | a0001c0001t0001g0009a0001c0001t0001g0031a0001c0001t0001g0035others(39): Show | 42 | HG00280.hp1 HG00438.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.817-10404dupT | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76241801 | ||||||
| chr15:76241801
|
C | CAA | 8 | a0001c0001t0003g0016a0001c0001t0003g0024a0001c0001t0003g0025others(5): Show | 8 | HG02055.hp2 HG02145.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.817-10405_817-1040 others(6): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76241801 | ||||||
| chr15:76241801
|
CA | C | 113 | a0001c0001t0001g0010a0001c0001t0001g0082a0001c0001t0002g0002others(110): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.817-10404delT | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76241801 | ||||||
| chr15:76241842
|
A | T | 9 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0019others(6): Show | 9 | HG02145.hp2 HG02258.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-10444T>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76241842 | ||||||
| chr15:76241843
|
A | AT | 142 | a0001c0001t0001g0010a0001c0001t0001g0046a0001c0001t0002g0002others(139): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.817-10446dupA | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76241843 | ||||||
| chr15:76241876
|
C | CA | 9 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0019others(6): Show | 9 | HG02145.hp2 HG02258.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-10479_817-1047 others(5): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76241876 | ||||||
| chr15:76241877
|
G | C | 9 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0019others(6): Show | 9 | HG02145.hp2 HG02258.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-10479C>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76241877 | ||||||
| chr15:76241877
|
G | GC | 323 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(320): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.817-10480dupG | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76241877 | ||||||
| chr15:76241905
|
C | T | 1 | a0001c0001t0011g0330 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.817-10507G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76241905 | ||||||
| chr15:76241985
|
C | T | 1 | a0001c0001t0003g0024 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.817-10587G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76241985 | ||||||
| chr15:76242672
|
A | G | 1 | a0001c0001t0003g0324 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.817-11274T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76242672 | ||||||
| chr15:76242880
|
C | T | 1 | a0001c0001t0002g0128 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.817-11482G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76242880 | ||||||
| chr15:76243073
|
G | A | 2 | a0001c0001t0003g0273a0001c0001t0003g0274 | 2 | HG01255.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.817-11675C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76243073 | ||||||
| chr15:76243112
|
A | G | 3 | a0001c0001t0003g0264a0001c0001t0003g0275a0001c0001t0003g0277 | 3 | HG02145.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.817-11714T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76243112 | ||||||
| chr15:76243270
|
C | CA | 121 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(118): Show | 122 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.817-11873dupT | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76243270 | ||||||
| chr15:76243342
|
A | G | 1 | a0001c0001t0004g0102 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.817-11944T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76243342 | ||||||
| chr15:76243355
|
C | T | 131 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(128): Show | 132 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.817-11957G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76243355 | ||||||
| chr15:76243402
|
C | T | 38 | a0001c0001t0004g0102a0001c0001t0004g0231a0001c0001t0004g0232others(35): Show | 38 | HG00438.hp2 HG00621.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.817-12004G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76243402 | ||||||
| chr15:76243442
|
A | AAAT | 131 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(128): Show | 132 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.817-12047_817-1204 others(7): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76243442 | ||||||
| chr15:76243561
|
GC | G | 115 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(112): Show | 116 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.817-12164delG | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76243561 | ||||||
| chr15:76243582
|
C | T | 7 | a0001c0001t0003g0324a0001c0001t0003g0325a0001c0001t0003g0326others(4): Show | 7 | HG02109.hp2 HG02451.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.817-12184G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76243582 | ||||||
| chr15:76243633
|
T | C | 121 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(118): Show | 122 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.817-12235A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76243633 | ||||||
| chr15:76243816
|
C | CA | 5 | a0001c0001t0001g0049a0001c0001t0001g0065a0001c0001t0001g0289others(2): Show | 5 | HG01884.hp1 HG02027.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.817-12419dupT | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76243816 | ||||||
| chr15:76243820
|
C | A | 109 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(106): Show | 110 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.817-12422G>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76243820 | ||||||
| chr15:76243820
|
C | CA | 15 | a0001c0001t0003g0015a0001c0001t0003g0018a0001c0001t0003g0020others(12): Show | 15 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.817-12423dupT | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76243820 | ||||||
| chr15:76243823
|
A | AC | 116 | a0001c0001t0001g0010a0001c0001t0002g0002a0001c0001t0002g0054others(113): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.817-12426_817-1242 others(5): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76243823 | ||||||
| chr15:76243949
|
C | T | 3 | a0001c0001t0003g0264a0001c0001t0003g0275a0001c0001t0003g0277 | 3 | HG02145.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.817-12551G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76243949 | ||||||
| chr15:76243973
|
G | T | 2 | a0001c0001t0003g0273a0001c0001t0003g0274 | 2 | HG01255.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.817-12575C>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76243973 | ||||||
| chr15:76243996
|
C | T | 187 | a0001c0001t0001g0010a0001c0001t0002g0002a0001c0001t0002g0054others(184): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.817-12598G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76243996 | ||||||
| chr15:76244036
|
C | A | 1 | a0001c0001t0001g0093 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.817-12638G>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76244036 | ||||||
| chr15:76244165
|
G | A | 131 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(128): Show | 132 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.817-12767C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76244165 | ||||||
| chr15:76244310
|
A | T | 14 | a0001c0001t0003g0015a0001c0001t0003g0018a0001c0001t0003g0020others(11): Show | 14 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.817-12912T>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76244310 | ||||||
| chr15:76244335
|
A | G | 1 | a0001c0001t0012g0268 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.817-12937T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76244335 | ||||||
| chr15:76244664
|
GA | G | 133 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(130): Show | 134 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.817-13267delT | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76244664 | ||||||
| chr15:76244666
|
A | G | 3 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287 | 3 | HG02572.hp1 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.817-13268T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76244666 | ||||||
| chr15:76244668
|
A | G | 1 | a0001c0001t0001g0063 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.817-13270T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76244668 | ||||||
| chr15:76244991
|
G | A | 1 | a0001c0001t0001g0307 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.817-13593C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76244991 | ||||||
| chr15:76245104
|
C | T | 1 | a0001c0001t0003g0276 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.817-13706G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76245104 | ||||||
| chr15:76245135
|
C | T | 16 | a0001c0001t0004g0102a0002c0002t0004g0228a0002c0002t0004g0229others(13): Show | 16 | HG00438.hp2 HG00621.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.817-13737G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76245135 | ||||||
| chr15:76245169
|
C | T | 1 | a0001c0001t0002g0210 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.817-13771G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76245169 | ||||||
| chr15:76245308
|
A | T | 1 | a0001c0001t0002g0129 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.817-13910T>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76245308 | ||||||
| chr15:76245874
|
C | T | 5 | a0001c0001t0001g0044a0001c0001t0001g0047a0001c0001t0001g0048others(2): Show | 5 | NA18945.hp1 NA18972.hp1 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.817-14476G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76245874 | ||||||
| chr15:76246015
|
C | T | 2 | a0001c0001t0002g0222a0001c0001t0002g0227 | 2 | HG01081.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.817-14617G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76246015 | ||||||
| chr15:76246060
|
C | T | 9 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0019others(6): Show | 9 | HG02145.hp2 HG02258.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-14662G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76246060 | ||||||
| chr15:76246118
|
G | C | 15 | a0002c0002t0004g0228a0002c0002t0004g0229a0002c0002t0004g0247others(12): Show | 15 | HG00438.hp2 HG00621.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.817-14720C>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76246118 | ||||||
| chr15:76246214
|
G | C | 3 | a0001c0001t0001g0321a0001c0001t0001g0322a0001c0001t0001g0323 | 3 | HG01243.hp2 HG01496.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.817-14816C>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76246214 | ||||||
| chr15:76246251
|
A | T | 3 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287 | 3 | HG02572.hp1 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.817-14853T>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76246251 | ||||||
| chr15:76246649
|
G | C | 16 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0015others(13): Show | 16 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.817-15251C>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76246649 | ||||||
| chr15:76246690
|
G | A | 2 | a0001c0001t0001g0080a0001c0001t0001g0322 | 2 | HG01243.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.817-15292C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76246690 | ||||||
| chr15:76246908
|
G | A | 2 | a0001c0001t0004g0241a0001c0001t0004g0244 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.817-15510C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76246908 | ||||||
| chr15:76246917
|
T | G | 1 | a0001c0001t0003g0108 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.817-15519A>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76246917 | ||||||
| chr15:76247062
|
G | A | 1 | a0001c0001t0003g0332 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.817-15664C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76247062 | ||||||
| chr15:76247112
|
T | G | 1 | a0001c0001t0001g0085 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.817-15714A>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76247112 | ||||||
| chr15:76247149
|
G | A | 325 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(322): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.817-15751C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76247149 | ||||||
| chr15:76247199
|
T | A | 1 | a0001c0001t0001g0310 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.817-15801A>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76247199 | ||||||
| chr15:76247199
|
T | TA | 129 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(126): Show | 130 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.817-15802dupT | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76247199 | ||||||
| chr15:76247221
|
T | G | 1 | a0001c0001t0003g0276 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.817-15823A>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76247221 | ||||||
| chr15:76247319
|
T | C | 1 | a0001c0001t0002g0166 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.817-15921A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76247319 | ||||||
| chr15:76247497
|
C | G | 120 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(117): Show | 121 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.817-16099G>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76247497 | ||||||
| chr15:76247612
|
G | A | 1 | a0001c0001t0003g0112 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.817-16214C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76247612 | ||||||
| chr15:76247797
|
C | T | 1 | a0001c0001t0002g0166 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.817-16399G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76247797 | ||||||
| chr15:76247890
|
G | A | 128 | a0001c0001t0002g0002a0001c0001t0002g0116a0001c0001t0002g0117others(125): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.817-16492C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76247890 | ||||||
| chr15:76247974
|
T | A | 1 | a0001c0001t0002g0127 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.817-16576A>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76247974 | ||||||
| chr15:76248019
|
C | A | 3 | a0001c0001t0003g0264a0001c0001t0003g0275a0001c0001t0003g0277 | 3 | HG02145.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.817-16621G>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76248019 | ||||||
| chr15:76248085
|
G | A | 1 | a0002c0002t0004g0259 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.817-16687C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76248085 | ||||||
| chr15:76248257
|
T | C | 9 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0019others(6): Show | 9 | HG02145.hp2 HG02258.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-16859A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76248257 | ||||||
| chr15:76248500
|
C | A | 1 | a0001c0001t0003g0326 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.817-17102G>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76248500 | ||||||
| chr15:76248581
|
A | T | 1 | a0002c0002t0004g0229 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.817-17183T>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76248581 | ||||||
| chr15:76248760
|
C | T | 132 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(129): Show | 133 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.817-17362G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76248760 | ||||||
| chr15:76248883
|
T | TA | 56 | a0001c0001t0001g0292a0001c0001t0002g0192a0001c0001t0003g0015others(53): Show | 56 | HG00438.hp2 HG00621.hp2 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.817-17486dupT | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76248883 | ||||||
| chr15:76248970
|
G | GA | 4 | a0001c0001t0003g0106a0001c0001t0003g0107a0001c0001t0003g0108others(1): Show | 4 | HG02630.hp2 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.817-17573dupT | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76248970 | ||||||
| chr15:76249129
|
A | AT | 176 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0083others(173): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.817-17732dupA | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76249129 | ||||||
| chr15:76249129
|
A | ATT | 25 | a0001c0001t0002g0126a0001c0001t0002g0134a0001c0001t0002g0135others(22): Show | 25 | HG00438.hp2 HG00621.hp2 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.817-17733_817-1773 others(6): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76249129 | ||||||
| chr15:76249285
|
C | A | 9 | a0001c0001t0003g0324a0001c0001t0003g0325a0001c0001t0003g0326others(6): Show | 9 | HG02109.hp2 HG02451.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-17887G>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76249285 | ||||||
| chr15:76249435
|
A | ATC | 149 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(146): Show | 150 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.817-18038_817-1803 others(6): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76249435 | ||||||
| chr15:76249435
|
A | ATCT | 26 | a0001c0001t0001g0007a0001c0001t0001g0042a0001c0001t0001g0043others(23): Show | 26 | HG00438.hp1 HG00597.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.817-18038_817-1803 others(7): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76249435 | ||||||
| chr15:76249435
|
ATTTTTTT others(7): Show |
A | 1 | a0001c0001t0003g0114 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.817-18051_817-1803 others(18): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76249435 | ||||||
| chr15:76249436
|
T | TC | 52 | a0001c0001t0001g0013a0001c0001t0002g0134a0001c0001t0002g0145others(49): Show | 52 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(49): Show |
intron_variant | MODIFIER | c.817-18039_817-1803 others(5): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76249436 | ||||||
| chr15:76249437
|
T | C | 90 | a0001c0001t0002g0002a0001c0001t0002g0116a0001c0001t0002g0117others(87): Show | 91 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.817-18039A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76249437 | ||||||
| chr15:76249438
|
T | C | 1 | a0001c0001t0002g0141 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.817-18040A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76249438 | ||||||
| chr15:76249451
|
T | C | 1 | a0001c0001t0003g0114 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.817-18053A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76249451 | ||||||
| chr15:76249527
|
C | T | 3 | a0001c0001t0003g0264a0001c0001t0003g0275a0001c0001t0003g0277 | 3 | HG02145.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.817-18129G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76249527 | ||||||
| chr15:76249534
|
C | T | 2 | a0001c0001t0001g0030a0001c0001t0001g0031 | 2 | HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.817-18136G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76249534 | ||||||
| chr15:76249542
|
T | A | 2 | a0001c0001t0003g0273a0001c0001t0003g0274 | 2 | HG01255.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.817-18144A>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76249542 | ||||||
| chr15:76249639
|
C | T | 1 | a0001c0001t0003g0087 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.817-18241G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76249639 | ||||||
| chr15:76249773
|
C | A | 115 | a0001c0001t0002g0002a0001c0001t0002g0116a0001c0001t0002g0117others(112): Show | 116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.817-18375G>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76249773 | ||||||
| chr15:76250001
|
T | C | 1 | a0001c0001t0003g0115 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.817-18603A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76250001 | ||||||
| chr15:76250062
|
T | C | 1 | a0001c0001t0001g0296 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.817-18664A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76250062 | ||||||
| chr15:76250133
|
A | G | 2 | a0001c0001t0001g0035a0001c0001t0001g0065 | 2 | HG02027.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.817-18735T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76250133 | ||||||
| chr15:76250222
|
G | GA | 187 | a0001c0001t0002g0002a0001c0001t0002g0054a0001c0001t0002g0116others(184): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.817-18825dupT | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76250222 | ||||||
| chr15:76250278
|
C | T | 4 | a0001c0001t0002g0163a0001c0001t0002g0164a0001c0001t0002g0174others(1): Show | 4 | HG00738.hp1 HG01884.hp2 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.817-18880G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76250278 | ||||||
| chr15:76250335
|
A | T | 3 | a0002c0002t0004g0228a0002c0002t0004g0257a0002c0002t0004g0260 | 3 | HG00621.hp2 NA18946.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.817-18937T>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76250335 | ||||||
| chr15:76250355
|
G | A | 1 | a0002c0002t0004g0256 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.817-18957C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76250355 | ||||||
| chr15:76250539
|
G | A | 9 | a0001c0001t0002g0198a0001c0001t0002g0199a0001c0001t0002g0201others(6): Show | 9 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(6): Show |
intron_variant | MODIFIER | c.817-19141C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76250539 | ||||||
| chr15:76250733
|
C | T | 1 | a0001c0001t0002g0210 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.817-19335G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76250733 | ||||||
| chr15:76251184
|
G | T | 1 | a0001c0001t0001g0043 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.817-19786C>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76251184 | ||||||
| chr15:76251433
|
A | C | 3 | a0001c0001t0003g0264a0001c0001t0003g0275a0001c0001t0003g0277 | 3 | HG02145.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.817-20035T>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76251433 | ||||||
| chr15:76251487
|
C | T | 1 | a0001c0001t0012g0268 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.817-20089G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76251487 | ||||||
| chr15:76251534
|
G | T | 1 | a0001c0001t0002g0130 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.817-20136C>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76251534 | ||||||
| chr15:76251569
|
A | C | 187 | a0001c0001t0002g0002a0001c0001t0002g0054a0001c0001t0002g0116others(184): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.817-20171T>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76251569 | ||||||
| chr15:76251603
|
C | T | 131 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(128): Show | 132 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.817-20205G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76251603 | ||||||
| chr15:76251783
|
A | G | 9 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0092others(6): Show | 9 | HG00597.hp1 HG03490.hp2 NA18944.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-20385T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76251783 | ||||||
| chr15:76251987
|
C | G | 1 | a0001c0001t0002g0140 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.817-20589G>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76251987 | ||||||
| chr15:76252231
|
C | A | 1 | a0001c0001t0001g0057 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.817-20833G>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76252231 | ||||||
| chr15:76252320
|
G | T | 3 | a0001c0001t0003g0264a0001c0001t0003g0275a0001c0001t0003g0277 | 3 | HG02145.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.817-20922C>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76252320 | ||||||
| chr15:76252523
|
G | A | 2 | a0001c0001t0003g0005a0001c0001t0003g0006 | 2 | HG01243.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.817-21125C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76252523 | ||||||
| chr15:76252659
|
G | A | 9 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0019others(6): Show | 9 | HG02145.hp2 HG02258.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.817-21261C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76252659 | ||||||
| chr15:76252809
|
C | T | 2 | a0002c0002t0004g0261a0002c0002t0004g0262 | 2 | HG00438.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.817-21411G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76252809 | ||||||
| chr15:76252829
|
G | T | 3 | a0001c0001t0003g0264a0001c0001t0003g0275a0001c0001t0003g0277 | 3 | HG02145.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.817-21431C>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76252829 | ||||||
| chr15:76252876
|
T | TACACACA others(1): Show |
68 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(65): Show | 69 | HG00280.hp1 HG00597.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.817-21486_817-2147 others(12): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76252876 | ||||||
| chr15:76252876
|
T | TACACACA others(3): Show |
3 | a0001c0001t0001g0036a0001c0001t0001g0088a0001c0001t0001g0091 | 3 | HG01433.hp2 HG04115.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.817-21488_817-2147 others(14): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76252876 | ||||||
| chr15:76252876
|
T | TACACACA others(5): Show |
6 | a0001c0001t0001g0033a0001c0001t0001g0285a0001c0001t0001g0286others(3): Show | 6 | HG01243.hp2 HG02257.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.817-21490_817-2147 others(16): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76252876 | ||||||
| chr15:76252876
|
T | TACACACA others(7): Show |
44 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(41): Show | 44 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.817-21492_817-2147 others(18): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76252876 | ||||||
| chr15:76252876
|
T | TACACACA others(9): Show |
4 | a0001c0001t0001g0317a0001c0001t0003g0332a0001c0001t0003g0333others(1): Show | 4 | HG02922.hp2 HG03041.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.817-21479_817-2147 others(20): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76252876 | ||||||
| chr15:76252876
|
T | TACACACA others(11): Show |
7 | a0001c0001t0003g0324a0001c0001t0003g0325a0001c0001t0003g0326others(4): Show | 7 | HG02109.hp2 HG02451.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.817-21479_817-2147 others(22): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76252876 | ||||||
| chr15:76252897
|
C | CT | 17 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(14): Show | 17 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.817-21500dupA | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76252897 | ||||||
| chr15:76252897
|
CT | C | 241 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(238): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.817-21500delA | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76252897 | ||||||
| chr15:76252897
|
CTT | C | 19 | a0001c0001t0001g0066a0001c0001t0001g0071a0001c0001t0001g0096others(16): Show | 19 | HG01074.hp2 HG01167.hp2 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.817-21501_817-2150 others(6): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76252897 | ||||||
| chr15:76252915
|
T | C | 1 | a0001c0001t0005g0271 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.816+21497A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76252915 | ||||||
| chr15:76253434
|
T | C | 1 | a0001c0001t0001g0294 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.816+20978A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76253434 | ||||||
| chr15:76253503
|
A | G | 53 | a0001c0001t0003g0015a0001c0001t0003g0018a0001c0001t0003g0020others(50): Show | 53 | HG00438.hp2 HG00621.hp2 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.816+20909T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76253503 | ||||||
| chr15:76253680
|
C | T | 325 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(322): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.816+20732G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76253680 | ||||||
| chr15:76254058
|
T | C | 1 | a0001c0001t0012g0268 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.816+20354A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76254058 | ||||||
| chr15:76254071
|
A | G | 1 | a0001c0001t0011g0330 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.816+20341T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76254071 | ||||||
| chr15:76254076
|
A | G | 1 | a0001c0001t0006g0280 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.816+20336T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76254076 | ||||||
| chr15:76254198
|
G | C | 3 | a0001c0001t0003g0264a0001c0001t0003g0275a0001c0001t0003g0277 | 3 | HG02145.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.816+20214C>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76254198 | ||||||
| chr15:76254374
|
C | T | 5 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0094others(2): Show | 5 | HG03490.hp2 NA18945.hp2 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.816+20038G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76254374 | ||||||
| chr15:76254390
|
C | G | 5 | a0001c0001t0006g0278a0001c0001t0006g0279a0001c0001t0006g0280others(2): Show | 5 | HG02055.hp1 HG02559.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.816+20022G>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76254390 | ||||||
| chr15:76254482
|
G | A | 1 | a0001c0001t0003g0332 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.816+19930C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76254482 | ||||||
| chr15:76254592
|
G | A | 59 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0015others(56): Show | 59 | HG00438.hp2 HG00621.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.816+19820C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76254592 | ||||||
| chr15:76254598
|
C | T | 1 | a0001c0001t0002g0172 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.816+19814G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76254598 | ||||||
| chr15:76254680
|
G | A | 1 | a0001c0001t0012g0268 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.816+19732C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76254680 | ||||||
| chr15:76254720
|
T | C | 1 | a0001c0001t0001g0290 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.816+19692A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76254720 | ||||||
| chr15:76254932
|
G | C | 5 | a0001c0001t0006g0278a0001c0001t0006g0279a0001c0001t0006g0280others(2): Show | 5 | HG02055.hp1 HG02559.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.816+19480C>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76254932 | ||||||
| chr15:76255006
|
T | A | 1 | a0001c0001t0003g0108 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.816+19406A>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76255006 | ||||||
| chr15:76255077
|
C | G | 19 | a0001c0001t0002g0120a0001c0001t0002g0136a0001c0001t0002g0137others(16): Show | 19 | HG00673.hp2 HG00733.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.816+19335G>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76255077 | ||||||
| chr15:76255434
|
A | T | 1 | a0001c0001t0002g0145 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.816+18978T>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76255434 | ||||||
| chr15:76255606
|
T | C | 17 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(14): Show | 17 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.816+18806A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76255606 | ||||||
| chr15:76255675
|
G | T | 1 | a0001c0001t0001g0083 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.816+18737C>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76255675 | ||||||
| chr15:76255796
|
A | G | 1 | a0001c0001t0003g0103 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.816+18616T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76255796 | ||||||
| chr15:76255908
|
G | T | 2 | a0001c0001t0005g0270a0001c0001t0005g0271 | 2 | HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.816+18504C>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76255908 | ||||||
| chr15:76255911
|
G | T | 5 | a0001c0001t0003g0018a0001c0001t0003g0020a0001c0001t0003g0021others(2): Show | 5 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.816+18501C>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76255911 | ||||||
| chr15:76255986
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.816+18426C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76255986 | ||||||
| chr15:76256238
|
A | G | 10 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0019others(7): Show | 10 | HG02145.hp2 HG02258.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.816+18174T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76256238 | ||||||
| chr15:76256254
|
G | A | 1 | a0001c0001t0011g0330 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.816+18158C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76256254 | ||||||
| chr15:76256262
|
G | GA | 29 | a0001c0001t0001g0049a0001c0001t0001g0061a0001c0001t0001g0068others(26): Show | 29 | HG00673.hp1 HG01081.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.816+18149dupT | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76256262 | ||||||
| chr15:76256262
|
G | GAA | 33 | a0001c0001t0003g0023a0001c0001t0004g0102a0001c0001t0004g0231others(30): Show | 33 | HG00438.hp2 HG00621.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.816+18148_816+1814 others(6): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76256262 | ||||||
| chr15:76256262
|
GA | G | 15 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(12): Show | 15 | HG00438.hp1 HG00733.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.816+18149delT | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76256262 | ||||||
| chr15:76256282
|
A | T | 1 | a0001c0001t0012g0268 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.816+18130T>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76256282 | ||||||
| chr15:76256284
|
T | G | 324 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(321): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.816+18128A>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76256284 | ||||||
| chr15:76256630
|
C | T | 3 | a0001c0001t0001g0038a0001c0001t0001g0063a0001c0001t0001g0064 | 3 | NA18939.hp1 NA18986.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.816+17782G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76256630 | ||||||
| chr15:76256774
|
C | T | 1 | a0001c0001t0001g0053 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.816+17638G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76256774 | ||||||
| chr15:76257040
|
T | C | 1 | a0001c0001t0001g0082 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.816+17372A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76257040 | ||||||
| chr15:76257077
|
CTTT | C | 63 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0015others(60): Show | 63 | HG00438.hp2 HG00621.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.816+17332_816+1733 others(7): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76257077 | ||||||
| chr15:76257155
|
C | A | 1 | a0001c0001t0002g0226 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.816+17257G>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76257155 | ||||||
| chr15:76257191
|
C | T | 325 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(322): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.816+17221G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76257191 | ||||||
| chr15:76257194
|
A | G | 2 | a0001c0001t0003g0015a0001c0001t0003g0028 | 2 | HG02602.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.816+17218T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76257194 | ||||||
| chr15:76257208
|
C | A | 1 | a0001c0001t0012g0268 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.816+17204G>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76257208 | ||||||
| chr15:76257460
|
A | G | 13 | a0001c0001t0003g0015a0001c0001t0003g0018a0001c0001t0003g0020others(10): Show | 13 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.816+16952T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76257460 | ||||||
| chr15:76257481
|
C | T | 2 | a0001c0001t0003g0005a0001c0001t0003g0006 | 2 | HG01243.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.816+16931G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76257481 | ||||||
| chr15:76257545
|
G | T | 1 | a0001c0001t0003g0276 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.816+16867C>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76257545 | ||||||
| chr15:76257723
|
G | A | 122 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(119): Show | 123 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.816+16689C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76257723 | ||||||
| chr15:76257749
|
A | C | 1 | a0001c0001t0001g0291 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.816+16663T>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76257749 | ||||||
| chr15:76257837
|
C | T | 1 | a0001c0001t0002g0224 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.816+16575G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76257837 | ||||||
| chr15:76257912
|
G | T | 3 | a0001c0001t0003g0264a0001c0001t0003g0275a0001c0001t0003g0277 | 3 | HG02145.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.816+16500C>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76257912 | ||||||
| chr15:76257934
|
A | C | 101 | a0001c0001t0002g0002a0001c0001t0002g0116a0001c0001t0002g0117others(98): Show | 102 | HG00099.hp1 HG00544.hp1 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.816+16478T>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76257934 | ||||||
| chr15:76258031
|
A | AG | 29 | a0001c0001t0001g0029a0001c0001t0001g0034a0001c0001t0001g0035others(26): Show | 29 | HG00544.hp1 HG00738.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.816+16380dupC | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76258031 | ||||||
| chr15:76258170
|
T | TAATA | 62 | a0001c0001t0002g0196a0001c0001t0003g0005a0001c0001t0003g0006others(59): Show | 62 | HG00438.hp2 HG00621.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.816+16238_816+1624 others(8): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76258170 | ||||||
| chr15:76258170
|
T | TAATAAAT others(1): Show |
12 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0019others(9): Show | 12 | HG02145.hp1 HG02145.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.816+16234_816+1624 others(12): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76258170 | ||||||
| chr15:76258170
|
TAATA | T | 38 | a0001c0001t0002g0002a0001c0001t0002g0116a0001c0001t0002g0117others(35): Show | 39 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.816+16238_816+1624 others(8): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76258170 | ||||||
| chr15:76258189
|
T | G | 1 | a0001c0001t0005g0271 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.816+16223A>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76258189 | ||||||
| chr15:76258432
|
C | T | 3 | a0001c0001t0003g0264a0001c0001t0003g0275a0001c0001t0003g0277 | 3 | HG02145.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.816+15980G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76258432 | ||||||
| chr15:76258592
|
G | A | 13 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0071others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.816+15820C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76258592 | ||||||
| chr15:76258597
|
C | T | 325 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(322): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.816+15815G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76258597 | ||||||
| chr15:76258632
|
C | T | 121 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(118): Show | 122 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.816+15780G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76258632 | ||||||
| chr15:76259133
|
G | A | 1 | a0001c0001t0003g0276 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.816+15279C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76259133 | ||||||
| chr15:76259354
|
A | G | 10 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0019others(7): Show | 10 | HG02145.hp2 HG02258.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.816+15058T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76259354 | ||||||
| chr15:76259436
|
G | A | 3 | a0001c0001t0003g0324a0001c0001t0003g0326a0001c0001t0003g0327 | 3 | HG02109.hp2 HG02451.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.816+14976C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76259436 | ||||||
| chr15:76259507
|
C | T | 2 | a0001c0001t0001g0060a0001c0001t0001g0078 | 2 | HG00280.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.816+14905G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76259507 | ||||||
| chr15:76259511
|
G | A | 113 | a0001c0001t0002g0002a0001c0001t0002g0116a0001c0001t0002g0117others(110): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.816+14901C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76259511 | ||||||
| chr15:76259669
|
G | T | 2 | a0001c0001t0003g0273a0001c0001t0003g0274 | 2 | HG01255.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.816+14743C>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76259669 | ||||||
| chr15:76259788
|
T | C | 1 | a0001c0001t0003g0027 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.816+14624A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76259788 | ||||||
| chr15:76259814
|
C | T | 1 | a0001c0001t0003g0006 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.816+14598G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76259814 | ||||||
| chr15:76259850
|
G | A | 1 | a0001c0001t0001g0291 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.816+14562C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76259850 | ||||||
| chr15:76259938
|
G | C | 1 | a0001c0001t0004g0102 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.816+14474C>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76259938 | ||||||
| chr15:76260111
|
G | T | 1 | a0002c0002t0004g0261 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.816+14301C>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76260111 | ||||||
| chr15:76260200
|
C | T | 1 | a0001c0001t0002g0188 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.816+14212G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76260200 | ||||||
| chr15:76260320
|
C | T | 1 | a0001c0001t0001g0053 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.816+14092G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76260320 | ||||||
| chr15:76260646
|
G | A | 1 | a0001c0001t0002g0146 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.816+13766C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76260646 | ||||||
| chr15:76260734
|
C | T | 1 | a0001c0001t0001g0099 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.816+13678G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76260734 | ||||||
| chr15:76260851
|
G | A | 1 | a0002c0002t0004g0284 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.816+13561C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76260851 | ||||||
| chr15:76260992
|
C | T | 6 | a0001c0001t0001g0321a0001c0001t0003g0018a0001c0001t0003g0020others(3): Show | 6 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.816+13420G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76260992 | ||||||
| chr15:76261158
|
C | G | 122 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(119): Show | 123 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.816+13254G>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76261158 | ||||||
| chr15:76261168
|
G | A | 3 | a0001c0001t0003g0264a0001c0001t0003g0275a0001c0001t0003g0277 | 3 | HG02145.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.816+13244C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76261168 | ||||||
| chr15:76261247
|
G | A | 116 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(113): Show | 117 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.816+13165C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76261247 | ||||||
| chr15:76261338
|
C | T | 1 | a0002c0002t0004g0228 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.816+13074G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76261338 | ||||||
| chr15:76261449
|
C | T | 115 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(112): Show | 116 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.816+12963G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76261449 | ||||||
| chr15:76261493
|
C | T | 1 | a0001c0001t0003g0276 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.816+12919G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76261493 | ||||||
| chr15:76261549
|
C | T | 7 | a0001c0001t0003g0015a0001c0001t0003g0018a0001c0001t0003g0020others(4): Show | 7 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.816+12863G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76261549 | ||||||
| chr15:76261616
|
C | T | 2 | a0002c0002t0004g0247a0002c0002t0004g0258 | 2 | NA18972.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.816+12796G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76261616 | ||||||
| chr15:76261618
|
CCAGCAGC others(20): Show |
C | 3 | a0001c0001t0003g0264a0001c0001t0003g0275a0001c0001t0003g0277 | 3 | HG02145.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.816+12767_816+1279 others(31): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76261618 | ||||||
| chr15:76261652
|
C | G | 1 | a0001c0001t0006g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.816+12760G>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76261652 | ||||||
| chr15:76261766
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.816+12646G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76261766 | ||||||
| chr15:76261873
|
G | A | 9 | a0001c0001t0001g0291a0001c0001t0001g0292a0001c0001t0001g0293others(6): Show | 9 | NA18941.hp2 NA18967.hp2 NA18971.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+12539C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76261873 | ||||||
| chr15:76261948
|
G | A | 1 | a0001c0001t0003g0114 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.816+12464C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76261948 | ||||||
| chr15:76262221
|
G | A | 3 | a0001c0001t0003g0264a0001c0001t0003g0275a0001c0001t0003g0277 | 3 | HG02145.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.816+12191C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76262221 | ||||||
| chr15:76262329
|
G | GA | 10 | a0001c0001t0001g0096a0001c0001t0003g0016a0001c0001t0003g0017others(7): Show | 10 | HG02145.hp2 HG02258.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.816+12082dupT | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76262329 | ||||||
| chr15:76262414
|
C | T | 53 | a0001c0001t0003g0015a0001c0001t0003g0018a0001c0001t0003g0020others(50): Show | 53 | HG00438.hp2 HG00621.hp2 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.816+11998G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76262414 | ||||||
| chr15:76262449
|
C | A | 116 | a0001c0001t0002g0002a0001c0001t0002g0054a0001c0001t0002g0116others(113): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.816+11963G>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76262449 | ||||||
| chr15:76262474
|
C | CT | 21 | a0001c0001t0002g0130a0001c0001t0002g0144a0001c0001t0002g0154others(18): Show | 21 | HG00099.hp1 HG00735.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.816+11937dupA | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76262474 | ||||||
| chr15:76262474
|
C | CTT | 94 | a0001c0001t0002g0002a0001c0001t0002g0116a0001c0001t0002g0117others(91): Show | 95 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.816+11936_816+1193 others(6): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76262474 | ||||||
| chr15:76262474
|
C | CTTT | 17 | a0001c0001t0002g0054a0001c0001t0002g0122a0001c0001t0002g0126others(14): Show | 17 | HG00735.hp2 HG01081.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.816+11935_816+1193 others(7): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76262474 | ||||||
| chr15:76262474
|
CT | C | 12 | a0001c0001t0003g0025a0001c0001t0003g0026a0001c0001t0003g0324others(9): Show | 12 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.816+11937delA | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76262474 | ||||||
| chr15:76262474
|
CTT | C | 17 | a0001c0001t0001g0036a0001c0001t0001g0041a0001c0001t0001g0052others(14): Show | 17 | HG00280.hp1 HG01346.hp2 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.816+11936_816+1193 others(6): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76262474 | ||||||
| chr15:76262474
|
CTTT | C | 100 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(97): Show | 101 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.816+11935_816+1193 others(7): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76262474 | ||||||
| chr15:76262476
|
T | C | 4 | a0001c0001t0003g0324a0001c0001t0003g0325a0001c0001t0003g0326others(1): Show | 4 | HG02109.hp2 HG02451.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.816+11936A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76262476 | ||||||
| chr15:76262588
|
T | G | 3 | a0001c0001t0004g0245a0001c0001t0004g0246a0001c0001t0004g0249 | 3 | HG02896.hp1 HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.816+11824A>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76262588 | ||||||
| chr15:76262650
|
T | C | 174 | a0001c0001t0002g0002a0001c0001t0002g0054a0001c0001t0002g0116others(171): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.816+11762A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76262650 | ||||||
| chr15:76262672
|
C | T | 1 | a0001c0001t0001g0317 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.816+11740G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76262672 | ||||||
| chr15:76262673
|
G | A | 9 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0019others(6): Show | 9 | HG02145.hp2 HG02258.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+11739C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76262673 | ||||||
| chr15:76262687
|
T | G | 1 | a0001c0001t0005g0270 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.816+11725A>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76262687 | ||||||
| chr15:76262688
|
A | T | 324 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(321): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.816+11724T>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76262688 | ||||||
| chr15:76262935
|
T | G | 1 | a0001c0001t0003g0276 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.816+11477A>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76262935 | ||||||
| chr15:76263006
|
CAT | C | 3 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287 | 3 | HG02572.hp1 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.816+11404_816+1140 others(6): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76263006 | ||||||
| chr15:76263080
|
C | A | 27 | a0001c0001t0001g0098a0001c0001t0001g0288a0001c0001t0001g0289others(24): Show | 27 | HG00140.hp2 HG00544.hp2 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.816+11332G>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76263080 | ||||||
| chr15:76263198
|
G | C | 116 | a0001c0001t0002g0002a0001c0001t0002g0054a0001c0001t0002g0116others(113): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.816+11214C>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76263198 | ||||||
| chr15:76263258
|
T | C | 39 | a0001c0001t0004g0102a0001c0001t0004g0231a0001c0001t0004g0232others(36): Show | 39 | HG00438.hp2 HG00621.hp2 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.816+11154A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76263258 | ||||||
| chr15:76263274
|
G | A | 1 | a0001c0001t0004g0237 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.816+11138C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76263274 | ||||||
| chr15:76263347
|
G | A | 14 | a0001c0001t0002g0139a0001c0001t0002g0155a0001c0001t0002g0161others(11): Show | 14 | HG02071.hp2 HG03831.hp2 HG03927.hp1 others(11): Show |
intron_variant | MODIFIER | c.816+11065C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76263347 | ||||||
| chr15:76263369
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.816+11043G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76263369 | ||||||
| chr15:76263370
|
G | A | 1 | a0001c0001t0002g0141 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.816+11042C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76263370 | ||||||
| chr15:76263379
|
T | C | 132 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(129): Show | 133 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.816+11033A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76263379 | ||||||
| chr15:76263400
|
G | A | 6 | a0001c0001t0002g0162a0001c0001t0002g0175a0001c0001t0002g0184others(3): Show | 6 | HG02071.hp2 NA18939.hp2 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.816+11012C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76263400 | ||||||
| chr15:76263574
|
T | C | 4 | a0001c0001t0003g0106a0001c0001t0003g0107a0001c0001t0003g0108others(1): Show | 4 | HG02630.hp2 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+10838A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76263574 | ||||||
| chr15:76263645
|
C | T | 52 | a0001c0001t0003g0015a0001c0001t0003g0018a0001c0001t0003g0020others(49): Show | 52 | HG00438.hp2 HG00621.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.816+10767G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76263645 | ||||||
| chr15:76263789
|
T | C | 13 | a0001c0001t0003g0015a0001c0001t0003g0018a0001c0001t0003g0020others(10): Show | 13 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.816+10623A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76263789 | ||||||
| chr15:76263830
|
C | T | 1 | a0001c0001t0001g0321 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.816+10582G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76263830 | ||||||
| chr15:76263895
|
C | A | 1 | a0001c0001t0001g0295 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.816+10517G>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76263895 | ||||||
| chr15:76263933
|
C | G | 1 | a0001c0001t0002g0146 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.816+10479G>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76263933 | ||||||
| chr15:76264006
|
T | C | 2 | a0001c0001t0002g0190a0001c0001t0002g0192 | 2 | NA18965.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.816+10406A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76264006 | ||||||
| chr15:76264161
|
C | T | 1 | a0001c0001t0003g0276 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.816+10251G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76264161 | ||||||
| chr15:76264162
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.816+10250C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76264162 | ||||||
| chr15:76264358
|
T | G | 133 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(130): Show | 134 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.816+10054A>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76264358 | ||||||
| chr15:76264625
|
C | A | 1 | a0001c0001t0003g0028 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.816+9787G>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76264625 | ||||||
| chr15:76265028
|
G | C | 1 | a0001c0001t0002g0168 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.816+9384C>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76265028 | ||||||
| chr15:76265079
|
G | A | 1 | a0001c0001t0003g0276 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.816+9333C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76265079 | ||||||
| chr15:76265135
|
A | G | 195 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(192): Show | 196 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(193): Show |
intron_variant | MODIFIER | c.816+9277T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76265135 | ||||||
| chr15:76265212
|
T | G | 196 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(193): Show | 197 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(194): Show |
intron_variant | MODIFIER | c.816+9200A>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76265212 | ||||||
| chr15:76265214
|
C | T | 13 | a0001c0001t0003g0015a0001c0001t0003g0018a0001c0001t0003g0020others(10): Show | 13 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.816+9198G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76265214 | ||||||
| chr15:76265274
|
G | A | 1 | a0001c0001t0004g0272 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.816+9138C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76265274 | ||||||
| chr15:76265307
|
C | T | 1 | a0002c0002t0004g0253 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.816+9105G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76265307 | ||||||
| chr15:76265454
|
A | G | 1 | a0001c0001t0006g0278 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.816+8958T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76265454 | ||||||
| chr15:76265556
|
C | A | 5 | a0001c0001t0006g0278a0001c0001t0006g0279a0001c0001t0006g0280others(2): Show | 5 | HG02055.hp1 HG02559.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.816+8856G>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76265556 | ||||||
| chr15:76265593
|
T | C | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0321others(1): Show | 4 | HG02015.hp2 HG02132.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.816+8819A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76265593 | ||||||
| chr15:76265648
|
G | A | 1 | a0001c0001t0001g0079 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.816+8764C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76265648 | ||||||
| chr15:76265802
|
T | C | 132 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(129): Show | 133 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.816+8610A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76265802 | ||||||
| chr15:76265828
|
C | T | 324 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(321): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.816+8584G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76265828 | ||||||
| chr15:76266041
|
G | A | 3 | a0001c0001t0003g0264a0001c0001t0003g0275a0001c0001t0003g0277 | 3 | HG02145.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.816+8371C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76266041 | ||||||
| chr15:76266117
|
A | G | 1 | a0001c0001t0003g0017 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.816+8295T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76266117 | ||||||
| chr15:76266148
|
G | A | 3 | a0001c0001t0003g0264a0001c0001t0003g0275a0001c0001t0003g0277 | 3 | HG02145.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.816+8264C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76266148 | ||||||
| chr15:76266150
|
T | C | 116 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(113): Show | 117 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.816+8262A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76266150 | ||||||
| chr15:76266529
|
T | C | 52 | a0001c0001t0003g0015a0001c0001t0003g0018a0001c0001t0003g0020others(49): Show | 52 | HG00438.hp2 HG00621.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.816+7883A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76266529 | ||||||
| chr15:76266631
|
C | A | 1 | a0001c0001t0009g0239 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.816+7781G>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76266631 | ||||||
| chr15:76266631
|
C | T | 2 | a0001c0001t0003g0005a0001c0001t0003g0006 | 2 | HG01243.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.816+7781G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76266631 | ||||||
| chr15:76266632
|
G | A | 1 | a0001c0001t0002g0158 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.816+7780C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76266632 | ||||||
| chr15:76266762
|
G | T | 1 | a0001c0001t0001g0101 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.816+7650C>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76266762 | ||||||
| chr15:76266776
|
C | T | 3 | a0001c0001t0003g0264a0001c0001t0003g0275a0001c0001t0003g0277 | 3 | HG02145.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.816+7636G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76266776 | ||||||
| chr15:76266777
|
G | A | 4 | a0001c0001t0003g0106a0001c0001t0003g0107a0001c0001t0003g0108others(1): Show | 4 | HG02630.hp2 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+7635C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76266777 | ||||||
| chr15:76266860
|
C | T | 1 | a0001c0001t0002g0180 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.816+7552G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76266860 | ||||||
| chr15:76266902
|
T | TA | 132 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(129): Show | 133 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.816+7509dupT | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76266902 | ||||||
| chr15:76267005
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.816+7407C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76267005 | ||||||
| chr15:76267265
|
A | C | 1 | a0001c0001t0003g0103 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.816+7147T>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76267265 | ||||||
| chr15:76267320
|
G | A | 1 | a0001c0001t0004g0237 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.816+7092C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76267320 | ||||||
| chr15:76267345
|
T | A | 3 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0091 | 3 | HG01168.hp1 HG01433.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.816+7067A>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76267345 | ||||||
| chr15:76267547
|
A | G | 1 | a0001c0001t0001g0098 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.816+6865T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76267547 | ||||||
| chr15:76267603
|
G | T | 5 | a0001c0001t0001g0303a0001c0001t0001g0305a0001c0001t0001g0314others(2): Show | 5 | HG01346.hp2 HG01433.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.816+6809C>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76267603 | ||||||
| chr15:76267651
|
A | T | 1 | a0001c0001t0003g0115 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.816+6761T>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76267651 | ||||||
| chr15:76267763
|
G | A | 2 | a0002c0002t0004g0283a0002c0002t0004g0284 | 2 | NA18943.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.816+6649C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76267763 | ||||||
| chr15:76267906
|
C | A | 1 | a0001c0001t0003g0115 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.816+6506G>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76267906 | ||||||
| chr15:76267924
|
G | A | 113 | a0001c0001t0002g0002a0001c0001t0002g0116a0001c0001t0002g0117others(110): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.816+6488C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76267924 | ||||||
| chr15:76267951
|
T | A | 1 | a0001c0001t0002g0194 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.816+6461A>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76267951 | ||||||
| chr15:76267984
|
G | A | 1 | a0001c0001t0001g0056 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.816+6428C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76267984 | ||||||
| chr15:76268189
|
C | CA | 13 | a0001c0001t0002g0120a0001c0001t0002g0136a0001c0001t0002g0149others(10): Show | 13 | HG00733.hp1 HG00735.hp1 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.816+6222dupT | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76268189 | ||||||
| chr15:76268189
|
C | CAAAA | 13 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287others(10): Show | 13 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.816+6219_816+6222d others(6): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76268189 | ||||||
| chr15:76268189
|
C | CAAAAA | 109 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(106): Show | 110 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.816+6218_816+6222d others(7): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76268189 | ||||||
| chr15:76268189
|
C | CAAAAAA | 10 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0050others(7): Show | 10 | HG01074.hp2 HG01243.hp2 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.816+6217_816+6222d others(8): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76268189 | ||||||
| chr15:76268189
|
CA | C | 50 | a0001c0001t0003g0110a0001c0001t0003g0111a0001c0001t0003g0112others(47): Show | 50 | HG00438.hp2 HG01109.hp2 HG01123.hp2 others(47): Show |
intron_variant | MODIFIER | c.816+6222delT | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76268189 | ||||||
| chr15:76268241
|
A | T | 2 | a0001c0001t0004g0245a0001c0001t0004g0246 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.816+6171T>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76268241 | ||||||
| chr15:76268620
|
G | A | 5 | a0001c0001t0002g0175a0001c0001t0002g0184a0001c0001t0002g0185others(2): Show | 5 | NA18939.hp2 NA18960.hp2 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.816+5792C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76268620 | ||||||
| chr15:76268898
|
T | C | 1 | a0001c0001t0001g0046 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.816+5514A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76268898 | ||||||
| chr15:76268976
|
C | T | 1 | a0001c0001t0001g0060 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.816+5436G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76268976 | ||||||
| chr15:76269147
|
C | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | NA18969.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.816+5265G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76269147 | ||||||
| chr15:76269148
|
G | A | 1 | a0001c0001t0003g0005 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.816+5264C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76269148 | ||||||
| chr15:76269203
|
C | T | 115 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(112): Show | 116 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.816+5209G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76269203 | ||||||
| chr15:76269204
|
G | A | 7 | a0001c0001t0002g0002a0001c0001t0002g0116a0001c0001t0002g0128others(4): Show | 8 | HG00544.hp1 HG00621.hp1 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.816+5208C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76269204 | ||||||
| chr15:76269224
|
G | A | 1 | a0002c0002t0004g0254 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.816+5188C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76269224 | ||||||
| chr15:76269467
|
C | T | 2 | a0001c0001t0003g0273a0001c0001t0003g0274 | 2 | HG01255.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.816+4945G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76269467 | ||||||
| chr15:76269693
|
A | G | 1 | a0001c0001t0003g0331 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.816+4719T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76269693 | ||||||
| chr15:76269777
|
C | T | 187 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(184): Show | 188 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.816+4635G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76269777 | ||||||
| chr15:76269848
|
G | A | 12 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0044others(9): Show | 12 | NA18945.hp1 NA18968.hp1 NA18971.hp2 others(9): Show |
intron_variant | MODIFIER | c.816+4564C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76269848 | ||||||
| chr15:76270327
|
A | G | 1 | a0001c0001t0001g0286 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.816+4085T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76270327 | ||||||
| chr15:76270397
|
T | C | 17 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(14): Show | 17 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.816+4015A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76270397 | ||||||
| chr15:76270745
|
G | C | 1 | a0001c0001t0001g0088 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.816+3667C>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76270745 | ||||||
| chr15:76270962
|
G | A | 1 | a0001c0001t0001g0096 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.816+3450C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76270962 | ||||||
| chr15:76271031
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.816+3381C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76271031 | ||||||
| chr15:76271093
|
C | T | 1 | a0001c0001t0002g0180 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.816+3319G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76271093 | ||||||
| chr15:76271137
|
T | C | 19 | a0001c0001t0002g0120a0001c0001t0002g0136a0001c0001t0002g0137others(16): Show | 19 | HG00673.hp2 HG00733.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.816+3275A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76271137 | ||||||
| chr15:76271169
|
C | CA | 14 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0098others(11): Show | 14 | HG00673.hp1 HG01081.hp1 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.816+3242dupT | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76271169 | ||||||
| chr15:76271169
|
C | CAA | 6 | a0001c0001t0003g0006a0001c0001t0003g0110a0001c0001t0003g0111others(3): Show | 6 | HG01243.hp1 HG01891.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.816+3241_816+3242d others(4): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76271169 | ||||||
| chr15:76271169
|
CA | C | 28 | a0001c0001t0001g0037a0001c0001t0001g0047a0001c0001t0001g0077others(25): Show | 28 | HG00673.hp2 HG00733.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.816+3242delT | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76271169 | ||||||
| chr15:76271176
|
A | C | 1 | a0001c0001t0002g0227 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.816+3236T>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76271176 | ||||||
| chr15:76271286
|
G | A | 1 | a0001c0001t0001g0322 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.816+3126C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76271286 | ||||||
| chr15:76271618
|
C | T | 1 | a0001c0001t0004g0235 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.816+2794G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76271618 | ||||||
| chr15:76271726
|
G | A | 6 | a0001c0001t0003g0110a0001c0001t0003g0111a0001c0001t0003g0112others(3): Show | 6 | HG01891.hp2 HG02280.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.816+2686C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76271726 | ||||||
| chr15:76271738
|
A | C | 1 | a0001c0001t0002g0151 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.816+2674T>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76271738 | ||||||
| chr15:76271755
|
G | A | 1 | a0001c0001t0002g0158 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.816+2657C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76271755 | ||||||
| chr15:76271814
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.816+2598A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76271814 | ||||||
| chr15:76271914
|
TAC | T | 179 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(176): Show | 180 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(177): Show |
intron_variant | MODIFIER | c.816+2496_816+2497d others(4): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76271914 | ||||||
| chr15:76271914
|
TACAC | T | 3 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287 | 3 | HG02572.hp1 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.816+2494_816+2497d others(6): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76271914 | ||||||
| chr15:76271916
|
C | T | 2 | a0001c0001t0003g0273a0001c0001t0003g0274 | 2 | HG01255.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.816+2496G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76271916 | ||||||
| chr15:76271920
|
C | T | 1 | a0001c0001t0001g0098 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.816+2492G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76271920 | ||||||
| chr15:76271941
|
C | A | 2 | a0001c0001t0003g0273a0001c0001t0003g0274 | 2 | HG01255.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.816+2471G>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76271941 | ||||||
| chr15:76271943
|
T | C | 2 | a0001c0001t0003g0273a0001c0001t0003g0274 | 2 | HG01255.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.816+2469A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76271943 | ||||||
| chr15:76272000
|
A | C | 1 | a0001c0001t0003g0021 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.816+2412T>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76272000 | ||||||
| chr15:76272051
|
T | C | 6 | a0001c0001t0003g0110a0001c0001t0003g0111a0001c0001t0003g0112others(3): Show | 6 | HG01891.hp2 HG02280.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.816+2361A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76272051 | ||||||
| chr15:76272222
|
C | CT | 40 | a0001c0001t0003g0112a0001c0001t0003g0276a0001c0001t0004g0102others(37): Show | 40 | HG00438.hp2 HG00621.hp2 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.816+2189dupA | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76272222 | ||||||
| chr15:76272677
|
C | T | 2 | a0001c0001t0003g0005a0001c0001t0003g0006 | 2 | HG01243.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.816+1735G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76272677 | ||||||
| chr15:76272685
|
G | C | 114 | a0001c0001t0001g0088a0001c0001t0002g0002a0001c0001t0002g0116others(111): Show | 115 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(112): Show |
intron_variant | MODIFIER | c.816+1727C>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76272685 | ||||||
| chr15:76272748
|
C | A | 1 | a0001c0001t0002g0184 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.816+1664G>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76272748 | ||||||
| chr15:76272805
|
A | AATATATA others(29): Show |
1 | a0001c0001t0004g0272 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.816+1606_816+1607i others(38): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76272805 | ||||||
| chr15:76272813
|
C | CAT | 19 | a0001c0001t0001g0043a0001c0001t0001g0068a0001c0001t0001g0098others(16): Show | 19 | HG01175.hp2 HG01243.hp2 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.816+1597_816+1598d others(4): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76272813 | ||||||
| chr15:76272813
|
C | CATAT | 7 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287others(4): Show | 7 | HG02145.hp1 HG02572.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.816+1595_816+1598d others(6): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76272813 | ||||||
| chr15:76272813
|
C | CATATAT | 77 | a0001c0001t0001g0088a0001c0001t0002g0002a0001c0001t0002g0116others(74): Show | 78 | HG00544.hp1 HG00621.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.816+1593_816+1598d others(8): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76272813 | ||||||
| chr15:76272813
|
C | CATATATA others(1): Show |
28 | a0001c0001t0002g0117a0001c0001t0002g0122a0001c0001t0002g0123others(25): Show | 28 | HG00099.hp1 HG00597.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.816+1591_816+1598d others(10): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76272813 | ||||||
| chr15:76272813
|
C | CATATATA others(3): Show |
10 | a0001c0001t0002g0159a0001c0001t0002g0198a0001c0001t0002g0199others(7): Show | 10 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(7): Show |
intron_variant | MODIFIER | c.816+1589_816+1598d others(12): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76272813 | ||||||
| chr15:76272813
|
C | CATATATA others(5): Show |
4 | a0001c0001t0002g0126a0001c0001t0002g0143a0002c0002t0004g0261others(1): Show | 4 | HG00438.hp2 HG02165.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+1587_816+1598d others(14): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76272813 | ||||||
| chr15:76272813
|
C | CATATATA others(7): Show |
13 | a0001c0001t0004g0235a0001c0001t0004g0248a0002c0002t0001g0252others(10): Show | 13 | HG00621.hp2 HG01175.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.816+1585_816+1598d others(16): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76272813 | ||||||
| chr15:76272813
|
C | CATATATA others(9): Show |
5 | a0001c0001t0004g0249a0001c0001t0004g0250a0001c0001t0004g0251others(2): Show | 5 | HG01255.hp2 HG02886.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.816+1583_816+1598d others(18): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76272813 | ||||||
| chr15:76272813
|
C | CATATATA others(11): Show |
1 | a0002c0002t0004g0259 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.816+1581_816+1598d others(20): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76272813 | ||||||
| chr15:76272813
|
C | CATATATA others(15): Show |
2 | a0001c0001t0004g0234a0001c0001t0004g0237 | 2 | HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.816+1598_816+1599i others(24): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76272813 | ||||||
| chr15:76272813
|
C | CATATATA others(17): Show |
4 | a0001c0001t0004g0231a0001c0001t0004g0240a0001c0001t0004g0241others(1): Show | 4 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.816+1598_816+1599i others(26): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76272813 | ||||||
| chr15:76272813
|
C | CATATATA others(19): Show |
5 | a0001c0001t0004g0232a0001c0001t0004g0233a0001c0001t0004g0236others(2): Show | 5 | HG02258.hp1 HG02717.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.816+1598_816+1599i others(28): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76272813 | ||||||
| chr15:76272813
|
C | CATATATA others(23): Show |
4 | a0001c0001t0004g0242a0001c0001t0004g0245a0001c0001t0004g0246others(1): Show | 4 | HG02055.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+1598_816+1599i others(32): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76272813 | ||||||
| chr15:76272813
|
C | CATATATA others(29): Show |
1 | a0001c0001t0009g0230 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.816+1598_816+1599i others(38): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76272813 | ||||||
| chr15:76272813
|
C | CATATATA others(31): Show |
1 | a0001c0001t0004g0102 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.816+1598_816+1599i others(40): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76272813 | ||||||
| chr15:76272813
|
C | T | 1 | a0001c0001t0004g0272 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.816+1599G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76272813 | ||||||
| chr15:76272913
|
C | T | 1 | a0001c0001t0013g0301 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.816+1499G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76272913 | ||||||
| chr15:76273042
|
C | T | 1 | a0001c0001t0002g0129 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.816+1370G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76273042 | ||||||
| chr15:76273071
|
C | T | 3 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287 | 3 | HG02572.hp1 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.816+1341G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76273071 | ||||||
| chr15:76273150
|
C | T | 1 | a0001c0001t0001g0295 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.816+1262G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76273150 | ||||||
| chr15:76273238
|
G | C | 1 | a0001c0001t0004g0245 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.816+1174C>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76273238 | ||||||
| chr15:76273262
|
G | A | 131 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(128): Show | 132 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.816+1150C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76273262 | ||||||
| chr15:76273375
|
G | A | 14 | a0001c0001t0002g0139a0001c0001t0002g0155a0001c0001t0002g0161others(11): Show | 14 | HG02071.hp2 HG03831.hp2 HG03927.hp1 others(11): Show |
intron_variant | MODIFIER | c.816+1037C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76273375 | ||||||
| chr15:76273391
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.816+1021A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76273391 | ||||||
| chr15:76273437
|
T | A | 1 | a0001c0001t0001g0086 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.816+975A>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76273437 | ||||||
| chr15:76273538
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.816+874C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76273538 | ||||||
| chr15:76273553
|
C | CAAACA | 108 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(105): Show | 109 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.816+854_816+858dup others(5): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76273553 | ||||||
| chr15:76273553
|
C | CAAACAAA others(3): Show |
2 | a0001c0001t0001g0052a0001c0001t0001g0322 | 2 | HG01243.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.816+849_816+858dup others(10): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76273553 | ||||||
| chr15:76273553
|
C | CAAACAAA others(8): Show |
3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0076 | 3 | HG00738.hp2 HG00741.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.816+844_816+858dup others(15): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76273553 | ||||||
| chr15:76273553
|
CAAACAAA others(3): Show |
C | 3 | a0001c0001t0003g0264a0001c0001t0003g0275a0001c0001t0003g0277 | 3 | HG02145.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.816+849_816+858del others(10): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76273553 | ||||||
| chr15:76273590
|
A | G | 9 | a0001c0001t0003g0324a0001c0001t0003g0325a0001c0001t0003g0326others(6): Show | 9 | HG02109.hp2 HG02451.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.816+822T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76273590 | ||||||
| chr15:76273727
|
T | TA | 114 | a0001c0001t0001g0088a0001c0001t0002g0002a0001c0001t0002g0116others(111): Show | 115 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(112): Show |
intron_variant | MODIFIER | c.816+684dupT | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76273727 | ||||||
| chr15:76273792
|
T | C | 1 | a0001c0001t0001g0322 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.816+620A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76273792 | ||||||
| chr15:76274011
|
C | T | 1 | a0001c0001t0002g0135 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.816+401G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76274011 | ||||||
| chr15:76274356
|
C | T | 1 | a0001c0001t0011g0330 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.816+56G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 9/11 | chr15 | 76274356 | ||||||
| chr15:76274514
|
G | T | 2 | a0001c0001t0004g0236a0001c0001t0004g0237 | 2 | HG02922.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.734-20C>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76274514 | ||||||
| chr15:76274546
|
T | C | 3 | a0001c0001t0002g0002a0001c0001t0002g0116a0001c0001t0002g0193 | 4 | HG02132.hp1 NA18942.hp2 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.734-52A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76274546 | ||||||
| chr15:76274601
|
T | C | 3 | a0001c0001t0003g0264a0001c0001t0003g0275a0001c0001t0003g0277 | 3 | HG02145.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.734-107A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76274601 | ||||||
| chr15:76274649
|
C | A | 1 | a0001c0001t0001g0079 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.734-155G>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76274649 | ||||||
| chr15:76274797
|
A | G | 7 | a0001c0001t0003g0110a0001c0001t0003g0111a0001c0001t0003g0112others(4): Show | 7 | HG01891.hp2 HG02280.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.734-303T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76274797 | ||||||
| chr15:76274801
|
T | C | 116 | a0001c0001t0001g0088a0001c0001t0002g0002a0001c0001t0002g0116others(113): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.734-307A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76274801 | ||||||
| chr15:76274909
|
C | T | 1 | a0001c0001t0003g0276 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.734-415G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76274909 | ||||||
| chr15:76274987
|
A | G | 16 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(13): Show | 16 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.734-493T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76274987 | ||||||
| chr15:76275021
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.734-527T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76275021 | ||||||
| chr15:76275043
|
C | G | 3 | a0001c0001t0001g0321a0001c0001t0001g0322a0001c0001t0001g0323 | 3 | HG01243.hp2 HG01496.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.734-549G>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76275043 | ||||||
| chr15:76275058
|
C | A | 9 | a0001c0001t0003g0324a0001c0001t0003g0325a0001c0001t0003g0326others(6): Show | 9 | HG02109.hp2 HG02451.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.734-564G>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76275058 | ||||||
| chr15:76275143
|
A | G | 39 | a0001c0001t0004g0102a0001c0001t0004g0231a0001c0001t0004g0232others(36): Show | 39 | HG00438.hp2 HG00621.hp2 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.734-649T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76275143 | ||||||
| chr15:76275151
|
A | G | 1 | a0001c0001t0001g0080 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.734-657T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76275151 | ||||||
| chr15:76275607
|
C | T | 1 | a0001c0001t0001g0321 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.734-1113G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76275607 | ||||||
| chr15:76275868
|
G | A | 73 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0015others(70): Show | 73 | HG00438.hp2 HG00621.hp2 HG00735.hp1 others(70): Show |
intron_variant | MODIFIER | c.734-1374C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76275868 | ||||||
| chr15:76275948
|
A | G | 1 | a0001c0001t0001g0317 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.734-1454T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76275948 | ||||||
| chr15:76276057
|
T | A | 40 | a0001c0001t0002g0129a0001c0001t0002g0131a0001c0001t0002g0135others(37): Show | 40 | HG00099.hp1 HG00738.hp1 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.734-1563A>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76276057 | ||||||
| chr15:76276135
|
A | C | 1 | a0002c0002t0004g0255 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.734-1641T>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76276135 | ||||||
| chr15:76276174
|
A | G | 1 | a0002c0002t0004g0256 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.734-1680T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76276174 | ||||||
| chr15:76276238
|
G | A | 116 | a0001c0001t0001g0088a0001c0001t0002g0002a0001c0001t0002g0116others(113): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.734-1744C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76276238 | ||||||
| chr15:76276428
|
T | C | 1 | a0001c0001t0003g0024 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.734-1934A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76276428 | ||||||
| chr15:76276451
|
C | G | 115 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(112): Show | 116 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.734-1957G>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76276451 | ||||||
| chr15:76276512
|
G | A | 1 | a0001c0001t0002g0218 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.734-2018C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76276512 | ||||||
| chr15:76276624
|
G | T | 136 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(133): Show | 137 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.734-2130C>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76276624 | ||||||
| chr15:76276625
|
T | C | 27 | a0001c0001t0001g0098a0001c0001t0001g0288a0001c0001t0001g0289others(24): Show | 27 | HG00140.hp2 HG00544.hp2 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.734-2131A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76276625 | ||||||
| chr15:76276632
|
T | C | 131 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(128): Show | 132 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.734-2138A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76276632 | ||||||
| chr15:76276633
|
G | T | 4 | a0001c0001t0003g0106a0001c0001t0003g0107a0001c0001t0003g0108others(1): Show | 4 | HG02630.hp2 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.734-2139C>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76276633 | ||||||
| chr15:76276636
|
T | G | 134 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(131): Show | 135 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.734-2142A>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76276636 | ||||||
| chr15:76276723
|
G | A | 1 | a0001c0001t0001g0321 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.734-2229C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76276723 | ||||||
| chr15:76276751
|
T | C | 1 | a0001c0001t0002g0138 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.734-2257A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76276751 | ||||||
| chr15:76276792
|
T | C | 1 | a0001c0001t0002g0129 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.734-2298A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76276792 | ||||||
| chr15:76276810
|
C | T | 16 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(13): Show | 16 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.734-2316G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76276810 | ||||||
| chr15:76276891
|
T | G | 1 | a0001c0001t0012g0268 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.734-2397A>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76276891 | ||||||
| chr15:76277128
|
G | A | 7 | a0001c0001t0003g0110a0001c0001t0003g0111a0001c0001t0003g0112others(4): Show | 7 | HG01891.hp2 HG02280.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.734-2634C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76277128 | ||||||
| chr15:76277372
|
G | A | 1 | a0001c0001t0003g0328 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.734-2878C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76277372 | ||||||
| chr15:76277483
|
G | GT | 46 | a0001c0001t0003g0110a0001c0001t0003g0111a0001c0001t0003g0112others(43): Show | 46 | HG00438.hp2 HG00621.hp2 HG01109.hp2 others(43): Show |
intron_variant | MODIFIER | c.734-2990dupA | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76277483 | ||||||
| chr15:76277504
|
CA | C | 119 | a0001c0001t0001g0088a0001c0001t0002g0002a0001c0001t0002g0116others(116): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.734-3011delT | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76277504 | ||||||
| chr15:76277504
|
CAA | C | 203 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(200): Show | 204 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.734-3012_734-3011d others(4): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76277504 | ||||||
| chr15:76277511
|
A | C | 3 | a0001c0001t0002g0136a0001c0001t0002g0149a0001c0001t0002g0191 | 3 | HG00621.hp1 HG00733.hp1 HG00735.hp2 |
intron_variant | MODIFIER | c.734-3017T>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76277511 | ||||||
| chr15:76277512
|
A | C | 121 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(118): Show | 122 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.734-3018T>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76277512 | ||||||
| chr15:76277542
|
G | A | 1 | a0001c0001t0003g0276 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.734-3048C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76277542 | ||||||
| chr15:76277574
|
C | A | 16 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(13): Show | 16 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.734-3080G>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76277574 | ||||||
| chr15:76277650
|
G | C | 4 | a0001c0001t0003g0106a0001c0001t0003g0107a0001c0001t0003g0108others(1): Show | 4 | HG02630.hp2 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.734-3156C>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76277650 | ||||||
| chr15:76277699
|
C | T | 1 | a0001c0001t0002g0210 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.734-3205G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76277699 | ||||||
| chr15:76277700
|
G | C | 3 | a0001c0001t0001g0292a0001c0001t0001g0307a0001c0001t0001g0319 | 3 | NA18941.hp2 NA18967.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.734-3206C>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76277700 | ||||||
| chr15:76277792
|
C | T | 2 | a0001c0001t0003g0273a0001c0001t0003g0274 | 2 | HG01255.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.734-3298G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76277792 | ||||||
| chr15:76277802
|
C | T | 39 | a0001c0001t0004g0102a0001c0001t0004g0231a0001c0001t0004g0232others(36): Show | 39 | HG00438.hp2 HG00621.hp2 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.734-3308G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76277802 | ||||||
| chr15:76277821
|
C | T | 4 | a0001c0001t0003g0106a0001c0001t0003g0107a0001c0001t0003g0108others(1): Show | 4 | HG02630.hp2 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.734-3327G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76277821 | ||||||
| chr15:76278079
|
T | C | 1 | a0001c0001t0002g0153 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.734-3585A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76278079 | ||||||
| chr15:76278243
|
A | G | 2 | a0001c0001t0003g0005a0001c0001t0003g0006 | 2 | HG01243.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.734-3749T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76278243 | ||||||
| chr15:76278250
|
C | T | 325 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(322): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.734-3756G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76278250 | ||||||
| chr15:76278502
|
G | C | 318 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(315): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.734-4008C>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76278502 | ||||||
| chr15:76278634
|
C | T | 1 | a0001c0001t0003g0276 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.734-4140G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76278634 | ||||||
| chr15:76278712
|
A | T | 131 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(128): Show | 132 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.734-4218T>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76278712 | ||||||
| chr15:76278770
|
G | C | 6 | a0001c0001t0003g0110a0001c0001t0003g0111a0001c0001t0003g0112others(3): Show | 6 | HG01891.hp2 HG02280.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.734-4276C>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76278770 | ||||||
| chr15:76278783
|
C | T | 121 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(118): Show | 122 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.734-4289G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76278783 | ||||||
| chr15:76278903
|
GGAGTGAC others(6): Show |
G | 3 | a0001c0001t0002g0211a0001c0001t0002g0215a0001c0001t0002g0216 | 3 | HG01070.hp2 HG01257.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.734-4422_734-4410d others(15): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76278903 | ||||||
| chr15:76278941
|
G | A | 1 | a0001c0001t0001g0299 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.734-4447C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76278941 | ||||||
| chr15:76279027
|
C | A | 17 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(14): Show | 17 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.734-4533G>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76279027 | ||||||
| chr15:76279165
|
A | G | 2 | a0001c0001t0003g0005a0001c0001t0003g0006 | 2 | HG01243.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.733+4592T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76279165 | ||||||
| chr15:76279269
|
C | T | 53 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0110others(50): Show | 53 | HG00438.hp2 HG00621.hp2 HG01109.hp2 others(50): Show |
intron_variant | MODIFIER | c.733+4488G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76279269 | ||||||
| chr15:76279302
|
G | C | 2 | a0001c0001t0001g0300a0001c0001t0001g0318 | 2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.733+4455C>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76279302 | ||||||
| chr15:76279329
|
G | A | 2 | a0001c0001t0002g0214a0001c0001t0002g0226 | 2 | HG02622.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.733+4428C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76279329 | ||||||
| chr15:76279333
|
T | G | 17 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(14): Show | 17 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.733+4424A>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76279333 | ||||||
| chr15:76279465
|
C | T | 1 | a0001c0001t0003g0276 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.733+4292G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76279465 | ||||||
| chr15:76279517
|
TCCTCCCA others(6): Show |
T | 11 | a0001c0001t0001g0045a0001c0001t0001g0056a0001c0001t0001g0058others(8): Show | 11 | HG00673.hp1 HG01361.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.733+4227_733+4239d others(15): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76279517 | ||||||
| chr15:76279674
|
T | C | 3 | a0001c0001t0003g0264a0001c0001t0003g0275a0001c0001t0003g0277 | 3 | HG02145.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.733+4083A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76279674 | ||||||
| chr15:76279696
|
G | A | 1 | a0001c0001t0001g0053 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.733+4061C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76279696 | ||||||
| chr15:76280060
|
G | A | 5 | a0001c0001t0002g0175a0001c0001t0002g0184a0001c0001t0002g0185others(2): Show | 5 | NA18939.hp2 NA18960.hp2 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.733+3697C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76280060 | ||||||
| chr15:76280389
|
A | C | 1 | a0001c0001t0002g0160 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.733+3368T>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76280389 | ||||||
| chr15:76280587
|
T | G | 1 | a0001c0001t0013g0301 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.733+3170A>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76280587 | ||||||
| chr15:76280593
|
A | G | 1 | a0001c0001t0002g0224 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.733+3164T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76280593 | ||||||
| chr15:76280645
|
C | T | 9 | a0001c0001t0003g0324a0001c0001t0003g0325a0001c0001t0003g0326others(6): Show | 9 | HG02109.hp2 HG02451.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.733+3112G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76280645 | ||||||
| chr15:76280917
|
C | CT | 236 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(233): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.733+2839dupA | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76280917 | ||||||
| chr15:76280917
|
C | CTT | 81 | a0001c0001t0001g0011a0001c0001t0001g0044a0001c0001t0001g0057others(78): Show | 81 | HG00438.hp2 HG00621.hp2 HG00738.hp2 others(78): Show |
intron_variant | MODIFIER | c.733+2838_733+2839d others(4): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76280917 | ||||||
| chr15:76280973
|
T | C | 1 | a0001c0001t0001g0040 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.733+2784A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76280973 | ||||||
| chr15:76281074
|
C | T | 1 | a0001c0001t0011g0330 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.733+2683G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76281074 | ||||||
| chr15:76281119
|
C | T | 1 | a0001c0001t0001g0306 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.733+2638G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76281119 | ||||||
| chr15:76281194
|
G | A | 1 | a0001c0001t0001g0321 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.733+2563C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76281194 | ||||||
| chr15:76281207
|
G | A | 1 | a0001c0001t0002g0169 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.733+2550C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76281207 | ||||||
| chr15:76281291
|
C | T | 1 | a0001c0001t0001g0093 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.733+2466G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76281291 | ||||||
| chr15:76281366
|
T | C | 1 | a0001c0001t0001g0311 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.733+2391A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76281366 | ||||||
| chr15:76281428
|
AT | A | 10 | a0001c0001t0001g0104a0001c0001t0001g0322a0001c0001t0001g0323others(7): Show | 10 | HG01243.hp2 HG01496.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.733+2328delA | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76281428 | ||||||
| chr15:76281443
|
TGA | T | 3 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287 | 3 | HG02572.hp1 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.733+2312_733+2313d others(4): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76281443 | ||||||
| chr15:76281891
|
C | T | 114 | a0001c0001t0001g0088a0001c0001t0002g0002a0001c0001t0002g0116others(111): Show | 115 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(112): Show |
intron_variant | MODIFIER | c.733+1866G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76281891 | ||||||
| chr15:76281897
|
C | CT | 266 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(263): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.733+1859dupA | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76281897 | ||||||
| chr15:76281897
|
C | CTT | 38 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(35): Show | 38 | HG00140.hp2 HG00544.hp2 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.733+1858_733+1859d others(4): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76281897 | ||||||
| chr15:76281926
|
C | T | 1 | a0001c0001t0011g0330 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.733+1831G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76281926 | ||||||
| chr15:76282105
|
C | T | 1 | a0001c0001t0012g0268 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.733+1652G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76282105 | ||||||
| chr15:76282146
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.733+1611G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76282146 | ||||||
| chr15:76282155
|
T | C | 2 | a0001c0001t0005g0265a0001c0001t0005g0266 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.733+1602A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76282155 | ||||||
| chr15:76282287
|
G | A | 53 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0110others(50): Show | 53 | HG00438.hp2 HG00621.hp2 HG01109.hp2 others(50): Show |
intron_variant | MODIFIER | c.733+1470C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76282287 | ||||||
| chr15:76282332
|
C | G | 1 | a0001c0001t0002g0217 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.733+1425G>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76282332 | ||||||
| chr15:76282616
|
C | T | 1 | a0001c0001t0003g0016 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.733+1141G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76282616 | ||||||
| chr15:76282619
|
T | C | 1 | a0001c0001t0006g0278 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.733+1138A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76282619 | ||||||
| chr15:76282680
|
C | T | 15 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0148others(12): Show | 15 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(12): Show |
intron_variant | MODIFIER | c.733+1077G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76282680 | ||||||
| chr15:76282691
|
C | G | 1 | a0001c0001t0002g0144 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.733+1066G>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76282691 | ||||||
| chr15:76282713
|
C | G | 325 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(322): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.733+1044G>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76282713 | ||||||
| chr15:76282829
|
A | T | 2 | a0001c0001t0008g0165a0001c0001t0008g0173 | 2 | HG03491.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.733+928T>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76282829 | ||||||
| chr15:76283029
|
C | T | 1 | a0001c0001t0011g0330 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.733+728G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76283029 | ||||||
| chr15:76283054
|
A | T | 1 | a0001c0001t0001g0074 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.733+703T>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76283054 | ||||||
| chr15:76283368
|
G | A | 6 | a0001c0001t0003g0110a0001c0001t0003g0111a0001c0001t0003g0112others(3): Show | 6 | HG01891.hp2 HG02280.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.733+389C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76283368 | ||||||
| chr15:76283507
|
A | G | 3 | a0001c0001t0001g0321a0001c0001t0001g0322a0001c0001t0001g0323 | 3 | HG01243.hp2 HG01496.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.733+250T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76283507 | ||||||
| chr15:76283719
|
A | G | 2 | a0001c0001t0001g0303a0001c0001t0001g0305 | 2 | HG01433.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.733+38T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 8/11 | chr15 | 76283719 | ||||||
| chr15:76284032
|
T | C | 2 | a0001c0001t0007g0132a0001c0001t0007g0133 | 2 | HG02080.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.665-207A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 7/11 | chr15 | 76284032 | ||||||
| chr15:76284143
|
A | G | 1 | a0001c0001t0002g0191 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.665-318T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 7/11 | chr15 | 76284143 | ||||||
| chr15:76284200
|
G | A | 4 | a0001c0001t0003g0106a0001c0001t0003g0107a0001c0001t0003g0108others(1): Show | 4 | HG02630.hp2 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.665-375C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 7/11 | chr15 | 76284200 | ||||||
| chr15:76284293
|
C | T | 13 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287others(10): Show | 13 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.665-468G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 7/11 | chr15 | 76284293 | ||||||
| chr15:76284371
|
T | A | 10 | a0001c0001t0003g0324a0001c0001t0003g0325a0001c0001t0003g0326others(7): Show | 10 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.665-546A>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 7/11 | chr15 | 76284371 | ||||||
| chr15:76284454
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.665-629C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 7/11 | chr15 | 76284454 | ||||||
| chr15:76284498
|
A | T | 1 | a0001c0001t0002g0158 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.665-673T>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 7/11 | chr15 | 76284498 | ||||||
| chr15:76284553
|
C | T | 3 | a0001c0001t0001g0314a0001c0001t0001g0315a0001c0001t0001g0316 | 3 | HG01346.hp2 HG01515.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.665-728G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 7/11 | chr15 | 76284553 | ||||||
| chr15:76284644
|
C | T | 1 | a0001c0001t0004g0248 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.665-819G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 7/11 | chr15 | 76284644 | ||||||
| chr15:76284739
|
G | A | 1 | a0001c0001t0005g0271 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.664+898C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 7/11 | chr15 | 76284739 | ||||||
| chr15:76284781
|
C | T | 3 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014 | 3 | NA18960.hp1 NA18969.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.664+856G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 7/11 | chr15 | 76284781 | ||||||
| chr15:76284823
|
G | C | 4 | a0001c0001t0003g0106a0001c0001t0003g0107a0001c0001t0003g0108others(1): Show | 4 | HG02630.hp2 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.664+814C>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 7/11 | chr15 | 76284823 | ||||||
| chr15:76285272
|
T | C | 2 | a0001c0001t0003g0005a0001c0001t0003g0006 | 2 | HG01243.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.664+365A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 7/11 | chr15 | 76285272 | ||||||
| chr15:76285548
|
T | G | 1 | a0001c0001t0001g0041 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.664+89A>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 7/11 | chr15 | 76285548 | ||||||
| chr15:76285610
|
A | T | 2 | a0001c0001t0003g0273a0001c0001t0003g0274 | 2 | HG01255.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.664+27T>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 7/11 | chr15 | 76285610 | ||||||
| chr15:76286043
|
C | A | 5 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0205others(2): Show | 5 | HG02080.hp2 HG02083.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.563-305G>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 6/11 | chr15 | 76286043 | ||||||
| chr15:76286267
|
T | G | 2 | a0001c0001t0003g0005a0001c0001t0003g0006 | 2 | HG01243.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.562+104A>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 6/11 | chr15 | 76286267 | ||||||
| chr15:76286271
|
A | G | 3 | a0001c0001t0003g0264a0001c0001t0003g0275a0001c0001t0003g0277 | 3 | HG02145.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.562+100T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 6/11 | chr15 | 76286271 | ||||||
| chr15:76286345
|
C | T | 1 | a0001c0001t0003g0276 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.562+26G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 6/11 | chr15 | 76286345 | ||||||
| chr15:76286360
|
T | A | 1 | a0001c0001t0011g0330 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.562+11A>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 6/11 | chr15 | 76286360 | ||||||
| chr15:76286546
|
T | G | 1 | a0001c0001t0001g0322 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.452-65A>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 5/11 | chr15 | 76286546 | ||||||
| chr15:76286637
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.452-156G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 5/11 | chr15 | 76286637 | ||||||
| chr15:76286656
|
C | T | 325 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(322): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.452-175G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 5/11 | chr15 | 76286656 | ||||||
| chr15:76286693
|
G | A | 2 | a0001c0001t0003g0273a0001c0001t0003g0274 | 2 | HG01255.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.452-212C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 5/11 | chr15 | 76286693 | ||||||
| chr15:76286749
|
G | A | 8 | a0001c0001t0002g0211a0001c0001t0002g0213a0001c0001t0002g0214others(5): Show | 8 | HG00639.hp2 HG01070.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.452-268C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 5/11 | chr15 | 76286749 | ||||||
| chr15:76286868
|
A | G | 1 | a0001c0001t0004g0102 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.452-387T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 5/11 | chr15 | 76286868 | ||||||
| chr15:76286893
|
A | G | 17 | a0001c0001t0004g0102a0002c0002t0001g0252a0002c0002t0004g0228others(14): Show | 17 | HG00438.hp2 HG00621.hp2 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.452-412T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 5/11 | chr15 | 76286893 | ||||||
| chr15:76286945
|
A | G | 9 | a0001c0001t0003g0324a0001c0001t0003g0325a0001c0001t0003g0326others(6): Show | 9 | HG02109.hp2 HG02451.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.452-464T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 5/11 | chr15 | 76286945 | ||||||
| chr15:76287036
|
A | AT | 10 | a0001c0001t0003g0324a0001c0001t0003g0325a0001c0001t0003g0326others(7): Show | 10 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.452-556_452-555ins others(1): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 5/11 | chr15 | 76287036 | ||||||
| chr15:76287195
|
G | T | 121 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(118): Show | 122 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.451+651C>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 5/11 | chr15 | 76287195 | ||||||
| chr15:76287323
|
T | C | 324 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(321): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.451+523A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 5/11 | chr15 | 76287323 | ||||||
| chr15:76287337
|
T | A | 1 | a0001c0001t0001g0105 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.451+509A>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 5/11 | chr15 | 76287337 | ||||||
| chr15:76287559
|
A | G | 3 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287 | 3 | HG02572.hp1 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.451+287T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 5/11 | chr15 | 76287559 | ||||||
| chr15:76287593
|
T | C | 2 | a0001c0001t0001g0322a0001c0001t0001g0323 | 2 | HG01243.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.451+253A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 5/11 | chr15 | 76287593 | ||||||
| chr15:76287751
|
T | C | 1 | a0001c0001t0002g0118 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.451+95A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 5/11 | chr15 | 76287751 | ||||||
| chr15:76287772
|
T | C | 2 | a0001c0001t0001g0084a0001c0001t0001g0104 | 2 | NA19068.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.451+74A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 5/11 | chr15 | 76287772 | ||||||
| chr15:76288186
|
C | T | 131 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(128): Show | 132 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.352-241G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76288186 | ||||||
| chr15:76288206
|
C | T | 325 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(322): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.352-261G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76288206 | ||||||
| chr15:76288304
|
G | A | 1 | a0002c0002t0001g0252 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.352-359C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76288304 | ||||||
| chr15:76288317
|
A | T | 1 | a0001c0001t0009g0230 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.352-372T>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76288317 | ||||||
| chr15:76288716
|
G | GA | 149 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(146): Show | 150 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.352-772dupT | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76288716 | ||||||
| chr15:76288857
|
C | T | 324 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(321): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.352-912G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76288857 | ||||||
| chr15:76288917
|
C | T | 3 | a0001c0001t0001g0310a0001c0001t0002g0205a0002c0002t0004g0247 | 3 | HG02040.hp1 NA18972.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.352-972G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76288917 | ||||||
| chr15:76288920
|
C | CT | 16 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(13): Show | 16 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.352-976dupA | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76288920 | ||||||
| chr15:76288920
|
C | CTTCTTCT | 9 | a0001c0001t0003g0324a0001c0001t0003g0325a0001c0001t0003g0326others(6): Show | 9 | HG02109.hp2 HG02451.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.352-976_352-975ins others(7): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76288920 | ||||||
| chr15:76288920
|
C | CTTTTTT | 165 | a0001c0001t0001g0034a0001c0001t0001g0051a0001c0001t0001g0066others(162): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.352-981_352-976dup others(6): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76288920 | ||||||
| chr15:76288920
|
C | CTTTTTTT | 97 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(94): Show | 98 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.352-982_352-976dup others(7): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76288920 | ||||||
| chr15:76288920
|
C | CTTTTTTT others(1): Show |
14 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(11): Show | 14 | HG00733.hp2 HG01106.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.352-983_352-976dup others(8): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76288920 | ||||||
| chr15:76288920
|
C | CTTTTTTT others(4): Show |
7 | a0001c0001t0003g0110a0001c0001t0003g0111a0001c0001t0003g0112others(4): Show | 7 | HG01891.hp2 HG02280.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.352-986_352-976dup others(11): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76288920 | ||||||
| chr15:76288920
|
C | T | 3 | a0001c0001t0001g0310a0001c0001t0002g0205a0002c0002t0004g0247 | 3 | HG02040.hp1 NA18972.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.352-975G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76288920 | ||||||
| chr15:76289027
|
A | G | 16 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(13): Show | 16 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.352-1082T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76289027 | ||||||
| chr15:76289077
|
G | A | 39 | a0001c0001t0004g0102a0001c0001t0004g0231a0001c0001t0004g0232others(36): Show | 39 | HG00438.hp2 HG00621.hp2 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.352-1132C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76289077 | ||||||
| chr15:76289105
|
G | GA | 7 | a0001c0001t0003g0324a0001c0001t0003g0325a0001c0001t0003g0326others(4): Show | 7 | HG02109.hp2 HG02451.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.352-1161_352-1160i others(3): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76289105 | ||||||
| chr15:76289153
|
C | T | 3 | a0002c0002t0004g0228a0002c0002t0004g0257a0002c0002t0004g0260 | 3 | HG00621.hp2 NA18946.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.352-1208G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76289153 | ||||||
| chr15:76289251
|
C | T | 116 | a0001c0001t0001g0088a0001c0001t0002g0002a0001c0001t0002g0116others(113): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.352-1306G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76289251 | ||||||
| chr15:76289357
|
C | T | 1 | a0001c0001t0003g0276 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.352-1412G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76289357 | ||||||
| chr15:76289708
|
T | C | 1 | a0001c0001t0003g0019 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.352-1763A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76289708 | ||||||
| chr15:76289810
|
C | T | 1 | a0001c0001t0003g0276 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.352-1865G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76289810 | ||||||
| chr15:76289866
|
G | A | 1 | a0001c0001t0003g0276 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.352-1921C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76289866 | ||||||
| chr15:76290119
|
A | G | 1 | a0001c0001t0001g0294 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.352-2174T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76290119 | ||||||
| chr15:76290276
|
C | T | 3 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287 | 3 | HG02572.hp1 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.351+2155G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76290276 | ||||||
| chr15:76290331
|
C | A | 1 | a0001c0001t0001g0086 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.351+2100G>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76290331 | ||||||
| chr15:76290333
|
C | CT | 13 | a0001c0001t0001g0029a0001c0001t0001g0055a0001c0001t0001g0073others(10): Show | 13 | HG00741.hp1 HG01167.hp1 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.351+2097dupA | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76290333 | ||||||
| chr15:76290333
|
C | CTT | 46 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(43): Show | 46 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.351+2096_351+2097d others(4): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76290333 | ||||||
| chr15:76290333
|
C | CTTT | 24 | a0001c0001t0003g0015a0001c0001t0003g0111a0001c0001t0003g0112others(21): Show | 24 | HG00438.hp2 HG00621.hp2 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.351+2095_351+2097d others(5): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76290333 | ||||||
| chr15:76290333
|
C | CTTTTTT | 95 | a0001c0001t0001g0088a0001c0001t0002g0002a0001c0001t0002g0116others(92): Show | 96 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(93): Show |
intron_variant | MODIFIER | c.351+2092_351+2097d others(8): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76290333 | ||||||
| chr15:76290333
|
C | CTTTTTTT | 14 | a0001c0001t0002g0134a0001c0001t0002g0139a0001c0001t0002g0145others(11): Show | 14 | HG00738.hp1 HG00741.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.351+2091_351+2097d others(9): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76290333 | ||||||
| chr15:76290333
|
C | CTTTTTTT others(4): Show |
2 | a0001c0001t0003g0275a0001c0001t0003g0277 | 2 | HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.351+2087_351+2097d others(13): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76290333 | ||||||
| chr15:76290333
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0003g0264 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.351+2086_351+2097d others(14): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76290333 | ||||||
| chr15:76290333
|
CT | C | 8 | a0001c0001t0001g0051a0001c0001t0001g0072a0001c0001t0001g0285others(5): Show | 8 | HG02572.hp1 HG02809.hp1 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.351+2097delA | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76290333 | ||||||
| chr15:76290401
|
G | A | 7 | a0001c0001t0003g0110a0001c0001t0003g0111a0001c0001t0003g0112others(4): Show | 7 | HG01891.hp2 HG02280.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.351+2030C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76290401 | ||||||
| chr15:76290566
|
G | A | 1 | a0001c0001t0002g0143 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.351+1865C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76290566 | ||||||
| chr15:76290631
|
C | T | 3 | a0001c0001t0003g0264a0001c0001t0003g0275a0001c0001t0003g0277 | 3 | HG02145.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.351+1800G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76290631 | ||||||
| chr15:76290667
|
T | C | 16 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(13): Show | 16 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.351+1764A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76290667 | ||||||
| chr15:76290716
|
T | C | 1 | a0001c0001t0003g0115 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.351+1715A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76290716 | ||||||
| chr15:76290718
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.351+1713A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76290718 | ||||||
| chr15:76290766
|
A | G | 1 | a0001c0001t0002g0054 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.351+1665T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76290766 | ||||||
| chr15:76290915
|
A | G | 1 | a0001c0001t0011g0330 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.351+1516T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76290915 | ||||||
| chr15:76290951
|
T | C | 131 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(128): Show | 132 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.351+1480A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76290951 | ||||||
| chr15:76290957
|
T | G | 1 | a0001c0001t0001g0317 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.351+1474A>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76290957 | ||||||
| chr15:76291337
|
C | A | 2 | a0001c0001t0003g0273a0001c0001t0003g0274 | 2 | HG01255.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.351+1094G>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76291337 | ||||||
| chr15:76291369
|
C | A | 2 | a0001c0001t0003g0273a0001c0001t0003g0274 | 2 | HG01255.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.351+1062G>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76291369 | ||||||
| chr15:76291446
|
G | GA | 258 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(255): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.351+984dupT | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76291446 | ||||||
| chr15:76291446
|
G | GAA | 52 | a0001c0001t0001g0067a0001c0001t0002g0145a0001c0001t0002g0159others(49): Show | 52 | HG00438.hp1 HG00438.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.351+983_351+984dup others(2): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76291446 | ||||||
| chr15:76291446
|
G | GAAA | 7 | a0001c0001t0002g0174a0001c0001t0003g0264a0001c0001t0003g0275others(4): Show | 7 | HG01175.hp1 HG01884.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.351+982_351+984dup others(3): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76291446 | ||||||
| chr15:76291449
|
A | AG | 5 | a0001c0001t0006g0278a0001c0001t0006g0279a0001c0001t0006g0280others(2): Show | 5 | HG02055.hp1 HG02559.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.351+981_351+982ins others(1): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76291449 | ||||||
| chr15:76291473
|
A | G | 3 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287 | 3 | HG02572.hp1 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.351+958T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76291473 | ||||||
| chr15:76291479
|
G | A | 1 | a0001c0001t0001g0317 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.351+952C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76291479 | ||||||
| chr15:76291533
|
G | A | 2 | a0001c0001t0003g0005a0001c0001t0003g0006 | 2 | HG01243.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.351+898C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76291533 | ||||||
| chr15:76291557
|
T | C | 1 | a0001c0001t0002g0191 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.351+874A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76291557 | ||||||
| chr15:76291601
|
T | C | 1 | a0001c0001t0006g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.351+830A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76291601 | ||||||
| chr15:76291606
|
C | T | 324 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(321): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.351+825G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76291606 | ||||||
| chr15:76291622
|
C | A | 1 | a0001c0001t0001g0321 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.351+809G>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76291622 | ||||||
| chr15:76291703
|
ATGGCGCC others(14): Show |
A | 17 | a0001c0001t0004g0102a0002c0002t0001g0252a0002c0002t0004g0228others(14): Show | 17 | HG00438.hp2 HG00621.hp2 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.351+707_351+727del others(21): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76291703 | ||||||
| chr15:76291721
|
A | C | 1 | a0001c0001t0003g0327 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.351+710T>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76291721 | ||||||
| chr15:76291847
|
G | A | 1 | a0001c0001t0003g0024 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.351+584C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76291847 | ||||||
| chr15:76291879
|
C | T | 1 | a0001c0001t0001g0303 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.351+552G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76291879 | ||||||
| chr15:76292345
|
T | TA | 122 | a0001c0001t0002g0002a0001c0001t0002g0116a0001c0001t0002g0117others(119): Show | 123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.351+85dupT | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 4/11 | chr15 | 76292345 | ||||||
| chr15:76293448
|
A | G | 5 | a0001c0001t0004g0235a0001c0001t0004g0248a0001c0001t0004g0249others(2): Show | 5 | HG02809.hp2 HG02886.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.187-748T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 2/11 | chr15 | 76293448 | ||||||
| chr15:76293456
|
A | G | 5 | a0001c0001t0006g0278a0001c0001t0006g0279a0001c0001t0006g0280others(2): Show | 5 | HG02055.hp1 HG02559.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.187-756T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 2/11 | chr15 | 76293456 | ||||||
| chr15:76293839
|
G | A | 2 | a0001c0001t0003g0328a0001c0001t0003g0329 | 2 | HG02723.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.187-1139C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 2/11 | chr15 | 76293839 | ||||||
| chr15:76293991
|
C | CA | 132 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(129): Show | 133 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.187-1292dupT | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 2/11 | chr15 | 76293991 | ||||||
| chr15:76294039
|
T | C | 9 | a0001c0001t0003g0324a0001c0001t0003g0325a0001c0001t0003g0326others(6): Show | 9 | HG02109.hp2 HG02451.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.187-1339A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 2/11 | chr15 | 76294039 | ||||||
| chr15:76294071
|
A | G | 3 | a0001c0001t0003g0264a0001c0001t0003g0275a0001c0001t0003g0277 | 3 | HG02145.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.187-1371T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 2/11 | chr15 | 76294071 | ||||||
| chr15:76294179
|
A | G | 1 | a0001c0001t0002g0167 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.186+1412T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 2/11 | chr15 | 76294179 | ||||||
| chr15:76294268
|
C | A | 1 | a0001c0001t0002g0140 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.186+1323G>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 2/11 | chr15 | 76294268 | ||||||
| chr15:76294356
|
A | G | 2 | a0001c0001t0001g0322a0001c0001t0001g0323 | 2 | HG01243.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.186+1235T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 2/11 | chr15 | 76294356 | ||||||
| chr15:76294490
|
T | C | 1 | a0001c0001t0003g0276 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.186+1101A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 2/11 | chr15 | 76294490 | ||||||
| chr15:76294642
|
A | C | 132 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(129): Show | 133 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.186+949T>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 2/11 | chr15 | 76294642 | ||||||
| chr15:76294817
|
G | A | 9 | a0001c0001t0003g0324a0001c0001t0003g0325a0001c0001t0003g0326others(6): Show | 9 | HG02109.hp2 HG02451.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.186+774C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 2/11 | chr15 | 76294817 | ||||||
| chr15:76294978
|
G | C | 132 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(129): Show | 133 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.186+613C>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 2/11 | chr15 | 76294978 | ||||||
| chr15:76295030
|
T | C | 39 | a0001c0001t0004g0102a0001c0001t0004g0231a0001c0001t0004g0232others(36): Show | 39 | HG00438.hp2 HG00621.hp2 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.186+561A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 2/11 | chr15 | 76295030 | ||||||
| chr15:76295090
|
A | G | 2 | a0001c0001t0002g0222a0001c0001t0002g0227 | 2 | HG01081.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.186+501T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 2/11 | chr15 | 76295090 | ||||||
| chr15:76295146
|
T | C | 132 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(129): Show | 133 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.186+445A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 2/11 | chr15 | 76295146 | ||||||
| chr15:76295318
|
C | G | 1 | a0001c0001t0002g0210 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.186+273G>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 2/11 | chr15 | 76295318 | ||||||
| chr15:76295436
|
C | T | 113 | a0001c0001t0002g0002a0001c0001t0002g0116a0001c0001t0002g0117others(110): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.186+155G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 2/11 | chr15 | 76295436 | ||||||
| chr15:76295439
|
T | C | 1 | a0001c0001t0012g0268 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.186+152A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 2/11 | chr15 | 76295439 | ||||||
| chr15:76295575
|
C | A | 1 | a0001c0001t0011g0330 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.186+16G>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 2/11 | chr15 | 76295575 | ||||||
| chr15:76295584
|
T | C | 1 | a0001c0001t0002g0198 | 1 | HG00099.hp2 | splice_region_variant&intron_variant | LOW | c.186+7A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 2/11 | chr15 | 76295584 | ||||||
| chr15:76295786
|
G | GT | 54 | a0001c0001t0001g0035a0001c0001t0001g0043a0001c0001t0001g0046others(51): Show | 54 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.40-50dupA | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76295786 | ||||||
| chr15:76295786
|
G | GTT | 17 | a0001c0001t0001g0293a0001c0001t0001g0317a0001c0001t0003g0015others(14): Show | 17 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.40-51_40-50dupAA | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76295786 | ||||||
| chr15:76295786
|
GT | G | 6 | a0001c0001t0001g0068a0001c0001t0001g0082a0001c0001t0001g0287others(3): Show | 6 | HG01361.hp1 HG02965.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.40-50delA | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76295786 | ||||||
| chr15:76295809
|
T | A | 1 | a0001c0001t0003g0115 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.40-72A>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76295809 | ||||||
| chr15:76295936
|
C | CCTTTTTT others(8): Show |
3 | a0001c0001t0004g0233a0001c0001t0004g0243a0001c0001t0004g0245 | 3 | HG02896.hp1 HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.40-200_40-199insAA others(13): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76295936 | ||||||
| chr15:76295936
|
C | CCTTTTTT others(9): Show |
3 | a0001c0001t0004g0232a0001c0001t0004g0242a0001c0001t0004g0246 | 3 | HG02055.hp2 HG02717.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.40-200_40-199insAA others(14): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76295936 | ||||||
| chr15:76295936
|
C | CTTT | 14 | a0001c0001t0002g0126a0001c0001t0003g0015a0001c0001t0003g0020others(11): Show | 14 | HG00735.hp1 HG01081.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.40-202_40-200dupAA others(1): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76295936 | ||||||
| chr15:76295936
|
C | CTTTT | 8 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(5): Show | 8 | HG01106.hp2 HG02055.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.40-203_40-200dupAA others(2): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76295936 | ||||||
| chr15:76295936
|
C | CTTTTTTT others(8): Show |
6 | a0001c0001t0004g0231a0001c0001t0004g0234a0001c0001t0004g0237others(3): Show | 6 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.40-214_40-200dupAA others(13): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76295936 | ||||||
| chr15:76295936
|
C | CTTTTTTT others(9): Show |
1 | a0001c0001t0004g0236 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.40-215_40-200dupAA others(14): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76295936 | ||||||
| chr15:76295936
|
C | CTTTTTTT others(10): Show |
3 | a0001c0001t0002g0143a0001c0001t0003g0276a0002c0002t0004g0262 | 3 | HG03239.hp2 NA18957.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.40-216_40-200dupAA others(15): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76295936 | ||||||
| chr15:76295936
|
C | CTTTTTTT others(11): Show |
8 | a0001c0001t0004g0272a0002c0002t0004g0228a0002c0002t0004g0229others(5): Show | 8 | HG00438.hp2 HG01123.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.40-217_40-200dupAA others(16): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76295936 | ||||||
| chr15:76295936
|
C | CTTTTTTT others(12): Show |
3 | a0001c0001t0002g0135a0001c0001t0002g0142a0002c0002t0004g0260 | 3 | HG00621.hp2 NA18970.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.40-218_40-200dupAA others(17): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76295936 | ||||||
| chr15:76295936
|
C | CTTTTTTT others(13): Show |
15 | a0001c0001t0002g0129a0001c0001t0002g0137a0001c0001t0002g0141others(12): Show | 15 | HG01081.hp1 HG01175.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.40-219_40-200dupAA others(18): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76295936 | ||||||
| chr15:76295936
|
C | CTTTTTTT others(14): Show |
29 | a0001c0001t0002g0002a0001c0001t0002g0116a0001c0001t0002g0117others(26): Show | 30 | HG00544.hp1 HG00639.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.40-220_40-200dupAA others(19): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76295936 | ||||||
| chr15:76295936
|
C | CTTTTTTT others(15): Show |
27 | a0001c0001t0002g0118a0001c0001t0002g0120a0001c0001t0002g0131others(24): Show | 27 | HG00099.hp1 HG00597.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.40-221_40-200dupAA others(20): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76295936 | ||||||
| chr15:76295936
|
C | CTTTTTTT others(16): Show |
15 | a0001c0001t0002g0136a0001c0001t0002g0149a0001c0001t0002g0150others(12): Show | 15 | HG00673.hp2 HG00733.hp1 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.40-222_40-200dupAA others(21): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76295936 | ||||||
| chr15:76295936
|
C | CTTTTTTT others(17): Show |
6 | a0001c0001t0002g0138a0001c0001t0002g0174a0001c0001t0002g0187others(3): Show | 6 | HG01074.hp1 HG01256.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.40-200_40-199insAA others(22): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76295936 | ||||||
| chr15:76295936
|
C | CTTTTTTT others(18): Show |
3 | a0001c0001t0002g0212a0001c0001t0003g0264a0001c0001t0003g0277 | 3 | HG02145.hp1 HG02630.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.40-200_40-199insAA others(23): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76295936 | ||||||
| chr15:76295936
|
C | CTTTTTTT others(19): Show |
8 | a0001c0001t0002g0155a0001c0001t0002g0167a0001c0001t0002g0181others(5): Show | 8 | HG01978.hp1 HG01993.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.40-200_40-199insAA others(24): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76295936 | ||||||
| chr15:76295936
|
C | CTTTTTTT others(20): Show |
1 | a0001c0001t0002g0204 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.40-200_40-199insAA others(25): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76295936 | ||||||
| chr15:76295936
|
C | CTTTTTTT others(21): Show |
3 | a0001c0001t0002g0148a0001c0001t0004g0235a0001c0001t0009g0239 | 3 | HG01256.hp2 HG02965.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.40-200_40-199insAA others(26): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76295936 | ||||||
| chr15:76295936
|
C | CTTTTTTT others(22): Show |
1 | a0001c0001t0002g0225 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.40-200_40-199insAA others(27): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76295936 | ||||||
| chr15:76295936
|
C | CTTTTTTT others(23): Show |
2 | a0001c0001t0002g0147a0001c0001t0002g0190 | 2 | HG01123.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.40-200_40-199insAA others(28): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76295936 | ||||||
| chr15:76295936
|
C | CTTTTTTT others(25): Show |
1 | a0001c0001t0002g0207 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.40-200_40-199insAA others(30): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76295936 | ||||||
| chr15:76295936
|
C | CTTTTTTT others(26): Show |
2 | a0001c0001t0002g0220a0002c0002t0004g0247 | 2 | HG03688.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.40-200_40-199insAA others(31): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76295936 | ||||||
| chr15:76295936
|
C | CTTTTTTT others(29): Show |
1 | a0001c0001t0002g0195 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.40-200_40-199insAA others(34): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76295936 | ||||||
| chr15:76295936
|
CT | C | 8 | a0001c0001t0001g0053a0001c0001t0001g0081a0001c0001t0001g0084others(5): Show | 8 | HG02258.hp1 NA18985.hp1 NA19030.hp1 others(5): Show |
intron_variant | MODIFIER | c.40-200delA | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76295936 | ||||||
| chr15:76295936
|
CTT | C | 116 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(113): Show | 117 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.40-201_40-200delAA | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76295936 | ||||||
| chr15:76295936
|
CTTT | C | 10 | a0001c0001t0001g0052a0001c0001t0001g0069a0001c0001t0001g0086others(7): Show | 10 | HG01496.hp1 HG01943.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.40-202_40-200delAA others(1): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76295936 | ||||||
| chr15:76295981
|
G | A | 6 | a0001c0001t0003g0110a0001c0001t0003g0111a0001c0001t0003g0112others(3): Show | 6 | HG01891.hp2 HG02280.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.40-244C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76295981 | ||||||
| chr15:76296002
|
CGCGT | C | 132 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(129): Show | 133 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.40-269_40-266delAC others(2): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76296002 | ||||||
| chr15:76296006
|
T | C | 186 | a0001c0001t0002g0002a0001c0001t0002g0116a0001c0001t0002g0117others(183): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.40-269A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76296006 | ||||||
| chr15:76296046
|
T | C | 1 | a0001c0001t0001g0322 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.40-309A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76296046 | ||||||
| chr15:76296058
|
G | A | 1 | a0002c0002t0004g0247 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.40-321C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76296058 | ||||||
| chr15:76296279
|
G | A | 1 | a0001c0001t0002g0144 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.40-542C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76296279 | ||||||
| chr15:76296465
|
T | C | 17 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(14): Show | 17 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.40-728A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76296465 | ||||||
| chr15:76296513
|
T | C | 132 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(129): Show | 133 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.40-776A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76296513 | ||||||
| chr15:76296745
|
T | C | 1 | a0001c0001t0002g0166 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.40-1008A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76296745 | ||||||
| chr15:76296871
|
C | A | 1 | a0001c0001t0003g0113 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.40-1134G>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76296871 | ||||||
| chr15:76296910
|
G | A | 3 | a0001c0001t0003g0264a0001c0001t0003g0275a0001c0001t0003g0277 | 3 | HG02145.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.40-1173C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76296910 | ||||||
| chr15:76296921
|
A | G | 113 | a0001c0001t0002g0002a0001c0001t0002g0116a0001c0001t0002g0117others(110): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.40-1184T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76296921 | ||||||
| chr15:76296938
|
T | C | 122 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(119): Show | 123 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.40-1201A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76296938 | ||||||
| chr15:76296975
|
A | G | 132 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(129): Show | 133 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.40-1238T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76296975 | ||||||
| chr15:76297104
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.40-1367C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76297104 | ||||||
| chr15:76297137
|
A | G | 1 | a0002c0002t0004g0260 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.40-1400T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76297137 | ||||||
| chr15:76297154
|
G | A | 132 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(129): Show | 133 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.40-1417C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76297154 | ||||||
| chr15:76297426
|
A | T | 113 | a0001c0001t0002g0002a0001c0001t0002g0116a0001c0001t0002g0117others(110): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.40-1689T>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76297426 | ||||||
| chr15:76297489
|
T | A | 1 | a0001c0001t0003g0276 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.40-1752A>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76297489 | ||||||
| chr15:76297526
|
A | T | 15 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0148others(12): Show | 15 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(12): Show |
intron_variant | MODIFIER | c.40-1789T>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76297526 | ||||||
| chr15:76297882
|
C | T | 9 | a0001c0001t0003g0324a0001c0001t0003g0325a0001c0001t0003g0326others(6): Show | 9 | HG02109.hp2 HG02451.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.40-2145G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76297882 | ||||||
| chr15:76297996
|
T | C | 1 | a0001c0001t0002g0220 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.40-2259A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76297996 | ||||||
| chr15:76298060
|
TGA | T | 115 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(112): Show | 116 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.40-2325_40-2324del others(2): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76298060 | ||||||
| chr15:76298067
|
G | C | 5 | a0001c0001t0006g0278a0001c0001t0006g0279a0001c0001t0006g0280others(2): Show | 5 | HG02055.hp1 HG02559.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.40-2330C>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76298067 | ||||||
| chr15:76298095
|
T | C | 1 | a0001c0001t0001g0321 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.40-2358A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76298095 | ||||||
| chr15:76298165
|
G | C | 1 | a0001c0001t0003g0028 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.40-2428C>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76298165 | ||||||
| chr15:76298509
|
G | A | 325 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(322): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.40-2772C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76298509 | ||||||
| chr15:76298604
|
G | A | 16 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(13): Show | 16 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.40-2867C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76298604 | ||||||
| chr15:76298745
|
C | G | 306 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(303): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.40-3008G>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76298745 | ||||||
| chr15:76298769
|
C | T | 12 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0044others(9): Show | 12 | NA18945.hp1 NA18968.hp1 NA18971.hp2 others(9): Show |
intron_variant | MODIFIER | c.40-3032G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76298769 | ||||||
| chr15:76298848
|
C | A | 1 | a0001c0001t0003g0114 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.40-3111G>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76298848 | ||||||
| chr15:76298852
|
A | G | 132 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(129): Show | 133 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.40-3115T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76298852 | ||||||
| chr15:76298933
|
C | G | 327 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(324): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.40-3196G>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76298933 | ||||||
| chr15:76299016
|
T | C | 10 | a0001c0001t0003g0324a0001c0001t0003g0325a0001c0001t0003g0326others(7): Show | 10 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.40-3279A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76299016 | ||||||
| chr15:76299052
|
T | G | 1 | a0001c0001t0003g0276 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.40-3315A>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76299052 | ||||||
| chr15:76299240
|
C | G | 1 | a0001c0001t0001g0092 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.40-3503G>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76299240 | ||||||
| chr15:76299432
|
C | T | 1 | a0001c0001t0001g0046 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.40-3695G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76299432 | ||||||
| chr15:76299479
|
T | C | 132 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(129): Show | 133 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.40-3742A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76299479 | ||||||
| chr15:76299528
|
G | A | 1 | a0001c0001t0001g0070 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.40-3791C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76299528 | ||||||
| chr15:76299546
|
G | A | 132 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(129): Show | 133 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.40-3809C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76299546 | ||||||
| chr15:76299561
|
G | T | 1 | a0001c0001t0001g0321 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.40-3824C>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76299561 | ||||||
| chr15:76299708
|
G | A | 15 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0148others(12): Show | 15 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(12): Show |
intron_variant | MODIFIER | c.40-3971C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76299708 | ||||||
| chr15:76299947
|
G | A | 2 | a0001c0001t0003g0273a0001c0001t0003g0274 | 2 | HG01255.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.40-4210C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76299947 | ||||||
| chr15:76300263
|
C | T | 1 | a0001c0001t0003g0276 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.40-4526G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76300263 | ||||||
| chr15:76300327
|
C | A | 16 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(13): Show | 16 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.40-4590G>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76300327 | ||||||
| chr15:76300382
|
T | C | 1 | a0001c0001t0001g0310 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.40-4645A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76300382 | ||||||
| chr15:76300397
|
G | C | 132 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(129): Show | 133 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.40-4660C>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76300397 | ||||||
| chr15:76300557
|
C | T | 3 | a0001c0001t0001g0321a0001c0001t0001g0322a0001c0001t0001g0323 | 3 | HG01243.hp2 HG01496.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.40-4820G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76300557 | ||||||
| chr15:76300742
|
T | C | 1 | a0001c0001t0003g0276 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.40-5005A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76300742 | ||||||
| chr15:76300833
|
A | C | 1 | a0001c0001t0003g0276 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.40-5096T>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76300833 | ||||||
| chr15:76301027
|
G | A | 1 | a0001c0001t0001g0323 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.40-5290C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76301027 | ||||||
| chr15:76301044
|
C | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | NA18969.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.40-5307G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76301044 | ||||||
| chr15:76301231
|
T | C | 1 | a0001c0001t0001g0041 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.40-5494A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76301231 | ||||||
| chr15:76301286
|
T | C | 10 | a0001c0001t0003g0324a0001c0001t0003g0325a0001c0001t0003g0326others(7): Show | 10 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.40-5549A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76301286 | ||||||
| chr15:76301299
|
G | T | 132 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(129): Show | 133 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.40-5562C>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76301299 | ||||||
| chr15:76301313
|
C | T | 132 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(129): Show | 133 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.40-5576G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76301313 | ||||||
| chr15:76301437
|
G | A | 17 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(14): Show | 17 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.40-5700C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76301437 | ||||||
| chr15:76301526
|
T | C | 1 | a0001c0001t0012g0268 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.40-5789A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76301526 | ||||||
| chr15:76301535
|
A | T | 132 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(129): Show | 133 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.40-5798T>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76301535 | ||||||
| chr15:76301537
|
C | T | 132 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(129): Show | 133 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.40-5800G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76301537 | ||||||
| chr15:76301659
|
G | A | 17 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(14): Show | 17 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.40-5922C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76301659 | ||||||
| chr15:76301704
|
TCAAAA | T | 56 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0110others(53): Show | 56 | HG00438.hp2 HG00621.hp2 HG01109.hp2 others(53): Show |
intron_variant | MODIFIER | c.40-5972_40-5968del others(5): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76301704 | ||||||
| chr15:76301704
|
TCAAAACA others(3): Show |
T | 133 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(130): Show | 134 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.40-5977_40-5968del others(10): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76301704 | ||||||
| chr15:76302154
|
T | C | 1 | a0001c0001t0011g0330 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.40-6417A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76302154 | ||||||
| chr15:76302254
|
A | C | 17 | a0001c0001t0004g0102a0002c0002t0001g0252a0002c0002t0004g0228others(14): Show | 17 | HG00438.hp2 HG00621.hp2 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.40-6517T>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76302254 | ||||||
| chr15:76302383
|
G | GA | 287 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(284): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.40-6647dupT | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76302383 | ||||||
| chr15:76302383
|
G | GAA | 10 | a0001c0001t0001g0043a0001c0001t0002g0118a0001c0001t0002g0119others(7): Show | 10 | HG01175.hp2 HG02559.hp2 HG03098.hp2 others(7): Show |
intron_variant | MODIFIER | c.40-6648_40-6647dup others(2): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76302383 | ||||||
| chr15:76302576
|
CT | C | 39 | a0001c0001t0004g0102a0001c0001t0004g0231a0001c0001t0004g0232others(36): Show | 39 | HG00438.hp2 HG00621.hp2 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.40-6840delA | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76302576 | ||||||
| chr15:76302612
|
C | A | 132 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(129): Show | 133 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.40-6875G>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76302612 | ||||||
| chr15:76302730
|
G | C | 1 | a0001c0001t0002g0211 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.40-6993C>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76302730 | ||||||
| chr15:76302733
|
G | C | 1 | a0001c0001t0001g0310 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.40-6996C>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76302733 | ||||||
| chr15:76302786
|
T | C | 1 | a0001c0001t0003g0276 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.40-7049A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76302786 | ||||||
| chr15:76302828
|
A | C | 19 | a0001c0001t0002g0120a0001c0001t0002g0136a0001c0001t0002g0137others(16): Show | 19 | HG00673.hp2 HG00733.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.40-7091T>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76302828 | ||||||
| chr15:76302874
|
T | C | 1 | a0001c0001t0003g0028 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.40-7137A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76302874 | ||||||
| chr15:76302898
|
G | A | 1 | a0001c0001t0004g0272 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.40-7161C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76302898 | ||||||
| chr15:76302898
|
G | C | 132 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(129): Show | 133 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.40-7161C>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76302898 | ||||||
| chr15:76303063
|
G | C | 132 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(129): Show | 133 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.40-7326C>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76303063 | ||||||
| chr15:76303198
|
T | C | 132 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(129): Show | 133 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.40-7461A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76303198 | ||||||
| chr15:76303208
|
T | C | 46 | a0001c0001t0003g0110a0001c0001t0003g0111a0001c0001t0003g0112others(43): Show | 46 | HG00438.hp2 HG00621.hp2 HG01109.hp2 others(43): Show |
intron_variant | MODIFIER | c.40-7471A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76303208 | ||||||
| chr15:76303210
|
C | T | 135 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(132): Show | 136 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.40-7473G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76303210 | ||||||
| chr15:76303375
|
A | G | 324 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(321): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.40-7638T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76303375 | ||||||
| chr15:76303519
|
GT | G | 56 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0110others(53): Show | 56 | HG00438.hp2 HG00621.hp2 HG01109.hp2 others(53): Show |
intron_variant | MODIFIER | c.40-7783delA | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76303519 | ||||||
| chr15:76303539
|
A | T | 1 | a0001c0001t0001g0288 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.40-7802T>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76303539 | ||||||
| chr15:76303752
|
T | C | 13 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0071others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.39+7598A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76303752 | ||||||
| chr15:76303868
|
A | C | 3 | a0001c0001t0003g0264a0001c0001t0003g0275a0001c0001t0003g0277 | 3 | HG02145.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.39+7482T>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76303868 | ||||||
| chr15:76303874
|
G | C | 132 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(129): Show | 133 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.39+7476C>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76303874 | ||||||
| chr15:76303909
|
C | T | 122 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(119): Show | 123 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.39+7441G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76303909 | ||||||
| chr15:76304149
|
A | G | 132 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(129): Show | 133 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.39+7201T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76304149 | ||||||
| chr15:76304191
|
G | GA | 10 | a0001c0001t0003g0324a0001c0001t0003g0325a0001c0001t0003g0326others(7): Show | 10 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.39+7158dupT | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76304191 | ||||||
| chr15:76304217
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.39+7133G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76304217 | ||||||
| chr15:76304359
|
G | A | 122 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(119): Show | 123 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.39+6991C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76304359 | ||||||
| chr15:76304401
|
A | G | 3 | a0001c0001t0003g0264a0001c0001t0003g0275a0001c0001t0003g0277 | 3 | HG02145.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.39+6949T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76304401 | ||||||
| chr15:76304449
|
G | C | 3 | a0001c0001t0003g0264a0001c0001t0003g0275a0001c0001t0003g0277 | 3 | HG02145.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.39+6901C>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76304449 | ||||||
| chr15:76304532
|
C | T | 1 | a0001c0001t0011g0330 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.39+6818G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76304532 | ||||||
| chr15:76304661
|
CA | C | 51 | a0001c0001t0001g0045a0001c0001t0002g0002a0001c0001t0002g0116others(48): Show | 52 | HG00438.hp2 HG00544.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.39+6688delT | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76304661 | ||||||
| chr15:76304681
|
T | G | 1 | a0001c0001t0001g0315 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.39+6669A>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76304681 | ||||||
| chr15:76304716
|
G | C | 172 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287others(169): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.39+6634C>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76304716 | ||||||
| chr15:76304763
|
G | A | 3 | a0001c0001t0003g0264a0001c0001t0003g0275a0001c0001t0003g0277 | 3 | HG02145.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.39+6587C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76304763 | ||||||
| chr15:76304912
|
G | A | 3 | a0001c0001t0001g0043a0001c0001t0001g0078a0001c0001t0001g0105 | 3 | HG00280.hp1 HG01175.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.39+6438C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76304912 | ||||||
| chr15:76304914
|
G | A | 5 | a0001c0001t0004g0235a0001c0001t0004g0248a0001c0001t0004g0249others(2): Show | 5 | HG02809.hp2 HG02886.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.39+6436C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76304914 | ||||||
| chr15:76304960
|
G | A | 3 | a0001c0001t0003g0264a0001c0001t0003g0275a0001c0001t0003g0277 | 3 | HG02145.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.39+6390C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76304960 | ||||||
| chr15:76304975
|
A | G | 325 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(322): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.39+6375T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76304975 | ||||||
| chr15:76305040
|
CA | C | 129 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(126): Show | 130 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.39+6309delT | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76305040 | ||||||
| chr15:76305049
|
A | G | 3 | a0001c0001t0003g0264a0001c0001t0003g0275a0001c0001t0003g0277 | 3 | HG02145.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.39+6301T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76305049 | ||||||
| chr15:76305073
|
A | ATCCTCCG others(32): Show |
3 | a0001c0001t0003g0264a0001c0001t0003g0275a0001c0001t0003g0277 | 3 | HG02145.hp1 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.39+6238_39+6276dup others(39): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76305073 | ||||||
| chr15:76305456
|
C | T | 1 | a0001c0001t0003g0276 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.39+5894G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76305456 | ||||||
| chr15:76305480
|
A | G | 1 | a0001c0001t0004g0238 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.39+5870T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76305480 | ||||||
| chr15:76305498
|
T | C | 2 | a0001c0001t0003g0005a0001c0001t0003g0006 | 2 | HG01243.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.39+5852A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76305498 | ||||||
| chr15:76305808
|
T | C | 1 | a0001c0001t0002g0209 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.39+5542A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76305808 | ||||||
| chr15:76305859
|
G | GTT | 3 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0322 | 3 | HG01243.hp2 HG02735.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.39+5489_39+5490dup others(2): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76305859 | ||||||
| chr15:76305859
|
G | GTTT | 127 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(124): Show | 128 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.39+5490_39+5491ins others(3): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76305859 | ||||||
| chr15:76305862
|
G | T | 132 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(129): Show | 133 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.39+5488C>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76305862 | ||||||
| chr15:76305862
|
GT | G | 7 | a0001c0001t0002g0127a0001c0001t0003g0005a0001c0001t0003g0006others(4): Show | 7 | HG01243.hp1 HG02080.hp2 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.39+5487delA | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76305862 | ||||||
| chr15:76305911
|
T | C | 2 | a0001c0001t0003g0273a0001c0001t0003g0274 | 2 | HG01255.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.39+5439A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76305911 | ||||||
| chr15:76305981
|
G | A | 1 | a0001c0001t0001g0083 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.39+5369C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76305981 | ||||||
| chr15:76306075
|
A | G | 1 | a0001c0001t0001g0044 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.39+5275T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76306075 | ||||||
| chr15:76306109
|
T | C | 2 | a0001c0001t0004g0245a0001c0001t0004g0246 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.39+5241A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76306109 | ||||||
| chr15:76306211
|
T | C | 131 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(128): Show | 132 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.39+5139A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76306211 | ||||||
| chr15:76306267
|
C | CT | 110 | a0001c0001t0002g0002a0001c0001t0002g0116a0001c0001t0002g0117others(107): Show | 111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.39+5082dupA | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76306267 | ||||||
| chr15:76306267
|
C | CTTTTTTT others(1): Show |
8 | a0001c0001t0003g0324a0001c0001t0003g0325a0001c0001t0003g0326others(5): Show | 8 | HG02109.hp2 HG02257.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.39+5075_39+5082dup others(8): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76306267 | ||||||
| chr15:76306267
|
C | CTTTTTTT others(3): Show |
7 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0308others(4): Show | 7 | HG01168.hp2 HG01346.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.39+5073_39+5082dup others(10): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76306267 | ||||||
| chr15:76306267
|
C | CTTTTTTT others(4): Show |
90 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(87): Show | 91 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.39+5072_39+5082dup others(11): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76306267 | ||||||
| chr15:76306267
|
C | CTTTTTTT others(5): Show |
24 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0033others(21): Show | 24 | HG01070.hp1 HG01175.hp2 HG01978.hp2 others(21): Show |
intron_variant | MODIFIER | c.39+5071_39+5082dup others(12): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76306267 | ||||||
| chr15:76306267
|
CT | C | 69 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(66): Show | 69 | HG00438.hp2 HG00621.hp2 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.39+5082delA | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76306267 | ||||||
| chr15:76306302
|
A | T | 317 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(314): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.39+5048T>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76306302 | ||||||
| chr15:76306353
|
G | A | 8 | a0001c0001t0003g0324a0001c0001t0003g0325a0001c0001t0003g0326others(5): Show | 8 | HG02109.hp2 HG02723.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.39+4997C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76306353 | ||||||
| chr15:76306553
|
T | C | 1 | a0001c0001t0001g0321 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.39+4797A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76306553 | ||||||
| chr15:76306577
|
C | T | 122 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(119): Show | 123 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.39+4773G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76306577 | ||||||
| chr15:76306700
|
A | G | 39 | a0001c0001t0004g0102a0001c0001t0004g0231a0001c0001t0004g0232others(36): Show | 39 | HG00438.hp2 HG00621.hp2 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.39+4650T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76306700 | ||||||
| chr15:76306765
|
T | C | 1 | a0001c0001t0003g0109 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.39+4585A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76306765 | ||||||
| chr15:76306838
|
A | G | 4 | a0001c0001t0003g0106a0001c0001t0003g0107a0001c0001t0003g0108others(1): Show | 4 | HG02630.hp2 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.39+4512T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76306838 | ||||||
| chr15:76306928
|
GCTCT | G | 8 | a0001c0001t0003g0324a0001c0001t0003g0325a0001c0001t0003g0326others(5): Show | 8 | HG02109.hp2 HG02723.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.39+4418_39+4421del others(4): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76306928 | ||||||
| chr15:76307055
|
T | C | 6 | a0001c0001t0003g0324a0001c0001t0003g0325a0001c0001t0003g0326others(3): Show | 6 | HG02109.hp2 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.39+4295A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76307055 | ||||||
| chr15:76307134
|
CATAA | C | 3 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0001g0311 | 3 | HG01346.hp1 HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.39+4212_39+4215del others(4): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76307134 | ||||||
| chr15:76307159
|
ATTC | A | 5 | a0001c0001t0006g0278a0001c0001t0006g0279a0001c0001t0006g0280others(2): Show | 5 | HG02055.hp1 HG02559.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.39+4188_39+4190del others(3): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76307159 | ||||||
| chr15:76307184
|
G | A | 2 | a0001c0001t0004g0236a0001c0001t0004g0237 | 2 | HG02922.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.39+4166C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76307184 | ||||||
| chr15:76307260
|
G | T | 323 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(320): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.39+4090C>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76307260 | ||||||
| chr15:76307487
|
AC | A | 17 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(14): Show | 17 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.39+3862delG | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76307487 | ||||||
| chr15:76307534
|
C | T | 1 | a0001c0001t0001g0323 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.39+3816G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76307534 | ||||||
| chr15:76307551
|
A | T | 39 | a0001c0001t0004g0102a0001c0001t0004g0231a0001c0001t0004g0232others(36): Show | 39 | HG00438.hp2 HG00621.hp2 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.39+3799T>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76307551 | ||||||
| chr15:76307575
|
T | C | 132 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(129): Show | 133 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.39+3775A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76307575 | ||||||
| chr15:76307622
|
G | A | 3 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014 | 3 | NA18960.hp1 NA18969.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.39+3728C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76307622 | ||||||
| chr15:76307653
|
A | AT | 17 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0017others(14): Show | 17 | HG00735.hp1 HG01081.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.39+3696dupA | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76307653 | ||||||
| chr15:76307794
|
C | A | 1 | a0001c0001t0001g0310 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.39+3556G>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76307794 | ||||||
| chr15:76307818
|
T | G | 1 | a0001c0001t0002g0204 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.39+3532A>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76307818 | ||||||
| chr15:76307881
|
A | T | 54 | a0001c0001t0003g0005a0001c0001t0003g0006a0001c0001t0003g0110others(51): Show | 54 | HG00438.hp2 HG00621.hp2 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.39+3469T>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76307881 | ||||||
| chr15:76307983
|
T | C | 1 | a0002c0002t0004g0283 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.39+3367A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76307983 | ||||||
| chr15:76308264
|
G | A | 1 | a0001c0001t0003g0276 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.39+3086C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76308264 | ||||||
| chr15:76308290
|
C | G | 325 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(322): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.39+3060G>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76308290 | ||||||
| chr15:76308421
|
T | C | 1 | a0001c0001t0001g0086 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.39+2929A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76308421 | ||||||
| chr15:76308513
|
A | G | 15 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0148others(12): Show | 15 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(12): Show |
intron_variant | MODIFIER | c.39+2837T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76308513 | ||||||
| chr15:76308573
|
G | GC | 10 | a0001c0001t0003g0324a0001c0001t0003g0325a0001c0001t0003g0326others(7): Show | 10 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.39+2776dupG | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76308573 | ||||||
| chr15:76308708
|
T | C | 46 | a0001c0001t0003g0110a0001c0001t0003g0111a0001c0001t0003g0112others(43): Show | 46 | HG00438.hp2 HG00621.hp2 HG01109.hp2 others(43): Show |
intron_variant | MODIFIER | c.39+2642A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76308708 | ||||||
| chr15:76308734
|
A | C | 46 | a0001c0001t0003g0110a0001c0001t0003g0111a0001c0001t0003g0112others(43): Show | 46 | HG00438.hp2 HG00621.hp2 HG01109.hp2 others(43): Show |
intron_variant | MODIFIER | c.39+2616T>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76308734 | ||||||
| chr15:76308761
|
C | T | 4 | a0001c0001t0003g0106a0001c0001t0003g0107a0001c0001t0003g0108others(1): Show | 4 | HG02630.hp2 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.39+2589G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76308761 | ||||||
| chr15:76308875
|
A | C | 9 | a0001c0001t0003g0324a0001c0001t0003g0325a0001c0001t0003g0326others(6): Show | 9 | HG02109.hp2 HG02451.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.39+2475T>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76308875 | ||||||
| chr15:76309175
|
C | T | 167 | a0001c0001t0001g0032a0001c0001t0002g0002a0001c0001t0002g0116others(164): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.39+2175G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76309175 | ||||||
| chr15:76309222
|
G | C | 1 | a0001c0001t0012g0268 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.39+2128C>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76309222 | ||||||
| chr15:76309246
|
G | C | 1 | a0001c0001t0003g0276 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.39+2104C>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76309246 | ||||||
| chr15:76309258
|
G | A | 1 | a0001c0001t0002g0198 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.39+2092C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76309258 | ||||||
| chr15:76309259
|
C | A | 1 | a0001c0001t0002g0198 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.39+2091G>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76309259 | ||||||
| chr15:76309260
|
T | A | 1 | a0001c0001t0002g0198 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.39+2090A>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76309260 | ||||||
| chr15:76309264
|
A | T | 1 | a0001c0001t0002g0198 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.39+2086T>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76309264 | ||||||
| chr15:76309265
|
C | A | 1 | a0001c0001t0002g0198 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.39+2085G>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76309265 | ||||||
| chr15:76309269
|
G | A | 1 | a0001c0001t0002g0198 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.39+2081C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76309269 | ||||||
| chr15:76309273
|
C | T | 1 | a0001c0001t0002g0198 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.39+2077G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76309273 | ||||||
| chr15:76309274
|
C | T | 1 | a0001c0001t0002g0198 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.39+2076G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76309274 | ||||||
| chr15:76309275
|
C | A | 1 | a0001c0001t0002g0198 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.39+2075G>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76309275 | ||||||
| chr15:76309276
|
C | G | 1 | a0001c0001t0002g0198 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.39+2074G>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76309276 | ||||||
| chr15:76309307
|
G | T | 1 | a0001c0001t0002g0167 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.39+2043C>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76309307 | ||||||
| chr15:76309325
|
C | A | 1 | a0001c0001t0002g0198 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.39+2025G>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76309325 | ||||||
| chr15:76309340
|
A | G | 1 | a0001c0001t0002g0198 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.39+2010T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76309340 | ||||||
| chr15:76309375
|
C | T | 2 | a0001c0001t0001g0030a0001c0001t0001g0031 | 2 | HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.39+1975G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76309375 | ||||||
| chr15:76309407
|
C | G | 1 | a0001c0001t0002g0198 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.39+1943G>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76309407 | ||||||
| chr15:76309408
|
G | C | 1 | a0001c0001t0002g0198 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.39+1942C>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76309408 | ||||||
| chr15:76309409
|
C | G | 1 | a0001c0001t0002g0198 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.39+1941G>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76309409 | ||||||
| chr15:76309420
|
C | G | 1 | a0001c0001t0002g0198 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.39+1930G>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76309420 | ||||||
| chr15:76309422
|
G | A | 1 | a0001c0001t0002g0198 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.39+1928C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76309422 | ||||||
| chr15:76309433
|
A | T | 1 | a0001c0001t0002g0198 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.39+1917T>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76309433 | ||||||
| chr15:76309434
|
G | C | 1 | a0001c0001t0002g0198 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.39+1916C>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76309434 | ||||||
| chr15:76309448
|
C | G | 1 | a0001c0001t0002g0198 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.39+1902G>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76309448 | ||||||
| chr15:76309449
|
T | G | 1 | a0001c0001t0002g0198 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.39+1901A>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76309449 | ||||||
| chr15:76309453
|
A | T | 1 | a0001c0001t0002g0198 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.39+1897T>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76309453 | ||||||
| chr15:76309475
|
A | C | 1 | a0001c0001t0001g0029 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.39+1875T>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76309475 | ||||||
| chr15:76309530
|
A | G | 122 | a0001c0001t0002g0002a0001c0001t0002g0116a0001c0001t0002g0117others(119): Show | 123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.39+1820T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76309530 | ||||||
| chr15:76309703
|
G | A | 5 | a0001c0001t0003g0110a0001c0001t0003g0111a0001c0001t0003g0112others(2): Show | 5 | HG01891.hp2 HG02486.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.39+1647C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76309703 | ||||||
| chr15:76309790
|
T | C | 322 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(319): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.39+1560A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76309790 | ||||||
| chr15:76309803
|
A | G | 1 | a0001c0001t0006g0278 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.39+1547T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76309803 | ||||||
| chr15:76309869
|
A | T | 1 | a0001c0001t0001g0287 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.39+1481T>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76309869 | ||||||
| chr15:76309871
|
G | A | 83 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(80): Show | 84 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.39+1479C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76309871 | ||||||
| chr15:76309997
|
C | T | 2 | a0001c0001t0001g0322a0001c0001t0001g0323 | 2 | HG01243.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.39+1353G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76309997 | ||||||
| chr15:76310005
|
G | A | 46 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0001g0290others(43): Show | 46 | HG00140.hp2 HG00544.hp2 HG01074.hp2 others(43): Show |
intron_variant | MODIFIER | c.39+1345C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310005 | ||||||
| chr15:76310068
|
C | CA | 13 | a0001c0001t0003g0273a0001c0001t0003g0274a0001c0001t0004g0238others(10): Show | 13 | HG01167.hp1 HG01169.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.39+1281dupT | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310068 | ||||||
| chr15:76310068
|
C | CAA | 7 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0004g0102others(4): Show | 7 | HG01123.hp2 HG02647.hp1 HG03540.hp2 others(4): Show |
intron_variant | MODIFIER | c.39+1280_39+1281dup others(2): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310068 | ||||||
| chr15:76310068
|
C | CAAAAAAA others(3): Show |
20 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0002g0137others(17): Show | 20 | HG00099.hp1 HG00639.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.39+1272_39+1281dup others(10): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310068 | ||||||
| chr15:76310068
|
C | CAAAAAAA others(4): Show |
27 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0148others(24): Show | 27 | HG00735.hp2 HG00738.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.39+1271_39+1281dup others(11): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310068 | ||||||
| chr15:76310068
|
C | CAAAAAAA others(5): Show |
17 | a0001c0001t0002g0167a0001c0001t0002g0168a0001c0001t0002g0169others(14): Show | 17 | HG00673.hp2 HG01884.hp2 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.39+1270_39+1281dup others(12): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310068 | ||||||
| chr15:76310068
|
C | CAAAAAAA others(6): Show |
6 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(3): Show | 6 | HG01978.hp1 HG02135.hp1 NA18989.hp2 others(3): Show |
intron_variant | MODIFIER | c.39+1269_39+1281dup others(13): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310068 | ||||||
| chr15:76310068
|
C | CAAAAAAA others(7): Show |
3 | a0001c0001t0002g0187a0001c0001t0002g0188a0001c0001t0002g0189 | 3 | NA18980.hp1 NA18986.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.39+1268_39+1281dup others(14): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310068 | ||||||
| chr15:76310068
|
C | CAAAAAAA others(8): Show |
7 | a0001c0001t0002g0190a0001c0001t0002g0191a0001c0001t0002g0192others(4): Show | 7 | HG00621.hp1 HG01516.hp2 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.39+1267_39+1281dup others(15): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310068 | ||||||
| chr15:76310068
|
C | CAAAAAAA others(9): Show |
4 | a0001c0001t0002g0002a0001c0001t0002g0196a0001c0001t0002g0197others(1): Show | 5 | HG01081.hp1 NA18939.hp2 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.39+1266_39+1281dup others(16): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310068 | ||||||
| chr15:76310068
|
C | CAAAAAAA others(10): Show |
1 | a0002c0002t0004g0283 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.39+1265_39+1281dup others(17): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310068 | ||||||
| chr15:76310068
|
C | CAAAAAAA others(11): Show |
4 | a0001c0001t0002g0198a0001c0001t0002g0199a0001c0001t0002g0200others(1): Show | 4 | HG00099.hp2 HG00280.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.39+1264_39+1281dup others(18): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310068 | ||||||
| chr15:76310068
|
C | CAAAAAAA others(12): Show |
3 | a0001c0001t0002g0201a0001c0001t0002g0202a0001c0001t0002g0223 | 3 | HG00140.hp1 NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.39+1263_39+1281dup others(19): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310068 | ||||||
| chr15:76310068
|
C | CAAAAAAA others(13): Show |
2 | a0001c0001t0002g0203a0001c0001t0002g0204 | 2 | HG02074.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.39+1262_39+1281dup others(20): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310068 | ||||||
| chr15:76310068
|
C | CAAAAAAA others(14): Show |
3 | a0001c0001t0002g0205a0001c0001t0003g0115a0002c0002t0004g0253 | 3 | HG01255.hp2 HG02280.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.39+1261_39+1281dup others(21): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310068 | ||||||
| chr15:76310068
|
C | CAAAAAAA others(15): Show |
1 | a0001c0001t0002g0206 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.39+1260_39+1281dup others(22): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310068 | ||||||
| chr15:76310068
|
C | CAAAAAAA others(17): Show |
3 | a0001c0001t0002g0207a0001c0001t0002g0208a0002c0002t0004g0254 | 3 | HG02602.hp1 HG02717.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.39+1258_39+1281dup others(24): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310068 | ||||||
| chr15:76310068
|
C | CAAAAAAA others(18): Show |
4 | a0002c0002t0004g0255a0002c0002t0004g0256a0002c0002t0004g0257others(1): Show | 4 | HG03710.hp2 NA18946.hp1 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.39+1257_39+1281dup others(25): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310068 | ||||||
| chr15:76310068
|
C | CAAAAAAA others(19): Show |
2 | a0002c0002t0004g0258a0002c0002t0004g0259 | 2 | HG02027.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.39+1256_39+1281dup others(26): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310068 | ||||||
| chr15:76310068
|
C | CAAAAAAA others(20): Show |
3 | a0001c0001t0002g0209a0002c0002t0004g0260a0002c0002t0004g0261 | 3 | HG00438.hp2 HG00621.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.39+1255_39+1281dup others(27): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310068 | ||||||
| chr15:76310068
|
C | CAAAAAAA others(31): Show |
1 | a0002c0002t0004g0262 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.39+1281_39+1282ins others(38): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310068 | ||||||
| chr15:76310068
|
CA | C | 12 | a0001c0001t0002g0117a0001c0001t0002g0118a0001c0001t0002g0119others(9): Show | 12 | HG00597.hp2 HG02015.hp1 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.39+1281delT | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310068 | ||||||
| chr15:76310068
|
CAAAAA | C | 7 | a0001c0001t0001g0321a0001c0001t0001g0323a0001c0001t0003g0112others(4): Show | 7 | HG01496.hp1 HG01891.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.39+1277_39+1281del others(5): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310068 | ||||||
| chr15:76310068
|
CAAAAAAA others(1): Show |
C | 16 | a0001c0001t0001g0001a0001c0001t0001g0088a0001c0001t0001g0089others(13): Show | 17 | HG00597.hp1 HG01257.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.39+1274_39+1281del others(8): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310068 | ||||||
| chr15:76310068
|
CAAAAAAA others(2): Show |
C | 78 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(75): Show | 78 | HG00280.hp1 HG00438.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.39+1273_39+1281del others(9): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310068 | ||||||
| chr15:76310068
|
CAAAAAAA others(3): Show |
C | 9 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(6): Show | 9 | HG00733.hp2 HG01106.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.39+1272_39+1281del others(10): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310068 | ||||||
| chr15:76310068
|
CAAAAAAA others(4): Show |
C | 5 | a0001c0001t0001g0311a0001c0001t0001g0312a0001c0001t0001g0313others(2): Show | 5 | HG01168.hp2 HG01169.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.39+1271_39+1281del others(11): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310068 | ||||||
| chr15:76310068
|
CAAAAAAA others(5): Show |
C | 41 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0001g0290others(38): Show | 41 | HG00140.hp2 HG00544.hp2 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.39+1270_39+1281del others(12): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310068 | ||||||
| chr15:76310138
|
C | G | 1 | a0001c0001t0001g0323 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.39+1212G>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310138 | ||||||
| chr15:76310149
|
G | A | 3 | a0001c0001t0001g0314a0001c0001t0001g0315a0001c0001t0001g0316 | 3 | HG01346.hp2 HG01515.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.39+1201C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310149 | ||||||
| chr15:76310252
|
T | TAAAC | 5 | a0001c0001t0006g0278a0001c0001t0006g0279a0001c0001t0006g0280others(2): Show | 5 | HG02055.hp1 HG02559.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.39+1094_39+1097dup others(4): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310252 | ||||||
| chr15:76310268
|
C | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG02015.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.39+1082G>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310268 | ||||||
| chr15:76310366
|
C | A | 332 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(329): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.39+984G>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310366 | ||||||
| chr15:76310369
|
G | GA | 6 | a0001c0001t0003g0110a0001c0001t0003g0111a0001c0001t0003g0112others(3): Show | 6 | HG01891.hp2 HG02280.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.39+980dupT | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310369 | ||||||
| chr15:76310369
|
G | GAA | 128 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0001g0290others(125): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.39+979_39+980dupTT | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310369 | ||||||
| chr15:76310369
|
G | GAAA | 25 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0319others(22): Show | 25 | HG00639.hp2 HG00673.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.39+978_39+980dupTT others(1): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310369 | ||||||
| chr15:76310369
|
G | GAAAA | 7 | a0001c0001t0001g0287a0001c0001t0002g0224a0001c0001t0002g0225others(4): Show | 7 | HG01074.hp1 HG01496.hp2 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.39+977_39+980dupTT others(2): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310369 | ||||||
| chr15:76310369
|
G | GAAAAAAA others(3): Show |
1 | a0001c0001t0003g0275 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.39+971_39+980dupTT others(8): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310369 | ||||||
| chr15:76310369
|
G | GAAAAAAA others(5): Show |
1 | a0001c0001t0011g0330 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.39+969_39+980dupTT others(10): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310369 | ||||||
| chr15:76310369
|
G | GAAAAAAA others(7): Show |
2 | a0001c0001t0003g0276a0001c0001t0003g0331 | 2 | NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.39+967_39+980dupTT others(12): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310369 | ||||||
| chr15:76310369
|
G | GAAAAAAA others(8): Show |
1 | a0001c0001t0003g0277 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.39+966_39+980dupTT others(13): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310369 | ||||||
| chr15:76310369
|
G | GAAAAAAA others(10): Show |
1 | a0001c0001t0003g0332 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.39+964_39+980dupTT others(15): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310369 | ||||||
| chr15:76310369
|
G | GAAAAAAA others(12): Show |
1 | a0001c0001t0006g0278 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.39+962_39+980dupTT others(17): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310369 | ||||||
| chr15:76310369
|
G | GAAAAAAA others(21): Show |
1 | a0001c0001t0003g0333 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.39+980_39+981insTT others(26): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310369 | ||||||
| chr15:76310369
|
G | GAAAAAAA others(24): Show |
1 | a0001c0001t0006g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.39+980_39+981insTT others(29): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310369 | ||||||
| chr15:76310369
|
G | GAAAAAAA others(25): Show |
2 | a0001c0001t0006g0280a0001c0001t0006g0281 | 2 | HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.39+980_39+981insTT others(30): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310369 | ||||||
| chr15:76310369
|
G | GAAAAAAA others(31): Show |
1 | a0001c0001t0006g0282 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.39+980_39+981insTT others(36): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310369 | ||||||
| chr15:76310369
|
GAAAAAA | G | 135 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(132): Show | 136 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.39+975_39+980delTT others(4): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310369 | ||||||
| chr15:76310596
|
A | C | 122 | a0001c0001t0002g0002a0001c0001t0002g0116a0001c0001t0002g0117others(119): Show | 123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.39+754T>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310596 | ||||||
| chr15:76310823
|
A | G | 49 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287others(46): Show | 49 | HG00140.hp2 HG00544.hp2 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.39+527T>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310823 | ||||||
| chr15:76310828
|
T | C | 36 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0001g0290others(33): Show | 36 | HG00140.hp2 HG00544.hp2 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.39+522A>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310828 | ||||||
| chr15:76310830
|
G | A | 1 | a0001c0001t0001g0323 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.39+520C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310830 | ||||||
| chr15:76310834
|
C | T | 4 | a0001c0001t0003g0106a0001c0001t0003g0107a0001c0001t0003g0108others(1): Show | 4 | HG02630.hp2 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.39+516G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310834 | ||||||
| chr15:76310835
|
G | A | 1 | a0001c0001t0001g0323 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.39+515C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310835 | ||||||
| chr15:76310836
|
C | A | 1 | a0001c0001t0001g0323 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.39+514G>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310836 | ||||||
| chr15:76310841
|
T | TCCCAC | 10 | a0001c0001t0003g0324a0001c0001t0003g0325a0001c0001t0003g0326others(7): Show | 10 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.39+504_39+508dupGT others(3): Show |
ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310841 | ||||||
| chr15:76310998
|
C | A | 10 | a0001c0001t0003g0324a0001c0001t0003g0325a0001c0001t0003g0326others(7): Show | 10 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.39+352G>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76310998 | ||||||
| chr15:76311116
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.39+234G>A | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76311116 | ||||||
| chr15:76311247
|
G | A | 2 | a0002c0002t0004g0283a0002c0002t0004g0284 | 2 | NA18943.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.39+103C>T | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76311247 | ||||||
| chr15:76311265
|
G | C | 1 | a0001c0001t0001g0105 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.39+85C>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76311265 | ||||||
| chr15:76311269
|
CA | C | 100 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(97): Show | 101 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.39+80delT | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76311269 | ||||||
| chr15:76311319
|
C | G | 2 | a0001c0001t0003g0005a0001c0001t0003g0006 | 2 | HG01243.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.39+31G>C | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76311319 | ||||||
| chr15:76311338
|
G | C | 49 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287others(46): Show | 49 | HG00140.hp2 HG00544.hp2 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.39+12C>G | ETFA | ENSG00000140374.17 | transcript | ENST00000557943.6 | protein_coding | 1/11 | chr15 | 76311338 |