Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 2196 |
|---|---|
| ensemblid | ENSG00000086570.13 |
| hgncid | 3596 |
| symbol | FAT2 |
| name | FAT atypical cadherin 2 |
| refseq_nuc | NM_001447.3 |
| refseq_prot | NP_001438.1 |
| ensembl_nuc | ENST00000261800.6 |
| ensembl_prot | ENSP00000261800.5 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 151504092 |
| end | 151591331 |
| strand | - |
| ver | v1.2 |
| region | chr5:151504092-151591331 |
| region5000 | chr5:151499092-151596331 |
| regionname0 | FAT2_chr5_151504092_151591331 |
| regionname5000 | FAT2_chr5_151499092_151596331 |
| 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 | 0/0 | 4349 | 81 | 17 | 10 | 40 | 4 | 10 | 33 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0002 | 0/1 | 4349 | 59 | 6 | 8 | 35 | 1 | 8 | 24 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0003 | 0/0 | 4349 | 43 | 6 | 11 | 25 | 0 | 1 | 16 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0004 | 0/0 | 4349 | 19 | 11 | 5 | 3 | 0 | 0 | 3 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0005 | 0/0 | 4349 | 17 | 9 | 1 | 6 | 0 | 1 | 6 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0006 | 0/0 | 4349 | 16 | 1 | 3 | 10 | 1 | 1 | 9 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0007 | 0/0 | 4349 | 14 | 0 | 6 | 8 | 0 | 0 | 6 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0008 | 0/0 | 4349 | 13 | 6 | 4 | 0 | 3 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0009 | 0/0 | 4349 | 10 | 0 | 0 | 10 | 0 | 0 | 10 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0010 | 0/0 | 4349 | 8 | 3 | 2 | 2 | 0 | 1 | 2 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0011 | 0/0 | 4349 | 7 | 0 | 2 | 0 | 2 | 3 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0012 | 0/0 | 4349 | 5 | 0 | 2 | 1 | 0 | 2 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0013 | 0/0 | 4349 | 5 | 1 | 0 | 4 | 0 | 0 | 3 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0014 | 0/0 | 4349 | 4 | 0 | 1 | 1 | 0 | 2 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0015 | 0/0 | 4349 | 4 | 2 | 2 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0016 | 0/0 | 4349 | 4 | 0 | 0 | 3 | 0 | 1 | 2 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0017 | 0/0 | 4349 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0018 | 0/0 | 4349 | 4 | 0 | 0 | 4 | 0 | 0 | 2 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0019 | 0/0 | 4349 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0020 | 0/0 | 4349 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0021 | 0/0 | 4349 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0022 | 0/0 | 4349 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0023 | 0/0 | 4349 | 2 | 0 | 1 | 1 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0024 | 0/0 | 4349 | 2 | 1 | 0 | 1 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0025 | 0/0 | 4349 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0026 | 0/0 | 4349 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0027 | 0/0 | 4349 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0028 | 0/0 | 4349 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0029 | 0/0 | 4349 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0030 | 0/0 | 4349 | 2 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0031 | 0/0 | 4349 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0032 | 0/0 | 4349 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0033 | 0/0 | 4349 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0034 | 0/0 | 4349 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0035 | 0/0 | 4349 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0036 | 0/0 | 4349 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0037 | 0/0 | 4349 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0038 | 0/0 | 4349 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0039 | 0/0 | 4349 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0040 | 0/0 | 4349 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0041 | 0/0 | 4349 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0042 | 0/0 | 4349 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0043 | 0/0 | 4349 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0044 | 0/0 | 4349 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0045 | 0/0 | 4349 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0046 | 0/0 | 4349 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0047 | 0/0 | 4349 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0048 | 0/0 | 4349 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0049 | 0/0 | 4349 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0050 | 0/0 | 4349 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0051 | 0/0 | 4349 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0052 | 0/0 | 4349 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0053 | 0/0 | 4349 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0054 | 0/0 | 4349 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0055 | 0/0 | 4349 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0056 | 0/0 | 4349 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0057 | 0/0 | 4349 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0058 | 0/0 | 4349 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0059 | 0/0 | 4349 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0060 | 0/0 | 4349 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0061 | 0/0 | 4349 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0062 | 0/0 | 4349 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0063 | 0/0 | 4349 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0064 | 0/0 | 4349 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0065 | 0/0 | 4349 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0066 | 0/0 | 4349 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0067 | 0/0 | 4349 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0068 | 0/0 | 4349 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0069 | 0/0 | 4349 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0070 | 0/0 | 4349 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0071 | 0/0 | 4349 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0072 | 0/0 | 4349 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0073 | 0/0 | 4349 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0074 | 0/0 | 4349 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0075 | 0/0 | 4349 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0076 | 0/0 | 4349 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0077 | 1/0 | 4349 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0078 | 0/0 | 4349 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0079 | 0/0 | 4349 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0080 | 0/0 | 4349 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0081 | 0/0 | 4349 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0082 | 0/0 | 4349 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| 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 | 0/0 | 13050 | 31 | 1 | 2 | 23 | 1 | 4 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0002 | 0/0 | 13050 | 21 | 1 | 9 | 11 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0003 | 0/0 | 13050 | 18 | 1 | 2 | 10 | 0 | 5 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0004 | 0/0 | 13050 | 13 | 0 | 2 | 10 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0005 | 0/0 | 13050 | 13 | 0 | 3 | 9 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0006 | 0/1 | 13050 | 10 | 2 | 3 | 4 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0007 | 0/0 | 13050 | 9 | 0 | 0 | 9 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0008 | 0/0 | 13050 | 8 | 0 | 0 | 5 | 0 | 3 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0009 | 0/0 | 13050 | 7 | 0 | 0 | 6 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0010 | 0/0 | 13050 | 7 | 5 | 0 | 2 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0011 | 0/0 | 13050 | 6 | 3 | 0 | 2 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0012 | 0/0 | 13050 | 6 | 4 | 0 | 0 | 2 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0013 | 0/0 | 13050 | 6 | 1 | 1 | 4 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0014 | 0/0 | 13050 | 6 | 6 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0015 | 0/0 | 13050 | 6 | 0 | 0 | 5 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0016 | 0/0 | 13050 | 6 | 0 | 1 | 2 | 2 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0017 | 0/0 | 13050 | 4 | 1 | 0 | 2 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0018 | 0/0 | 13050 | 4 | 0 | 1 | 1 | 0 | 2 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0019 | 0/0 | 13050 | 4 | 4 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0020 | 0/0 | 13050 | 4 | 2 | 0 | 1 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0021 | 0/0 | 13050 | 4 | 0 | 0 | 4 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0022 | 0/0 | 13050 | 4 | 0 | 0 | 4 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0023 | 0/0 | 13050 | 3 | 0 | 2 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0024 | 0/0 | 13050 | 3 | 0 | 0 | 3 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0025 | 0/0 | 13050 | 3 | 1 | 2 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0026 | 0/0 | 13050 | 3 | 0 | 1 | 1 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0027 | 0/0 | 13050 | 3 | 0 | 0 | 3 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0028 | 0/0 | 13050 | 3 | 0 | 0 | 3 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0029 | 0/0 | 13050 | 3 | 3 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0030 | 0/0 | 13050 | 3 | 3 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0031 | 0/0 | 13050 | 3 | 0 | 0 | 3 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0032 | 0/0 | 13050 | 2 | 0 | 0 | 2 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0033 | 0/0 | 13050 | 2 | 0 | 2 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0034 | 0/0 | 13050 | 2 | 1 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0035 | 0/0 | 13050 | 2 | 1 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0036 | 0/0 | 13050 | 2 | 2 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0037 | 0/0 | 13050 | 2 | 1 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0038 | 0/0 | 13050 | 2 | 0 | 2 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0039 | 0/0 | 13050 | 2 | 0 | 0 | 2 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0040 | 0/0 | 13050 | 2 | 0 | 0 | 2 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0041 | 0/0 | 13050 | 2 | 0 | 2 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0042 | 0/0 | 13050 | 2 | 0 | 0 | 2 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0043 | 0/0 | 13050 | 2 | 2 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0044 | 0/0 | 13050 | 2 | 1 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0045 | 0/0 | 13050 | 2 | 0 | 0 | 2 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0046 | 0/0 | 13050 | 2 | 0 | 0 | 2 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0047 | 0/0 | 13050 | 2 | 2 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0048 | 0/0 | 13050 | 2 | 0 | 0 | 0 | 0 | 2 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0049 | 0/0 | 13050 | 2 | 0 | 1 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0050 | 0/0 | 13050 | 2 | 2 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0051 | 0/0 | 13050 | 2 | 0 | 1 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0052 | 0/0 | 13050 | 2 | 2 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0053 | 0/0 | 13050 | 2 | 2 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0054 | 0/0 | 13050 | 2 | 0 | 2 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0055 | 0/0 | 13050 | 2 | 0 | 0 | 2 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0056 | 0/0 | 13050 | 2 | 2 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0057 | 0/0 | 13050 | 2 | 0 | 2 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0058 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0059 | 0/0 | 13050 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0060 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0061 | 0/0 | 13050 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0062 | 0/0 | 13050 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0063 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0064 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0065 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0066 | 0/0 | 13050 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0067 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0068 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0069 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0070 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0071 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0072 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0073 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0074 | 0/0 | 13050 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0075 | 0/0 | 13050 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0076 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0077 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0078 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0079 | 0/0 | 13050 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0080 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0081 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0082 | 0/0 | 13050 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0083 | 0/0 | 13050 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0084 | 0/0 | 13050 | 1 | 0 | 0 | 0 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0085 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0086 | 0/0 | 13050 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0087 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0088 | 0/0 | 13050 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0089 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0090 | 0/0 | 13050 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0091 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0092 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0093 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0094 | 0/0 | 13050 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0095 | 0/0 | 13050 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0096 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0097 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0098 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0099 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0100 | 0/0 | 13050 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0101 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0102 | 0/0 | 13050 | 1 | 0 | 0 | 0 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0103 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0104 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0105 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0106 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0107 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0108 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0109 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0110 | 0/0 | 13050 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0111 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0112 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0113 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0114 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0115 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0116 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0117 | 0/0 | 13050 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0118 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0119 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0120 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0121 | 0/0 | 13050 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0122 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0123 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0124 | 0/0 | 13050 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0125 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0126 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0127 | 1/0 | 13050 | 1 | 0 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0128 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0129 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0130 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0131 | 0/0 | 13050 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0132 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0133 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0134 | 0/0 | 13050 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0135 | 0/0 | 13050 | 1 | 0 | 0 | 0 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0136 | 0/0 | 13050 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0137 | 0/0 | 13050 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0138 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0139 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0140 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0141 | 0/0 | 13050 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0142 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0143 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0144 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0145 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0146 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0147 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0148 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0149 | 0/0 | 13050 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0150 | 0/0 | 13050 | 1 | 0 | 0 | 0 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0151 | 0/0 | 13050 | 1 | 0 | 0 | 0 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0152 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0153 | 0/0 | 13050 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0154 | 0/0 | 13050 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0155 | 0/0 | 13050 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0156 | 0/0 | 13050 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0157 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0158 | 0/0 | 13050 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0159 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0160 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0161 | 0/0 | 13050 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0162 | 0/0 | 13050 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0163 | 0/0 | 13050 | 1 | 0 | 0 | 0 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0164 | 0/0 | 13050 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0165 | 0/0 | 13050 | 1 | 0 | 0 | 0 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0166 | 0/0 | 13050 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0167 | 0/0 | 13050 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0168 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0169 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0170 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0171 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0172 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0173 | 0/0 | 13050 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0174 | 0/0 | 13050 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0175 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0176 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0177 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0178 | 0/0 | 13050 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| c0179 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| 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 | 1/0 | 1661 | 228 | 45 | 47 | 109 | 8 | 18 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| t0002 | 0/0 | 1661 | 51 | 5 | 5 | 32 | 2 | 7 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| t0003 | 0/0 | 1662 | 18 | 0 | 0 | 18 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| t0004 | 0/0 | 1662 | 14 | 1 | 5 | 0 | 3 | 5 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| t0005 | 0/0 | 1661 | 12 | 11 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| t0006 | 0/0 | 1662 | 11 | 0 | 0 | 10 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| t0007 | 0/0 | 1661 | 9 | 9 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| t0008 | 0/0 | 1661 | 7 | 0 | 0 | 7 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| t0009 | 0/0 | 1661 | 6 | 5 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| t0010 | 0/0 | 1665 | 6 | 6 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| t0011 | 0/0 | 1662 | 6 | 0 | 3 | 1 | 1 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| t0012 | 0/0 | 1661 | 2 | 0 | 0 | 2 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| t0013 | 0/0 | 1661 | 2 | 2 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| t0014 | 0/0 | 1661 | 2 | 0 | 2 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| t0015 | 0/1 | 1661 | 2 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| t0016 | 0/0 | 1619 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| t0017 | 0/0 | 1665 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| t0018 | 0/0 | 1661 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| t0019 | 0/0 | 1661 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| t0020 | 0/0 | 1661 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| t0021 | 0/0 | 1661 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| t0022 | 0/0 | 1661 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| t0023 | 0/0 | 1661 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| t0024 | 0/0 | 1661 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| t0025 | 0/0 | 1662 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| t0026 | 0/0 | 1661 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| t0027 | 0/0 | 1661 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| t0028 | 0/0 | 1661 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| t0029 | 0/0 | 1661 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| t0030 | 0/0 | 1661 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| t0031 | 0/0 | 1661 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| t0032 | 0/0 | 1661 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| t0033 | 0/0 | 1661 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| t0034 | 0/0 | 1661 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| t0035 | 0/0 | 1661 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| t0036 | 0/0 | 1661 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| t0037 | 0/0 | 1661 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| 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 | 2 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0105 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0369 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0385 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0386 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0387 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0388 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0389 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0390 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| g0391 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0003 | 0/0 | 13050 | 18 | 1 | 2 | 10 | 0 | 5 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0004 | 0/0 | 13050 | 13 | 0 | 2 | 10 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0010 | 0/0 | 13050 | 7 | 5 | 0 | 2 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0016 | 0/0 | 13050 | 6 | 0 | 1 | 2 | 2 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0017 | 0/0 | 13050 | 4 | 1 | 0 | 2 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0020 | 0/0 | 13050 | 4 | 2 | 0 | 1 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0021 | 0/0 | 13050 | 4 | 0 | 0 | 4 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0032 | 0/0 | 13050 | 2 | 0 | 0 | 2 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0044 | 0/0 | 13050 | 2 | 1 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0047 | 0/0 | 13050 | 2 | 2 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0048 | 0/0 | 13050 | 2 | 0 | 0 | 0 | 0 | 2 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0049 | 0/0 | 13050 | 2 | 0 | 1 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0059 | 0/0 | 13050 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0065 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0110 | 0/0 | 13050 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0123 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0124 | 0/0 | 13050 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0125 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0128 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0129 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0130 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0142 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0144 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0147 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0159 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0174 | 0/0 | 13050 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0179 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0002c0001 | 0/0 | 13050 | 31 | 1 | 2 | 23 | 1 | 4 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0002c0006 | 0/1 | 13050 | 10 | 2 | 3 | 4 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0002c0008 | 0/0 | 13050 | 8 | 0 | 0 | 5 | 0 | 3 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0002c0026 | 0/0 | 13050 | 3 | 0 | 1 | 1 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0002c0037 | 0/0 | 13050 | 2 | 1 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0002c0085 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0002c0092 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0002c0099 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0002c0100 | 0/0 | 13050 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0002c0170 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0003c0002 | 0/0 | 13050 | 21 | 1 | 9 | 11 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0003c0009 | 0/0 | 13050 | 7 | 0 | 0 | 6 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0003c0013 | 0/0 | 13050 | 6 | 1 | 1 | 4 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0003c0029 | 0/0 | 13050 | 3 | 3 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0003c0109 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0003c0114 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0003c0117 | 0/0 | 13050 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0003c0138 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0003c0139 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0003c0140 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0004c0019 | 0/0 | 13050 | 4 | 4 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0004c0033 | 0/0 | 13050 | 2 | 0 | 2 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0004c0052 | 0/0 | 13050 | 2 | 2 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0004c0053 | 0/0 | 13050 | 2 | 2 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0004c0055 | 0/0 | 13050 | 2 | 0 | 0 | 2 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0004c0064 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0004c0143 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0004c0148 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0004c0152 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0004c0153 | 0/0 | 13050 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0004c0156 | 0/0 | 13050 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0004c0161 | 0/0 | 13050 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0005c0014 | 0/0 | 13050 | 6 | 6 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0005c0015 | 0/0 | 13050 | 6 | 0 | 0 | 5 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0005c0030 | 0/0 | 13050 | 3 | 3 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0005c0063 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0005c0173 | 0/0 | 13050 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0006c0005 | 0/0 | 13050 | 13 | 0 | 3 | 9 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0006c0091 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0006c0093 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0006c0102 | 0/0 | 13050 | 1 | 0 | 0 | 0 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0007c0022 | 0/0 | 13050 | 4 | 0 | 0 | 4 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0007c0023 | 0/0 | 13050 | 3 | 0 | 2 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0007c0045 | 0/0 | 13050 | 2 | 0 | 0 | 2 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0007c0051 | 0/0 | 13050 | 2 | 0 | 1 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0007c0054 | 0/0 | 13050 | 2 | 0 | 2 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0007c0154 | 0/0 | 13050 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0008c0012 | 0/0 | 13050 | 6 | 4 | 0 | 0 | 2 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0008c0025 | 0/0 | 13050 | 3 | 1 | 2 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0008c0038 | 0/0 | 13050 | 2 | 0 | 2 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0008c0084 | 0/0 | 13050 | 1 | 0 | 0 | 0 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0008c0087 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0009c0007 | 0/0 | 13050 | 9 | 0 | 0 | 9 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0009c0132 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0010c0011 | 0/0 | 13050 | 6 | 3 | 0 | 2 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0010c0082 | 0/0 | 13050 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0010c0094 | 0/0 | 13050 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0011c0061 | 0/0 | 13050 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0011c0136 | 0/0 | 13050 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0011c0137 | 0/0 | 13050 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0011c0149 | 0/0 | 13050 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0011c0150 | 0/0 | 13050 | 1 | 0 | 0 | 0 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0011c0155 | 0/0 | 13050 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0011c0163 | 0/0 | 13050 | 1 | 0 | 0 | 0 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0012c0018 | 0/0 | 13050 | 4 | 0 | 1 | 1 | 0 | 2 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0012c0090 | 0/0 | 13050 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0013c0024 | 0/0 | 13050 | 3 | 0 | 0 | 3 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0013c0035 | 0/0 | 13050 | 2 | 1 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0014c0083 | 0/0 | 13050 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0014c0086 | 0/0 | 13050 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0014c0088 | 0/0 | 13050 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0014c0089 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0015c0041 | 0/0 | 13050 | 2 | 0 | 2 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0015c0043 | 0/0 | 13050 | 2 | 2 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0016c0042 | 0/0 | 13050 | 2 | 0 | 0 | 2 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0016c0118 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0016c0121 | 0/0 | 13050 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0017c0027 | 0/0 | 13050 | 3 | 0 | 0 | 3 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0017c0108 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0018c0031 | 0/0 | 13050 | 3 | 0 | 0 | 3 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0018c0177 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0019c0036 | 0/0 | 13050 | 2 | 2 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0019c0101 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0020c0028 | 0/0 | 13050 | 3 | 0 | 0 | 3 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0021c0056 | 0/0 | 13050 | 2 | 2 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0021c0167 | 0/0 | 13050 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0022c0096 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0022c0098 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0023c0078 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0023c0079 | 0/0 | 13050 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0024c0034 | 0/0 | 13050 | 2 | 1 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0025c0069 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0025c0071 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0026c0046 | 0/0 | 13050 | 2 | 0 | 0 | 2 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0027c0040 | 0/0 | 13050 | 2 | 0 | 0 | 2 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0028c0039 | 0/0 | 13050 | 2 | 0 | 0 | 2 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0029c0050 | 0/0 | 13050 | 2 | 2 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0030c0146 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0030c0151 | 0/0 | 13050 | 1 | 0 | 0 | 0 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0031c0104 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0031c0105 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0032c0057 | 0/0 | 13050 | 2 | 0 | 2 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0033c0058 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0034c0178 | 0/0 | 13050 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0035c0066 | 0/0 | 13050 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0036c0172 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0037c0171 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0038c0097 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0039c0073 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0040c0074 | 0/0 | 13050 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0041c0075 | 0/0 | 13050 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0042c0077 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0043c0076 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0044c0081 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0045c0080 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0046c0095 | 0/0 | 13050 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0047c0072 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0048c0070 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0049c0068 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0050c0067 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0051c0131 | 0/0 | 13050 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0052c0169 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0053c0133 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0054c0134 | 0/0 | 13050 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0055c0112 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0056c0113 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0057c0122 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0058c0120 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0059c0119 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0060c0116 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0061c0115 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0062c0165 | 0/0 | 13050 | 1 | 0 | 0 | 0 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0063c0062 | 0/0 | 13050 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0064c0060 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0065c0145 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0066c0162 | 0/0 | 13050 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0067c0160 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0068c0135 | 0/0 | 13050 | 1 | 0 | 0 | 0 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0069c0164 | 0/0 | 13050 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0070c0157 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0071c0158 | 0/0 | 13050 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0072c0166 | 0/0 | 13050 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0073c0141 | 0/0 | 13050 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0074c0168 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0075c0126 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0076c0111 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0077c0127 | 1/0 | 13050 | 1 | 0 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0078c0107 | 0/0 | 13050 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0079c0175 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0080c0176 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0081c0103 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0082c0106 | 0/0 | 13050 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0003t0001 | 0/0 | 14710 | 13 | 0 | 2 | 7 | 0 | 4 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0003t0002 | 0/0 | 14710 | 2 | 1 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0003t0012 | 0/0 | 14710 | 2 | 0 | 0 | 2 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0003t0020 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0004t0001 | 0/0 | 14710 | 12 | 0 | 2 | 9 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0004t0002 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0010t0001 | 0/0 | 14710 | 2 | 1 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0010t0002 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0010t0005 | 0/0 | 14710 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0010t0007 | 0/0 | 14710 | 2 | 2 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0010t0009 | 0/0 | 14710 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0016t0001 | 0/0 | 14710 | 3 | 0 | 1 | 2 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0016t0002 | 0/0 | 14710 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0016t0004 | 0/0 | 14711 | 2 | 0 | 0 | 0 | 2 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0017t0001 | 0/0 | 14710 | 3 | 1 | 0 | 1 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0017t0002 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0020t0001 | 0/0 | 14710 | 2 | 0 | 0 | 1 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0020t0005 | 0/0 | 14710 | 2 | 2 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0021t0002 | 0/0 | 14710 | 2 | 0 | 0 | 2 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0021t0003 | 0/0 | 14711 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0021t0008 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0032t0001 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0032t0008 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0044t0001 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0044t0007 | 0/0 | 14710 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0047t0005 | 0/0 | 14710 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0047t0007 | 0/0 | 14710 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0048t0001 | 0/0 | 14710 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0048t0021 | 0/0 | 14710 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0049t0001 | 0/0 | 14710 | 2 | 0 | 1 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0059t0001 | 0/0 | 14710 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0065t0001 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0110t0001 | 0/0 | 14710 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0123t0007 | 0/0 | 14710 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0124t0001 | 0/0 | 14710 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0125t0010 | 0/0 | 14714 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0128t0002 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0129t0001 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0130t0001 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0142t0007 | 0/0 | 14710 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0144t0001 | 0/0 | 14710 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0147t0013 | 0/0 | 14710 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0159t0001 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0174t0002 | 0/0 | 14710 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0001c0179t0001 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0002c0001t0001 | 0/0 | 14710 | 15 | 0 | 1 | 11 | 1 | 2 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0002c0001t0002 | 0/0 | 14710 | 13 | 0 | 0 | 11 | 0 | 2 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0002c0001t0005 | 0/0 | 14710 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0002c0001t0017 | 0/0 | 14714 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0002c0001t0036 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0002c0006t0001 | 0/0 | 14710 | 5 | 0 | 3 | 2 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0002c0006t0002 | 0/0 | 14710 | 2 | 0 | 0 | 2 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0002c0006t0005 | 0/0 | 14710 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0002c0006t0015 | 0/1 | 14710 | 1 | 0 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0002c0006t0034 | 0/0 | 14710 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0002c0008t0001 | 0/0 | 14710 | 3 | 0 | 0 | 2 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0002c0008t0002 | 0/0 | 14710 | 3 | 0 | 0 | 1 | 0 | 2 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0002c0008t0008 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0002c0008t0029 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0002c0026t0001 | 0/0 | 14710 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0002c0026t0002 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0002c0026t0024 | 0/0 | 14710 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0002c0037t0002 | 0/0 | 14710 | 2 | 1 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0002c0085t0037 | 0/0 | 14710 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0002c0092t0002 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0002c0099t0007 | 0/0 | 14710 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0002c0100t0001 | 0/0 | 14710 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0002c0170t0002 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0003c0002t0001 | 0/0 | 14710 | 17 | 1 | 8 | 8 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0003c0002t0002 | 0/0 | 14710 | 3 | 0 | 0 | 3 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0003c0002t0023 | 0/0 | 14710 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0003c0009t0001 | 0/0 | 14710 | 5 | 0 | 0 | 5 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0003c0009t0002 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0003c0009t0026 | 0/0 | 14710 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0003c0013t0001 | 0/0 | 14710 | 5 | 0 | 1 | 4 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0003c0013t0009 | 0/0 | 14710 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0003c0029t0005 | 0/0 | 14710 | 3 | 3 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0003c0109t0001 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0003c0114t0001 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0003c0117t0001 | 0/0 | 14710 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0003c0138t0025 | 0/0 | 14711 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0003c0139t0008 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0003c0140t0001 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0004c0019t0001 | 0/0 | 14710 | 3 | 3 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0004c0019t0007 | 0/0 | 14710 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0004c0033t0001 | 0/0 | 14710 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0004c0033t0004 | 0/0 | 14711 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0004c0052t0001 | 0/0 | 14710 | 2 | 2 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0004c0053t0001 | 0/0 | 14710 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0004c0053t0010 | 0/0 | 14714 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0004c0055t0001 | 0/0 | 14710 | 2 | 0 | 0 | 2 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0004c0064t0001 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0004c0143t0001 | 0/0 | 14710 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0004c0148t0001 | 0/0 | 14710 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0004c0152t0001 | 0/0 | 14710 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0004c0153t0027 | 0/0 | 14710 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0004c0156t0001 | 0/0 | 14710 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0004c0161t0004 | 0/0 | 14711 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0005c0014t0001 | 0/0 | 14710 | 6 | 6 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0005c0015t0001 | 0/0 | 14710 | 6 | 0 | 0 | 5 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0005c0030t0001 | 0/0 | 14710 | 3 | 3 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0005c0063t0001 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0005c0173t0002 | 0/0 | 14710 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0006c0005t0001 | 0/0 | 14710 | 3 | 0 | 2 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0006c0005t0003 | 0/0 | 14711 | 5 | 0 | 0 | 5 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0006c0005t0006 | 0/0 | 14711 | 3 | 0 | 0 | 3 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0006c0005t0015 | 0/0 | 14710 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0006c0005t0016 | 0/0 | 14668 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0006c0091t0001 | 0/0 | 14710 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0006c0093t0003 | 0/0 | 14711 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0006c0102t0001 | 0/0 | 14710 | 1 | 0 | 0 | 0 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0007c0022t0003 | 0/0 | 14711 | 3 | 0 | 0 | 3 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0007c0022t0006 | 0/0 | 14711 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0007c0023t0001 | 0/0 | 14710 | 2 | 0 | 2 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0007c0023t0003 | 0/0 | 14711 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0007c0045t0003 | 0/0 | 14711 | 2 | 0 | 0 | 2 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0007c0051t0001 | 0/0 | 14710 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0007c0051t0006 | 0/0 | 14711 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0007c0054t0001 | 0/0 | 14710 | 2 | 0 | 2 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0007c0154t0001 | 0/0 | 14710 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0008c0012t0001 | 0/0 | 14710 | 2 | 2 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0008c0012t0002 | 0/0 | 14710 | 3 | 1 | 0 | 0 | 2 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0008c0012t0022 | 0/0 | 14710 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0008c0025t0002 | 0/0 | 14710 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0008c0025t0014 | 0/0 | 14710 | 2 | 0 | 2 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0008c0038t0001 | 0/0 | 14710 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0008c0038t0004 | 0/0 | 14711 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0008c0084t0001 | 0/0 | 14710 | 1 | 0 | 0 | 0 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0008c0087t0002 | 0/0 | 14710 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0009c0007t0001 | 0/0 | 14710 | 7 | 0 | 0 | 7 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0009c0007t0002 | 0/0 | 14710 | 2 | 0 | 0 | 2 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0009c0132t0028 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0010c0011t0001 | 0/0 | 14710 | 6 | 3 | 0 | 2 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0010c0082t0001 | 0/0 | 14710 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0010c0094t0002 | 0/0 | 14710 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0011c0061t0004 | 0/0 | 14711 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0011c0136t0004 | 0/0 | 14711 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0011c0137t0011 | 0/0 | 14711 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0011c0149t0004 | 0/0 | 14711 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0011c0150t0001 | 0/0 | 14710 | 1 | 0 | 0 | 0 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0011c0155t0004 | 0/0 | 14711 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0011c0163t0011 | 0/0 | 14711 | 1 | 0 | 0 | 0 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0012c0018t0004 | 0/0 | 14711 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0012c0018t0011 | 0/0 | 14711 | 2 | 0 | 1 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0012c0018t0031 | 0/0 | 14710 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0012c0090t0011 | 0/0 | 14711 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0013c0024t0001 | 0/0 | 14710 | 2 | 0 | 0 | 2 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0013c0024t0008 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0013c0035t0001 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0013c0035t0010 | 0/0 | 14714 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0014c0083t0004 | 0/0 | 14711 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0014c0086t0002 | 0/0 | 14710 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0014c0088t0001 | 0/0 | 14710 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0014c0089t0006 | 0/0 | 14711 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0015c0041t0001 | 0/0 | 14710 | 2 | 0 | 2 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0015c0043t0001 | 0/0 | 14710 | 2 | 2 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0016c0042t0006 | 0/0 | 14711 | 2 | 0 | 0 | 2 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0016c0118t0006 | 0/0 | 14711 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0016c0121t0006 | 0/0 | 14711 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0017c0027t0001 | 0/0 | 14710 | 3 | 0 | 0 | 3 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0017c0108t0001 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0018c0031t0001 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0018c0031t0008 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0018c0031t0033 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0018c0177t0002 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0019c0036t0001 | 0/0 | 14710 | 2 | 2 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0019c0101t0001 | 0/0 | 14710 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0020c0028t0001 | 0/0 | 14710 | 3 | 0 | 0 | 3 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0021c0056t0005 | 0/0 | 14710 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0021c0056t0030 | 0/0 | 14710 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0021c0167t0005 | 0/0 | 14710 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0022c0096t0001 | 0/0 | 14710 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0022c0098t0010 | 0/0 | 14714 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0023c0078t0001 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0023c0079t0002 | 0/0 | 14710 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0024c0034t0001 | 0/0 | 14710 | 2 | 1 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0025c0069t0001 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0025c0071t0001 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0026c0046t0003 | 0/0 | 14711 | 2 | 0 | 0 | 2 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0027c0040t0001 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0027c0040t0019 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0028c0039t0003 | 0/0 | 14711 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0028c0039t0006 | 0/0 | 14711 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0029c0050t0004 | 0/0 | 14711 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0029c0050t0032 | 0/0 | 14710 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0030c0146t0018 | 0/0 | 14710 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0030c0151t0001 | 0/0 | 14710 | 1 | 0 | 0 | 0 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0031c0104t0001 | 0/0 | 14710 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0031c0105t0001 | 0/0 | 14710 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0032c0057t0001 | 0/0 | 14710 | 2 | 0 | 2 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0033c0058t0005 | 0/0 | 14710 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0034c0178t0001 | 0/0 | 14710 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0035c0066t0001 | 0/0 | 14710 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0036c0172t0009 | 0/0 | 14710 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0037c0171t0001 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0038c0097t0001 | 0/0 | 14710 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0039c0073t0002 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0040c0074t0001 | 0/0 | 14710 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0041c0075t0009 | 0/0 | 14710 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0042c0077t0010 | 0/0 | 14714 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0043c0076t0007 | 0/0 | 14710 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0044c0081t0035 | 0/0 | 14710 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0045c0080t0009 | 0/0 | 14710 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0046c0095t0011 | 0/0 | 14711 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0047c0072t0001 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0048c0070t0001 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0049c0068t0003 | 0/0 | 14711 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0050c0067t0001 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0051c0131t0001 | 0/0 | 14710 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0052c0169t0001 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0053c0133t0013 | 0/0 | 14710 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0054c0134t0004 | 0/0 | 14711 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0055c0112t0001 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0056c0113t0001 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0057c0122t0001 | 0/0 | 14710 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0058c0120t0001 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0059c0119t0001 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0060c0116t0003 | 0/0 | 14711 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0061c0115t0002 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0062c0165t0004 | 0/0 | 14711 | 1 | 0 | 0 | 0 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0063c0062t0001 | 0/0 | 14710 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0064c0060t0001 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0065c0145t0001 | 0/0 | 14710 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0066c0162t0001 | 0/0 | 14710 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0067c0160t0008 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0068c0135t0001 | 0/0 | 14710 | 1 | 0 | 0 | 0 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0069c0164t0001 | 0/0 | 14710 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0070c0157t0001 | 0/0 | 14710 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0071c0158t0001 | 0/0 | 14710 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0072c0166t0001 | 0/0 | 14710 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0073c0141t0001 | 0/0 | 14710 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0074c0168t0009 | 0/0 | 14710 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0075c0126t0001 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0076c0111t0001 | 0/0 | 14710 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0077c0127t0001 | 1/0 | 14710 | 1 | 0 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0078c0107t0001 | 0/0 | 14710 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0079c0175t0010 | 0/0 | 14714 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0080c0176t0001 | 0/0 | 14710 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0081c0103t0001 | 0/0 | 14710 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| a0082c0106t0001 | 0/0 | 14710 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | copy fasta | chr5 | 151499092 | 151596331 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0003t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0003t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0003t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0003t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0003t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0003t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0003t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0003t0002g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0003t0002g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0003t0012g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0003t0012g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0003t0020g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0004t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0004t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0004t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0004t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0004t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0004t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0004t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0004t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0004t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0004t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0004t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0004t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0004t0002g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0010t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0010t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0010t0002g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0010t0005g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0010t0007g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0010t0009g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0016t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0016t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0016t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0016t0002g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0016t0004g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0017t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0017t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0017t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0017t0002g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0020t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0020t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0020t0005g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0020t0005g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0021t0002g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0021t0002g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0021t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0021t0008g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0032t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0032t0008g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0044t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0044t0007g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0047t0005g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0047t0007g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0048t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0048t0021g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0049t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0049t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0059t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0065t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0110t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0123t0007g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0124t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0125t0010g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0128t0002g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0129t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0130t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0142t0007g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0144t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0147t0013g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0159t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0174t0002g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0001c0179t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0001t0002g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0001t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0001t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0001t0002g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0001t0002g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0001t0002g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0001t0002g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0001t0002g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0001t0002g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0001t0002g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0001t0002g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0001t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0001t0017g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0001t0036g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0006t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0006t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0006t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0006t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0006t0002g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0006t0002g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0006t0005g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0006t0015g0390 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0006t0034g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0008t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0008t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0008t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0008t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0008t0002g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0008t0002g0369 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0008t0008g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0008t0029g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0026t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0026t0002g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0026t0024g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0037t0002g0386 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0037t0002g0389 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0085t0037g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0092t0002g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0099t0007g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0100t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0002c0170t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0003c0002t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0003c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0003c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0003c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0003c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0003c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0003c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0003c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0003c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0003c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0003c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0003c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0003c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0003c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0003c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0003c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0003c0002t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0003c0002t0002g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0003c0002t0002g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0003c0002t0023g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0003c0009t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0003c0009t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0003c0009t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0003c0009t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0003c0009t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0003c0009t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0003c0009t0026g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0003c0013t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0003c0013t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0003c0013t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0003c0013t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0003c0013t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0003c0013t0009g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0003c0029t0005g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0003c0029t0005g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0003c0029t0005g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0003c0109t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0003c0114t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0003c0117t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0003c0138t0025g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0003c0139t0008g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0003c0140t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0004c0019t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0004c0019t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0004c0019t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0004c0019t0007g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0004c0033t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0004c0033t0004g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0004c0052t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0004c0052t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0004c0053t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0004c0053t0010g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0004c0055t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0004c0055t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0004c0064t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0004c0143t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0004c0148t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0004c0152t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0004c0153t0027g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0004c0156t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0004c0161t0004g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0005c0014t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0005c0014t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0005c0014t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0005c0014t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0005c0014t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0005c0014t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0005c0015t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0005c0015t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0005c0015t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0005c0015t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0005c0015t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0005c0015t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0005c0030t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0005c0030t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0005c0030t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0005c0063t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0005c0173t0002g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0006c0005t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0006c0005t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0006c0005t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0006c0005t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0006c0005t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0006c0005t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0006c0005t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0006c0005t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0006c0005t0006g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0006c0005t0006g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0006c0005t0006g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0006c0005t0015g0391 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0006c0005t0016g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0006c0091t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0006c0093t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0006c0102t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0007c0022t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0007c0022t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0007c0022t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0007c0022t0006g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0007c0023t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0007c0023t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0007c0023t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0007c0045t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0007c0045t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0007c0051t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0007c0051t0006g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0007c0054t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0007c0054t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0007c0154t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0008c0012t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0008c0012t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0008c0012t0002g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0008c0012t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0008c0012t0022g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0008c0025t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0008c0025t0014g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0008c0025t0014g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0008c0038t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0008c0038t0004g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0008c0084t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0008c0087t0002g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0009c0007t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0009c0007t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0009c0007t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0009c0007t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0009c0007t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0009c0007t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0009c0007t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0009c0007t0002g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0009c0007t0002g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0009c0132t0028g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0010c0011t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0010c0011t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0010c0011t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0010c0011t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0010c0011t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0010c0011t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0010c0082t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0010c0094t0002g0385 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0011c0061t0004g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0011c0136t0004g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0011c0137t0011g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0011c0149t0004g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0011c0150t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0011c0155t0004g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0011c0163t0011g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0012c0018t0004g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0012c0018t0011g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0012c0018t0011g0387 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0012c0018t0031g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0012c0090t0011g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0013c0024t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0013c0024t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0013c0024t0008g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0013c0035t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0013c0035t0010g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0014c0083t0004g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0014c0086t0002g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0014c0088t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0014c0089t0006g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0015c0041t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0015c0041t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0015c0043t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0015c0043t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0016c0042t0006g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0016c0042t0006g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0016c0118t0006g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0016c0121t0006g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0017c0027t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0017c0027t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0017c0108t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0018c0031t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0018c0031t0008g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0018c0031t0033g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0018c0177t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0019c0036t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0019c0036t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0019c0101t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0020c0028t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0020c0028t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0020c0028t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0021c0056t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0021c0056t0030g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0021c0167t0005g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0022c0096t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0022c0098t0010g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0023c0078t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0023c0079t0002g0388 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0024c0034t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0024c0034t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0025c0069t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0025c0071t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0026c0046t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0026c0046t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0027c0040t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0027c0040t0019g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0028c0039t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0028c0039t0006g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0029c0050t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0029c0050t0032g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0030c0146t0018g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0030c0151t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0031c0104t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0031c0105t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0032c0057t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0032c0057t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0033c0058t0005g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0034c0178t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0035c0066t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0036c0172t0009g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0037c0171t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0038c0097t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0039c0073t0002g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0040c0074t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0041c0075t0009g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0042c0077t0010g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0043c0076t0007g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0044c0081t0035g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0045c0080t0009g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0046c0095t0011g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0047c0072t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0048c0070t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0049c0068t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0050c0067t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0051c0131t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0052c0169t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0053c0133t0013g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0054c0134t0004g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0055c0112t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0056c0113t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0057c0122t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0058c0120t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0059c0119t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0060c0116t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0061c0115t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0062c0165t0004g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0063c0062t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0064c0060t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0065c0145t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0066c0162t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0067c0160t0008g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0068c0135t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0069c0164t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0070c0157t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0071c0158t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0072c0166t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0073c0141t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0074c0168t0009g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0075c0126t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0076c0111t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0077c0127t0001g0105 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0078c0107t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0079c0175t0010g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0080c0176t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0081c0103t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| a0082c0106t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0030 | c0151 | t0001 | g0168 | EUR | GBR | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG00140 | hp2 | a0006 | c0102 | t0001 | g0306 | EUR | GBR | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG00323 | hp1 | a0011 | c0150 | t0001 | g0189 | EUR | FIN | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG00323 | hp2 | a0062 | c0165 | t0004 | g0208 | EUR | FIN | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG00423 | hp1 | a0003 | c0002 | t0001 | g0113 | EAS | CHS | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG00423 | hp2 | a0002 | c0008 | t0008 | g0277 | EAS | CHS | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG00558 | hp1 | a0006 | c0005 | t0016 | g0008 | EAS | CHS | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG00558 | hp2 | a0001 | c0004 | t0001 | g0259 | EAS | CHS | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG00597 | hp1 | a0002 | c0008 | t0001 | g0276 | EAS | CHS | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG00597 | hp2 | a0007 | c0022 | t0003 | g0207 | EAS | CHS | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG00609 | hp1 | a0002 | c0001 | t0001 | g0132 | EAS | CHS | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG00609 | hp2 | a0052 | c0169 | t0001 | g0074 | EAS | CHS | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG00621 | hp1 | a0002 | c0001 | t0002 | g0007 | EAS | CHS | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG00621 | hp2 | a0003 | c0002 | t0001 | g0095 | EAS | CHS | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG00639 | hp1 | a0007 | c0051 | t0001 | g0174 | AMR | PUR | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG00639 | hp2 | a0011 | c0061 | t0004 | g0282 | AMR | PUR | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG00642 | hp1 | a0006 | c0005 | t0001 | g0301 | AMR | PUR | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG00642 | hp2 | a0005 | c0173 | t0002 | g0336 | AMR | PUR | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG00673 | hp1 | a0002 | c0001 | t0002 | g0368 | EAS | CHS | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG00673 | hp2 | a0039 | c0073 | t0002 | g0356 | EAS | CHS | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG00735 | hp1 | a0012 | c0018 | t0011 | g0387 | AMR | PUR | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG00735 | hp2 | a0040 | c0074 | t0001 | g0244 | AMR | PUR | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG00741 | hp1 | a0023 | c0079 | t0002 | g0388 | AMR | PUR | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG00741 | hp2 | a0001 | c0174 | t0002 | g0337 | AMR | PUR | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01069 | hp1 | a0008 | c0025 | t0014 | g0339 | AMR | PUR | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01069 | hp2 | a0007 | c0023 | t0001 | g0314 | AMR | PUR | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01070 | hp1 | a0007 | c0054 | t0001 | g0021 | AMR | PUR | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01070 | hp2 | a0002 | c0006 | t0001 | g0005 | AMR | PUR | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01071 | hp1 | a0008 | c0025 | t0014 | g0341 | AMR | PUR | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01071 | hp2 | a0002 | c0006 | t0001 | g0005 | AMR | PUR | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01074 | hp1 | a0001 | c0003 | t0001 | g0202 | AMR | PUR | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01074 | hp2 | a0007 | c0054 | t0001 | g0024 | AMR | PUR | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01081 | hp1 | a0002 | c0026 | t0001 | g0298 | AMR | PUR | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01081 | hp2 | a0001 | c0003 | t0001 | g0295 | AMR | PUR | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01106 | hp1 | a0007 | c0154 | t0001 | g0165 | AMR | PUR | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01106 | hp2 | a0003 | c0002 | t0001 | g0116 | AMR | PUR | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01109 | hp1 | a0011 | c0149 | t0004 | g0190 | AMR | PUR | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01109 | hp2 | a0021 | c0167 | t0005 | g0048 | AMR | PUR | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01167 | hp1 | a0008 | c0038 | t0004 | g0305 | AMR | PUR | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01167 | hp2 | a0001 | c0110 | t0001 | g0119 | AMR | PUR | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01168 | hp1 | a0035 | c0066 | t0001 | g0299 | AMR | PUR | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01168 | hp2 | a0004 | c0033 | t0001 | g0280 | AMR | PUR | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01169 | hp1 | a0004 | c0033 | t0004 | g0281 | AMR | PUR | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01169 | hp2 | a0008 | c0038 | t0001 | g0304 | AMR | PUR | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01175 | hp1 | a0007 | c0023 | t0001 | g0285 | AMR | PUR | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01175 | hp2 | a0002 | c0001 | t0001 | g0309 | AMR | PUR | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01192 | hp1 | a0004 | c0161 | t0004 | g0205 | AMR | PUR | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01192 | hp2 | a0001 | c0004 | t0001 | g0264 | AMR | PUR | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01243 | hp1 | a0041 | c0075 | t0009 | g0249 | AMR | PUR | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01243 | hp2 | a0072 | c0166 | t0001 | g0047 | AMR | PUR | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01255 | hp1 | a0003 | c0002 | t0001 | g0106 | AMR | CLM | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01255 | hp2 | a0004 | c0156 | t0001 | g0023 | AMR | CLM | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01256 | hp1 | a0012 | c0090 | t0011 | g0338 | AMR | CLM | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01256 | hp2 | a0003 | c0002 | t0001 | g0001 | AMR | CLM | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01257 | hp1 | a0032 | c0057 | t0001 | g0017 | AMR | CLM | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01257 | hp2 | a0046 | c0095 | t0011 | g0354 | AMR | CLM | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01258 | hp1 | a0032 | c0057 | t0001 | g0018 | AMR | CLM | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01258 | hp2 | a0003 | c0002 | t0001 | g0001 | AMR | CLM | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01261 | hp1 | a0002 | c0100 | t0001 | g0307 | AMR | CLM | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01261 | hp2 | a0006 | c0005 | t0001 | g0135 | AMR | CLM | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01358 | hp1 | a0001 | c0016 | t0001 | g0247 | AMR | CLM | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01358 | hp2 | a0014 | c0088 | t0001 | g0310 | AMR | CLM | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01433 | hp1 | a0003 | c0002 | t0023 | g0094 | AMR | CLM | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01433 | hp2 | a0010 | c0082 | t0001 | g0162 | AMR | CLM | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01496 | hp1 | a0002 | c0001 | t0017 | g0009 | AMR | CLM | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01496 | hp2 | a0003 | c0013 | t0001 | g0092 | AMR | CLM | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01515 | hp1 | a0001 | c0016 | t0004 | g0004 | EUR | IBS | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01515 | hp2 | a0011 | c0163 | t0011 | g0335 | EUR | IBS | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01516 | hp1 | a0001 | c0004 | t0001 | g0262 | EUR | IBS | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01516 | hp2 | a0008 | c0012 | t0002 | g0006 | EUR | IBS | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01517 | hp1 | a0008 | c0012 | t0002 | g0006 | EUR | IBS | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01517 | hp2 | a0001 | c0016 | t0004 | g0004 | EUR | IBS | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01884 | hp1 | a0008 | c0025 | t0002 | g0321 | AFR | ACB | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01884 | hp2 | a0024 | c0034 | t0001 | g0241 | AFR | ACB | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01891 | hp1 | a0001 | c0017 | t0001 | g0279 | AFR | ACB | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01891 | hp2 | a0001 | c0010 | t0001 | g0289 | AFR | ACB | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01928 | hp1 | a0003 | c0002 | t0001 | g0078 | AMR | PEL | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01928 | hp2 | a0001 | c0049 | t0001 | g0030 | AMR | PEL | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01934 | hp1 | a0006 | c0005 | t0015 | g0391 | AMR | PEL | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01934 | hp2 | a0003 | c0002 | t0001 | g0088 | AMR | PEL | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01952 | hp1 | a0003 | c0002 | t0001 | g0091 | AMR | PEL | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01952 | hp2 | a0051 | c0131 | t0001 | g0199 | AMR | PEL | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01978 | hp1 | a0015 | c0041 | t0001 | g0114 | AMR | PEL | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01978 | hp2 | a0002 | c0037 | t0002 | g0386 | AMR | PEL | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01981 | hp1 | a0071 | c0158 | t0001 | g0173 | AMR | PEL | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01981 | hp2 | a0002 | c0006 | t0001 | g0022 | AMR | PEL | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01993 | hp1 | a0001 | c0004 | t0001 | g0284 | AMR | PEL | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG01993 | hp2 | a0001 | c0124 | t0001 | g0104 | AMR | PEL | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02015 | hp1 | a0016 | c0042 | t0006 | g0383 | EAS | KHV | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02015 | hp2 | a0013 | c0024 | t0001 | g0225 | EAS | KHV | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02027 | hp1 | a0001 | c0003 | t0020 | g0221 | EAS | KHV | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02027 | hp2 | a0001 | c0016 | t0001 | g0273 | EAS | KHV | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02040 | hp1 | a0002 | c0001 | t0002 | g0345 | EAS | KHV | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02040 | hp2 | a0014 | c0089 | t0006 | g0359 | EAS | KHV | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02055 | hp1 | a0043 | c0076 | t0007 | g0037 | AFR | ACB | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02055 | hp2 | a0065 | c0145 | t0001 | g0061 | AFR | ACB | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02056 | hp1 | a0002 | c0026 | t0002 | g0370 | EAS | KHV | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02056 | hp2 | a0018 | c0177 | t0002 | g0328 | EAS | KHV | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02071 | hp1 | a0003 | c0002 | t0001 | g0062 | EAS | KHV | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02071 | hp2 | a0001 | c0003 | t0001 | g0204 | EAS | KHV | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02080 | hp1 | a0049 | c0068 | t0003 | g0236 | EAS | KHV | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02080 | hp2 | a0018 | c0031 | t0008 | g0118 | EAS | KHV | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02083 | hp1 | a0003 | c0109 | t0001 | g0087 | EAS | KHV | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02083 | hp2 | a0001 | c0128 | t0002 | g0371 | EAS | KHV | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02132 | hp1 | a0001 | c0021 | t0002 | g0375 | EAS | KHV | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02132 | hp2 | a0012 | c0018 | t0011 | g0347 | EAS | KHV | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02135 | hp1 | a0003 | c0002 | t0001 | g0081 | EAS | KHV | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02135 | hp2 | a0002 | c0006 | t0002 | g0367 | EAS | KHV | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02145 | hp1 | a0004 | c0052 | t0001 | g0193 | AFR | ACB | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02145 | hp2 | a0022 | c0098 | t0010 | g0039 | AFR | ACB | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02148 | hp1 | a0010 | c0094 | t0002 | g0385 | AMR | PEL | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02148 | hp2 | a0001 | c0059 | t0001 | g0267 | AMR | PEL | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02155 | hp1 | a0001 | c0010 | t0001 | g0212 | EAS | CDX | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02155 | hp2 | a0028 | c0039 | t0006 | g0376 | EAS | CDX | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02165 | hp1 | a0003 | c0013 | t0001 | g0109 | EAS | CDX | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02165 | hp2 | a0007 | c0022 | t0006 | g0322 | EAS | CDX | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02258 | hp1 | a0005 | c0014 | t0001 | g0182 | AFR | ACB | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02258 | hp2 | a0045 | c0080 | t0009 | g0150 | AFR | ACB | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02273 | hp1 | a0015 | c0041 | t0001 | g0097 | AMR | PEL | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02273 | hp2 | a0003 | c0002 | t0001 | g0089 | AMR | PEL | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02280 | hp1 | a0005 | c0014 | t0001 | g0056 | AFR | ACB | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02280 | hp2 | a0001 | c0020 | t0005 | g0167 | AFR | ACB | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02293 | hp1 | a0003 | c0117 | t0001 | g0111 | AMR | PEL | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02293 | hp2 | a0004 | c0153 | t0027 | g0166 | AMR | PEL | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02451 | hp1 | a0003 | c0138 | t0025 | g0042 | AFR | ACB | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02451 | hp2 | a0029 | c0050 | t0032 | g0052 | AFR | ACB | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02523 | hp1 | a0002 | c0001 | t0002 | g0350 | EAS | KHV | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02523 | hp2 | a0002 | c0001 | t0002 | g0384 | EAS | KHV | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02572 | hp1 | a0001 | c0020 | t0005 | g0172 | AFR | GWD | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02572 | hp2 | a0001 | c0147 | t0013 | g0161 | AFR | GWD | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02602 | hp1 | a0066 | c0162 | t0001 | g0214 | SAS | PJL | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02602 | hp2 | a0054 | c0134 | t0004 | g0083 | SAS | PJL | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02622 | hp1 | a0003 | c0013 | t0009 | g0312 | AFR | GWD | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02622 | hp2 | a0029 | c0050 | t0004 | g0177 | AFR | GWD | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02647 | hp1 | a0003 | c0029 | t0005 | g0292 | AFR | GWD | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02647 | hp2 | a0001 | c0003 | t0002 | g0329 | AFR | GWD | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02683 | hp1 | a0002 | c0001 | t0001 | g0300 | SAS | PJL | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02683 | hp2 | a0012 | c0018 | t0004 | g0142 | SAS | PJL | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02698 | hp1 | a0011 | c0136 | t0004 | g0031 | SAS | PJL | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02698 | hp2 | a0002 | c0026 | t0024 | g0146 | SAS | PJL | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02717 | hp1 | a0004 | c0053 | t0001 | g0169 | AFR | GWD | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02717 | hp2 | a0008 | c0012 | t0022 | g0318 | AFR | GWD | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02723 | hp1 | a0001 | c0010 | t0007 | g0003 | AFR | GWD | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02723 | hp2 | a0057 | c0122 | t0001 | g0082 | AFR | GWD | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02735 | hp1 | a0003 | c0009 | t0026 | g0117 | SAS | PJL | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02735 | hp2 | a0069 | c0164 | t0001 | g0201 | SAS | PJL | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02738 | hp1 | a0014 | c0086 | t0002 | g0340 | SAS | PJL | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02738 | hp2 | a0006 | c0005 | t0001 | g0302 | SAS | PJL | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02809 | hp1 | a0004 | c0019 | t0007 | g0170 | AFR | GWD | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02809 | hp2 | a0004 | c0143 | t0001 | g0043 | AFR | GWD | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02818 | hp1 | a0010 | c0011 | t0001 | g0035 | AFR | GWD | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02818 | hp2 | a0030 | c0146 | t0018 | g0057 | AFR | GWD | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02886 | hp1 | a0001 | c0047 | t0005 | g0290 | AFR | GWD | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02886 | hp2 | a0005 | c0030 | t0001 | g0180 | AFR | GWD | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02895 | hp1 | a0005 | c0030 | t0001 | g0060 | AFR | GWD | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02895 | hp2 | a0021 | c0056 | t0005 | g0046 | AFR | GWD | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02896 | hp1 | a0005 | c0030 | t0001 | g0015 | AFR | GWD | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02896 | hp2 | a0001 | c0142 | t0007 | g0044 | AFR | GWD | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02922 | hp1 | a0081 | c0103 | t0001 | g0315 | AFR | ESN | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02922 | hp2 | a0003 | c0029 | t0005 | g0291 | AFR | ESN | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02965 | hp1 | a0002 | c0006 | t0034 | g0358 | AFR | ESN | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02965 | hp2 | a0053 | c0133 | t0013 | g0016 | AFR | ESN | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02970 | hp1 | a0033 | c0058 | t0005 | g0243 | AFR | ESN | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02970 | hp2 | a0004 | c0052 | t0001 | g0175 | AFR | ESN | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02976 | hp1 | a0005 | c0014 | t0001 | g0051 | AFR | ESN | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02976 | hp2 | a0001 | c0123 | t0007 | g0077 | AFR | ESN | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG03041 | hp1 | a0008 | c0012 | t0002 | g0320 | AFR | GWD | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG03041 | hp2 | a0080 | c0176 | t0001 | g0311 | AFR | GWD | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG03098 | hp1 | a0008 | c0087 | t0002 | g0365 | AFR | MSL | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG03098 | hp2 | a0044 | c0081 | t0035 | g0357 | AFR | MSL | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG03130 | hp1 | a0004 | c0053 | t0010 | g0019 | AFR | ESN | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG03130 | hp2 | a0015 | c0043 | t0001 | g0141 | AFR | ESN | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG03139 | hp1 | a0002 | c0001 | t0005 | g0036 | AFR | ESN | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG03139 | hp2 | a0038 | c0097 | t0001 | g0038 | AFR | ESN | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG03195 | hp1 | a0042 | c0077 | t0010 | g0248 | AFR | ESN | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG03195 | hp2 | a0001 | c0144 | t0001 | g0179 | AFR | ESN | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG03209 | hp1 | a0021 | c0056 | t0030 | g0050 | AFR | MSL | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG03209 | hp2 | a0005 | c0014 | t0001 | g0178 | AFR | MSL | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG03225 | hp1 | a0001 | c0047 | t0007 | g0294 | AFR | MSL | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG03225 | hp2 | a0001 | c0010 | t0005 | g0058 | AFR | MSL | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG03453 | hp1 | a0005 | c0014 | t0001 | g0059 | AFR | MSL | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG03453 | hp2 | a0008 | c0012 | t0001 | g0045 | AFR | MSL | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG03486 | hp1 | a0008 | c0012 | t0001 | g0049 | AFR | MSL | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG03486 | hp2 | a0022 | c0096 | t0001 | g0041 | AFR | MSL | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG03492 | hp1 | a0001 | c0020 | t0001 | g0209 | SAS | PJL | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG03492 | hp2 | a0001 | c0003 | t0001 | g0230 | SAS | PJL | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG03516 | hp1 | a0031 | c0104 | t0001 | g0010 | AFR | ESN | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG03516 | hp2 | a0002 | c0006 | t0005 | g0163 | AFR | ESN | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG03540 | hp1 | a0013 | c0035 | t0010 | g0242 | AFR | GWD | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG03540 | hp2 | a0003 | c0029 | t0005 | g0293 | AFR | GWD | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG03579 | hp1 | a0005 | c0014 | t0001 | g0055 | AFR | MSL | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG03579 | hp2 | a0001 | c0125 | t0010 | g0286 | AFR | MSL | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG03669 | hp1 | a0016 | c0121 | t0006 | g0326 | SAS | PJL | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG03669 | hp2 | a0010 | c0011 | t0001 | g0303 | SAS | PJL | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG03688 | hp1 | a0002 | c0008 | t0001 | g0149 | SAS | STU | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG03688 | hp2 | a0001 | c0048 | t0001 | g0026 | SAS | STU | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG03704 | hp1 | a0011 | c0137 | t0011 | g0319 | SAS | PJL | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG03704 | hp2 | a0002 | c0001 | t0002 | g0353 | SAS | PJL | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG03710 | hp1 | a0011 | c0155 | t0004 | g0028 | SAS | PJL | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG03710 | hp2 | a0002 | c0008 | t0002 | g0369 | SAS | PJL | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG03831 | hp1 | a0063 | c0062 | t0001 | g0266 | SAS | BEB | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG03831 | hp2 | a0073 | c0141 | t0001 | g0200 | SAS | BEB | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG03834 | hp1 | a0034 | c0178 | t0001 | g0229 | SAS | BEB | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG03834 | hp2 | a0012 | c0018 | t0031 | g0139 | SAS | BEB | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG03927 | hp1 | a0005 | c0015 | t0001 | g0217 | SAS | BEB | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG03927 | hp2 | a0002 | c0008 | t0002 | g0348 | SAS | BEB | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG04115 | hp1 | a0001 | c0048 | t0021 | g0025 | SAS | STU | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG04115 | hp2 | a0001 | c0016 | t0002 | g0331 | SAS | STU | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG04184 | hp1 | a0001 | c0003 | t0001 | g0147 | SAS | BEB | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG04184 | hp2 | a0014 | c0083 | t0004 | g0137 | SAS | BEB | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG04199 | hp1 | a0001 | c0049 | t0001 | g0020 | SAS | STU | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG04199 | hp2 | a0001 | c0003 | t0001 | g0313 | SAS | STU | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG04204 | hp1 | a0001 | c0003 | t0002 | g0332 | SAS | STU | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG04204 | hp2 | a0002 | c0001 | t0002 | g0342 | SAS | STU | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18522 | hp1 | a0004 | c0019 | t0001 | g0053 | AFR | YRI | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18522 | hp2 | a0019 | c0036 | t0001 | g0040 | AFR | YRI | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18612 | hp1 | a0003 | c0013 | t0001 | g0100 | EAS | CHB | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18612 | hp2 | a0003 | c0013 | t0001 | g0079 | EAS | CHB | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18747 | hp1 | a0002 | c0001 | t0002 | g0344 | EAS | CHB | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18747 | hp2 | a0003 | c0002 | t0001 | g0065 | EAS | CHB | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18906 | hp1 | a0001 | c0010 | t0009 | g0171 | AFR | YRI | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18906 | hp2 | a0010 | c0011 | t0001 | g0032 | AFR | YRI | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18939 | hp1 | a0001 | c0020 | t0001 | g0187 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18939 | hp2 | a0017 | c0027 | t0001 | g0107 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18941 | hp1 | a0017 | c0027 | t0001 | g0002 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18941 | hp2 | a0005 | c0015 | t0001 | g0011 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18942 | hp1 | a0020 | c0028 | t0001 | g0073 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18942 | hp2 | a0007 | c0045 | t0003 | g0191 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18943 | hp1 | a0016 | c0042 | t0006 | g0381 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18943 | hp2 | a0002 | c0001 | t0002 | g0361 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18944 | hp1 | a0048 | c0070 | t0001 | g0226 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18944 | hp2 | a0002 | c0006 | t0001 | g0145 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18945 | hp1 | a0002 | c0001 | t0002 | g0007 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18945 | hp2 | a0003 | c0009 | t0001 | g0098 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18948 | hp1 | a0024 | c0034 | t0001 | g0288 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18948 | hp2 | a0001 | c0003 | t0001 | g0123 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18951 | hp1 | a0005 | c0015 | t0001 | g0232 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18951 | hp2 | a0056 | c0113 | t0001 | g0072 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18952 | hp1 | a0002 | c0001 | t0001 | g0251 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18952 | hp2 | a0009 | c0007 | t0001 | g0216 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18954 | hp1 | a0013 | c0024 | t0008 | g0228 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18954 | hp2 | a0001 | c0004 | t0001 | g0256 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18956 | hp1 | a0003 | c0002 | t0001 | g0254 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18956 | hp2 | a0001 | c0004 | t0002 | g0380 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18957 | hp1 | a0010 | c0011 | t0001 | g0143 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18957 | hp2 | a0047 | c0072 | t0001 | g0155 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18959 | hp1 | a0001 | c0021 | t0002 | g0374 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18959 | hp2 | a0001 | c0004 | t0001 | g0260 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18962 | hp1 | a0001 | c0004 | t0001 | g0253 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18962 | hp2 | a0009 | c0007 | t0001 | g0197 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18963 | hp1 | a0001 | c0003 | t0001 | g0185 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18963 | hp2 | a0037 | c0171 | t0001 | g0213 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18964 | hp1 | a0001 | c0003 | t0001 | g0121 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18964 | hp2 | a0002 | c0008 | t0002 | g0343 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18965 | hp1 | a0002 | c0001 | t0001 | g0239 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18965 | hp2 | a0006 | c0005 | t0003 | g0126 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18967 | hp1 | a0001 | c0129 | t0001 | g0218 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18967 | hp2 | a0002 | c0001 | t0002 | g0366 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18968 | hp1 | a0002 | c0001 | t0001 | g0130 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18968 | hp2 | a0006 | c0005 | t0006 | g0333 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18969 | hp1 | a0075 | c0126 | t0001 | g0096 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18969 | hp2 | a0001 | c0159 | t0001 | g0186 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18970 | hp1 | a0001 | c0004 | t0001 | g0252 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18970 | hp2 | a0060 | c0116 | t0003 | g0101 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18971 | hp1 | a0025 | c0069 | t0001 | g0240 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18971 | hp2 | a0002 | c0006 | t0001 | g0129 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18972 | hp1 | a0009 | c0007 | t0001 | g0215 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18972 | hp2 | a0001 | c0017 | t0001 | g0261 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18973 | hp1 | a0009 | c0132 | t0028 | g0196 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18973 | hp2 | a0001 | c0004 | t0001 | g0156 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18975 | hp1 | a0003 | c0009 | t0001 | g0270 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18975 | hp2 | a0007 | c0051 | t0006 | g0351 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18977 | hp1 | a0009 | c0007 | t0001 | g0220 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18977 | hp2 | a0001 | c0065 | t0001 | g0268 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18980 | hp1 | a0001 | c0021 | t0008 | g0122 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18980 | hp2 | a0001 | c0130 | t0001 | g0192 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18982 | hp1 | a0003 | c0009 | t0002 | g0330 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18982 | hp2 | a0006 | c0005 | t0003 | g0128 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18983 | hp1 | a0001 | c0003 | t0001 | g0183 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18983 | hp2 | a0058 | c0120 | t0001 | g0099 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18984 | hp1 | a0006 | c0005 | t0003 | g0125 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18984 | hp2 | a0017 | c0027 | t0001 | g0002 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18985 | hp1 | a0003 | c0114 | t0001 | g0160 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18985 | hp2 | a0023 | c0078 | t0001 | g0297 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18987 | hp1 | a0001 | c0003 | t0012 | g0206 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18987 | hp2 | a0025 | c0071 | t0001 | g0287 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18989 | hp1 | a0003 | c0009 | t0001 | g0120 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18989 | hp2 | a0009 | c0007 | t0002 | g0372 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18990 | hp1 | a0006 | c0005 | t0003 | g0140 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18990 | hp2 | a0001 | c0004 | t0001 | g0265 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18991 | hp1 | a0003 | c0009 | t0001 | g0063 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18991 | hp2 | a0005 | c0063 | t0001 | g0257 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18992 | hp1 | a0020 | c0028 | t0001 | g0070 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18992 | hp2 | a0006 | c0005 | t0003 | g0127 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18994 | hp1 | a0006 | c0005 | t0006 | g0362 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18994 | hp2 | a0003 | c0009 | t0001 | g0103 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18997 | hp1 | a0010 | c0011 | t0001 | g0274 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18997 | hp2 | a0002 | c0001 | t0036 | g0349 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18998 | hp1 | a0001 | c0021 | t0003 | g0184 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA18998 | hp2 | a0002 | c0001 | t0001 | g0133 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19000 | hp1 | a0028 | c0039 | t0003 | g0066 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19000 | hp2 | a0002 | c0001 | t0001 | g0144 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19001 | hp1 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19001 | hp2 | a0001 | c0004 | t0001 | g0271 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19002 | hp1 | a0003 | c0002 | t0002 | g0378 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19002 | hp2 | a0009 | c0007 | t0002 | g0373 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19003 | hp1 | a0007 | c0022 | t0003 | g0158 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19003 | hp2 | a0002 | c0092 | t0002 | g0382 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19004 | hp1 | a0002 | c0001 | t0001 | g0250 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19004 | hp2 | a0006 | c0005 | t0006 | g0364 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19005 | hp1 | a0001 | c0017 | t0002 | g0379 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19005 | hp2 | a0007 | c0022 | t0003 | g0014 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19007 | hp1 | a0004 | c0064 | t0001 | g0263 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19007 | hp2 | a0055 | c0112 | t0001 | g0067 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19010 | hp1 | a0001 | c0004 | t0001 | g0255 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19010 | hp2 | a0001 | c0016 | t0001 | g0203 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19011 | hp1 | a0016 | c0118 | t0006 | g0325 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19011 | hp2 | a0050 | c0067 | t0001 | g0224 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19012 | hp1 | a0001 | c0032 | t0008 | g0108 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19012 | hp2 | a0003 | c0013 | t0001 | g0090 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19030 | hp1 | a0076 | c0111 | t0001 | g0076 | AFR | LWK | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19030 | hp2 | a0074 | c0168 | t0009 | g0029 | AFR | LWK | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19043 | hp1 | a0015 | c0043 | t0001 | g0075 | AFR | LWK | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19043 | hp2 | a0001 | c0044 | t0007 | g0085 | AFR | LWK | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19054 | hp1 | a0002 | c0008 | t0001 | g0237 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19054 | hp2 | a0005 | c0015 | t0001 | g0159 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19055 | hp1 | a0067 | c0160 | t0008 | g0211 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19055 | hp2 | a0002 | c0001 | t0001 | g0131 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19056 | hp1 | a0026 | c0046 | t0003 | g0219 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19056 | hp2 | a0004 | c0055 | t0001 | g0234 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19057 | hp1 | a0061 | c0115 | t0002 | g0324 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19057 | hp2 | a0017 | c0108 | t0001 | g0112 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19058 | hp1 | a0026 | c0046 | t0003 | g0198 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19058 | hp2 | a0027 | c0040 | t0001 | g0071 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19060 | hp1 | a0001 | c0044 | t0001 | g0110 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19060 | hp2 | a0003 | c0002 | t0001 | g0093 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19062 | hp1 | a0018 | c0031 | t0033 | g0327 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19062 | hp2 | a0002 | c0001 | t0001 | g0124 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19066 | hp1 | a0059 | c0119 | t0001 | g0102 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19066 | hp2 | a0001 | c0003 | t0012 | g0222 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19068 | hp1 | a0001 | c0003 | t0001 | g0231 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19068 | hp2 | a0007 | c0045 | t0003 | g0153 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19070 | hp1 | a0027 | c0040 | t0019 | g0068 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19070 | hp2 | a0009 | c0007 | t0001 | g0195 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19072 | hp1 | a0006 | c0093 | t0003 | g0275 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19072 | hp2 | a0064 | c0060 | t0001 | g0272 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19074 | hp1 | a0003 | c0002 | t0002 | g0323 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19074 | hp2 | a0001 | c0179 | t0001 | g0233 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19075 | hp1 | a0005 | c0015 | t0001 | g0151 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19075 | hp2 | a0002 | c0001 | t0002 | g0346 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19077 | hp1 | a0003 | c0002 | t0001 | g0064 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19077 | hp2 | a0002 | c0001 | t0002 | g0363 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19079 | hp1 | a0009 | c0007 | t0001 | g0154 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19079 | hp2 | a0002 | c0001 | t0001 | g0138 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19080 | hp1 | a0078 | c0107 | t0001 | g0086 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19080 | hp2 | a0003 | c0139 | t0008 | g0238 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19081 | hp1 | a0002 | c0001 | t0001 | g0278 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19081 | hp2 | a0013 | c0035 | t0001 | g0227 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19083 | hp1 | a0002 | c0170 | t0002 | g0334 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19083 | hp2 | a0009 | c0007 | t0001 | g0194 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19086 | hp1 | a0001 | c0032 | t0001 | g0269 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19086 | hp2 | a0001 | c0010 | t0002 | g0352 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19087 | hp1 | a0013 | c0024 | t0001 | g0235 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19087 | hp2 | a0002 | c0008 | t0029 | g0246 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19088 | hp1 | a0005 | c0015 | t0001 | g0157 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19088 | hp2 | a0020 | c0028 | t0001 | g0069 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19089 | hp1 | a0003 | c0140 | t0001 | g0223 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19089 | hp2 | a0002 | c0006 | t0002 | g0360 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19090 | hp1 | a0004 | c0055 | t0001 | g0012 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19090 | hp2 | a0007 | c0023 | t0003 | g0258 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19091 | hp1 | a0003 | c0002 | t0002 | g0377 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19091 | hp2 | a0018 | c0031 | t0001 | g0080 | EAS | JPT | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19240 | hp1 | a0082 | c0106 | t0001 | g0317 | AFR | YRI | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA19240 | hp2 | a0004 | c0148 | t0001 | g0152 | AFR | YRI | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA20129 | hp1 | a0002 | c0099 | t0007 | g0033 | AFR | ASW | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA20129 | hp2 | a0070 | c0157 | t0001 | g0164 | AFR | ASW | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA20752 | hp1 | a0008 | c0084 | t0001 | g0134 | EUR | TSI | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA20752 | hp2 | a0001 | c0017 | t0001 | g0283 | EUR | TSI | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA20805 | hp1 | a0002 | c0001 | t0001 | g0084 | EUR | TSI | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA20805 | hp2 | a0068 | c0135 | t0001 | g0027 | EUR | TSI | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA20905 | hp1 | a0002 | c0001 | t0001 | g0296 | SAS | GIH | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA20905 | hp2 | a0001 | c0003 | t0001 | g0210 | SAS | GIH | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02109 | hp1 | a0004 | c0019 | t0001 | g0181 | AFR | ACB | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02109 | hp2 | a0031 | c0105 | t0001 | g0316 | AFR | ACB | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02486 | hp1 | a0004 | c0019 | t0001 | g0054 | AFR | ACB | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02486 | hp2 | a0006 | c0091 | t0001 | g0308 | AFR | ACB | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02559 | hp1 | a0004 | c0152 | t0001 | g0176 | AFR | ACB | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG02559 | hp2 | a0019 | c0101 | t0001 | g0136 | AFR | ACB | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG03471 | hp1 | a0010 | c0011 | t0001 | g0034 | AFR | MSL | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG03471 | hp2 | a0079 | c0175 | t0010 | g0148 | AFR | MSL | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG06807 | hp1 | a0001 | c0010 | t0007 | g0003 | AFR | USA | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| HG06807 | hp2 | a0003 | c0002 | t0001 | g0115 | AFR | USA | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA20300 | hp1 | a0002 | c0037 | t0002 | g0389 | AFR | USA | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA20300 | hp2 | a0036 | c0172 | t0009 | g0245 | AFR | USA | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA21309 | hp1 | a0002 | c0085 | t0037 | g0355 | AFR | LWK | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| NA21309 | hp2 | a0019 | c0036 | t0001 | g0188 | AFR | LWK | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0006 | t0015 | g0390 | REF | REF | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| homoSapiens_grch38 | hp1 | a0077 | c0127 | t0001 | g0105 | REF | REF | FAT2_chr5_151499092_151596331 | FAT2 | chr5 | 151499092 | 151596331 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:151505890
|
C | T | 1 | a0065 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.12725G>A | p.Arg4242His | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 24/24 | 12912/14710 | 12725/13050 | 4242/4349 | chr5 | 151505890 | ||
| chr5:151507321
|
G | A | 58 | a0001a0002a0003others(55): Show | 322 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(319): Show |
missense_variant | MODERATE | c.12350C>T | p.Pro4117Leu | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 23/24 | 12537/14710 | 12350/13050 | 4117/4349 | chr5 | 151507321 | ||
| chr5:151512207
|
T | G | 1 | a0029 | 2 | HG02451.hp2 HG02622.hp2 |
missense_variant | MODERATE | c.11863A>C | p.Thr3955Pro | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 21/24 | 12050/14710 | 11863/13050 | 3955/4349 | chr5 | 151512207 | ||
| chr5:151512211
|
C | G | 7 | a0019a0027a0030others(4): Show | 12 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(9): Show |
missense_variant | MODERATE | c.11859G>C | p.Gln3953His | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 21/24 | 12046/14710 | 11859/13050 | 3953/4349 | chr5 | 151512211 | ||
| chr5:151512245
|
G | C | 1 | a0029 | 2 | HG02451.hp2 HG02622.hp2 |
missense_variant | MODERATE | c.11825C>G | p.Thr3942Ser | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 21/24 | 12012/14710 | 11825/13050 | 3942/4349 | chr5 | 151512245 | ||
| chr5:151521401
|
G | A | 1 | a0050 | 1 | NA19011.hp2 | missense_variant | MODERATE | c.11192C>T | p.Thr3731Ile | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/24 | 11379/14710 | 11192/13050 | 3731/4349 | chr5 | 151521401 | ||
| chr5:151521401
|
G | T | 1 | a0067 | 1 | NA19055.hp1 | missense_variant | MODERATE | c.11192C>A | p.Thr3731Asn | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/24 | 11379/14710 | 11192/13050 | 3731/4349 | chr5 | 151521401 | ||
| chr5:151521700
|
C | T | 63 | a0001a0002a0003others(60): Show | 334 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(331): Show |
missense_variant | MODERATE | c.10893G>A | p.Met3631Ile | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/24 | 11080/14710 | 10893/13050 | 3631/4349 | chr5 | 151521700 | ||
| chr5:151521761
|
G | A | 1 | a0033 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.10832C>T | p.Thr3611Met | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/24 | 11019/14710 | 10832/13050 | 3611/4349 | chr5 | 151521761 | ||
| chr5:151521905
|
G | A | 1 | a0066 | 1 | HG02602.hp1 | missense_variant | MODERATE | c.10688C>T | p.Thr3563Met | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/24 | 10875/14710 | 10688/13050 | 3563/4349 | chr5 | 151521905 | ||
| chr5:151522052
|
A | G | 63 | a0001a0002a0003others(60): Show | 334 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(331): Show |
missense_variant | MODERATE | c.10541T>C | p.Leu3514Ser | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/24 | 10728/14710 | 10541/13050 | 3514/4349 | chr5 | 151522052 | ||
| chr5:151525870
|
C | G | 1 | a0061 | 1 | NA19057.hp1 | missense_variant | MODERATE | c.10404G>C | p.Lys3468Asn | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 18/24 | 10591/14710 | 10404/13050 | 3468/4349 | chr5 | 151525870 | ||
| chr5:151529189
|
C | T | 1 | a0065 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.10015G>A | p.Val3339Ile | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 15/24 | 10202/14710 | 10015/13050 | 3339/4349 | chr5 | 151529189 | ||
| chr5:151529251
|
C | T | 9 | a0005a0010a0015others(6): Show | 36 | HG00642.hp2 HG01243.hp2 HG01433.hp2 others(33): Show |
missense_variant | MODERATE | c.9953G>A | p.Arg3318Gln | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 15/24 | 10140/14710 | 9953/13050 | 3318/4349 | chr5 | 151529251 | ||
| chr5:151529252
|
G | A | 7 | a0006a0007a0016others(4): Show | 40 | HG00140.hp2 HG00558.hp1 HG00597.hp2 others(37): Show |
missense_variant | MODERATE | c.9952C>T | p.Arg3318Trp | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 15/24 | 10139/14710 | 9952/13050 | 3318/4349 | chr5 | 151529252 | ||
| chr5:151529287
|
G | A | 2 | a0042a0079 | 2 | HG03195.hp1 HG03471.hp2 |
missense_variant | MODERATE | c.9917C>T | p.Thr3306Ile | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 15/24 | 10104/14710 | 9917/13050 | 3306/4349 | chr5 | 151529287 | ||
| chr5:151529294
|
C | T | 1 | a0064 | 1 | NA19072.hp2 | missense_variant | MODERATE | c.9910G>A | p.Val3304Met | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 15/24 | 10097/14710 | 9910/13050 | 3304/4349 | chr5 | 151529294 | ||
| chr5:151531593
|
G | A | 1 | a0063 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.9805C>T | p.Arg3269Cys | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 14/24 | 9992/14710 | 9805/13050 | 3269/4349 | chr5 | 151531593 | ||
| chr5:151534423
|
C | T | 1 | a0057 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.9413G>A | p.Arg3138Gln | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 13/24 | 9600/14710 | 9413/13050 | 3138/4349 | chr5 | 151534423 | ||
| chr5:151534546
|
G | T | 1 | a0061 | 1 | NA19057.hp1 | missense_variant | MODERATE | c.9290C>A | p.Ala3097Glu | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 13/24 | 9477/14710 | 9290/13050 | 3097/4349 | chr5 | 151534546 | ||
| chr5:151534547
|
C | T | 1 | a0061 | 1 | NA19057.hp1 | missense_variant | MODERATE | c.9289G>A | p.Ala3097Thr | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 13/24 | 9476/14710 | 9289/13050 | 3097/4349 | chr5 | 151534547 | ||
| chr5:151542408
|
C | T | 1 | a0018 | 4 | HG02056.hp2 HG02080.hp2 NA19062.hp1 others(1): Show |
missense_variant | MODERATE | c.8719G>A | p.Ala2907Thr | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 10/24 | 8906/14710 | 8719/13050 | 2907/4349 | chr5 | 151542408 | ||
| chr5:151542413
|
C | T | 1 | a0044 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.8714G>A | p.Arg2905Gln | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 10/24 | 8901/14710 | 8714/13050 | 2905/4349 | chr5 | 151542413 | ||
| chr5:151543071
|
C | G | 1 | a0041 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.8056G>C | p.Val2686Leu | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 10/24 | 8243/14710 | 8056/13050 | 2686/4349 | chr5 | 151543071 | ||
| chr5:151543844
|
A | G | 80 | a0001a0002a0003others(77): Show | 396 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(393): Show |
missense_variant | MODERATE | c.7283T>C | p.Phe2428Ser | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 10/24 | 7470/14710 | 7283/13050 | 2428/4349 | chr5 | 151543844 | ||
| chr5:151544966
|
C | G | 3 | a0076a0079a0080 | 3 | HG03041.hp2 HG03471.hp2 NA19030.hp1 |
missense_variant | MODERATE | c.6161G>C | p.Gly2054Ala | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 10/24 | 6348/14710 | 6161/13050 | 2054/4349 | chr5 | 151544966 | ||
| chr5:151545444
|
G | A | 2 | a0070a0071 | 2 | HG01981.hp1 NA20129.hp2 |
missense_variant | MODERATE | c.5683C>T | p.Arg1895Trp | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 10/24 | 5870/14710 | 5683/13050 | 1895/4349 | chr5 | 151545444 | ||
| chr5:151545485
|
A | G | 1 | a0045 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.5642T>C | p.Ile1881Thr | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 10/24 | 5829/14710 | 5642/13050 | 1881/4349 | chr5 | 151545485 | ||
| chr5:151545582
|
C | T | 3 | a0076a0079a0080 | 3 | HG03041.hp2 HG03471.hp2 NA19030.hp1 |
missense_variant | MODERATE | c.5545G>A | p.Val1849Ile | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 10/24 | 5732/14710 | 5545/13050 | 1849/4349 | chr5 | 151545582 | ||
| chr5:151546167
|
C | G | 5 | a0020a0027a0028others(2): Show | 9 | HG02155.hp2 NA18942.hp1 NA18951.hp2 others(6): Show |
missense_variant | MODERATE | c.4960G>C | p.Asp1654His | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 10/24 | 5147/14710 | 4960/13050 | 1654/4349 | chr5 | 151546167 | ||
| chr5:151546167
|
C | T | 1 | a0050 | 1 | NA19011.hp2 | missense_variant | MODERATE | c.4960G>A | p.Asp1654Asn | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 10/24 | 5147/14710 | 4960/13050 | 1654/4349 | chr5 | 151546167 | ||
| chr5:151546179
|
C | T | 1 | a0040 | 1 | HG00735.hp2 | missense_variant | MODERATE | c.4948G>A | p.Val1650Ile | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 10/24 | 5135/14710 | 4948/13050 | 1650/4349 | chr5 | 151546179 | ||
| chr5:151546259
|
T | C | 1 | a0046 | 1 | HG01257.hp2 | missense_variant | MODERATE | c.4868A>G | p.His1623Arg | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 10/24 | 5055/14710 | 4868/13050 | 1623/4349 | chr5 | 151546259 | ||
| chr5:151546287
|
G | C | 2 | a0021a0072 | 4 | HG01109.hp2 HG01243.hp2 HG02895.hp2 others(1): Show |
missense_variant | MODERATE | c.4840C>G | p.Leu1614Val | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 10/24 | 5027/14710 | 4840/13050 | 1614/4349 | chr5 | 151546287 | ||
| chr5:151546322
|
A | G | 1 | a0038 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.4805T>C | p.Phe1602Ser | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 10/24 | 4992/14710 | 4805/13050 | 1602/4349 | chr5 | 151546322 | ||
| chr5:151549373
|
C | T | 10 | a0013a0022a0024others(7): Show | 17 | HG01884.hp2 HG02015.hp2 HG02080.hp1 others(14): Show |
missense_variant | MODERATE | c.4711G>A | p.Gly1571Ser | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 9/24 | 4898/14710 | 4711/13050 | 1571/4349 | chr5 | 151549373 | ||
| chr5:151550625
|
C | T | 14 | a0003a0015a0016others(11): Show | 69 | HG00423.hp1 HG00621.hp2 HG00741.hp1 others(66): Show |
missense_variant | MODERATE | c.4543G>A | p.Gly1515Ser | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 8/24 | 4730/14710 | 4543/13050 | 1515/4349 | chr5 | 151550625 | ||
| chr5:151550631
|
C | T | 3 | a0076a0079a0080 | 3 | HG03041.hp2 HG03471.hp2 NA19030.hp1 |
missense_variant | MODERATE | c.4537G>A | p.Asp1513Asn | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 8/24 | 4724/14710 | 4537/13050 | 1513/4349 | chr5 | 151550631 | ||
| chr5:151550750
|
A | G | 1 | a0073 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.4418T>C | p.Ile1473Thr | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 8/24 | 4605/14710 | 4418/13050 | 1473/4349 | chr5 | 151550750 | ||
| chr5:151550781
|
G | A | 1 | a0074 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.4387C>T | p.Pro1463Ser | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 8/24 | 4574/14710 | 4387/13050 | 1463/4349 | chr5 | 151550781 | ||
| chr5:151550784
|
C | T | 24 | a0003a0015a0016others(21): Show | 83 | HG00423.hp1 HG00621.hp2 HG00735.hp2 others(80): Show |
missense_variant | MODERATE | c.4384G>A | p.Val1462Met | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 8/24 | 4571/14710 | 4384/13050 | 1462/4349 | chr5 | 151550784 | ||
| chr5:151550799
|
C | T | 3 | a0076a0079a0080 | 3 | HG03041.hp2 HG03471.hp2 NA19030.hp1 |
missense_variant | MODERATE | c.4369G>A | p.Val1457Ile | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 8/24 | 4556/14710 | 4369/13050 | 1457/4349 | chr5 | 151550799 | ||
| chr5:151553247
|
G | C | 1 | a0075 | 1 | NA18969.hp1 | missense_variant | MODERATE | c.4086C>G | p.Asp1362Glu | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 6/24 | 4273/14710 | 4086/13050 | 1362/4349 | chr5 | 151553247 | ||
| chr5:151553311
|
C | T | 1 | a0054 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.4022G>A | p.Arg1341Gln | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 6/24 | 4209/14710 | 4022/13050 | 1341/4349 | chr5 | 151553311 | ||
| chr5:151553318
|
A | G | 3 | a0076a0079a0080 | 3 | HG03041.hp2 HG03471.hp2 NA19030.hp1 |
missense_variant | MODERATE | c.4015T>C | p.Trp1339Arg | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 6/24 | 4202/14710 | 4015/13050 | 1339/4349 | chr5 | 151553318 | ||
| chr5:151553357
|
G | A | 1 | a0076 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.3976C>T | p.Leu1326Phe | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 6/24 | 4163/14710 | 3976/13050 | 1326/4349 | chr5 | 151553357 | ||
| chr5:151554423
|
A | G | 3 | a0076a0079a0080 | 3 | HG03041.hp2 HG03471.hp2 NA19030.hp1 |
missense_variant | MODERATE | c.3884T>C | p.Leu1295Pro | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 5/24 | 4071/14710 | 3884/13050 | 1295/4349 | chr5 | 151554423 | ||
| chr5:151554604
|
C | T | 1 | a0039 | 1 | HG00673.hp2 | missense_variant | MODERATE | c.3703G>A | p.Val1235Ile | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 5/24 | 3890/14710 | 3703/13050 | 1235/4349 | chr5 | 151554604 | ||
| chr5:151554648
|
G | T | 1 | a0053 | 1 | HG02965.hp2 | missense_variant | MODERATE | c.3659C>A | p.Pro1220His | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 5/24 | 3846/14710 | 3659/13050 | 1220/4349 | chr5 | 151554648 | ||
| chr5:151563358
|
A | G | 81 | a0001a0002a0003others(78): Show | 397 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(394): Show |
missense_variant | MODERATE | c.3541T>C | p.Tyr1181His | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/24 | 3728/14710 | 3541/13050 | 1181/4349 | chr5 | 151563358 | ||
| chr5:151563408
|
G | A | 17 | a0002a0006a0008others(14): Show | 119 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(116): Show |
missense_variant | MODERATE | c.3491C>T | p.Pro1164Leu | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/24 | 3678/14710 | 3491/13050 | 1164/4349 | chr5 | 151563408 | ||
| chr5:151563516
|
G | A | 1 | a0052 | 1 | HG00609.hp2 | missense_variant | MODERATE | c.3383C>T | p.Thr1128Met | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/24 | 3570/14710 | 3383/13050 | 1128/4349 | chr5 | 151563516 | ||
| chr5:151565922
|
C | T | 28 | a0002a0006a0008others(25): Show | 137 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(134): Show |
missense_variant | MODERATE | c.3010G>A | p.Gly1004Ser | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/24 | 3197/14710 | 3010/13050 | 1004/4349 | chr5 | 151565922 | ||
| chr5:151565957
|
C | T | 3 | a0009a0026a0051 | 13 | HG01952.hp2 NA18952.hp2 NA18962.hp2 others(10): Show |
missense_variant | MODERATE | c.2975G>A | p.Arg992Gln | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/24 | 3162/14710 | 2975/13050 | 992/4349 | chr5 | 151565957 | ||
| chr5:151566263
|
A | G | 1 | a0017 | 4 | NA18939.hp2 NA18941.hp1 NA18984.hp2 others(1): Show |
missense_variant | MODERATE | c.2669T>C | p.Ile890Thr | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/24 | 2856/14710 | 2669/13050 | 890/4349 | chr5 | 151566263 | ||
| chr5:151566297
|
C | G | 1 | a0078 | 1 | NA19080.hp1 | missense_variant | MODERATE | c.2635G>C | p.Gly879Arg | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/24 | 2822/14710 | 2635/13050 | 879/4349 | chr5 | 151566297 | ||
| chr5:151566468
|
G | A | 2 | a0079a0080 | 2 | HG03041.hp2 HG03471.hp2 |
missense_variant | MODERATE | c.2464C>T | p.Pro822Ser | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/24 | 2651/14710 | 2464/13050 | 822/4349 | chr5 | 151566468 | ||
| chr5:151566512
|
G | A | 1 | a0036 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.2420C>T | p.Thr807Ile | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/24 | 2607/14710 | 2420/13050 | 807/4349 | chr5 | 151566512 | ||
| chr5:151566875
|
A | G | 32 | a0002a0006a0008others(29): Show | 142 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(139): Show |
missense_variant | MODERATE | c.2057T>C | p.Phe686Ser | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/24 | 2244/14710 | 2057/13050 | 686/4349 | chr5 | 151566875 | ||
| chr5:151567212
|
G | A | 32 | a0002a0006a0008others(29): Show | 142 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(139): Show |
missense_variant | MODERATE | c.1720C>T | p.Arg574Cys | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/24 | 1907/14710 | 1720/13050 | 574/4349 | chr5 | 151567212 | ||
| chr5:151567269
|
T | C | 1 | a0037 | 1 | NA18963.hp2 | missense_variant | MODERATE | c.1663A>G | p.Arg555Gly | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/24 | 1850/14710 | 1663/13050 | 555/4349 | chr5 | 151567269 | ||
| chr5:151567478
|
C | A | 1 | a0036 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.1454G>T | p.Arg485Leu | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/24 | 1641/14710 | 1454/13050 | 485/4349 | chr5 | 151567478 | ||
| chr5:151567601
|
A | G | 1 | a0035 | 1 | HG01168.hp1 | missense_variant | MODERATE | c.1331T>C | p.Val444Ala | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/24 | 1518/14710 | 1331/13050 | 444/4349 | chr5 | 151567601 | ||
| chr5:151567659
|
C | T | 3 | a0031a0081a0082 | 4 | HG02109.hp2 HG02922.hp1 HG03516.hp1 others(1): Show |
missense_variant | MODERATE | c.1273G>A | p.Asp425Asn | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/24 | 1460/14710 | 1273/13050 | 425/4349 | chr5 | 151567659 | ||
| chr5:151568190
|
G | A | 1 | a0018 | 4 | HG02056.hp2 HG02080.hp2 NA19062.hp1 others(1): Show |
missense_variant | MODERATE | c.742C>T | p.Pro248Ser | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/24 | 929/14710 | 742/13050 | 248/4349 | chr5 | 151568190 | ||
| chr5:151568451
|
T | G | 1 | a0034 | 1 | HG03834.hp1 | missense_variant | MODERATE | c.481A>C | p.Met161Leu | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/24 | 668/14710 | 481/13050 | 161/4349 | chr5 | 151568451 | ||
| chr5:151568727
|
C | T | 1 | a0033 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.205G>A | p.Val69Met | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/24 | 392/14710 | 205/13050 | 69/4349 | chr5 | 151568727 | ||
| chr5:151568744
|
G | A | 1 | a0032 | 2 | HG01257.hp1 HG01258.hp1 |
missense_variant | MODERATE | c.188C>T | p.Ala63Val | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/24 | 375/14710 | 188/13050 | 63/4349 | chr5 | 151568744 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:151507164
|
G | A | 165 | a0001c0003a0001c0004a0001c0010others(162): Show | 380 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(377): Show |
synonymous_variant | LOW | c.12507C>T | p.Ser4169Ser | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 23/24 | 12694/14710 | 12507/13050 | 4169/4349 | chr5 | 151507164 | ||
| chr5:151507185
|
G | A | 1 | a0017c0108 | 1 | NA19057.hp2 | synonymous_variant | LOW | c.12486C>T | p.Val4162Val | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 23/24 | 12673/14710 | 12486/13050 | 4162/4349 | chr5 | 151507185 | ||
| chr5:151512172
|
A | G | 140 | a0001c0003a0001c0004a0001c0010others(137): Show | 339 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(336): Show |
synonymous_variant | LOW | c.11898T>C | p.His3966His | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 21/24 | 12085/14710 | 11898/13050 | 3966/4349 | chr5 | 151512172 | ||
| chr5:151521334
|
G | A | 1 | a0016c0118 | 1 | NA19011.hp1 | synonymous_variant | LOW | c.11259C>T | p.Thr3753Thr | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/24 | 11446/14710 | 11259/13050 | 3753/4349 | chr5 | 151521334 | ||
| chr5:151521352
|
A | G | 2 | a0042c0077a0079c0175 | 2 | HG03195.hp1 HG03471.hp2 |
synonymous_variant | LOW | c.11241T>C | p.Val3747Val | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/24 | 11428/14710 | 11241/13050 | 3747/4349 | chr5 | 151521352 | ||
| chr5:151521550
|
A | G | 139 | a0001c0003a0001c0004a0001c0010others(136): Show | 338 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(335): Show |
synonymous_variant | LOW | c.11043T>C | p.Asp3681Asp | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/24 | 11230/14710 | 11043/13050 | 3681/4349 | chr5 | 151521550 | ||
| chr5:151521739
|
G | A | 132 | a0001c0003a0001c0004a0001c0010others(129): Show | 331 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(328): Show |
synonymous_variant | LOW | c.10854C>T | p.Tyr3618Tyr | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/24 | 11041/14710 | 10854/13050 | 3618/4349 | chr5 | 151521739 | ||
| chr5:151521790
|
G | A | 1 | a0003c0117 | 1 | HG02293.hp1 | synonymous_variant | LOW | c.10803C>T | p.Asn3601Asn | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/24 | 10990/14710 | 10803/13050 | 3601/4349 | chr5 | 151521790 | ||
| chr5:151522036
|
G | C | 19 | a0006c0005a0006c0091a0006c0093others(16): Show | 42 | HG00140.hp2 HG00558.hp1 HG00597.hp2 others(39): Show |
synonymous_variant | LOW | c.10557C>G | p.Val3519Val | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/24 | 10744/14710 | 10557/13050 | 3519/4349 | chr5 | 151522036 | ||
| chr5:151522057
|
C | T | 1 | a0010c0082 | 1 | HG01433.hp2 | synonymous_variant | LOW | c.10536G>A | p.Ser3512Ser | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/24 | 10723/14710 | 10536/13050 | 3512/4349 | chr5 | 151522057 | ||
| chr5:151522069
|
G | T | 19 | a0006c0005a0006c0091a0006c0093others(16): Show | 42 | HG00140.hp2 HG00558.hp1 HG00597.hp2 others(39): Show |
synonymous_variant | LOW | c.10524C>A | p.Ile3508Ile | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/24 | 10711/14710 | 10524/13050 | 3508/4349 | chr5 | 151522069 | ||
| chr5:151522084
|
C | T | 2 | a0001c0142a0002c0099 | 2 | HG02896.hp2 NA20129.hp1 |
splice_region_variant&synonymous_variant | LOW | c.10509G>A | p.Ala3503Ala | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/24 | 10696/14710 | 10509/13050 | 3503/4349 | chr5 | 151522084 | ||
| chr5:151525837
|
C | T | 38 | a0001c0142a0002c0099a0003c0138others(35): Show | 70 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(67): Show |
synonymous_variant | LOW | c.10437G>A | p.Pro3479Pro | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 18/24 | 10624/14710 | 10437/13050 | 3479/4349 | chr5 | 151525837 | ||
| chr5:151525924
|
C | T | 20 | a0001c0021a0001c0032a0001c0048others(17): Show | 44 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(41): Show |
synonymous_variant | LOW | c.10350G>A | p.Leu3450Leu | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 18/24 | 10537/14710 | 10350/13050 | 3450/4349 | chr5 | 151525924 | ||
| chr5:151529274
|
G | A | 1 | a0082c0106 | 1 | NA19240.hp1 | synonymous_variant | LOW | c.9930C>T | p.Asn3310Asn | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 15/24 | 10117/14710 | 9930/13050 | 3310/4349 | chr5 | 151529274 | ||
| chr5:151534413
|
G | A | 1 | a0002c0085 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.9423C>T | p.Asp3141Asp | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 13/24 | 9610/14710 | 9423/13050 | 3141/4349 | chr5 | 151534413 | ||
| chr5:151534542
|
G | A | 2 | a0005c0063a0045c0080 | 2 | HG02258.hp2 NA18991.hp2 |
synonymous_variant | LOW | c.9294C>T | p.Asp3098Asp | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 13/24 | 9481/14710 | 9294/13050 | 3098/4349 | chr5 | 151534542 | ||
| chr5:151534623
|
A | T | 115 | a0001c0003a0001c0004a0001c0010others(112): Show | 291 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(288): Show |
synonymous_variant | LOW | c.9213T>A | p.Thr3071Thr | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 13/24 | 9400/14710 | 9213/13050 | 3071/4349 | chr5 | 151534623 | ||
| chr5:151537923
|
A | G | 3 | a0001c0144a0003c0138a0057c0122 | 3 | HG02451.hp1 HG02723.hp2 HG03195.hp2 |
synonymous_variant | LOW | c.9063T>C | p.His3021His | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/24 | 9250/14710 | 9063/13050 | 3021/4349 | chr5 | 151537923 | ||
| chr5:151542640
|
A | G | 1 | a0003c0114 | 1 | NA18985.hp1 | synonymous_variant | LOW | c.8487T>C | p.Asp2829Asp | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 10/24 | 8674/14710 | 8487/13050 | 2829/4349 | chr5 | 151542640 | ||
| chr5:151543183
|
G | A | 1 | a0002c0092 | 1 | NA19003.hp2 | synonymous_variant | LOW | c.7944C>T | p.Ser2648Ser | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 10/24 | 8131/14710 | 7944/13050 | 2648/4349 | chr5 | 151543183 | ||
| chr5:151543714
|
A | G | 2 | a0001c0142a0004c0143 | 2 | HG02809.hp2 HG02896.hp2 |
synonymous_variant | LOW | c.7413T>C | p.Thr2471Thr | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 10/24 | 7600/14710 | 7413/13050 | 2471/4349 | chr5 | 151543714 | ||
| chr5:151544275
|
G | A | 1 | a0057c0122 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.6852C>T | p.Gly2284Gly | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 10/24 | 7039/14710 | 6852/13050 | 2284/4349 | chr5 | 151544275 | ||
| chr5:151544533
|
T | C | 3 | a0076c0111a0079c0175a0080c0176 | 3 | HG03041.hp2 HG03471.hp2 NA19030.hp1 |
synonymous_variant | LOW | c.6594A>G | p.Pro2198Pro | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 10/24 | 6781/14710 | 6594/13050 | 2198/4349 | chr5 | 151544533 | ||
| chr5:151544779
|
G | A | 3 | a0004c0156a0007c0054a0011c0155 | 4 | HG01070.hp1 HG01074.hp2 HG01255.hp2 others(1): Show |
synonymous_variant | LOW | c.6348C>T | p.Phe2116Phe | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 10/24 | 6535/14710 | 6348/13050 | 2116/4349 | chr5 | 151544779 | ||
| chr5:151544872
|
T | C | 3 | a0076c0111a0079c0175a0080c0176 | 3 | HG03041.hp2 HG03471.hp2 NA19030.hp1 |
synonymous_variant | LOW | c.6255A>G | p.Pro2085Pro | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 10/24 | 6442/14710 | 6255/13050 | 2085/4349 | chr5 | 151544872 | ||
| chr5:151545208
|
G | A | 37 | a0001c0004a0001c0017a0001c0032others(34): Show | 64 | HG00558.hp2 HG00639.hp2 HG00735.hp2 others(61): Show |
synonymous_variant | LOW | c.5919C>T | p.Tyr1973Tyr | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 10/24 | 6106/14710 | 5919/13050 | 1973/4349 | chr5 | 151545208 | ||
| chr5:151545481
|
G | C | 3 | a0076c0111a0079c0175a0080c0176 | 3 | HG03041.hp2 HG03471.hp2 NA19030.hp1 |
synonymous_variant | LOW | c.5646C>G | p.Val1882Val | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 10/24 | 5833/14710 | 5646/13050 | 1882/4349 | chr5 | 151545481 | ||
| chr5:151545583
|
A | G | 151 | a0001c0004a0001c0010a0001c0017others(148): Show | 326 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(323): Show |
synonymous_variant | LOW | c.5544T>C | p.Pro1848Pro | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 10/24 | 5731/14710 | 5544/13050 | 1848/4349 | chr5 | 151545583 | ||
| chr5:151545706
|
C | T | 1 | a0001c0123 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.5421G>A | p.Pro1807Pro | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 10/24 | 5608/14710 | 5421/13050 | 1807/4349 | chr5 | 151545706 | ||
| chr5:151546120
|
G | T | 3 | a0076c0111a0079c0175a0080c0176 | 3 | HG03041.hp2 HG03471.hp2 NA19030.hp1 |
synonymous_variant | LOW | c.5007C>A | p.Ile1669Ile | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 10/24 | 5194/14710 | 5007/13050 | 1669/4349 | chr5 | 151546120 | ||
| chr5:151551521
|
C | G | 5 | a0001c0048a0001c0049a0011c0136others(2): Show | 7 | HG01928.hp2 HG02698.hp1 HG03688.hp2 others(4): Show |
synonymous_variant | LOW | c.4242G>C | p.Ser1414Ser | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 7/24 | 4429/14710 | 4242/13050 | 1414/4349 | chr5 | 151551521 | ||
| chr5:151553241
|
C | T | 24 | a0013c0024a0013c0035a0020c0028others(21): Show | 32 | HG00735.hp2 HG01243.hp1 HG01884.hp2 others(29): Show |
synonymous_variant | LOW | c.4092G>A | p.Val1364Val | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 6/24 | 4279/14710 | 4092/13050 | 1364/4349 | chr5 | 151553241 | ||
| chr5:151553283
|
A | G | 3 | a0076c0111a0079c0175a0080c0176 | 3 | HG03041.hp2 HG03471.hp2 NA19030.hp1 |
synonymous_variant | LOW | c.4050T>C | p.Asp1350Asp | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 6/24 | 4237/14710 | 4050/13050 | 1350/4349 | chr5 | 151553283 | ||
| chr5:151563524
|
G | A | 58 | a0002c0001a0002c0006a0002c0008others(55): Show | 140 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(137): Show |
synonymous_variant | LOW | c.3375C>T | p.Ile1125Ile | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/24 | 3562/14710 | 3375/13050 | 1125/4349 | chr5 | 151563524 | ||
| chr5:151563545
|
A | G | 1 | a0001c0047 | 2 | HG02886.hp1 HG03225.hp1 |
synonymous_variant | LOW | c.3354T>C | p.Ser1118Ser | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/24 | 3541/14710 | 3354/13050 | 1118/4349 | chr5 | 151563545 | ||
| chr5:151565791
|
C | T | 2 | a0079c0175a0080c0176 | 2 | HG03041.hp2 HG03471.hp2 |
synonymous_variant | LOW | c.3141G>A | p.Ser1047Ser | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/24 | 3328/14710 | 3141/13050 | 1047/4349 | chr5 | 151565791 | ||
| chr5:151565923
|
A | G | 1 | a0001c0110 | 1 | HG01167.hp2 | synonymous_variant | LOW | c.3009T>C | p.Asp1003Asp | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/24 | 3196/14710 | 3009/13050 | 1003/4349 | chr5 | 151565923 | ||
| chr5:151566112
|
G | T | 2 | a0001c0130a0007c0045 | 3 | NA18942.hp2 NA18980.hp2 NA19068.hp2 |
synonymous_variant | LOW | c.2820C>A | p.Pro940Pro | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/24 | 3007/14710 | 2820/13050 | 940/4349 | chr5 | 151566112 | ||
| chr5:151566138
|
G | A | 60 | a0002c0001a0002c0006a0002c0008others(57): Show | 142 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(139): Show |
synonymous_variant | LOW | c.2794C>T | p.Leu932Leu | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/24 | 2981/14710 | 2794/13050 | 932/4349 | chr5 | 151566138 | ||
| chr5:151566259
|
G | T | 1 | a0003c0109 | 1 | HG02083.hp1 | synonymous_variant | LOW | c.2673C>A | p.Leu891Leu | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/24 | 2860/14710 | 2673/13050 | 891/4349 | chr5 | 151566259 | ||
| chr5:151566301
|
A | G | 60 | a0002c0001a0002c0006a0002c0008others(57): Show | 142 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(139): Show |
synonymous_variant | LOW | c.2631T>C | p.Val877Val | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/24 | 2818/14710 | 2631/13050 | 877/4349 | chr5 | 151566301 | ||
| chr5:151566361
|
G | A | 1 | a0002c0099 | 1 | NA20129.hp1 | synonymous_variant | LOW | c.2571C>T | p.Tyr857Tyr | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/24 | 2758/14710 | 2571/13050 | 857/4349 | chr5 | 151566361 | ||
| chr5:151566370
|
C | T | 59 | a0002c0001a0002c0006a0002c0008others(56): Show | 141 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(138): Show |
synonymous_variant | LOW | c.2562G>A | p.Arg854Arg | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/24 | 2749/14710 | 2562/13050 | 854/4349 | chr5 | 151566370 | ||
| chr5:151566460
|
C | T | 2 | a0079c0175a0080c0176 | 2 | HG03041.hp2 HG03471.hp2 |
synonymous_variant | LOW | c.2472G>A | p.Gly824Gly | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/24 | 2659/14710 | 2472/13050 | 824/4349 | chr5 | 151566460 | ||
| chr5:151566571
|
G | A | 60 | a0002c0001a0002c0006a0002c0008others(57): Show | 142 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(139): Show |
synonymous_variant | LOW | c.2361C>T | p.Ile787Ile | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/24 | 2548/14710 | 2361/13050 | 787/4349 | chr5 | 151566571 | ||
| chr5:151566874
|
A | G | 1 | a0001c0129 | 1 | NA18967.hp1 | synonymous_variant | LOW | c.2058T>C | p.Phe686Phe | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/24 | 2245/14710 | 2058/13050 | 686/4349 | chr5 | 151566874 | ||
| chr5:151567219
|
C | A | 4 | a0002c0100a0006c0102a0008c0038others(1): Show | 5 | HG00140.hp2 HG01167.hp1 HG01169.hp2 others(2): Show |
synonymous_variant | LOW | c.1713G>T | p.Gly571Gly | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/24 | 1900/14710 | 1713/13050 | 571/4349 | chr5 | 151567219 | ||
| chr5:151567246
|
A | G | 1 | a0001c0128 | 1 | HG02083.hp2 | synonymous_variant | LOW | c.1686T>C | p.Pro562Pro | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/24 | 1873/14710 | 1686/13050 | 562/4349 | chr5 | 151567246 | ||
| chr5:151567405
|
G | A | 143 | a0001c0003a0001c0004a0001c0010others(140): Show | 319 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(316): Show |
synonymous_variant | LOW | c.1527C>T | p.Pro509Pro | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/24 | 1714/14710 | 1527/13050 | 509/4349 | chr5 | 151567405 | ||
| chr5:151567567
|
G | A | 2 | a0001c0174a0005c0173 | 2 | HG00642.hp2 HG00741.hp2 |
synonymous_variant | LOW | c.1365C>T | p.Ala455Ala | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/24 | 1552/14710 | 1365/13050 | 455/4349 | chr5 | 151567567 | ||
| chr5:151567939
|
G | A | 2 | a0079c0175a0080c0176 | 2 | HG03041.hp2 HG03471.hp2 |
synonymous_variant | LOW | c.993C>T | p.Leu331Leu | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/24 | 1180/14710 | 993/13050 | 331/4349 | chr5 | 151567939 | ||
| chr5:151568143
|
T | C | 4 | a0031c0104a0031c0105a0081c0103others(1): Show | 4 | HG02109.hp2 HG02922.hp1 HG03516.hp1 others(1): Show |
synonymous_variant | LOW | c.789A>G | p.Pro263Pro | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/24 | 976/14710 | 789/13050 | 263/4349 | chr5 | 151568143 | ||
| chr5:151568158
|
C | T | 58 | a0002c0001a0002c0006a0002c0008others(55): Show | 140 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(137): Show |
synonymous_variant | LOW | c.774G>A | p.Ser258Ser | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/24 | 961/14710 | 774/13050 | 258/4349 | chr5 | 151568158 | ||
| chr5:151568455
|
C | T | 12 | a0001c0004a0001c0017a0001c0032others(9): Show | 31 | HG00558.hp2 HG00639.hp2 HG01069.hp2 others(28): Show |
synonymous_variant | LOW | c.477G>A | p.Glu159Glu | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/24 | 664/14710 | 477/13050 | 159/4349 | chr5 | 151568455 | ||
| chr5:151568767
|
G | A | 1 | a0001c0179 | 1 | NA19074.hp2 | synonymous_variant | LOW | c.165C>T | p.Phe55Phe | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/24 | 352/14710 | 165/13050 | 55/4349 | chr5 | 151568767 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:151504119
|
T | TA | 38 | a0001c0016t0004a0001c0021t0003a0003c0138t0025others(35): Show | 51 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*1445dupT | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 24/24 | 1445 | chr5 | 151504119 | |||||
| chr5:151504139
|
A | G | 2 | a0001c0147t0013a0053c0133t0013 | 2 | HG02572.hp2 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1426T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 24/24 | 1426 | chr5 | 151504139 | |||||
| chr5:151504153
|
T | C | 1 | a0003c0009t0026 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1412A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 24/24 | 1412 | chr5 | 151504153 | |||||
| chr5:151504279
|
T | TTCTG | 7 | a0001c0125t0010a0002c0001t0017a0004c0053t0010others(4): Show | 7 | HG01496.hp1 HG02145.hp2 HG03130.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1282_*1285dupCAGA | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 24/24 | 1285 | chr5 | 151504279 | |||||
| chr5:151504311
|
C | T | 19 | a0001c0021t0003a0006c0005t0003a0006c0005t0006others(16): Show | 30 | HG00558.hp1 HG00597.hp2 HG02015.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1254G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 24/24 | 1254 | chr5 | 151504311 | |||||
| chr5:151504354
|
T | G | 10 | a0001c0010t0005a0001c0020t0005a0001c0047t0005others(7): Show | 13 | HG01109.hp2 HG02280.hp2 HG02572.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1211A>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 24/24 | 1211 | chr5 | 151504354 | |||||
| chr5:151504496
|
C | T | 20 | a0001c0016t0004a0002c0026t0024a0004c0033t0004others(17): Show | 22 | HG00323.hp2 HG00639.hp2 HG00735.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1069G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 24/24 | 1069 | chr5 | 151504496 | |||||
| chr5:151504528
|
A | G | 19 | a0001c0016t0004a0004c0033t0004a0004c0161t0004others(16): Show | 21 | HG00323.hp2 HG00639.hp2 HG00735.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1037T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 24/24 | 1037 | chr5 | 151504528 | |||||
| chr5:151504563
|
C | T | 1 | a0003c0002t0023 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1002G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 24/24 | 1002 | chr5 | 151504563 | |||||
| chr5:151504591
|
C | T | 1 | a0009c0132t0028 | 1 | NA18973.hp1 | 3_prime_UTR_variant | MODIFIER | c.*974G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 24/24 | 974 | chr5 | 151504591 | |||||
| chr5:151504608
|
T | C | 1 | a0004c0153t0027 | 1 | HG02293.hp2 | 3_prime_UTR_variant | MODIFIER | c.*957A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 24/24 | 957 | chr5 | 151504608 | |||||
| chr5:151504685
|
G | A | 1 | a0044c0081t0035 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*880C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 24/24 | 880 | chr5 | 151504685 | |||||
| chr5:151504837
|
C | T | 6 | a0001c0010t0009a0003c0013t0009a0036c0172t0009others(3): Show | 6 | HG01243.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*728G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 24/24 | 728 | chr5 | 151504837 | |||||
| chr5:151504889
|
T | C | 19 | a0001c0016t0004a0004c0033t0004a0004c0161t0004others(16): Show | 21 | HG00323.hp2 HG00639.hp2 HG00735.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*676A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 24/24 | 676 | chr5 | 151504889 | |||||
| chr5:151504914
|
G | T | 2 | a0008c0012t0022a0008c0025t0014 | 3 | HG01069.hp1 HG01071.hp1 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*651C>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 24/24 | 651 | chr5 | 151504914 | |||||
| chr5:151504925
|
C | T | 1 | a0018c0031t0033 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*640G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 24/24 | 640 | chr5 | 151504925 | |||||
| chr5:151504929
|
G | A | 8 | a0001c0021t0008a0001c0032t0008a0002c0008t0008others(5): Show | 8 | HG00423.hp2 HG02080.hp2 NA18954.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*636C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 24/24 | 636 | chr5 | 151504929 | |||||
| chr5:151505094
|
G | A | 2 | a0002c0001t0036a0002c0008t0029 | 2 | NA18997.hp2 NA19087.hp2 |
3_prime_UTR_variant | MODIFIER | c.*471C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 24/24 | 471 | chr5 | 151505094 | |||||
| chr5:151505124
|
G | C | 1 | a0021c0056t0030 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*441C>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 24/24 | 441 | chr5 | 151505124 | |||||
| chr5:151505200
|
G | C | 10 | a0001c0010t0007a0001c0044t0007a0001c0047t0007others(7): Show | 11 | HG02055.hp1 HG02723.hp1 HG02809.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*365C>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 24/24 | 365 | chr5 | 151505200 | |||||
| chr5:151505232
|
C | T | 20 | a0001c0016t0004a0004c0033t0004a0004c0161t0004others(17): Show | 22 | HG00323.hp2 HG00639.hp2 HG00735.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*333G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 24/24 | 333 | chr5 | 151505232 | |||||
| chr5:151505278
|
C | G | 20 | a0001c0016t0004a0004c0033t0004a0004c0161t0004others(17): Show | 22 | HG00323.hp2 HG00639.hp2 HG00735.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*287G>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 24/24 | 287 | chr5 | 151505278 | |||||
| chr5:151505290
|
G | A | 20 | a0001c0016t0004a0004c0033t0004a0004c0161t0004others(17): Show | 22 | HG00323.hp2 HG00639.hp2 HG00735.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*275C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 24/24 | 275 | chr5 | 151505290 | |||||
| chr5:151505298
|
A | G | 1 | a0001c0003t0012 | 2 | NA18987.hp1 NA19066.hp2 |
3_prime_UTR_variant | MODIFIER | c.*267T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 24/24 | 267 | chr5 | 151505298 | |||||
| chr5:151505343
|
C | G | 1 | a0001c0003t0020 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*222G>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 24/24 | 222 | chr5 | 151505343 | |||||
| chr5:151505404
|
A | G | 1 | a0001c0048t0021 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*161T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 24/24 | 161 | chr5 | 151505404 | |||||
| chr5:151505408
|
G | T | 1 | a0001c0003t0020 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*157C>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 24/24 | 157 | chr5 | 151505408 | |||||
| chr5:151505492
|
C | G | 1 | a0027c0040t0019 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*73G>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 24/24 | 73 | chr5 | 151505492 | |||||
| chr5:151505493
|
C | G | 1 | a0030c0146t0018 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*72G>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 24/24 | 72 | chr5 | 151505493 | |||||
| chr5:151591238
|
TGACAGGC others(36): Show |
T | 1 | a0006c0005t0016 | 1 | HG00558.hp1 | 5_prime_UTR_variant | MODIFIER | c.-137_-95delGCCTTCC others(36): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/24 | 22308 | chr5 | 151591238 | |||||
| chr5:151591268
|
C | T | 1 | a0002c0001t0017 | 1 | HG01496.hp1 | 5_prime_UTR_variant | MODIFIER | c.-124G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/24 | 22337 | chr5 | 151591268 | |||||
| chr5:151591276
|
G | A | 49 | a0001c0003t0002a0001c0004t0002a0001c0010t0002others(46): Show | 77 | HG00621.hp1 HG00642.hp2 HG00673.hp1 others(74): Show |
5_prime_UTR_variant | MODIFIER | c.-132C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/24 | 22345 | chr5 | 151591276 | |||||
| chr5:151591280
|
G | A | 2 | a0002c0006t0015a0006c0005t0015 | 2 | HG01934.hp1 homoSapiens_chm13v2.hp1 |
5_prime_UTR_variant | MODIFIER | c.-136C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/24 | 22349 | chr5 | 151591280 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:151506113
|
A | AAGAT | 14 | a0001c0010t0009g0171a0001c0125t0010g0286a0002c0001t0017g0009others(11): Show | 14 | HG01243.hp1 HG01496.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.12518-20_12518-17d others(6): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 23/23 | chr5 | 151506113 | ||||||
| chr5:151506129
|
A | AT | 3 | a0005c0015t0001g0217a0005c0173t0002g0336a0010c0011t0001g0303 | 3 | HG00642.hp2 HG03669.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.12518-33dupA | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 23/23 | chr5 | 151506129 | ||||||
| chr5:151506220
|
C | T | 1 | a0008c0012t0022g0318 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.12518-123G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 23/23 | chr5 | 151506220 | ||||||
| chr5:151506227
|
G | T | 20 | a0004c0033t0004g0281a0004c0161t0004g0205a0008c0038t0004g0305others(17): Show | 20 | HG00323.hp2 HG00639.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.12518-130C>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 23/23 | chr5 | 151506227 | ||||||
| chr5:151506258
|
A | G | 1 | a0004c0152t0001g0176 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.12518-161T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 23/23 | chr5 | 151506258 | ||||||
| chr5:151506400
|
G | A | 1 | a0031c0104t0001g0010 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.12518-303C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 23/23 | chr5 | 151506400 | ||||||
| chr5:151506420
|
A | C | 20 | a0004c0033t0004g0281a0004c0161t0004g0205a0008c0038t0004g0305others(17): Show | 20 | HG00323.hp2 HG00639.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.12518-323T>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 23/23 | chr5 | 151506420 | ||||||
| chr5:151506468
|
GACTC | G | 20 | a0004c0033t0004g0281a0004c0161t0004g0205a0008c0038t0004g0305others(17): Show | 20 | HG00323.hp2 HG00639.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.12518-375_12518-37 others(8): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 23/23 | chr5 | 151506468 | ||||||
| chr5:151506482
|
T | C | 1 | a0018c0031t0001g0080 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.12518-385A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 23/23 | chr5 | 151506482 | ||||||
| chr5:151506524
|
C | A | 6 | a0001c0010t0009g0171a0003c0013t0009g0312a0036c0172t0009g0245others(3): Show | 6 | HG01243.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.12518-427G>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 23/23 | chr5 | 151506524 | ||||||
| chr5:151506581
|
G | A | 1 | a0074c0168t0009g0029 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.12518-484C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 23/23 | chr5 | 151506581 | ||||||
| chr5:151506587
|
T | A | 2 | a0004c0053t0010g0019a0022c0098t0010g0039 | 2 | HG02145.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.12518-490A>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 23/23 | chr5 | 151506587 | ||||||
| chr5:151506592
|
T | C | 20 | a0004c0033t0004g0281a0004c0161t0004g0205a0008c0038t0004g0305others(17): Show | 20 | HG00323.hp2 HG00639.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.12518-495A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 23/23 | chr5 | 151506592 | ||||||
| chr5:151506638
|
C | G | 20 | a0004c0033t0004g0281a0004c0161t0004g0205a0008c0038t0004g0305others(17): Show | 20 | HG00323.hp2 HG00639.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.12517+516G>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 23/23 | chr5 | 151506638 | ||||||
| chr5:151506700
|
A | C | 100 | a0001c0003t0001g0013a0001c0003t0001g0183a0001c0003t0001g0185others(97): Show | 102 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.12517+454T>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 23/23 | chr5 | 151506700 | ||||||
| chr5:151506726
|
G | A | 1 | a0064c0060t0001g0272 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.12517+428C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 23/23 | chr5 | 151506726 | ||||||
| chr5:151506958
|
A | G | 262 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(259): Show | 269 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(266): Show |
intron_variant | MODIFIER | c.12517+196T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 23/23 | chr5 | 151506958 | ||||||
| chr5:151507055
|
G | A | 325 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(322): Show | 332 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(329): Show |
intron_variant | MODIFIER | c.12517+99C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 23/23 | chr5 | 151507055 | ||||||
| chr5:151507089
|
G | T | 1 | a0078c0107t0001g0086 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.12517+65C>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 23/23 | chr5 | 151507089 | ||||||
| chr5:151507615
|
C | T | 2 | a0002c0001t0002g0007a0003c0002t0001g0093 | 3 | HG00621.hp1 NA18945.hp1 NA19060.hp2 |
splice_region_variant&intron_variant | LOW | c.12060-4G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 22/23 | chr5 | 151507615 | ||||||
| chr5:151507623
|
G | GAGA | 374 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(371): Show | 381 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(378): Show |
intron_variant | MODIFIER | c.12060-13_12060-12i others(5): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 22/23 | chr5 | 151507623 | ||||||
| chr5:151507639
|
A | G | 48 | a0001c0125t0010g0286a0002c0001t0017g0009a0006c0005t0001g0301others(45): Show | 48 | HG00140.hp2 HG00558.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.12060-28T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 22/23 | chr5 | 151507639 | ||||||
| chr5:151507716
|
A | G | 2 | a0029c0050t0004g0177a0029c0050t0032g0052 | 2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.12060-105T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 22/23 | chr5 | 151507716 | ||||||
| chr5:151507723
|
G | A | 21 | a0004c0019t0001g0053a0004c0019t0001g0054a0004c0019t0001g0181others(18): Show | 21 | HG01069.hp1 HG01071.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.12060-112C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 22/23 | chr5 | 151507723 | ||||||
| chr5:151507858
|
G | A | 1 | a0057c0122t0001g0082 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.12060-247C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 22/23 | chr5 | 151507858 | ||||||
| chr5:151507860
|
A | T | 2 | a0029c0050t0004g0177a0029c0050t0032g0052 | 2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.12060-249T>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 22/23 | chr5 | 151507860 | ||||||
| chr5:151507893
|
A | G | 2 | a0029c0050t0004g0177a0029c0050t0032g0052 | 2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.12060-282T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 22/23 | chr5 | 151507893 | ||||||
| chr5:151508004
|
A | G | 1 | a0008c0012t0022g0318 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.12060-393T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 22/23 | chr5 | 151508004 | ||||||
| chr5:151508032
|
G | A | 30 | a0005c0014t0001g0051a0005c0014t0001g0055a0005c0014t0001g0056others(27): Show | 30 | HG00140.hp1 HG01243.hp2 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.12060-421C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 22/23 | chr5 | 151508032 | ||||||
| chr5:151508058
|
C | T | 1 | a0004c0019t0007g0170 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.12060-447G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 22/23 | chr5 | 151508058 | ||||||
| chr5:151508106
|
A | T | 2 | a0029c0050t0004g0177a0029c0050t0032g0052 | 2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.12060-495T>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 22/23 | chr5 | 151508106 | ||||||
| chr5:151508174
|
T | C | 2 | a0029c0050t0004g0177a0029c0050t0032g0052 | 2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.12060-563A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 22/23 | chr5 | 151508174 | ||||||
| chr5:151508197
|
G | C | 1 | a0008c0012t0002g0006 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.12060-586C>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 22/23 | chr5 | 151508197 | ||||||
| chr5:151508341
|
C | A | 1 | a0037c0171t0001g0213 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.12060-730G>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 22/23 | chr5 | 151508341 | ||||||
| chr5:151508364
|
A | G | 245 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(242): Show | 251 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(248): Show |
intron_variant | MODIFIER | c.12060-753T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 22/23 | chr5 | 151508364 | ||||||
| chr5:151508424
|
A | G | 2 | a0029c0050t0004g0177a0029c0050t0032g0052 | 2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.12060-813T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 22/23 | chr5 | 151508424 | ||||||
| chr5:151508476
|
G | A | 2 | a0029c0050t0004g0177a0029c0050t0032g0052 | 2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.12060-865C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 22/23 | chr5 | 151508476 | ||||||
| chr5:151508539
|
G | C | 1 | a0005c0014t0001g0178 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.12060-928C>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 22/23 | chr5 | 151508539 | ||||||
| chr5:151508659
|
G | A | 2 | a0029c0050t0004g0177a0029c0050t0032g0052 | 2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.12060-1048C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 22/23 | chr5 | 151508659 | ||||||
| chr5:151508864
|
T | G | 2 | a0029c0050t0004g0177a0029c0050t0032g0052 | 2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.12059+1157A>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 22/23 | chr5 | 151508864 | ||||||
| chr5:151508978
|
C | A | 12 | a0019c0036t0001g0040a0019c0036t0001g0188a0019c0101t0001g0136others(9): Show | 12 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.12059+1043G>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 22/23 | chr5 | 151508978 | ||||||
| chr5:151509014
|
C | G | 2 | a0029c0050t0004g0177a0029c0050t0032g0052 | 2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.12059+1007G>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 22/23 | chr5 | 151509014 | ||||||
| chr5:151509122
|
C | T | 2 | a0011c0136t0004g0031a0012c0018t0031g0139 | 2 | HG02698.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.12059+899G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 22/23 | chr5 | 151509122 | ||||||
| chr5:151509126
|
A | G | 2 | a0029c0050t0004g0177a0029c0050t0032g0052 | 2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.12059+895T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 22/23 | chr5 | 151509126 | ||||||
| chr5:151509142
|
C | T | 1 | a0011c0155t0004g0028 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.12059+879G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 22/23 | chr5 | 151509142 | ||||||
| chr5:151509260
|
G | C | 354 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(351): Show | 360 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(357): Show |
intron_variant | MODIFIER | c.12059+761C>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 22/23 | chr5 | 151509260 | ||||||
| chr5:151509374
|
A | G | 332 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(329): Show | 338 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(335): Show |
intron_variant | MODIFIER | c.12059+647T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 22/23 | chr5 | 151509374 | ||||||
| chr5:151509378
|
T | C | 13 | a0001c0010t0005g0058a0001c0020t0005g0167a0001c0020t0005g0172others(10): Show | 13 | HG01109.hp2 HG02280.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.12059+643A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 22/23 | chr5 | 151509378 | ||||||
| chr5:151509403
|
G | T | 1 | a0001c0010t0007g0003 | 2 | HG02723.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.12059+618C>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 22/23 | chr5 | 151509403 | ||||||
| chr5:151509411
|
C | T | 1 | a0004c0153t0027g0166 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.12059+610G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 22/23 | chr5 | 151509411 | ||||||
| chr5:151509697
|
G | A | 1 | a0001c0010t0001g0289 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.12059+324C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 22/23 | chr5 | 151509697 | ||||||
| chr5:151509863
|
A | G | 1 | a0011c0150t0001g0189 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.12059+158T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 22/23 | chr5 | 151509863 | ||||||
| chr5:151509984
|
C | CGGTGCAA others(10): Show |
2 | a0029c0050t0004g0177a0029c0050t0032g0052 | 2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.12059+36_12059+37i others(19): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 22/23 | chr5 | 151509984 | ||||||
| chr5:151510244
|
A | T | 237 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(234): Show | 243 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(240): Show |
intron_variant | MODIFIER | c.11906-70T>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 21/23 | chr5 | 151510244 | ||||||
| chr5:151510313
|
G | A | 2 | a0029c0050t0004g0177a0029c0050t0032g0052 | 2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.11906-139C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 21/23 | chr5 | 151510313 | ||||||
| chr5:151510365
|
A | G | 1 | a0003c0138t0025g0042 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.11906-191T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 21/23 | chr5 | 151510365 | ||||||
| chr5:151510392
|
C | T | 1 | a0018c0031t0001g0080 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.11906-218G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 21/23 | chr5 | 151510392 | ||||||
| chr5:151510412
|
A | G | 3 | a0001c0125t0010g0286a0002c0001t0017g0009a0013c0035t0010g0242 | 3 | HG01496.hp1 HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.11906-238T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 21/23 | chr5 | 151510412 | ||||||
| chr5:151510497
|
G | A | 1 | a0065c0145t0001g0061 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.11906-323C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 21/23 | chr5 | 151510497 | ||||||
| chr5:151510540
|
C | G | 1 | a0010c0094t0002g0385 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.11906-366G>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 21/23 | chr5 | 151510540 | ||||||
| chr5:151510563
|
A | G | 2 | a0029c0050t0004g0177a0029c0050t0032g0052 | 2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.11906-389T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 21/23 | chr5 | 151510563 | ||||||
| chr5:151510591
|
A | T | 2 | a0042c0077t0010g0248a0079c0175t0010g0148 | 2 | HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.11906-417T>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 21/23 | chr5 | 151510591 | ||||||
| chr5:151510631
|
C | G | 13 | a0001c0010t0005g0058a0001c0020t0005g0167a0001c0020t0005g0172others(10): Show | 13 | HG01109.hp2 HG02280.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.11906-457G>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 21/23 | chr5 | 151510631 | ||||||
| chr5:151510648
|
A | G | 4 | a0004c0055t0001g0012a0004c0055t0001g0234a0025c0069t0001g0240others(1): Show | 4 | NA18971.hp1 NA18987.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.11906-474T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 21/23 | chr5 | 151510648 | ||||||
| chr5:151510680
|
A | G | 328 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(325): Show | 334 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(331): Show |
intron_variant | MODIFIER | c.11906-506T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 21/23 | chr5 | 151510680 | ||||||
| chr5:151510742
|
G | A | 1 | a0001c0048t0001g0026 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.11906-568C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 21/23 | chr5 | 151510742 | ||||||
| chr5:151510769
|
A | G | 2 | a0029c0050t0004g0177a0029c0050t0032g0052 | 2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.11906-595T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 21/23 | chr5 | 151510769 | ||||||
| chr5:151510823
|
G | A | 3 | a0008c0012t0022g0318a0008c0025t0014g0339a0008c0025t0014g0341 | 3 | HG01069.hp1 HG01071.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.11906-649C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 21/23 | chr5 | 151510823 | ||||||
| chr5:151510840
|
C | T | 325 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(322): Show | 331 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(328): Show |
intron_variant | MODIFIER | c.11906-666G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 21/23 | chr5 | 151510840 | ||||||
| chr5:151510852
|
A | G | 64 | a0001c0003t0012g0206a0001c0003t0012g0222a0001c0004t0001g0156others(61): Show | 64 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.11906-678T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 21/23 | chr5 | 151510852 | ||||||
| chr5:151510983
|
G | A | 2 | a0029c0050t0004g0177a0029c0050t0032g0052 | 2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.11906-809C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 21/23 | chr5 | 151510983 | ||||||
| chr5:151510989
|
T | C | 2 | a0029c0050t0004g0177a0029c0050t0032g0052 | 2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.11906-815A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 21/23 | chr5 | 151510989 | ||||||
| chr5:151511051
|
T | C | 3 | a0008c0012t0022g0318a0008c0025t0014g0339a0008c0025t0014g0341 | 3 | HG01069.hp1 HG01071.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.11906-877A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 21/23 | chr5 | 151511051 | ||||||
| chr5:151511057
|
C | T | 1 | a0001c0003t0001g0230 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.11906-883G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 21/23 | chr5 | 151511057 | ||||||
| chr5:151511122
|
G | T | 1 | a0001c0049t0001g0020 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.11906-948C>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 21/23 | chr5 | 151511122 | ||||||
| chr5:151511160
|
A | G | 2 | a0029c0050t0004g0177a0029c0050t0032g0052 | 2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.11906-986T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 21/23 | chr5 | 151511160 | ||||||
| chr5:151511325
|
A | G | 45 | a0002c0006t0001g0129a0006c0005t0001g0135a0006c0005t0001g0301others(42): Show | 45 | HG00140.hp2 HG00558.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.11905+840T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 21/23 | chr5 | 151511325 | ||||||
| chr5:151511366
|
G | C | 2 | a0029c0050t0004g0177a0029c0050t0032g0052 | 2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.11905+799C>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 21/23 | chr5 | 151511366 | ||||||
| chr5:151511366
|
G | T | 324 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(321): Show | 330 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(327): Show |
intron_variant | MODIFIER | c.11905+799C>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 21/23 | chr5 | 151511366 | ||||||
| chr5:151511489
|
G | T | 1 | a0002c0001t0001g0084 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.11905+676C>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 21/23 | chr5 | 151511489 | ||||||
| chr5:151511764
|
T | G | 66 | a0001c0003t0012g0206a0001c0003t0012g0222a0001c0004t0001g0156others(63): Show | 66 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.11905+401A>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 21/23 | chr5 | 151511764 | ||||||
| chr5:151511913
|
C | T | 2 | a0029c0050t0004g0177a0029c0050t0032g0052 | 2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.11905+252G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 21/23 | chr5 | 151511913 | ||||||
| chr5:151511983
|
A | G | 48 | a0002c0001t0017g0009a0002c0006t0001g0129a0003c0138t0025g0042others(45): Show | 48 | HG00140.hp2 HG00558.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.11905+182T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 21/23 | chr5 | 151511983 | ||||||
| chr5:151512025
|
C | CA | 13 | a0001c0010t0005g0058a0001c0020t0005g0167a0001c0020t0005g0172others(10): Show | 13 | HG01109.hp2 HG02280.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.11905+139dupT | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 21/23 | chr5 | 151512025 | ||||||
| chr5:151512043
|
T | A | 2 | a0029c0050t0004g0177a0029c0050t0032g0052 | 2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.11905+122A>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 21/23 | chr5 | 151512043 | ||||||
| chr5:151512102
|
T | C | 332 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(329): Show | 338 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(335): Show |
intron_variant | MODIFIER | c.11905+63A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 21/23 | chr5 | 151512102 | ||||||
| chr5:151512118
|
G | A | 1 | a0079c0175t0010g0148 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.11905+47C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 21/23 | chr5 | 151512118 | ||||||
| chr5:151512619
|
T | C | 2 | a0029c0050t0004g0177a0029c0050t0032g0052 | 2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.11464-13A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151512619 | ||||||
| chr5:151512751
|
C | T | 1 | a0006c0005t0003g0126 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.11464-145G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151512751 | ||||||
| chr5:151512829
|
G | C | 2 | a0029c0050t0004g0177a0029c0050t0032g0052 | 2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.11464-223C>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151512829 | ||||||
| chr5:151512928
|
T | C | 285 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(282): Show | 291 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(288): Show |
intron_variant | MODIFIER | c.11464-322A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151512928 | ||||||
| chr5:151512989
|
C | T | 1 | a0003c0138t0025g0042 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.11464-383G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151512989 | ||||||
| chr5:151513004
|
A | G | 47 | a0002c0006t0001g0129a0003c0138t0025g0042a0006c0005t0001g0135others(44): Show | 47 | HG00140.hp2 HG00558.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.11464-398T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151513004 | ||||||
| chr5:151513202
|
G | A | 1 | a0001c0125t0010g0286 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.11464-596C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151513202 | ||||||
| chr5:151513222
|
A | G | 66 | a0001c0003t0012g0206a0001c0003t0012g0222a0001c0004t0001g0156others(63): Show | 66 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.11464-616T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151513222 | ||||||
| chr5:151513269
|
T | C | 46 | a0002c0006t0001g0129a0003c0138t0025g0042a0006c0005t0001g0135others(43): Show | 46 | HG00140.hp2 HG00558.hp1 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.11464-663A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151513269 | ||||||
| chr5:151513557
|
C | T | 1 | a0001c0003t0002g0332 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.11464-951G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151513557 | ||||||
| chr5:151513607
|
G | A | 6 | a0004c0053t0010g0019a0004c0152t0001g0176a0022c0098t0010g0039others(3): Show | 6 | HG02145.hp2 HG02559.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.11464-1001C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151513607 | ||||||
| chr5:151513615
|
T | G | 329 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(326): Show | 335 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(332): Show |
intron_variant | MODIFIER | c.11464-1009A>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151513615 | ||||||
| chr5:151513621
|
A | AC | 329 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(326): Show | 335 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(332): Show |
intron_variant | MODIFIER | c.11464-1016dupG | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151513621 | ||||||
| chr5:151513686
|
C | T | 2 | a0029c0050t0004g0177a0029c0050t0032g0052 | 2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.11464-1080G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151513686 | ||||||
| chr5:151513694
|
T | C | 329 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(326): Show | 335 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(332): Show |
intron_variant | MODIFIER | c.11464-1088A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151513694 | ||||||
| chr5:151513700
|
G | A | 2 | a0001c0004t0001g0284a0001c0110t0001g0119 | 2 | HG01167.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.11464-1094C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151513700 | ||||||
| chr5:151513708
|
G | T | 1 | a0005c0014t0001g0178 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.11464-1102C>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151513708 | ||||||
| chr5:151513726
|
T | G | 2 | a0029c0050t0004g0177a0029c0050t0032g0052 | 2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.11464-1120A>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151513726 | ||||||
| chr5:151513855
|
C | T | 1 | a0004c0019t0007g0170 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.11464-1249G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151513855 | ||||||
| chr5:151513989
|
T | C | 47 | a0002c0006t0001g0129a0006c0005t0001g0135a0006c0005t0001g0301others(44): Show | 47 | HG00140.hp2 HG00558.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.11464-1383A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151513989 | ||||||
| chr5:151514032
|
T | C | 30 | a0005c0014t0001g0051a0005c0014t0001g0055a0005c0014t0001g0056others(27): Show | 30 | HG00140.hp1 HG01243.hp2 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.11464-1426A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151514032 | ||||||
| chr5:151514079
|
C | A | 18 | a0005c0014t0001g0051a0005c0014t0001g0055a0005c0014t0001g0056others(15): Show | 18 | HG01243.hp2 HG01433.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.11464-1473G>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151514079 | ||||||
| chr5:151514138
|
A | G | 47 | a0002c0006t0001g0129a0006c0005t0001g0135a0006c0005t0001g0301others(44): Show | 47 | HG00140.hp2 HG00558.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.11464-1532T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151514138 | ||||||
| chr5:151514350
|
G | A | 6 | a0004c0053t0010g0019a0004c0152t0001g0176a0022c0098t0010g0039others(3): Show | 6 | HG02145.hp2 HG02559.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.11464-1744C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151514350 | ||||||
| chr5:151514434
|
TCTTA | T | 4 | a0001c0003t0001g0204a0001c0128t0002g0371a0002c0001t0001g0124others(1): Show | 4 | HG02071.hp2 HG02083.hp2 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.11464-1832_11464-1 others(10): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151514434 | ||||||
| chr5:151514443
|
G | A | 4 | a0027c0040t0001g0071a0027c0040t0019g0068a0048c0070t0001g0226others(1): Show | 4 | NA18944.hp1 NA19058.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.11464-1837C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151514443 | ||||||
| chr5:151514492
|
C | T | 1 | a0004c0148t0001g0152 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.11464-1886G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151514492 | ||||||
| chr5:151514551
|
C | T | 13 | a0001c0010t0005g0058a0001c0020t0005g0167a0001c0020t0005g0172others(10): Show | 13 | HG01109.hp2 HG02280.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.11464-1945G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151514551 | ||||||
| chr5:151514591
|
G | C | 2 | a0001c0144t0001g0179a0080c0176t0001g0311 | 2 | HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.11464-1985C>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151514591 | ||||||
| chr5:151514664
|
G | A | 1 | a0022c0096t0001g0041 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.11464-2058C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151514664 | ||||||
| chr5:151514764
|
C | T | 3 | a0007c0154t0001g0165a0014c0086t0002g0340a0069c0164t0001g0201 | 3 | HG01106.hp1 HG02735.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.11464-2158G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151514764 | ||||||
| chr5:151514832
|
C | T | 1 | a0004c0148t0001g0152 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.11464-2226G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151514832 | ||||||
| chr5:151514872
|
T | C | 331 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(328): Show | 337 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(334): Show |
intron_variant | MODIFIER | c.11464-2266A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151514872 | ||||||
| chr5:151514896
|
A | G | 1 | a0003c0002t0001g0062 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.11464-2290T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151514896 | ||||||
| chr5:151514922
|
G | C | 351 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(348): Show | 357 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(354): Show |
intron_variant | MODIFIER | c.11464-2316C>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151514922 | ||||||
| chr5:151514933
|
C | G | 55 | a0001c0004t0001g0255a0001c0004t0001g0256a0001c0021t0002g0374others(52): Show | 55 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.11464-2327G>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151514933 | ||||||
| chr5:151515253
|
G | A | 1 | a0001c0010t0007g0003 | 2 | HG02723.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.11463+2367C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151515253 | ||||||
| chr5:151515359
|
A | G | 353 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(350): Show | 359 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(356): Show |
intron_variant | MODIFIER | c.11463+2261T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151515359 | ||||||
| chr5:151515396
|
C | G | 2 | a0029c0050t0004g0177a0029c0050t0032g0052 | 2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.11463+2224G>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151515396 | ||||||
| chr5:151515427
|
T | G | 5 | a0001c0010t0002g0352a0001c0021t0003g0184a0003c0002t0002g0323others(2): Show | 5 | NA18989.hp2 NA18998.hp1 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.11463+2193A>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151515427 | ||||||
| chr5:151515465
|
A | T | 352 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(349): Show | 358 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(355): Show |
intron_variant | MODIFIER | c.11463+2155T>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151515465 | ||||||
| chr5:151515512
|
G | A | 7 | a0001c0004t0001g0284a0001c0016t0002g0331a0001c0059t0001g0267others(4): Show | 7 | HG01167.hp2 HG01261.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.11463+2108C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151515512 | ||||||
| chr5:151515537
|
C | T | 1 | a0078c0107t0001g0086 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.11463+2083G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151515537 | ||||||
| chr5:151515556
|
A | G | 1 | a0003c0002t0001g0062 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.11463+2064T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151515556 | ||||||
| chr5:151515725
|
A | G | 2 | a0002c0001t0005g0036a0021c0056t0005g0046 | 2 | HG02895.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.11463+1895T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151515725 | ||||||
| chr5:151515860
|
C | A | 4 | a0004c0055t0001g0012a0004c0055t0001g0234a0025c0069t0001g0240others(1): Show | 4 | NA18971.hp1 NA18987.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.11463+1760G>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151515860 | ||||||
| chr5:151515948
|
A | G | 45 | a0002c0006t0001g0129a0006c0005t0001g0135a0006c0005t0001g0301others(42): Show | 45 | HG00140.hp2 HG00558.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.11463+1672T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151515948 | ||||||
| chr5:151516213
|
G | A | 1 | a0001c0021t0002g0375 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.11463+1407C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151516213 | ||||||
| chr5:151516229
|
G | A | 1 | a0002c0001t0001g0296 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.11463+1391C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151516229 | ||||||
| chr5:151516290
|
G | A | 317 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(314): Show | 323 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(320): Show |
intron_variant | MODIFIER | c.11463+1330C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151516290 | ||||||
| chr5:151516353
|
C | T | 1 | a0002c0008t0002g0369 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.11463+1267G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151516353 | ||||||
| chr5:151516372
|
T | C | 2 | a0004c0152t0001g0176a0057c0122t0001g0082 | 2 | HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.11463+1248A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151516372 | ||||||
| chr5:151516464
|
T | C | 327 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(324): Show | 333 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(330): Show |
intron_variant | MODIFIER | c.11463+1156A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151516464 | ||||||
| chr5:151516598
|
C | A | 322 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(319): Show | 328 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(325): Show |
intron_variant | MODIFIER | c.11463+1022G>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151516598 | ||||||
| chr5:151516672
|
A | C | 1 | a0018c0031t0033g0327 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.11463+948T>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151516672 | ||||||
| chr5:151516872
|
G | A | 1 | a0001c0021t0008g0122 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.11463+748C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151516872 | ||||||
| chr5:151516910
|
A | G | 1 | a0002c0001t0001g0278 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.11463+710T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151516910 | ||||||
| chr5:151516978
|
T | G | 1 | a0024c0034t0001g0288 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.11463+642A>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151516978 | ||||||
| chr5:151517107
|
C | CA | 15 | a0001c0010t0005g0058a0001c0020t0005g0167a0001c0020t0005g0172others(12): Show | 15 | HG00673.hp2 HG01109.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.11463+512dupT | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151517107 | ||||||
| chr5:151517235
|
T | A | 4 | a0001c0010t0007g0003a0001c0142t0007g0044a0002c0099t0007g0033others(1): Show | 5 | HG02723.hp1 HG02896.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.11463+385A>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151517235 | ||||||
| chr5:151517256
|
C | G | 44 | a0006c0005t0001g0135a0006c0005t0001g0301a0006c0005t0001g0302others(41): Show | 44 | HG00140.hp2 HG00558.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.11463+364G>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151517256 | ||||||
| chr5:151517337
|
C | T | 41 | a0001c0021t0002g0374a0001c0021t0002g0375a0001c0021t0003g0184others(38): Show | 41 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.11463+283G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151517337 | ||||||
| chr5:151517364
|
A | G | 1 | a0003c0002t0023g0094 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.11463+256T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151517364 | ||||||
| chr5:151517422
|
C | T | 1 | a0002c0008t0002g0348 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.11463+198G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151517422 | ||||||
| chr5:151517528
|
G | C | 1 | a0003c0138t0025g0042 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.11463+92C>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151517528 | ||||||
| chr5:151517585
|
C | A | 1 | a0001c0010t0002g0352 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.11463+35G>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 20/23 | chr5 | 151517585 | ||||||
| chr5:151517814
|
G | A | 1 | a0024c0034t0001g0288 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.11318-49C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/23 | chr5 | 151517814 | ||||||
| chr5:151517935
|
C | T | 2 | a0019c0101t0001g0136a0030c0151t0001g0168 | 2 | HG00140.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.11318-170G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/23 | chr5 | 151517935 | ||||||
| chr5:151517965
|
C | G | 1 | a0002c0008t0029g0246 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.11318-200G>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/23 | chr5 | 151517965 | ||||||
| chr5:151518348
|
C | CTAA | 10 | a0004c0152t0001g0176a0008c0012t0022g0318a0008c0025t0014g0339others(7): Show | 10 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.11318-586_11318-58 others(7): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/23 | chr5 | 151518348 | ||||||
| chr5:151518348
|
C | CTAATAA | 13 | a0002c0006t0005g0163a0003c0029t0005g0291a0015c0043t0001g0075others(10): Show | 13 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.11318-589_11318-58 others(10): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/23 | chr5 | 151518348 | ||||||
| chr5:151518348
|
C | CTAATAAT others(2): Show |
18 | a0001c0147t0013g0161a0004c0019t0001g0053a0004c0019t0001g0054others(15): Show | 18 | HG01109.hp2 HG01884.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.11318-592_11318-58 others(13): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/23 | chr5 | 151518348 | ||||||
| chr5:151518348
|
C | CTAATAAT others(5): Show |
18 | a0001c0020t0005g0167a0001c0020t0005g0172a0003c0029t0005g0292others(15): Show | 18 | HG01243.hp2 HG01433.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.11318-595_11318-58 others(16): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/23 | chr5 | 151518348 | ||||||
| chr5:151518348
|
C | CTAATAAT others(8): Show |
7 | a0002c0001t0017g0009a0010c0011t0001g0032a0010c0011t0001g0034others(4): Show | 7 | HG01496.hp1 HG02055.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.11318-598_11318-58 others(19): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/23 | chr5 | 151518348 | ||||||
| chr5:151518348
|
C | CTAATAAT others(14): Show |
4 | a0001c0010t0005g0058a0001c0047t0005g0290a0002c0001t0005g0036others(1): Show | 4 | HG02886.hp1 HG02970.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.11318-604_11318-58 others(25): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/23 | chr5 | 151518348 | ||||||
| chr5:151518348
|
C | CTAATAAT others(17): Show |
3 | a0002c0006t0034g0358a0003c0138t0025g0042a0021c0056t0005g0046 | 3 | HG02451.hp1 HG02895.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.11318-607_11318-58 others(28): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/23 | chr5 | 151518348 | ||||||
| chr5:151518362
|
A | AATTATTA others(8): Show |
6 | a0002c0001t0001g0132a0002c0001t0002g0361a0009c0007t0001g0195others(3): Show | 6 | HG00609.hp1 NA18939.hp2 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.11318-598_11318-59 others(19): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/23 | chr5 | 151518362 | ||||||
| chr5:151518365
|
A | AATTATTA others(5): Show |
2 | a0003c0013t0009g0312a0036c0172t0009g0245 | 2 | HG02622.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.11318-601_11318-60 others(16): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/23 | chr5 | 151518365 | ||||||
| chr5:151518365
|
A | AATTATTA others(8): Show |
48 | a0001c0003t0001g0123a0001c0003t0001g0147a0001c0003t0001g0183others(45): Show | 51 | HG00423.hp1 HG00621.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.11318-601_11318-60 others(19): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/23 | chr5 | 151518365 | ||||||
| chr5:151518365
|
A | AATTATTA others(11): Show |
7 | a0001c0003t0001g0313a0001c0004t0002g0380a0001c0017t0001g0279others(4): Show | 8 | HG01070.hp2 HG01071.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.11318-601_11318-60 others(22): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/23 | chr5 | 151518365 | ||||||
| chr5:151518365
|
A | T | 6 | a0002c0001t0001g0132a0002c0001t0002g0361a0009c0007t0001g0195others(3): Show | 6 | HG00609.hp1 NA18939.hp2 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.11318-600T>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/23 | chr5 | 151518365 | ||||||
| chr5:151518368
|
A | AATTATTA others(8): Show |
109 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0204others(106): Show | 111 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.11318-604_11318-60 others(19): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/23 | chr5 | 151518368 | ||||||
| chr5:151518368
|
A | AATTATTA others(11): Show |
13 | a0001c0004t0001g0255a0001c0004t0001g0256a0001c0021t0008g0122others(10): Show | 13 | HG00423.hp2 HG02080.hp2 NA18954.hp1 others(10): Show |
intron_variant | MODIFIER | c.11318-604_11318-60 others(22): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/23 | chr5 | 151518368 | ||||||
| chr5:151518368
|
A | T | 63 | a0001c0003t0001g0123a0001c0003t0001g0147a0001c0003t0001g0183others(60): Show | 67 | HG00423.hp1 HG00609.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.11318-603T>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/23 | chr5 | 151518368 | ||||||
| chr5:151518371
|
A | AATTATTA others(8): Show |
39 | a0001c0004t0001g0253a0001c0004t0001g0284a0001c0010t0001g0212others(36): Show | 39 | HG01167.hp2 HG01261.hp1 HG01891.hp2 others(36): Show |
intron_variant | MODIFIER | c.11318-607_11318-60 others(19): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/23 | chr5 | 151518371 | ||||||
| chr5:151518371
|
A | AATTATTA others(11): Show |
2 | a0001c0021t0002g0374a0064c0060t0001g0272 | 2 | NA18959.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.11318-607_11318-60 others(22): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/23 | chr5 | 151518371 | ||||||
| chr5:151518371
|
A | T | 185 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(182): Show | 191 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(188): Show |
intron_variant | MODIFIER | c.11318-606T>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/23 | chr5 | 151518371 | ||||||
| chr5:151518374
|
A | AATTATTA others(8): Show |
6 | a0001c0004t0001g0265a0002c0001t0002g0345a0002c0006t0002g0367others(3): Show | 6 | HG02040.hp1 HG02135.hp2 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.11318-610_11318-60 others(19): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/23 | chr5 | 151518374 | ||||||
| chr5:151518374
|
A | T | 226 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(223): Show | 232 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(229): Show |
intron_variant | MODIFIER | c.11318-609T>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/23 | chr5 | 151518374 | ||||||
| chr5:151518694
|
G | A | 2 | a0001c0016t0004g0004a0023c0079t0002g0388 | 3 | HG00741.hp1 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.11318-929C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/23 | chr5 | 151518694 | ||||||
| chr5:151518813
|
C | T | 1 | a0001c0125t0010g0286 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.11318-1048G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/23 | chr5 | 151518813 | ||||||
| chr5:151518837
|
C | G | 10 | a0001c0010t0007g0003a0001c0044t0007g0085a0001c0047t0007g0294others(7): Show | 11 | HG02055.hp1 HG02723.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.11318-1072G>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/23 | chr5 | 151518837 | ||||||
| chr5:151519172
|
C | T | 1 | a0003c0009t0026g0117 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.11318-1407G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/23 | chr5 | 151519172 | ||||||
| chr5:151519394
|
A | G | 1 | a0063c0062t0001g0266 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.11318-1629T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/23 | chr5 | 151519394 | ||||||
| chr5:151519586
|
G | A | 283 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(280): Show | 289 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(286): Show |
intron_variant | MODIFIER | c.11317+1690C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/23 | chr5 | 151519586 | ||||||
| chr5:151519651
|
C | A | 42 | a0006c0005t0001g0135a0006c0005t0001g0301a0006c0005t0001g0302others(39): Show | 42 | HG00140.hp2 HG00558.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.11317+1625G>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/23 | chr5 | 151519651 | ||||||
| chr5:151519684
|
T | C | 1 | a0001c0004t0001g0260 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.11317+1592A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/23 | chr5 | 151519684 | ||||||
| chr5:151519822
|
A | G | 4 | a0019c0101t0001g0136a0030c0151t0001g0168a0032c0057t0001g0017others(1): Show | 4 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.11317+1454T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/23 | chr5 | 151519822 | ||||||
| chr5:151519857
|
T | C | 1 | a0065c0145t0001g0061 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.11317+1419A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/23 | chr5 | 151519857 | ||||||
| chr5:151519939
|
G | A | 1 | a0003c0009t0001g0103 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.11317+1337C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/23 | chr5 | 151519939 | ||||||
| chr5:151520035
|
T | G | 28 | a0001c0147t0013g0161a0004c0019t0001g0053a0004c0019t0001g0054others(25): Show | 28 | HG00735.hp2 HG01069.hp1 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.11317+1241A>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/23 | chr5 | 151520035 | ||||||
| chr5:151520071
|
A | C | 3 | a0005c0015t0001g0217a0005c0173t0002g0336a0010c0011t0001g0303 | 3 | HG00642.hp2 HG03669.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.11317+1205T>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/23 | chr5 | 151520071 | ||||||
| chr5:151520084
|
A | G | 1 | a0007c0045t0003g0191 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.11317+1192T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/23 | chr5 | 151520084 | ||||||
| chr5:151520214
|
C | T | 40 | a0006c0005t0001g0135a0006c0005t0001g0301a0006c0005t0001g0302others(37): Show | 40 | HG00140.hp2 HG00558.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.11317+1062G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/23 | chr5 | 151520214 | ||||||
| chr5:151520249
|
G | A | 1 | a0015c0043t0001g0075 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.11317+1027C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/23 | chr5 | 151520249 | ||||||
| chr5:151520396
|
A | G | 354 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(351): Show | 360 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(357): Show |
intron_variant | MODIFIER | c.11317+880T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/23 | chr5 | 151520396 | ||||||
| chr5:151520542
|
C | T | 1 | a0001c0004t0001g0264 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.11317+734G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/23 | chr5 | 151520542 | ||||||
| chr5:151520615
|
C | T | 6 | a0004c0053t0010g0019a0008c0012t0001g0045a0008c0012t0001g0049others(3): Show | 6 | HG02145.hp2 HG03130.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.11317+661G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/23 | chr5 | 151520615 | ||||||
| chr5:151520630
|
G | A | 2 | a0022c0096t0001g0041a0065c0145t0001g0061 | 2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.11317+646C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/23 | chr5 | 151520630 | ||||||
| chr5:151520719
|
A | G | 2 | a0004c0152t0001g0176a0057c0122t0001g0082 | 2 | HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.11317+557T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/23 | chr5 | 151520719 | ||||||
| chr5:151521134
|
G | A | 2 | a0004c0152t0001g0176a0057c0122t0001g0082 | 2 | HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.11317+142C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/23 | chr5 | 151521134 | ||||||
| chr5:151521226
|
G | A | 13 | a0019c0036t0001g0040a0019c0036t0001g0188a0019c0101t0001g0136others(10): Show | 13 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.11317+50C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/23 | chr5 | 151521226 | ||||||
| chr5:151521250
|
G | A | 1 | a0009c0007t0001g0216 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.11317+26C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 19/23 | chr5 | 151521250 | ||||||
| chr5:151522138
|
C | T | 47 | a0005c0014t0001g0051a0005c0014t0001g0055a0005c0014t0001g0056others(44): Show | 47 | HG00140.hp1 HG00642.hp2 HG01243.hp2 others(44): Show |
intron_variant | MODIFIER | c.10507-52G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 18/23 | chr5 | 151522138 | ||||||
| chr5:151522227
|
G | GA | 223 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(220): Show | 229 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(226): Show |
intron_variant | MODIFIER | c.10507-142dupT | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 18/23 | chr5 | 151522227 | ||||||
| chr5:151522275
|
C | T | 1 | a0061c0115t0002g0324 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.10507-189G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 18/23 | chr5 | 151522275 | ||||||
| chr5:151522312
|
CCTATACC others(3): Show |
C | 25 | a0001c0021t0002g0374a0001c0021t0008g0122a0001c0032t0008g0108others(22): Show | 25 | HG00423.hp2 HG01081.hp1 HG01993.hp2 others(22): Show |
intron_variant | MODIFIER | c.10507-236_10507-22 others(14): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 18/23 | chr5 | 151522312 | ||||||
| chr5:151522365
|
C | G | 13 | a0001c0147t0013g0161a0004c0019t0001g0053a0004c0019t0001g0054others(10): Show | 13 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.10507-279G>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 18/23 | chr5 | 151522365 | ||||||
| chr5:151522448
|
T | A | 1 | a0045c0080t0009g0150 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.10507-362A>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 18/23 | chr5 | 151522448 | ||||||
| chr5:151522495
|
C | T | 1 | a0058c0120t0001g0099 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.10507-409G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 18/23 | chr5 | 151522495 | ||||||
| chr5:151522626
|
T | C | 223 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(220): Show | 229 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(226): Show |
intron_variant | MODIFIER | c.10507-540A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 18/23 | chr5 | 151522626 | ||||||
| chr5:151522716
|
G | A | 3 | a0004c0153t0027g0166a0011c0137t0011g0319a0011c0163t0011g0335 | 3 | HG01515.hp2 HG02293.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.10507-630C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 18/23 | chr5 | 151522716 | ||||||
| chr5:151522872
|
C | T | 13 | a0019c0036t0001g0040a0019c0036t0001g0188a0019c0101t0001g0136others(10): Show | 13 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.10507-786G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 18/23 | chr5 | 151522872 | ||||||
| chr5:151522922
|
G | A | 1 | a0001c0048t0001g0026 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.10507-836C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 18/23 | chr5 | 151522922 | ||||||
| chr5:151522982
|
C | A | 1 | a0002c0008t0001g0237 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.10507-896G>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 18/23 | chr5 | 151522982 | ||||||
| chr5:151523002
|
C | T | 4 | a0019c0101t0001g0136a0030c0151t0001g0168a0032c0057t0001g0017others(1): Show | 4 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.10507-916G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 18/23 | chr5 | 151523002 | ||||||
| chr5:151523009
|
A | C | 6 | a0005c0015t0001g0157a0005c0015t0001g0159a0005c0015t0001g0232others(3): Show | 6 | NA18948.hp1 NA18951.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.10507-923T>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 18/23 | chr5 | 151523009 | ||||||
| chr5:151523051
|
A | G | 1 | a0008c0012t0022g0318 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.10507-965T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 18/23 | chr5 | 151523051 | ||||||
| chr5:151523162
|
A | G | 1 | a0003c0002t0001g0106 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.10507-1076T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 18/23 | chr5 | 151523162 | ||||||
| chr5:151523224
|
C | G | 2 | a0022c0096t0001g0041a0065c0145t0001g0061 | 2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.10507-1138G>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 18/23 | chr5 | 151523224 | ||||||
| chr5:151523262
|
ATAC | A | 3 | a0001c0003t0001g0313a0001c0049t0001g0020a0002c0006t0001g0005 | 4 | HG01070.hp2 HG01071.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.10507-1179_10507-1 others(9): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 18/23 | chr5 | 151523262 | ||||||
| chr5:151523324
|
T | C | 223 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(220): Show | 229 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(226): Show |
intron_variant | MODIFIER | c.10507-1238A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 18/23 | chr5 | 151523324 | ||||||
| chr5:151523631
|
A | G | 355 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(352): Show | 361 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(358): Show |
intron_variant | MODIFIER | c.10507-1545T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 18/23 | chr5 | 151523631 | ||||||
| chr5:151523633
|
G | C | 36 | a0005c0014t0001g0051a0005c0014t0001g0055a0005c0014t0001g0056others(33): Show | 36 | HG00642.hp2 HG01243.hp2 HG01433.hp2 others(33): Show |
intron_variant | MODIFIER | c.10507-1547C>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 18/23 | chr5 | 151523633 | ||||||
| chr5:151523770
|
C | T | 354 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(351): Show | 360 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(357): Show |
intron_variant | MODIFIER | c.10507-1684G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 18/23 | chr5 | 151523770 | ||||||
| chr5:151523814
|
T | C | 304 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(301): Show | 310 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(307): Show |
intron_variant | MODIFIER | c.10507-1728A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 18/23 | chr5 | 151523814 | ||||||
| chr5:151523831
|
C | T | 212 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(209): Show | 218 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(215): Show |
intron_variant | MODIFIER | c.10507-1745G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 18/23 | chr5 | 151523831 | ||||||
| chr5:151523900
|
G | C | 87 | a0001c0142t0007g0044a0001c0147t0013g0161a0002c0006t0001g0129others(84): Show | 87 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.10507-1814C>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 18/23 | chr5 | 151523900 | ||||||
| chr5:151523913
|
G | A | 1 | a0012c0018t0004g0142 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.10507-1827C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 18/23 | chr5 | 151523913 | ||||||
| chr5:151523962
|
T | C | 304 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(301): Show | 310 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(307): Show |
intron_variant | MODIFIER | c.10506+1806A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 18/23 | chr5 | 151523962 | ||||||
| chr5:151524040
|
A | C | 44 | a0001c0142t0007g0044a0001c0147t0013g0161a0002c0099t0007g0033others(41): Show | 44 | HG00140.hp1 HG00735.hp2 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.10506+1728T>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 18/23 | chr5 | 151524040 | ||||||
| chr5:151524111
|
T | C | 6 | a0001c0142t0007g0044a0002c0099t0007g0033a0003c0138t0025g0042others(3): Show | 6 | HG01069.hp1 HG01071.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.10506+1657A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 18/23 | chr5 | 151524111 | ||||||
| chr5:151524197
|
T | G | 1 | a0003c0013t0001g0090 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.10506+1571A>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 18/23 | chr5 | 151524197 | ||||||
| chr5:151524317
|
C | G | 1 | a0001c0021t0002g0375 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.10506+1451G>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 18/23 | chr5 | 151524317 | ||||||
| chr5:151524442
|
G | GAGC | 305 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(302): Show | 311 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(308): Show |
intron_variant | MODIFIER | c.10506+1325_10506+1 others(9): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 18/23 | chr5 | 151524442 | ||||||
| chr5:151524446
|
C | T | 3 | a0003c0002t0001g0062a0018c0177t0002g0328a0039c0073t0002g0356 | 3 | HG00673.hp2 HG02056.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.10506+1322G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 18/23 | chr5 | 151524446 | ||||||
| chr5:151524567
|
G | A | 1 | a0003c0009t0001g0063 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.10506+1201C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 18/23 | chr5 | 151524567 | ||||||
| chr5:151524678
|
C | T | 3 | a0001c0004t0001g0259a0001c0004t0001g0271a0075c0126t0001g0096 | 3 | HG00558.hp2 NA18969.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.10506+1090G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 18/23 | chr5 | 151524678 | ||||||
| chr5:151524739
|
G | A | 36 | a0005c0014t0001g0051a0005c0014t0001g0055a0005c0014t0001g0056others(33): Show | 36 | HG00642.hp2 HG01243.hp2 HG01433.hp2 others(33): Show |
intron_variant | MODIFIER | c.10506+1029C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 18/23 | chr5 | 151524739 | ||||||
| chr5:151524780
|
T | C | 44 | a0001c0142t0007g0044a0001c0147t0013g0161a0002c0099t0007g0033others(41): Show | 44 | HG00140.hp1 HG00735.hp2 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.10506+988A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 18/23 | chr5 | 151524780 | ||||||
| chr5:151525033
|
C | T | 5 | a0001c0010t0009g0171a0003c0013t0009g0312a0036c0172t0009g0245others(2): Show | 5 | HG01243.hp1 HG02622.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.10506+735G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 18/23 | chr5 | 151525033 | ||||||
| chr5:151525228
|
G | C | 305 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(302): Show | 311 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(308): Show |
intron_variant | MODIFIER | c.10506+540C>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 18/23 | chr5 | 151525228 | ||||||
| chr5:151525236
|
T | C | 2 | a0004c0152t0001g0176a0057c0122t0001g0082 | 2 | HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.10506+532A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 18/23 | chr5 | 151525236 | ||||||
| chr5:151525332
|
A | G | 34 | a0005c0014t0001g0051a0005c0014t0001g0055a0005c0014t0001g0056others(31): Show | 34 | HG00642.hp2 HG01243.hp2 HG01433.hp2 others(31): Show |
intron_variant | MODIFIER | c.10506+436T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 18/23 | chr5 | 151525332 | ||||||
| chr5:151525514
|
T | C | 13 | a0019c0036t0001g0040a0019c0036t0001g0188a0019c0101t0001g0136others(10): Show | 13 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.10506+254A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 18/23 | chr5 | 151525514 | ||||||
| chr5:151525551
|
CCT | C | 13 | a0001c0010t0005g0058a0001c0020t0005g0167a0001c0020t0005g0172others(10): Show | 13 | HG01109.hp2 HG02280.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.10506+215_10506+21 others(6): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 18/23 | chr5 | 151525551 | ||||||
| chr5:151526024
|
G | A | 1 | a0004c0019t0007g0170 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.10309-59C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 17/23 | chr5 | 151526024 | ||||||
| chr5:151526038
|
A | G | 1 | a0004c0053t0001g0169 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.10309-73T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 17/23 | chr5 | 151526038 | ||||||
| chr5:151526124
|
T | C | 3 | a0001c0003t0012g0206a0001c0003t0012g0222a0002c0001t0002g0350 | 3 | HG02523.hp1 NA18987.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.10309-159A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 17/23 | chr5 | 151526124 | ||||||
| chr5:151526389
|
A | G | 3 | a0002c0008t0029g0246a0003c0009t0001g0120a0061c0115t0002g0324 | 3 | NA18989.hp1 NA19057.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.10309-424T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 17/23 | chr5 | 151526389 | ||||||
| chr5:151526405
|
A | G | 1 | a0008c0012t0001g0049 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.10309-440T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 17/23 | chr5 | 151526405 | ||||||
| chr5:151526636
|
G | A | 1 | a0003c0013t0001g0079 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.10308+598C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 17/23 | chr5 | 151526636 | ||||||
| chr5:151526637
|
A | C | 221 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(218): Show | 227 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(224): Show |
intron_variant | MODIFIER | c.10308+597T>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 17/23 | chr5 | 151526637 | ||||||
| chr5:151527028
|
G | A | 44 | a0001c0021t0002g0374a0001c0021t0002g0375a0001c0021t0008g0122others(41): Show | 44 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.10308+206C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 17/23 | chr5 | 151527028 | ||||||
| chr5:151527038
|
A | T | 1 | a0003c0002t0001g0064 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.10308+196T>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 17/23 | chr5 | 151527038 | ||||||
| chr5:151527160
|
A | G | 58 | a0001c0003t0012g0206a0001c0003t0012g0222a0001c0004t0001g0156others(55): Show | 58 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.10308+74T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 17/23 | chr5 | 151527160 | ||||||
| chr5:151527402
|
T | G | 41 | a0001c0010t0001g0289a0001c0142t0007g0044a0002c0001t0017g0009others(38): Show | 41 | HG00140.hp1 HG00735.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.10165-25A>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 16/23 | chr5 | 151527402 | ||||||
| chr5:151527434
|
C | A | 1 | a0019c0036t0001g0188 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.10165-57G>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 16/23 | chr5 | 151527434 | ||||||
| chr5:151527434
|
C | T | 1 | a0026c0046t0003g0198 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.10165-57G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 16/23 | chr5 | 151527434 | ||||||
| chr5:151527510
|
G | A | 7 | a0001c0004t0001g0255a0001c0004t0001g0256a0002c0001t0001g0130others(4): Show | 7 | NA18954.hp2 NA18956.hp1 NA18957.hp2 others(4): Show |
intron_variant | MODIFIER | c.10165-133C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 16/23 | chr5 | 151527510 | ||||||
| chr5:151527694
|
T | A | 2 | a0001c0142t0007g0044a0003c0138t0025g0042 | 2 | HG02451.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.10164+302A>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 16/23 | chr5 | 151527694 | ||||||
| chr5:151527738
|
A | C | 59 | a0001c0004t0001g0255a0001c0004t0001g0256a0001c0021t0002g0374others(56): Show | 59 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.10164+258T>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 16/23 | chr5 | 151527738 | ||||||
| chr5:151528180
|
C | T | 15 | a0014c0086t0002g0340a0019c0036t0001g0040a0019c0036t0001g0188others(12): Show | 15 | HG00140.hp1 HG01257.hp1 HG01258.hp1 others(12): Show |
intron_variant | MODIFIER | c.10027-47G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 15/23 | chr5 | 151528180 | ||||||
| chr5:151528192
|
C | T | 2 | a0004c0156t0001g0023a0008c0084t0001g0134 | 2 | HG01255.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.10027-59G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 15/23 | chr5 | 151528192 | ||||||
| chr5:151528258
|
T | C | 295 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(292): Show | 301 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(298): Show |
intron_variant | MODIFIER | c.10027-125A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 15/23 | chr5 | 151528258 | ||||||
| chr5:151528475
|
C | T | 1 | a0021c0167t0005g0048 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.10027-342G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 15/23 | chr5 | 151528475 | ||||||
| chr5:151528609
|
C | T | 1 | a0016c0118t0006g0325 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.10027-476G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 15/23 | chr5 | 151528609 | ||||||
| chr5:151528616
|
T | C | 2 | a0022c0096t0001g0041a0065c0145t0001g0061 | 2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.10027-483A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 15/23 | chr5 | 151528616 | ||||||
| chr5:151528711
|
G | A | 2 | a0029c0050t0004g0177a0029c0050t0032g0052 | 2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.10026+467C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 15/23 | chr5 | 151528711 | ||||||
| chr5:151528717
|
G | A | 132 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(129): Show | 137 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(134): Show |
intron_variant | MODIFIER | c.10026+461C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 15/23 | chr5 | 151528717 | ||||||
| chr5:151529003
|
G | A | 3 | a0002c0099t0007g0033a0008c0025t0014g0339a0008c0025t0014g0341 | 3 | HG01069.hp1 HG01071.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.10026+175C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 15/23 | chr5 | 151529003 | ||||||
| chr5:151529098
|
T | C | 38 | a0005c0014t0001g0051a0005c0014t0001g0055a0005c0014t0001g0056others(35): Show | 38 | HG00642.hp2 HG01243.hp2 HG01433.hp2 others(35): Show |
intron_variant | MODIFIER | c.10026+80A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 15/23 | chr5 | 151529098 | ||||||
| chr5:151529414
|
G | A | 3 | a0001c0142t0007g0044a0003c0138t0025g0042a0015c0043t0001g0075 | 3 | HG02451.hp1 HG02896.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.9812-22C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 14/23 | chr5 | 151529414 | ||||||
| chr5:151529554
|
C | T | 14 | a0004c0019t0001g0053a0004c0019t0001g0054a0004c0019t0001g0181others(11): Show | 14 | HG01884.hp1 HG02055.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.9812-162G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 14/23 | chr5 | 151529554 | ||||||
| chr5:151529577
|
AT | A | 50 | a0001c0010t0001g0289a0001c0021t0008g0122a0001c0142t0007g0044others(47): Show | 50 | HG00140.hp2 HG00558.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.9812-186delA | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 14/23 | chr5 | 151529577 | ||||||
| chr5:151529586
|
T | C | 2 | a0004c0153t0027g0166a0034c0178t0001g0229 | 2 | HG02293.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.9812-194A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 14/23 | chr5 | 151529586 | ||||||
| chr5:151529614
|
C | T | 3 | a0001c0142t0007g0044a0003c0138t0025g0042a0015c0043t0001g0075 | 3 | HG02451.hp1 HG02896.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.9812-222G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 14/23 | chr5 | 151529614 | ||||||
| chr5:151529779
|
A | G | 50 | a0001c0010t0001g0289a0001c0021t0008g0122a0001c0142t0007g0044others(47): Show | 50 | HG00140.hp2 HG00558.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.9812-387T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 14/23 | chr5 | 151529779 | ||||||
| chr5:151529851
|
A | T | 50 | a0001c0010t0001g0289a0001c0021t0008g0122a0001c0142t0007g0044others(47): Show | 50 | HG00140.hp2 HG00558.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.9812-459T>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 14/23 | chr5 | 151529851 | ||||||
| chr5:151529948
|
G | A | 110 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(107): Show | 114 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(111): Show |
intron_variant | MODIFIER | c.9812-556C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 14/23 | chr5 | 151529948 | ||||||
| chr5:151530011
|
T | C | 37 | a0001c0010t0001g0289a0001c0142t0007g0044a0001c0147t0013g0161others(34): Show | 37 | HG00140.hp1 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.9812-619A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 14/23 | chr5 | 151530011 | ||||||
| chr5:151530111
|
T | C | 293 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(290): Show | 299 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(296): Show |
intron_variant | MODIFIER | c.9812-719A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 14/23 | chr5 | 151530111 | ||||||
| chr5:151530112
|
A | G | 13 | a0001c0010t0005g0058a0001c0020t0005g0167a0001c0020t0005g0172others(10): Show | 13 | HG01109.hp2 HG02280.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.9812-720T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 14/23 | chr5 | 151530112 | ||||||
| chr5:151530188
|
T | C | 13 | a0001c0010t0005g0058a0001c0020t0005g0167a0001c0020t0005g0172others(10): Show | 13 | HG01109.hp2 HG02280.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.9812-796A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 14/23 | chr5 | 151530188 | ||||||
| chr5:151530215
|
T | C | 1 | a0001c0124t0001g0104 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.9812-823A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 14/23 | chr5 | 151530215 | ||||||
| chr5:151530251
|
G | GA | 7 | a0001c0010t0002g0352a0001c0020t0005g0172a0001c0142t0007g0044others(4): Show | 7 | HG01981.hp1 HG02451.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.9812-860dupT | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 14/23 | chr5 | 151530251 | ||||||
| chr5:151530251
|
GA | G | 79 | a0001c0003t0001g0123a0001c0003t0001g0202a0001c0003t0001g0204others(76): Show | 81 | HG00140.hp1 HG00609.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.9812-860delT | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 14/23 | chr5 | 151530251 | ||||||
| chr5:151530406
|
T | A | 1 | a0003c0009t0001g0063 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.9812-1014A>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 14/23 | chr5 | 151530406 | ||||||
| chr5:151530406
|
T | C | 342 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(339): Show | 348 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(345): Show |
intron_variant | MODIFIER | c.9812-1014A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 14/23 | chr5 | 151530406 | ||||||
| chr5:151530719
|
CTTA | C | 4 | a0001c0179t0001g0233a0003c0009t0001g0098a0003c0009t0002g0330others(1): Show | 4 | NA18945.hp2 NA18982.hp1 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.9811+865_9811+867d others(5): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 14/23 | chr5 | 151530719 | ||||||
| chr5:151530777
|
G | A | 41 | a0003c0002t0001g0064a0006c0005t0001g0135a0006c0005t0001g0301others(38): Show | 41 | HG00140.hp2 HG00558.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.9811+810C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 14/23 | chr5 | 151530777 | ||||||
| chr5:151530790
|
A | G | 43 | a0001c0021t0008g0122a0003c0002t0001g0064a0006c0005t0001g0135others(40): Show | 43 | HG00140.hp2 HG00558.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.9811+797T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 14/23 | chr5 | 151530790 | ||||||
| chr5:151530830
|
A | T | 65 | a0001c0010t0001g0289a0001c0021t0008g0122a0001c0142t0007g0044others(62): Show | 65 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.9811+757T>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 14/23 | chr5 | 151530830 | ||||||
| chr5:151530867
|
T | C | 355 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(352): Show | 361 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(358): Show |
intron_variant | MODIFIER | c.9811+720A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 14/23 | chr5 | 151530867 | ||||||
| chr5:151530884
|
T | C | 1 | a0001c0017t0001g0261 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.9811+703A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 14/23 | chr5 | 151530884 | ||||||
| chr5:151530892
|
A | G | 1 | a0013c0035t0001g0227 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.9811+695T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 14/23 | chr5 | 151530892 | ||||||
| chr5:151530986
|
G | A | 1 | a0001c0142t0007g0044 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.9811+601C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 14/23 | chr5 | 151530986 | ||||||
| chr5:151531098
|
C | T | 2 | a0022c0096t0001g0041a0065c0145t0001g0061 | 2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.9811+489G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 14/23 | chr5 | 151531098 | ||||||
| chr5:151531363
|
G | T | 39 | a0003c0002t0001g0064a0006c0005t0001g0135a0006c0005t0001g0301others(36): Show | 39 | HG00140.hp2 HG00558.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.9811+224C>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 14/23 | chr5 | 151531363 | ||||||
| chr5:151531381
|
T | C | 5 | a0001c0016t0002g0331a0001c0124t0001g0104a0002c0026t0001g0298others(2): Show | 5 | HG00323.hp1 HG01081.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.9811+206A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 14/23 | chr5 | 151531381 | ||||||
| chr5:151531999
|
C | T | 2 | a0004c0148t0001g0152a0040c0074t0001g0244 | 2 | HG00735.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.9428-29G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 13/23 | chr5 | 151531999 | ||||||
| chr5:151532225
|
G | C | 5 | a0004c0052t0001g0193a0004c0152t0001g0176a0005c0030t0001g0060others(2): Show | 5 | HG02145.hp1 HG02559.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.9428-255C>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 13/23 | chr5 | 151532225 | ||||||
| chr5:151532342
|
A | G | 19 | a0002c0001t0001g0131a0002c0001t0001g0138a0002c0001t0002g0345others(16): Show | 19 | HG00597.hp2 HG01109.hp1 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.9428-372T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 13/23 | chr5 | 151532342 | ||||||
| chr5:151532388
|
AAC | A | 34 | a0001c0003t0001g0123a0001c0003t0001g0230a0001c0003t0001g0295others(31): Show | 35 | HG00621.hp2 HG00642.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.9428-420_9428-419d others(4): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 13/23 | chr5 | 151532388 | ||||||
| chr5:151532388
|
AACAC | A | 58 | a0001c0003t0001g0313a0001c0004t0001g0156a0001c0010t0002g0352others(55): Show | 58 | HG00597.hp2 HG01433.hp2 HG01496.hp1 others(55): Show |
intron_variant | MODIFIER | c.9428-422_9428-419d others(6): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 13/23 | chr5 | 151532388 | ||||||
| chr5:151532388
|
AACACAC | A | 29 | a0001c0010t0005g0058a0001c0016t0002g0331a0001c0124t0001g0104others(26): Show | 29 | HG00323.hp1 HG00673.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.9428-424_9428-419d others(8): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 13/23 | chr5 | 151532388 | ||||||
| chr5:151532388
|
AACACACA others(1): Show |
A | 212 | a0001c0003t0001g0147a0001c0003t0001g0202a0001c0003t0001g0204others(209): Show | 216 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.9428-426_9428-419d others(10): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 13/23 | chr5 | 151532388 | ||||||
| chr5:151532388
|
AACACACA others(3): Show |
A | 5 | a0022c0096t0001g0041a0042c0077t0010g0248a0045c0080t0009g0150others(2): Show | 5 | HG02055.hp2 HG02258.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.9428-428_9428-419d others(12): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 13/23 | chr5 | 151532388 | ||||||
| chr5:151532388
|
AACACACA others(5): Show |
A | 1 | a0004c0052t0001g0193 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.9428-430_9428-419d others(14): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 13/23 | chr5 | 151532388 | ||||||
| chr5:151532388
|
AACACACA others(9): Show |
A | 1 | a0003c0029t0005g0293 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.9428-434_9428-419d others(18): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 13/23 | chr5 | 151532388 | ||||||
| chr5:151532694
|
GT | G | 39 | a0001c0003t0001g0123a0001c0003t0001g0230a0001c0003t0001g0295others(36): Show | 40 | HG00323.hp1 HG00621.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.9428-725delA | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 13/23 | chr5 | 151532694 | ||||||
| chr5:151532754
|
G | T | 81 | a0001c0003t0012g0206a0001c0003t0012g0222a0001c0004t0001g0156others(78): Show | 81 | HG00597.hp2 HG00673.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.9428-784C>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 13/23 | chr5 | 151532754 | ||||||
| chr5:151532784
|
T | C | 1 | a0045c0080t0009g0150 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.9428-814A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 13/23 | chr5 | 151532784 | ||||||
| chr5:151532813
|
C | T | 1 | a0004c0053t0001g0169 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.9428-843G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 13/23 | chr5 | 151532813 | ||||||
| chr5:151532959
|
T | C | 1 | a0045c0080t0009g0150 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.9428-989A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 13/23 | chr5 | 151532959 | ||||||
| chr5:151533088
|
T | C | 1 | a0028c0039t0003g0066 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.9428-1118A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 13/23 | chr5 | 151533088 | ||||||
| chr5:151533282
|
G | A | 4 | a0022c0096t0001g0041a0042c0077t0010g0248a0065c0145t0001g0061others(1): Show | 4 | HG02055.hp2 HG03195.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.9427+1127C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 13/23 | chr5 | 151533282 | ||||||
| chr5:151533337
|
A | G | 1 | a0023c0079t0002g0388 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.9427+1072T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 13/23 | chr5 | 151533337 | ||||||
| chr5:151533392
|
C | CAA | 8 | a0001c0004t0001g0262a0001c0010t0001g0289a0001c0048t0021g0025others(5): Show | 8 | HG01516.hp1 HG01891.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.9427+1015_9427+101 others(6): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 13/23 | chr5 | 151533392 | ||||||
| chr5:151533393
|
A | AAAAC | 70 | a0001c0003t0001g0202a0001c0003t0001g0210a0001c0003t0002g0329others(67): Show | 70 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.9427+1015_9427+101 others(8): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 13/23 | chr5 | 151533393 | ||||||
| chr5:151533393
|
A | AAAACAC | 40 | a0001c0003t0001g0121a0001c0003t0001g0204a0001c0003t0001g0231others(37): Show | 40 | HG00609.hp1 HG00639.hp2 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.9427+1015_9427+101 others(10): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 13/23 | chr5 | 151533393 | ||||||
| chr5:151533393
|
A | AAAACACA others(1): Show |
11 | a0001c0004t0001g0156a0002c0001t0001g0130a0006c0005t0001g0301others(8): Show | 11 | HG00597.hp2 HG00642.hp1 NA18948.hp1 others(8): Show |
intron_variant | MODIFIER | c.9427+1015_9427+101 others(12): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 13/23 | chr5 | 151533393 | ||||||
| chr5:151533393
|
A | AAAACACA others(3): Show |
5 | a0001c0021t0002g0374a0002c0001t0001g0084a0003c0002t0001g0081others(2): Show | 5 | HG02135.hp1 NA18942.hp2 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.9427+1015_9427+101 others(14): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 13/23 | chr5 | 151533393 | ||||||
| chr5:151533393
|
A | AAAACACA others(5): Show |
1 | a0002c0001t0002g0384 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.9427+1015_9427+101 others(16): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 13/23 | chr5 | 151533393 | ||||||
| chr5:151533393
|
A | AAC | 44 | a0001c0003t0001g0123a0001c0003t0012g0206a0001c0003t0020g0221others(41): Show | 46 | HG00140.hp1 HG00323.hp1 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.9427+1014_9427+101 others(6): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 13/23 | chr5 | 151533393 | ||||||
| chr5:151533393
|
A | AACAC | 53 | a0001c0003t0001g0013a0001c0003t0001g0147a0001c0003t0001g0183others(50): Show | 54 | HG00423.hp1 HG00609.hp2 HG00741.hp2 others(51): Show |
intron_variant | MODIFIER | c.9427+1012_9427+101 others(8): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 13/23 | chr5 | 151533393 | ||||||
| chr5:151533393
|
A | AACACAC | 9 | a0001c0003t0001g0185a0002c0001t0002g0363a0002c0001t0036g0349others(6): Show | 9 | HG00621.hp2 HG02132.hp2 HG02273.hp2 others(6): Show |
intron_variant | MODIFIER | c.9427+1010_9427+101 others(10): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 13/23 | chr5 | 151533393 | ||||||
| chr5:151533393
|
AAC | A | 44 | a0001c0016t0001g0247a0001c0016t0002g0331a0001c0017t0001g0279others(41): Show | 46 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(43): Show |
intron_variant | MODIFIER | c.9427+1014_9427+101 others(6): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 13/23 | chr5 | 151533393 | ||||||
| chr5:151533393
|
AACAC | A | 17 | a0001c0010t0002g0352a0001c0016t0004g0004a0001c0017t0001g0261others(14): Show | 18 | HG01243.hp1 HG01257.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.9427+1012_9427+101 others(8): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 13/23 | chr5 | 151533393 | ||||||
| chr5:151533393
|
AACACACA others(9): Show |
A | 1 | a0004c0156t0001g0023 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.9427+1000_9427+101 others(20): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 13/23 | chr5 | 151533393 | ||||||
| chr5:151533393
|
AACACACA others(11): Show |
A | 33 | a0001c0010t0005g0058a0001c0010t0009g0171a0001c0047t0005g0290others(30): Show | 33 | HG00673.hp1 HG00741.hp1 HG01433.hp2 others(30): Show |
intron_variant | MODIFIER | c.9427+998_9427+1015 others(21): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 13/23 | chr5 | 151533393 | ||||||
| chr5:151533395
|
C | A | 7 | a0001c0049t0001g0030a0001c0110t0001g0119a0003c0139t0008g0238others(4): Show | 7 | HG00735.hp2 HG01167.hp2 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.9427+1014G>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 13/23 | chr5 | 151533395 | ||||||
| chr5:151533397
|
C | A | 1 | a0003c0009t0001g0270 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.9427+1012G>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 13/23 | chr5 | 151533397 | ||||||
| chr5:151533399
|
C | A | 6 | a0001c0010t0002g0352a0001c0044t0007g0085a0001c0047t0007g0294others(3): Show | 6 | HG02055.hp1 HG03209.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.9427+1010G>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 13/23 | chr5 | 151533399 | ||||||
| chr5:151533403
|
C | A | 1 | a0013c0035t0001g0227 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.9427+1006G>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 13/23 | chr5 | 151533403 | ||||||
| chr5:151533437
|
C | G | 4 | a0004c0052t0001g0193a0004c0152t0001g0176a0005c0030t0001g0060others(1): Show | 4 | HG02145.hp1 HG02559.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.9427+972G>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 13/23 | chr5 | 151533437 | ||||||
| chr5:151533454
|
C | T | 154 | a0001c0003t0001g0121a0001c0003t0001g0202a0001c0003t0001g0204others(151): Show | 154 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(151): Show |
intron_variant | MODIFIER | c.9427+955G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 13/23 | chr5 | 151533454 | ||||||
| chr5:151533741
|
A | G | 2 | a0004c0143t0001g0043a0072c0166t0001g0047 | 2 | HG01243.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.9427+668T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 13/23 | chr5 | 151533741 | ||||||
| chr5:151533757
|
GAT | G | 10 | a0001c0003t0012g0206a0001c0003t0012g0222a0003c0002t0001g0064others(7): Show | 10 | HG01978.hp1 HG02155.hp2 NA18969.hp1 others(7): Show |
intron_variant | MODIFIER | c.9427+650_9427+651d others(4): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 13/23 | chr5 | 151533757 | ||||||
| chr5:151533802
|
A | G | 1 | a0001c0142t0007g0044 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.9427+607T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 13/23 | chr5 | 151533802 | ||||||
| chr5:151533823
|
C | T | 2 | a0004c0152t0001g0176a0005c0030t0001g0180 | 2 | HG02559.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.9427+586G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 13/23 | chr5 | 151533823 | ||||||
| chr5:151533845
|
G | A | 4 | a0004c0052t0001g0193a0004c0152t0001g0176a0005c0030t0001g0060others(1): Show | 4 | HG02145.hp1 HG02559.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.9427+564C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 13/23 | chr5 | 151533845 | ||||||
| chr5:151533904
|
T | A | 118 | a0001c0003t0001g0013a0001c0003t0001g0123a0001c0003t0001g0183others(115): Show | 122 | HG00323.hp1 HG00423.hp1 HG00609.hp2 others(119): Show |
intron_variant | MODIFIER | c.9427+505A>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 13/23 | chr5 | 151533904 | ||||||
| chr5:151534033
|
A | G | 276 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(273): Show | 280 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(277): Show |
intron_variant | MODIFIER | c.9427+376T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 13/23 | chr5 | 151534033 | ||||||
| chr5:151534311
|
G | A | 2 | a0006c0005t0001g0135a0011c0149t0004g0190 | 2 | HG01109.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.9427+98C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 13/23 | chr5 | 151534311 | ||||||
| chr5:151534330
|
A | G | 1 | a0018c0031t0001g0080 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.9427+79T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 13/23 | chr5 | 151534330 | ||||||
| chr5:151534649
|
G | A | 1 | a0001c0004t0001g0271 | 1 | NA19001.hp2 | splice_region_variant&intron_variant | LOW | c.9194-7C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151534649 | ||||||
| chr5:151534669
|
G | A | 2 | a0015c0043t0001g0075a0057c0122t0001g0082 | 2 | HG02723.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.9194-27C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151534669 | ||||||
| chr5:151534708
|
A | G | 2 | a0001c0142t0007g0044a0005c0014t0001g0182 | 2 | HG02258.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.9194-66T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151534708 | ||||||
| chr5:151534859
|
A | G | 1 | a0008c0087t0002g0365 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.9194-217T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151534859 | ||||||
| chr5:151534883
|
T | C | 92 | a0001c0003t0001g0013a0001c0003t0001g0123a0001c0003t0001g0183others(89): Show | 96 | HG00323.hp1 HG00423.hp1 HG00621.hp1 others(93): Show |
intron_variant | MODIFIER | c.9194-241A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151534883 | ||||||
| chr5:151534951
|
G | A | 4 | a0022c0096t0001g0041a0042c0077t0010g0248a0065c0145t0001g0061others(1): Show | 4 | HG02055.hp2 HG03195.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.9194-309C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151534951 | ||||||
| chr5:151534968
|
A | AATATATA others(5): Show |
1 | a0005c0173t0002g0336 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.9194-327_9194-326i others(14): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151534968 | ||||||
| chr5:151534968
|
A | AATATATA others(25): Show |
2 | a0011c0136t0004g0031a0012c0018t0004g0142 | 2 | HG02683.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.9194-327_9194-326i others(34): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151534968 | ||||||
| chr5:151534968
|
A | AATATATA others(29): Show |
1 | a0006c0005t0015g0391 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.9194-327_9194-326i others(38): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151534968 | ||||||
| chr5:151534968
|
A | AATATATA others(33): Show |
1 | a0010c0011t0001g0303 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.9194-327_9194-326i others(42): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151534968 | ||||||
| chr5:151534970
|
A | AAAATATA others(17): Show |
1 | a0003c0002t0001g0081 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.9194-329_9194-328i others(26): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151534970 | ||||||
| chr5:151534970
|
A | AAATATAT others(6): Show |
1 | a0002c0170t0002g0334 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.9194-329_9194-328i others(15): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151534970 | ||||||
| chr5:151534970
|
A | AAT | 18 | a0001c0016t0002g0331a0001c0020t0005g0167a0002c0006t0002g0360others(15): Show | 18 | HG01243.hp2 HG02280.hp2 HG02293.hp2 others(15): Show |
intron_variant | MODIFIER | c.9194-330_9194-329d others(4): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151534970 | ||||||
| chr5:151534970
|
A | AATAT | 26 | a0001c0016t0001g0203a0001c0016t0001g0273a0001c0017t0001g0283others(23): Show | 26 | HG00609.hp2 HG01106.hp1 HG01358.hp2 others(23): Show |
intron_variant | MODIFIER | c.9194-332_9194-329d others(6): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151534970 | ||||||
| chr5:151534970
|
A | AATATAT | 25 | a0001c0010t0009g0171a0001c0020t0001g0209a0001c0047t0005g0290others(22): Show | 25 | HG01255.hp2 HG01884.hp1 HG02080.hp2 others(22): Show |
intron_variant | MODIFIER | c.9194-334_9194-329d others(8): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151534970 | ||||||
| chr5:151534970
|
A | AATATATA others(1): Show |
11 | a0001c0124t0001g0104a0001c0179t0001g0233a0002c0001t0002g0368others(8): Show | 11 | HG00673.hp1 HG01081.hp1 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.9194-336_9194-329d others(10): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151534970 | ||||||
| chr5:151534970
|
A | AATATATA others(3): Show |
7 | a0001c0010t0005g0058a0001c0123t0007g0077a0002c0001t0002g0344others(4): Show | 7 | HG00741.hp1 HG02818.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.9194-338_9194-329d others(12): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151534970 | ||||||
| chr5:151534970
|
A | AATATATA others(5): Show |
1 | a0001c0142t0007g0044 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.9194-340_9194-329d others(14): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151534970 | ||||||
| chr5:151534970
|
A | AATATATA others(7): Show |
5 | a0001c0003t0001g0121a0001c0010t0002g0352a0001c0020t0005g0172others(2): Show | 5 | HG02572.hp1 HG03540.hp2 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.9194-342_9194-329d others(16): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151534970 | ||||||
| chr5:151534970
|
A | AATATATA others(9): Show |
6 | a0002c0006t0034g0358a0004c0052t0001g0175a0005c0014t0001g0182others(3): Show | 6 | HG00558.hp1 HG00639.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.9194-344_9194-329d others(18): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151534970 | ||||||
| chr5:151534970
|
A | AATATATA others(11): Show |
8 | a0001c0003t0001g0147a0002c0006t0005g0163a0003c0029t0005g0291others(5): Show | 8 | HG02258.hp2 HG02647.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.9194-346_9194-329d others(20): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151534970 | ||||||
| chr5:151534970
|
A | AATATATA others(13): Show |
9 | a0001c0003t0002g0329a0001c0004t0001g0156a0007c0023t0001g0285others(6): Show | 9 | HG00639.hp2 HG01069.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.9194-348_9194-329d others(22): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151534970 | ||||||
| chr5:151534970
|
A | AATATATA others(15): Show |
7 | a0001c0003t0001g0313a0001c0004t0001g0271a0004c0161t0004g0205others(4): Show | 7 | HG01167.hp1 HG01168.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.9194-350_9194-329d others(24): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151534970 | ||||||
| chr5:151534970
|
A | AATATATA others(17): Show |
5 | a0001c0021t0003g0184a0001c0065t0001g0268a0002c0001t0001g0084others(2): Show | 5 | HG00597.hp2 HG02523.hp2 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.9194-352_9194-329d others(26): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151534970 | ||||||
| chr5:151534970
|
A | AATATATA others(19): Show |
7 | a0002c0008t0001g0276a0002c0008t0008g0277a0002c0100t0001g0307others(4): Show | 7 | HG00423.hp2 HG00597.hp1 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.9194-354_9194-329d others(28): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151534970 | ||||||
| chr5:151534970
|
A | AATATATA others(21): Show |
5 | a0001c0032t0008g0108a0002c0001t0001g0300a0002c0008t0002g0348others(2): Show | 5 | HG02683.hp1 HG02738.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.9194-329_9194-328i others(30): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151534970 | ||||||
| chr5:151534970
|
A | AATATATA others(23): Show |
6 | a0001c0003t0001g0210a0001c0004t0001g0256a0006c0005t0003g0128others(3): Show | 6 | HG02818.hp2 NA18954.hp1 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.9194-329_9194-328i others(32): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151534970 | ||||||
| chr5:151534970
|
A | AATATATA others(25): Show |
6 | a0001c0003t0001g0231a0001c0048t0021g0025a0001c0049t0001g0030others(3): Show | 6 | HG01928.hp2 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.9194-329_9194-328i others(34): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151534970 | ||||||
| chr5:151534970
|
A | AATATATA others(27): Show |
18 | a0001c0048t0001g0026a0001c0110t0001g0119a0002c0001t0001g0296others(15): Show | 18 | HG01070.hp1 HG01074.hp2 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.9194-329_9194-328i others(36): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151534970 | ||||||
| chr5:151534970
|
A | AATATATA others(29): Show |
11 | a0001c0003t0001g0202a0001c0004t0001g0262a0001c0004t0001g0265others(8): Show | 11 | HG01074.hp1 HG01516.hp1 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.9194-329_9194-328i others(38): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151534970 | ||||||
| chr5:151534970
|
A | AATATATA others(31): Show |
7 | a0001c0004t0002g0380a0002c0001t0001g0124a0002c0001t0001g0131others(4): Show | 7 | NA18956.hp1 NA18956.hp2 NA18972.hp1 others(4): Show |
intron_variant | MODIFIER | c.9194-329_9194-328i others(40): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151534970 | ||||||
| chr5:151534970
|
A | AATATATA others(33): Show |
9 | a0001c0003t0001g0204a0002c0001t0001g0138a0003c0009t0001g0120others(6): Show | 9 | HG00642.hp1 HG02071.hp2 HG02273.hp1 others(6): Show |
intron_variant | MODIFIER | c.9194-329_9194-328i others(42): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151534970 | ||||||
| chr5:151534970
|
A | AATATATA others(35): Show |
5 | a0001c0004t0001g0255a0001c0128t0002g0371a0002c0001t0001g0278others(2): Show | 5 | HG02083.hp2 HG02165.hp2 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.9194-329_9194-328i others(44): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151534970 | ||||||
| chr5:151534970
|
A | AATATATA others(37): Show |
5 | a0002c0008t0029g0246a0007c0023t0003g0258a0007c0045t0003g0153others(2): Show | 5 | HG02015.hp1 NA19068.hp2 NA19083.hp2 others(2): Show |
intron_variant | MODIFIER | c.9194-329_9194-328i others(46): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151534970 | ||||||
| chr5:151534970
|
A | AATATATA others(39): Show |
3 | a0002c0001t0001g0132a0002c0008t0002g0343a0003c0002t0002g0377 | 3 | HG00609.hp1 NA18964.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.9194-329_9194-328i others(48): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151534970 | ||||||
| chr5:151534970
|
A | AATATATA others(41): Show |
3 | a0002c0001t0001g0130a0055c0112t0001g0067a0061c0115t0002g0324 | 3 | NA18968.hp1 NA19007.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.9194-329_9194-328i others(50): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151534970 | ||||||
| chr5:151534970
|
A | ATATATAT others(28): Show |
1 | a0003c0009t0001g0103 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.9194-329_9194-328i others(37): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151534970 | ||||||
| chr5:151534970
|
A | ATATATAT others(30): Show |
1 | a0073c0141t0001g0200 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.9194-329_9194-328i others(39): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151534970 | ||||||
| chr5:151534970
|
A | T | 5 | a0005c0173t0002g0336a0006c0005t0015g0391a0010c0011t0001g0303others(2): Show | 5 | HG00642.hp2 HG01934.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.9194-328T>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151534970 | ||||||
| chr5:151534970
|
AAT | A | 6 | a0001c0010t0001g0289a0002c0099t0007g0033a0008c0025t0014g0339others(3): Show | 6 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.9194-330_9194-329d others(4): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151534970 | ||||||
| chr5:151534970
|
AATAT | A | 104 | a0001c0003t0001g0013a0001c0003t0001g0123a0001c0003t0001g0183others(101): Show | 108 | HG00323.hp1 HG00423.hp1 HG00621.hp1 others(105): Show |
intron_variant | MODIFIER | c.9194-332_9194-329d others(6): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151534970 | ||||||
| chr5:151534970
|
AATATAT | A | 17 | a0001c0003t0012g0206a0001c0003t0012g0222a0003c0002t0001g0064others(14): Show | 17 | HG01109.hp1 HG01261.hp2 HG01978.hp1 others(14): Show |
intron_variant | MODIFIER | c.9194-334_9194-329d others(8): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151534970 | ||||||
| chr5:151534970
|
AATATATA others(1): Show |
A | 3 | a0001c0021t0002g0374a0002c0001t0001g0251a0017c0108t0001g0112 | 3 | NA18952.hp1 NA18959.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.9194-336_9194-329d others(10): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151534970 | ||||||
| chr5:151534970
|
AATATATA others(3): Show |
A | 1 | a0001c0010t0001g0212 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.9194-338_9194-329d others(12): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151534970 | ||||||
| chr5:151534978
|
T | TATATATA others(3): Show |
1 | a0001c0004t0001g0259 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.9194-337_9194-336i others(12): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151534978 | ||||||
| chr5:151535058
|
T | C | 3 | a0001c0004t0001g0252a0002c0001t0002g0007a0002c0001t0002g0350 | 4 | HG00621.hp1 HG02523.hp1 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.9194-416A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151535058 | ||||||
| chr5:151535335
|
A | T | 2 | a0004c0033t0001g0280a0004c0033t0004g0281 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.9194-693T>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151535335 | ||||||
| chr5:151535384
|
T | G | 286 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(283): Show | 290 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(287): Show |
intron_variant | MODIFIER | c.9194-742A>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151535384 | ||||||
| chr5:151535408
|
A | G | 106 | a0001c0003t0001g0013a0001c0003t0001g0123a0001c0003t0001g0183others(103): Show | 110 | HG00323.hp1 HG00423.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.9194-766T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151535408 | ||||||
| chr5:151535443
|
C | T | 1 | a0082c0106t0001g0317 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.9194-801G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151535443 | ||||||
| chr5:151535507
|
C | T | 10 | a0001c0003t0012g0206a0001c0003t0012g0222a0003c0002t0001g0064others(7): Show | 10 | HG01978.hp1 HG02155.hp2 NA18969.hp1 others(7): Show |
intron_variant | MODIFIER | c.9194-865G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151535507 | ||||||
| chr5:151535545
|
C | T | 1 | a0010c0011t0001g0034 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.9194-903G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151535545 | ||||||
| chr5:151535567
|
G | A | 111 | a0001c0003t0001g0121a0001c0003t0001g0147a0001c0003t0001g0202others(108): Show | 111 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.9194-925C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151535567 | ||||||
| chr5:151535728
|
G | C | 2 | a0004c0148t0001g0152a0040c0074t0001g0244 | 2 | HG00735.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.9194-1086C>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151535728 | ||||||
| chr5:151535746
|
A | C | 1 | a0006c0093t0003g0275 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.9194-1104T>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151535746 | ||||||
| chr5:151535843
|
C | A | 79 | a0001c0003t0001g0013a0001c0003t0001g0123a0001c0003t0001g0183others(76): Show | 83 | HG00323.hp1 HG00423.hp1 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.9194-1201G>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151535843 | ||||||
| chr5:151535953
|
C | A | 2 | a0019c0036t0001g0040a0071c0158t0001g0173 | 2 | HG01981.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.9194-1311G>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151535953 | ||||||
| chr5:151535963
|
A | G | 1 | a0003c0138t0025g0042 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.9194-1321T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151535963 | ||||||
| chr5:151536025
|
A | G | 4 | a0022c0096t0001g0041a0042c0077t0010g0248a0065c0145t0001g0061others(1): Show | 4 | HG02055.hp2 HG03195.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.9194-1383T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151536025 | ||||||
| chr5:151536173
|
T | A | 1 | a0021c0056t0005g0046 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.9194-1531A>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151536173 | ||||||
| chr5:151536221
|
GA | G | 267 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(264): Show | 271 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(268): Show |
intron_variant | MODIFIER | c.9193+1571delT | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151536221 | ||||||
| chr5:151536362
|
A | G | 2 | a0001c0147t0013g0161a0053c0133t0013g0016 | 2 | HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.9193+1431T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151536362 | ||||||
| chr5:151536383
|
A | T | 239 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(236): Show | 243 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(240): Show |
intron_variant | MODIFIER | c.9193+1410T>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151536383 | ||||||
| chr5:151536397
|
C | T | 1 | a0013c0024t0001g0235 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.9193+1396G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151536397 | ||||||
| chr5:151536884
|
C | T | 1 | a0003c0002t0001g0088 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.9193+909G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151536884 | ||||||
| chr5:151536969
|
A | G | 4 | a0002c0001t0036g0349a0009c0007t0001g0197a0009c0132t0028g0196others(1): Show | 4 | HG02056.hp2 NA18962.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.9193+824T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151536969 | ||||||
| chr5:151536991
|
C | T | 1 | a0001c0010t0009g0171 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.9193+802G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151536991 | ||||||
| chr5:151537000
|
C | T | 1 | a0021c0056t0005g0046 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.9193+793G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151537000 | ||||||
| chr5:151537028
|
T | C | 14 | a0001c0003t0012g0206a0001c0003t0012g0222a0001c0017t0001g0261others(11): Show | 14 | HG01109.hp1 HG01261.hp2 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.9193+765A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151537028 | ||||||
| chr5:151537066
|
T | C | 7 | a0001c0142t0007g0044a0003c0013t0009g0312a0004c0053t0010g0019others(4): Show | 7 | HG02258.hp1 HG02622.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.9193+727A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151537066 | ||||||
| chr5:151537089
|
G | A | 3 | a0001c0142t0007g0044a0005c0014t0001g0182a0036c0172t0009g0245 | 3 | HG02258.hp1 HG02896.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.9193+704C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151537089 | ||||||
| chr5:151537095
|
A | C | 264 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(261): Show | 268 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(265): Show |
intron_variant | MODIFIER | c.9193+698T>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151537095 | ||||||
| chr5:151537123
|
C | T | 1 | a0002c0037t0002g0389 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.9193+670G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151537123 | ||||||
| chr5:151537174
|
CAGAA | C | 6 | a0002c0001t0002g0368a0003c0140t0001g0223a0006c0005t0006g0364others(3): Show | 6 | HG00673.hp1 HG02080.hp2 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.9193+615_9193+618d others(6): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151537174 | ||||||
| chr5:151537214
|
A | G | 4 | a0004c0152t0001g0176a0005c0030t0001g0060a0005c0030t0001g0180others(1): Show | 4 | HG02109.hp2 HG02559.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.9193+579T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151537214 | ||||||
| chr5:151537220
|
A | AGAG | 163 | a0001c0003t0001g0121a0001c0003t0001g0123a0001c0003t0001g0185others(160): Show | 164 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(161): Show |
intron_variant | MODIFIER | c.9193+570_9193+572d others(5): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151537220 | ||||||
| chr5:151537220
|
AGAG | A | 4 | a0002c0001t0002g0368a0003c0140t0001g0223a0016c0042t0006g0381others(1): Show | 4 | HG00673.hp1 HG02080.hp2 NA18943.hp1 others(1): Show |
intron_variant | MODIFIER | c.9193+570_9193+572d others(5): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151537220 | ||||||
| chr5:151537277
|
T | A | 66 | a0001c0003t0001g0123a0001c0003t0001g0185a0001c0003t0001g0230others(63): Show | 67 | HG00558.hp1 HG00597.hp2 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.9193+516A>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151537277 | ||||||
| chr5:151537292
|
A | AG | 14 | a0001c0003t0001g0231a0001c0017t0001g0261a0001c0125t0010g0286others(11): Show | 14 | HG01109.hp1 HG01261.hp2 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.9193+500dupC | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151537292 | ||||||
| chr5:151537313
|
A | AAG | 13 | a0001c0004t0001g0253a0001c0016t0001g0247a0001c0016t0002g0331others(10): Show | 13 | HG00323.hp1 HG00735.hp2 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.9193+478_9193+479d others(4): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151537313 | ||||||
| chr5:151537317
|
A | G | 117 | a0001c0003t0001g0121a0001c0003t0001g0202a0001c0003t0001g0204others(114): Show | 117 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.9193+476T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151537317 | ||||||
| chr5:151537319
|
G | GAA | 100 | a0001c0003t0001g0121a0001c0003t0001g0202a0001c0003t0001g0204others(97): Show | 100 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.9193+473_9193+474i others(4): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151537319 | ||||||
| chr5:151537321
|
G | A | 1 | a0004c0055t0001g0012 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.9193+472C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151537321 | ||||||
| chr5:151537323
|
A | G | 3 | a0004c0152t0001g0176a0005c0030t0001g0180a0031c0105t0001g0316 | 3 | HG02109.hp2 HG02559.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.9193+470T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151537323 | ||||||
| chr5:151537325
|
A | G | 1 | a0006c0093t0003g0275 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.9193+468T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151537325 | ||||||
| chr5:151537329
|
G | A | 1 | a0006c0093t0003g0275 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.9193+464C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151537329 | ||||||
| chr5:151537329
|
GAAAGA | G | 106 | a0001c0003t0020g0221a0001c0004t0001g0284a0001c0010t0005g0058others(103): Show | 109 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.9193+459_9193+463d others(7): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151537329 | ||||||
| chr5:151537333
|
GA | G | 179 | a0001c0003t0001g0013a0001c0003t0001g0123a0001c0003t0001g0147others(176): Show | 183 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(180): Show |
intron_variant | MODIFIER | c.9193+459delT | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151537333 | ||||||
| chr5:151537340
|
AAAG | A | 13 | a0002c0001t0002g0368a0003c0140t0001g0223a0005c0015t0001g0157others(10): Show | 13 | HG00673.hp1 HG00741.hp1 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.9193+450_9193+452d others(5): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151537340 | ||||||
| chr5:151537343
|
GAAAAGAA others(2): Show |
G | 101 | a0001c0003t0001g0121a0001c0003t0001g0202a0001c0003t0001g0204others(98): Show | 101 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.9193+441_9193+449d others(11): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151537343 | ||||||
| chr5:151537352
|
A | G | 1 | a0067c0160t0008g0211 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.9193+441T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151537352 | ||||||
| chr5:151537378
|
C | T | 1 | a0016c0042t0006g0381 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.9193+415G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151537378 | ||||||
| chr5:151537385
|
C | T | 120 | a0001c0004t0001g0284a0001c0010t0001g0289a0001c0010t0005g0058others(117): Show | 123 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.9193+408G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151537385 | ||||||
| chr5:151537439
|
AGAGGG | A | 238 | a0001c0003t0001g0013a0001c0003t0001g0123a0001c0003t0001g0147others(235): Show | 245 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(242): Show |
intron_variant | MODIFIER | c.9193+349_9193+353d others(7): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151537439 | ||||||
| chr5:151537447
|
G | A | 1 | a0004c0053t0010g0019 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.9193+346C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151537447 | ||||||
| chr5:151537509
|
GAATAA | G | 54 | a0001c0003t0001g0185a0001c0003t0001g0295a0001c0003t0002g0332others(51): Show | 55 | HG00597.hp2 HG00621.hp2 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.9193+279_9193+283d others(7): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151537509 | ||||||
| chr5:151537578
|
T | C | 8 | a0001c0142t0007g0044a0001c0144t0001g0179a0001c0147t0013g0161others(5): Show | 8 | HG01109.hp2 HG02258.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.9193+215A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151537578 | ||||||
| chr5:151537633
|
T | C | 4 | a0008c0012t0001g0045a0008c0012t0001g0049a0015c0043t0001g0075others(1): Show | 4 | HG02258.hp2 HG03453.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.9193+160A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 12/23 | chr5 | 151537633 | ||||||
| chr5:151537984
|
G | A | 137 | a0001c0003t0001g0121a0001c0003t0001g0123a0001c0003t0001g0202others(134): Show | 140 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(137): Show |
intron_variant | MODIFIER | c.9040-38C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 11/23 | chr5 | 151537984 | ||||||
| chr5:151538020
|
A | G | 1 | a0001c0047t0005g0290 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.9040-74T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 11/23 | chr5 | 151538020 | ||||||
| chr5:151538066
|
C | T | 1 | a0066c0162t0001g0214 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.9040-120G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 11/23 | chr5 | 151538066 | ||||||
| chr5:151538089
|
A | G | 2 | a0011c0155t0004g0028a0054c0134t0004g0083 | 2 | HG02602.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.9040-143T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 11/23 | chr5 | 151538089 | ||||||
| chr5:151538094
|
CAGAG | C | 2 | a0002c0026t0001g0298a0008c0012t0002g0006 | 3 | HG01081.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.9040-152_9040-149d others(6): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 11/23 | chr5 | 151538094 | ||||||
| chr5:151538173
|
C | T | 103 | a0001c0003t0001g0013a0001c0003t0001g0123a0001c0003t0001g0147others(100): Show | 104 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(101): Show |
intron_variant | MODIFIER | c.9040-227G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 11/23 | chr5 | 151538173 | ||||||
| chr5:151538235
|
T | C | 85 | a0001c0003t0001g0185a0001c0004t0001g0264a0001c0004t0001g0265others(82): Show | 86 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.9040-289A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 11/23 | chr5 | 151538235 | ||||||
| chr5:151538476
|
G | A | 3 | a0001c0065t0001g0268a0004c0052t0001g0175a0005c0014t0001g0182 | 3 | HG02258.hp1 HG02970.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.9040-530C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 11/23 | chr5 | 151538476 | ||||||
| chr5:151538508
|
G | A | 226 | a0001c0003t0001g0013a0001c0003t0001g0123a0001c0003t0001g0185others(223): Show | 230 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.9040-562C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 11/23 | chr5 | 151538508 | ||||||
| chr5:151538597
|
G | C | 99 | a0001c0004t0001g0156a0001c0004t0001g0252a0001c0004t0001g0264others(96): Show | 100 | HG00558.hp1 HG00609.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.9040-651C>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 11/23 | chr5 | 151538597 | ||||||
| chr5:151538779
|
A | G | 48 | a0001c0048t0001g0026a0001c0048t0021g0025a0001c0049t0001g0020others(45): Show | 48 | HG00735.hp2 HG01243.hp1 HG01433.hp2 others(45): Show |
intron_variant | MODIFIER | c.9040-833T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 11/23 | chr5 | 151538779 | ||||||
| chr5:151538823
|
C | T | 1 | a0051c0131t0001g0199 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.9040-877G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 11/23 | chr5 | 151538823 | ||||||
| chr5:151538824
|
G | A | 2 | a0079c0175t0010g0148a0080c0176t0001g0311 | 2 | HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.9040-878C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 11/23 | chr5 | 151538824 | ||||||
| chr5:151538843
|
A | AT | 18 | a0001c0003t0001g0295a0001c0003t0002g0329a0001c0017t0002g0379others(15): Show | 18 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.9040-898dupA | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 11/23 | chr5 | 151538843 | ||||||
| chr5:151538843
|
ATT | A | 12 | a0001c0048t0001g0026a0001c0048t0021g0025a0001c0049t0001g0020others(9): Show | 12 | HG01928.hp2 HG02055.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.9040-899_9040-898d others(4): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 11/23 | chr5 | 151538843 | ||||||
| chr5:151538874
|
C | T | 1 | a0065c0145t0001g0061 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.9040-928G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 11/23 | chr5 | 151538874 | ||||||
| chr5:151538875
|
G | A | 1 | a0003c0002t0001g0089 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.9040-929C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 11/23 | chr5 | 151538875 | ||||||
| chr5:151538882
|
C | T | 1 | a0015c0043t0001g0075 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.9040-936G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 11/23 | chr5 | 151538882 | ||||||
| chr5:151538883
|
A | G | 15 | a0001c0048t0001g0026a0001c0048t0021g0025a0001c0049t0001g0020others(12): Show | 15 | HG01109.hp2 HG01243.hp2 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.9040-937T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 11/23 | chr5 | 151538883 | ||||||
| chr5:151538995
|
T | C | 1 | a0076c0111t0001g0076 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.9040-1049A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 11/23 | chr5 | 151538995 | ||||||
| chr5:151539080
|
G | A | 1 | a0073c0141t0001g0200 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.9040-1134C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 11/23 | chr5 | 151539080 | ||||||
| chr5:151539121
|
A | G | 1 | a0031c0104t0001g0010 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.9040-1175T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 11/23 | chr5 | 151539121 | ||||||
| chr5:151539186
|
T | A | 7 | a0036c0172t0009g0245a0040c0074t0001g0244a0041c0075t0009g0249others(4): Show | 7 | HG00735.hp2 HG01243.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.9040-1240A>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 11/23 | chr5 | 151539186 | ||||||
| chr5:151539425
|
A | G | 1 | a0076c0111t0001g0076 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.9039+1142T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 11/23 | chr5 | 151539425 | ||||||
| chr5:151539582
|
T | C | 1 | a0040c0074t0001g0244 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.9039+985A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 11/23 | chr5 | 151539582 | ||||||
| chr5:151539911
|
G | C | 1 | a0076c0111t0001g0076 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.9039+656C>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 11/23 | chr5 | 151539911 | ||||||
| chr5:151539970
|
G | T | 1 | a0076c0111t0001g0076 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.9039+597C>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 11/23 | chr5 | 151539970 | ||||||
| chr5:151540024
|
G | A | 1 | a0076c0111t0001g0076 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.9039+543C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 11/23 | chr5 | 151540024 | ||||||
| chr5:151540047
|
A | G | 2 | a0013c0024t0001g0225a0034c0178t0001g0229 | 2 | HG02015.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.9039+520T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 11/23 | chr5 | 151540047 | ||||||
| chr5:151540216
|
C | A | 1 | a0076c0111t0001g0076 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.9039+351G>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 11/23 | chr5 | 151540216 | ||||||
| chr5:151540263
|
G | A | 1 | a0003c0013t0009g0312 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.9039+304C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 11/23 | chr5 | 151540263 | ||||||
| chr5:151540331
|
T | C | 1 | a0076c0111t0001g0076 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.9039+236A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 11/23 | chr5 | 151540331 | ||||||
| chr5:151540345
|
T | TTTCTCCT others(37): Show |
1 | a0006c0005t0006g0364 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.9039+178_9039+221d others(46): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 11/23 | chr5 | 151540345 | ||||||
| chr5:151540345
|
TTTCTCCT others(37): Show |
T | 1 | a0001c0044t0007g0085 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.9039+178_9039+221d others(46): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 11/23 | chr5 | 151540345 | ||||||
| chr5:151540370
|
C | T | 1 | a0076c0111t0001g0076 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.9039+197G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 11/23 | chr5 | 151540370 | ||||||
| chr5:151540453
|
C | G | 1 | a0076c0111t0001g0076 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.9039+114G>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 11/23 | chr5 | 151540453 | ||||||
| chr5:151540547
|
A | G | 60 | a0001c0003t0001g0202a0001c0004t0001g0156a0001c0004t0001g0252others(57): Show | 60 | HG00558.hp2 HG00639.hp2 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.9039+20T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 11/23 | chr5 | 151540547 | ||||||
| chr5:151540550
|
C | A | 1 | a0023c0079t0002g0388 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.9039+17G>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 11/23 | chr5 | 151540550 | ||||||
| chr5:151540888
|
A | G | 1 | a0003c0002t0001g0089 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.8843-125T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 10/23 | chr5 | 151540888 | ||||||
| chr5:151540902
|
G | A | 2 | a0013c0035t0010g0242a0024c0034t0001g0241 | 2 | HG01884.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.8843-139C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 10/23 | chr5 | 151540902 | ||||||
| chr5:151540919
|
A | G | 1 | a0076c0111t0001g0076 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.8843-156T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 10/23 | chr5 | 151540919 | ||||||
| chr5:151541001
|
A | G | 2 | a0001c0003t0002g0332a0001c0016t0002g0331 | 2 | HG04115.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.8843-238T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 10/23 | chr5 | 151541001 | ||||||
| chr5:151541005
|
G | A | 75 | a0001c0020t0001g0209a0001c0130t0001g0192a0002c0001t0001g0084others(72): Show | 78 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.8843-242C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 10/23 | chr5 | 151541005 | ||||||
| chr5:151541020
|
G | GT | 7 | a0022c0096t0001g0041a0033c0058t0005g0243a0036c0172t0009g0245others(4): Show | 7 | HG00735.hp2 HG01243.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.8843-258dupA | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 10/23 | chr5 | 151541020 | ||||||
| chr5:151541330
|
G | T | 2 | a0001c0044t0007g0085a0001c0125t0010g0286 | 2 | HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.8843-567C>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 10/23 | chr5 | 151541330 | ||||||
| chr5:151541771
|
C | G | 1 | a0076c0111t0001g0076 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.8842+514G>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 10/23 | chr5 | 151541771 | ||||||
| chr5:151541796
|
C | T | 3 | a0076c0111t0001g0076a0079c0175t0010g0148a0080c0176t0001g0311 | 3 | HG03041.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.8842+489G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 10/23 | chr5 | 151541796 | ||||||
| chr5:151541820
|
AG | A | 3 | a0076c0111t0001g0076a0079c0175t0010g0148a0080c0176t0001g0311 | 3 | HG03041.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.8842+464delC | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 10/23 | chr5 | 151541820 | ||||||
| chr5:151541876
|
A | G | 2 | a0022c0098t0010g0039a0038c0097t0001g0038 | 2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.8842+409T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 10/23 | chr5 | 151541876 | ||||||
| chr5:151541911
|
AT | A | 15 | a0002c0001t0001g0130a0013c0024t0001g0225a0013c0024t0008g0228others(12): Show | 15 | HG01884.hp2 HG02015.hp2 HG02080.hp1 others(12): Show |
intron_variant | MODIFIER | c.8842+373delA | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 10/23 | chr5 | 151541911 | ||||||
| chr5:151541923
|
G | A | 3 | a0076c0111t0001g0076a0079c0175t0010g0148a0080c0176t0001g0311 | 3 | HG03041.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.8842+362C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 10/23 | chr5 | 151541923 | ||||||
| chr5:151541989
|
G | A | 3 | a0076c0111t0001g0076a0079c0175t0010g0148a0080c0176t0001g0311 | 3 | HG03041.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.8842+296C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 10/23 | chr5 | 151541989 | ||||||
| chr5:151542052
|
A | G | 14 | a0013c0024t0001g0235a0020c0028t0001g0069a0020c0028t0001g0070others(11): Show | 14 | HG00735.hp2 HG01243.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.8842+233T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 10/23 | chr5 | 151542052 | ||||||
| chr5:151542080
|
A | C | 1 | a0003c0140t0001g0223 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.8842+205T>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 10/23 | chr5 | 151542080 | ||||||
| chr5:151542244
|
G | A | 249 | a0001c0004t0001g0156a0001c0004t0001g0252a0001c0004t0001g0253others(246): Show | 254 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(251): Show |
intron_variant | MODIFIER | c.8842+41C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 10/23 | chr5 | 151542244 | ||||||
| chr5:151542246
|
T | C | 2 | a0002c0008t0002g0348a0012c0018t0011g0347 | 2 | HG02132.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.8842+39A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 10/23 | chr5 | 151542246 | ||||||
| chr5:151546358
|
A | G | 1 | a0003c0002t0001g0088 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.4790-21T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 9/23 | chr5 | 151546358 | ||||||
| chr5:151546494
|
T | G | 1 | a0016c0121t0006g0326 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.4790-157A>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 9/23 | chr5 | 151546494 | ||||||
| chr5:151546517
|
T | C | 3 | a0076c0111t0001g0076a0079c0175t0010g0148a0080c0176t0001g0311 | 3 | HG03041.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4790-180A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 9/23 | chr5 | 151546517 | ||||||
| chr5:151546664
|
CT | C | 3 | a0076c0111t0001g0076a0079c0175t0010g0148a0080c0176t0001g0311 | 3 | HG03041.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4790-328delA | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 9/23 | chr5 | 151546664 | ||||||
| chr5:151546692
|
C | T | 3 | a0076c0111t0001g0076a0079c0175t0010g0148a0080c0176t0001g0311 | 3 | HG03041.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4790-355G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 9/23 | chr5 | 151546692 | ||||||
| chr5:151546707
|
A | T | 13 | a0013c0024t0001g0225a0013c0024t0001g0235a0013c0024t0008g0228others(10): Show | 13 | HG01884.hp2 HG02015.hp2 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.4790-370T>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 9/23 | chr5 | 151546707 | ||||||
| chr5:151546770
|
A | G | 3 | a0076c0111t0001g0076a0079c0175t0010g0148a0080c0176t0001g0311 | 3 | HG03041.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4790-433T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 9/23 | chr5 | 151546770 | ||||||
| chr5:151546821
|
C | T | 1 | a0046c0095t0011g0354 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.4790-484G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 9/23 | chr5 | 151546821 | ||||||
| chr5:151546879
|
CATTTTTA others(5): Show |
C | 1 | a0003c0138t0025g0042 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4790-554_4790-543d others(14): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 9/23 | chr5 | 151546879 | ||||||
| chr5:151546907
|
G | C | 40 | a0003c0002t0001g0064a0003c0013t0001g0079a0003c0117t0001g0111others(37): Show | 40 | HG00735.hp2 HG01243.hp1 HG01884.hp2 others(37): Show |
intron_variant | MODIFIER | c.4790-570C>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 9/23 | chr5 | 151546907 | ||||||
| chr5:151546947
|
T | C | 1 | a0044c0081t0035g0357 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4790-610A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 9/23 | chr5 | 151546947 | ||||||
| chr5:151547061
|
T | C | 3 | a0001c0130t0001g0192a0007c0045t0003g0153a0007c0045t0003g0191 | 3 | NA18942.hp2 NA18980.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.4790-724A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 9/23 | chr5 | 151547061 | ||||||
| chr5:151547140
|
C | T | 3 | a0076c0111t0001g0076a0079c0175t0010g0148a0080c0176t0001g0311 | 3 | HG03041.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4790-803G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 9/23 | chr5 | 151547140 | ||||||
| chr5:151547181
|
G | A | 2 | a0022c0098t0010g0039a0038c0097t0001g0038 | 2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.4790-844C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 9/23 | chr5 | 151547181 | ||||||
| chr5:151547424
|
G | A | 1 | a0044c0081t0035g0357 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4790-1087C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 9/23 | chr5 | 151547424 | ||||||
| chr5:151547488
|
T | C | 1 | a0019c0101t0001g0136 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4790-1151A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 9/23 | chr5 | 151547488 | ||||||
| chr5:151547556
|
T | C | 3 | a0001c0044t0007g0085a0001c0125t0010g0286a0010c0011t0001g0032 | 3 | HG03579.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.4790-1219A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 9/23 | chr5 | 151547556 | ||||||
| chr5:151547785
|
T | C | 13 | a0013c0024t0001g0225a0013c0024t0001g0235a0013c0024t0008g0228others(10): Show | 13 | HG01884.hp2 HG02015.hp2 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.4790-1448A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 9/23 | chr5 | 151547785 | ||||||
| chr5:151547826
|
G | A | 1 | a0007c0023t0001g0285 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.4789+1469C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 9/23 | chr5 | 151547826 | ||||||
| chr5:151547970
|
A | G | 2 | a0007c0154t0001g0165a0011c0150t0001g0189 | 2 | HG00323.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.4789+1325T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 9/23 | chr5 | 151547970 | ||||||
| chr5:151547981
|
A | T | 3 | a0076c0111t0001g0076a0079c0175t0010g0148a0080c0176t0001g0311 | 3 | HG03041.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4789+1314T>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 9/23 | chr5 | 151547981 | ||||||
| chr5:151548040
|
G | T | 3 | a0076c0111t0001g0076a0079c0175t0010g0148a0080c0176t0001g0311 | 3 | HG03041.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4789+1255C>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 9/23 | chr5 | 151548040 | ||||||
| chr5:151548128
|
C | T | 3 | a0076c0111t0001g0076a0079c0175t0010g0148a0080c0176t0001g0311 | 3 | HG03041.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4789+1167G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 9/23 | chr5 | 151548128 | ||||||
| chr5:151548163
|
C | T | 1 | a0066c0162t0001g0214 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.4789+1132G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 9/23 | chr5 | 151548163 | ||||||
| chr5:151548200
|
A | G | 132 | a0001c0004t0001g0156a0001c0004t0001g0252a0001c0004t0001g0253others(129): Show | 134 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(131): Show |
intron_variant | MODIFIER | c.4789+1095T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 9/23 | chr5 | 151548200 | ||||||
| chr5:151548207
|
A | G | 2 | a0003c0013t0009g0312a0015c0043t0001g0075 | 2 | HG02622.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4789+1088T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 9/23 | chr5 | 151548207 | ||||||
| chr5:151548605
|
C | T | 10 | a0002c0001t0005g0036a0002c0001t0017g0009a0002c0099t0007g0033others(7): Show | 10 | HG01496.hp1 HG01884.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.4789+690G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 9/23 | chr5 | 151548605 | ||||||
| chr5:151548631
|
T | C | 3 | a0076c0111t0001g0076a0079c0175t0010g0148a0080c0176t0001g0311 | 3 | HG03041.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4789+664A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 9/23 | chr5 | 151548631 | ||||||
| chr5:151548700
|
C | T | 2 | a0003c0114t0001g0160a0028c0039t0006g0376 | 2 | HG02155.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.4789+595G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 9/23 | chr5 | 151548700 | ||||||
| chr5:151548701
|
G | A | 6 | a0022c0096t0001g0041a0033c0058t0005g0243a0040c0074t0001g0244others(3): Show | 6 | HG00735.hp2 HG01243.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.4789+594C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 9/23 | chr5 | 151548701 | ||||||
| chr5:151548723
|
C | T | 3 | a0076c0111t0001g0076a0079c0175t0010g0148a0080c0176t0001g0311 | 3 | HG03041.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4789+572G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 9/23 | chr5 | 151548723 | ||||||
| chr5:151548728
|
G | A | 3 | a0076c0111t0001g0076a0079c0175t0010g0148a0080c0176t0001g0311 | 3 | HG03041.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4789+567C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 9/23 | chr5 | 151548728 | ||||||
| chr5:151548761
|
G | A | 1 | a0004c0053t0010g0019 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.4789+534C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 9/23 | chr5 | 151548761 | ||||||
| chr5:151548841
|
G | A | 1 | a0040c0074t0001g0244 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.4789+454C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 9/23 | chr5 | 151548841 | ||||||
| chr5:151548925
|
A | C | 117 | a0001c0020t0001g0209a0001c0044t0007g0085a0001c0110t0001g0119others(114): Show | 120 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.4789+370T>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 9/23 | chr5 | 151548925 | ||||||
| chr5:151549157
|
G | T | 1 | a0006c0102t0001g0306 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.4789+138C>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 9/23 | chr5 | 151549157 | ||||||
| chr5:151549192
|
T | A | 4 | a0001c0003t0001g0210a0005c0015t0001g0217a0066c0162t0001g0214others(1): Show | 4 | HG02602.hp1 HG02735.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.4789+103A>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 9/23 | chr5 | 151549192 | ||||||
| chr5:151549623
|
C | T | 7 | a0001c0003t0001g0210a0005c0015t0001g0217a0066c0162t0001g0214others(4): Show | 7 | HG02602.hp1 HG02735.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.4579-118G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 8/23 | chr5 | 151549623 | ||||||
| chr5:151549713
|
T | G | 2 | a0079c0175t0010g0148a0080c0176t0001g0311 | 2 | HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.4579-208A>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 8/23 | chr5 | 151549713 | ||||||
| chr5:151549774
|
A | G | 1 | a0001c0004t0001g0156 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.4579-269T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 8/23 | chr5 | 151549774 | ||||||
| chr5:151549922
|
C | T | 1 | a0002c0001t0001g0250 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.4579-417G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 8/23 | chr5 | 151549922 | ||||||
| chr5:151550027
|
G | A | 1 | a0076c0111t0001g0076 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4579-522C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 8/23 | chr5 | 151550027 | ||||||
| chr5:151550103
|
G | C | 4 | a0005c0015t0001g0151a0005c0015t0001g0157a0005c0015t0001g0159others(1): Show | 4 | NA19003.hp1 NA19054.hp2 NA19075.hp1 others(1): Show |
intron_variant | MODIFIER | c.4578+487C>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 8/23 | chr5 | 151550103 | ||||||
| chr5:151550176
|
C | T | 1 | a0009c0007t0001g0216 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.4578+414G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 8/23 | chr5 | 151550176 | ||||||
| chr5:151550181
|
C | A | 2 | a0001c0003t0002g0332a0001c0016t0002g0331 | 2 | HG04115.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.4578+409G>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 8/23 | chr5 | 151550181 | ||||||
| chr5:151550184
|
A | G | 9 | a0020c0028t0001g0069a0020c0028t0001g0070a0020c0028t0001g0073others(6): Show | 9 | HG02155.hp2 NA18942.hp1 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.4578+406T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 8/23 | chr5 | 151550184 | ||||||
| chr5:151550288
|
T | C | 3 | a0076c0111t0001g0076a0079c0175t0010g0148a0080c0176t0001g0311 | 3 | HG03041.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4578+302A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 8/23 | chr5 | 151550288 | ||||||
| chr5:151550471
|
C | T | 2 | a0002c0001t0002g0350a0002c0006t0002g0367 | 2 | HG02135.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.4578+119G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 8/23 | chr5 | 151550471 | ||||||
| chr5:151551109
|
ATGT | A | 4 | a0031c0104t0001g0010a0031c0105t0001g0316a0081c0103t0001g0315others(1): Show | 4 | HG02109.hp2 HG02922.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.4297-241_4297-239d others(5): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 7/23 | chr5 | 151551109 | ||||||
| chr5:151551121
|
A | C | 7 | a0001c0142t0007g0044a0004c0143t0001g0043a0021c0056t0005g0046others(4): Show | 7 | HG01109.hp2 HG01243.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.4297-250T>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 7/23 | chr5 | 151551121 | ||||||
| chr5:151551159
|
T | C | 3 | a0076c0111t0001g0076a0079c0175t0010g0148a0080c0176t0001g0311 | 3 | HG03041.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4297-288A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 7/23 | chr5 | 151551159 | ||||||
| chr5:151551181
|
A | G | 2 | a0079c0175t0010g0148a0080c0176t0001g0311 | 2 | HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.4296+286T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 7/23 | chr5 | 151551181 | ||||||
| chr5:151551193
|
A | G | 3 | a0076c0111t0001g0076a0079c0175t0010g0148a0080c0176t0001g0311 | 3 | HG03041.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4296+274T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 7/23 | chr5 | 151551193 | ||||||
| chr5:151551367
|
G | A | 4 | a0001c0010t0001g0212a0001c0128t0002g0371a0007c0022t0006g0322others(1): Show | 4 | HG02083.hp2 HG02155.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.4296+100C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 7/23 | chr5 | 151551367 | ||||||
| chr5:151551449
|
C | A | 1 | a0075c0126t0001g0096 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.4296+18G>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 7/23 | chr5 | 151551449 | ||||||
| chr5:151551620
|
G | A | 3 | a0076c0111t0001g0076a0079c0175t0010g0148a0080c0176t0001g0311 | 3 | HG03041.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4157-14C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 6/23 | chr5 | 151551620 | ||||||
| chr5:151551863
|
C | CAT | 3 | a0076c0111t0001g0076a0079c0175t0010g0148a0080c0176t0001g0311 | 3 | HG03041.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4157-258_4157-257i others(4): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 6/23 | chr5 | 151551863 | ||||||
| chr5:151551867
|
A | G | 2 | a0001c0125t0010g0286a0065c0145t0001g0061 | 2 | HG02055.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.4157-261T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 6/23 | chr5 | 151551867 | ||||||
| chr5:151551968
|
A | T | 1 | a0076c0111t0001g0076 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4157-362T>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 6/23 | chr5 | 151551968 | ||||||
| chr5:151551976
|
G | GGGGTGTG others(1): Show |
7 | a0020c0028t0001g0073a0027c0040t0001g0071a0027c0040t0019g0068others(4): Show | 7 | HG02155.hp2 NA18942.hp1 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.4157-371_4157-370i others(10): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 6/23 | chr5 | 151551976 | ||||||
| chr5:151551976
|
G | GGGGTGTG others(3): Show |
3 | a0020c0028t0001g0069a0020c0028t0001g0070a0036c0172t0009g0245 | 3 | NA18992.hp1 NA19088.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.4157-371_4157-370i others(12): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 6/23 | chr5 | 151551976 | ||||||
| chr5:151551976
|
G | GGT | 121 | a0001c0003t0001g0230a0001c0003t0001g0231a0001c0010t0001g0289others(118): Show | 124 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.4157-372_4157-371d others(4): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 6/23 | chr5 | 151551976 | ||||||
| chr5:151551976
|
G | GGTGT | 54 | a0001c0003t0001g0185a0001c0003t0020g0221a0001c0004t0001g0156others(51): Show | 55 | HG00558.hp2 HG00639.hp2 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.4157-374_4157-371d others(6): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 6/23 | chr5 | 151551976 | ||||||
| chr5:151551976
|
G | GGTGTGT | 10 | a0001c0003t0001g0183a0001c0044t0001g0110a0002c0001t0002g0353others(7): Show | 10 | HG01081.hp1 HG01884.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.4157-376_4157-371d others(8): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 6/23 | chr5 | 151551976 | ||||||
| chr5:151551976
|
G | GGTGTGTG others(1): Show |
14 | a0013c0024t0001g0235a0013c0024t0008g0228a0013c0035t0001g0227others(11): Show | 14 | HG01243.hp1 HG01884.hp2 HG03041.hp2 others(11): Show |
intron_variant | MODIFIER | c.4157-378_4157-371d others(10): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 6/23 | chr5 | 151551976 | ||||||
| chr5:151551976
|
G | GGTGTGTG others(3): Show |
3 | a0013c0024t0001g0225a0049c0068t0003g0236a0050c0067t0001g0224 | 3 | HG02015.hp2 HG02080.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.4157-380_4157-371d others(12): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 6/23 | chr5 | 151551976 | ||||||
| chr5:151551976
|
G | GGTGTGTG others(7): Show |
1 | a0047c0072t0001g0155 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.4157-384_4157-371d others(16): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 6/23 | chr5 | 151551976 | ||||||
| chr5:151551976
|
GGT | G | 15 | a0001c0123t0007g0077a0004c0053t0010g0019a0004c0055t0001g0234others(12): Show | 15 | HG02976.hp2 HG03130.hp1 NA18952.hp2 others(12): Show |
intron_variant | MODIFIER | c.4157-372_4157-371d others(4): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 6/23 | chr5 | 151551976 | ||||||
| chr5:151551978
|
T | G | 1 | a0003c0139t0008g0238 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.4157-372A>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 6/23 | chr5 | 151551978 | ||||||
| chr5:151552371
|
G | A | 31 | a0001c0004t0001g0156a0001c0004t0001g0252a0001c0004t0001g0253others(28): Show | 31 | HG00558.hp2 HG00639.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.4157-765C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 6/23 | chr5 | 151552371 | ||||||
| chr5:151552581
|
G | T | 32 | a0013c0024t0001g0225a0013c0024t0001g0235a0013c0024t0008g0228others(29): Show | 32 | HG00735.hp2 HG01243.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.4156+596C>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 6/23 | chr5 | 151552581 | ||||||
| chr5:151552590
|
A | G | 3 | a0076c0111t0001g0076a0079c0175t0010g0148a0080c0176t0001g0311 | 3 | HG03041.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4156+587T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 6/23 | chr5 | 151552590 | ||||||
| chr5:151552600
|
A | T | 32 | a0013c0024t0001g0225a0013c0024t0001g0235a0013c0024t0008g0228others(29): Show | 32 | HG00735.hp2 HG01243.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.4156+577T>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 6/23 | chr5 | 151552600 | ||||||
| chr5:151552893
|
A | G | 3 | a0076c0111t0001g0076a0079c0175t0010g0148a0080c0176t0001g0311 | 3 | HG03041.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4156+284T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 6/23 | chr5 | 151552893 | ||||||
| chr5:151552951
|
G | A | 1 | a0009c0007t0001g0220 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.4156+226C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 6/23 | chr5 | 151552951 | ||||||
| chr5:151552961
|
G | A | 2 | a0079c0175t0010g0148a0080c0176t0001g0311 | 2 | HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.4156+216C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 6/23 | chr5 | 151552961 | ||||||
| chr5:151553072
|
G | A | 1 | a0001c0174t0002g0337 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.4156+105C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 6/23 | chr5 | 151553072 | ||||||
| chr5:151553434
|
G | A | 3 | a0076c0111t0001g0076a0079c0175t0010g0148a0080c0176t0001g0311 | 3 | HG03041.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3946-47C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 5/23 | chr5 | 151553434 | ||||||
| chr5:151553498
|
A | G | 3 | a0076c0111t0001g0076a0079c0175t0010g0148a0080c0176t0001g0311 | 3 | HG03041.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3946-111T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 5/23 | chr5 | 151553498 | ||||||
| chr5:151553609
|
C | T | 1 | a0076c0111t0001g0076 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3946-222G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 5/23 | chr5 | 151553609 | ||||||
| chr5:151553786
|
C | T | 32 | a0013c0024t0001g0225a0013c0024t0001g0235a0013c0024t0008g0228others(29): Show | 32 | HG00735.hp2 HG01243.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.3946-399G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 5/23 | chr5 | 151553786 | ||||||
| chr5:151553811
|
A | G | 2 | a0079c0175t0010g0148a0080c0176t0001g0311 | 2 | HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3946-424T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 5/23 | chr5 | 151553811 | ||||||
| chr5:151553850
|
A | G | 136 | a0001c0004t0001g0156a0001c0004t0001g0252a0001c0004t0001g0253others(133): Show | 138 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(135): Show |
intron_variant | MODIFIER | c.3946-463T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 5/23 | chr5 | 151553850 | ||||||
| chr5:151553862
|
A | G | 3 | a0076c0111t0001g0076a0079c0175t0010g0148a0080c0176t0001g0311 | 3 | HG03041.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3946-475T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 5/23 | chr5 | 151553862 | ||||||
| chr5:151553986
|
A | G | 3 | a0076c0111t0001g0076a0079c0175t0010g0148a0080c0176t0001g0311 | 3 | HG03041.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3945+376T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 5/23 | chr5 | 151553986 | ||||||
| chr5:151554093
|
G | A | 3 | a0076c0111t0001g0076a0079c0175t0010g0148a0080c0176t0001g0311 | 3 | HG03041.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3945+269C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 5/23 | chr5 | 151554093 | ||||||
| chr5:151554215
|
A | G | 3 | a0076c0111t0001g0076a0079c0175t0010g0148a0080c0176t0001g0311 | 3 | HG03041.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3945+147T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 5/23 | chr5 | 151554215 | ||||||
| chr5:151554254
|
T | C | 3 | a0076c0111t0001g0076a0079c0175t0010g0148a0080c0176t0001g0311 | 3 | HG03041.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3945+108A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 5/23 | chr5 | 151554254 | ||||||
| chr5:151554272
|
G | C | 2 | a0022c0098t0010g0039a0038c0097t0001g0038 | 2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3945+90C>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 5/23 | chr5 | 151554272 | ||||||
| chr5:151554324
|
G | A | 1 | a0001c0179t0001g0233 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.3945+38C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 5/23 | chr5 | 151554324 | ||||||
| chr5:151554723
|
T | G | 1 | a0002c0001t0001g0309 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3634-50A>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 4/23 | chr5 | 151554723 | ||||||
| chr5:151554731
|
C | CTTTGCCA others(23): Show |
3 | a0076c0111t0001g0076a0079c0175t0010g0148a0080c0176t0001g0311 | 3 | HG03041.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3634-59_3634-58ins others(30): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 4/23 | chr5 | 151554731 | ||||||
| chr5:151554839
|
T | A | 3 | a0076c0111t0001g0076a0079c0175t0010g0148a0080c0176t0001g0311 | 3 | HG03041.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3634-166A>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 4/23 | chr5 | 151554839 | ||||||
| chr5:151554888
|
G | C | 1 | a0076c0111t0001g0076 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3634-215C>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 4/23 | chr5 | 151554888 | ||||||
| chr5:151555011
|
C | T | 18 | a0013c0024t0001g0225a0013c0024t0001g0235a0013c0024t0008g0228others(15): Show | 18 | HG01884.hp2 HG02015.hp2 HG02080.hp1 others(15): Show |
intron_variant | MODIFIER | c.3634-338G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 4/23 | chr5 | 151555011 | ||||||
| chr5:151555036
|
T | C | 3 | a0076c0111t0001g0076a0079c0175t0010g0148a0080c0176t0001g0311 | 3 | HG03041.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3634-363A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 4/23 | chr5 | 151555036 | ||||||
| chr5:151555087
|
T | C | 3 | a0076c0111t0001g0076a0079c0175t0010g0148a0080c0176t0001g0311 | 3 | HG03041.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3634-414A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 4/23 | chr5 | 151555087 | ||||||
| chr5:151555367
|
C | CT | 25 | a0001c0021t0002g0374a0002c0006t0002g0367a0005c0015t0001g0159others(22): Show | 25 | HG00735.hp2 HG01884.hp2 HG02015.hp2 others(22): Show |
intron_variant | MODIFIER | c.3634-695dupA | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 4/23 | chr5 | 151555367 | ||||||
| chr5:151555367
|
CT | C | 70 | a0001c0044t0007g0085a0001c0110t0001g0119a0001c0123t0007g0077others(67): Show | 72 | HG00423.hp1 HG00621.hp2 HG00741.hp1 others(69): Show |
intron_variant | MODIFIER | c.3634-695delA | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 4/23 | chr5 | 151555367 | ||||||
| chr5:151555367
|
CTT | C | 32 | a0001c0004t0001g0156a0001c0004t0001g0252a0001c0004t0001g0253others(29): Show | 32 | HG00558.hp2 HG00639.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.3634-696_3634-695d others(4): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 4/23 | chr5 | 151555367 | ||||||
| chr5:151555443
|
T | A | 1 | a0005c0015t0001g0159 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.3634-770A>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 4/23 | chr5 | 151555443 | ||||||
| chr5:151555457
|
G | GT | 6 | a0001c0142t0007g0044a0004c0143t0001g0043a0021c0056t0005g0046others(3): Show | 6 | HG01109.hp2 HG01243.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.3634-785dupA | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 4/23 | chr5 | 151555457 | ||||||
| chr5:151555495
|
C | T | 1 | a0076c0111t0001g0076 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3634-822G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 4/23 | chr5 | 151555495 | ||||||
| chr5:151555570
|
A | C | 1 | a0027c0040t0019g0068 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.3633+774T>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 4/23 | chr5 | 151555570 | ||||||
| chr5:151555858
|
G | A | 32 | a0001c0010t0005g0058a0001c0010t0007g0003a0001c0010t0009g0171others(29): Show | 33 | HG00140.hp1 HG00323.hp1 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.3633+486C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 4/23 | chr5 | 151555858 | ||||||
| chr5:151555944
|
A | G | 1 | a0040c0074t0001g0244 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3633+400T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 4/23 | chr5 | 151555944 | ||||||
| chr5:151555954
|
A | G | 3 | a0076c0111t0001g0076a0079c0175t0010g0148a0080c0176t0001g0311 | 3 | HG03041.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3633+390T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 4/23 | chr5 | 151555954 | ||||||
| chr5:151555962
|
G | T | 2 | a0004c0033t0001g0280a0004c0033t0004g0281 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.3633+382C>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 4/23 | chr5 | 151555962 | ||||||
| chr5:151556025
|
G | C | 1 | a0004c0019t0001g0181 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3633+319C>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 4/23 | chr5 | 151556025 | ||||||
| chr5:151556029
|
G | C | 3 | a0076c0111t0001g0076a0079c0175t0010g0148a0080c0176t0001g0311 | 3 | HG03041.hp2 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3633+315C>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 4/23 | chr5 | 151556029 | ||||||
| chr5:151556417
|
A | T | 32 | a0013c0024t0001g0225a0013c0024t0001g0235a0013c0024t0008g0228others(29): Show | 32 | HG00735.hp2 HG01243.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.3575-15T>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151556417 | ||||||
| chr5:151556430
|
A | G | 1 | a0082c0106t0001g0317 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3575-28T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151556430 | ||||||
| chr5:151556495
|
T | C | 2 | a0002c0001t0002g0350a0002c0006t0002g0367 | 2 | HG02135.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.3575-93A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151556495 | ||||||
| chr5:151556636
|
T | G | 2 | a0079c0175t0010g0148a0080c0176t0001g0311 | 2 | HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3575-234A>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151556636 | ||||||
| chr5:151556800
|
G | C | 268 | a0001c0004t0001g0156a0001c0004t0001g0252a0001c0004t0001g0253others(265): Show | 273 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(270): Show |
intron_variant | MODIFIER | c.3575-398C>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151556800 | ||||||
| chr5:151557067
|
G | A | 1 | a0007c0023t0001g0314 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.3575-665C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151557067 | ||||||
| chr5:151557319
|
G | C | 31 | a0001c0004t0001g0156a0001c0004t0001g0252a0001c0004t0001g0253others(28): Show | 31 | HG00558.hp2 HG00639.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.3575-917C>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151557319 | ||||||
| chr5:151557350
|
C | T | 1 | a0010c0082t0001g0162 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3575-948G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151557350 | ||||||
| chr5:151557494
|
CT | C | 4 | a0031c0104t0001g0010a0031c0105t0001g0316a0081c0103t0001g0315others(1): Show | 4 | HG02109.hp2 HG02922.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.3575-1093delA | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151557494 | ||||||
| chr5:151557632
|
A | G | 39 | a0001c0044t0001g0110a0013c0024t0001g0225a0013c0024t0001g0235others(36): Show | 39 | HG00735.hp2 HG01243.hp1 HG01884.hp2 others(36): Show |
intron_variant | MODIFIER | c.3575-1230T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151557632 | ||||||
| chr5:151557633
|
C | T | 1 | a0036c0172t0009g0245 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3575-1231G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151557633 | ||||||
| chr5:151557719
|
C | A | 1 | a0024c0034t0001g0288 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3575-1317G>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151557719 | ||||||
| chr5:151557938
|
G | T | 1 | a0076c0111t0001g0076 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3575-1536C>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151557938 | ||||||
| chr5:151558055
|
C | G | 1 | a0036c0172t0009g0245 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3575-1653G>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151558055 | ||||||
| chr5:151558070
|
T | C | 2 | a0001c0110t0001g0119a0001c0124t0001g0104 | 2 | HG01167.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.3575-1668A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151558070 | ||||||
| chr5:151558170
|
C | A | 1 | a0001c0003t0001g0210 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3575-1768G>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151558170 | ||||||
| chr5:151558382
|
G | A | 6 | a0031c0104t0001g0010a0031c0105t0001g0316a0079c0175t0010g0148others(3): Show | 6 | HG02109.hp2 HG02922.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.3575-1980C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151558382 | ||||||
| chr5:151558390
|
C | A | 1 | a0015c0041t0001g0097 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.3575-1988G>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151558390 | ||||||
| chr5:151558470
|
T | A | 2 | a0003c0002t0001g0062a0003c0009t0001g0063 | 2 | HG02071.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.3575-2068A>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151558470 | ||||||
| chr5:151558599
|
G | A | 5 | a0001c0010t0001g0289a0005c0014t0001g0051a0005c0014t0001g0055others(2): Show | 5 | HG01891.hp2 HG02280.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.3575-2197C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151558599 | ||||||
| chr5:151558609
|
T | TA | 6 | a0001c0130t0001g0192a0007c0045t0003g0153a0007c0045t0003g0191others(3): Show | 6 | HG02080.hp2 NA18522.hp2 NA18906.hp2 others(3): Show |
intron_variant | MODIFIER | c.3575-2208dupT | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151558609 | ||||||
| chr5:151558651
|
A | G | 1 | a0036c0172t0009g0245 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3575-2249T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151558651 | ||||||
| chr5:151558922
|
C | T | 4 | a0005c0014t0001g0051a0005c0014t0001g0055a0005c0014t0001g0056others(1): Show | 4 | HG02280.hp1 HG02976.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.3575-2520G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151558922 | ||||||
| chr5:151558946
|
G | A | 58 | a0001c0110t0001g0119a0001c0124t0001g0104a0003c0002t0001g0001others(55): Show | 60 | HG00423.hp1 HG00621.hp2 HG01106.hp2 others(57): Show |
intron_variant | MODIFIER | c.3575-2544C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151558946 | ||||||
| chr5:151559120
|
G | A | 1 | a0052c0169t0001g0074 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3575-2718C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151559120 | ||||||
| chr5:151559139
|
A | G | 4 | a0031c0104t0001g0010a0031c0105t0001g0316a0081c0103t0001g0315others(1): Show | 4 | HG02109.hp2 HG02922.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.3575-2737T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151559139 | ||||||
| chr5:151559274
|
G | A | 2 | a0032c0057t0001g0017a0032c0057t0001g0018 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.3575-2872C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151559274 | ||||||
| chr5:151559293
|
G | C | 22 | a0013c0024t0001g0225a0013c0024t0001g0235a0013c0024t0008g0228others(19): Show | 22 | HG00735.hp2 HG01243.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.3575-2891C>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151559293 | ||||||
| chr5:151559356
|
A | G | 10 | a0001c0044t0001g0110a0020c0028t0001g0069a0020c0028t0001g0070others(7): Show | 10 | HG02155.hp2 NA18942.hp1 NA18951.hp2 others(7): Show |
intron_variant | MODIFIER | c.3575-2954T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151559356 | ||||||
| chr5:151559363
|
C | G | 1 | a0025c0069t0001g0240 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.3575-2961G>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151559363 | ||||||
| chr5:151559377
|
G | A | 1 | a0014c0088t0001g0310 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.3575-2975C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151559377 | ||||||
| chr5:151559477
|
G | T | 61 | a0001c0044t0007g0085a0001c0110t0001g0119a0001c0124t0001g0104others(58): Show | 63 | HG00423.hp1 HG00621.hp2 HG01106.hp2 others(60): Show |
intron_variant | MODIFIER | c.3575-3075C>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151559477 | ||||||
| chr5:151559543
|
C | T | 27 | a0013c0024t0001g0225a0013c0024t0001g0235a0013c0024t0008g0228others(24): Show | 27 | HG00735.hp2 HG01243.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.3575-3141G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151559543 | ||||||
| chr5:151559619
|
C | T | 27 | a0013c0024t0001g0225a0013c0024t0001g0235a0013c0024t0008g0228others(24): Show | 27 | HG00735.hp2 HG01243.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.3575-3217G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151559619 | ||||||
| chr5:151559647
|
C | CTCTGTGT others(1): Show |
15 | a0013c0024t0001g0225a0013c0024t0001g0235a0013c0024t0008g0228others(12): Show | 15 | HG01884.hp2 HG02015.hp2 HG02080.hp1 others(12): Show |
intron_variant | MODIFIER | c.3575-3246_3575-324 others(12): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151559647 | ||||||
| chr5:151559647
|
C | CTGTGTGT others(1): Show |
12 | a0022c0096t0001g0041a0022c0098t0010g0039a0031c0104t0001g0010others(9): Show | 12 | HG00735.hp2 HG01243.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.3575-3253_3575-324 others(12): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151559647 | ||||||
| chr5:151559647
|
C | G | 1 | a0016c0042t0006g0383 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.3575-3245G>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151559647 | ||||||
| chr5:151559674
|
C | T | 1 | a0002c0170t0002g0334 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.3575-3272G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151559674 | ||||||
| chr5:151559740
|
C | T | 2 | a0002c0006t0015g0390a0006c0005t0015g0391 | 2 | HG01934.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.3575-3338G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151559740 | ||||||
| chr5:151559767
|
C | T | 26 | a0013c0024t0001g0225a0013c0024t0001g0235a0013c0024t0008g0228others(23): Show | 26 | HG00735.hp2 HG01243.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.3575-3365G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151559767 | ||||||
| chr5:151559820
|
C | A | 5 | a0003c0002t0001g0254a0003c0002t0002g0377a0003c0002t0002g0378others(2): Show | 5 | NA18943.hp1 NA18956.hp1 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.3575-3418G>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151559820 | ||||||
| chr5:151559834
|
T | A | 27 | a0013c0024t0001g0225a0013c0024t0001g0235a0013c0024t0008g0228others(24): Show | 27 | HG00735.hp2 HG01243.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.3575-3432A>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151559834 | ||||||
| chr5:151559870
|
C | T | 27 | a0013c0024t0001g0225a0013c0024t0001g0235a0013c0024t0008g0228others(24): Show | 27 | HG00735.hp2 HG01243.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.3574+3455G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151559870 | ||||||
| chr5:151559871
|
A | G | 27 | a0013c0024t0001g0225a0013c0024t0001g0235a0013c0024t0008g0228others(24): Show | 27 | HG00735.hp2 HG01243.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.3574+3454T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151559871 | ||||||
| chr5:151560033
|
A | G | 2 | a0004c0033t0001g0280a0004c0033t0004g0281 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.3574+3292T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151560033 | ||||||
| chr5:151560036
|
T | C | 27 | a0013c0024t0001g0225a0013c0024t0001g0235a0013c0024t0008g0228others(24): Show | 27 | HG00735.hp2 HG01243.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.3574+3289A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151560036 | ||||||
| chr5:151560042
|
C | A | 2 | a0008c0025t0014g0339a0008c0025t0014g0341 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.3574+3283G>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151560042 | ||||||
| chr5:151560131
|
A | T | 18 | a0013c0024t0001g0225a0013c0024t0001g0235a0013c0024t0008g0228others(15): Show | 18 | HG01884.hp2 HG02015.hp2 HG02080.hp1 others(15): Show |
intron_variant | MODIFIER | c.3574+3194T>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151560131 | ||||||
| chr5:151560146
|
A | C | 256 | a0001c0004t0001g0156a0001c0004t0001g0252a0001c0004t0001g0253others(253): Show | 261 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(258): Show |
intron_variant | MODIFIER | c.3574+3179T>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151560146 | ||||||
| chr5:151560189
|
G | A | 2 | a0002c0001t0002g0350a0002c0006t0002g0367 | 2 | HG02135.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.3574+3136C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151560189 | ||||||
| chr5:151560257
|
T | C | 27 | a0013c0024t0001g0225a0013c0024t0001g0235a0013c0024t0008g0228others(24): Show | 27 | HG00735.hp2 HG01243.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.3574+3068A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151560257 | ||||||
| chr5:151560384
|
C | T | 390 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(387): Show | 397 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(394): Show |
intron_variant | MODIFIER | c.3574+2941G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151560384 | ||||||
| chr5:151560503
|
G | A | 27 | a0013c0024t0001g0225a0013c0024t0001g0235a0013c0024t0008g0228others(24): Show | 27 | HG00735.hp2 HG01243.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.3574+2822C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151560503 | ||||||
| chr5:151560543
|
C | G | 56 | a0002c0001t0001g0124a0002c0001t0001g0130a0002c0001t0001g0131others(53): Show | 57 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.3574+2782G>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151560543 | ||||||
| chr5:151560638
|
G | T | 27 | a0013c0024t0001g0225a0013c0024t0001g0235a0013c0024t0008g0228others(24): Show | 27 | HG00735.hp2 HG01243.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.3574+2687C>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151560638 | ||||||
| chr5:151560673
|
T | C | 27 | a0013c0024t0001g0225a0013c0024t0001g0235a0013c0024t0008g0228others(24): Show | 27 | HG00735.hp2 HG01243.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.3574+2652A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151560673 | ||||||
| chr5:151560816
|
C | T | 27 | a0013c0024t0001g0225a0013c0024t0001g0235a0013c0024t0008g0228others(24): Show | 27 | HG00735.hp2 HG01243.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.3574+2509G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151560816 | ||||||
| chr5:151560968
|
G | A | 71 | a0001c0044t0001g0110a0001c0110t0001g0119a0001c0124t0001g0104others(68): Show | 73 | HG00423.hp1 HG00621.hp2 HG01106.hp2 others(70): Show |
intron_variant | MODIFIER | c.3574+2357C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151560968 | ||||||
| chr5:151561068
|
G | A | 2 | a0003c0002t0001g0062a0003c0009t0001g0063 | 2 | HG02071.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.3574+2257C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151561068 | ||||||
| chr5:151561189
|
G | A | 27 | a0013c0024t0001g0225a0013c0024t0001g0235a0013c0024t0008g0228others(24): Show | 27 | HG00735.hp2 HG01243.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.3574+2136C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151561189 | ||||||
| chr5:151561204
|
G | A | 1 | a0002c0006t0001g0022 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3574+2121C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151561204 | ||||||
| chr5:151561222
|
A | G | 27 | a0013c0024t0001g0225a0013c0024t0001g0235a0013c0024t0008g0228others(24): Show | 27 | HG00735.hp2 HG01243.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.3574+2103T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151561222 | ||||||
| chr5:151561311
|
G | A | 1 | a0057c0122t0001g0082 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3574+2014C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151561311 | ||||||
| chr5:151561390
|
C | G | 5 | a0003c0002t0001g0254a0003c0002t0002g0377a0003c0002t0002g0378others(2): Show | 5 | NA18943.hp1 NA18956.hp1 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.3574+1935G>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151561390 | ||||||
| chr5:151561453
|
C | T | 4 | a0004c0156t0001g0023a0007c0054t0001g0021a0007c0054t0001g0024others(1): Show | 4 | HG01070.hp1 HG01074.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.3574+1872G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151561453 | ||||||
| chr5:151561469
|
T | C | 27 | a0013c0024t0001g0225a0013c0024t0001g0235a0013c0024t0008g0228others(24): Show | 27 | HG00735.hp2 HG01243.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.3574+1856A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151561469 | ||||||
| chr5:151561572
|
G | A | 5 | a0003c0002t0001g0254a0003c0002t0002g0377a0003c0002t0002g0378others(2): Show | 5 | NA18943.hp1 NA18956.hp1 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.3574+1753C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151561572 | ||||||
| chr5:151561607
|
T | C | 27 | a0013c0024t0001g0225a0013c0024t0001g0235a0013c0024t0008g0228others(24): Show | 27 | HG00735.hp2 HG01243.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.3574+1718A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151561607 | ||||||
| chr5:151561628
|
C | T | 4 | a0040c0074t0001g0244a0041c0075t0009g0249a0042c0077t0010g0248others(1): Show | 4 | HG00735.hp2 HG01243.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.3574+1697G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151561628 | ||||||
| chr5:151561665
|
G | A | 27 | a0013c0024t0001g0225a0013c0024t0001g0235a0013c0024t0008g0228others(24): Show | 27 | HG00735.hp2 HG01243.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.3574+1660C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151561665 | ||||||
| chr5:151561733
|
T | C | 8 | a0001c0125t0010g0286a0001c0142t0007g0044a0004c0143t0001g0043others(5): Show | 8 | HG01109.hp2 HG01243.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.3574+1592A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151561733 | ||||||
| chr5:151561883
|
A | C | 25 | a0013c0024t0001g0225a0013c0024t0001g0235a0013c0024t0008g0228others(22): Show | 25 | HG00735.hp2 HG01243.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.3574+1442T>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151561883 | ||||||
| chr5:151561975
|
A | C | 1 | a0036c0172t0009g0245 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3574+1350T>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151561975 | ||||||
| chr5:151561990
|
C | T | 4 | a0003c0002t0001g0254a0003c0002t0002g0377a0003c0002t0002g0378others(1): Show | 4 | NA18943.hp1 NA18956.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.3574+1335G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151561990 | ||||||
| chr5:151562065
|
A | G | 137 | a0002c0001t0001g0084a0002c0001t0001g0124a0002c0001t0001g0130others(134): Show | 140 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.3574+1260T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151562065 | ||||||
| chr5:151562129
|
T | C | 137 | a0002c0001t0001g0084a0002c0001t0001g0124a0002c0001t0001g0130others(134): Show | 140 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.3574+1196A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151562129 | ||||||
| chr5:151562140
|
A | C | 137 | a0002c0001t0001g0084a0002c0001t0001g0124a0002c0001t0001g0130others(134): Show | 140 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.3574+1185T>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151562140 | ||||||
| chr5:151562157
|
C | T | 137 | a0002c0001t0001g0084a0002c0001t0001g0124a0002c0001t0001g0130others(134): Show | 140 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.3574+1168G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151562157 | ||||||
| chr5:151562168
|
C | A | 32 | a0001c0010t0005g0058a0001c0010t0007g0003a0001c0010t0009g0171others(29): Show | 33 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.3574+1157G>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151562168 | ||||||
| chr5:151562181
|
T | G | 1 | a0001c0059t0001g0267 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.3574+1144A>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151562181 | ||||||
| chr5:151562188
|
G | C | 137 | a0002c0001t0001g0084a0002c0001t0001g0124a0002c0001t0001g0130others(134): Show | 140 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.3574+1137C>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151562188 | ||||||
| chr5:151562214
|
A | C | 137 | a0002c0001t0001g0084a0002c0001t0001g0124a0002c0001t0001g0130others(134): Show | 140 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.3574+1111T>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151562214 | ||||||
| chr5:151562235
|
G | A | 22 | a0002c0001t0001g0084a0002c0001t0001g0300a0002c0001t0001g0309others(19): Show | 24 | HG00140.hp2 HG00642.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.3574+1090C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151562235 | ||||||
| chr5:151562244
|
C | A | 6 | a0003c0013t0009g0312a0003c0029t0005g0291a0003c0029t0005g0292others(3): Show | 6 | HG02622.hp1 HG02647.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.3574+1081G>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151562244 | ||||||
| chr5:151562245
|
G | A | 1 | a0074c0168t0009g0029 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3574+1080C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151562245 | ||||||
| chr5:151562249
|
G | A | 1 | a0031c0105t0001g0316 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3574+1076C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151562249 | ||||||
| chr5:151562268
|
A | G | 1 | a0005c0030t0001g0060 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3574+1057T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151562268 | ||||||
| chr5:151562278
|
G | A | 112 | a0002c0001t0001g0084a0002c0001t0001g0124a0002c0001t0001g0130others(109): Show | 115 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.3574+1047C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151562278 | ||||||
| chr5:151562463
|
G | A | 2 | a0004c0019t0001g0181a0005c0030t0001g0180 | 2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3574+862C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151562463 | ||||||
| chr5:151562486
|
G | A | 4 | a0001c0010t0001g0212a0001c0128t0002g0371a0007c0022t0006g0322others(1): Show | 4 | HG02083.hp2 HG02155.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.3574+839C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151562486 | ||||||
| chr5:151562577
|
G | A | 24 | a0013c0024t0001g0225a0013c0024t0001g0235a0013c0024t0008g0228others(21): Show | 24 | HG00735.hp2 HG01243.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.3574+748C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151562577 | ||||||
| chr5:151562618
|
A | C | 137 | a0002c0001t0001g0084a0002c0001t0001g0124a0002c0001t0001g0130others(134): Show | 140 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.3574+707T>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151562618 | ||||||
| chr5:151562650
|
C | T | 137 | a0002c0001t0001g0084a0002c0001t0001g0124a0002c0001t0001g0130others(134): Show | 140 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.3574+675G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151562650 | ||||||
| chr5:151562668
|
A | G | 2 | a0008c0038t0001g0304a0008c0038t0004g0305 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.3574+657T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151562668 | ||||||
| chr5:151562725
|
A | T | 1 | a0014c0089t0006g0359 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.3574+600T>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151562725 | ||||||
| chr5:151562743
|
C | G | 1 | a0055c0112t0001g0067 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.3574+582G>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151562743 | ||||||
| chr5:151562800
|
C | T | 6 | a0001c0142t0007g0044a0004c0143t0001g0043a0021c0056t0005g0046others(3): Show | 6 | HG01109.hp2 HG01243.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.3574+525G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151562800 | ||||||
| chr5:151562885
|
T | C | 4 | a0040c0074t0001g0244a0041c0075t0009g0249a0042c0077t0010g0248others(1): Show | 4 | HG00735.hp2 HG01243.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.3574+440A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151562885 | ||||||
| chr5:151563213
|
A | G | 137 | a0002c0001t0001g0084a0002c0001t0001g0124a0002c0001t0001g0130others(134): Show | 140 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.3574+112T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151563213 | ||||||
| chr5:151563230
|
A | G | 2 | a0002c0001t0001g0130a0006c0005t0006g0333 | 2 | NA18968.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.3574+95T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 3/23 | chr5 | 151563230 | ||||||
| chr5:151563694
|
G | C | 1 | a0036c0172t0009g0245 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3260-55C>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/23 | chr5 | 151563694 | ||||||
| chr5:151563761
|
T | C | 1 | a0076c0111t0001g0076 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3260-122A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/23 | chr5 | 151563761 | ||||||
| chr5:151563791
|
A | G | 1 | a0070c0157t0001g0164 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3260-152T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/23 | chr5 | 151563791 | ||||||
| chr5:151563964
|
T | C | 1 | a0005c0014t0001g0182 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3260-325A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/23 | chr5 | 151563964 | ||||||
| chr5:151563969
|
C | G | 141 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(138): Show | 143 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.3260-330G>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/23 | chr5 | 151563969 | ||||||
| chr5:151564225
|
G | C | 139 | a0002c0001t0001g0084a0002c0001t0001g0124a0002c0001t0001g0130others(136): Show | 142 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.3260-586C>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/23 | chr5 | 151564225 | ||||||
| chr5:151564229
|
T | C | 139 | a0002c0001t0001g0084a0002c0001t0001g0124a0002c0001t0001g0130others(136): Show | 142 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.3260-590A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/23 | chr5 | 151564229 | ||||||
| chr5:151564286
|
A | C | 23 | a0003c0002t0001g0001a0003c0002t0001g0065a0003c0002t0001g0078others(20): Show | 24 | HG00423.hp1 HG00621.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.3260-647T>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/23 | chr5 | 151564286 | ||||||
| chr5:151564314
|
T | G | 1 | a0076c0111t0001g0076 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3260-675A>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/23 | chr5 | 151564314 | ||||||
| chr5:151564343
|
C | T | 139 | a0002c0001t0001g0084a0002c0001t0001g0124a0002c0001t0001g0130others(136): Show | 142 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.3260-704G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/23 | chr5 | 151564343 | ||||||
| chr5:151564352
|
C | T | 139 | a0002c0001t0001g0084a0002c0001t0001g0124a0002c0001t0001g0130others(136): Show | 142 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.3260-713G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/23 | chr5 | 151564352 | ||||||
| chr5:151564442
|
A | G | 138 | a0002c0001t0001g0084a0002c0001t0001g0124a0002c0001t0001g0130others(135): Show | 141 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(138): Show |
intron_variant | MODIFIER | c.3260-803T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/23 | chr5 | 151564442 | ||||||
| chr5:151564502
|
A | AAAATAAC others(9): Show |
1 | a0003c0009t0001g0063 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3260-864_3260-863i others(18): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/23 | chr5 | 151564502 | ||||||
| chr5:151564508
|
T | C | 1 | a0003c0009t0001g0063 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3260-869A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/23 | chr5 | 151564508 | ||||||
| chr5:151564646
|
G | T | 1 | a0001c0003t0001g0231 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.3260-1007C>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/23 | chr5 | 151564646 | ||||||
| chr5:151564715
|
C | T | 139 | a0002c0001t0001g0084a0002c0001t0001g0124a0002c0001t0001g0130others(136): Show | 142 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.3259+958G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/23 | chr5 | 151564715 | ||||||
| chr5:151564756
|
C | G | 1 | a0014c0083t0004g0137 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3259+917G>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/23 | chr5 | 151564756 | ||||||
| chr5:151564775
|
T | C | 2 | a0041c0075t0009g0249a0042c0077t0010g0248 | 2 | HG01243.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3259+898A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/23 | chr5 | 151564775 | ||||||
| chr5:151564780
|
A | G | 6 | a0002c0006t0001g0129a0006c0005t0003g0125a0006c0005t0003g0126others(3): Show | 6 | NA18957.hp1 NA18965.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.3259+893T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/23 | chr5 | 151564780 | ||||||
| chr5:151564794
|
C | T | 1 | a0001c0123t0007g0077 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3259+879G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/23 | chr5 | 151564794 | ||||||
| chr5:151564797
|
G | A | 1 | a0002c0037t0002g0386 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.3259+876C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/23 | chr5 | 151564797 | ||||||
| chr5:151564811
|
G | A | 1 | a0036c0172t0009g0245 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3259+862C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/23 | chr5 | 151564811 | ||||||
| chr5:151564815
|
G | C | 2 | a0041c0075t0009g0249a0042c0077t0010g0248 | 2 | HG01243.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3259+858C>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/23 | chr5 | 151564815 | ||||||
| chr5:151564847
|
T | C | 31 | a0001c0004t0001g0156a0001c0004t0001g0252a0001c0004t0001g0253others(28): Show | 31 | HG00558.hp2 HG00639.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.3259+826A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/23 | chr5 | 151564847 | ||||||
| chr5:151564894
|
A | G | 139 | a0002c0001t0001g0084a0002c0001t0001g0124a0002c0001t0001g0130others(136): Show | 142 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.3259+779T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/23 | chr5 | 151564894 | ||||||
| chr5:151564902
|
G | A | 11 | a0001c0048t0001g0026a0001c0048t0021g0025a0001c0049t0001g0020others(8): Show | 11 | HG01070.hp1 HG01074.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.3259+771C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/23 | chr5 | 151564902 | ||||||
| chr5:151564967
|
C | T | 4 | a0001c0130t0001g0192a0007c0045t0003g0153a0007c0045t0003g0191others(1): Show | 4 | NA18942.hp2 NA18980.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.3259+706G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/23 | chr5 | 151564967 | ||||||
| chr5:151565000
|
G | A | 22 | a0013c0024t0001g0225a0013c0024t0001g0235a0013c0024t0008g0228others(19): Show | 22 | HG00735.hp2 HG01243.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.3259+673C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/23 | chr5 | 151565000 | ||||||
| chr5:151565188
|
A | G | 139 | a0002c0001t0001g0084a0002c0001t0001g0124a0002c0001t0001g0130others(136): Show | 142 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.3259+485T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/23 | chr5 | 151565188 | ||||||
| chr5:151565458
|
C | A | 138 | a0002c0001t0001g0084a0002c0001t0001g0124a0002c0001t0001g0130others(135): Show | 141 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(138): Show |
intron_variant | MODIFIER | c.3259+215G>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/23 | chr5 | 151565458 | ||||||
| chr5:151565465
|
G | A | 2 | a0013c0024t0008g0228a0013c0035t0001g0227 | 2 | NA18954.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.3259+208C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/23 | chr5 | 151565465 | ||||||
| chr5:151565511
|
C | A | 139 | a0002c0001t0001g0084a0002c0001t0001g0124a0002c0001t0001g0130others(136): Show | 142 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.3259+162G>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/23 | chr5 | 151565511 | ||||||
| chr5:151565531
|
C | G | 133 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(130): Show | 135 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.3259+142G>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/23 | chr5 | 151565531 | ||||||
| chr5:151565562
|
A | G | 2 | a0001c0016t0001g0247a0001c0016t0004g0004 | 3 | HG01358.hp1 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.3259+111T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/23 | chr5 | 151565562 | ||||||
| chr5:151565563
|
TTTCAGCC others(21): Show |
T | 2 | a0079c0175t0010g0148a0080c0176t0001g0311 | 2 | HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3259+82_3259+109de others(29): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 2/23 | chr5 | 151565563 | ||||||
| chr5:151568976
|
T | C | 313 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(310): Show | 318 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(315): Show |
intron_variant | MODIFIER | c.-20-25A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151568976 | ||||||
| chr5:151569024
|
G | C | 1 | a0002c0006t0034g0358 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-20-73C>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151569024 | ||||||
| chr5:151569092
|
A | G | 388 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(385): Show | 395 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(392): Show |
intron_variant | MODIFIER | c.-20-141T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151569092 | ||||||
| chr5:151569100
|
T | C | 4 | a0031c0104t0001g0010a0031c0105t0001g0316a0081c0103t0001g0315others(1): Show | 4 | HG02109.hp2 HG02922.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20-149A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151569100 | ||||||
| chr5:151569116
|
C | T | 2 | a0022c0098t0010g0039a0038c0097t0001g0038 | 2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-20-165G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151569116 | ||||||
| chr5:151569240
|
T | C | 1 | a0003c0002t0001g0106 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-20-289A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151569240 | ||||||
| chr5:151569255
|
G | A | 1 | a0045c0080t0009g0150 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-20-304C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151569255 | ||||||
| chr5:151569301
|
G | A | 1 | a0002c0085t0037g0355 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-20-350C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151569301 | ||||||
| chr5:151569363
|
T | G | 31 | a0001c0004t0001g0156a0001c0004t0001g0252a0001c0004t0001g0253others(28): Show | 31 | HG00558.hp2 HG00639.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.-20-412A>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151569363 | ||||||
| chr5:151569416
|
A | G | 323 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(320): Show | 328 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(325): Show |
intron_variant | MODIFIER | c.-20-465T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151569416 | ||||||
| chr5:151569431
|
C | T | 139 | a0001c0003t0001g0147a0002c0001t0001g0084a0002c0001t0001g0124others(136): Show | 142 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.-20-480G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151569431 | ||||||
| chr5:151569471
|
A | T | 330 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(327): Show | 335 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.-20-520T>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151569471 | ||||||
| chr5:151569592
|
G | A | 1 | a0002c0006t0005g0163 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-20-641C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151569592 | ||||||
| chr5:151569620
|
A | G | 1 | a0015c0043t0001g0075 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-20-669T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151569620 | ||||||
| chr5:151569666
|
C | CT | 139 | a0001c0003t0001g0147a0002c0001t0001g0084a0002c0001t0001g0124others(136): Show | 142 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.-20-716dupA | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151569666 | ||||||
| chr5:151569699
|
C | T | 1 | a0053c0133t0013g0016 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-20-748G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151569699 | ||||||
| chr5:151569757
|
G | T | 4 | a0031c0104t0001g0010a0031c0105t0001g0316a0081c0103t0001g0315others(1): Show | 4 | HG02109.hp2 HG02922.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20-806C>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151569757 | ||||||
| chr5:151569961
|
C | T | 4 | a0001c0004t0001g0255a0001c0004t0001g0256a0001c0004t0001g0271others(1): Show | 4 | NA18954.hp2 NA18991.hp2 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20-1010G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151569961 | ||||||
| chr5:151570206
|
C | T | 1 | a0033c0058t0005g0243 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-20-1255G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151570206 | ||||||
| chr5:151570326
|
G | A | 14 | a0013c0024t0001g0225a0013c0024t0001g0235a0013c0024t0008g0228others(11): Show | 14 | HG01884.hp2 HG02015.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.-20-1375C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151570326 | ||||||
| chr5:151570327
|
A | G | 2 | a0001c0044t0007g0085a0001c0125t0010g0286 | 2 | HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-20-1376T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151570327 | ||||||
| chr5:151570499
|
G | A | 4 | a0003c0114t0001g0160a0017c0027t0001g0002a0017c0027t0001g0107others(1): Show | 5 | NA18939.hp2 NA18941.hp1 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-1548C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151570499 | ||||||
| chr5:151570531
|
G | T | 133 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(130): Show | 135 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.-20-1580C>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151570531 | ||||||
| chr5:151570664
|
T | C | 2 | a0001c0159t0001g0186a0004c0055t0001g0234 | 2 | NA18969.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.-20-1713A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151570664 | ||||||
| chr5:151570742
|
C | T | 4 | a0031c0104t0001g0010a0031c0105t0001g0316a0081c0103t0001g0315others(1): Show | 4 | HG02109.hp2 HG02922.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20-1791G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151570742 | ||||||
| chr5:151570810
|
G | T | 1 | a0004c0052t0001g0193 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-20-1859C>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151570810 | ||||||
| chr5:151570854
|
A | G | 33 | a0001c0004t0001g0156a0001c0004t0001g0252a0001c0004t0001g0253others(30): Show | 33 | HG00558.hp2 HG00639.hp2 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.-20-1903T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151570854 | ||||||
| chr5:151570894
|
C | A | 136 | a0001c0003t0001g0147a0002c0001t0001g0084a0002c0001t0001g0124others(133): Show | 139 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(136): Show |
intron_variant | MODIFIER | c.-20-1943G>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151570894 | ||||||
| chr5:151570970
|
G | A | 140 | a0001c0003t0001g0147a0002c0001t0001g0084a0002c0001t0001g0124others(137): Show | 143 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(140): Show |
intron_variant | MODIFIER | c.-20-2019C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151570970 | ||||||
| chr5:151570998
|
C | T | 1 | a0001c0003t0001g0230 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-20-2047G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151570998 | ||||||
| chr5:151571050
|
A | C | 31 | a0001c0004t0001g0156a0001c0004t0001g0252a0001c0004t0001g0253others(28): Show | 31 | HG00558.hp2 HG00639.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.-20-2099T>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151571050 | ||||||
| chr5:151571149
|
C | T | 1 | a0065c0145t0001g0061 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-20-2198G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151571149 | ||||||
| chr5:151571178
|
A | G | 31 | a0001c0004t0001g0156a0001c0004t0001g0252a0001c0004t0001g0253others(28): Show | 31 | HG00558.hp2 HG00639.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.-20-2227T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151571178 | ||||||
| chr5:151571223
|
G | A | 183 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(180): Show | 185 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.-20-2272C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151571223 | ||||||
| chr5:151571251
|
G | A | 2 | a0041c0075t0009g0249a0042c0077t0010g0248 | 2 | HG01243.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-20-2300C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151571251 | ||||||
| chr5:151571292
|
C | A | 110 | a0001c0003t0001g0147a0002c0001t0001g0084a0002c0001t0001g0124others(107): Show | 113 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.-20-2341G>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151571292 | ||||||
| chr5:151571309
|
C | G | 110 | a0001c0003t0001g0147a0002c0001t0001g0084a0002c0001t0001g0124others(107): Show | 113 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.-20-2358G>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151571309 | ||||||
| chr5:151571384
|
C | G | 56 | a0002c0001t0001g0124a0002c0001t0001g0130a0002c0001t0001g0131others(53): Show | 57 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.-20-2433G>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151571384 | ||||||
| chr5:151571505
|
G | A | 31 | a0001c0004t0001g0156a0001c0004t0001g0252a0001c0004t0001g0253others(28): Show | 31 | HG00558.hp2 HG00639.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.-20-2554C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151571505 | ||||||
| chr5:151571807
|
G | A | 166 | a0001c0003t0001g0147a0001c0010t0005g0058a0001c0010t0007g0003others(163): Show | 170 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.-20-2856C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151571807 | ||||||
| chr5:151571928
|
C | G | 1 | a0033c0058t0005g0243 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-20-2977G>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151571928 | ||||||
| chr5:151571936
|
G | T | 1 | a0001c0020t0001g0187 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-20-2985C>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151571936 | ||||||
| chr5:151572020
|
A | G | 174 | a0001c0003t0001g0147a0001c0004t0001g0156a0001c0004t0001g0252others(171): Show | 177 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(174): Show |
intron_variant | MODIFIER | c.-20-3069T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151572020 | ||||||
| chr5:151572037
|
A | G | 14 | a0013c0024t0001g0225a0013c0024t0001g0235a0013c0024t0008g0228others(11): Show | 14 | HG01884.hp2 HG02015.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.-20-3086T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151572037 | ||||||
| chr5:151572182
|
T | A | 292 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(289): Show | 296 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(293): Show |
intron_variant | MODIFIER | c.-20-3231A>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151572182 | ||||||
| chr5:151572312
|
A | C | 138 | a0001c0003t0001g0147a0001c0003t0001g0230a0001c0003t0001g0231others(135): Show | 141 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(138): Show |
intron_variant | MODIFIER | c.-20-3361T>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151572312 | ||||||
| chr5:151572472
|
G | A | 5 | a0036c0172t0009g0245a0040c0074t0001g0244a0041c0075t0009g0249others(2): Show | 5 | HG00735.hp2 HG01243.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.-20-3521C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151572472 | ||||||
| chr5:151572561
|
T | C | 139 | a0001c0003t0001g0147a0001c0003t0001g0230a0001c0003t0001g0231others(136): Show | 142 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.-20-3610A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151572561 | ||||||
| chr5:151572598
|
C | A | 139 | a0001c0003t0001g0147a0001c0003t0001g0230a0001c0003t0001g0231others(136): Show | 142 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.-20-3647G>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151572598 | ||||||
| chr5:151572637
|
G | GA | 3 | a0002c0099t0007g0033a0008c0012t0002g0320a0008c0025t0002g0321 | 3 | HG01884.hp1 HG03041.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-20-3687dupT | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151572637 | ||||||
| chr5:151572651
|
G | A | 139 | a0001c0003t0001g0147a0001c0003t0001g0230a0001c0003t0001g0231others(136): Show | 142 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.-20-3700C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151572651 | ||||||
| chr5:151572656
|
C | T | 4 | a0031c0104t0001g0010a0031c0105t0001g0316a0081c0103t0001g0315others(1): Show | 4 | HG02109.hp2 HG02922.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20-3705G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151572656 | ||||||
| chr5:151573065
|
A | G | 1 | a0003c0013t0009g0312 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-20-4114T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151573065 | ||||||
| chr5:151573095
|
A | G | 5 | a0036c0172t0009g0245a0040c0074t0001g0244a0041c0075t0009g0249others(2): Show | 5 | HG00735.hp2 HG01243.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.-20-4144T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151573095 | ||||||
| chr5:151573158
|
G | T | 2 | a0001c0003t0002g0329a0054c0134t0004g0083 | 2 | HG02602.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-20-4207C>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151573158 | ||||||
| chr5:151573159
|
C | T | 2 | a0001c0003t0002g0329a0054c0134t0004g0083 | 2 | HG02602.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-20-4208G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151573159 | ||||||
| chr5:151573233
|
A | G | 138 | a0001c0003t0001g0147a0001c0003t0001g0230a0001c0003t0001g0231others(135): Show | 141 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(138): Show |
intron_variant | MODIFIER | c.-20-4282T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151573233 | ||||||
| chr5:151573257
|
A | G | 1 | a0047c0072t0001g0155 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-20-4306T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151573257 | ||||||
| chr5:151573323
|
T | C | 133 | a0001c0003t0001g0147a0001c0003t0001g0230a0001c0003t0001g0231others(130): Show | 136 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(133): Show |
intron_variant | MODIFIER | c.-20-4372A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151573323 | ||||||
| chr5:151573326
|
C | G | 19 | a0001c0003t0001g0230a0001c0003t0001g0231a0001c0179t0001g0233others(16): Show | 19 | HG01884.hp2 HG02015.hp2 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.-20-4375G>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151573326 | ||||||
| chr5:151573547
|
G | C | 1 | a0063c0062t0001g0266 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-20-4596C>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151573547 | ||||||
| chr5:151573596
|
G | A | 1 | a0003c0013t0001g0109 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-20-4645C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151573596 | ||||||
| chr5:151573603
|
G | A | 2 | a0041c0075t0009g0249a0042c0077t0010g0248 | 2 | HG01243.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-20-4652C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151573603 | ||||||
| chr5:151573616
|
T | C | 133 | a0001c0003t0001g0147a0001c0003t0001g0230a0001c0003t0001g0231others(130): Show | 136 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(133): Show |
intron_variant | MODIFIER | c.-20-4665A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151573616 | ||||||
| chr5:151573619
|
A | T | 4 | a0022c0096t0001g0041a0022c0098t0010g0039a0033c0058t0005g0243others(1): Show | 4 | HG02145.hp2 HG02970.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20-4668T>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151573619 | ||||||
| chr5:151573667
|
CAAA | C | 26 | a0001c0004t0001g0156a0001c0004t0001g0252a0001c0004t0001g0253others(23): Show | 26 | HG00558.hp2 HG01192.hp2 HG01516.hp1 others(23): Show |
intron_variant | MODIFIER | c.-20-4719_-20-4717d others(5): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151573667 | ||||||
| chr5:151573859
|
T | C | 1 | a0001c0016t0002g0331 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-20-4908A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151573859 | ||||||
| chr5:151574025
|
A | G | 1 | a0001c0020t0001g0187 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-20-5074T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151574025 | ||||||
| chr5:151574083
|
A | G | 2 | a0008c0012t0001g0045a0008c0012t0001g0049 | 2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-20-5132T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151574083 | ||||||
| chr5:151574084
|
T | C | 139 | a0001c0003t0001g0147a0001c0003t0001g0230a0001c0003t0001g0231others(136): Show | 142 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.-20-5133A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151574084 | ||||||
| chr5:151574372
|
T | C | 10 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(7): Show | 10 | HG00609.hp2 HG02027.hp2 NA18941.hp2 others(7): Show |
intron_variant | MODIFIER | c.-20-5421A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151574372 | ||||||
| chr5:151574476
|
A | G | 1 | a0057c0122t0001g0082 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-20-5525T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151574476 | ||||||
| chr5:151574483
|
T | C | 1 | a0013c0035t0010g0242 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-20-5532A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151574483 | ||||||
| chr5:151574556
|
T | C | 19 | a0001c0003t0001g0230a0001c0003t0001g0231a0001c0179t0001g0233others(16): Show | 19 | HG01884.hp2 HG02015.hp2 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.-20-5605A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151574556 | ||||||
| chr5:151574613
|
A | G | 139 | a0001c0003t0001g0147a0001c0003t0001g0230a0001c0003t0001g0231others(136): Show | 142 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.-20-5662T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151574613 | ||||||
| chr5:151574728
|
A | T | 130 | a0001c0003t0001g0147a0001c0003t0001g0230a0001c0003t0001g0231others(127): Show | 133 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.-20-5777T>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151574728 | ||||||
| chr5:151574813
|
G | C | 24 | a0001c0003t0001g0230a0001c0003t0001g0231a0001c0179t0001g0233others(21): Show | 24 | HG01884.hp2 HG02015.hp2 HG02080.hp1 others(21): Show |
intron_variant | MODIFIER | c.-20-5862C>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151574813 | ||||||
| chr5:151574835
|
C | CAAAT | 139 | a0001c0003t0001g0147a0001c0003t0001g0230a0001c0003t0001g0231others(136): Show | 142 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.-20-5885_-20-5884i others(6): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151574835 | ||||||
| chr5:151574867
|
C | T | 1 | a0065c0145t0001g0061 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-20-5916G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151574867 | ||||||
| chr5:151574927
|
C | T | 139 | a0001c0003t0001g0147a0001c0003t0001g0230a0001c0003t0001g0231others(136): Show | 142 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.-20-5976G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151574927 | ||||||
| chr5:151574928
|
T | C | 139 | a0001c0003t0001g0147a0001c0003t0001g0230a0001c0003t0001g0231others(136): Show | 142 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.-20-5977A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151574928 | ||||||
| chr5:151575026
|
A | G | 139 | a0001c0003t0001g0147a0001c0003t0001g0230a0001c0003t0001g0231others(136): Show | 142 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.-20-6075T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151575026 | ||||||
| chr5:151575087
|
G | A | 332 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(329): Show | 337 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(334): Show |
intron_variant | MODIFIER | c.-20-6136C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151575087 | ||||||
| chr5:151575091
|
G | A | 1 | a0003c0013t0001g0079 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-20-6140C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151575091 | ||||||
| chr5:151575270
|
T | A | 4 | a0022c0096t0001g0041a0022c0098t0010g0039a0033c0058t0005g0243others(1): Show | 4 | HG02145.hp2 HG02970.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20-6319A>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151575270 | ||||||
| chr5:151575275
|
T | C | 28 | a0001c0003t0001g0230a0001c0003t0001g0231a0001c0179t0001g0233others(25): Show | 28 | HG01884.hp2 HG02015.hp2 HG02080.hp1 others(25): Show |
intron_variant | MODIFIER | c.-20-6324A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151575275 | ||||||
| chr5:151575325
|
C | T | 139 | a0001c0003t0001g0147a0001c0003t0001g0230a0001c0003t0001g0231others(136): Show | 142 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.-20-6374G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151575325 | ||||||
| chr5:151575380
|
C | T | 139 | a0001c0003t0001g0147a0001c0003t0001g0230a0001c0003t0001g0231others(136): Show | 142 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.-20-6429G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151575380 | ||||||
| chr5:151575391
|
A | G | 6 | a0004c0053t0010g0019a0032c0057t0001g0017a0032c0057t0001g0018others(3): Show | 6 | HG01257.hp1 HG01258.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20-6440T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151575391 | ||||||
| chr5:151575397
|
C | G | 6 | a0004c0053t0010g0019a0032c0057t0001g0017a0032c0057t0001g0018others(3): Show | 6 | HG01257.hp1 HG01258.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20-6446G>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151575397 | ||||||
| chr5:151575414
|
G | C | 139 | a0001c0003t0001g0147a0001c0003t0001g0230a0001c0003t0001g0231others(136): Show | 142 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.-20-6463C>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151575414 | ||||||
| chr5:151575566
|
C | T | 139 | a0001c0003t0001g0147a0001c0003t0001g0230a0001c0003t0001g0231others(136): Show | 142 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.-20-6615G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151575566 | ||||||
| chr5:151575580
|
G | C | 139 | a0001c0003t0001g0147a0001c0003t0001g0230a0001c0003t0001g0231others(136): Show | 142 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.-20-6629C>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151575580 | ||||||
| chr5:151575602
|
C | A | 139 | a0001c0003t0001g0147a0001c0003t0001g0230a0001c0003t0001g0231others(136): Show | 142 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.-20-6651G>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151575602 | ||||||
| chr5:151575681
|
G | A | 139 | a0001c0003t0001g0147a0001c0003t0001g0230a0001c0003t0001g0231others(136): Show | 142 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.-20-6730C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151575681 | ||||||
| chr5:151575721
|
G | A | 139 | a0001c0003t0001g0147a0001c0003t0001g0230a0001c0003t0001g0231others(136): Show | 142 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.-20-6770C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151575721 | ||||||
| chr5:151575744
|
C | T | 1 | a0003c0002t0001g0081 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-20-6793G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151575744 | ||||||
| chr5:151575771
|
T | C | 139 | a0001c0003t0001g0147a0001c0003t0001g0230a0001c0003t0001g0231others(136): Show | 142 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.-20-6820A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151575771 | ||||||
| chr5:151575786
|
C | T | 139 | a0001c0003t0001g0147a0001c0003t0001g0230a0001c0003t0001g0231others(136): Show | 142 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.-20-6835G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151575786 | ||||||
| chr5:151575805
|
C | G | 22 | a0002c0001t0001g0300a0002c0001t0001g0309a0002c0001t0002g0342others(19): Show | 23 | HG00140.hp2 HG00642.hp1 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.-20-6854G>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151575805 | ||||||
| chr5:151575854
|
G | A | 3 | a0001c0059t0001g0267a0001c0159t0001g0186a0004c0055t0001g0234 | 3 | HG02148.hp2 NA18969.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.-20-6903C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151575854 | ||||||
| chr5:151575891
|
G | A | 1 | a0002c0001t0001g0239 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-20-6940C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151575891 | ||||||
| chr5:151575960
|
C | T | 139 | a0001c0003t0001g0147a0001c0003t0001g0230a0001c0003t0001g0231others(136): Show | 142 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.-20-7009G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151575960 | ||||||
| chr5:151575983
|
C | T | 2 | a0001c0010t0007g0003a0004c0148t0001g0152 | 3 | HG02723.hp1 HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-20-7032G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151575983 | ||||||
| chr5:151576009
|
G | A | 12 | a0001c0048t0001g0026a0001c0048t0021g0025a0001c0049t0001g0020others(9): Show | 12 | HG01070.hp1 HG01074.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.-20-7058C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151576009 | ||||||
| chr5:151576012
|
T | C | 139 | a0001c0003t0001g0147a0001c0003t0001g0230a0001c0003t0001g0231others(136): Show | 142 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.-20-7061A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151576012 | ||||||
| chr5:151576153
|
A | G | 4 | a0022c0096t0001g0041a0022c0098t0010g0039a0033c0058t0005g0243others(1): Show | 4 | HG02145.hp2 HG02970.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20-7202T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151576153 | ||||||
| chr5:151576208
|
A | G | 24 | a0002c0001t0002g0353a0002c0001t0005g0036a0002c0001t0017g0009others(21): Show | 25 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.-20-7257T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151576208 | ||||||
| chr5:151576252
|
T | C | 19 | a0002c0001t0002g0353a0002c0001t0005g0036a0002c0001t0017g0009others(16): Show | 20 | HG00735.hp1 HG00741.hp1 HG01256.hp1 others(17): Show |
intron_variant | MODIFIER | c.-20-7301A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151576252 | ||||||
| chr5:151576360
|
G | A | 138 | a0001c0003t0001g0147a0001c0003t0001g0230a0001c0003t0001g0231others(135): Show | 141 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(138): Show |
intron_variant | MODIFIER | c.-20-7409C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151576360 | ||||||
| chr5:151576397
|
G | A | 1 | a0002c0085t0037g0355 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-20-7446C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151576397 | ||||||
| chr5:151576498
|
T | C | 139 | a0001c0003t0001g0147a0001c0003t0001g0230a0001c0003t0001g0231others(136): Show | 142 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.-20-7547A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151576498 | ||||||
| chr5:151576556
|
G | A | 1 | a0043c0076t0007g0037 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-20-7605C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151576556 | ||||||
| chr5:151576657
|
A | G | 2 | a0015c0043t0001g0075a0076c0111t0001g0076 | 2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-20-7706T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151576657 | ||||||
| chr5:151576681
|
G | A | 3 | a0003c0029t0005g0291a0003c0029t0005g0292a0003c0029t0005g0293 | 3 | HG02647.hp1 HG02922.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-20-7730C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151576681 | ||||||
| chr5:151576789
|
T | C | 6 | a0004c0053t0010g0019a0032c0057t0001g0017a0032c0057t0001g0018others(3): Show | 6 | HG01257.hp1 HG01258.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-20-7838A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151576789 | ||||||
| chr5:151576865
|
C | A | 332 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(329): Show | 337 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(334): Show |
intron_variant | MODIFIER | c.-20-7914G>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151576865 | ||||||
| chr5:151576900
|
A | G | 3 | a0001c0159t0001g0186a0004c0055t0001g0234a0009c0007t0001g0216 | 3 | NA18952.hp2 NA18969.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.-20-7949T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151576900 | ||||||
| chr5:151576925
|
C | T | 4 | a0004c0053t0010g0019a0032c0057t0001g0017a0032c0057t0001g0018others(1): Show | 4 | HG01257.hp1 HG01258.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20-7974G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151576925 | ||||||
| chr5:151576939
|
A | G | 5 | a0002c0001t0001g0132a0002c0001t0001g0133a0002c0001t0001g0144others(2): Show | 5 | HG00609.hp1 NA18944.hp2 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-7988T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151576939 | ||||||
| chr5:151577012
|
G | A | 8 | a0003c0013t0009g0312a0022c0096t0001g0041a0022c0098t0010g0039others(5): Show | 8 | HG02109.hp2 HG02145.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-20-8061C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151577012 | ||||||
| chr5:151577224
|
A | G | 140 | a0001c0003t0001g0147a0001c0003t0001g0230a0001c0003t0001g0231others(137): Show | 143 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(140): Show |
intron_variant | MODIFIER | c.-20-8273T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151577224 | ||||||
| chr5:151577437
|
C | A | 1 | a0066c0162t0001g0214 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-20-8486G>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151577437 | ||||||
| chr5:151577467
|
G | A | 2 | a0001c0179t0001g0233a0005c0015t0001g0232 | 2 | NA18951.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.-20-8516C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151577467 | ||||||
| chr5:151577527
|
C | T | 1 | a0009c0007t0001g0216 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-20-8576G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151577527 | ||||||
| chr5:151577709
|
TG | T | 8 | a0003c0013t0009g0312a0022c0096t0001g0041a0022c0098t0010g0039others(5): Show | 8 | HG02109.hp2 HG02145.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-20-8759delC | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151577709 | ||||||
| chr5:151577764
|
A | G | 4 | a0004c0053t0010g0019a0032c0057t0001g0017a0032c0057t0001g0018others(1): Show | 4 | HG01257.hp1 HG01258.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-20-8813T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151577764 | ||||||
| chr5:151577824
|
C | T | 8 | a0003c0013t0009g0312a0022c0096t0001g0041a0022c0098t0010g0039others(5): Show | 8 | HG02109.hp2 HG02145.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-20-8873G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151577824 | ||||||
| chr5:151577859
|
C | G | 1 | a0001c0147t0013g0161 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-20-8908G>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151577859 | ||||||
| chr5:151577890
|
G | A | 1 | a0009c0007t0001g0215 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-20-8939C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151577890 | ||||||
| chr5:151578020
|
CA | C | 12 | a0001c0003t0001g0147a0002c0001t0001g0131a0002c0008t0002g0369others(9): Show | 12 | HG01257.hp1 HG01258.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-20-9070delT | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151578020 | ||||||
| chr5:151578099
|
G | A | 8 | a0003c0013t0009g0312a0022c0096t0001g0041a0022c0098t0010g0039others(5): Show | 8 | HG02109.hp2 HG02145.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-20-9148C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151578099 | ||||||
| chr5:151578113
|
C | T | 1 | a0003c0002t0001g0113 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-20-9162G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151578113 | ||||||
| chr5:151578498
|
G | A | 1 | a0019c0036t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-20-9547C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151578498 | ||||||
| chr5:151578545
|
C | T | 1 | a0002c0008t0002g0369 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-20-9594G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151578545 | ||||||
| chr5:151578627
|
C | T | 1 | a0002c0026t0001g0298 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-20-9676G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151578627 | ||||||
| chr5:151578820
|
G | A | 2 | a0001c0142t0007g0044a0004c0143t0001g0043 | 2 | HG02809.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-20-9869C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151578820 | ||||||
| chr5:151578993
|
G | A | 1 | a0041c0075t0009g0249 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-20-10042C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151578993 | ||||||
| chr5:151579139
|
C | G | 1 | a0023c0078t0001g0297 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-20-10188G>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151579139 | ||||||
| chr5:151579305
|
C | T | 3 | a0022c0096t0001g0041a0022c0098t0010g0039a0038c0097t0001g0038 | 3 | HG02145.hp2 HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-20-10354G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151579305 | ||||||
| chr5:151579312
|
C | T | 3 | a0002c0099t0007g0033a0008c0012t0002g0320a0008c0025t0002g0321 | 3 | HG01884.hp1 HG03041.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-20-10361G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151579312 | ||||||
| chr5:151579495
|
C | T | 1 | a0001c0017t0001g0279 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-20-10544G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151579495 | ||||||
| chr5:151579737
|
TA | T | 8 | a0001c0010t0005g0058a0001c0047t0005g0290a0001c0047t0007g0294others(5): Show | 8 | HG01069.hp1 HG02451.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-20-10787delT | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151579737 | ||||||
| chr5:151579782
|
A | G | 1 | a0002c0001t0001g0296 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-20-10831T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151579782 | ||||||
| chr5:151580025
|
A | G | 20 | a0001c0010t0001g0289a0001c0125t0010g0286a0001c0142t0007g0044others(17): Show | 20 | HG01109.hp2 HG01243.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-20-11074T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151580025 | ||||||
| chr5:151580144
|
C | T | 4 | a0022c0096t0001g0041a0022c0098t0010g0039a0033c0058t0005g0243others(1): Show | 4 | HG02145.hp2 HG02970.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-21+11021G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151580144 | ||||||
| chr5:151580155
|
G | A | 133 | a0001c0003t0001g0147a0001c0003t0001g0230a0001c0003t0001g0231others(130): Show | 136 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(133): Show |
intron_variant | MODIFIER | c.-21+11010C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151580155 | ||||||
| chr5:151580506
|
A | C | 1 | a0002c0006t0015g0390 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-21+10659T>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151580506 | ||||||
| chr5:151580545
|
A | T | 1 | a0003c0013t0009g0312 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-21+10620T>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151580545 | ||||||
| chr5:151580593
|
G | A | 5 | a0031c0104t0001g0010a0031c0105t0001g0316a0039c0073t0002g0356others(2): Show | 5 | HG00673.hp2 HG02109.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-21+10572C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151580593 | ||||||
| chr5:151580657
|
A | T | 2 | a0003c0002t0002g0323a0003c0013t0001g0079 | 2 | NA18612.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.-21+10508T>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151580657 | ||||||
| chr5:151580718
|
G | A | 1 | a0003c0013t0009g0312 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-21+10447C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151580718 | ||||||
| chr5:151580720
|
A | G | 1 | a0003c0013t0009g0312 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-21+10445T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151580720 | ||||||
| chr5:151580745
|
G | A | 135 | a0001c0003t0001g0147a0001c0003t0001g0230a0001c0003t0001g0231others(132): Show | 138 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(135): Show |
intron_variant | MODIFIER | c.-21+10420C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151580745 | ||||||
| chr5:151580813
|
C | T | 4 | a0022c0096t0001g0041a0022c0098t0010g0039a0033c0058t0005g0243others(1): Show | 4 | HG02145.hp2 HG02970.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-21+10352G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151580813 | ||||||
| chr5:151581091
|
C | T | 1 | a0003c0013t0009g0312 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-21+10074G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151581091 | ||||||
| chr5:151581258
|
G | C | 1 | a0002c0001t0002g0368 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-21+9907C>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151581258 | ||||||
| chr5:151581272
|
G | A | 3 | a0002c0006t0034g0358a0044c0081t0035g0357a0045c0080t0009g0150 | 3 | HG02258.hp2 HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-21+9893C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151581272 | ||||||
| chr5:151581288
|
A | G | 4 | a0001c0003t0001g0147a0002c0008t0002g0369a0002c0026t0024g0146others(1): Show | 4 | HG02451.hp1 HG02698.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.-21+9877T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151581288 | ||||||
| chr5:151581367
|
C | T | 1 | a0003c0013t0009g0312 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-21+9798G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151581367 | ||||||
| chr5:151581368
|
G | A | 2 | a0001c0016t0001g0247a0001c0016t0004g0004 | 3 | HG01358.hp1 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-21+9797C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151581368 | ||||||
| chr5:151581478
|
G | A | 10 | a0002c0001t0002g0007a0002c0001t0002g0361a0002c0001t0002g0363others(7): Show | 11 | HG00621.hp1 HG02015.hp1 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.-21+9687C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151581478 | ||||||
| chr5:151581577
|
C | T | 1 | a0003c0013t0009g0312 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-21+9588G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151581577 | ||||||
| chr5:151581703
|
C | G | 1 | a0002c0170t0002g0334 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-21+9462G>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151581703 | ||||||
| chr5:151581772
|
C | T | 4 | a0031c0104t0001g0010a0031c0105t0001g0316a0081c0103t0001g0315others(1): Show | 4 | HG02109.hp2 HG02922.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-21+9393G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151581772 | ||||||
| chr5:151581843
|
A | G | 1 | a0011c0137t0011g0319 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-21+9322T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151581843 | ||||||
| chr5:151581909
|
C | T | 19 | a0001c0003t0001g0230a0001c0003t0001g0231a0001c0179t0001g0233others(16): Show | 19 | HG01884.hp2 HG02015.hp2 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.-21+9256G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151581909 | ||||||
| chr5:151581934
|
C | T | 114 | a0001c0003t0001g0147a0001c0010t0002g0352a0002c0001t0001g0124others(111): Show | 117 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.-21+9231G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151581934 | ||||||
| chr5:151582048
|
C | T | 3 | a0001c0003t0001g0183a0001c0003t0001g0185a0001c0021t0003g0184 | 3 | NA18963.hp1 NA18983.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.-21+9117G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151582048 | ||||||
| chr5:151582293
|
T | C | 4 | a0036c0172t0009g0245a0040c0074t0001g0244a0041c0075t0009g0249others(1): Show | 4 | HG00735.hp2 HG01243.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-21+8872A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151582293 | ||||||
| chr5:151582400
|
G | A | 1 | a0010c0011t0001g0032 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-21+8765C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151582400 | ||||||
| chr5:151582442
|
G | A | 137 | a0001c0003t0001g0147a0001c0003t0001g0230a0001c0003t0001g0231others(134): Show | 140 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.-21+8723C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151582442 | ||||||
| chr5:151582536
|
C | G | 21 | a0001c0003t0001g0230a0001c0003t0001g0231a0001c0142t0007g0044others(18): Show | 21 | HG01884.hp2 HG02015.hp2 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.-21+8629G>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151582536 | ||||||
| chr5:151582622
|
C | T | 114 | a0001c0003t0001g0147a0001c0010t0002g0352a0002c0001t0001g0124others(111): Show | 117 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.-21+8543G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151582622 | ||||||
| chr5:151582624
|
C | T | 1 | a0043c0076t0007g0037 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-21+8541G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151582624 | ||||||
| chr5:151582688
|
A | G | 20 | a0001c0003t0001g0230a0001c0003t0001g0231a0001c0179t0001g0233others(17): Show | 20 | HG01884.hp2 HG02015.hp2 HG02080.hp1 others(17): Show |
intron_variant | MODIFIER | c.-21+8477T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151582688 | ||||||
| chr5:151582745
|
C | T | 9 | a0001c0142t0007g0044a0004c0143t0001g0043a0008c0012t0001g0045others(6): Show | 9 | HG01109.hp2 HG01243.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.-21+8420G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151582745 | ||||||
| chr5:151582837
|
T | C | 6 | a0004c0053t0010g0019a0032c0057t0001g0017a0032c0057t0001g0018others(3): Show | 6 | HG01257.hp1 HG01258.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-21+8328A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151582837 | ||||||
| chr5:151582867
|
A | T | 1 | a0019c0036t0001g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-21+8298T>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151582867 | ||||||
| chr5:151582966
|
C | A | 109 | a0001c0003t0001g0147a0001c0010t0002g0352a0002c0001t0001g0124others(106): Show | 112 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.-21+8199G>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151582966 | ||||||
| chr5:151582980
|
A | C | 7 | a0002c0001t0001g0130a0002c0006t0001g0129a0006c0005t0003g0125others(4): Show | 7 | NA18957.hp1 NA18965.hp2 NA18968.hp1 others(4): Show |
intron_variant | MODIFIER | c.-21+8185T>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151582980 | ||||||
| chr5:151583015
|
G | A | 2 | a0079c0175t0010g0148a0080c0176t0001g0311 | 2 | HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-21+8150C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151583015 | ||||||
| chr5:151583069
|
T | A | 2 | a0032c0057t0001g0017a0032c0057t0001g0018 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-21+8096A>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151583069 | ||||||
| chr5:151583086
|
T | C | 1 | a0022c0098t0010g0039 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-21+8079A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151583086 | ||||||
| chr5:151583325
|
T | C | 1 | a0003c0117t0001g0111 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-21+7840A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151583325 | ||||||
| chr5:151583630
|
C | A | 5 | a0001c0003t0001g0231a0001c0179t0001g0233a0004c0055t0001g0234others(2): Show | 5 | HG02155.hp2 NA18951.hp1 NA19056.hp2 others(2): Show |
intron_variant | MODIFIER | c.-21+7535G>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151583630 | ||||||
| chr5:151583666
|
G | A | 1 | a0003c0009t0001g0120 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-21+7499C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151583666 | ||||||
| chr5:151583767
|
T | C | 1 | a0013c0024t0001g0235 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-21+7398A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151583767 | ||||||
| chr5:151583924
|
G | A | 1 | a0017c0108t0001g0112 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-21+7241C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151583924 | ||||||
| chr5:151583980
|
G | A | 1 | a0002c0037t0002g0386 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-21+7185C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151583980 | ||||||
| chr5:151583997
|
C | CA | 111 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(108): Show | 112 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.-21+7167dupT | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151583997 | ||||||
| chr5:151583997
|
C | CAA | 22 | a0001c0003t0002g0332a0001c0003t0012g0222a0001c0003t0020g0221others(19): Show | 22 | HG00735.hp2 HG00741.hp2 HG01258.hp1 others(19): Show |
intron_variant | MODIFIER | c.-21+7166_-21+7167d others(4): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151583997 | ||||||
| chr5:151583997
|
C | CAAA | 12 | a0013c0035t0010g0242a0020c0028t0001g0069a0020c0028t0001g0070others(9): Show | 12 | HG02109.hp2 HG03041.hp2 HG03195.hp1 others(9): Show |
intron_variant | MODIFIER | c.-21+7165_-21+7167d others(5): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151583997 | ||||||
| chr5:151583997
|
CA | C | 101 | a0001c0004t0001g0253a0001c0010t0002g0352a0001c0142t0007g0044others(98): Show | 104 | HG00140.hp2 HG00558.hp1 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.-21+7167delT | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151583997 | ||||||
| chr5:151583997
|
CAA | C | 6 | a0001c0123t0007g0077a0002c0001t0001g0124a0010c0011t0001g0032others(3): Show | 6 | HG01256.hp1 HG02976.hp2 NA18906.hp2 others(3): Show |
intron_variant | MODIFIER | c.-21+7166_-21+7167d others(4): Show |
FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151583997 | ||||||
| chr5:151584097
|
C | T | 1 | a0003c0013t0009g0312 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-21+7068G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151584097 | ||||||
| chr5:151584098
|
G | A | 1 | a0003c0140t0001g0223 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-21+7067C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151584098 | ||||||
| chr5:151584169
|
A | G | 9 | a0003c0013t0009g0312a0022c0096t0001g0041a0022c0098t0010g0039others(6): Show | 9 | HG02109.hp2 HG02145.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-21+6996T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151584169 | ||||||
| chr5:151584229
|
C | T | 2 | a0036c0172t0009g0245a0040c0074t0001g0244 | 2 | HG00735.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-21+6936G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151584229 | ||||||
| chr5:151584241
|
G | A | 125 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(122): Show | 127 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.-21+6924C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151584241 | ||||||
| chr5:151584294
|
C | T | 5 | a0005c0015t0001g0151a0005c0015t0001g0157a0005c0015t0001g0159others(2): Show | 5 | HG02717.hp2 NA19003.hp1 NA19054.hp2 others(2): Show |
intron_variant | MODIFIER | c.-21+6871G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151584294 | ||||||
| chr5:151584295
|
G | A | 1 | a0002c0006t0001g0145 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-21+6870C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151584295 | ||||||
| chr5:151584296
|
C | T | 1 | a0001c0049t0001g0020 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-21+6869G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151584296 | ||||||
| chr5:151584351
|
G | A | 1 | a0002c0006t0001g0005 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-21+6814C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151584351 | ||||||
| chr5:151584410
|
T | C | 1 | a0043c0076t0007g0037 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-21+6755A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151584410 | ||||||
| chr5:151584443
|
A | G | 1 | a0003c0013t0009g0312 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-21+6722T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151584443 | ||||||
| chr5:151584536
|
C | T | 1 | a0002c0037t0002g0386 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-21+6629G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151584536 | ||||||
| chr5:151584540
|
A | G | 2 | a0079c0175t0010g0148a0080c0176t0001g0311 | 2 | HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-21+6625T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151584540 | ||||||
| chr5:151584559
|
C | T | 2 | a0079c0175t0010g0148a0080c0176t0001g0311 | 2 | HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-21+6606G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151584559 | ||||||
| chr5:151584599
|
G | C | 1 | a0004c0053t0010g0019 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-21+6566C>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151584599 | ||||||
| chr5:151584604
|
G | A | 4 | a0001c0003t0001g0147a0002c0008t0002g0369a0002c0026t0024g0146others(1): Show | 4 | HG02451.hp1 HG02698.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.-21+6561C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151584604 | ||||||
| chr5:151584782
|
C | T | 1 | a0043c0076t0007g0037 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-21+6383G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151584782 | ||||||
| chr5:151585086
|
A | G | 8 | a0002c0001t0005g0036a0002c0001t0017g0009a0002c0099t0007g0033others(5): Show | 8 | HG01496.hp1 HG01884.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.-21+6079T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151585086 | ||||||
| chr5:151585137
|
A | G | 4 | a0036c0172t0009g0245a0040c0074t0001g0244a0041c0075t0009g0249others(1): Show | 4 | HG00735.hp2 HG01243.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-21+6028T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151585137 | ||||||
| chr5:151585216
|
G | A | 154 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(151): Show | 156 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.-21+5949C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151585216 | ||||||
| chr5:151585237
|
C | G | 153 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(150): Show | 155 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.-21+5928G>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151585237 | ||||||
| chr5:151585421
|
C | T | 287 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(284): Show | 292 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.-21+5744G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151585421 | ||||||
| chr5:151585533
|
A | G | 20 | a0001c0003t0001g0230a0001c0003t0001g0231a0001c0179t0001g0233others(17): Show | 20 | HG01884.hp2 HG02015.hp2 HG02080.hp1 others(17): Show |
intron_variant | MODIFIER | c.-21+5632T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151585533 | ||||||
| chr5:151585539
|
G | A | 2 | a0013c0035t0010g0242a0024c0034t0001g0241 | 2 | HG01884.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-21+5626C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151585539 | ||||||
| chr5:151586155
|
C | G | 4 | a0004c0053t0010g0019a0032c0057t0001g0017a0032c0057t0001g0018others(1): Show | 4 | HG01257.hp1 HG01258.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-21+5010G>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151586155 | ||||||
| chr5:151586414
|
A | G | 297 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(294): Show | 302 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(299): Show |
intron_variant | MODIFIER | c.-21+4751T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151586414 | ||||||
| chr5:151586450
|
C | G | 8 | a0020c0028t0001g0069a0020c0028t0001g0070a0020c0028t0001g0073others(5): Show | 8 | NA18942.hp1 NA18951.hp2 NA18992.hp1 others(5): Show |
intron_variant | MODIFIER | c.-21+4715G>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151586450 | ||||||
| chr5:151586766
|
A | G | 34 | a0001c0004t0001g0156a0001c0004t0001g0252a0001c0004t0001g0253others(31): Show | 34 | HG00558.hp2 HG00639.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.-21+4399T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151586766 | ||||||
| chr5:151586827
|
A | C | 114 | a0001c0003t0001g0121a0001c0003t0001g0123a0001c0003t0001g0147others(111): Show | 117 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.-21+4338T>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151586827 | ||||||
| chr5:151586844
|
A | C | 165 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(162): Show | 167 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.-21+4321T>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151586844 | ||||||
| chr5:151586945
|
A | G | 1 | a0006c0005t0006g0333 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-21+4220T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151586945 | ||||||
| chr5:151587166
|
C | CA | 125 | a0001c0003t0001g0013a0001c0003t0001g0183a0001c0003t0001g0185others(122): Show | 127 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.-21+3998dupT | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151587166 | ||||||
| chr5:151587171
|
A | C | 5 | a0001c0047t0005g0290a0003c0002t0001g0065a0003c0029t0005g0291others(2): Show | 5 | HG02647.hp1 HG02886.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-21+3994T>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151587171 | ||||||
| chr5:151587176
|
A | C | 2 | a0036c0172t0009g0245a0040c0074t0001g0244 | 2 | HG00735.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-21+3989T>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151587176 | ||||||
| chr5:151587177
|
C | A | 1 | a0042c0077t0010g0248 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-21+3988G>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151587177 | ||||||
| chr5:151587254
|
A | G | 1 | a0001c0004t0001g0252 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-21+3911T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151587254 | ||||||
| chr5:151587378
|
T | A | 2 | a0036c0172t0009g0245a0040c0074t0001g0244 | 2 | HG00735.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-21+3787A>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151587378 | ||||||
| chr5:151587517
|
A | G | 1 | a0042c0077t0010g0248 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-21+3648T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151587517 | ||||||
| chr5:151587557
|
C | T | 27 | a0001c0048t0001g0026a0001c0048t0021g0025a0001c0049t0001g0020others(24): Show | 27 | HG01070.hp1 HG01074.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.-21+3608G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151587557 | ||||||
| chr5:151587706
|
T | C | 8 | a0001c0016t0001g0273a0002c0001t0001g0239a0002c0001t0001g0278others(5): Show | 8 | HG00423.hp2 HG00597.hp1 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.-21+3459A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151587706 | ||||||
| chr5:151587833
|
C | T | 4 | a0001c0047t0005g0290a0003c0029t0005g0291a0003c0029t0005g0292others(1): Show | 4 | HG02647.hp1 HG02886.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-21+3332G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151587833 | ||||||
| chr5:151587884
|
A | T | 1 | a0031c0104t0001g0010 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-21+3281T>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151587884 | ||||||
| chr5:151587900
|
G | T | 1 | a0010c0094t0002g0385 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-21+3265C>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151587900 | ||||||
| chr5:151587978
|
A | G | 322 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(319): Show | 327 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(324): Show |
intron_variant | MODIFIER | c.-21+3187T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151587978 | ||||||
| chr5:151588123
|
G | A | 1 | a0025c0069t0001g0240 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-21+3042C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151588123 | ||||||
| chr5:151588181
|
T | C | 1 | a0003c0013t0009g0312 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-21+2984A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151588181 | ||||||
| chr5:151588203
|
G | C | 1 | a0005c0030t0001g0060 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-21+2962C>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151588203 | ||||||
| chr5:151588275
|
C | T | 134 | a0001c0003t0001g0121a0001c0003t0001g0123a0001c0003t0001g0147others(131): Show | 137 | HG00140.hp2 HG00558.hp1 HG00609.hp1 others(134): Show |
intron_variant | MODIFIER | c.-21+2890G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151588275 | ||||||
| chr5:151588371
|
T | C | 1 | a0045c0080t0009g0150 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-21+2794A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151588371 | ||||||
| chr5:151588393
|
G | T | 120 | a0001c0003t0001g0013a0001c0003t0001g0183a0001c0003t0001g0185others(117): Show | 122 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.-21+2772C>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151588393 | ||||||
| chr5:151588574
|
C | G | 145 | a0001c0003t0001g0121a0001c0003t0001g0123a0001c0003t0001g0147others(142): Show | 148 | HG00140.hp2 HG00558.hp1 HG00609.hp1 others(145): Show |
intron_variant | MODIFIER | c.-21+2591G>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151588574 | ||||||
| chr5:151588685
|
C | G | 2 | a0024c0034t0001g0288a0025c0071t0001g0287 | 2 | NA18948.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.-21+2480G>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151588685 | ||||||
| chr5:151588742
|
G | A | 313 | a0001c0003t0001g0013a0001c0003t0001g0121a0001c0003t0001g0123others(310): Show | 318 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(315): Show |
intron_variant | MODIFIER | c.-21+2423C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151588742 | ||||||
| chr5:151588839
|
A | C | 20 | a0001c0010t0001g0289a0001c0010t0005g0058a0001c0142t0007g0044others(17): Show | 20 | HG01109.hp2 HG01243.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-21+2326T>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151588839 | ||||||
| chr5:151588856
|
C | T | 1 | a0003c0138t0025g0042 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-21+2309G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151588856 | ||||||
| chr5:151588897
|
G | A | 2 | a0001c0016t0001g0247a0001c0016t0004g0004 | 3 | HG01358.hp1 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-21+2268C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151588897 | ||||||
| chr5:151589236
|
C | G | 2 | a0031c0105t0001g0316a0081c0103t0001g0315 | 2 | HG02109.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-21+1929G>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151589236 | ||||||
| chr5:151589548
|
A | G | 2 | a0002c0001t0001g0250a0002c0001t0001g0251 | 2 | NA18952.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.-21+1617T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151589548 | ||||||
| chr5:151589645
|
C | T | 5 | a0019c0036t0001g0040a0022c0096t0001g0041a0022c0098t0010g0039others(2): Show | 5 | HG02055.hp1 HG02145.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-21+1520G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151589645 | ||||||
| chr5:151589732
|
C | A | 2 | a0041c0075t0009g0249a0042c0077t0010g0248 | 2 | HG01243.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-21+1433G>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151589732 | ||||||
| chr5:151589741
|
A | AT | 26 | a0001c0048t0001g0026a0001c0048t0021g0025a0001c0049t0001g0020others(23): Show | 26 | HG01070.hp1 HG01074.hp2 HG01255.hp2 others(23): Show |
intron_variant | MODIFIER | c.-21+1423dupA | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151589741 | ||||||
| chr5:151589764
|
G | A | 5 | a0002c0037t0002g0386a0002c0037t0002g0389a0010c0094t0002g0385others(2): Show | 5 | HG00735.hp1 HG00741.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.-21+1401C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151589764 | ||||||
| chr5:151589765
|
G | A | 29 | a0001c0004t0001g0252a0001c0004t0001g0253a0001c0004t0001g0255others(26): Show | 29 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.-21+1400C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151589765 | ||||||
| chr5:151589767
|
G | A | 8 | a0001c0004t0001g0284a0001c0017t0001g0279a0001c0017t0001g0283others(5): Show | 8 | HG00639.hp2 HG01069.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.-21+1398C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151589767 | ||||||
| chr5:151589924
|
A | G | 6 | a0001c0010t0001g0289a0001c0047t0005g0290a0001c0047t0007g0294others(3): Show | 6 | HG01891.hp2 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-21+1241T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151589924 | ||||||
| chr5:151590029
|
T | G | 4 | a0001c0125t0010g0286a0031c0105t0001g0316a0081c0103t0001g0315others(1): Show | 4 | HG02109.hp2 HG02922.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-21+1136A>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151590029 | ||||||
| chr5:151590066
|
C | A | 2 | a0024c0034t0001g0288a0025c0071t0001g0287 | 2 | NA18948.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.-21+1099G>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151590066 | ||||||
| chr5:151590260
|
C | T | 4 | a0001c0003t0001g0013a0004c0055t0001g0012a0005c0015t0001g0011others(1): Show | 4 | NA18941.hp2 NA19001.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.-21+905G>A | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151590260 | ||||||
| chr5:151590330
|
C | A | 6 | a0001c0010t0001g0289a0001c0047t0005g0290a0001c0047t0007g0294others(3): Show | 6 | HG01891.hp2 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-21+835G>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151590330 | ||||||
| chr5:151590741
|
T | C | 1 | a0008c0012t0022g0318 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-21+424A>G | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151590741 | ||||||
| chr5:151590872
|
A | G | 1 | a0031c0104t0001g0010 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-21+293T>C | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151590872 | ||||||
| chr5:151591084
|
G | A | 27 | a0001c0003t0001g0295a0001c0003t0001g0313a0002c0001t0001g0296others(24): Show | 28 | HG00140.hp2 HG00642.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.-21+81C>T | FAT2 | ENSG00000086570.13 | transcript | ENST00000261800.6 | protein_coding | 1/23 | chr5 | 151591084 |