Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 23017 |
|---|---|
| ensemblid | ENSG00000135472.9 |
| hgncid | 17067 |
| symbol | FAIM2 |
| name | Fas apoptotic inhibitory molecule 2 |
| refseq_nuc | NM_012306.4 |
| refseq_prot | NP_036438.2 |
| ensembl_nuc | ENST00000320634.8 |
| ensembl_prot | ENSP00000321951.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 49866896 |
| end | 49903900 |
| strand | - |
| ver | v1.2 |
| region | chr12:49866896-49903900 |
| region5000 | chr12:49861896-49908900 |
| regionname0 | FAIM2_chr12_49866896_49903900 |
| regionname5000 | FAIM2_chr12_49861896_49908900 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 316 | 432 | 94 | 67 | 205 | 18 | 46 | 156 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0002 | 0/0 | 316 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0003 | 0/0 | 305 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0004 | 0/0 | 316 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 951 | 422 | 85 | 66 | 205 | 18 | 46 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| c0002 | 0/0 | 951 | 10 | 9 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| c0003 | 0/0 | 951 | 2 | 2 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| c0004 | 0/0 | 918 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| c0005 | 0/0 | 951 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 3717 | 52 | 14 | 1 | 34 | 1 | 2 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0002 | 0/0 | 3717 | 51 | 0 | 8 | 35 | 5 | 3 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0003 | 0/0 | 3717 | 32 | 1 | 10 | 12 | 4 | 5 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0004 | 0/0 | 3717 | 31 | 4 | 2 | 23 | 0 | 2 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0005 | 0/0 | 3717 | 30 | 0 | 5 | 19 | 0 | 6 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0006 | 0/0 | 3717 | 29 | 1 | 9 | 17 | 0 | 2 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0007 | 0/0 | 3717 | 23 | 0 | 2 | 18 | 0 | 3 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0008 | 0/0 | 3717 | 20 | 1 | 2 | 12 | 2 | 3 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0009 | 0/0 | 3717 | 16 | 12 | 0 | 3 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0010 | 0/0 | 3717 | 14 | 0 | 6 | 4 | 0 | 4 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0011 | 0/0 | 3717 | 13 | 0 | 2 | 7 | 1 | 3 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0012 | 0/1 | 3717 | 13 | 2 | 2 | 1 | 2 | 5 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0013 | 1/0 | 3717 | 9 | 2 | 2 | 1 | 1 | 2 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0014 | 0/0 | 3717 | 6 | 5 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0015 | 0/0 | 3717 | 5 | 2 | 3 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0016 | 0/0 | 3713 | 5 | 5 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0017 | 0/0 | 3717 | 4 | 4 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0018 | 0/0 | 3717 | 4 | 0 | 0 | 4 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0019 | 0/0 | 3717 | 4 | 4 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0020 | 0/0 | 3717 | 4 | 4 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0021 | 0/0 | 3717 | 4 | 1 | 0 | 2 | 1 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0022 | 0/0 | 3717 | 3 | 3 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0023 | 0/0 | 3717 | 3 | 2 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0024 | 0/0 | 3717 | 3 | 3 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0025 | 0/0 | 3717 | 3 | 0 | 3 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0026 | 0/0 | 3717 | 3 | 0 | 0 | 3 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0027 | 0/0 | 3717 | 2 | 2 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0028 | 0/0 | 3717 | 2 | 2 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0029 | 0/0 | 3717 | 2 | 2 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0030 | 0/0 | 3717 | 2 | 2 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0031 | 0/0 | 3717 | 2 | 0 | 0 | 2 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0032 | 0/0 | 3717 | 2 | 0 | 2 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0033 | 0/0 | 3717 | 2 | 2 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0034 | 0/0 | 3713 | 2 | 2 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0035 | 0/0 | 3717 | 2 | 2 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0036 | 0/0 | 3717 | 2 | 0 | 0 | 0 | 0 | 2 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0037 | 0/0 | 3717 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0038 | 0/0 | 3717 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0039 | 0/0 | 3717 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0040 | 0/0 | 3717 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0041 | 0/0 | 3717 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0042 | 0/0 | 3717 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0043 | 0/0 | 3717 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0044 | 0/0 | 3717 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0045 | 0/0 | 3717 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0046 | 0/0 | 3717 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0047 | 0/0 | 3717 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0048 | 0/0 | 3717 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0049 | 0/0 | 3717 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0050 | 0/0 | 3717 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0051 | 0/0 | 3717 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0052 | 0/0 | 3717 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0053 | 0/0 | 3717 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0054 | 0/0 | 3717 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0055 | 0/0 | 3717 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0056 | 0/0 | 3717 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0057 | 0/0 | 3717 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0058 | 0/0 | 3717 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0059 | 0/0 | 3717 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0060 | 0/0 | 3717 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0061 | 0/0 | 3717 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0062 | 0/0 | 3717 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0063 | 0/0 | 3717 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0064 | 0/0 | 3717 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0065 | 0/0 | 3717 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0066 | 0/0 | 3717 | 1 | 0 | 0 | 0 | 1 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0067 | 0/0 | 3717 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| t0068 | 0/0 | 3717 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0003 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0005 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0009 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0010 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0013 | 0/0 | 3 | 0 | 0 | 1 | 1 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0016 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0035 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0038 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0041 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0044 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0224 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0257 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0340 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0346 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0352 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0353 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0368 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0369 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 951 | 422 | 85 | 66 | 205 | 18 | 46 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0002 | 0/0 | 951 | 10 | 9 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0002c0003 | 0/0 | 951 | 2 | 2 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0003c0004 | 0/0 | 918 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0004c0005 | 0/0 | 951 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4667 | 49 | 12 | 0 | 34 | 1 | 2 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0002 | 0/0 | 4667 | 51 | 0 | 8 | 35 | 5 | 3 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0003 | 0/0 | 4667 | 32 | 1 | 10 | 12 | 4 | 5 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0004 | 0/0 | 4667 | 29 | 3 | 2 | 22 | 0 | 2 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0005 | 0/0 | 4667 | 30 | 0 | 5 | 19 | 0 | 6 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0006 | 0/0 | 4667 | 29 | 1 | 9 | 17 | 0 | 2 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0007 | 0/0 | 4667 | 23 | 0 | 2 | 18 | 0 | 3 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0008 | 0/0 | 4667 | 20 | 1 | 2 | 12 | 2 | 3 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0009 | 0/0 | 4667 | 16 | 12 | 0 | 3 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0010 | 0/0 | 4667 | 14 | 0 | 6 | 4 | 0 | 4 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0011 | 0/0 | 4667 | 13 | 0 | 2 | 7 | 1 | 3 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0012 | 0/1 | 4667 | 13 | 2 | 2 | 1 | 2 | 5 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0013 | 1/0 | 4667 | 9 | 2 | 2 | 1 | 1 | 2 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0014 | 0/0 | 4667 | 3 | 2 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0015 | 0/0 | 4667 | 5 | 2 | 3 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0016 | 0/0 | 4663 | 5 | 5 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0017 | 0/0 | 4667 | 3 | 3 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0018 | 0/0 | 4667 | 4 | 0 | 0 | 4 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0019 | 0/0 | 4667 | 3 | 3 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0020 | 0/0 | 4667 | 3 | 3 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0021 | 0/0 | 4667 | 4 | 1 | 0 | 2 | 1 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0022 | 0/0 | 4667 | 3 | 3 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0023 | 0/0 | 4667 | 2 | 2 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0024 | 0/0 | 4667 | 3 | 3 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0025 | 0/0 | 4667 | 3 | 0 | 3 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0026 | 0/0 | 4667 | 3 | 0 | 0 | 3 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0027 | 0/0 | 4667 | 2 | 2 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0028 | 0/0 | 4667 | 2 | 2 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0029 | 0/0 | 4667 | 2 | 2 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0030 | 0/0 | 4667 | 2 | 2 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0031 | 0/0 | 4667 | 2 | 0 | 0 | 2 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0032 | 0/0 | 4667 | 2 | 0 | 2 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0033 | 0/0 | 4667 | 2 | 2 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0034 | 0/0 | 4663 | 2 | 2 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0035 | 0/0 | 4667 | 2 | 2 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0036 | 0/0 | 4667 | 2 | 0 | 0 | 0 | 0 | 2 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0037 | 0/0 | 4667 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0039 | 0/0 | 4667 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0040 | 0/0 | 4667 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0042 | 0/0 | 4667 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0043 | 0/0 | 4667 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0044 | 0/0 | 4667 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0045 | 0/0 | 4667 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0046 | 0/0 | 4667 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0047 | 0/0 | 4667 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0048 | 0/0 | 4667 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0049 | 0/0 | 4667 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0050 | 0/0 | 4667 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0051 | 0/0 | 4667 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0052 | 0/0 | 4667 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0053 | 0/0 | 4667 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0054 | 0/0 | 4667 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0055 | 0/0 | 4667 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0056 | 0/0 | 4667 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0057 | 0/0 | 4667 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0058 | 0/0 | 4667 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0059 | 0/0 | 4667 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0060 | 0/0 | 4667 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0061 | 0/0 | 4667 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0062 | 0/0 | 4667 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0063 | 0/0 | 4667 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0064 | 0/0 | 4667 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0065 | 0/0 | 4667 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0066 | 0/0 | 4667 | 1 | 0 | 0 | 0 | 1 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0067 | 0/0 | 4667 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0001t0068 | 0/0 | 4667 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0002t0001 | 0/0 | 4667 | 2 | 2 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0002t0004 | 0/0 | 4667 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0002t0014 | 0/0 | 4667 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0002t0017 | 0/0 | 4667 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0002t0019 | 0/0 | 4667 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0002t0020 | 0/0 | 4667 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0002t0023 | 0/0 | 4667 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0002t0038 | 0/0 | 4667 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0001c0002t0041 | 0/0 | 4667 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0002c0003t0014 | 0/0 | 4667 | 2 | 2 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0003c0004t0001 | 0/0 | 4634 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| a0004c0005t0004 | 0/0 | 4667 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | copy fasta | chr12 | 49861896 | 49908900 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0002g0001 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0002g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0002g0010 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0002g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0003g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0003g0013 | 0/0 | 3 | 0 | 0 | 1 | 1 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0003g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0003g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0003g0038 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0003g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0003g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0003g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0003g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0003g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0003g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0003g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0003g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0003g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0003g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0003g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0003g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0003g0368 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0003g0369 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0004g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0004g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0004g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0004g0044 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0004g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0004g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0004g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0004g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0004g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0004g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0004g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0004g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0004g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0004g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0004g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0004g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0004g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0004g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0004g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0005g0005 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0005g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0005g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0005g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0005g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0005g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0005g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0005g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0005g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0005g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0005g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0005g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0005g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0005g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0005g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0005g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0005g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0005g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0005g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0005g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0005g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0005g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0005g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0005g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0005g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0005g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0005g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0006g0003 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0006g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0006g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0006g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0006g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0006g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0006g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0006g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0006g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0006g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0006g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0006g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0006g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0006g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0006g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0006g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0006g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0006g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0006g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0006g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0006g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0006g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0006g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0007g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0007g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0007g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0007g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0007g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0007g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0007g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0007g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0007g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0007g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0007g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0007g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0007g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0007g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0007g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0007g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0007g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0007g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0007g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0007g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0007g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0008g0035 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0008g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0008g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0008g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0008g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0008g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0008g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0008g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0008g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0008g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0008g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0008g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0008g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0008g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0008g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0008g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0008g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0008g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0009g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0009g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0009g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0009g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0009g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0009g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0009g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0009g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0009g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0009g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0009g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0009g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0009g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0009g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0009g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0009g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0010g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0010g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0010g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0010g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0010g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0010g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0010g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0010g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0010g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0010g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0010g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0010g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0011g0041 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0011g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0011g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0011g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0011g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0011g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0011g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0011g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0011g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0011g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0011g0352 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0011g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0012g0257 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0012g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0012g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0012g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0012g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0012g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0012g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0012g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0012g0340 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0012g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0012g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0012g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0012g0353 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0013g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0013g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0013g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0013g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0013g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0013g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0013g0224 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0013g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0014g0009 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0015g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0015g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0015g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0015g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0016g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0016g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0016g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0016g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0016g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0017g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0017g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0018g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0018g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0019g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0019g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0019g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0020g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0020g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0021g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0021g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0021g0346 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0021g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0022g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0022g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0023g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0024g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0025g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0025g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0026g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0026g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0027g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0027g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0028g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0028g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0029g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0029g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0030g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0030g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0031g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0031g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0032g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0033g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0033g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0034g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0034g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0035g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0035g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0036g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0036g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0037g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0039g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0040g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0042g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0043g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0044g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0045g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0046g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0047g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0048g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0049g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0050g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0051g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0052g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0053g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0054g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0055g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0056g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0057g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0058g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0059g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0060g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0061g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0062g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0063g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0064g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0065g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0066g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0067g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0068g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0002t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0002t0004g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0002t0014g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0002t0017g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0002t0019g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0002t0020g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0002t0023g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0002t0038g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0002t0041g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0002c0003t0014g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0003c0004t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0004c0005t0004g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0066 | g0316 | EUR | GBR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0010 | EUR | GBR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG00140 | hp1 | a0001 | c0001 | t0012 | g0353 | EUR | GBR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0369 | EUR | GBR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0187 | EUR | FIN | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG00280 | hp2 | a0001 | c0001 | t0013 | g0120 | EUR | FIN | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0016 | EUR | FIN | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0235 | EUR | FIN | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG00408 | hp1 | a0001 | c0001 | t0008 | g0305 | EAS | CHS | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG00408 | hp2 | a0001 | c0001 | t0009 | g0169 | EAS | CHS | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG00423 | hp1 | a0001 | c0001 | t0007 | g0055 | EAS | CHS | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG00423 | hp2 | a0001 | c0001 | t0048 | g0073 | EAS | CHS | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG00438 | hp1 | a0001 | c0001 | t0007 | g0007 | EAS | CHS | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG00438 | hp2 | a0001 | c0001 | t0008 | g0291 | EAS | CHS | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG00544 | hp1 | a0001 | c0001 | t0004 | g0286 | EAS | CHS | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG00544 | hp2 | a0001 | c0001 | t0013 | g0178 | EAS | CHS | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG00558 | hp1 | a0001 | c0001 | t0004 | g0264 | EAS | CHS | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | CHS | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG00609 | hp2 | a0001 | c0001 | t0011 | g0348 | EAS | CHS | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG00621 | hp1 | a0001 | c0001 | t0007 | g0064 | EAS | CHS | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG00621 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | CHS | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0327 | AMR | PUR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0111 | AMR | PUR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG00642 | hp1 | a0001 | c0001 | t0011 | g0335 | AMR | PUR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG00642 | hp2 | a0001 | c0001 | t0012 | g0345 | AMR | PUR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG00673 | hp1 | a0001 | c0001 | t0005 | g0278 | EAS | CHS | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0293 | EAS | CHS | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG00733 | hp1 | a0001 | c0001 | t0015 | g0027 | AMR | PUR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG00733 | hp2 | a0001 | c0001 | t0007 | g0231 | AMR | PUR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG00735 | hp1 | a0001 | c0001 | t0015 | g0027 | AMR | PUR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG00735 | hp2 | a0001 | c0001 | t0006 | g0003 | AMR | PUR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG00738 | hp1 | a0003 | c0004 | t0001 | g0227 | AMR | PUR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG00738 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | PUR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0358 | AMR | PUR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG00741 | hp2 | a0001 | c0001 | t0060 | g0349 | AMR | PUR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01069 | hp1 | a0001 | c0001 | t0010 | g0018 | AMR | PUR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0188 | AMR | PUR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0037 | AMR | PUR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01070 | hp2 | a0001 | c0001 | t0005 | g0302 | AMR | PUR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01071 | hp1 | a0001 | c0001 | t0010 | g0018 | AMR | PUR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0037 | AMR | PUR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01074 | hp1 | a0001 | c0001 | t0025 | g0273 | AMR | PUR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01074 | hp2 | a0001 | c0001 | t0008 | g0254 | AMR | PUR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01081 | hp1 | a0001 | c0001 | t0008 | g0274 | AMR | PUR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01081 | hp2 | a0001 | c0001 | t0015 | g0232 | AMR | PUR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0189 | AMR | PUR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01099 | hp2 | a0001 | c0001 | t0010 | g0216 | AMR | PUR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0313 | AMR | PUR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01106 | hp2 | a0001 | c0001 | t0053 | g0220 | AMR | PUR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01109 | hp1 | a0001 | c0002 | t0023 | g0157 | AMR | PUR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01109 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | PUR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01167 | hp1 | a0001 | c0001 | t0010 | g0020 | AMR | PUR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01167 | hp2 | a0001 | c0001 | t0014 | g0009 | AMR | PUR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01168 | hp1 | a0001 | c0001 | t0032 | g0023 | AMR | PUR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01168 | hp2 | a0001 | c0001 | t0051 | g0173 | AMR | PUR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01169 | hp1 | a0001 | c0001 | t0032 | g0023 | AMR | PUR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01169 | hp2 | a0001 | c0001 | t0010 | g0020 | AMR | PUR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0249 | AMR | PUR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0312 | AMR | PUR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01192 | hp1 | a0001 | c0001 | t0045 | g0211 | AMR | PUR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0233 | AMR | PUR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0135 | AMR | PUR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0318 | AMR | PUR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01257 | hp1 | a0001 | c0001 | t0025 | g0034 | AMR | CLM | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0217 | AMR | CLM | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01258 | hp1 | a0001 | c0001 | t0025 | g0034 | AMR | CLM | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01258 | hp2 | a0001 | c0001 | t0010 | g0193 | AMR | CLM | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01261 | hp1 | a0001 | c0001 | t0012 | g0298 | AMR | CLM | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01261 | hp2 | a0001 | c0001 | t0006 | g0194 | AMR | CLM | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0199 | AMR | CLM | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01346 | hp2 | a0001 | c0001 | t0007 | g0094 | AMR | CLM | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0289 | AMR | CLM | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0341 | AMR | CLM | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01361 | hp1 | a0001 | c0001 | t0011 | g0252 | AMR | CLM | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01361 | hp2 | a0001 | c0001 | t0006 | g0003 | AMR | CLM | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01433 | hp1 | a0001 | c0001 | t0013 | g0032 | AMR | CLM | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01433 | hp2 | a0001 | c0001 | t0056 | g0354 | AMR | CLM | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01496 | hp1 | a0001 | c0001 | t0006 | g0003 | AMR | CLM | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01496 | hp2 | a0001 | c0001 | t0013 | g0032 | AMR | CLM | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0013 | EUR | IBS | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01515 | hp2 | a0001 | c0001 | t0008 | g0035 | EUR | IBS | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0010 | EUR | IBS | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01516 | hp2 | a0001 | c0001 | t0011 | g0352 | EUR | IBS | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01517 | hp1 | a0001 | c0001 | t0008 | g0035 | EUR | IBS | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0010 | EUR | IBS | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01884 | hp1 | a0001 | c0001 | t0034 | g0238 | AFR | ACB | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01891 | hp1 | a0001 | c0001 | t0017 | g0022 | AFR | ACB | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01891 | hp2 | a0001 | c0001 | t0012 | g0315 | AFR | ACB | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01928 | hp1 | a0001 | c0001 | t0004 | g0336 | AMR | PEL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01928 | hp2 | a0001 | c0001 | t0006 | g0003 | AMR | PEL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01975 | hp1 | a0001 | c0001 | t0005 | g0005 | AMR | PEL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01975 | hp2 | a0001 | c0001 | t0006 | g0229 | AMR | PEL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01978 | hp1 | a0001 | c0001 | t0068 | g0321 | AMR | PEL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01978 | hp2 | a0001 | c0001 | t0006 | g0221 | AMR | PEL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02015 | hp1 | a0001 | c0001 | t0008 | g0308 | EAS | KHV | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02015 | hp2 | a0001 | c0001 | t0005 | g0319 | EAS | KHV | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02027 | hp2 | a0004 | c0005 | t0004 | g0259 | EAS | KHV | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02040 | hp1 | a0001 | c0001 | t0021 | g0275 | EAS | KHV | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02040 | hp2 | a0001 | c0001 | t0005 | g0329 | EAS | KHV | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02055 | hp1 | a0001 | c0001 | t0016 | g0098 | AFR | ACB | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02055 | hp2 | a0001 | c0002 | t0020 | g0106 | AFR | ACB | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02056 | hp1 | a0001 | c0001 | t0005 | g0301 | EAS | KHV | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | KHV | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02071 | hp1 | a0001 | c0001 | t0040 | g0156 | EAS | KHV | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02071 | hp2 | a0001 | c0001 | t0007 | g0007 | EAS | KHV | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | KHV | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02080 | hp2 | a0001 | c0001 | t0050 | g0058 | EAS | KHV | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02083 | hp1 | a0001 | c0001 | t0004 | g0043 | EAS | KHV | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02083 | hp2 | a0001 | c0001 | t0008 | g0295 | EAS | KHV | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | KHV | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02132 | hp1 | a0001 | c0001 | t0065 | g0242 | EAS | KHV | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02132 | hp2 | a0001 | c0001 | t0010 | g0059 | EAS | KHV | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02135 | hp1 | a0001 | c0001 | t0004 | g0292 | EAS | KHV | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02135 | hp2 | a0001 | c0001 | t0012 | g0350 | EAS | KHV | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02145 | hp1 | a0001 | c0001 | t0021 | g0365 | AFR | ACB | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0141 | AFR | ACB | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02148 | hp1 | a0001 | c0001 | t0005 | g0269 | AMR | PEL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02148 | hp2 | a0001 | c0001 | t0006 | g0218 | AMR | PEL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02155 | hp1 | a0001 | c0001 | t0005 | g0270 | EAS | CDX | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02155 | hp2 | a0001 | c0001 | t0007 | g0078 | EAS | CDX | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02165 | hp1 | a0001 | c0001 | t0007 | g0047 | EAS | CDX | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | CDX | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02257 | hp1 | a0001 | c0001 | t0022 | g0021 | AFR | ACB | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02257 | hp2 | a0001 | c0001 | t0009 | g0103 | AFR | ACB | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02258 | hp1 | a0001 | c0001 | t0024 | g0008 | AFR | ACB | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02258 | hp2 | a0001 | c0001 | t0020 | g0145 | AFR | ACB | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02280 | hp1 | a0001 | c0001 | t0062 | g0311 | AFR | ACB | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02280 | hp2 | a0001 | c0001 | t0033 | g0148 | AFR | ACB | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02293 | hp1 | a0001 | c0001 | t0039 | g0092 | AMR | PEL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02293 | hp2 | a0001 | c0001 | t0006 | g0230 | AMR | PEL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0317 | AMR | PEL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0133 | AMR | PEL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02451 | hp2 | a0001 | c0001 | t0035 | g0271 | AFR | ACB | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | KHV | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02523 | hp2 | a0001 | c0001 | t0004 | g0337 | EAS | KHV | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02572 | hp1 | a0001 | c0001 | t0028 | g0163 | AFR | GWD | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02572 | hp2 | a0001 | c0001 | t0058 | g0310 | AFR | GWD | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0368 | SAS | PJL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0013 | SAS | PJL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02615 | hp1 | a0001 | c0001 | t0009 | g0152 | AFR | GWD | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02622 | hp1 | a0001 | c0001 | t0009 | g0162 | AFR | GWD | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02622 | hp2 | a0001 | c0001 | t0044 | g0241 | AFR | GWD | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02630 | hp2 | a0001 | c0001 | t0029 | g0160 | AFR | GWD | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02647 | hp2 | a0001 | c0001 | t0063 | g0362 | AFR | GWD | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02683 | hp1 | a0001 | c0001 | t0012 | g0272 | SAS | PJL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0191 | SAS | PJL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02698 | hp1 | a0001 | c0001 | t0004 | g0044 | SAS | PJL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02698 | hp2 | a0001 | c0001 | t0036 | g0347 | SAS | PJL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02717 | hp1 | a0001 | c0001 | t0009 | g0240 | AFR | GWD | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02717 | hp2 | a0001 | c0002 | t0014 | g0093 | AFR | GWD | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02723 | hp1 | a0001 | c0001 | t0034 | g0146 | AFR | GWD | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02723 | hp2 | a0001 | c0001 | t0030 | g0109 | AFR | GWD | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02735 | hp1 | a0001 | c0001 | t0012 | g0314 | SAS | PJL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02809 | hp1 | a0001 | c0001 | t0030 | g0125 | AFR | GWD | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02809 | hp2 | a0001 | c0001 | t0028 | g0164 | AFR | GWD | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0281 | AFR | GWD | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02895 | hp1 | a0001 | c0001 | t0033 | g0131 | AFR | GWD | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02895 | hp2 | a0002 | c0003 | t0014 | g0019 | AFR | GWD | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02896 | hp1 | a0001 | c0001 | t0020 | g0025 | AFR | GWD | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02897 | hp1 | a0001 | c0001 | t0020 | g0025 | AFR | GWD | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02897 | hp2 | a0002 | c0003 | t0014 | g0019 | AFR | GWD | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02922 | hp1 | a0001 | c0001 | t0015 | g0225 | AFR | ESN | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02922 | hp2 | a0001 | c0001 | t0052 | g0095 | AFR | ESN | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02965 | hp2 | a0001 | c0001 | t0009 | g0112 | AFR | ESN | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02970 | hp1 | a0001 | c0001 | t0023 | g0024 | AFR | ESN | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02970 | hp2 | a0001 | c0001 | t0009 | g0122 | AFR | ESN | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02976 | hp1 | a0001 | c0001 | t0016 | g0136 | AFR | ESN | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02976 | hp2 | a0001 | c0001 | t0042 | g0107 | AFR | ESN | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0192 | SAS | PJL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03017 | hp2 | a0001 | c0001 | t0005 | g0283 | SAS | PJL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03041 | hp2 | a0001 | c0001 | t0009 | g0100 | AFR | GWD | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03098 | hp1 | a0001 | c0001 | t0016 | g0237 | AFR | MSL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0139 | AFR | MSL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03130 | hp1 | a0001 | c0001 | t0035 | g0342 | AFR | ESN | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03130 | hp2 | a0001 | c0002 | t0019 | g0143 | AFR | ESN | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ESN | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03139 | hp2 | a0001 | c0001 | t0015 | g0209 | AFR | ESN | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03209 | hp1 | a0001 | c0001 | t0054 | g0151 | AFR | MSL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03209 | hp2 | a0001 | c0001 | t0043 | g0101 | AFR | MSL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03225 | hp1 | a0001 | c0001 | t0009 | g0144 | AFR | MSL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0255 | AFR | MSL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03239 | hp1 | a0001 | c0001 | t0036 | g0359 | SAS | PJL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03239 | hp2 | a0001 | c0001 | t0037 | g0132 | SAS | PJL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03453 | hp1 | a0001 | c0001 | t0019 | g0150 | AFR | MSL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | MSL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03486 | hp1 | a0001 | c0001 | t0022 | g0123 | AFR | MSL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03486 | hp2 | a0001 | c0001 | t0006 | g0130 | AFR | MSL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0036 | SAS | PJL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03491 | hp1 | a0001 | c0001 | t0004 | g0044 | SAS | PJL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03491 | hp2 | a0001 | c0001 | t0010 | g0114 | SAS | PJL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03492 | hp1 | a0001 | c0001 | t0010 | g0113 | SAS | PJL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0036 | SAS | PJL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03516 | hp1 | a0001 | c0002 | t0041 | g0142 | AFR | ESN | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03516 | hp2 | a0001 | c0001 | t0014 | g0009 | AFR | ESN | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03540 | hp1 | a0001 | c0001 | t0019 | g0124 | AFR | GWD | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03540 | hp2 | a0001 | c0002 | t0004 | g0250 | AFR | GWD | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03579 | hp1 | a0001 | c0001 | t0009 | g0159 | AFR | MSL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03579 | hp2 | a0001 | c0001 | t0029 | g0127 | AFR | MSL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03654 | hp1 | a0001 | c0001 | t0012 | g0296 | SAS | PJL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03654 | hp2 | a0001 | c0001 | t0008 | g0287 | SAS | PJL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03669 | hp1 | a0001 | c0001 | t0012 | g0285 | SAS | PJL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03669 | hp2 | a0001 | c0001 | t0006 | g0134 | SAS | PJL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03688 | hp1 | a0001 | c0001 | t0010 | g0190 | SAS | STU | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03688 | hp2 | a0001 | c0001 | t0012 | g0339 | SAS | STU | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0203 | SAS | PJL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03704 | hp2 | a0001 | c0001 | t0011 | g0041 | SAS | PJL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03710 | hp1 | a0001 | c0001 | t0010 | g0208 | SAS | PJL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03710 | hp2 | a0001 | c0001 | t0005 | g0288 | SAS | PJL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03831 | hp1 | a0001 | c0001 | t0005 | g0300 | SAS | BEB | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03831 | hp2 | a0001 | c0001 | t0007 | g0110 | SAS | BEB | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03834 | hp1 | a0001 | c0001 | t0007 | g0082 | SAS | BEB | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03834 | hp2 | a0001 | c0001 | t0067 | g0266 | SAS | BEB | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03927 | hp1 | a0001 | c0001 | t0013 | g0195 | SAS | BEB | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03927 | hp2 | a0001 | c0001 | t0005 | g0303 | SAS | BEB | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG04115 | hp1 | a0001 | c0001 | t0009 | g0118 | SAS | STU | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG04115 | hp2 | a0001 | c0001 | t0064 | g0299 | SAS | STU | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG04184 | hp1 | a0001 | c0001 | t0008 | g0343 | SAS | BEB | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG04184 | hp2 | a0001 | c0001 | t0011 | g0041 | SAS | BEB | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG04199 | hp1 | a0001 | c0001 | t0006 | g0212 | SAS | STU | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG04199 | hp2 | a0001 | c0001 | t0007 | g0117 | SAS | STU | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG04204 | hp1 | a0001 | c0001 | t0005 | g0290 | SAS | STU | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG04204 | hp2 | a0001 | c0001 | t0011 | g0333 | SAS | STU | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG04228 | hp1 | a0001 | c0001 | t0013 | g0119 | SAS | STU | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG04228 | hp2 | a0001 | c0001 | t0005 | g0280 | SAS | STU | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0363 | AFR | YRI | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18522 | hp2 | a0001 | c0001 | t0016 | g0099 | AFR | YRI | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18612 | hp1 | a0001 | c0001 | t0005 | g0320 | EAS | CHB | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18747 | hp1 | a0001 | c0001 | t0007 | g0051 | EAS | CHB | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18747 | hp2 | a0001 | c0001 | t0011 | g0370 | EAS | CHB | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18906 | hp1 | a0001 | c0001 | t0024 | g0008 | AFR | YRI | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18906 | hp2 | a0001 | c0001 | t0009 | g0184 | AFR | YRI | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18939 | hp1 | a0001 | c0001 | t0005 | g0256 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18940 | hp1 | a0001 | c0001 | t0010 | g0176 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18940 | hp2 | a0001 | c0001 | t0026 | g0039 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18941 | hp1 | a0001 | c0001 | t0046 | g0196 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18941 | hp2 | a0001 | c0001 | t0004 | g0332 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18942 | hp2 | a0001 | c0001 | t0005 | g0355 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18943 | hp1 | a0001 | c0001 | t0007 | g0069 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0367 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18944 | hp1 | a0001 | c0001 | t0018 | g0011 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0338 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18945 | hp1 | a0001 | c0001 | t0010 | g0155 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18945 | hp2 | a0001 | c0001 | t0006 | g0228 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18946 | hp2 | a0001 | c0001 | t0059 | g0263 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18947 | hp2 | a0001 | c0001 | t0006 | g0206 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18948 | hp1 | a0001 | c0001 | t0005 | g0324 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18950 | hp1 | a0001 | c0001 | t0008 | g0307 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18950 | hp2 | a0001 | c0001 | t0006 | g0029 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18953 | hp2 | a0001 | c0001 | t0006 | g0067 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18954 | hp2 | a0001 | c0001 | t0007 | g0089 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18956 | hp1 | a0001 | c0001 | t0031 | g0087 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18957 | hp1 | a0001 | c0001 | t0006 | g0210 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18960 | hp1 | a0001 | c0001 | t0006 | g0029 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18960 | hp2 | a0001 | c0001 | t0006 | g0180 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18961 | hp1 | a0001 | c0001 | t0006 | g0031 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18961 | hp2 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18962 | hp2 | a0001 | c0001 | t0018 | g0154 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18963 | hp1 | a0001 | c0001 | t0011 | g0247 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18963 | hp2 | a0001 | c0001 | t0005 | g0268 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18966 | hp1 | a0001 | c0001 | t0011 | g0244 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18966 | hp2 | a0001 | c0001 | t0026 | g0039 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18967 | hp2 | a0001 | c0001 | t0004 | g0306 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0326 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0334 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18970 | hp1 | a0001 | c0001 | t0008 | g0294 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18971 | hp2 | a0001 | c0001 | t0007 | g0057 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18972 | hp2 | a0001 | c0001 | t0005 | g0360 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18973 | hp1 | a0001 | c0001 | t0006 | g0056 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18973 | hp2 | a0001 | c0001 | t0047 | g0081 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18975 | hp2 | a0001 | c0001 | t0055 | g0061 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0328 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18977 | hp2 | a0001 | c0001 | t0006 | g0070 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18979 | hp2 | a0001 | c0001 | t0007 | g0053 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18980 | hp1 | a0001 | c0001 | t0007 | g0054 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18980 | hp2 | a0001 | c0001 | t0011 | g0246 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18981 | hp1 | a0001 | c0001 | t0008 | g0261 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18983 | hp1 | a0001 | c0001 | t0006 | g0197 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0265 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18986 | hp1 | a0001 | c0001 | t0004 | g0040 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18988 | hp2 | a0001 | c0001 | t0004 | g0045 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0309 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18991 | hp2 | a0001 | c0001 | t0010 | g0205 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18992 | hp1 | a0001 | c0001 | t0008 | g0243 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18993 | hp1 | a0001 | c0001 | t0009 | g0172 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18993 | hp2 | a0001 | c0001 | t0008 | g0042 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18994 | hp2 | a0001 | c0001 | t0008 | g0245 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18998 | hp1 | a0001 | c0001 | t0005 | g0361 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18998 | hp2 | a0001 | c0001 | t0004 | g0366 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18999 | hp1 | a0001 | c0001 | t0018 | g0011 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18999 | hp2 | a0001 | c0001 | t0004 | g0262 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19000 | hp1 | a0001 | c0001 | t0026 | g0325 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19000 | hp2 | a0001 | c0001 | t0006 | g0030 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19002 | hp1 | a0001 | c0001 | t0057 | g0351 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19002 | hp2 | a0001 | c0001 | t0006 | g0167 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19003 | hp1 | a0001 | c0001 | t0004 | g0267 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19003 | hp2 | a0001 | c0001 | t0007 | g0083 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19005 | hp1 | a0001 | c0001 | t0006 | g0031 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19007 | hp2 | a0001 | c0001 | t0007 | g0007 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19010 | hp2 | a0001 | c0001 | t0031 | g0084 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19011 | hp2 | a0001 | c0001 | t0004 | g0282 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19012 | hp1 | a0001 | c0001 | t0009 | g0077 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19012 | hp2 | a0001 | c0001 | t0005 | g0284 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19030 | hp1 | a0001 | c0001 | t0009 | g0129 | AFR | LWK | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19030 | hp2 | a0001 | c0001 | t0016 | g0236 | AFR | LWK | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19043 | hp1 | a0001 | c0001 | t0027 | g0161 | AFR | LWK | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19043 | hp2 | a0001 | c0001 | t0024 | g0008 | AFR | LWK | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19057 | hp2 | a0001 | c0001 | t0005 | g0248 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19058 | hp1 | a0001 | c0001 | t0004 | g0043 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19060 | hp1 | a0001 | c0001 | t0005 | g0356 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19060 | hp2 | a0001 | c0001 | t0004 | g0040 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19063 | hp2 | a0001 | c0001 | t0005 | g0279 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19064 | hp2 | a0001 | c0001 | t0006 | g0068 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19066 | hp1 | a0001 | c0001 | t0004 | g0253 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19066 | hp2 | a0001 | c0001 | t0005 | g0304 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19067 | hp1 | a0001 | c0001 | t0005 | g0258 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19067 | hp2 | a0001 | c0001 | t0004 | g0045 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19072 | hp2 | a0001 | c0001 | t0021 | g0260 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19074 | hp2 | a0001 | c0001 | t0007 | g0207 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19077 | hp1 | a0001 | c0001 | t0004 | g0357 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19077 | hp2 | a0001 | c0001 | t0006 | g0121 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19079 | hp1 | a0001 | c0001 | t0007 | g0075 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19085 | hp2 | a0001 | c0001 | t0007 | g0215 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19086 | hp1 | a0001 | c0001 | t0008 | g0042 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19086 | hp2 | a0001 | c0001 | t0011 | g0331 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19089 | hp2 | a0001 | c0001 | t0011 | g0330 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19090 | hp2 | a0001 | c0001 | t0007 | g0060 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19091 | hp1 | a0001 | c0001 | t0018 | g0011 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19091 | hp2 | a0001 | c0001 | t0008 | g0297 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0276 | AFR | YRI | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19240 | hp2 | a0001 | c0001 | t0017 | g0022 | AFR | YRI | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA20129 | hp1 | a0001 | c0001 | t0014 | g0009 | AFR | ASW | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA20129 | hp2 | a0001 | c0001 | t0027 | g0097 | AFR | ASW | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA20752 | hp1 | a0001 | c0001 | t0012 | g0340 | EUR | TSI | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0038 | EUR | TSI | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0322 | EUR | TSI | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA20805 | hp2 | a0001 | c0001 | t0021 | g0346 | EUR | TSI | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0038 | SAS | GIH | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA20905 | hp2 | a0001 | c0001 | t0008 | g0277 | SAS | GIH | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02109 | hp1 | a0001 | c0001 | t0022 | g0021 | AFR | ACB | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02109 | hp2 | a0001 | c0002 | t0017 | g0138 | AFR | ACB | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02486 | hp1 | a0001 | c0001 | t0061 | g0364 | AFR | ACB | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02486 | hp2 | a0001 | c0001 | t0009 | g0158 | AFR | ACB | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02559 | hp2 | a0001 | c0001 | t0019 | g0104 | AFR | ACB | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03471 | hp1 | a0001 | c0001 | t0049 | g0183 | AFR | MSL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03471 | hp2 | a0001 | c0002 | t0038 | g0140 | AFR | MSL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG06807 | hp1 | a0001 | c0001 | t0013 | g0116 | AFR | USA | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG06807 | hp2 | a0001 | c0001 | t0023 | g0024 | AFR | USA | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18955 | hp1 | a0001 | c0001 | t0006 | g0030 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA20300 | hp1 | a0001 | c0001 | t0012 | g0344 | AFR | USA | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA20300 | hp2 | a0001 | c0001 | t0008 | g0323 | AFR | USA | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA21309 | hp1 | a0001 | c0001 | t0017 | g0214 | AFR | LWK | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA21309 | hp2 | a0001 | c0001 | t0013 | g0226 | AFR | LWK | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0012 | g0257 | REF | REF | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0013 | g0224 | REF | REF | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:49889524
|
G | C | 1 | a0004 | 1 | HG02027.hp2 | missense_variant | MODERATE | c.608C>G | p.Ala203Gly | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 9/12 | 716/4667 | 608/951 | 203/316 | chr12 | 49889524 | ||
| chr12:49897549
|
GTCACCAG others(26): Show |
G | 1 | a0003 | 1 | HG00738.hp1 | disruptive_inframe_deletion&splice_region_variant | MODERATE | c.317_349delTCTACACC others(25): Show |
p.Val106_Thr117delin others(4): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 4/12 | 457/4667 | 317/951 | 106/316 | chr12 | 49897549 | ||
| chr12:49901139
|
C | T | 1 | a0002 | 2 | HG02895.hp2 HG02897.hp2 |
missense_variant | MODERATE | c.202G>A | p.Val68Met | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 2/12 | 310/4667 | 202/951 | 68/316 | chr12 | 49901139 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:49901140
|
A | G | 2 | a0001c0002a0002c0003 | 12 | HG01109.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
synonymous_variant | LOW | c.201T>C | p.Tyr67Tyr | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 2/12 | 309/4667 | 201/951 | 67/316 | chr12 | 49901140 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:49867042
|
T | C | 67 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(64): Show | 376 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(373): Show |
3_prime_UTR_variant | MODIFIER | c.*3462A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 12/12 | 3462 | chr12 | 49867042 | |||||
| chr12:49867059
|
G | C | 1 | a0001c0001t0051 | 1 | HG01168.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3445C>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 12/12 | 3445 | chr12 | 49867059 | |||||
| chr12:49867250
|
G | T | 1 | a0001c0001t0052 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3254C>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 12/12 | 3254 | chr12 | 49867250 | |||||
| chr12:49867274
|
C | T | 2 | a0001c0001t0032a0001c0001t0036 | 4 | HG01168.hp1 HG01169.hp1 HG02698.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3230G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 12/12 | 3230 | chr12 | 49867274 | |||||
| chr12:49867331
|
G | A | 6 | a0001c0001t0019a0001c0001t0022a0001c0001t0028others(3): Show | 12 | HG02109.hp1 HG02257.hp1 HG02486.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3173C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 12/12 | 3173 | chr12 | 49867331 | |||||
| chr12:49867498
|
A | C | 1 | a0001c0001t0044 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3006T>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 12/12 | 3006 | chr12 | 49867498 | |||||
| chr12:49867532
|
C | T | 1 | a0001c0001t0045 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2972G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 12/12 | 2972 | chr12 | 49867532 | |||||
| chr12:49867538
|
T | C | 1 | a0001c0001t0051 | 1 | HG01168.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2966A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 12/12 | 2966 | chr12 | 49867538 | |||||
| chr12:49867546
|
G | T | 33 | a0001c0001t0006a0001c0001t0008a0001c0001t0009others(30): Show | 146 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(143): Show |
3_prime_UTR_variant | MODIFIER | c.*2958C>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 12/12 | 2958 | chr12 | 49867546 | |||||
| chr12:49867691
|
T | C | 7 | a0001c0001t0014a0001c0001t0017a0001c0001t0042others(4): Show | 12 | HG01167.hp2 HG01891.hp1 HG02109.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2813A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 12/12 | 2813 | chr12 | 49867691 | |||||
| chr12:49867691
|
T | G | 1 | a0001c0001t0024 | 3 | HG02258.hp1 NA18906.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2813A>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 12/12 | 2813 | chr12 | 49867691 | |||||
| chr12:49867707
|
T | G | 1 | a0001c0001t0046 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2797A>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 12/12 | 2797 | chr12 | 49867707 | |||||
| chr12:49867899
|
C | G | 2 | a0001c0001t0018a0001c0001t0066 | 5 | HG00099.hp1 NA18944.hp1 NA18962.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2605G>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 12/12 | 2605 | chr12 | 49867899 | |||||
| chr12:49867924
|
C | T | 1 | a0001c0001t0057 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2580G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 12/12 | 2580 | chr12 | 49867924 | |||||
| chr12:49867938
|
C | T | 1 | a0001c0001t0043 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2566G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 12/12 | 2566 | chr12 | 49867938 | |||||
| chr12:49867986
|
C | T | 23 | a0001c0001t0005a0001c0001t0006a0001c0001t0007others(20): Show | 132 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(129): Show |
3_prime_UTR_variant | MODIFIER | c.*2518G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 12/12 | 2518 | chr12 | 49867986 | |||||
| chr12:49868008
|
C | A | 1 | a0001c0001t0059 | 1 | NA18946.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2496G>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 12/12 | 2496 | chr12 | 49868008 | |||||
| chr12:49868026
|
C | T | 13 | a0001c0001t0002a0001c0001t0003a0001c0001t0015others(10): Show | 102 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*2478G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 12/12 | 2478 | chr12 | 49868026 | |||||
| chr12:49868285
|
G | A | 1 | a0001c0001t0060 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2219C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 12/12 | 2219 | chr12 | 49868285 | |||||
| chr12:49868389
|
G | A | 23 | a0001c0001t0005a0001c0001t0006a0001c0001t0007others(20): Show | 133 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*2115C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 12/12 | 2115 | chr12 | 49868389 | |||||
| chr12:49868439
|
T | C | 3 | a0001c0001t0020a0001c0001t0063a0001c0002t0020 | 5 | HG02055.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2065A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 12/12 | 2065 | chr12 | 49868439 | |||||
| chr12:49868478
|
G | A | 1 | a0001c0001t0064 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2026C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 12/12 | 2026 | chr12 | 49868478 | |||||
| chr12:49868564
|
C | T | 1 | a0001c0001t0040 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1940G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 12/12 | 1940 | chr12 | 49868564 | |||||
| chr12:49868846
|
C | T | 1 | a0001c0001t0027 | 2 | NA19043.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1658G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 12/12 | 1658 | chr12 | 49868846 | |||||
| chr12:49868933
|
T | C | 1 | a0001c0001t0048 | 1 | HG00423.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1571A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 12/12 | 1571 | chr12 | 49868933 | |||||
| chr12:49869178
|
G | A | 1 | a0001c0001t0026 | 3 | NA18940.hp2 NA18966.hp2 NA19000.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1326C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 12/12 | 1326 | chr12 | 49869178 | |||||
| chr12:49869192
|
T | C | 1 | a0001c0001t0049 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1312A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 12/12 | 1312 | chr12 | 49869192 | |||||
| chr12:49869210
|
C | A | 2 | a0001c0001t0031a0001c0001t0065 | 3 | HG02132.hp1 NA18956.hp1 NA19010.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1294G>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 12/12 | 1294 | chr12 | 49869210 | |||||
| chr12:49869234
|
G | A | 1 | a0001c0001t0050 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1270C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 12/12 | 1270 | chr12 | 49869234 | |||||
| chr12:49869365
|
G | A | 13 | a0001c0001t0002a0001c0001t0003a0001c0001t0015others(10): Show | 102 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*1139C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 12/12 | 1139 | chr12 | 49869365 | |||||
| chr12:49869487
|
A | G | 1 | a0001c0001t0039 | 1 | HG02293.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1017T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 12/12 | 1017 | chr12 | 49869487 | |||||
| chr12:49869542
|
G | A | 3 | a0001c0001t0024a0001c0001t0033a0001c0001t0052 | 6 | HG02258.hp1 HG02280.hp2 HG02895.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*962C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 12/12 | 962 | chr12 | 49869542 | |||||
| chr12:49869587
|
C | G | 1 | a0001c0002t0038 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*917G>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 12/12 | 917 | chr12 | 49869587 | |||||
| chr12:49869668
|
AAGTG | A | 2 | a0001c0001t0016a0001c0001t0034 | 7 | HG01884.hp1 HG02055.hp1 HG02723.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*832_*835delCACT | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 12/12 | 832 | chr12 | 49869668 | |||||
| chr12:49869728
|
G | A | 1 | a0001c0001t0053 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*776C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 12/12 | 776 | chr12 | 49869728 | |||||
| chr12:49869801
|
G | A | 1 | a0001c0001t0054 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*703C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 12/12 | 703 | chr12 | 49869801 | |||||
| chr12:49869945
|
T | C | 1 | a0001c0001t0055 | 1 | NA18975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*559A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 12/12 | 559 | chr12 | 49869945 | |||||
| chr12:49870295
|
G | C | 1 | a0001c0001t0068 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*209C>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 12/12 | 209 | chr12 | 49870295 | |||||
| chr12:49870483
|
C | T | 2 | a0001c0001t0037a0001c0001t0056 | 2 | HG01433.hp2 HG03239.hp2 |
3_prime_UTR_variant | MODIFIER | c.*21G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 12/12 | 21 | chr12 | 49870483 | |||||
| chr12:49903887
|
T | C | 26 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(23): Show | 166 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(163): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-95A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 1/12 | chr12 | 49903887 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:49870838
|
G | C | 1 | a0001c0001t0001g0147 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.802-185C>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49870838 | ||||||
| chr12:49871019
|
G | A | 291 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0052others(288): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.802-366C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49871019 | ||||||
| chr12:49871027
|
C | T | 1 | a0001c0001t0045g0211 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.802-374G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49871027 | ||||||
| chr12:49871133
|
C | G | 3 | a0001c0001t0009g0152a0001c0001t0009g0240a0001c0001t0044g0241 | 3 | HG02615.hp1 HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.802-480G>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49871133 | ||||||
| chr12:49871277
|
C | A | 1 | a0001c0001t0011g0041 | 2 | HG03704.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.802-624G>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49871277 | ||||||
| chr12:49871576
|
T | C | 1 | a0001c0001t0006g0210 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.802-923A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49871576 | ||||||
| chr12:49871616
|
G | A | 8 | a0001c0001t0009g0100a0001c0001t0009g0103a0001c0001t0009g0129others(5): Show | 8 | HG02145.hp1 HG02257.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.802-963C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49871616 | ||||||
| chr12:49871640
|
T | C | 1 | a0001c0001t0007g0047 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.802-987A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49871640 | ||||||
| chr12:49871646
|
T | C | 1 | a0001c0001t0028g0164 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.802-993A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49871646 | ||||||
| chr12:49871649
|
T | C | 3 | a0001c0001t0003g0309a0001c0001t0003g0328a0001c0001t0003g0367 | 3 | NA18943.hp2 NA18977.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.802-996A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49871649 | ||||||
| chr12:49871669
|
C | CT | 8 | a0001c0001t0009g0152a0001c0001t0009g0240a0001c0001t0017g0022others(5): Show | 10 | HG01891.hp1 HG02109.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.802-1017dupA | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49871669 | ||||||
| chr12:49871669
|
C | CTTTT | 8 | a0001c0001t0009g0100a0001c0001t0009g0103a0001c0001t0009g0129others(5): Show | 8 | HG02145.hp1 HG02257.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.802-1020_802-1017d others(6): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49871669 | ||||||
| chr12:49871669
|
CT | C | 124 | a0001c0001t0004g0276a0001c0001t0004g0306a0001c0001t0004g0337others(121): Show | 142 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.802-1017delA | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49871669 | ||||||
| chr12:49871714
|
C | G | 1 | a0001c0001t0008g0294 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.802-1061G>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49871714 | ||||||
| chr12:49871769
|
C | T | 6 | a0001c0001t0004g0276a0001c0001t0022g0021a0001c0001t0022g0123others(3): Show | 7 | HG02109.hp1 HG02257.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.802-1116G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49871769 | ||||||
| chr12:49871770
|
G | A | 6 | a0001c0001t0007g0094a0001c0001t0019g0104a0001c0001t0019g0124others(3): Show | 6 | HG01346.hp2 HG02486.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.802-1117C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49871770 | ||||||
| chr12:49872070
|
C | T | 276 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0052others(273): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.802-1417G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49872070 | ||||||
| chr12:49872148
|
G | A | 3 | a0001c0001t0009g0152a0001c0001t0009g0240a0001c0001t0044g0241 | 3 | HG02615.hp1 HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.802-1495C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49872148 | ||||||
| chr12:49872174
|
G | A | 1 | a0001c0001t0042g0107 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.802-1521C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49872174 | ||||||
| chr12:49872294
|
CTGAGGCT others(5): Show |
C | 1 | a0001c0001t0002g0189 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.802-1653_802-1642d others(14): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49872294 | ||||||
| chr12:49872381
|
G | A | 237 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0052others(234): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.802-1728C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49872381 | ||||||
| chr12:49872432
|
T | C | 8 | a0001c0001t0009g0100a0001c0001t0009g0103a0001c0001t0009g0129others(5): Show | 8 | HG02145.hp1 HG02257.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.802-1779A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49872432 | ||||||
| chr12:49872441
|
C | T | 1 | a0001c0001t0021g0365 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.802-1788G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49872441 | ||||||
| chr12:49872466
|
G | A | 8 | a0001c0001t0009g0100a0001c0001t0009g0103a0001c0001t0009g0129others(5): Show | 8 | HG02145.hp1 HG02257.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.802-1813C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49872466 | ||||||
| chr12:49872488
|
C | T | 3 | a0001c0001t0009g0158a0001c0001t0009g0159a0001c0001t0009g0162 | 3 | HG02486.hp2 HG02622.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.802-1835G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49872488 | ||||||
| chr12:49872496
|
T | C | 281 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0052others(278): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.802-1843A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49872496 | ||||||
| chr12:49872589
|
A | G | 1 | a0001c0001t0001g0086 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.802-1936T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49872589 | ||||||
| chr12:49872590
|
A | G | 43 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0052others(40): Show | 49 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.802-1937T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49872590 | ||||||
| chr12:49872987
|
A | G | 8 | a0001c0001t0009g0100a0001c0001t0009g0103a0001c0001t0009g0129others(5): Show | 8 | HG02145.hp1 HG02257.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.802-2334T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49872987 | ||||||
| chr12:49873075
|
C | G | 281 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0052others(278): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.802-2422G>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49873075 | ||||||
| chr12:49873345
|
T | A | 1 | a0001c0001t0009g0112 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.802-2692A>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49873345 | ||||||
| chr12:49873464
|
T | C | 1 | a0001c0001t0016g0236 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.802-2811A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49873464 | ||||||
| chr12:49873552
|
C | T | 162 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0052others(159): Show | 186 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.802-2899G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49873552 | ||||||
| chr12:49873564
|
A | G | 1 | a0001c0001t0009g0122 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.802-2911T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49873564 | ||||||
| chr12:49873654
|
C | T | 4 | a0001c0001t0017g0022a0001c0002t0014g0093a0001c0002t0017g0138others(1): Show | 6 | HG01891.hp1 HG02109.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.802-3001G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49873654 | ||||||
| chr12:49873830
|
G | C | 281 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0052others(278): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.802-3177C>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49873830 | ||||||
| chr12:49874203
|
A | G | 5 | a0001c0001t0009g0100a0001c0001t0009g0103a0001c0001t0009g0129others(2): Show | 5 | HG02145.hp1 HG02257.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.802-3550T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49874203 | ||||||
| chr12:49874216
|
G | C | 1 | a0001c0001t0004g0363 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.802-3563C>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49874216 | ||||||
| chr12:49874238
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.802-3585C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49874238 | ||||||
| chr12:49874341
|
AGGAAAGG others(3): Show |
A | 1 | a0001c0001t0004g0255 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.802-3698_802-3689d others(12): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49874341 | ||||||
| chr12:49874371
|
C | CTGA | 4 | a0001c0001t0001g0096a0001c0001t0001g0102a0001c0001t0001g0105others(1): Show | 4 | HG01884.hp2 HG02451.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.802-3721_802-3719d others(5): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49874371 | ||||||
| chr12:49874509
|
T | C | 1 | a0001c0001t0030g0109 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.802-3856A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49874509 | ||||||
| chr12:49874523
|
G | C | 1 | a0001c0001t0007g0094 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.802-3870C>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49874523 | ||||||
| chr12:49874749
|
G | A | 1 | a0001c0001t0010g0018 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.802-4096C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49874749 | ||||||
| chr12:49874856
|
G | A | 6 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0177others(3): Show | 14 | HG00609.hp1 NA18939.hp2 NA18947.hp1 others(11): Show |
intron_variant | MODIFIER | c.802-4203C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49874856 | ||||||
| chr12:49874951
|
G | A | 1 | a0001c0001t0007g0078 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.802-4298C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49874951 | ||||||
| chr12:49874985
|
C | T | 1 | a0001c0001t0003g0037 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.802-4332G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49874985 | ||||||
| chr12:49875217
|
T | C | 1 | a0001c0001t0003g0338 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.802-4564A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49875217 | ||||||
| chr12:49875428
|
T | C | 1 | a0001c0001t0011g0252 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.802-4775A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49875428 | ||||||
| chr12:49875516
|
C | T | 6 | a0001c0001t0001g0149a0001c0001t0016g0136a0001c0001t0049g0183others(3): Show | 6 | HG02145.hp2 HG02896.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.802-4863G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49875516 | ||||||
| chr12:49875635
|
G | A | 1 | a0001c0001t0009g0077 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.802-4982C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49875635 | ||||||
| chr12:49875780
|
G | A | 41 | a0001c0001t0001g0015a0001c0001t0001g0076a0001c0001t0001g0088others(38): Show | 47 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.802-5127C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49875780 | ||||||
| chr12:49875962
|
T | C | 59 | a0001c0001t0001g0015a0001c0001t0001g0076a0001c0001t0001g0088others(56): Show | 68 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.802-5309A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49875962 | ||||||
| chr12:49875975
|
C | T | 3 | a0001c0001t0009g0152a0001c0001t0009g0240a0001c0001t0044g0241 | 3 | HG02615.hp1 HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.802-5322G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49875975 | ||||||
| chr12:49875979
|
A | G | 58 | a0001c0001t0001g0015a0001c0001t0001g0076a0001c0001t0001g0088others(55): Show | 67 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.802-5326T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49875979 | ||||||
| chr12:49876080
|
C | T | 9 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0048others(6): Show | 20 | HG00609.hp1 NA18939.hp2 NA18947.hp1 others(17): Show |
intron_variant | MODIFIER | c.802-5427G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49876080 | ||||||
| chr12:49876112
|
A | G | 58 | a0001c0001t0001g0015a0001c0001t0001g0076a0001c0001t0001g0088others(55): Show | 67 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.802-5459T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49876112 | ||||||
| chr12:49876329
|
C | A | 4 | a0001c0001t0002g0133a0001c0001t0003g0249a0001c0001t0003g0322others(1): Show | 4 | HG01175.hp1 HG01978.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.802-5676G>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49876329 | ||||||
| chr12:49876330
|
G | A | 1 | a0001c0001t0015g0027 | 2 | HG00733.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.802-5677C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49876330 | ||||||
| chr12:49876379
|
T | C | 2 | a0001c0001t0027g0097a0001c0001t0027g0161 | 2 | NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.802-5726A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49876379 | ||||||
| chr12:49876385
|
A | G | 12 | a0001c0001t0004g0276a0001c0001t0014g0009a0001c0001t0016g0236others(9): Show | 15 | HG01167.hp2 HG01884.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.802-5732T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49876385 | ||||||
| chr12:49876470
|
G | A | 1 | a0001c0001t0051g0173 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.802-5817C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49876470 | ||||||
| chr12:49876548
|
T | G | 299 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0052others(296): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.802-5895A>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49876548 | ||||||
| chr12:49876581
|
G | C | 72 | a0001c0001t0001g0185a0001c0001t0002g0001a0001c0001t0002g0002others(69): Show | 98 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.802-5928C>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49876581 | ||||||
| chr12:49876591
|
G | A | 1 | a0001c0001t0009g0112 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.802-5938C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49876591 | ||||||
| chr12:49876599
|
T | TA | 19 | a0001c0001t0002g0187a0001c0001t0004g0255a0001c0001t0004g0336others(16): Show | 21 | HG00280.hp1 HG00642.hp1 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.802-5947dupT | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49876599 | ||||||
| chr12:49876599
|
TA | T | 134 | a0001c0001t0001g0028a0001c0001t0001g0052a0001c0001t0001g0074others(131): Show | 152 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.802-5947delT | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49876599 | ||||||
| chr12:49876633
|
G | A | 3 | a0001c0001t0003g0369a0001c0001t0015g0232a0001c0001t0067g0266 | 3 | HG00140.hp2 HG01081.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.802-5980C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49876633 | ||||||
| chr12:49876638
|
G | T | 5 | a0001c0001t0017g0022a0001c0002t0014g0093a0001c0002t0017g0138others(2): Show | 7 | HG01891.hp1 HG02109.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.802-5985C>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49876638 | ||||||
| chr12:49876771
|
A | T | 1 | a0001c0001t0043g0101 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.802-6118T>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49876771 | ||||||
| chr12:49876920
|
T | G | 2 | a0001c0001t0011g0252a0001c0001t0012g0340 | 2 | HG01361.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.802-6267A>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49876920 | ||||||
| chr12:49877054
|
C | T | 1 | a0001c0001t0008g0308 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.802-6401G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49877054 | ||||||
| chr12:49877072
|
T | G | 78 | a0001c0001t0001g0096a0001c0001t0001g0115a0001c0001t0001g0185others(75): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.802-6419A>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49877072 | ||||||
| chr12:49877204
|
A | AG | 6 | a0001c0001t0014g0009a0001c0001t0016g0236a0001c0001t0016g0237others(3): Show | 8 | HG01167.hp2 HG01884.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.802-6552dupC | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49877204 | ||||||
| chr12:49877262
|
G | T | 291 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0052others(288): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.802-6609C>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49877262 | ||||||
| chr12:49877340
|
G | A | 1 | a0001c0001t0027g0161 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.802-6687C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49877340 | ||||||
| chr12:49877346
|
T | A | 1 | a0001c0001t0027g0161 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.802-6693A>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49877346 | ||||||
| chr12:49877367
|
G | A | 1 | a0001c0001t0002g0049 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.802-6714C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49877367 | ||||||
| chr12:49877421
|
G | A | 2 | a0001c0001t0031g0087a0001c0001t0065g0242 | 2 | HG02132.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.802-6768C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49877421 | ||||||
| chr12:49877509
|
T | TAAGTCTA others(102): Show |
285 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0052others(282): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.802-6857_802-6856i others(111): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49877509 | ||||||
| chr12:49877509
|
T | TAAGTCTA others(211): Show |
7 | a0001c0001t0004g0044a0001c0001t0009g0158a0001c0001t0009g0159others(4): Show | 10 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.802-6857_802-6856i others(220): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49877509 | ||||||
| chr12:49877589
|
G | T | 293 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0052others(290): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.802-6936C>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49877589 | ||||||
| chr12:49877685
|
GC | G | 6 | a0001c0001t0014g0009a0001c0001t0016g0236a0001c0001t0016g0237others(3): Show | 8 | HG01167.hp2 HG01884.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.802-7033delG | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49877685 | ||||||
| chr12:49877687
|
C | G | 6 | a0001c0001t0014g0009a0001c0001t0016g0236a0001c0001t0016g0237others(3): Show | 8 | HG01167.hp2 HG01884.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.802-7034G>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49877687 | ||||||
| chr12:49877712
|
C | A | 3 | a0001c0001t0031g0084a0001c0001t0031g0087a0001c0001t0065g0242 | 3 | HG02132.hp1 NA18956.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.802-7059G>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49877712 | ||||||
| chr12:49877713
|
G | A | 1 | a0001c0001t0001g0050 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.802-7060C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49877713 | ||||||
| chr12:49877714
|
C | T | 135 | a0001c0001t0001g0028a0001c0001t0001g0052a0001c0001t0001g0074others(132): Show | 153 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.802-7061G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49877714 | ||||||
| chr12:49877767
|
T | C | 1 | a0001c0001t0004g0255 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.802-7114A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49877767 | ||||||
| chr12:49877770
|
G | C | 1 | a0001c0002t0017g0138 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.802-7117C>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49877770 | ||||||
| chr12:49877782
|
G | A | 6 | a0001c0001t0009g0152a0001c0001t0009g0240a0001c0001t0015g0209others(3): Show | 6 | HG01168.hp2 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.802-7129C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49877782 | ||||||
| chr12:49877826
|
CTA | C | 11 | a0001c0001t0001g0128a0001c0001t0001g0137a0001c0001t0001g0149others(8): Show | 11 | HG02145.hp2 HG02896.hp2 HG02976.hp1 others(8): Show |
intron_variant | MODIFIER | c.802-7175_802-7174d others(4): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49877826 | ||||||
| chr12:49877833
|
C | T | 1 | a0001c0001t0036g0347 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.802-7180G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49877833 | ||||||
| chr12:49877834
|
G | A | 16 | a0001c0001t0001g0126a0001c0001t0001g0128a0001c0001t0001g0137others(13): Show | 18 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.802-7181C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49877834 | ||||||
| chr12:49877884
|
G | GTATACAT others(1): Show |
4 | a0001c0001t0020g0025a0001c0001t0020g0145a0001c0001t0063g0362others(1): Show | 5 | HG02055.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.802-7232_802-7231i others(10): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49877884 | ||||||
| chr12:49877892
|
G | A | 1 | a0001c0001t0026g0325 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.802-7239C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49877892 | ||||||
| chr12:49877933
|
T | C | 6 | a0001c0001t0014g0009a0001c0001t0016g0236a0001c0001t0016g0237others(3): Show | 8 | HG01167.hp2 HG01884.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.802-7280A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49877933 | ||||||
| chr12:49877949
|
CGTATGTG others(3): Show |
C | 3 | a0001c0001t0009g0152a0001c0001t0009g0240a0001c0001t0044g0241 | 3 | HG02615.hp1 HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.802-7306_802-7297d others(12): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49877949 | ||||||
| chr12:49877956
|
GTGTGTA | G | 16 | a0001c0001t0001g0126a0001c0001t0001g0128a0001c0001t0001g0137others(13): Show | 18 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.802-7309_802-7304d others(8): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49877956 | ||||||
| chr12:49877970
|
G | GTGTATGT others(9): Show |
6 | a0001c0001t0004g0276a0001c0001t0022g0021a0001c0001t0022g0123others(3): Show | 7 | HG02109.hp1 HG02257.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.802-7318_802-7317i others(18): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49877970 | ||||||
| chr12:49877997
|
T | C | 56 | a0001c0001t0001g0015a0001c0001t0001g0076a0001c0001t0001g0088others(53): Show | 66 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.802-7344A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49877997 | ||||||
| chr12:49878061
|
C | CGT | 153 | a0001c0001t0001g0015a0001c0001t0001g0076a0001c0001t0001g0088others(150): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.802-7410_802-7409d others(4): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878061 | ||||||
| chr12:49878061
|
CGT | C | 6 | a0001c0001t0009g0152a0001c0001t0009g0240a0001c0001t0015g0209others(3): Show | 6 | HG01168.hp2 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.802-7410_802-7409d others(4): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878061 | ||||||
| chr12:49878063
|
TGTATGTG others(1255): Show |
T | 134 | a0001c0001t0001g0028a0001c0001t0001g0052a0001c0001t0001g0074others(131): Show | 152 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.801+8061_802-7411d others(2): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878063 | ||||||
| chr12:49878079
|
TGTGCATG others(1267): Show |
T | 1 | a0001c0001t0006g0230 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.801+8033_802-7427d others(2): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878079 | ||||||
| chr12:49878089
|
AGTGCATG others(3): Show |
A | 44 | a0001c0001t0001g0015a0001c0001t0001g0076a0001c0001t0001g0088others(41): Show | 50 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.802-7446_802-7437d others(12): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878089 | ||||||
| chr12:49878099
|
T | A | 6 | a0001c0001t0014g0009a0001c0001t0016g0236a0001c0001t0016g0237others(3): Show | 8 | HG01167.hp2 HG01884.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.802-7446A>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878099 | ||||||
| chr12:49878111
|
T | TGC | 6 | a0001c0001t0014g0009a0001c0001t0016g0236a0001c0001t0016g0237others(3): Show | 8 | HG01167.hp2 HG01884.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.802-7459_802-7458i others(4): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878111 | ||||||
| chr12:49878117
|
G | T | 22 | a0001c0001t0001g0126a0001c0001t0001g0128a0001c0001t0001g0137others(19): Show | 26 | HG01167.hp2 HG01884.hp1 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.802-7464C>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878117 | ||||||
| chr12:49878155
|
T | A | 6 | a0001c0001t0014g0009a0001c0001t0016g0236a0001c0001t0016g0237others(3): Show | 8 | HG01167.hp2 HG01884.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.802-7502A>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878155 | ||||||
| chr12:49878177
|
T | C | 2 | a0001c0001t0014g0009a0001c0001t0058g0310 | 4 | HG01167.hp2 HG02572.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.802-7524A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878177 | ||||||
| chr12:49878184
|
ATG | A | 158 | a0001c0001t0001g0015a0001c0001t0001g0076a0001c0001t0001g0088others(155): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.802-7533_802-7532d others(4): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878184 | ||||||
| chr12:49878262
|
ATG | A | 50 | a0001c0001t0001g0015a0001c0001t0001g0076a0001c0001t0001g0088others(47): Show | 58 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.802-7611_802-7610d others(4): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878262 | ||||||
| chr12:49878280
|
C | G | 158 | a0001c0001t0001g0015a0001c0001t0001g0076a0001c0001t0001g0088others(155): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.802-7627G>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878280 | ||||||
| chr12:49878291
|
T | C | 1 | a0001c0001t0002g0188 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.802-7638A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878291 | ||||||
| chr12:49878312
|
G | A | 1 | a0001c0001t0013g0226 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.802-7659C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878312 | ||||||
| chr12:49878377
|
C | A | 158 | a0001c0001t0001g0015a0001c0001t0001g0076a0001c0001t0001g0088others(155): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.802-7724G>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878377 | ||||||
| chr12:49878392
|
G | GTGTGTGC others(7): Show |
8 | a0001c0001t0001g0128a0001c0001t0001g0137a0001c0001t0001g0149others(5): Show | 8 | HG02145.hp2 HG02896.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.802-7740_802-7739i others(16): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878392 | ||||||
| chr12:49878392
|
G | GTGTGTGC others(9): Show |
8 | a0001c0001t0002g0048a0001c0001t0003g0004a0001c0001t0014g0009others(5): Show | 13 | HG01167.hp2 HG01884.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.802-7740_802-7739i others(18): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878392 | ||||||
| chr12:49878392
|
G | GTGTGTGT others(7): Show |
1 | a0001c0001t0033g0131 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.802-7740_802-7739i others(16): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878392 | ||||||
| chr12:49878392
|
G | GTGTGTGT others(9): Show |
7 | a0001c0001t0001g0126a0001c0001t0017g0022a0001c0001t0017g0214others(4): Show | 9 | HG01891.hp1 HG02109.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.802-7740_802-7739i others(18): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878392 | ||||||
| chr12:49878392
|
G | GTGTGTGT others(11): Show |
134 | a0001c0001t0001g0015a0001c0001t0001g0076a0001c0001t0001g0088others(131): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.802-7740_802-7739i others(20): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878392 | ||||||
| chr12:49878416
|
ATG | A | 74 | a0001c0001t0001g0015a0001c0001t0001g0076a0001c0001t0001g0088others(71): Show | 86 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.802-7765_802-7764d others(4): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878416 | ||||||
| chr12:49878440
|
GTGTC | G | 9 | a0001c0001t0001g0128a0001c0001t0001g0137a0001c0001t0001g0149others(6): Show | 9 | HG02145.hp2 HG02896.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.802-7791_802-7788d others(6): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878440 | ||||||
| chr12:49878477
|
CAT | C | 78 | a0001c0001t0001g0096a0001c0001t0001g0115a0001c0001t0001g0185others(75): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.802-7826_802-7825d others(4): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878477 | ||||||
| chr12:49878489
|
T | C | 1 | a0001c0001t0012g0285 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.802-7836A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878489 | ||||||
| chr12:49878502
|
G | A | 6 | a0001c0001t0004g0276a0001c0001t0022g0021a0001c0001t0022g0123others(3): Show | 7 | HG02109.hp1 HG02257.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.802-7849C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878502 | ||||||
| chr12:49878522
|
CTG | C | 148 | a0001c0001t0001g0015a0001c0001t0001g0076a0001c0001t0001g0088others(145): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.802-7871_802-7870d others(4): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878522 | ||||||
| chr12:49878522
|
CTGTG | C | 9 | a0001c0001t0009g0118a0001c0001t0014g0009a0001c0001t0016g0236others(6): Show | 11 | HG01167.hp2 HG01884.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.802-7873_802-7870d others(6): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878522 | ||||||
| chr12:49878530
|
G | A | 1 | a0001c0001t0016g0099 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.802-7877C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878530 | ||||||
| chr12:49878559
|
AGT | A | 157 | a0001c0001t0001g0015a0001c0001t0001g0076a0001c0001t0001g0088others(154): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.802-7908_802-7907d others(4): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878559 | ||||||
| chr12:49878563
|
T | A | 1 | a0001c0001t0002g0213 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.802-7910A>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878563 | ||||||
| chr12:49878581
|
T | C | 2 | a0001c0001t0027g0097a0001c0001t0027g0161 | 2 | NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.802-7928A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878581 | ||||||
| chr12:49878600
|
G | GTGCA | 6 | a0001c0001t0001g0096a0001c0001t0001g0115a0001c0001t0010g0020others(3): Show | 7 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.802-7948_802-7947i others(6): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878600 | ||||||
| chr12:49878600
|
G | GTGTGCA | 74 | a0001c0001t0001g0185a0001c0001t0002g0001a0001c0001t0002g0002others(71): Show | 100 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.802-7953_802-7948d others(8): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878600 | ||||||
| chr12:49878600
|
G | GTGTGCAT others(13): Show |
84 | a0001c0001t0001g0015a0001c0001t0001g0076a0001c0001t0001g0088others(81): Show | 97 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.802-7967_802-7948d others(22): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878600 | ||||||
| chr12:49878674
|
ATG | A | 2 | a0001c0001t0004g0363a0001c0001t0023g0024 | 3 | HG02970.hp1 HG06807.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.802-8023_802-8022d others(4): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878674 | ||||||
| chr12:49878715
|
C | CGT | 6 | a0001c0001t0004g0276a0001c0001t0022g0021a0001c0001t0022g0123others(3): Show | 7 | HG02109.hp1 HG02257.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.802-8064_802-8063d others(4): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878715 | ||||||
| chr12:49878718
|
G | A | 73 | a0001c0001t0001g0185a0001c0001t0002g0001a0001c0001t0002g0002others(70): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.802-8065C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878718 | ||||||
| chr12:49878718
|
G | GTGTA | 85 | a0001c0001t0001g0015a0001c0001t0001g0076a0001c0001t0001g0088others(82): Show | 98 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.802-8066_802-8065i others(6): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878718 | ||||||
| chr12:49878724
|
C | T | 1 | a0001c0001t0009g0112 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.802-8071G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878724 | ||||||
| chr12:49878725
|
T | G | 50 | a0001c0001t0001g0015a0001c0001t0001g0076a0001c0001t0001g0088others(47): Show | 58 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.802-8072A>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878725 | ||||||
| chr12:49878735
|
TGA | T | 4 | a0001c0001t0017g0022a0001c0002t0014g0093a0001c0002t0017g0138others(1): Show | 6 | HG01891.hp1 HG02109.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.802-8084_802-8083d others(4): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878735 | ||||||
| chr12:49878742
|
A | G | 2 | a0001c0001t0027g0097a0001c0001t0027g0161 | 2 | NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.802-8089T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878742 | ||||||
| chr12:49878800
|
A | ATGTGCGT others(9): Show |
158 | a0001c0001t0001g0015a0001c0001t0001g0076a0001c0001t0001g0088others(155): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.802-8148_802-8147i others(18): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878800 | ||||||
| chr12:49878852
|
ATG | A | 157 | a0001c0001t0001g0015a0001c0001t0001g0076a0001c0001t0001g0088others(154): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.802-8201_802-8200d others(4): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878852 | ||||||
| chr12:49878869
|
TGTGA | T | 158 | a0001c0001t0001g0015a0001c0001t0001g0076a0001c0001t0001g0088others(155): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.802-8220_802-8217d others(6): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878869 | ||||||
| chr12:49878884
|
A | AGG | 50 | a0001c0001t0001g0015a0001c0001t0001g0076a0001c0001t0001g0088others(47): Show | 58 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.802-8232_802-8231i others(4): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878884 | ||||||
| chr12:49878887
|
T | C | 50 | a0001c0001t0001g0015a0001c0001t0001g0076a0001c0001t0001g0088others(47): Show | 58 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.802-8234A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878887 | ||||||
| chr12:49878887
|
T | TGC | 108 | a0001c0001t0001g0096a0001c0001t0001g0115a0001c0001t0001g0126others(105): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.802-8235_802-8234i others(4): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878887 | ||||||
| chr12:49878907
|
C | T | 157 | a0001c0001t0001g0015a0001c0001t0001g0076a0001c0001t0001g0088others(154): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.802-8254G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878907 | ||||||
| chr12:49878966
|
G | T | 2 | a0001c0001t0027g0097a0001c0001t0027g0161 | 2 | NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.802-8313C>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878966 | ||||||
| chr12:49878979
|
T | G | 4 | a0001c0001t0010g0205a0001c0001t0011g0244a0001c0001t0011g0246others(1): Show | 4 | NA18963.hp1 NA18966.hp1 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.802-8326A>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878979 | ||||||
| chr12:49878983
|
CAT | C | 4 | a0001c0001t0001g0076a0001c0001t0001g0198a0001c0001t0004g0045others(1): Show | 5 | HG00558.hp1 HG02074.hp2 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.802-8332_802-8331d others(4): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49878983 | ||||||
| chr12:49879008
|
ATGTG | A | 6 | a0001c0001t0009g0152a0001c0001t0009g0240a0001c0001t0015g0209others(3): Show | 6 | HG01168.hp2 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.802-8359_802-8356d others(6): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879008 | ||||||
| chr12:49879028
|
GTGTC | G | 6 | a0001c0001t0014g0009a0001c0001t0016g0236a0001c0001t0016g0237others(3): Show | 8 | HG01167.hp2 HG01884.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.801+8354_801+8357d others(6): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879028 | ||||||
| chr12:49879046
|
T | G | 78 | a0001c0001t0001g0096a0001c0001t0001g0115a0001c0001t0001g0185others(75): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.801+8340A>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879046 | ||||||
| chr12:49879052
|
A | G | 78 | a0001c0001t0001g0096a0001c0001t0001g0115a0001c0001t0001g0185others(75): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.801+8334T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879052 | ||||||
| chr12:49879080
|
ATG | A | 12 | a0001c0001t0001g0096a0001c0001t0001g0115a0001c0001t0010g0020others(9): Show | 15 | HG01167.hp1 HG01167.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.801+8304_801+8305d others(4): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879080 | ||||||
| chr12:49879222
|
ATGTG | A | 157 | a0001c0001t0001g0015a0001c0001t0001g0076a0001c0001t0001g0088others(154): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.801+8160_801+8163d others(6): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879222 | ||||||
| chr12:49879229
|
T | C | 5 | a0001c0001t0002g0010a0001c0001t0002g0135a0001c0001t0002g0192others(2): Show | 7 | HG00099.hp2 HG00639.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.801+8157A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879229 | ||||||
| chr12:49879242
|
ATG | A | 22 | a0001c0001t0001g0126a0001c0001t0001g0128a0001c0001t0001g0137others(19): Show | 26 | HG01167.hp2 HG01884.hp1 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.801+8142_801+8143d others(4): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879242 | ||||||
| chr12:49879274
|
ATATGTG | A | 5 | a0001c0001t0001g0234a0001c0001t0024g0008a0001c0001t0033g0131others(2): Show | 7 | HG02258.hp1 HG02280.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.801+8106_801+8111d others(8): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879274 | ||||||
| chr12:49879278
|
GTGTGTA | G | 71 | a0001c0001t0001g0185a0001c0001t0002g0001a0001c0001t0002g0002others(68): Show | 97 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.801+8102_801+8107d others(8): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879278 | ||||||
| chr12:49879280
|
GTGTA | G | 65 | a0001c0001t0001g0015a0001c0001t0001g0076a0001c0001t0001g0088others(62): Show | 74 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.801+8102_801+8105d others(6): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879280 | ||||||
| chr12:49879282
|
G | GTGTGGGT others(25): Show |
1 | a0001c0001t0037g0132 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.801+8103_801+8104i others(34): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879282 | ||||||
| chr12:49879282
|
GTA | G | 16 | a0001c0001t0001g0128a0001c0001t0001g0137a0001c0001t0001g0149others(13): Show | 18 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.801+8102_801+8103d others(4): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879282 | ||||||
| chr12:49879284
|
A | G | 7 | a0001c0001t0001g0234a0001c0001t0009g0122a0001c0001t0024g0008others(4): Show | 9 | HG02258.hp1 HG02280.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.801+8102T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879284 | ||||||
| chr12:49879328
|
G | A | 50 | a0001c0001t0001g0015a0001c0001t0001g0076a0001c0001t0001g0088others(47): Show | 58 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.801+8058C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879328 | ||||||
| chr12:49879330
|
G | A | 134 | a0001c0001t0001g0028a0001c0001t0001g0052a0001c0001t0001g0074others(131): Show | 152 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.801+8056C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879330 | ||||||
| chr12:49879330
|
GTA | G | 6 | a0001c0001t0004g0276a0001c0001t0022g0021a0001c0001t0022g0123others(3): Show | 7 | HG02109.hp1 HG02257.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.801+8054_801+8055d others(4): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879330 | ||||||
| chr12:49879332
|
A | ATG | 154 | a0001c0001t0001g0015a0001c0001t0001g0076a0001c0001t0001g0088others(151): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.801+8052_801+8053d others(4): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879332 | ||||||
| chr12:49879332
|
A | ATGTGTGT others(49): Show |
1 | a0001c0001t0009g0122 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.801+8053_801+8054i others(58): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879332 | ||||||
| chr12:49879332
|
A | G | 134 | a0001c0001t0001g0028a0001c0001t0001g0052a0001c0001t0001g0074others(131): Show | 152 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.801+8054T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879332 | ||||||
| chr12:49879378
|
A | G | 3 | a0001c0001t0001g0096a0001c0001t0001g0115a0001c0001t0010g0020 | 4 | HG01167.hp1 HG01169.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.801+8008T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879378 | ||||||
| chr12:49879440
|
GTA | G | 145 | a0001c0001t0001g0028a0001c0001t0001g0052a0001c0001t0001g0074others(142): Show | 165 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.801+7944_801+7945d others(4): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879440 | ||||||
| chr12:49879452
|
G | A | 7 | a0001c0001t0002g0111a0001c0001t0003g0289a0001c0001t0005g0280others(4): Show | 8 | HG00639.hp2 HG01358.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.801+7934C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879452 | ||||||
| chr12:49879465
|
TGTGCATG others(4): Show |
T | 1 | a0001c0001t0002g0213 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.801+7910_801+7920d others(13): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879465 | ||||||
| chr12:49879469
|
CATGTGTA others(17): Show |
C | 292 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0052others(289): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.801+7893_801+7916d others(26): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879469 | ||||||
| chr12:49879481
|
CATGTGAG others(5): Show |
C | 1 | a0001c0001t0002g0213 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.801+7893_801+7904d others(14): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879481 | ||||||
| chr12:49879498
|
G | A | 5 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0213others(2): Show | 5 | NA18944.hp2 NA18951.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.801+7888C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879498 | ||||||
| chr12:49879512
|
A | ATG | 2 | a0001c0001t0002g0048a0001c0001t0003g0004 | 5 | NA18956.hp2 NA18992.hp2 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.801+7872_801+7873d others(4): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879512 | ||||||
| chr12:49879512
|
ATG | A | 16 | a0001c0001t0002g0091a0001c0001t0003g0318a0001c0001t0004g0276others(13): Show | 17 | HG01070.hp2 HG01074.hp2 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.801+7872_801+7873d others(4): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879512 | ||||||
| chr12:49879532
|
A | G | 293 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0052others(290): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.801+7854T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879532 | ||||||
| chr12:49879554
|
ATG | A | 6 | a0001c0001t0009g0158a0001c0001t0009g0159a0001c0001t0024g0008others(3): Show | 8 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.801+7830_801+7831d others(4): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879554 | ||||||
| chr12:49879560
|
A | C | 15 | a0001c0001t0001g0126a0001c0001t0001g0128a0001c0001t0001g0137others(12): Show | 17 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.801+7826T>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879560 | ||||||
| chr12:49879601
|
C | T | 299 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0052others(296): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.801+7785G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879601 | ||||||
| chr12:49879633
|
C | T | 1 | a0001c0001t0008g0042 | 2 | NA18993.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.801+7753G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879633 | ||||||
| chr12:49879637
|
T | C | 1 | a0001c0001t0054g0151 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.801+7749A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879637 | ||||||
| chr12:49879659
|
T | C | 1 | a0001c0001t0003g0318 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.801+7727A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879659 | ||||||
| chr12:49879665
|
TGA | T | 12 | a0001c0001t0006g0003a0001c0001t0006g0056a0001c0001t0006g0121others(9): Show | 15 | HG00733.hp2 HG00735.hp2 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.801+7719_801+7720d others(4): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879665 | ||||||
| chr12:49879667
|
A | T | 281 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0052others(278): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.801+7719T>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879667 | ||||||
| chr12:49879683
|
T | C | 4 | a0001c0001t0024g0008a0001c0001t0033g0131a0001c0001t0033g0148others(1): Show | 6 | HG02258.hp1 HG02280.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.801+7703A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879683 | ||||||
| chr12:49879690
|
GTC | G | 4 | a0001c0001t0020g0025a0001c0001t0020g0145a0001c0001t0063g0362others(1): Show | 5 | HG02055.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.801+7694_801+7695d others(4): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879690 | ||||||
| chr12:49879692
|
C | G | 1 | a0001c0001t0007g0215 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.801+7694G>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879692 | ||||||
| chr12:49879695
|
T | C | 1 | a0001c0001t0007g0215 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.801+7691A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879695 | ||||||
| chr12:49879696
|
G | A | 1 | a0001c0001t0007g0215 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.801+7690C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879696 | ||||||
| chr12:49879699
|
C | T | 1 | a0001c0001t0007g0215 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.801+7687G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879699 | ||||||
| chr12:49879700
|
A | G | 1 | a0001c0001t0007g0215 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.801+7686T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879700 | ||||||
| chr12:49879700
|
ATG | A | 5 | a0001c0001t0002g0187a0001c0001t0012g0272a0001c0001t0013g0226others(2): Show | 5 | HG00280.hp1 HG02683.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.801+7684_801+7685d others(4): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879700 | ||||||
| chr12:49879700
|
ATGTG | A | 6 | a0001c0001t0004g0276a0001c0001t0022g0021a0001c0001t0022g0123others(3): Show | 7 | HG02109.hp1 HG02257.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.801+7682_801+7685d others(6): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879700 | ||||||
| chr12:49879701
|
T | A | 1 | a0001c0001t0007g0215 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.801+7685A>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879701 | ||||||
| chr12:49879701
|
T | TGTGA | 151 | a0001c0001t0001g0015a0001c0001t0001g0076a0001c0001t0001g0088others(148): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.801+7684_801+7685i others(6): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879701 | ||||||
| chr12:49879703
|
T | TGA | 135 | a0001c0001t0001g0028a0001c0001t0001g0052a0001c0001t0001g0074others(132): Show | 153 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.801+7682_801+7683i others(4): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879703 | ||||||
| chr12:49879705
|
T | A | 6 | a0001c0001t0009g0152a0001c0001t0009g0240a0001c0001t0015g0209others(3): Show | 6 | HG01168.hp2 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.801+7681A>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879705 | ||||||
| chr12:49879706
|
G | A | 152 | a0001c0001t0001g0015a0001c0001t0001g0076a0001c0001t0001g0088others(149): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.801+7680C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879706 | ||||||
| chr12:49879708
|
G | A | 1 | a0001c0001t0003g0313 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.801+7678C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879708 | ||||||
| chr12:49879741
|
A | G | 1 | a0001c0001t0005g0329 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.801+7645T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879741 | ||||||
| chr12:49879742
|
A | C | 1 | a0001c0001t0007g0094 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.801+7644T>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879742 | ||||||
| chr12:49879756
|
A | G | 4 | a0001c0001t0024g0008a0001c0001t0033g0131a0001c0001t0033g0148others(1): Show | 6 | HG02258.hp1 HG02280.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.801+7630T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879756 | ||||||
| chr12:49879756
|
ATG | A | 7 | a0001c0001t0003g0368a0001c0001t0014g0009a0001c0001t0016g0236others(4): Show | 9 | HG01167.hp2 HG01884.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.801+7628_801+7629d others(4): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879756 | ||||||
| chr12:49879767
|
C | T | 298 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0052others(295): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.801+7619G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879767 | ||||||
| chr12:49879784
|
A | G | 6 | a0001c0001t0009g0152a0001c0001t0009g0240a0001c0001t0015g0209others(3): Show | 6 | HG01168.hp2 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.801+7602T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879784 | ||||||
| chr12:49879836
|
ATG | A | 5 | a0001c0001t0002g0187a0001c0001t0004g0255a0001c0001t0010g0216others(2): Show | 5 | HG00280.hp1 HG01099.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.801+7548_801+7549d others(4): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879836 | ||||||
| chr12:49879872
|
G | A | 2 | a0001c0001t0005g0284a0001c0001t0005g0304 | 2 | NA19012.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.801+7514C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879872 | ||||||
| chr12:49879875
|
TATGTGTA others(7): Show |
T | 43 | a0001c0001t0001g0015a0001c0001t0001g0076a0001c0001t0001g0088others(40): Show | 49 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.801+7497_801+7510d others(16): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879875 | ||||||
| chr12:49879884
|
GTGTGCAT others(5): Show |
G | 1 | a0001c0001t0001g0079 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.801+7490_801+7501d others(14): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879884 | ||||||
| chr12:49879917
|
CAT | C | 15 | a0001c0001t0001g0126a0001c0001t0001g0128a0001c0001t0001g0137others(12): Show | 17 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.801+7467_801+7468d others(4): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879917 | ||||||
| chr12:49879922
|
GTGTA | G | 3 | a0001c0001t0009g0158a0001c0001t0009g0159a0001c0001t0012g0339 | 3 | HG02486.hp2 HG03579.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.801+7460_801+7463d others(6): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879922 | ||||||
| chr12:49879956
|
G | A | 72 | a0001c0001t0001g0185a0001c0001t0002g0001a0001c0001t0002g0002others(69): Show | 98 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.801+7430C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879956 | ||||||
| chr12:49879966
|
G | GTGTGTA | 292 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0052others(289): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.801+7419_801+7420i others(8): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879966 | ||||||
| chr12:49879972
|
G | A | 4 | a0001c0001t0002g0133a0001c0001t0003g0322a0001c0001t0053g0220others(1): Show | 4 | HG01106.hp2 HG01978.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.801+7414C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49879972 | ||||||
| chr12:49880044
|
A | ATG | 292 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0052others(289): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.801+7340_801+7341d others(4): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880044 | ||||||
| chr12:49880050
|
A | G | 1 | a0001c0001t0013g0116 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.801+7336T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880050 | ||||||
| chr12:49880060
|
T | G | 1 | a0001c0001t0013g0116 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.801+7326A>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880060 | ||||||
| chr12:49880105
|
C | T | 1 | a0001c0001t0004g0267 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.801+7281G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880105 | ||||||
| chr12:49880106
|
G | A | 16 | a0001c0001t0001g0126a0001c0001t0001g0128a0001c0001t0001g0137others(13): Show | 18 | HG01891.hp1 HG02080.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.801+7280C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880106 | ||||||
| chr12:49880130
|
ATG | A | 5 | a0001c0001t0005g0290a0001c0001t0008g0035a0001c0001t0008g0277others(2): Show | 6 | HG01515.hp2 HG01517.hp1 HG04204.hp1 others(3): Show |
intron_variant | MODIFIER | c.801+7254_801+7255d others(4): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880130 | ||||||
| chr12:49880160
|
A | G | 1 | a0001c0001t0009g0112 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.801+7226T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880160 | ||||||
| chr12:49880167
|
T | TGTCTGTG others(3): Show |
4 | a0001c0001t0024g0008a0001c0001t0033g0131a0001c0001t0033g0148others(1): Show | 6 | HG02258.hp1 HG02280.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.801+7218_801+7219i others(12): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880167 | ||||||
| chr12:49880167
|
T | TGTGTCTG others(3): Show |
3 | a0001c0001t0001g0102a0001c0001t0001g0105a0001c0001t0001g0153 | 3 | HG01884.hp2 HG02451.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.801+7218_801+7219i others(12): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880167 | ||||||
| chr12:49880167
|
T | TGTGTCTG others(5): Show |
221 | a0001c0001t0001g0028a0001c0001t0001g0052a0001c0001t0001g0074others(218): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.801+7218_801+7219i others(14): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880167 | ||||||
| chr12:49880167
|
T | TGTGTGTC others(7): Show |
45 | a0001c0001t0001g0015a0001c0001t0001g0076a0001c0001t0001g0088others(42): Show | 51 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.801+7218_801+7219i others(16): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880167 | ||||||
| chr12:49880167
|
T | TGTGTGTG others(5): Show |
1 | a0001c0001t0015g0027 | 2 | HG00733.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.801+7218_801+7219i others(14): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880167 | ||||||
| chr12:49880167
|
T | TGTGTGTG others(7): Show |
2 | a0001c0001t0009g0158a0001c0001t0009g0159 | 2 | HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.801+7218_801+7219i others(16): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880167 | ||||||
| chr12:49880168
|
A | G | 16 | a0001c0001t0001g0126a0001c0001t0001g0128a0001c0001t0001g0137others(13): Show | 18 | HG01891.hp1 HG02109.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.801+7218T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880168 | ||||||
| chr12:49880169
|
T | TCTGTGTG others(1): Show |
7 | a0001c0001t0001g0126a0001c0001t0017g0022a0001c0001t0017g0214others(4): Show | 9 | HG01891.hp1 HG02109.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.801+7216_801+7217i others(10): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880169 | ||||||
| chr12:49880170
|
G | A | 7 | a0001c0001t0001g0126a0001c0001t0017g0022a0001c0001t0017g0214others(4): Show | 9 | HG01891.hp1 HG02109.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.801+7216C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880170 | ||||||
| chr12:49880170
|
G | GTCTGTGT others(3): Show |
9 | a0001c0001t0001g0128a0001c0001t0001g0137a0001c0001t0001g0149others(6): Show | 9 | HG02145.hp2 HG02896.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.801+7215_801+7216i others(12): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880170 | ||||||
| chr12:49880174
|
G | C | 1 | a0001c0001t0005g0280 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.801+7212C>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880174 | ||||||
| chr12:49880178
|
A | G | 2 | a0001c0001t0001g0170a0001c0001t0005g0280 | 2 | HG04228.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.801+7208T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880178 | ||||||
| chr12:49880181
|
C | T | 1 | a0001c0001t0034g0146 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.801+7205G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880181 | ||||||
| chr12:49880190
|
A | G | 1 | a0001c0001t0005g0280 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.801+7196T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880190 | ||||||
| chr12:49880198
|
ATG | A | 101 | a0001c0001t0001g0096a0001c0001t0001g0115a0001c0001t0001g0126others(98): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.801+7186_801+7187d others(4): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880198 | ||||||
| chr12:49880206
|
GTGCATGT others(13): Show |
G | 1 | a0001c0001t0008g0291 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.801+7160_801+7179d others(22): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880206 | ||||||
| chr12:49880294
|
CTG | C | 43 | a0001c0001t0001g0015a0001c0001t0001g0076a0001c0001t0001g0088others(40): Show | 49 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.801+7090_801+7091d others(4): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880294 | ||||||
| chr12:49880319
|
T | C | 11 | a0001c0001t0005g0248a0001c0001t0005g0270a0001c0001t0005g0284others(8): Show | 12 | HG02155.hp1 NA18942.hp2 NA18945.hp2 others(9): Show |
intron_variant | MODIFIER | c.801+7067A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880319 | ||||||
| chr12:49880320
|
ATG | A | 52 | a0001c0001t0001g0015a0001c0001t0001g0076a0001c0001t0001g0088others(49): Show | 60 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.801+7064_801+7065d others(4): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880320 | ||||||
| chr12:49880374
|
ATG | A | 73 | a0001c0001t0001g0185a0001c0001t0002g0001a0001c0001t0002g0002others(70): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.801+7010_801+7011d others(4): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880374 | ||||||
| chr12:49880374
|
ATGTGTGT others(17): Show |
A | 1 | a0001c0001t0009g0172 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.801+6988_801+7011d others(26): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880374 | ||||||
| chr12:49880382
|
CTA | C | 47 | a0001c0001t0001g0015a0001c0001t0001g0076a0001c0001t0001g0088others(44): Show | 55 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.801+7002_801+7003d others(4): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880382 | ||||||
| chr12:49880384
|
A | C | 1 | a0001c0001t0001g0234 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.801+7002T>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880384 | ||||||
| chr12:49880458
|
A | ATG | 262 | a0001c0001t0001g0028a0001c0001t0001g0052a0001c0001t0001g0074others(259): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.801+6926_801+6927d others(4): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880458 | ||||||
| chr12:49880477
|
C | T | 1 | a0001c0001t0062g0311 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.801+6909G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880477 | ||||||
| chr12:49880492
|
G | GTATGTGT others(3): Show |
2 | a0001c0001t0007g0083a0001c0001t0008g0291 | 2 | HG00438.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.801+6893_801+6894i others(12): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880492 | ||||||
| chr12:49880492
|
G | GTATGTGT others(5): Show |
4 | a0001c0001t0001g0096a0001c0001t0001g0115a0001c0001t0009g0122others(1): Show | 5 | HG01167.hp1 HG01169.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.801+6882_801+6893d others(14): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880492 | ||||||
| chr12:49880494
|
A | ATGTGTGT others(5): Show |
132 | a0001c0001t0001g0028a0001c0001t0001g0052a0001c0001t0001g0074others(129): Show | 150 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.801+6891_801+6892i others(14): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880494 | ||||||
| chr12:49880494
|
A | ATGTGTGT others(7): Show |
68 | a0001c0001t0001g0015a0001c0001t0001g0076a0001c0001t0001g0088others(65): Show | 77 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.801+6891_801+6892i others(16): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880494 | ||||||
| chr12:49880494
|
A | ATGTGTGT others(5): Show |
1 | a0003c0004t0001g0227 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.801+6880_801+6891d others(14): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880494 | ||||||
| chr12:49880496
|
G | GTGTGTGT others(3): Show |
72 | a0001c0001t0001g0185a0001c0001t0002g0001a0001c0001t0002g0002others(69): Show | 98 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.801+6889_801+6890i others(12): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880496 | ||||||
| chr12:49880502
|
G | GTA | 1 | a0001c0001t0024g0008 | 3 | HG02258.hp1 NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.801+6882_801+6883d others(4): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880502 | ||||||
| chr12:49880504
|
A | G | 1 | a0001c0001t0007g0083 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.801+6882T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880504 | ||||||
| chr12:49880505
|
TGA | T | 4 | a0001c0001t0020g0025a0001c0001t0020g0145a0001c0001t0063g0362others(1): Show | 5 | HG02055.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.801+6879_801+6880d others(4): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880505 | ||||||
| chr12:49880506
|
G | A | 9 | a0001c0001t0009g0152a0001c0001t0009g0240a0001c0001t0015g0209others(6): Show | 9 | HG01168.hp2 HG02055.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.801+6880C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880506 | ||||||
| chr12:49880507
|
A | T | 10 | a0001c0001t0009g0152a0001c0001t0009g0240a0001c0001t0015g0209others(7): Show | 12 | HG01168.hp2 HG02055.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.801+6879T>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880507 | ||||||
| chr12:49880508
|
G | A | 4 | a0001c0001t0020g0025a0001c0001t0020g0145a0001c0001t0063g0362others(1): Show | 5 | HG02055.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.801+6878C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880508 | ||||||
| chr12:49880514
|
A | G | 13 | a0001c0001t0009g0152a0001c0001t0009g0240a0001c0001t0015g0209others(10): Show | 14 | HG01168.hp2 HG02055.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.801+6872T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880514 | ||||||
| chr12:49880516
|
G | A | 3 | a0001c0001t0016g0098a0001c0001t0016g0099a0001c0001t0034g0146 | 3 | HG02055.hp1 HG02723.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.801+6870C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880516 | ||||||
| chr12:49880518
|
G | A | 6 | a0001c0001t0009g0152a0001c0001t0009g0240a0001c0001t0015g0209others(3): Show | 6 | HG01168.hp2 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.801+6868C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880518 | ||||||
| chr12:49880518
|
GCA | G | 3 | a0001c0001t0016g0098a0001c0001t0016g0099a0001c0001t0034g0146 | 3 | HG02055.hp1 HG02723.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.801+6866_801+6867d others(4): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880518 | ||||||
| chr12:49880519
|
C | T | 10 | a0001c0001t0009g0152a0001c0001t0009g0240a0001c0001t0015g0209others(7): Show | 11 | HG01168.hp2 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.801+6867G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880519 | ||||||
| chr12:49880520
|
A | G | 6 | a0001c0001t0009g0152a0001c0001t0009g0240a0001c0001t0015g0209others(3): Show | 6 | HG01168.hp2 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.801+6866T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880520 | ||||||
| chr12:49880521
|
T | A | 9 | a0001c0001t0009g0152a0001c0001t0009g0240a0001c0001t0015g0209others(6): Show | 9 | HG01168.hp2 HG02055.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.801+6865A>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880521 | ||||||
| chr12:49880526
|
A | G | 13 | a0001c0001t0009g0152a0001c0001t0009g0240a0001c0001t0015g0209others(10): Show | 14 | HG01168.hp2 HG02055.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.801+6860T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880526 | ||||||
| chr12:49880534
|
G | A | 13 | a0001c0001t0009g0152a0001c0001t0009g0240a0001c0001t0015g0209others(10): Show | 14 | HG01168.hp2 HG02055.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.801+6852C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880534 | ||||||
| chr12:49880540
|
ATG | A | 9 | a0001c0001t0009g0152a0001c0001t0009g0240a0001c0001t0015g0209others(6): Show | 9 | HG01168.hp2 HG02055.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.801+6844_801+6845d others(4): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880540 | ||||||
| chr12:49880542
|
G | A | 4 | a0001c0001t0020g0025a0001c0001t0020g0145a0001c0001t0063g0362others(1): Show | 5 | HG02055.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.801+6844C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880542 | ||||||
| chr12:49880544
|
A | G | 4 | a0001c0001t0020g0025a0001c0001t0020g0145a0001c0001t0063g0362others(1): Show | 5 | HG02055.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.801+6842T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880544 | ||||||
| chr12:49880546
|
GCA | G | 9 | a0001c0001t0009g0152a0001c0001t0009g0240a0001c0001t0015g0209others(6): Show | 9 | HG01168.hp2 HG02055.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.801+6838_801+6839d others(4): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880546 | ||||||
| chr12:49880548
|
A | G | 4 | a0001c0001t0020g0025a0001c0001t0020g0145a0001c0001t0063g0362others(1): Show | 5 | HG02055.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.801+6838T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880548 | ||||||
| chr12:49880551
|
C | T | 4 | a0001c0001t0020g0025a0001c0001t0020g0145a0001c0001t0063g0362others(1): Show | 5 | HG02055.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.801+6835G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880551 | ||||||
| chr12:49880554
|
G | A | 7 | a0001c0001t0016g0098a0001c0001t0016g0099a0001c0001t0020g0025others(4): Show | 8 | HG02055.hp1 HG02055.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.801+6832C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880554 | ||||||
| chr12:49880554
|
GTGTGTGC others(11): Show |
G | 280 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0052others(277): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.801+6814_801+6831d others(20): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880554 | ||||||
| chr12:49880558
|
G | A | 13 | a0001c0001t0009g0152a0001c0001t0009g0240a0001c0001t0015g0209others(10): Show | 14 | HG01168.hp2 HG02055.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.801+6828C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880558 | ||||||
| chr12:49880561
|
C | T | 6 | a0001c0001t0009g0152a0001c0001t0009g0240a0001c0001t0015g0209others(3): Show | 6 | HG01168.hp2 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.801+6825G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880561 | ||||||
| chr12:49880565
|
T | C | 13 | a0001c0001t0009g0152a0001c0001t0009g0240a0001c0001t0015g0209others(10): Show | 14 | HG01168.hp2 HG02055.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.801+6821A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880565 | ||||||
| chr12:49880566
|
G | A | 6 | a0001c0001t0009g0152a0001c0001t0009g0240a0001c0001t0015g0209others(3): Show | 6 | HG01168.hp2 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.801+6820C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880566 | ||||||
| chr12:49880568
|
GTATC | G | 7 | a0001c0001t0016g0098a0001c0001t0016g0099a0001c0001t0020g0025others(4): Show | 8 | HG02055.hp1 HG02055.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.801+6814_801+6817d others(6): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880568 | ||||||
| chr12:49880569
|
T | C | 6 | a0001c0001t0009g0152a0001c0001t0009g0240a0001c0001t0015g0209others(3): Show | 6 | HG01168.hp2 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.801+6817A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880569 | ||||||
| chr12:49880572
|
C | G | 6 | a0001c0001t0009g0152a0001c0001t0009g0240a0001c0001t0015g0209others(3): Show | 6 | HG01168.hp2 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.801+6814G>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880572 | ||||||
| chr12:49880572
|
CTGTGCAT others(7): Show |
C | 1 | a0001c0001t0011g0370 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.801+6800_801+6813d others(16): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880572 | ||||||
| chr12:49880609
|
T | C | 2 | a0001c0001t0002g0048a0001c0001t0003g0004 | 5 | NA18956.hp2 NA18992.hp2 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.801+6777A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880609 | ||||||
| chr12:49880628
|
GTGTA | G | 2 | a0001c0001t0002g0012a0001c0001t0003g0251 | 4 | HG00609.hp1 NA18948.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.801+6754_801+6757d others(6): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880628 | ||||||
| chr12:49880630
|
GTA | G | 291 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0052others(288): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.801+6754_801+6755d others(4): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880630 | ||||||
| chr12:49880660
|
A | C | 1 | a0001c0001t0004g0276 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.801+6726T>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880660 | ||||||
| chr12:49880690
|
A | G | 6 | a0001c0001t0009g0152a0001c0001t0009g0240a0001c0001t0015g0209others(3): Show | 6 | HG01168.hp2 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.801+6696T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880690 | ||||||
| chr12:49880703
|
C | A | 2 | a0001c0001t0015g0209a0001c0001t0015g0225 | 2 | HG02922.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.801+6683G>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880703 | ||||||
| chr12:49880717
|
C | T | 5 | a0001c0001t0017g0022a0001c0002t0014g0093a0001c0002t0017g0138others(2): Show | 7 | HG01891.hp1 HG02109.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.801+6669G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880717 | ||||||
| chr12:49880722
|
A | ATATGTG | 41 | a0001c0001t0001g0015a0001c0001t0001g0076a0001c0001t0001g0088others(38): Show | 46 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.801+6658_801+6663d others(8): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880722 | ||||||
| chr12:49880726
|
G | GTGTA | 245 | a0001c0001t0001g0028a0001c0001t0001g0052a0001c0001t0001g0074others(242): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.801+6659_801+6660i others(6): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880726 | ||||||
| chr12:49880728
|
G | GTA | 5 | a0001c0001t0017g0022a0001c0001t0033g0148a0001c0002t0014g0093others(2): Show | 7 | HG01891.hp1 HG02109.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.801+6657_801+6658i others(4): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880728 | ||||||
| chr12:49880736
|
A | G | 50 | a0001c0001t0001g0015a0001c0001t0001g0076a0001c0001t0001g0088others(47): Show | 58 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.801+6650T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880736 | ||||||
| chr12:49880755
|
C | T | 292 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0052others(289): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.801+6631G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880755 | ||||||
| chr12:49880778
|
G | C | 2 | a0001c0001t0004g0363a0001c0001t0023g0024 | 3 | HG02970.hp1 HG06807.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.801+6608C>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880778 | ||||||
| chr12:49880796
|
G | A | 1 | a0001c0002t0041g0142 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.801+6590C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880796 | ||||||
| chr12:49880800
|
G | T | 6 | a0001c0001t0014g0009a0001c0001t0016g0236a0001c0001t0016g0237others(3): Show | 8 | HG01167.hp2 HG01884.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.801+6586C>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880800 | ||||||
| chr12:49880812
|
A | G | 1 | a0001c0001t0010g0155 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.801+6574T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880812 | ||||||
| chr12:49880881
|
A | AGAGT | 46 | a0001c0001t0001g0015a0001c0001t0001g0076a0001c0001t0001g0088others(43): Show | 53 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.801+6504_801+6505i others(6): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880881 | ||||||
| chr12:49880881
|
A | AGAGTGT | 4 | a0001c0001t0020g0025a0001c0001t0020g0145a0001c0001t0063g0362others(1): Show | 5 | HG02055.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.801+6504_801+6505i others(8): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880881 | ||||||
| chr12:49880881
|
A | AGT | 8 | a0001c0001t0004g0276a0001c0001t0014g0009a0001c0001t0022g0021others(5): Show | 11 | HG01167.hp2 HG02109.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.801+6503_801+6504d others(4): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880881 | ||||||
| chr12:49880881
|
A | AGTGT | 87 | a0001c0001t0001g0096a0001c0001t0001g0115a0001c0001t0001g0128others(84): Show | 114 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.801+6501_801+6504d others(6): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880881 | ||||||
| chr12:49880881
|
A | AGTGTGT | 133 | a0001c0001t0001g0028a0001c0001t0001g0052a0001c0001t0001g0074others(130): Show | 151 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.801+6499_801+6504d others(8): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880881 | ||||||
| chr12:49880881
|
A | AGTGTGTG others(1): Show |
15 | a0001c0001t0001g0126a0001c0001t0004g0267a0001c0001t0004g0282others(12): Show | 17 | HG01192.hp1 HG01891.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.801+6497_801+6504d others(10): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880881 | ||||||
| chr12:49880881
|
A | AGTGTGTG others(5): Show |
1 | a0001c0001t0009g0122 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.801+6493_801+6504d others(14): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880881 | ||||||
| chr12:49880884
|
G | C | 4 | a0001c0001t0010g0205a0001c0001t0011g0244a0001c0001t0011g0246others(1): Show | 4 | NA18963.hp1 NA18966.hp1 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.801+6502C>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880884 | ||||||
| chr12:49880900
|
G | C | 1 | a0001c0001t0007g0094 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.801+6486C>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880900 | ||||||
| chr12:49880900
|
G | GTGTGTC | 4 | a0001c0001t0005g0290a0001c0001t0006g0067a0001c0001t0009g0162others(1): Show | 4 | HG02622.hp1 HG04204.hp1 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.801+6485_801+6486i others(8): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880900 | ||||||
| chr12:49880902
|
C | G | 1 | a0001c0001t0013g0120 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.801+6484G>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880902 | ||||||
| chr12:49880940
|
G | A | 1 | a0001c0001t0005g0248 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.801+6446C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880940 | ||||||
| chr12:49880958
|
C | G | 8 | a0001c0001t0001g0128a0001c0001t0001g0137a0001c0001t0001g0149others(5): Show | 8 | HG02145.hp2 HG02896.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.801+6428G>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49880958 | ||||||
| chr12:49881190
|
G | A | 1 | a0001c0001t0034g0238 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.801+6196C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49881190 | ||||||
| chr12:49881191
|
G | A | 1 | a0001c0001t0009g0169 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.801+6195C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49881191 | ||||||
| chr12:49881354
|
A | C | 293 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0052others(290): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.801+6032T>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49881354 | ||||||
| chr12:49881598
|
C | T | 4 | a0001c0001t0017g0022a0001c0002t0014g0093a0001c0002t0017g0138others(1): Show | 6 | HG01891.hp1 HG02109.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.801+5788G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49881598 | ||||||
| chr12:49881602
|
C | T | 71 | a0001c0001t0001g0185a0001c0001t0002g0001a0001c0001t0002g0002others(68): Show | 96 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.801+5784G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49881602 | ||||||
| chr12:49881746
|
G | A | 1 | a0001c0001t0003g0317 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.801+5640C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49881746 | ||||||
| chr12:49881991
|
G | A | 1 | a0001c0001t0002g0181 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.801+5395C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49881991 | ||||||
| chr12:49882036
|
T | A | 8 | a0001c0001t0001g0088a0001c0001t0001g0170a0001c0001t0009g0077others(5): Show | 8 | HG00408.hp2 HG02040.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.801+5350A>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49882036 | ||||||
| chr12:49882103
|
A | G | 1 | a0001c0001t0054g0151 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.801+5283T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49882103 | ||||||
| chr12:49882157
|
C | G | 1 | a0001c0001t0002g0062 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.801+5229G>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49882157 | ||||||
| chr12:49882248
|
G | A | 55 | a0001c0001t0001g0015a0001c0001t0001g0076a0001c0001t0001g0088others(52): Show | 64 | HG00408.hp2 HG00558.hp1 HG01167.hp2 others(61): Show |
intron_variant | MODIFIER | c.801+5138C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49882248 | ||||||
| chr12:49882469
|
T | C | 3 | a0001c0001t0001g0096a0001c0001t0001g0115a0001c0001t0010g0020 | 4 | HG01167.hp1 HG01169.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.801+4917A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49882469 | ||||||
| chr12:49882634
|
G | A | 2 | a0001c0001t0025g0034a0001c0001t0025g0273 | 3 | HG01074.hp1 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.801+4752C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49882634 | ||||||
| chr12:49882673
|
G | A | 1 | a0001c0001t0017g0214 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.801+4713C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49882673 | ||||||
| chr12:49882694
|
C | G | 6 | a0001c0001t0014g0009a0001c0001t0016g0236a0001c0001t0016g0237others(3): Show | 8 | HG01167.hp2 HG01884.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.801+4692G>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49882694 | ||||||
| chr12:49882846
|
A | C | 135 | a0001c0001t0001g0028a0001c0001t0001g0052a0001c0001t0001g0074others(132): Show | 153 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.801+4540T>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49882846 | ||||||
| chr12:49882948
|
G | A | 1 | a0001c0001t0004g0276 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.801+4438C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49882948 | ||||||
| chr12:49882953
|
G | A | 4 | a0001c0001t0006g0068a0001c0001t0006g0070a0001c0001t0007g0069others(1): Show | 4 | NA18943.hp1 NA18973.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.801+4433C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49882953 | ||||||
| chr12:49883006
|
C | T | 1 | a0001c0001t0004g0255 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.801+4380G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49883006 | ||||||
| chr12:49883104
|
C | A | 1 | a0001c0001t0006g0029 | 2 | NA18950.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.801+4282G>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49883104 | ||||||
| chr12:49883192
|
A | G | 1 | a0001c0001t0006g0206 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.801+4194T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49883192 | ||||||
| chr12:49883201
|
C | T | 1 | a0001c0001t0016g0237 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.801+4185G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49883201 | ||||||
| chr12:49883259
|
G | A | 135 | a0001c0001t0001g0028a0001c0001t0001g0052a0001c0001t0001g0074others(132): Show | 153 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.801+4127C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49883259 | ||||||
| chr12:49883315
|
C | A | 49 | a0001c0001t0001g0015a0001c0001t0001g0076a0001c0001t0001g0088others(46): Show | 57 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.801+4071G>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49883315 | ||||||
| chr12:49883346
|
T | G | 293 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0052others(290): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.801+4040A>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49883346 | ||||||
| chr12:49883447
|
C | T | 1 | a0001c0001t0009g0158 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.801+3939G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49883447 | ||||||
| chr12:49883616
|
A | C | 293 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0052others(290): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.801+3770T>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49883616 | ||||||
| chr12:49883629
|
T | C | 288 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0052others(285): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.801+3757A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49883629 | ||||||
| chr12:49883643
|
T | A | 49 | a0001c0001t0001g0015a0001c0001t0001g0076a0001c0001t0001g0088others(46): Show | 57 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.801+3743A>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49883643 | ||||||
| chr12:49883733
|
G | A | 3 | a0001c0001t0005g0290a0001c0001t0008g0035a0001c0001t0008g0277 | 4 | HG01515.hp2 HG01517.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.801+3653C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49883733 | ||||||
| chr12:49883996
|
C | T | 1 | a0001c0001t0004g0255 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.801+3390G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49883996 | ||||||
| chr12:49884053
|
C | A | 1 | a0001c0001t0008g0274 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.801+3333G>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49884053 | ||||||
| chr12:49884103
|
A | G | 1 | a0001c0001t0006g0221 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.801+3283T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49884103 | ||||||
| chr12:49884202
|
C | T | 2 | a0001c0001t0015g0209a0001c0001t0015g0225 | 2 | HG02922.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.801+3184G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49884202 | ||||||
| chr12:49884219
|
G | A | 25 | a0001c0001t0001g0015a0001c0001t0001g0076a0001c0001t0001g0088others(22): Show | 29 | HG00408.hp2 HG00558.hp1 HG01346.hp2 others(26): Show |
intron_variant | MODIFIER | c.801+3167C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49884219 | ||||||
| chr12:49884231
|
A | AC | 6 | a0001c0001t0001g0096a0001c0001t0001g0115a0001c0001t0010g0020others(3): Show | 7 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.801+3154_801+3155i others(3): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49884231 | ||||||
| chr12:49884235
|
A | AC | 288 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0052others(285): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.801+3150_801+3151i others(3): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49884235 | ||||||
| chr12:49884235
|
A | C | 6 | a0001c0001t0001g0096a0001c0001t0001g0115a0001c0001t0010g0020others(3): Show | 7 | HG01167.hp1 HG01169.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.801+3151T>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49884235 | ||||||
| chr12:49884381
|
T | C | 1 | a0001c0001t0009g0184 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.801+3005A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49884381 | ||||||
| chr12:49884517
|
G | A | 1 | a0001c0001t0013g0116 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.801+2869C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49884517 | ||||||
| chr12:49884701
|
A | G | 8 | a0001c0001t0001g0128a0001c0001t0001g0137a0001c0001t0001g0149others(5): Show | 8 | HG02145.hp2 HG02896.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.801+2685T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49884701 | ||||||
| chr12:49884705
|
T | A | 8 | a0001c0001t0001g0128a0001c0001t0001g0137a0001c0001t0001g0149others(5): Show | 8 | HG02145.hp2 HG02896.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.801+2681A>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49884705 | ||||||
| chr12:49884706
|
C | G | 9 | a0001c0001t0001g0128a0001c0001t0001g0137a0001c0001t0001g0149others(6): Show | 9 | HG02145.hp2 HG02896.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.801+2680G>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49884706 | ||||||
| chr12:49884707
|
A | G | 9 | a0001c0001t0001g0128a0001c0001t0001g0137a0001c0001t0001g0149others(6): Show | 9 | HG02145.hp2 HG02896.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.801+2679T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49884707 | ||||||
| chr12:49884741
|
A | G | 5 | a0001c0001t0002g0062a0001c0001t0024g0008a0001c0001t0033g0131others(2): Show | 7 | HG02258.hp1 HG02280.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.801+2645T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49884741 | ||||||
| chr12:49884771
|
G | A | 81 | a0001c0001t0001g0128a0001c0001t0001g0137a0001c0001t0001g0149others(78): Show | 93 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.801+2615C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49884771 | ||||||
| chr12:49884775
|
C | G | 1 | a0001c0001t0012g0272 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.801+2611G>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49884775 | ||||||
| chr12:49884778
|
T | C | 335 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(332): Show | 397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.801+2608A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49884778 | ||||||
| chr12:49884798
|
G | C | 13 | a0001c0001t0001g0128a0001c0001t0001g0137a0001c0001t0001g0149others(10): Show | 15 | HG02055.hp2 HG02145.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.801+2588C>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49884798 | ||||||
| chr12:49884800
|
T | C | 14 | a0001c0001t0001g0128a0001c0001t0001g0137a0001c0001t0001g0149others(11): Show | 16 | HG02055.hp2 HG02145.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.801+2586A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49884800 | ||||||
| chr12:49884840
|
G | A | 1 | a0001c0001t0005g0329 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.801+2546C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49884840 | ||||||
| chr12:49884845
|
G | A | 8 | a0001c0001t0001g0126a0001c0001t0009g0122a0001c0001t0009g0158others(5): Show | 8 | HG01168.hp2 HG02486.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.801+2541C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49884845 | ||||||
| chr12:49884872
|
A | G | 1 | a0001c0002t0041g0142 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.801+2514T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49884872 | ||||||
| chr12:49884939
|
A | T | 2 | a0001c0001t0005g0329a0001c0001t0007g0047 | 2 | HG02040.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.801+2447T>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49884939 | ||||||
| chr12:49884973
|
C | CA | 6 | a0001c0001t0002g0133a0001c0001t0005g0280a0001c0001t0008g0323others(3): Show | 7 | HG02300.hp2 HG02717.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.801+2412dupT | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49884973 | ||||||
| chr12:49885151
|
C | G | 2 | a0001c0002t0014g0093a0002c0003t0014g0019 | 3 | HG02717.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.801+2235G>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49885151 | ||||||
| chr12:49885285
|
A | G | 37 | a0001c0001t0001g0102a0001c0001t0001g0105a0001c0001t0001g0126others(34): Show | 38 | HG01070.hp2 HG01074.hp2 HG01168.hp2 others(35): Show |
intron_variant | MODIFIER | c.801+2101T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49885285 | ||||||
| chr12:49885403
|
C | T | 1 | a0001c0001t0013g0119 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.801+1983G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49885403 | ||||||
| chr12:49885572
|
GCCC | G | 12 | a0001c0001t0001g0126a0001c0001t0009g0112a0001c0001t0009g0122others(9): Show | 13 | HG01168.hp2 HG02486.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.801+1811_801+1813d others(5): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49885572 | ||||||
| chr12:49885611
|
G | A | 1 | a0001c0001t0021g0346 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.801+1775C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49885611 | ||||||
| chr12:49885919
|
G | A | 4 | a0001c0001t0024g0008a0001c0001t0033g0131a0001c0001t0033g0148others(1): Show | 6 | HG02258.hp1 HG02280.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.801+1467C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49885919 | ||||||
| chr12:49886002
|
C | T | 1 | a0001c0001t0021g0260 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.801+1384G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49886002 | ||||||
| chr12:49886165
|
C | T | 2 | a0001c0001t0005g0258a0001c0001t0055g0061 | 2 | NA18975.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.801+1221G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49886165 | ||||||
| chr12:49886166
|
G | T | 2 | a0001c0002t0014g0093a0002c0003t0014g0019 | 3 | HG02717.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.801+1220C>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49886166 | ||||||
| chr12:49886176
|
C | T | 2 | a0001c0001t0003g0312a0001c0001t0062g0311 | 2 | HG01175.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.801+1210G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49886176 | ||||||
| chr12:49886430
|
G | A | 135 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0017others(132): Show | 155 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.801+956C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49886430 | ||||||
| chr12:49886443
|
T | C | 6 | a0001c0001t0002g0062a0001c0001t0005g0248a0001c0001t0005g0270others(3): Show | 6 | HG02155.hp1 NA18942.hp2 NA18992.hp1 others(3): Show |
intron_variant | MODIFIER | c.801+943A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49886443 | ||||||
| chr12:49886635
|
C | T | 4 | a0001c0001t0020g0025a0001c0001t0020g0145a0001c0001t0063g0362others(1): Show | 5 | HG02055.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.801+751G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49886635 | ||||||
| chr12:49886647
|
T | C | 73 | a0001c0001t0001g0185a0001c0001t0002g0001a0001c0001t0002g0002others(70): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.801+739A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49886647 | ||||||
| chr12:49886680
|
G | T | 1 | a0001c0001t0004g0255 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.801+706C>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49886680 | ||||||
| chr12:49886688
|
G | A | 1 | a0001c0001t0030g0125 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.801+698C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49886688 | ||||||
| chr12:49886718
|
C | T | 1 | a0001c0001t0026g0325 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.801+668G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49886718 | ||||||
| chr12:49886753
|
G | A | 4 | a0001c0001t0020g0025a0001c0001t0020g0145a0001c0001t0063g0362others(1): Show | 5 | HG02055.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.801+633C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49886753 | ||||||
| chr12:49886763
|
A | C | 1 | a0001c0001t0051g0173 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.801+623T>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49886763 | ||||||
| chr12:49886772
|
G | A | 1 | a0001c0002t0041g0142 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.801+614C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49886772 | ||||||
| chr12:49886921
|
A | G | 1 | a0001c0001t0013g0195 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.801+465T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49886921 | ||||||
| chr12:49886933
|
G | A | 13 | a0001c0001t0001g0175a0001c0001t0001g0222a0001c0001t0001g0234others(10): Show | 14 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.801+453C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49886933 | ||||||
| chr12:49887016
|
T | G | 1 | a0001c0002t0041g0142 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.801+370A>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49887016 | ||||||
| chr12:49887031
|
G | C | 4 | a0001c0001t0004g0276a0001c0001t0028g0163a0001c0001t0028g0164others(1): Show | 4 | HG02572.hp1 HG02809.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.801+355C>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49887031 | ||||||
| chr12:49887061
|
G | A | 2 | a0001c0001t0035g0271a0001c0001t0035g0342 | 2 | HG02451.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.801+325C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49887061 | ||||||
| chr12:49887078
|
C | T | 4 | a0001c0001t0020g0025a0001c0001t0020g0145a0001c0001t0063g0362others(1): Show | 5 | HG02055.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.801+308G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49887078 | ||||||
| chr12:49887194
|
G | A | 3 | a0001c0001t0009g0112a0001c0002t0014g0093a0002c0003t0014g0019 | 4 | HG02717.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.801+192C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49887194 | ||||||
| chr12:49887236
|
C | A | 3 | a0001c0001t0002g0133a0001c0001t0005g0280a0001c0001t0008g0323 | 3 | HG02300.hp2 HG04228.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.801+150G>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49887236 | ||||||
| chr12:49887239
|
A | C | 3 | a0001c0001t0002g0133a0001c0001t0005g0280a0001c0001t0008g0323 | 3 | HG02300.hp2 HG04228.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.801+147T>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49887239 | ||||||
| chr12:49887266
|
C | A | 53 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0052others(50): Show | 63 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.801+120G>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49887266 | ||||||
| chr12:49887267
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.801+119G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 11/11 | chr12 | 49887267 | ||||||
| chr12:49887600
|
C | T | 1 | a0001c0001t0002g0135 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.748-161G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 10/11 | chr12 | 49887600 | ||||||
| chr12:49887615
|
G | A | 2 | a0001c0001t0012g0350a0001c0001t0013g0178 | 2 | HG00544.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.748-176C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 10/11 | chr12 | 49887615 | ||||||
| chr12:49887631
|
G | C | 153 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0017others(150): Show | 176 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.748-192C>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 10/11 | chr12 | 49887631 | ||||||
| chr12:49887634
|
C | T | 2 | a0001c0001t0006g0210a0001c0001t0008g0297 | 2 | NA18957.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.748-195G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 10/11 | chr12 | 49887634 | ||||||
| chr12:49887694
|
C | T | 1 | a0001c0001t0051g0173 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.748-255G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 10/11 | chr12 | 49887694 | ||||||
| chr12:49887864
|
G | A | 66 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0052others(63): Show | 75 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.748-425C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 10/11 | chr12 | 49887864 | ||||||
| chr12:49887873
|
T | C | 6 | a0001c0001t0004g0255a0001c0001t0009g0112a0001c0001t0027g0097others(3): Show | 7 | HG02717.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.748-434A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 10/11 | chr12 | 49887873 | ||||||
| chr12:49887880
|
G | T | 1 | a0001c0001t0001g0147 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.748-441C>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 10/11 | chr12 | 49887880 | ||||||
| chr12:49887895
|
C | T | 2 | a0001c0001t0033g0131a0001c0001t0033g0148 | 2 | HG02280.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.748-456G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 10/11 | chr12 | 49887895 | ||||||
| chr12:49887949
|
G | A | 1 | a0001c0001t0004g0337 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.748-510C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 10/11 | chr12 | 49887949 | ||||||
| chr12:49888156
|
C | T | 6 | a0001c0001t0004g0255a0001c0001t0009g0112a0001c0001t0027g0097others(3): Show | 7 | HG02717.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.748-717G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 10/11 | chr12 | 49888156 | ||||||
| chr12:49888429
|
T | C | 3 | a0001c0001t0004g0255a0001c0001t0027g0097a0001c0001t0027g0161 | 3 | HG03225.hp2 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.747+678A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 10/11 | chr12 | 49888429 | ||||||
| chr12:49888644
|
G | A | 1 | a0001c0002t0004g0250 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.747+463C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 10/11 | chr12 | 49888644 | ||||||
| chr12:49888661
|
G | A | 10 | a0001c0001t0004g0255a0001c0001t0009g0112a0001c0001t0020g0025others(7): Show | 12 | HG02055.hp2 HG02258.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.747+446C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 10/11 | chr12 | 49888661 | ||||||
| chr12:49888676
|
G | A | 1 | a0001c0001t0006g0070 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.747+431C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 10/11 | chr12 | 49888676 | ||||||
| chr12:49888680
|
G | C | 1 | a0001c0001t0008g0291 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.747+427C>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 10/11 | chr12 | 49888680 | ||||||
| chr12:49888690
|
C | A | 1 | a0001c0001t0005g0360 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.747+417G>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 10/11 | chr12 | 49888690 | ||||||
| chr12:49888827
|
T | A | 1 | a0001c0001t0002g0186 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.747+280A>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 10/11 | chr12 | 49888827 | ||||||
| chr12:49888837
|
C | T | 6 | a0001c0001t0004g0255a0001c0001t0009g0112a0001c0001t0027g0097others(3): Show | 7 | HG02717.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.747+270G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 10/11 | chr12 | 49888837 | ||||||
| chr12:49888980
|
G | A | 1 | a0001c0001t0027g0161 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.747+127C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 10/11 | chr12 | 49888980 | ||||||
| chr12:49889043
|
G | A | 1 | a0001c0001t0036g0359 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.747+64C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 10/11 | chr12 | 49889043 | ||||||
| chr12:49889080
|
G | T | 1 | a0001c0001t0001g0105 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.747+27C>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 10/11 | chr12 | 49889080 | ||||||
| chr12:49889241
|
G | C | 1 | a0001c0001t0002g0062 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.652-39C>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 9/11 | chr12 | 49889241 | ||||||
| chr12:49889320
|
C | T | 1 | a0001c0001t0066g0316 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.652-118G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 9/11 | chr12 | 49889320 | ||||||
| chr12:49889332
|
C | G | 3 | a0001c0001t0001g0096a0001c0001t0001g0115a0001c0001t0010g0020 | 4 | HG01167.hp1 HG01169.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.652-130G>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 9/11 | chr12 | 49889332 | ||||||
| chr12:49889341
|
C | G | 2 | a0001c0001t0006g0210a0001c0001t0008g0297 | 2 | NA18957.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.652-139G>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 9/11 | chr12 | 49889341 | ||||||
| chr12:49889395
|
G | A | 6 | a0001c0001t0014g0009a0001c0001t0016g0236a0001c0001t0016g0237others(3): Show | 8 | HG01167.hp2 HG01884.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.651+86C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 9/11 | chr12 | 49889395 | ||||||
| chr12:49889412
|
C | G | 1 | a0001c0002t0041g0142 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.651+69G>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 9/11 | chr12 | 49889412 | ||||||
| chr12:49889453
|
G | T | 1 | a0001c0001t0013g0195 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.651+28C>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 9/11 | chr12 | 49889453 | ||||||
| chr12:49889578
|
G | A | 1 | a0001c0001t0029g0127 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.564-10C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 8/11 | chr12 | 49889578 | ||||||
| chr12:49889586
|
G | A | 1 | a0001c0001t0001g0072 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.564-18C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 8/11 | chr12 | 49889586 | ||||||
| chr12:49889603
|
G | A | 1 | a0001c0001t0011g0247 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.564-35C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 8/11 | chr12 | 49889603 | ||||||
| chr12:49889682
|
G | A | 152 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0052others(149): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.564-114C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 8/11 | chr12 | 49889682 | ||||||
| chr12:49889724
|
C | A | 1 | a0001c0001t0020g0145 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.564-156G>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 8/11 | chr12 | 49889724 | ||||||
| chr12:49889752
|
C | A | 6 | a0001c0001t0014g0009a0001c0001t0016g0236a0001c0001t0016g0237others(3): Show | 8 | HG01167.hp2 HG01884.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.564-184G>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 8/11 | chr12 | 49889752 | ||||||
| chr12:49889777
|
G | C | 3 | a0001c0001t0009g0152a0001c0001t0009g0240a0001c0001t0044g0241 | 3 | HG02615.hp1 HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.564-209C>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 8/11 | chr12 | 49889777 | ||||||
| chr12:49889827
|
C | T | 2 | a0001c0001t0006g0210a0001c0001t0008g0297 | 2 | NA18957.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.564-259G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 8/11 | chr12 | 49889827 | ||||||
| chr12:49889893
|
G | A | 1 | a0001c0001t0010g0216 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.563+224C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 8/11 | chr12 | 49889893 | ||||||
| chr12:49889956
|
T | C | 5 | a0001c0001t0004g0255a0001c0001t0020g0025a0001c0001t0020g0145others(2): Show | 6 | HG02055.hp2 HG02258.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.563+161A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 8/11 | chr12 | 49889956 | ||||||
| chr12:49890049
|
G | A | 4 | a0001c0001t0020g0025a0001c0001t0020g0145a0001c0001t0063g0362others(1): Show | 5 | HG02055.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.563+68C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 8/11 | chr12 | 49890049 | ||||||
| chr12:49890196
|
C | T | 7 | a0001c0001t0004g0255a0001c0001t0004g0276a0001c0001t0027g0097others(4): Show | 7 | HG02572.hp1 HG02809.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.526-42G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 7/11 | chr12 | 49890196 | ||||||
| chr12:49890213
|
C | A | 8 | a0001c0001t0001g0128a0001c0001t0001g0137a0001c0001t0001g0153others(5): Show | 8 | HG02145.hp2 HG02647.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.526-59G>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 7/11 | chr12 | 49890213 | ||||||
| chr12:49890283
|
C | T | 1 | a0001c0001t0066g0316 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.526-129G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 7/11 | chr12 | 49890283 | ||||||
| chr12:49890480
|
G | A | 1 | a0001c0001t0001g0063 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.525+203C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 7/11 | chr12 | 49890480 | ||||||
| chr12:49890650
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.525+33C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 7/11 | chr12 | 49890650 | ||||||
| chr12:49890800
|
A | T | 8 | a0001c0001t0008g0343a0001c0001t0010g0113a0001c0001t0010g0114others(5): Show | 8 | HG00642.hp2 HG01258.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.486-78T>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 6/11 | chr12 | 49890800 | ||||||
| chr12:49890813
|
C | T | 1 | a0001c0001t0004g0332 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.486-91G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 6/11 | chr12 | 49890813 | ||||||
| chr12:49891135
|
G | A | 2 | a0001c0001t0015g0209a0001c0001t0015g0225 | 2 | HG02922.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.435-21C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49891135 | ||||||
| chr12:49891245
|
G | A | 1 | a0001c0001t0009g0112 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.435-131C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49891245 | ||||||
| chr12:49891248
|
C | T | 3 | a0001c0001t0009g0152a0001c0001t0009g0240a0001c0001t0044g0241 | 3 | HG02615.hp1 HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.435-134G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49891248 | ||||||
| chr12:49891278
|
T | C | 90 | a0001c0001t0001g0105a0001c0001t0001g0126a0001c0001t0001g0185others(87): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.435-164A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49891278 | ||||||
| chr12:49891319
|
G | A | 1 | a0001c0001t0013g0120 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.435-205C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49891319 | ||||||
| chr12:49891463
|
C | T | 1 | a0001c0001t0012g0344 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.435-349G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49891463 | ||||||
| chr12:49891624
|
TGCCCCAC others(3): Show |
T | 4 | a0001c0001t0020g0025a0001c0001t0020g0145a0001c0001t0063g0362others(1): Show | 5 | HG02055.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.435-520_435-511del others(10): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49891624 | ||||||
| chr12:49891692
|
G | C | 139 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0017others(136): Show | 160 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.435-578C>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49891692 | ||||||
| chr12:49891779
|
C | T | 73 | a0001c0001t0001g0126a0001c0001t0001g0185a0001c0001t0002g0001others(70): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.435-665G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49891779 | ||||||
| chr12:49891943
|
G | A | 1 | a0001c0001t0003g0322 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.435-829C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49891943 | ||||||
| chr12:49891997
|
T | G | 73 | a0001c0001t0001g0126a0001c0001t0001g0185a0001c0001t0002g0001others(70): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.435-883A>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49891997 | ||||||
| chr12:49892271
|
G | A | 4 | a0001c0001t0003g0249a0001c0001t0003g0322a0001c0001t0053g0220others(1): Show | 4 | HG01106.hp2 HG01175.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.435-1157C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49892271 | ||||||
| chr12:49892272
|
G | A | 138 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0017others(135): Show | 159 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.435-1158C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49892272 | ||||||
| chr12:49892339
|
G | A | 5 | a0001c0001t0020g0025a0001c0001t0020g0145a0001c0001t0057g0351others(2): Show | 6 | HG02055.hp2 HG02258.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.435-1225C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49892339 | ||||||
| chr12:49892371
|
A | G | 2 | a0001c0001t0027g0097a0001c0001t0027g0161 | 2 | NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.435-1257T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49892371 | ||||||
| chr12:49892399
|
C | T | 4 | a0001c0001t0020g0025a0001c0001t0020g0145a0001c0001t0063g0362others(1): Show | 5 | HG02055.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.435-1285G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49892399 | ||||||
| chr12:49892400
|
G | A | 1 | a0001c0001t0004g0363 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.435-1286C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49892400 | ||||||
| chr12:49892458
|
C | A | 6 | a0001c0001t0009g0122a0001c0001t0009g0158a0001c0001t0009g0159others(3): Show | 6 | HG01168.hp2 HG02486.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.435-1344G>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49892458 | ||||||
| chr12:49892501
|
C | T | 8 | a0001c0001t0001g0239a0001c0001t0009g0112a0001c0001t0024g0008others(5): Show | 11 | HG02258.hp1 HG02280.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.435-1387G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49892501 | ||||||
| chr12:49892503
|
T | C | 4 | a0001c0001t0020g0025a0001c0001t0020g0145a0001c0001t0063g0362others(1): Show | 5 | HG02055.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.435-1389A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49892503 | ||||||
| chr12:49892546
|
T | A | 3 | a0001c0001t0009g0152a0001c0001t0009g0240a0001c0001t0044g0241 | 3 | HG02615.hp1 HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.435-1432A>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49892546 | ||||||
| chr12:49892636
|
C | T | 1 | a0001c0001t0005g0279 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.435-1522G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49892636 | ||||||
| chr12:49892707
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.435-1593C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49892707 | ||||||
| chr12:49892736
|
C | A | 4 | a0001c0001t0020g0025a0001c0001t0020g0145a0001c0001t0063g0362others(1): Show | 5 | HG02055.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.435-1622G>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49892736 | ||||||
| chr12:49893054
|
A | G | 7 | a0001c0001t0001g0126a0001c0001t0004g0363a0001c0001t0020g0025others(4): Show | 9 | HG02055.hp2 HG02258.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.435-1940T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49893054 | ||||||
| chr12:49893163
|
G | T | 6 | a0001c0001t0009g0122a0001c0001t0009g0158a0001c0001t0009g0159others(3): Show | 6 | HG01168.hp2 HG02486.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.435-2049C>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49893163 | ||||||
| chr12:49893522
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.435-2408C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49893522 | ||||||
| chr12:49893602
|
C | T | 1 | a0001c0001t0007g0051 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.435-2488G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49893602 | ||||||
| chr12:49893701
|
T | C | 4 | a0001c0001t0020g0025a0001c0001t0020g0145a0001c0001t0063g0362others(1): Show | 5 | HG02055.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.435-2587A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49893701 | ||||||
| chr12:49893713
|
G | T | 4 | a0001c0001t0020g0025a0001c0001t0020g0145a0001c0001t0063g0362others(1): Show | 5 | HG02055.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.435-2599C>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49893713 | ||||||
| chr12:49893718
|
A | G | 6 | a0001c0001t0009g0152a0001c0001t0009g0240a0001c0001t0019g0150others(3): Show | 6 | HG02615.hp1 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.435-2604T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49893718 | ||||||
| chr12:49893809
|
G | A | 58 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0052others(55): Show | 67 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.435-2695C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49893809 | ||||||
| chr12:49893909
|
G | T | 4 | a0001c0001t0004g0276a0001c0001t0028g0163a0001c0001t0028g0164others(1): Show | 4 | HG02572.hp1 HG02809.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.435-2795C>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49893909 | ||||||
| chr12:49893915
|
T | G | 4 | a0001c0001t0004g0276a0001c0001t0028g0163a0001c0001t0028g0164others(1): Show | 4 | HG02572.hp1 HG02809.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.435-2801A>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49893915 | ||||||
| chr12:49894061
|
G | C | 170 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0052others(167): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.435-2947C>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49894061 | ||||||
| chr12:49894249
|
A | G | 12 | a0001c0001t0001g0102a0001c0001t0001g0105a0001c0001t0005g0302others(9): Show | 12 | HG01070.hp2 HG01074.hp2 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.434+2782T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49894249 | ||||||
| chr12:49894322
|
T | C | 6 | a0001c0001t0020g0025a0001c0001t0020g0145a0001c0001t0063g0362others(3): Show | 8 | HG02055.hp2 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.434+2709A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49894322 | ||||||
| chr12:49894384
|
G | A | 1 | a0001c0001t0011g0352 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.434+2647C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49894384 | ||||||
| chr12:49894514
|
T | C | 2 | a0001c0001t0005g0248a0001c0001t0008g0243 | 2 | NA18992.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.434+2517A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49894514 | ||||||
| chr12:49894531
|
C | CAG | 4 | a0001c0001t0004g0276a0001c0001t0028g0163a0001c0001t0028g0164others(1): Show | 4 | HG02572.hp1 HG02809.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.434+2498_434+2499d others(4): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49894531 | ||||||
| chr12:49894659
|
C | G | 2 | a0001c0001t0017g0214a0001c0002t0041g0142 | 2 | HG03516.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.434+2372G>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49894659 | ||||||
| chr12:49894695
|
A | C | 1 | a0001c0001t0023g0024 | 2 | HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.434+2336T>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49894695 | ||||||
| chr12:49894703
|
G | A | 142 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0017others(139): Show | 164 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.434+2328C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49894703 | ||||||
| chr12:49894832
|
G | C | 133 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0052others(130): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.434+2199C>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49894832 | ||||||
| chr12:49894855
|
AAC | A | 3 | a0001c0001t0016g0136a0001c0002t0001g0141a0001c0002t0038g0140 | 3 | HG02145.hp2 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.434+2174_434+2175d others(4): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49894855 | ||||||
| chr12:49894916
|
A | G | 2 | a0001c0001t0001g0102a0001c0001t0001g0105 | 2 | HG01884.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.434+2115T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49894916 | ||||||
| chr12:49895027
|
G | C | 15 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0017others(12): Show | 20 | HG00423.hp2 HG00673.hp2 HG02027.hp1 others(17): Show |
intron_variant | MODIFIER | c.434+2004C>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49895027 | ||||||
| chr12:49895058
|
A | G | 11 | a0001c0001t0004g0276a0001c0001t0009g0152a0001c0001t0009g0240others(8): Show | 11 | HG02572.hp1 HG02615.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.434+1973T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49895058 | ||||||
| chr12:49895060
|
C | CGGGCA | 133 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0052others(130): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.434+1966_434+1970d others(7): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49895060 | ||||||
| chr12:49895327
|
C | T | 8 | a0001c0001t0005g0278a0001c0001t0005g0301a0001c0001t0005g0356others(5): Show | 10 | HG00423.hp1 HG00673.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.434+1704G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49895327 | ||||||
| chr12:49895337
|
C | G | 1 | a0001c0001t0009g0112 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.434+1694G>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49895337 | ||||||
| chr12:49895337
|
C | T | 1 | a0001c0001t0008g0277 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.434+1694G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49895337 | ||||||
| chr12:49895374
|
C | G | 1 | a0001c0001t0009g0112 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.434+1657G>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49895374 | ||||||
| chr12:49895428
|
G | A | 5 | a0001c0001t0014g0009a0001c0001t0016g0237a0001c0001t0034g0238others(2): Show | 7 | HG01167.hp2 HG01884.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.434+1603C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49895428 | ||||||
| chr12:49895440
|
G | A | 8 | a0001c0001t0001g0175a0001c0001t0001g0222a0001c0001t0001g0234others(5): Show | 8 | HG00140.hp1 HG00738.hp1 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.434+1591C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49895440 | ||||||
| chr12:49895482
|
A | G | 4 | a0001c0001t0004g0276a0001c0001t0028g0163a0001c0001t0028g0164others(1): Show | 4 | HG02572.hp1 HG02809.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.434+1549T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49895482 | ||||||
| chr12:49895496
|
G | A | 2 | a0001c0001t0001g0102a0001c0001t0001g0105 | 2 | HG01884.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.434+1535C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49895496 | ||||||
| chr12:49895765
|
C | T | 5 | a0001c0001t0009g0158a0001c0001t0009g0159a0001c0001t0015g0209others(2): Show | 5 | HG01168.hp2 HG02486.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.434+1266G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49895765 | ||||||
| chr12:49895801
|
C | T | 4 | a0001c0001t0006g0068a0001c0001t0006g0070a0001c0001t0007g0069others(1): Show | 4 | NA18943.hp1 NA18973.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.434+1230G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49895801 | ||||||
| chr12:49895852
|
C | T | 22 | a0001c0001t0001g0149a0001c0001t0001g0153a0001c0001t0004g0255others(19): Show | 23 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.434+1179G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49895852 | ||||||
| chr12:49895874
|
T | C | 69 | a0001c0001t0001g0185a0001c0001t0001g0235a0001c0001t0002g0001others(66): Show | 92 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.434+1157A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49895874 | ||||||
| chr12:49895884
|
G | A | 68 | a0001c0001t0001g0185a0001c0001t0001g0235a0001c0001t0002g0001others(65): Show | 91 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.434+1147C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49895884 | ||||||
| chr12:49896014
|
G | C | 20 | a0001c0001t0001g0128a0001c0001t0001g0137a0001c0001t0001g0149others(17): Show | 21 | HG02145.hp2 HG02572.hp1 HG02615.hp1 others(18): Show |
intron_variant | MODIFIER | c.434+1017C>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49896014 | ||||||
| chr12:49896026
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.434+1005G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49896026 | ||||||
| chr12:49896240
|
T | C | 180 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0017others(177): Show | 206 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(203): Show |
intron_variant | MODIFIER | c.434+791A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49896240 | ||||||
| chr12:49896256
|
G | T | 1 | a0001c0001t0006g0229 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.434+775C>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49896256 | ||||||
| chr12:49896273
|
G | A | 8 | a0001c0001t0001g0175a0001c0001t0002g0010a0001c0001t0002g0135others(5): Show | 10 | HG00099.hp2 HG00639.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.434+758C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49896273 | ||||||
| chr12:49896445
|
G | T | 1 | a0001c0001t0006g0229 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.434+586C>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49896445 | ||||||
| chr12:49896654
|
G | A | 1 | a0001c0001t0005g0361 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.434+377C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49896654 | ||||||
| chr12:49896770
|
C | T | 2 | a0001c0001t0014g0009a0001c0001t0058g0310 | 4 | HG01167.hp2 HG02572.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.434+261G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49896770 | ||||||
| chr12:49896771
|
G | A | 222 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0063others(219): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.434+260C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49896771 | ||||||
| chr12:49896805
|
C | T | 8 | a0001c0001t0001g0102a0001c0001t0009g0158a0001c0001t0009g0159others(5): Show | 10 | HG01167.hp2 HG01884.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.434+226G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49896805 | ||||||
| chr12:49896945
|
A | G | 278 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(275): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.434+86T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49896945 | ||||||
| chr12:49897447
|
A | G | 1 | a0001c0001t0012g0257 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.380+72T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 4/11 | chr12 | 49897447 | ||||||
| chr12:49897668
|
T | A | 10 | a0001c0001t0001g0088a0001c0001t0001g0170a0001c0001t0006g0210others(7): Show | 12 | HG00408.hp2 HG02132.hp2 NA18944.hp1 others(9): Show |
intron_variant | MODIFIER | c.316-85A>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 3/11 | chr12 | 49897668 | ||||||
| chr12:49897674
|
T | C | 1 | a0001c0001t0006g0212 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.316-91A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 3/11 | chr12 | 49897674 | ||||||
| chr12:49897677
|
T | TCCTTTTT others(3): Show |
1 | a0001c0001t0006g0212 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.316-95_316-94insCC others(8): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 3/11 | chr12 | 49897677 | ||||||
| chr12:49897687
|
A | C | 1 | a0001c0001t0005g0258 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.316-104T>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 3/11 | chr12 | 49897687 | ||||||
| chr12:49897712
|
G | A | 1 | a0001c0001t0007g0215 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.316-129C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 3/11 | chr12 | 49897712 | ||||||
| chr12:49897764
|
A | AC | 204 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(201): Show | 235 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(232): Show |
intron_variant | MODIFIER | c.316-182dupG | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 3/11 | chr12 | 49897764 | ||||||
| chr12:49897767
|
C | CA | 4 | a0001c0001t0004g0306a0001c0001t0007g0064a0001c0001t0008g0245others(1): Show | 4 | HG00621.hp1 NA18950.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.316-185_316-184ins others(1): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 3/11 | chr12 | 49897767 | ||||||
| chr12:49897768
|
C | A | 45 | a0001c0001t0001g0072a0001c0001t0001g0149a0001c0001t0003g0037others(42): Show | 50 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.316-185G>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 3/11 | chr12 | 49897768 | ||||||
| chr12:49897842
|
A | C | 30 | a0001c0001t0001g0128a0001c0001t0001g0153a0001c0001t0001g0239others(27): Show | 35 | HG01109.hp1 HG02055.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.315+145T>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 3/11 | chr12 | 49897842 | ||||||
| chr12:49897884
|
G | T | 1 | a0001c0001t0042g0107 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.315+103C>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 3/11 | chr12 | 49897884 | ||||||
| chr12:49897952
|
G | C | 257 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(254): Show | 291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.315+35C>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 3/11 | chr12 | 49897952 | ||||||
| chr12:49897970
|
C | A | 5 | a0001c0001t0001g0015a0001c0001t0002g0065a0001c0001t0002g0066others(2): Show | 6 | NA18951.hp2 NA18975.hp1 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.315+17G>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 3/11 | chr12 | 49897970 | ||||||
| chr12:49898173
|
C | T | 5 | a0001c0001t0009g0144a0001c0001t0009g0158a0001c0001t0009g0159others(2): Show | 5 | HG02258.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.212-83G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 2/11 | chr12 | 49898173 | ||||||
| chr12:49898239
|
G | GCCCGGCT others(95): Show |
137 | a0001c0001t0001g0096a0001c0001t0001g0102a0001c0001t0001g0105others(134): Show | 170 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.212-251_212-150dup others(102): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 2/11 | chr12 | 49898239 | ||||||
| chr12:49898255
|
A | ATCCCCAG others(95): Show |
2 | a0001c0001t0002g0048a0001c0001t0003g0004 | 5 | NA18956.hp2 NA18992.hp2 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.212-166_212-165ins others(102): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 2/11 | chr12 | 49898255 | ||||||
| chr12:49898264
|
T | A | 1 | a0001c0001t0034g0146 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.212-174A>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 2/11 | chr12 | 49898264 | ||||||
| chr12:49898335
|
C | T | 14 | a0001c0001t0001g0072a0001c0001t0003g0338a0001c0001t0004g0040others(11): Show | 16 | HG00642.hp1 HG01928.hp1 HG02523.hp2 others(13): Show |
intron_variant | MODIFIER | c.212-245G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 2/11 | chr12 | 49898335 | ||||||
| chr12:49898345
|
G | A | 2 | a0001c0001t0009g0158a0001c0001t0009g0159 | 2 | HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.212-255C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 2/11 | chr12 | 49898345 | ||||||
| chr12:49898356
|
C | T | 1 | a0001c0001t0005g0256 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.212-266G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 2/11 | chr12 | 49898356 | ||||||
| chr12:49898449
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.212-359T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 2/11 | chr12 | 49898449 | ||||||
| chr12:49898503
|
C | T | 1 | a0001c0001t0013g0195 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.212-413G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 2/11 | chr12 | 49898503 | ||||||
| chr12:49898602
|
G | T | 11 | a0001c0001t0001g0153a0001c0001t0001g0239a0001c0001t0004g0255others(8): Show | 14 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.212-512C>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 2/11 | chr12 | 49898602 | ||||||
| chr12:49898641
|
C | T | 1 | a0001c0001t0007g0047 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.212-551G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 2/11 | chr12 | 49898641 | ||||||
| chr12:49898695
|
A | T | 315 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(312): Show | 376 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(373): Show |
intron_variant | MODIFIER | c.212-605T>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 2/11 | chr12 | 49898695 | ||||||
| chr12:49898800
|
T | G | 1 | a0001c0001t0005g0355 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.212-710A>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 2/11 | chr12 | 49898800 | ||||||
| chr12:49898803
|
C | T | 5 | a0001c0001t0009g0144a0001c0001t0009g0158a0001c0001t0009g0159others(2): Show | 5 | HG02258.hp2 HG02486.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.212-713G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 2/11 | chr12 | 49898803 | ||||||
| chr12:49898891
|
C | T | 1 | a0001c0001t0008g0254 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.212-801G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 2/11 | chr12 | 49898891 | ||||||
| chr12:49898896
|
G | A | 1 | a0001c0001t0048g0073 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.212-806C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 2/11 | chr12 | 49898896 | ||||||
| chr12:49898900
|
T | A | 1 | a0003c0004t0001g0227 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.212-810A>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 2/11 | chr12 | 49898900 | ||||||
| chr12:49898904
|
G | GGCTTTCC others(24): Show |
1 | a0003c0004t0001g0227 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.212-815_212-814ins others(31): Show |
FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 2/11 | chr12 | 49898904 | ||||||
| chr12:49898906
|
T | A | 1 | a0003c0004t0001g0227 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.212-816A>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 2/11 | chr12 | 49898906 | ||||||
| chr12:49898907
|
G | A | 1 | a0003c0004t0001g0227 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.212-817C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 2/11 | chr12 | 49898907 | ||||||
| chr12:49898910
|
A | C | 1 | a0003c0004t0001g0227 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.212-820T>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 2/11 | chr12 | 49898910 | ||||||
| chr12:49898914
|
A | C | 1 | a0003c0004t0001g0227 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.212-824T>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 2/11 | chr12 | 49898914 | ||||||
| chr12:49898917
|
G | A | 1 | a0003c0004t0001g0227 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.212-827C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 2/11 | chr12 | 49898917 | ||||||
| chr12:49899082
|
A | G | 2 | a0001c0001t0024g0008a0001c0001t0027g0097 | 4 | HG02258.hp1 NA18906.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.212-992T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 2/11 | chr12 | 49899082 | ||||||
| chr12:49899307
|
C | A | 43 | a0001c0001t0001g0017a0001c0001t0001g0074a0001c0001t0001g0076others(40): Show | 56 | HG00597.hp2 HG00733.hp2 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.212-1217G>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 2/11 | chr12 | 49899307 | ||||||
| chr12:49899316
|
C | T | 3 | a0001c0001t0001g0153a0001c0001t0009g0240a0001c0001t0044g0241 | 3 | HG02622.hp2 HG02647.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.212-1226G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 2/11 | chr12 | 49899316 | ||||||
| chr12:49899399
|
A | G | 1 | a0001c0001t0002g0187 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.212-1309T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 2/11 | chr12 | 49899399 | ||||||
| chr12:49899426
|
T | C | 20 | a0001c0001t0009g0152a0001c0001t0009g0184a0001c0001t0016g0136others(17): Show | 23 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.212-1336A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 2/11 | chr12 | 49899426 | ||||||
| chr12:49899450
|
G | A | 4 | a0001c0001t0004g0363a0001c0001t0009g0152a0001c0001t0020g0025others(1): Show | 5 | HG01109.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.212-1360C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 2/11 | chr12 | 49899450 | ||||||
| chr12:49899463
|
G | A | 3 | a0001c0001t0001g0105a0001c0001t0009g0103a0001c0001t0019g0104 | 3 | HG01884.hp2 HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.212-1373C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 2/11 | chr12 | 49899463 | ||||||
| chr12:49899475
|
A | G | 2 | a0001c0001t0002g0046a0001c0001t0004g0253 | 2 | NA19063.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.212-1385T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 2/11 | chr12 | 49899475 | ||||||
| chr12:49899517
|
A | G | 1 | a0001c0001t0032g0023 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.212-1427T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 2/11 | chr12 | 49899517 | ||||||
| chr12:49899525
|
T | C | 15 | a0001c0001t0001g0105a0001c0001t0001g0128a0001c0001t0001g0239others(12): Show | 17 | HG01069.hp1 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.212-1435A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 2/11 | chr12 | 49899525 | ||||||
| chr12:49899584
|
A | C | 2 | a0001c0001t0017g0022a0001c0001t0022g0021 | 4 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.212-1494T>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 2/11 | chr12 | 49899584 | ||||||
| chr12:49899738
|
T | C | 3 | a0001c0001t0003g0367a0001c0001t0004g0045a0001c0001t0004g0366 | 4 | NA18943.hp2 NA18988.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.211+1392A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 2/11 | chr12 | 49899738 | ||||||
| chr12:49899819
|
G | A | 2 | a0001c0001t0002g0233a0001c0001t0015g0232 | 2 | HG01081.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.211+1311C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 2/11 | chr12 | 49899819 | ||||||
| chr12:49899840
|
C | A | 2 | a0001c0001t0001g0153a0001c0001t0042g0107 | 2 | HG02647.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.211+1290G>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 2/11 | chr12 | 49899840 | ||||||
| chr12:49899938
|
C | T | 3 | a0001c0001t0017g0022a0001c0001t0022g0021a0001c0001t0033g0131 | 5 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.211+1192G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 2/11 | chr12 | 49899938 | ||||||
| chr12:49900000
|
G | T | 5 | a0001c0001t0001g0239a0001c0001t0016g0236a0001c0001t0016g0237others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.211+1130C>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 2/11 | chr12 | 49900000 | ||||||
| chr12:49900002
|
C | T | 1 | a0001c0001t0011g0252 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.211+1128G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 2/11 | chr12 | 49900002 | ||||||
| chr12:49900006
|
T | C | 12 | a0001c0001t0001g0102a0001c0001t0001g0105a0001c0001t0001g0137others(9): Show | 16 | HG01167.hp2 HG01884.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.211+1124A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 2/11 | chr12 | 49900006 | ||||||
| chr12:49900033
|
G | A | 2 | a0001c0001t0006g0130a0001c0001t0009g0129 | 2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.211+1097C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 2/11 | chr12 | 49900033 | ||||||
| chr12:49900167
|
C | G | 8 | a0001c0001t0009g0158a0001c0001t0009g0159a0001c0001t0009g0162others(5): Show | 9 | HG01069.hp1 HG01071.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.211+963G>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 2/11 | chr12 | 49900167 | ||||||
| chr12:49900181
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.211+949C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 2/11 | chr12 | 49900181 | ||||||
| chr12:49900239
|
A | G | 1 | a0001c0001t0042g0107 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.211+891T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 2/11 | chr12 | 49900239 | ||||||
| chr12:49900591
|
C | T | 1 | a0001c0001t0006g0194 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.211+539G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 2/11 | chr12 | 49900591 | ||||||
| chr12:49900671
|
C | T | 1 | a0001c0001t0003g0251 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.211+459G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 2/11 | chr12 | 49900671 | ||||||
| chr12:49901589
|
G | A | 1 | a0001c0001t0003g0368 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.16-264C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 1/11 | chr12 | 49901589 | ||||||
| chr12:49901927
|
A | G | 4 | a0001c0001t0010g0155a0001c0001t0018g0011a0001c0001t0018g0154others(1): Show | 6 | HG02071.hp1 NA18944.hp1 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.16-602T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 1/11 | chr12 | 49901927 | ||||||
| chr12:49902313
|
G | A | 10 | a0001c0001t0001g0137a0001c0001t0002g0010a0001c0001t0002g0133others(7): Show | 14 | HG00099.hp2 HG01243.hp1 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.16-988C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 1/11 | chr12 | 49902313 | ||||||
| chr12:49902376
|
T | C | 37 | a0001c0001t0001g0096a0001c0001t0001g0102a0001c0001t0001g0105others(34): Show | 47 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.16-1051A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 1/11 | chr12 | 49902376 | ||||||
| chr12:49902388
|
C | T | 35 | a0001c0001t0001g0108a0001c0001t0001g0115a0001c0001t0001g0126others(32): Show | 40 | HG00099.hp2 HG00280.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.16-1063G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 1/11 | chr12 | 49902388 | ||||||
| chr12:49902518
|
C | T | 280 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(277): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.16-1193G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 1/11 | chr12 | 49902518 | ||||||
| chr12:49902705
|
G | GC | 146 | a0001c0001t0001g0235a0001c0001t0002g0090a0001c0001t0003g0004others(143): Show | 167 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.15+1072dupG | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 1/11 | chr12 | 49902705 | ||||||
| chr12:49902802
|
T | C | 1 | a0001c0001t0001g0239 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.15+976A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 1/11 | chr12 | 49902802 | ||||||
| chr12:49902855
|
C | T | 2 | a0001c0002t0020g0106a0002c0003t0014g0019 | 3 | HG02055.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.15+923G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 1/11 | chr12 | 49902855 | ||||||
| chr12:49902856
|
G | A | 1 | a0001c0001t0011g0370 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.15+922C>T | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 1/11 | chr12 | 49902856 | ||||||
| chr12:49903020
|
T | C | 1 | a0001c0001t0002g0091 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.15+758A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 1/11 | chr12 | 49903020 | ||||||
| chr12:49903195
|
G | C | 55 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(52): Show | 66 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.15+583C>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 1/11 | chr12 | 49903195 | ||||||
| chr12:49903218
|
C | G | 243 | a0001c0001t0001g0108a0001c0001t0001g0115a0001c0001t0001g0126others(240): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.15+560G>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 1/11 | chr12 | 49903218 | ||||||
| chr12:49903251
|
T | C | 4 | a0001c0001t0001g0239a0001c0001t0016g0236a0001c0001t0016g0237others(1): Show | 4 | HG01884.hp1 HG02630.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+527A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 1/11 | chr12 | 49903251 | ||||||
| chr12:49903329
|
T | G | 1 | a0001c0001t0039g0092 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.15+449A>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 1/11 | chr12 | 49903329 | ||||||
| chr12:49903435
|
C | T | 1 | a0001c0001t0003g0249 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.15+343G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 1/11 | chr12 | 49903435 | ||||||
| chr12:49903557
|
C | G | 71 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(68): Show | 87 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.15+221G>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 1/11 | chr12 | 49903557 | ||||||
| chr12:49903592
|
A | G | 55 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0015others(52): Show | 66 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.15+186T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 1/11 | chr12 | 49903592 | ||||||
| chr12:49903630
|
C | T | 6 | a0001c0001t0008g0243a0001c0001t0008g0245a0001c0001t0011g0244others(3): Show | 6 | HG02132.hp1 NA18963.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.15+148G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 1/11 | chr12 | 49903630 | ||||||
| chr12:49903710
|
T | C | 2 | a0001c0001t0009g0240a0001c0001t0044g0241 | 2 | HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.15+68A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 1/11 | chr12 | 49903710 |