Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | MTQGK others(311): Show |
chr12 | 49861896 | 49908900 |
| a0002 | 0/0 | 316 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | MTQGK others(311): Show |
chr12 | 49861896 | 49908900 |
| a0003 | 0/0 | 305 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | MTQGK others(300): Show |
chr12 | 49861896 | 49908900 |
| a0004 | 0/0 | 316 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | MTQGK others(311): Show |
chr12 | 49861896 | 49908900 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 948 | 422 | 85 | 66 | 205 | 18 | 46 | FAIM2_chr12_49861896_49908900 | FAIM2 | ATGAC others(943): Show |
chr12 | 49861896 | 49908900 | ||
| a0001c0002 | 0/0 | 948 | 10 | 9 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | ATGAC others(943): Show |
chr12 | 49861896 | 49908900 | ||
| a0002c0003 | 0/0 | 948 | 2 | 2 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | ATGAC others(943): Show |
chr12 | 49861896 | 49908900 | ||
| a0003c0004 | 0/0 | 915 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | ATGAC others(910): Show |
chr12 | 49861896 | 49908900 | ||
| a0004c0005 | 0/0 | 948 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | ATGAC others(943): Show |
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 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0002 | 0/0 | 4667 | 51 | 0 | 8 | 35 | 5 | 3 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0003 | 0/0 | 4667 | 32 | 1 | 10 | 12 | 4 | 5 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0004 | 0/0 | 4667 | 29 | 3 | 2 | 22 | 0 | 2 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0005 | 0/0 | 4667 | 30 | 0 | 5 | 19 | 0 | 6 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0006 | 0/0 | 4667 | 29 | 1 | 9 | 17 | 0 | 2 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0007 | 0/0 | 4667 | 23 | 0 | 2 | 18 | 0 | 3 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0008 | 0/0 | 4667 | 20 | 1 | 2 | 12 | 2 | 3 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0009 | 0/0 | 4667 | 16 | 12 | 0 | 3 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0010 | 0/0 | 4667 | 14 | 0 | 6 | 4 | 0 | 4 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0011 | 0/0 | 4667 | 13 | 0 | 2 | 7 | 1 | 3 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0012 | 0/1 | 4667 | 13 | 2 | 2 | 1 | 2 | 5 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0013 | 1/0 | 4667 | 9 | 2 | 2 | 1 | 1 | 2 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0014 | 0/0 | 4667 | 3 | 2 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0015 | 0/0 | 4667 | 5 | 2 | 3 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0016 | 0/0 | 4663 | 5 | 5 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4658): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0017 | 0/0 | 4667 | 3 | 3 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0018 | 0/0 | 4667 | 4 | 0 | 0 | 4 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0019 | 0/0 | 4667 | 3 | 3 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0020 | 0/0 | 4667 | 3 | 3 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0021 | 0/0 | 4667 | 4 | 1 | 0 | 2 | 1 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0022 | 0/0 | 4667 | 3 | 3 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0023 | 0/0 | 4667 | 2 | 2 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0024 | 0/0 | 4667 | 3 | 3 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0025 | 0/0 | 4667 | 3 | 0 | 3 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0026 | 0/0 | 4667 | 3 | 0 | 0 | 3 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0027 | 0/0 | 4667 | 2 | 2 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0028 | 0/0 | 4667 | 2 | 2 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0029 | 0/0 | 4667 | 2 | 2 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0030 | 0/0 | 4667 | 2 | 2 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0031 | 0/0 | 4667 | 2 | 0 | 0 | 2 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0032 | 0/0 | 4667 | 2 | 0 | 2 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0033 | 0/0 | 4667 | 2 | 2 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0034 | 0/0 | 4663 | 2 | 2 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4658): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0035 | 0/0 | 4667 | 2 | 2 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0036 | 0/0 | 4667 | 2 | 0 | 0 | 0 | 0 | 2 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0037 | 0/0 | 4667 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0039 | 0/0 | 4667 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0040 | 0/0 | 4667 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0042 | 0/0 | 4667 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0043 | 0/0 | 4667 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0044 | 0/0 | 4667 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0045 | 0/0 | 4667 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0046 | 0/0 | 4667 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0047 | 0/0 | 4667 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0048 | 0/0 | 4667 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0049 | 0/0 | 4667 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0050 | 0/0 | 4667 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0051 | 0/0 | 4667 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0052 | 0/0 | 4667 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0053 | 0/0 | 4667 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0054 | 0/0 | 4667 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0055 | 0/0 | 4667 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0056 | 0/0 | 4667 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0057 | 0/0 | 4667 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0058 | 0/0 | 4667 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0059 | 0/0 | 4667 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0060 | 0/0 | 4667 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0061 | 0/0 | 4667 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0062 | 0/0 | 4667 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0063 | 0/0 | 4667 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0064 | 0/0 | 4667 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0065 | 0/0 | 4667 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0066 | 0/0 | 4667 | 1 | 0 | 0 | 0 | 1 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0067 | 0/0 | 4667 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0001t0068 | 0/0 | 4667 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0002t0001 | 0/0 | 4667 | 2 | 2 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0002t0004 | 0/0 | 4667 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0002t0014 | 0/0 | 4667 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0002t0017 | 0/0 | 4667 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0002t0019 | 0/0 | 4667 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0002t0020 | 0/0 | 4667 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0002t0023 | 0/0 | 4667 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0002t0038 | 0/0 | 4667 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0001c0002t0041 | 0/0 | 4667 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0002c0003t0014 | 0/0 | 4667 | 2 | 2 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
chr12 | 49861896 | 49908900 |
| a0003c0004t0001 | 0/0 | 4634 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4629): Show |
chr12 | 49861896 | 49908900 |
| a0004c0005t0004 | 0/0 | 4667 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | AGTGG others(4662): Show |
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 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 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 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0001g0075 | 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 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0001g0087 | 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 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0001g0098 | 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 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 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 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0002g0051 | 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 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0002g0093 | 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 |
| a0001c0001t0003g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0003g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0003g0040 | 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 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0003g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0003g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0003g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0003g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0003g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0003g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0003g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0003g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0003g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0003g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0003g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0003g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0003g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0003g0365 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0003g0366 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0004g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0004g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0004g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | 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 |
| a0001c0001t0004g0046 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0004g0047 | 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 |
| a0001c0001t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0004g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0004g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0004g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0004g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0004g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0004g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0004g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0004g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0004g0333 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0004g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0004g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0004g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0004g0363 | 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 |
| a0001c0001t0005g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0005g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0005g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0005g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0005g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0005g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0005g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0005g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0005g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0005g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0005g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0005g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0005g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 |
| a0001c0001t0005g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0005g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0005g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0005g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0005g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0005g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0005g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0005g0358 | 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 |
| 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 |
| a0001c0001t0006g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0006g0059 | 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 |
| a0001c0001t0006g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0006g0073 | 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 |
| a0001c0001t0006g0231 | 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 |
| a0001c0001t0007g0049 | 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 |
| a0001c0001t0007g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0007g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0007g0058 | 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 |
| a0001c0001t0007g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0007g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0007g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0007g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0007g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0007g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0007g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0007g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0007g0096 | 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 |
| a0001c0001t0007g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0008g0037 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0008g0044 | 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 |
| a0001c0001t0008g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0008g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0008g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0008g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0008g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0008g0292 | 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 |
| a0001c0001t0008g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0008g0304 | 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 |
| a0001c0001t0008g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0008g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0009g0079 | 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 |
| a0001c0001t0009g0241 | 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 |
| a0001c0001t0010g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0010g0062 | 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 |
| a0001c0001t0011g0043 | 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 |
| a0001c0001t0011g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0011g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0011g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0011g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0011g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0011g0349 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0011g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0012g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0012g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0012g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0012g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0012g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0012g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0012g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0012g0337 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0012g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0012g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0012g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0012g0350 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0012g0367 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0013g0033 | 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 |
| a0001c0001t0015g0028 | 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 |
| a0001c0001t0016g0019 | 0/0 | 2 | 2 | 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 |
| a0001c0001t0017g0023 | 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 |
| a0001c0001t0020g0026 | 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 |
| a0001c0001t0021g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0021g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0021g0343 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0021g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0022g0022 | 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 |
| a0001c0001t0023g0025 | 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 |
| a0001c0001t0025g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0025g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0026g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0026g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0027g0099 | 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 |
| a0001c0001t0031g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0031g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0032g0024 | 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 |
| a0001c0001t0035g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0035g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0036g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0036g0356 | 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 |
| a0001c0001t0039g0094 | 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 |
| a0001c0001t0044g0240 | 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 |
| a0001c0001t0047g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0048g0057 | 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 |
| a0001c0001t0050g0061 | 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 |
| a0001c0001t0052g0097 | 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 |
| a0001c0001t0055g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0056g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0057g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0058g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0059g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0060g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0061g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0062g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0063g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0064g0296 | 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 |
| a0001c0001t0066g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0067g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| a0001c0001t0068g0318 | 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 |
| a0001c0002t0014g0095 | 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 |
| a0002c0003t0014g0020 | 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 |
| a0004c0005t0004g0258 | 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 | g0313 | 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 | g0350 | EUR | GBR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0366 | 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 | g0302 | 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 | g0058 | EAS | CHS | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG00423 | hp2 | a0001 | c0001 | t0048 | g0057 | 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 | g0288 | EAS | CHS | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG00544 | hp1 | a0001 | c0001 | t0004 | g0283 | 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 | g0035 | EAS | CHS | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0054 | 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 | g0076 | 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 | g0345 | EAS | CHS | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG00621 | hp1 | a0001 | c0001 | t0007 | g0067 | 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 | g0324 | 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 | g0332 | AMR | PUR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG00642 | hp2 | a0001 | c0001 | t0012 | g0342 | AMR | PUR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG00673 | hp1 | a0001 | c0001 | t0005 | g0275 | EAS | CHS | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0290 | EAS | CHS | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG00733 | hp1 | a0001 | c0001 | t0015 | g0028 | AMR | PUR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG00733 | hp2 | a0001 | c0001 | t0007 | g0230 | AMR | PUR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG00735 | hp1 | a0001 | c0001 | t0015 | g0028 | 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 | g0355 | AMR | PUR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG00741 | hp2 | a0001 | c0001 | t0060 | g0346 | 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 | g0039 | AMR | PUR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01070 | hp2 | a0001 | c0001 | t0005 | g0299 | 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 | g0039 | AMR | PUR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01074 | hp1 | a0001 | c0001 | t0025 | g0270 | 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 | g0271 | 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 | g0310 | 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 | g0021 | 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 | g0024 | 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 | g0024 | AMR | PUR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01169 | hp2 | a0001 | c0001 | t0010 | g0021 | 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 | g0309 | 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 | g0315 | AMR | PUR | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01257 | hp1 | a0001 | c0001 | t0025 | g0036 | 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 | g0036 | 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 | g0295 | 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 | g0096 | AMR | CLM | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0286 | AMR | CLM | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0338 | 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 | g0033 | AMR | CLM | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01433 | hp2 | a0001 | c0001 | t0056 | g0351 | 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 | g0033 | 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 | g0037 | 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 | g0349 | EUR | IBS | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01517 | hp1 | a0001 | c0001 | t0008 | g0037 | 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 | g0023 | AFR | ACB | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01891 | hp2 | a0001 | c0001 | t0012 | g0312 | AFR | ACB | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG01928 | hp1 | a0001 | c0001 | t0004 | g0333 | 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 | g0318 | 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 | g0305 | EAS | KHV | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02015 | hp2 | a0001 | c0001 | t0005 | g0316 | EAS | KHV | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02027 | hp2 | a0004 | c0005 | t0004 | g0258 | EAS | KHV | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02040 | hp1 | a0001 | c0001 | t0021 | g0272 | EAS | KHV | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02040 | hp2 | a0001 | c0001 | t0005 | g0326 | EAS | KHV | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02055 | hp1 | a0001 | c0001 | t0016 | g0019 | 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 | g0298 | EAS | KHV | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0051 | 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 | g0074 | EAS | KHV | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02080 | hp2 | a0001 | c0001 | t0050 | g0061 | EAS | KHV | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02083 | hp1 | a0001 | c0001 | t0004 | g0045 | EAS | KHV | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02083 | hp2 | a0001 | c0001 | t0008 | g0292 | 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 | g0062 | EAS | KHV | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02135 | hp1 | a0001 | c0001 | t0004 | g0289 | EAS | KHV | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02135 | hp2 | a0001 | c0001 | t0012 | g0347 | EAS | KHV | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02145 | hp1 | a0001 | c0001 | t0021 | g0362 | 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 | g0266 | 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 | g0267 | EAS | CDX | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02155 | hp2 | a0001 | c0001 | t0007 | g0080 | EAS | CDX | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02165 | hp1 | a0001 | c0001 | t0007 | g0049 | 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 | g0022 | 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 | g0308 | 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 | g0094 | AMR | PEL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02293 | hp2 | a0001 | c0001 | t0006 | g0231 | AMR | PEL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0314 | 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 | g0268 | 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 | g0334 | 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 | g0307 | AFR | GWD | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0365 | 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 | g0240 | 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 | g0359 | AFR | GWD | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02683 | hp1 | a0001 | c0001 | t0012 | g0269 | 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 | g0046 | SAS | PJL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02698 | hp2 | a0001 | c0001 | t0036 | g0344 | SAS | PJL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02717 | hp1 | a0001 | c0001 | t0009 | g0241 | AFR | GWD | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02717 | hp2 | a0001 | c0002 | t0014 | g0095 | 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 | g0311 | 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 | g0278 | 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 | g0020 | AFR | GWD | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02896 | hp1 | a0001 | c0001 | t0020 | g0026 | 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 | g0026 | AFR | GWD | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02897 | hp2 | a0002 | c0003 | t0014 | g0020 | 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 | g0097 | AFR | ESN | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0098 | 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 | g0025 | 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 | g0280 | 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 | g0339 | 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 | g0356 | 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 | g0038 | 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 | g0046 | 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 | g0038 | 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 | g0293 | SAS | PJL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03654 | hp2 | a0001 | c0001 | t0008 | g0284 | SAS | PJL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03669 | hp1 | a0001 | c0001 | t0012 | g0282 | 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 | g0336 | 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 | g0043 | 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 | g0285 | SAS | PJL | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03831 | hp1 | a0001 | c0001 | t0005 | g0297 | 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 | g0084 | SAS | BEB | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG03834 | hp2 | a0001 | c0001 | t0067 | g0263 | 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 | g0300 | 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 | g0296 | SAS | STU | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG04184 | hp1 | a0001 | c0001 | t0008 | g0340 | SAS | BEB | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG04184 | hp2 | a0001 | c0001 | t0011 | g0043 | 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 | g0287 | SAS | STU | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG04204 | hp2 | a0001 | c0001 | t0011 | g0330 | 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 | g0277 | SAS | STU | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0360 | AFR | YRI | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18522 | hp2 | a0001 | c0001 | t0016 | g0019 | AFR | YRI | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18612 | hp1 | a0001 | c0001 | t0005 | g0317 | 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 | g0053 | EAS | CHB | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18747 | hp2 | a0001 | c0001 | t0011 | g0368 | 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 | g0041 | 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 | g0329 | 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 | g0352 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18943 | hp1 | a0001 | c0001 | t0007 | g0072 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0364 | 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 | g0335 | 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 | g0027 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18946 | hp2 | a0001 | c0001 | t0059 | g0261 | 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 | g0321 | 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 | g0304 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18950 | hp2 | a0001 | c0001 | t0006 | g0030 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0078 | 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 | g0029 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18953 | hp2 | a0001 | c0001 | t0006 | g0070 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18954 | hp2 | a0001 | c0001 | t0007 | g0091 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18956 | hp1 | a0001 | c0001 | t0031 | g0089 | 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 | g0082 | 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 | g0030 | 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 | g0032 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18961 | hp2 | a0001 | c0001 | t0004 | g0034 | 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 | g0265 | 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 | g0088 | 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 | g0041 | 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 | g0303 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0323 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0331 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18970 | hp1 | a0001 | c0001 | t0008 | g0291 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0034 | 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 | g0060 | 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 | g0357 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18973 | hp1 | a0001 | c0001 | t0006 | g0059 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18973 | hp2 | a0001 | c0001 | t0047 | g0083 | 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 | g0066 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18975 | hp2 | a0001 | c0001 | t0055 | g0064 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0325 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18977 | hp2 | a0001 | c0001 | t0006 | g0073 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0081 | 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 | g0055 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18980 | hp1 | a0001 | c0001 | t0007 | g0056 | 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 | g0260 | 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 | g0262 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18986 | hp1 | a0001 | c0001 | t0004 | g0042 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0027 | 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 | g0047 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0306 | 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 | g0044 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0093 | 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 | g0358 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18998 | hp2 | a0001 | c0001 | t0004 | g0363 | 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 | g0035 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19000 | hp1 | a0001 | c0001 | t0026 | g0322 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19000 | hp2 | a0001 | c0001 | t0006 | g0031 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19002 | hp1 | a0001 | c0001 | t0057 | g0348 | 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 | g0264 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19003 | hp2 | a0001 | c0001 | t0007 | g0085 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19005 | hp1 | a0001 | c0001 | t0006 | g0032 | 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 | g0086 | 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 | g0279 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19012 | hp1 | a0001 | c0001 | t0009 | g0079 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19012 | hp2 | a0001 | c0001 | t0005 | g0281 | 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 | g0045 | 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 | g0353 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19060 | hp2 | a0001 | c0001 | t0004 | g0042 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19063 | hp2 | a0001 | c0001 | t0005 | g0276 | 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 | g0071 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0065 | 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 | g0301 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19067 | hp1 | a0001 | c0001 | t0005 | g0257 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19067 | hp2 | a0001 | c0001 | t0004 | g0047 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0052 | 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 | g0259 | 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 | g0354 | 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 | g0077 | 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 | g0044 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19086 | hp2 | a0001 | c0001 | t0011 | g0328 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19089 | hp2 | a0001 | c0001 | t0011 | g0327 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19090 | hp2 | a0001 | c0001 | t0007 | g0063 | 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 | g0294 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0273 | AFR | YRI | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA19240 | hp2 | a0001 | c0001 | t0017 | g0023 | 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 | g0099 | AFR | ASW | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA20752 | hp1 | a0001 | c0001 | t0012 | g0337 | EUR | TSI | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0040 | EUR | TSI | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0319 | EUR | TSI | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA20805 | hp2 | a0001 | c0001 | t0021 | g0343 | EUR | TSI | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0040 | SAS | GIH | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA20905 | hp2 | a0001 | c0001 | t0008 | g0274 | SAS | GIH | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| HG02109 | hp1 | a0001 | c0001 | t0022 | g0022 | 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 | g0361 | 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 | g0025 | AFR | USA | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18955 | hp1 | a0001 | c0001 | t0006 | g0031 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA20300 | hp1 | a0001 | c0001 | t0012 | g0341 | AFR | USA | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| NA20300 | hp2 | a0001 | c0001 | t0008 | g0320 | 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 | a0001 | c0001 | t0012 | g0367 | REF | REF | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0013 | g0224 | REF | REF | FAIM2_chr12_49861896_49908900 | FAIM2 | chr12 | 49861896 | 49908900 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:49901140 | A | G | 2 | a0001c0002 a0002c0003 |
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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:49867042 | T | C | 67 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(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 | a0001c0001t0032 a0001c0001t0036 |
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 | a0001c0001t0019 a0001c0001t0022 a0001c0001t0028 others(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 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0009 others(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 | a0001c0001t0014 a0001c0001t0017 a0001c0001t0042 others(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 | a0001c0001t0018 a0001c0001t0066 |
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 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0007 others(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 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0015 others(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 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0007 others(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 | a0001c0001t0020 a0001c0001t0063 a0001c0002t0020 |
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 | a0001c0001t0031 a0001c0001t0065 |
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 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0015 others(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 | a0001c0001t0024 a0001c0001t0033 a0001c0001t0052 |
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 | a0001c0001t0016 a0001c0001t0034 |
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 | a0001c0001t0037 a0001c0001t0056 |
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 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(23): Show |
165 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(162): 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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | 289 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0054 others(286): 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 | a0001c0001t0009g0152 a0001c0001t0009g0241 a0001c0001t0044g0240 |
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 | a0001c0001t0011g0043 | 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 | a0001c0001t0009g0100 a0001c0001t0009g0103 a0001c0001t0009g0129 others(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 | a0001c0001t0007g0049 | 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 | a0001c0001t0003g0306 a0001c0001t0003g0325 a0001c0001t0003g0364 |
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 | a0001c0001t0009g0152 a0001c0001t0009g0241 a0001c0001t0017g0023 others(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 | a0001c0001t0009g0100 a0001c0001t0009g0103 a0001c0001t0009g0129 others(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 | a0001c0001t0004g0273 a0001c0001t0004g0303 a0001c0001t0004g0334 others(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 | a0001c0001t0008g0291 | 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 | a0001c0001t0004g0273 a0001c0001t0022g0022 a0001c0001t0022g0123 others(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 | a0001c0001t0007g0096 a0001c0001t0019g0104 a0001c0001t0019g0124 others(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 | 275 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0054 others(272): 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 | a0001c0001t0009g0152 a0001c0001t0009g0241 a0001c0001t0044g0240 |
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 | 236 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0054 others(233): 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 | a0001c0001t0009g0100 a0001c0001t0009g0103 a0001c0001t0009g0129 others(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 | a0001c0001t0021g0362 | 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 | a0001c0001t0009g0100 a0001c0001t0009g0103 a0001c0001t0009g0129 others(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 | a0001c0001t0009g0158 a0001c0001t0009g0159 a0001c0001t0009g0162 |
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 | 280 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0054 others(277): 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 | a0001c0001t0001g0088 | 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 | 42 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0054 others(39): 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 | a0001c0001t0009g0100 a0001c0001t0009g0103 a0001c0001t0009g0129 others(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 | 280 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0054 others(277): 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 | 161 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0054 others(158): 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 | a0001c0001t0017g0023 a0001c0002t0014g0095 a0001c0002t0017g0138 others(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 | 280 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0054 others(277): 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 | a0001c0001t0009g0100 a0001c0001t0009g0103 a0001c0001t0009g0129 others(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 | a0001c0001t0004g0360 | 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 | a0001c0001t0001g0098 a0001c0001t0001g0102 a0001c0001t0001g0105 others(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 | a0001c0001t0007g0096 | 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 | a0001c0001t0002g0001 a0001c0001t0002g0012 a0001c0001t0002g0177 others(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 | a0001c0001t0007g0080 | 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 | a0001c0001t0003g0039 | 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 | a0001c0001t0003g0335 | 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 | a0001c0001t0001g0149 a0001c0001t0016g0136 a0001c0001t0049g0183 others(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 | a0001c0001t0009g0079 | 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 | 40 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0001t0001g0090 others(37): 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 | 58 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0001t0001g0090 others(55): 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 | a0001c0001t0009g0152 a0001c0001t0009g0241 a0001c0001t0044g0240 |
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 | 57 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0001t0001g0090 others(54): 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 | a0001c0001t0002g0001 a0001c0001t0002g0012 a0001c0001t0002g0050 others(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 | 57 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0001t0001g0090 others(54): 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 | a0001c0001t0002g0133 a0001c0001t0003g0249 a0001c0001t0003g0319 others(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 | a0001c0001t0015g0028 | 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 | a0001c0001t0027g0099 a0001c0001t0027g0161 |
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 | a0001c0001t0004g0273 a0001c0001t0014g0009 a0001c0001t0016g0236 others(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 | 297 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0054 others(294): 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 | a0001c0001t0001g0185 a0001c0001t0002g0001 a0001c0001t0002g0002 others(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 | a0001c0001t0002g0187 a0001c0001t0004g0255 a0001c0001t0004g0333 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0054 a0001c0001t0001g0076 others(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 | a0001c0001t0003g0366 a0001c0001t0015g0232 a0001c0001t0067g0263 |
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 | a0001c0001t0017g0023 a0001c0002t0014g0095 a0001c0002t0017g0138 others(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 | a0001c0001t0011g0252 a0001c0001t0012g0337 |
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 | a0001c0001t0008g0305 | 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 | 77 | a0001c0001t0001g0098 a0001c0001t0001g0115 a0001c0001t0001g0185 others(74): 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 | a0001c0001t0014g0009 a0001c0001t0016g0236 a0001c0001t0016g0237 others(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 | 289 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0054 others(286): 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 | a0001c0001t0002g0051 | 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 | a0001c0001t0031g0089 a0001c0001t0065g0242 |
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 |
283 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0054 others(280): 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 | a0001c0001t0004g0046 a0001c0001t0009g0158 a0001c0001t0009g0159 others(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 | 291 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0054 others(288): 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 | a0001c0001t0014g0009 a0001c0001t0016g0236 a0001c0001t0016g0237 others(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 | a0001c0001t0014g0009 a0001c0001t0016g0236 a0001c0001t0016g0237 others(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 | a0001c0001t0031g0086 a0001c0001t0031g0089 a0001c0001t0065g0242 |
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 | a0001c0001t0001g0052 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0054 a0001c0001t0001g0076 others(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 | a0001c0001t0009g0152 a0001c0001t0009g0241 a0001c0001t0015g0209 others(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 | a0001c0001t0001g0128 a0001c0001t0001g0137 a0001c0001t0001g0149 others(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 | a0001c0001t0036g0344 | 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 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0137 others(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 | a0001c0001t0020g0026 a0001c0001t0020g0145 a0001c0001t0063g0359 others(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 | a0001c0001t0026g0322 | 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 | a0001c0001t0014g0009 a0001c0001t0016g0236 a0001c0001t0016g0237 others(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 | a0001c0001t0009g0152 a0001c0001t0009g0241 a0001c0001t0044g0240 |
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 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0137 others(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 | a0001c0001t0004g0273 a0001c0001t0022g0022 a0001c0001t0022g0123 others(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 | 55 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0001t0001g0090 others(52): 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 | 151 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0001t0001g0090 others(148): 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 | a0001c0001t0009g0152 a0001c0001t0009g0241 a0001c0001t0015g0209 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0054 a0001c0001t0001g0076 others(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 | a0001c0001t0006g0231 | 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 | 43 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0001t0001g0090 others(40): 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 | a0001c0001t0014g0009 a0001c0001t0016g0236 a0001c0001t0016g0237 others(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 | a0001c0001t0014g0009 a0001c0001t0016g0236 a0001c0001t0016g0237 others(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 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0137 others(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 | a0001c0001t0014g0009 a0001c0001t0016g0236 a0001c0001t0016g0237 others(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 | a0001c0001t0014g0009 a0001c0001t0058g0307 |
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 | 156 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0001t0001g0090 others(153): 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 | 49 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0001t0001g0090 others(46): 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 | 156 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0001t0001g0090 others(153): 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 | 156 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0001t0001g0090 others(153): 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 | a0001c0001t0001g0128 a0001c0001t0001g0137 a0001c0001t0001g0149 others(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 | a0001c0001t0002g0050 a0001c0001t0003g0004 a0001c0001t0014g0009 others(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 | a0001c0001t0001g0126 a0001c0001t0017g0023 a0001c0001t0017g0214 others(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 |
132 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0001t0001g0090 others(129): 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 | 73 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0001t0001g0090 others(70): 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 | a0001c0001t0001g0128 a0001c0001t0001g0137 a0001c0001t0001g0149 others(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 | 77 | a0001c0001t0001g0098 a0001c0001t0001g0115 a0001c0001t0001g0185 others(74): 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 | a0001c0001t0012g0282 | 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 | a0001c0001t0004g0273 a0001c0001t0022g0022 a0001c0001t0022g0123 others(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 | 147 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0001t0001g0090 others(144): 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 | a0001c0001t0009g0118 a0001c0001t0014g0009 a0001c0001t0016g0236 others(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 | a0001c0001t0016g0019 | 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 | 155 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0001t0001g0090 others(152): 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 | a0001c0001t0027g0099 a0001c0001t0027g0161 |
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 | 5 | a0001c0001t0001g0098 a0001c0001t0001g0115 a0001c0001t0010g0021 others(2): 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 | a0001c0001t0001g0185 a0001c0001t0002g0001 a0001c0001t0002g0002 others(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 |
83 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0001t0001g0090 others(80): 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 | a0001c0001t0004g0360 a0001c0001t0023g0025 |
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 | a0001c0001t0004g0273 a0001c0001t0022g0022 a0001c0001t0022g0123 others(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 | a0001c0001t0001g0185 a0001c0001t0002g0001 a0001c0001t0002g0002 others(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 | 83 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0001t0001g0090 others(80): 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 | 49 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0001t0001g0090 others(46): 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 | a0001c0001t0017g0023 a0001c0002t0014g0095 a0001c0002t0017g0138 others(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 | a0001c0001t0027g0099 a0001c0001t0027g0161 |
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 |
156 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0001t0001g0090 others(153): 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 | 155 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0001t0001g0090 others(152): 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 | 156 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0001t0001g0090 others(153): 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 | 49 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0001t0001g0090 others(46): 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 | 49 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0001t0001g0090 others(46): 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 | 107 | a0001c0001t0001g0098 a0001c0001t0001g0115 a0001c0001t0001g0126 others(104): 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 | 155 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0001t0001g0090 others(152): 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 | a0001c0001t0027g0099 a0001c0001t0027g0161 |
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 | a0001c0001t0010g0205 a0001c0001t0011g0244 a0001c0001t0011g0246 others(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 | a0001c0001t0001g0078 a0001c0001t0001g0198 a0001c0001t0004g0035 others(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 | a0001c0001t0009g0152 a0001c0001t0009g0241 a0001c0001t0015g0209 others(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 | a0001c0001t0014g0009 a0001c0001t0016g0236 a0001c0001t0016g0237 others(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 | 77 | a0001c0001t0001g0098 a0001c0001t0001g0115 a0001c0001t0001g0185 others(74): 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 | 77 | a0001c0001t0001g0098 a0001c0001t0001g0115 a0001c0001t0001g0185 others(74): 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 | 11 | a0001c0001t0001g0098 a0001c0001t0001g0115 a0001c0001t0010g0021 others(8): 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 | 155 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0001t0001g0090 others(152): 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 | a0001c0001t0002g0010 a0001c0001t0002g0135 a0001c0001t0002g0192 others(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 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0137 others(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 | a0001c0001t0001g0234 a0001c0001t0024g0008 a0001c0001t0033g0131 others(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 | a0001c0001t0001g0185 a0001c0001t0002g0001 a0001c0001t0002g0002 others(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 | 63 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0001t0001g0090 others(60): 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 | a0001c0001t0001g0128 a0001c0001t0001g0137 a0001c0001t0001g0149 others(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 | a0001c0001t0001g0234 a0001c0001t0009g0122 a0001c0001t0024g0008 others(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 | 49 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0001t0001g0090 others(46): 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 | a0001c0001t0001g0029 a0001c0001t0001g0054 a0001c0001t0001g0076 others(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 | a0001c0001t0004g0273 a0001c0001t0022g0022 a0001c0001t0022g0123 others(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 | 153 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0001t0001g0090 others(150): 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 | a0001c0001t0001g0029 a0001c0001t0001g0054 a0001c0001t0001g0076 others(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 | a0001c0001t0001g0098 a0001c0001t0001g0115 a0001c0001t0010g0021 |
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 | a0001c0001t0001g0029 a0001c0001t0001g0054 a0001c0001t0001g0076 others(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 | a0001c0001t0002g0111 a0001c0001t0003g0286 a0001c0001t0005g0277 others(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 | 290 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0054 others(287): 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 | a0001c0001t0002g0068 a0001c0001t0002g0069 a0001c0001t0002g0213 others(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 | a0001c0001t0002g0050 a0001c0001t0003g0004 |
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 | a0001c0001t0002g0093 a0001c0001t0003g0315 a0001c0001t0004g0273 others(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 | 291 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0054 others(288): 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 | a0001c0001t0009g0158 a0001c0001t0009g0159 a0001c0001t0024g0008 others(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 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0137 others(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 | 297 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0054 others(294): 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 | a0001c0001t0008g0044 | 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 | a0001c0001t0003g0315 | 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 | a0001c0001t0006g0003 a0001c0001t0006g0059 a0001c0001t0006g0121 others(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 | 279 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0054 others(276): 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 | a0001c0001t0024g0008 a0001c0001t0033g0131 a0001c0001t0033g0148 others(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 | a0001c0001t0020g0026 a0001c0001t0020g0145 a0001c0001t0063g0359 others(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 | a0001c0001t0002g0187 a0001c0001t0012g0269 a0001c0001t0013g0226 others(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 | a0001c0001t0004g0273 a0001c0001t0022g0022 a0001c0001t0022g0123 others(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 | 149 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0001t0001g0090 others(146): 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 | a0001c0001t0001g0029 a0001c0001t0001g0054 a0001c0001t0001g0076 others(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 | a0001c0001t0009g0152 a0001c0001t0009g0241 a0001c0001t0015g0209 others(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 | 150 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0001t0001g0090 others(147): 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 | a0001c0001t0003g0310 | 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 | a0001c0001t0005g0326 | 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 | a0001c0001t0007g0096 | 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 | a0001c0001t0024g0008 a0001c0001t0033g0131 a0001c0001t0033g0148 others(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 | a0001c0001t0003g0365 a0001c0001t0014g0009 a0001c0001t0016g0236 others(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 | 296 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0054 others(293): 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 | a0001c0001t0009g0152 a0001c0001t0009g0241 a0001c0001t0015g0209 others(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 | a0001c0001t0002g0187 a0001c0001t0004g0255 a0001c0001t0010g0216 others(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 | a0001c0001t0005g0281 a0001c0001t0005g0301 |
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 | 42 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0001t0001g0090 others(39): 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 | a0001c0001t0001g0081 | 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 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0137 others(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 | a0001c0001t0009g0158 a0001c0001t0009g0159 a0001c0001t0012g0336 |
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 | a0001c0001t0001g0185 a0001c0001t0002g0001 a0001c0001t0002g0002 others(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 | 290 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0054 others(287): 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 | a0001c0001t0002g0133 a0001c0001t0003g0319 a0001c0001t0053g0220 others(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 | 290 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0054 others(287): 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 | a0001c0001t0004g0264 | 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 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0137 others(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 | a0001c0001t0005g0287 a0001c0001t0008g0037 a0001c0001t0008g0274 others(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 | a0001c0001t0024g0008 a0001c0001t0033g0131 a0001c0001t0033g0148 others(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 | a0001c0001t0001g0102 a0001c0001t0001g0105 a0001c0001t0001g0153 |
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 |
220 | a0001c0001t0001g0029 a0001c0001t0001g0054 a0001c0001t0001g0076 others(217): 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 |
44 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0001t0001g0090 others(41): 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 | a0001c0001t0015g0028 | 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 | a0001c0001t0009g0158 a0001c0001t0009g0159 |
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 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0137 others(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 | a0001c0001t0001g0126 a0001c0001t0017g0023 a0001c0001t0017g0214 others(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 | a0001c0001t0001g0126 a0001c0001t0017g0023 a0001c0001t0017g0214 others(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 | a0001c0001t0001g0128 a0001c0001t0001g0137 a0001c0001t0001g0149 others(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 | a0001c0001t0005g0277 | 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 | a0001c0001t0001g0170 a0001c0001t0005g0277 |
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 | a0001c0001t0005g0277 | 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 | 100 | a0001c0001t0001g0098 a0001c0001t0001g0115 a0001c0001t0001g0126 others(97): 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 | a0001c0001t0008g0288 | 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 | 42 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0001t0001g0090 others(39): 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 | a0001c0001t0005g0248 a0001c0001t0005g0267 a0001c0001t0005g0281 others(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 | 51 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0001t0001g0090 others(48): 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 | a0001c0001t0001g0185 a0001c0001t0002g0001 a0001c0001t0002g0002 others(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 | 46 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0001t0001g0090 others(43): 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 | 261 | a0001c0001t0001g0029 a0001c0001t0001g0054 a0001c0001t0001g0076 others(258): 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 | a0001c0001t0062g0308 | 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 | a0001c0001t0007g0085 a0001c0001t0008g0288 |
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 | a0001c0001t0001g0098 a0001c0001t0001g0115 a0001c0001t0009g0122 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0054 a0001c0001t0001g0076 others(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 |
67 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0001t0001g0090 others(64): 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 | a0001c0001t0001g0185 a0001c0001t0002g0001 a0001c0001t0002g0002 others(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 | a0001c0001t0007g0085 | 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 | a0001c0001t0020g0026 a0001c0001t0020g0145 a0001c0001t0063g0359 others(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 | 8 | a0001c0001t0009g0152 a0001c0001t0009g0241 a0001c0001t0015g0209 others(5): 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 | 9 | a0001c0001t0009g0152 a0001c0001t0009g0241 a0001c0001t0015g0209 others(6): 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 | a0001c0001t0020g0026 a0001c0001t0020g0145 a0001c0001t0063g0359 others(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 | 12 | a0001c0001t0009g0152 a0001c0001t0009g0241 a0001c0001t0015g0209 others(9): 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 | 2 | a0001c0001t0016g0019 a0001c0001t0034g0146 |
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 | a0001c0001t0009g0152 a0001c0001t0009g0241 a0001c0001t0015g0209 others(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 | 2 | a0001c0001t0016g0019 a0001c0001t0034g0146 |
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 | a0001c0001t0009g0152 a0001c0001t0009g0241 a0001c0001t0015g0209 others(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 | a0001c0001t0009g0152 a0001c0001t0009g0241 a0001c0001t0015g0209 others(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 | 8 | a0001c0001t0009g0152 a0001c0001t0009g0241 a0001c0001t0015g0209 others(5): 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 | 12 | a0001c0001t0009g0152 a0001c0001t0009g0241 a0001c0001t0015g0209 others(9): 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 | 12 | a0001c0001t0009g0152 a0001c0001t0009g0241 a0001c0001t0015g0209 others(9): 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 | 8 | a0001c0001t0009g0152 a0001c0001t0009g0241 a0001c0001t0015g0209 others(5): 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 | a0001c0001t0020g0026 a0001c0001t0020g0145 a0001c0001t0063g0359 others(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 | a0001c0001t0020g0026 a0001c0001t0020g0145 a0001c0001t0063g0359 others(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 | 8 | a0001c0001t0009g0152 a0001c0001t0009g0241 a0001c0001t0015g0209 others(5): 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 | a0001c0001t0020g0026 a0001c0001t0020g0145 a0001c0001t0063g0359 others(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 | a0001c0001t0020g0026 a0001c0001t0020g0145 a0001c0001t0063g0359 others(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 | 6 | a0001c0001t0016g0019 a0001c0001t0020g0026 a0001c0001t0020g0145 others(3): 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 | 279 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0054 others(276): 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 | 12 | a0001c0001t0009g0152 a0001c0001t0009g0241 a0001c0001t0015g0209 others(9): 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 | a0001c0001t0009g0152 a0001c0001t0009g0241 a0001c0001t0015g0209 others(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 | 12 | a0001c0001t0009g0152 a0001c0001t0009g0241 a0001c0001t0015g0209 others(9): 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 | a0001c0001t0009g0152 a0001c0001t0009g0241 a0001c0001t0015g0209 others(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 | 6 | a0001c0001t0016g0019 a0001c0001t0020g0026 a0001c0001t0020g0145 others(3): 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 | a0001c0001t0009g0152 a0001c0001t0009g0241 a0001c0001t0015g0209 others(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 | a0001c0001t0009g0152 a0001c0001t0009g0241 a0001c0001t0015g0209 others(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 | a0001c0001t0011g0368 | 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 | a0001c0001t0002g0050 a0001c0001t0003g0004 |
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 | a0001c0001t0002g0012 a0001c0001t0003g0251 |
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 | 289 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0054 others(286): 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 | a0001c0001t0004g0273 | 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 | a0001c0001t0009g0152 a0001c0001t0009g0241 a0001c0001t0015g0209 others(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 | a0001c0001t0015g0209 a0001c0001t0015g0225 |
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 | a0001c0001t0017g0023 a0001c0002t0014g0095 a0001c0002t0017g0138 others(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 | 40 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0001t0001g0090 others(37): 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 | 244 | a0001c0001t0001g0029 a0001c0001t0001g0054 a0001c0001t0001g0076 others(241): 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 | a0001c0001t0017g0023 a0001c0001t0033g0148 a0001c0002t0014g0095 others(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 | 49 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0001t0001g0090 others(46): 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 | 290 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0054 others(287): 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 | a0001c0001t0004g0360 a0001c0001t0023g0025 |
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 | a0001c0001t0014g0009 a0001c0001t0016g0236 a0001c0001t0016g0237 others(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 | 45 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0001t0001g0090 others(42): 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 | a0001c0001t0020g0026 a0001c0001t0020g0145 a0001c0001t0063g0359 others(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 | a0001c0001t0004g0273 a0001c0001t0014g0009 a0001c0001t0022g0022 others(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 | 86 | a0001c0001t0001g0098 a0001c0001t0001g0115 a0001c0001t0001g0128 others(83): 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 | a0001c0001t0001g0029 a0001c0001t0001g0054 a0001c0001t0001g0076 others(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 | a0001c0001t0001g0126 a0001c0001t0004g0264 a0001c0001t0004g0279 others(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 | a0001c0001t0010g0205 a0001c0001t0011g0244 a0001c0001t0011g0246 others(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 | a0001c0001t0007g0096 | 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 | a0001c0001t0005g0287 a0001c0001t0006g0070 a0001c0001t0009g0162 others(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 | a0001c0001t0001g0128 a0001c0001t0001g0137 a0001c0001t0001g0149 others(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 | 291 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0054 others(288): 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 | a0001c0001t0017g0023 a0001c0002t0014g0095 a0001c0002t0017g0138 others(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 | a0001c0001t0001g0185 a0001c0001t0002g0001 a0001c0001t0002g0002 others(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 | a0001c0001t0003g0314 | 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 | a0001c0001t0001g0090 a0001c0001t0001g0170 a0001c0001t0009g0079 others(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 | a0001c0001t0002g0065 | 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 | 54 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0001t0001g0090 others(51): 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 | a0001c0001t0001g0098 a0001c0001t0001g0115 a0001c0001t0010g0021 |
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 | a0001c0001t0025g0036 a0001c0001t0025g0270 |
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 | a0001c0001t0014g0009 a0001c0001t0016g0236 a0001c0001t0016g0237 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0054 a0001c0001t0001g0076 others(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 | a0001c0001t0004g0273 | 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 | a0001c0001t0006g0071 a0001c0001t0006g0073 a0001c0001t0007g0072 others(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 | a0001c0001t0006g0030 | 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 | a0001c0001t0001g0029 a0001c0001t0001g0054 a0001c0001t0001g0076 others(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 | 48 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0001t0001g0090 others(45): 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 | 291 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0054 others(288): 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 | 291 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0054 others(288): 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 | 286 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0054 others(283): 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 | 48 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0001t0001g0090 others(45): 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 | a0001c0001t0005g0287 a0001c0001t0008g0037 a0001c0001t0008g0274 |
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 | a0001c0001t0008g0271 | 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 | a0001c0001t0015g0209 a0001c0001t0015g0225 |
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 | 24 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0001t0001g0090 others(21): 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 | 5 | a0001c0001t0001g0098 a0001c0001t0001g0115 a0001c0001t0010g0021 others(2): 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 | 287 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0054 others(284): 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 | 5 | a0001c0001t0001g0098 a0001c0001t0001g0115 a0001c0001t0010g0021 others(2): 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 | a0001c0001t0001g0128 a0001c0001t0001g0137 a0001c0001t0001g0149 others(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 | a0001c0001t0001g0128 a0001c0001t0001g0137 a0001c0001t0001g0149 others(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 | a0001c0001t0001g0128 a0001c0001t0001g0137 a0001c0001t0001g0149 others(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 | a0001c0001t0001g0128 a0001c0001t0001g0137 a0001c0001t0001g0149 others(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 | a0001c0001t0002g0065 a0001c0001t0024g0008 a0001c0001t0033g0131 others(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 | a0001c0001t0001g0128 a0001c0001t0001g0137 a0001c0001t0001g0149 others(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 | a0001c0001t0012g0269 | 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 | 333 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(330): 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 | a0001c0001t0001g0128 a0001c0001t0001g0137 a0001c0001t0001g0149 others(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 | a0001c0001t0001g0128 a0001c0001t0001g0137 a0001c0001t0001g0149 others(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 | a0001c0001t0005g0326 | 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 | a0001c0001t0001g0126 a0001c0001t0009g0122 a0001c0001t0009g0158 others(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 | a0001c0001t0005g0326 a0001c0001t0007g0049 |
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 | a0001c0001t0002g0133 a0001c0001t0005g0277 a0001c0001t0008g0320 others(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 | a0001c0002t0014g0095 a0002c0003t0014g0020 |
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 | a0001c0001t0001g0102 a0001c0001t0001g0105 a0001c0001t0001g0126 others(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 | a0001c0001t0001g0126 a0001c0001t0009g0112 a0001c0001t0009g0122 others(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 | a0001c0001t0021g0343 | 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 | a0001c0001t0024g0008 a0001c0001t0033g0131 a0001c0001t0033g0148 others(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 | a0001c0001t0021g0259 | 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 | a0001c0001t0005g0257 a0001c0001t0055g0064 |
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 | a0001c0002t0014g0095 a0002c0003t0014g0020 |
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 | a0001c0001t0003g0309 a0001c0001t0062g0308 |
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 | 134 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0017 others(131): 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 | a0001c0001t0002g0065 a0001c0001t0005g0248 a0001c0001t0005g0267 others(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 | a0001c0001t0020g0026 a0001c0001t0020g0145 a0001c0001t0063g0359 others(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 | a0001c0001t0001g0185 a0001c0001t0002g0001 a0001c0001t0002g0002 others(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 | a0001c0001t0026g0322 | 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 | a0001c0001t0020g0026 a0001c0001t0020g0145 a0001c0001t0063g0359 others(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 | a0001c0001t0001g0175 a0001c0001t0001g0222 a0001c0001t0001g0234 others(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 | a0001c0001t0004g0273 a0001c0001t0028g0163 a0001c0001t0028g0164 others(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 | a0001c0001t0035g0268 a0001c0001t0035g0339 |
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 | a0001c0001t0020g0026 a0001c0001t0020g0145 a0001c0001t0063g0359 others(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 | a0001c0001t0009g0112 a0001c0002t0014g0095 a0002c0003t0014g0020 |
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 | a0001c0001t0002g0133 a0001c0001t0005g0277 a0001c0001t0008g0320 |
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 | a0001c0001t0002g0133 a0001c0001t0005g0277 a0001c0001t0008g0320 |
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 | 52 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0054 others(49): 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 | a0001c0001t0012g0347 a0001c0001t0013g0178 |
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 | 152 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0017 others(149): 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 | a0001c0001t0006g0210 a0001c0001t0008g0294 |
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 | 65 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0054 others(62): 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 | a0001c0001t0004g0255 a0001c0001t0009g0112 a0001c0001t0027g0099 others(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 | a0001c0001t0033g0131 a0001c0001t0033g0148 |
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 | a0001c0001t0004g0334 | 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 | a0001c0001t0004g0255 a0001c0001t0009g0112 a0001c0001t0027g0099 others(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 | a0001c0001t0004g0255 a0001c0001t0027g0099 a0001c0001t0027g0161 |
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 | a0001c0001t0004g0255 a0001c0001t0009g0112 a0001c0001t0020g0026 others(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 | a0001c0001t0006g0073 | 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 | a0001c0001t0008g0288 | 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 | a0001c0001t0005g0357 | 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 | a0001c0001t0004g0255 a0001c0001t0009g0112 a0001c0001t0027g0099 others(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 | a0001c0001t0036g0356 | 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 | a0001c0001t0002g0065 | 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 | a0001c0001t0066g0313 | 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 | a0001c0001t0001g0098 a0001c0001t0001g0115 a0001c0001t0010g0021 |
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 | a0001c0001t0006g0210 a0001c0001t0008g0294 |
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 | a0001c0001t0014g0009 a0001c0001t0016g0236 a0001c0001t0016g0237 others(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 | a0001c0001t0001g0075 | 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 | 151 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0054 others(148): 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 | a0001c0001t0014g0009 a0001c0001t0016g0236 a0001c0001t0016g0237 others(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 | a0001c0001t0009g0152 a0001c0001t0009g0241 a0001c0001t0044g0240 |
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 | a0001c0001t0006g0210 a0001c0001t0008g0294 |
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 | a0001c0001t0004g0255 a0001c0001t0020g0026 a0001c0001t0020g0145 others(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 | a0001c0001t0020g0026 a0001c0001t0020g0145 a0001c0001t0063g0359 others(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 | a0001c0001t0004g0255 a0001c0001t0004g0273 a0001c0001t0027g0099 others(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 | a0001c0001t0001g0128 a0001c0001t0001g0137 a0001c0001t0001g0153 others(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 | a0001c0001t0066g0313 | 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 | a0001c0001t0001g0066 | 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 | a0001c0001t0008g0340 a0001c0001t0010g0113 a0001c0001t0010g0114 others(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 | a0001c0001t0004g0329 | 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 | a0001c0001t0015g0209 a0001c0001t0015g0225 |
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 | a0001c0001t0009g0152 a0001c0001t0009g0241 a0001c0001t0044g0240 |
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 | a0001c0001t0001g0105 a0001c0001t0001g0126 a0001c0001t0001g0185 others(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 | a0001c0001t0012g0341 | 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 | a0001c0001t0020g0026 a0001c0001t0020g0145 a0001c0001t0063g0359 others(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 | 138 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0017 others(135): 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 | a0001c0001t0001g0126 a0001c0001t0001g0185 a0001c0001t0002g0001 others(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 | a0001c0001t0003g0319 | 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 | a0001c0001t0001g0126 a0001c0001t0001g0185 a0001c0001t0002g0001 others(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 | a0001c0001t0003g0249 a0001c0001t0003g0319 a0001c0001t0053g0220 others(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 | 137 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0017 others(134): 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 | a0001c0001t0020g0026 a0001c0001t0020g0145 a0001c0001t0057g0348 others(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 | a0001c0001t0027g0099 a0001c0001t0027g0161 |
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 | a0001c0001t0020g0026 a0001c0001t0020g0145 a0001c0001t0063g0359 others(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 | a0001c0001t0004g0360 | 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 | a0001c0001t0009g0122 a0001c0001t0009g0158 a0001c0001t0009g0159 others(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 | a0001c0001t0001g0239 a0001c0001t0009g0112 a0001c0001t0024g0008 others(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 | a0001c0001t0020g0026 a0001c0001t0020g0145 a0001c0001t0063g0359 others(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 | a0001c0001t0009g0152 a0001c0001t0009g0241 a0001c0001t0044g0240 |
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 | a0001c0001t0005g0276 | 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 | a0001c0001t0020g0026 a0001c0001t0020g0145 a0001c0001t0063g0359 others(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 | a0001c0001t0001g0126 a0001c0001t0004g0360 a0001c0001t0020g0026 others(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 | a0001c0001t0009g0122 a0001c0001t0009g0158 a0001c0001t0009g0159 others(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 | a0001c0001t0007g0053 | 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 | a0001c0001t0020g0026 a0001c0001t0020g0145 a0001c0001t0063g0359 others(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 | a0001c0001t0020g0026 a0001c0001t0020g0145 a0001c0001t0063g0359 others(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 | a0001c0001t0009g0152 a0001c0001t0009g0241 a0001c0001t0019g0150 others(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 | 57 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0054 others(54): 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 | a0001c0001t0004g0273 a0001c0001t0028g0163 a0001c0001t0028g0164 others(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 | a0001c0001t0004g0273 a0001c0001t0028g0163 a0001c0001t0028g0164 others(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 | 169 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0054 others(166): 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 | a0001c0001t0001g0102 a0001c0001t0001g0105 a0001c0001t0005g0299 others(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 | a0001c0001t0020g0026 a0001c0001t0020g0145 a0001c0001t0063g0359 others(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 | a0001c0001t0011g0349 | 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 | a0001c0001t0005g0248 a0001c0001t0008g0243 |
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 | a0001c0001t0004g0273 a0001c0001t0028g0163 a0001c0001t0028g0164 others(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 | a0001c0001t0017g0214 a0001c0002t0041g0142 |
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 | a0001c0001t0023g0025 | 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 | 141 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0017 others(138): 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 | 132 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0054 others(129): 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 | a0001c0001t0016g0136 a0001c0002t0001g0141 a0001c0002t0038g0140 |
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 | a0001c0001t0001g0102 a0001c0001t0001g0105 |
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 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0017 others(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 | a0001c0001t0004g0273 a0001c0001t0009g0152 a0001c0001t0009g0241 others(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 | 132 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0054 others(129): 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 | a0001c0001t0005g0275 a0001c0001t0005g0298 a0001c0001t0005g0353 others(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 | a0001c0001t0008g0274 | 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 | a0001c0001t0014g0009 a0001c0001t0016g0237 a0001c0001t0034g0238 others(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 | a0001c0001t0001g0175 a0001c0001t0001g0222 a0001c0001t0001g0234 others(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 | a0001c0001t0004g0273 a0001c0001t0028g0163 a0001c0001t0028g0164 others(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 | a0001c0001t0001g0102 a0001c0001t0001g0105 |
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 | a0001c0001t0009g0158 a0001c0001t0009g0159 a0001c0001t0015g0209 others(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 | a0001c0001t0006g0071 a0001c0001t0006g0073 a0001c0001t0007g0072 others(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 | a0001c0001t0001g0149 a0001c0001t0001g0153 a0001c0001t0004g0255 others(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 | a0001c0001t0001g0185 a0001c0001t0001g0235 a0001c0001t0002g0001 others(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 | a0001c0001t0001g0185 a0001c0001t0001g0235 a0001c0001t0002g0001 others(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 | a0001c0001t0001g0128 a0001c0001t0001g0137 a0001c0001t0001g0149 others(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 | 179 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0017 others(176): 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 | a0001c0001t0001g0175 a0001c0001t0002g0010 a0001c0001t0002g0135 others(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 | a0001c0001t0005g0358 | 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 | a0001c0001t0014g0009 a0001c0001t0058g0307 |
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 | 221 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0066 others(218): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): 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 | a0001c0001t0001g0102 a0001c0001t0009g0158 a0001c0001t0009g0159 others(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 | 276 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(273): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.434+86T>C | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 5/11 | chr12 | 49896945 | |||||||
| chr12:49897668 | T | A | 10 | a0001c0001t0001g0090 a0001c0001t0001g0170 a0001c0001t0006g0210 others(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 | a0001c0001t0005g0257 | 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 | 202 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(199): 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 | a0001c0001t0004g0303 a0001c0001t0007g0067 a0001c0001t0008g0245 others(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 | a0001c0001t0001g0075 a0001c0001t0001g0149 a0001c0001t0003g0039 others(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 | a0001c0001t0001g0128 a0001c0001t0001g0153 a0001c0001t0001g0239 others(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 | 255 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(252): 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 | a0001c0001t0001g0015 a0001c0001t0002g0068 a0001c0001t0002g0069 others(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 | a0001c0001t0009g0144 a0001c0001t0009g0158 a0001c0001t0009g0159 others(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 | a0001c0001t0001g0098 a0001c0001t0001g0102 a0001c0001t0001g0105 others(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 | a0001c0001t0002g0050 a0001c0001t0003g0004 |
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 | a0001c0001t0001g0075 a0001c0001t0003g0335 a0001c0001t0004g0042 others(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 | a0001c0001t0009g0158 a0001c0001t0009g0159 |
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 | a0001c0001t0001g0153 a0001c0001t0001g0239 a0001c0001t0004g0255 others(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 | a0001c0001t0007g0049 | 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 | 312 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(309): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(372): 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 | a0001c0001t0005g0352 | 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 | a0001c0001t0009g0144 a0001c0001t0009g0158 a0001c0001t0009g0159 others(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 | a0001c0001t0048g0057 | 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 | a0001c0001t0024g0008 a0001c0001t0027g0099 |
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 | a0001c0001t0001g0017 a0001c0001t0001g0076 a0001c0001t0001g0078 others(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 | a0001c0001t0001g0153 a0001c0001t0009g0241 a0001c0001t0044g0240 |
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 | a0001c0001t0009g0152 a0001c0001t0009g0184 a0001c0001t0016g0136 others(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 | a0001c0001t0004g0360 a0001c0001t0009g0152 a0001c0001t0020g0026 others(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 | a0001c0001t0001g0105 a0001c0001t0009g0103 a0001c0001t0019g0104 |
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 | a0001c0001t0002g0048 a0001c0001t0004g0253 |
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 | a0001c0001t0032g0024 | 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 | a0001c0001t0001g0105 a0001c0001t0001g0128 a0001c0001t0001g0239 others(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 | a0001c0001t0017g0023 a0001c0001t0022g0022 |
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 | a0001c0001t0003g0364 a0001c0001t0004g0047 a0001c0001t0004g0363 |
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 | a0001c0001t0002g0233 a0001c0001t0015g0232 |
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 | a0001c0001t0001g0153 a0001c0001t0042g0107 |
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 | a0001c0001t0017g0023 a0001c0001t0022g0022 a0001c0001t0033g0131 |
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 | a0001c0001t0001g0239 a0001c0001t0016g0236 a0001c0001t0016g0237 others(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 | 11 | a0001c0001t0001g0102 a0001c0001t0001g0105 a0001c0001t0001g0137 others(8): 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 | a0001c0001t0006g0130 a0001c0001t0009g0129 |
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 | a0001c0001t0009g0158 a0001c0001t0009g0159 a0001c0001t0009g0162 others(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 | a0001c0001t0003g0365 | 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 | a0001c0001t0010g0155 a0001c0001t0018g0011 a0001c0001t0018g0154 others(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 | a0001c0001t0001g0137 a0001c0001t0002g0010 a0001c0001t0002g0133 others(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 | 36 | a0001c0001t0001g0098 a0001c0001t0001g0102 a0001c0001t0001g0105 others(33): 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 | a0001c0001t0001g0108 a0001c0001t0001g0115 a0001c0001t0001g0126 others(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 | 277 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(274): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.16-1193G>A | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 1/11 | chr12 | 49902518 | |||||||
| chr12:49902705 | G | GC | 144 | a0001c0001t0001g0235 a0001c0001t0002g0092 a0001c0001t0003g0004 others(141): Show |
166 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(163): 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 | a0001c0002t0020g0106 a0002c0003t0014g0020 |
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 | a0001c0001t0011g0368 | 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 | a0001c0001t0002g0093 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(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 | 241 | a0001c0001t0001g0108 a0001c0001t0001g0115 a0001c0001t0001g0126 others(238): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): 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 | a0001c0001t0001g0239 a0001c0001t0016g0236 a0001c0001t0016g0237 others(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 | a0001c0001t0039g0094 | 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 | 70 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(67): 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 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(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 | a0001c0001t0008g0243 a0001c0001t0008g0245 a0001c0001t0011g0244 others(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 | a0001c0001t0009g0241 a0001c0001t0044g0240 |
2 | HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.15+68A>G | FAIM2 | ENSG00000135472.9 | transcript | ENST00000320634.8 | protein_coding | 1/11 | chr12 | 49903710 |