Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2268 |
| ensemblid | ENSG00000000938.13 |
| hgncid | 3697 |
| symbol | FGR |
| name | FGR proto-oncogene, Src family tyrosine kinase |
| refseq_nuc | NM_005248.3 |
| refseq_prot | NP_005239.1 |
| ensembl_nuc | ENST00000374005.8 |
| ensembl_prot | ENSP00000363117.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 27612064 |
| end | 27635185 |
| strand | - |
| ver | v1.2 |
| region | chr1:27612064-27635185 |
| region5000 | chr1:27607064-27640185 |
| regionname0 | FGR_chr1_27612064_27635185 |
| regionname5000 | FGR_chr1_27607064_27640185 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 529 | 276 | 91 | 62 | 77 | 14 | 30 | 44 | FGR_chr1_27607064_27640185 | FGR | MGCVF others(524): Show |
chr1 | 27607064 | 27640185 |
| a0002 | 0/0 | 529 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | MGCVF others(524): Show |
chr1 | 27607064 | 27640185 |
| a0003 | 0/0 | 529 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | MGCVF others(524): Show |
chr1 | 27607064 | 27640185 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1587 | 267 | 86 | 62 | 76 | 14 | 27 | FGR_chr1_27607064_27640185 | FGR | ATGGG others(1582): Show |
chr1 | 27607064 | 27640185 | ||
| a0001c0002 | 0/0 | 1587 | 3 | 0 | 0 | 0 | 0 | 3 | FGR_chr1_27607064_27640185 | FGR | ATGGG others(1582): Show |
chr1 | 27607064 | 27640185 | ||
| a0001c0003 | 0/0 | 1587 | 2 | 2 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | ATGGG others(1582): Show |
chr1 | 27607064 | 27640185 | ||
| a0001c0004 | 0/0 | 1587 | 2 | 2 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | ATGGG others(1582): Show |
chr1 | 27607064 | 27640185 | ||
| a0001c0005 | 0/0 | 1587 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | ATGGG others(1582): Show |
chr1 | 27607064 | 27640185 | ||
| a0001c0007 | 0/0 | 1587 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | ATGGG others(1582): Show |
chr1 | 27607064 | 27640185 | ||
| a0002c0006 | 0/0 | 1587 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | ATGGG others(1582): Show |
chr1 | 27607064 | 27640185 | ||
| a0003c0008 | 0/0 | 1587 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | ATGGG others(1582): Show |
chr1 | 27607064 | 27640185 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2637 | 260 | 81 | 62 | 76 | 13 | 26 | FGR_chr1_27607064_27640185 | FGR | CCTGC others(2632): Show |
chr1 | 27607064 | 27640185 |
| a0001c0001t0002 | 0/0 | 2637 | 2 | 2 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | CCTGC others(2632): Show |
chr1 | 27607064 | 27640185 |
| a0001c0001t0003 | 0/0 | 2637 | 2 | 2 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | CCTGC others(2632): Show |
chr1 | 27607064 | 27640185 |
| a0001c0001t0004 | 0/0 | 2637 | 1 | 0 | 0 | 0 | 1 | 0 | FGR_chr1_27607064_27640185 | FGR | CCTGC others(2632): Show |
chr1 | 27607064 | 27640185 |
| a0001c0001t0005 | 0/0 | 2637 | 1 | 0 | 0 | 0 | 0 | 1 | FGR_chr1_27607064_27640185 | FGR | CCTGC others(2632): Show |
chr1 | 27607064 | 27640185 |
| a0001c0001t0006 | 0/0 | 2637 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | CCTGC others(2632): Show |
chr1 | 27607064 | 27640185 |
| a0001c0002t0001 | 0/0 | 2637 | 3 | 0 | 0 | 0 | 0 | 3 | FGR_chr1_27607064_27640185 | FGR | CCTGC others(2632): Show |
chr1 | 27607064 | 27640185 |
| a0001c0003t0008 | 0/0 | 2637 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | CCTGC others(2632): Show |
chr1 | 27607064 | 27640185 |
| a0001c0003t0009 | 0/0 | 2637 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | CCTGC others(2632): Show |
chr1 | 27607064 | 27640185 |
| a0001c0004t0002 | 0/0 | 2637 | 2 | 2 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | CCTGC others(2632): Show |
chr1 | 27607064 | 27640185 |
| a0001c0005t0001 | 0/0 | 2637 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | CCTGC others(2632): Show |
chr1 | 27607064 | 27640185 |
| a0001c0007t0001 | 0/0 | 2637 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | CCTGC others(2632): Show |
chr1 | 27607064 | 27640185 |
| a0002c0006t0007 | 0/0 | 2637 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | CCTGC others(2632): Show |
chr1 | 27607064 | 27640185 |
| a0003c0008t0001 | 0/0 | 2637 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | CCTGC others(2632): Show |
chr1 | 27607064 | 27640185 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0002 | 0/0 | 9 | 2 | 2 | 5 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0003 | 0/0 | 8 | 1 | 5 | 0 | 1 | 1 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0004 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0005 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0006 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0007 | 0/0 | 4 | 1 | 0 | 2 | 0 | 1 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0017 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0019 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0175 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0001g0214 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0004g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0005g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0001t0006g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0003t0008g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0003t0009g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0004t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0004t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0005t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0001c0007t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0002c0006t0007g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| a0003c0008t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0171 | EUR | GBR | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0028 | EUR | GBR | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0160 | EUR | GBR | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0170 | EUR | GBR | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | FIN | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0031 | EUR | FIN | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | CHS | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | CHS | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0029 | EUR | IBS | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0165 | EUR | IBS | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0159 | EUR | IBS | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0089 | EUR | IBS | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02015 | hp2 | a0002 | c0006 | t0007 | g0181 | EAS | KHV | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | CDX | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CDX | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0075 | AFR | ACB | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02451 | hp2 | a0001 | c0004 | t0002 | g0067 | AFR | ACB | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0057 | SAS | PJL | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02886 | hp1 | a0003 | c0008 | t0001 | g0166 | AFR | GWD | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0064 | AFR | ESN | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | ESN | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ESN | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ESN | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ESN | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | ESN | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | MSL | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ESN | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0066 | AFR | ESN | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | MSL | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | MSL | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | MSL | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | MSL | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | MSL | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | MSL | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | MSL | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG03490 | hp1 | a0001 | c0001 | t0005 | g0197 | SAS | PJL | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ESN | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0107 | AFR | ESN | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0058 | AFR | GWD | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG03579 | hp2 | a0001 | c0004 | t0002 | g0077 | AFR | MSL | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | STU | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | STU | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0055 | SAS | PJL | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0056 | SAS | BEB | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | BEB | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | STU | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | STU | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | STU | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | STU | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | STU | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | STU | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | YRI | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | YRI | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | CHB | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | YRI | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA18906 | hp2 | a0001 | c0003 | t0009 | g0061 | AFR | YRI | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA18964 | hp1 | a0001 | c0007 | t0001 | g0139 | EAS | JPT | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | LWK | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | LWK | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | LWK | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | YRI | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ASW | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ASW | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0163 | EUR | TSI | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0032 | EUR | TSI | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0098 | EUR | TSI | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02486 | hp2 | a0001 | c0005 | t0001 | g0071 | AFR | ACB | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | MSL | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | MSL | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | USA | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | USA | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| NA21309 | hp2 | a0001 | c0003 | t0008 | g0091 | AFR | LWK | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0214 | REF | REF | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0175 | REF | REF | FGR_chr1_27607064_27640185 | FGR | chr1 | 27607064 | 27640185 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:27612938 | C | A | 1 | a0002 | 1 | HG02015.hp2 | missense_variant | MODERATE | c.1566G>T | p.Gln522His | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 13/13 | 1763/2637 | 1566/1590 | 522/529 | chr1 | 27612938 | |||
| chr1:27613273 | A | C | 1 | a0002 | 1 | HG02015.hp2 | missense_variant | MODERATE | c.1327T>G | p.Ser443Ala | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 12/13 | 1524/2637 | 1327/1590 | 443/529 | chr1 | 27613273 | |||
| chr1:27614450 | T | C | 1 | a0002 | 1 | HG02015.hp2 | missense_variant | MODERATE | c.1229A>G | p.Asp410Gly | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 11/13 | 1426/2637 | 1229/1590 | 410/529 | chr1 | 27614450 | |||
| chr1:27614451 | C | G | 1 | a0002 | 1 | HG02015.hp2 | missense_variant | MODERATE | c.1228G>C | p.Asp410His | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 11/13 | 1425/2637 | 1228/1590 | 410/529 | chr1 | 27614451 | |||
| chr1:27614495 | G | A | 1 | a0003 | 1 | HG02886.hp1 | missense_variant | MODERATE | c.1184C>T | p.Ala395Val | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 11/13 | 1381/2637 | 1184/1590 | 395/529 | chr1 | 27614495 | |||
| chr1:27614516 | A | C | 1 | a0002 | 1 | HG02015.hp2 | missense_variant | MODERATE | c.1163T>G | p.Ile388Ser | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 11/13 | 1360/2637 | 1163/1590 | 388/529 | chr1 | 27614516 | |||
| chr1:27614520 | T | A | 1 | a0002 | 1 | HG02015.hp2 | missense_variant | MODERATE | c.1159A>T | p.Asn387Tyr | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 11/13 | 1356/2637 | 1159/1590 | 387/529 | chr1 | 27614520 | |||
| chr1:27614861 | T | C | 1 | a0002 | 1 | HG02015.hp2 | missense_variant | MODERATE | c.1084A>G | p.Met362Val | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 10/13 | 1281/2637 | 1084/1590 | 362/529 | chr1 | 27614861 | |||
| chr1:27615499 | A | C | 1 | a0002 | 1 | HG02015.hp2 | missense_variant | MODERATE | c.953T>G | p.Leu318Arg | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 9/13 | 1150/2637 | 953/1590 | 318/529 | chr1 | 27615499 | |||
| chr1:27615785 | T | G | 1 | a0002 | 1 | HG02015.hp2 | missense_variant | MODERATE | c.742A>C | p.Thr248Pro | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 8/13 | 939/2637 | 742/1590 | 248/529 | chr1 | 27615785 | |||
| chr1:27615799 | A | T | 1 | a0002 | 1 | HG02015.hp2 | missense_variant | MODERATE | c.728T>A | p.Ile243Asn | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 8/13 | 925/2637 | 728/1590 | 243/529 | chr1 | 27615799 | |||
| chr1:27616958 | T | A | 1 | a0002 | 1 | HG02015.hp2 | missense_variant | MODERATE | c.581A>T | p.His194Leu | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 7/13 | 778/2637 | 581/1590 | 194/529 | chr1 | 27616958 | |||
| chr1:27617273 | C | T | 1 | a0002 | 1 | HG02015.hp2 | missense_variant | MODERATE | c.452G>A | p.Arg151Lys | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 6/13 | 649/2637 | 452/1590 | 151/529 | chr1 | 27617273 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:27613304 | A | G | 1 | a0001c0007 | 1 | NA18964.hp1 | synonymous_variant | LOW | c.1296T>C | p.Phe432Phe | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 12/13 | 1493/2637 | 1296/1590 | 432/529 | chr1 | 27613304 | |||
| chr1:27613319 | T | G | 1 | a0002c0006 | 1 | HG02015.hp2 | synonymous_variant | LOW | c.1281A>C | p.Pro427Pro | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 12/13 | 1478/2637 | 1281/1590 | 427/529 | chr1 | 27613319 | |||
| chr1:27614515 | G | T | 1 | a0002c0006 | 1 | HG02015.hp2 | synonymous_variant | LOW | c.1164C>A | p.Ile388Ile | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 11/13 | 1361/2637 | 1164/1590 | 388/529 | chr1 | 27614515 | |||
| chr1:27615483 | G | T | 1 | a0001c0004 | 2 | HG02451.hp2 HG03579.hp2 |
synonymous_variant | LOW | c.969C>A | p.Ala323Ala | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 9/13 | 1166/2637 | 969/1590 | 323/529 | chr1 | 27615483 | |||
| chr1:27615765 | G | A | 1 | a0001c0002 | 3 | HG02698.hp2 HG03704.hp1 HG03831.hp1 |
synonymous_variant | LOW | c.762C>T | p.Asp254Asp | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 8/13 | 959/2637 | 762/1590 | 254/529 | chr1 | 27615765 | |||
| chr1:27616885 | C | T | 1 | a0001c0003 | 2 | NA18906.hp2 NA21309.hp2 |
synonymous_variant | LOW | c.654G>A | p.Ser218Ser | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 7/13 | 851/2637 | 654/1590 | 218/529 | chr1 | 27616885 | |||
| chr1:27623128 | C | G | 1 | a0001c0005 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.243G>C | p.Leu81Leu | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 4/13 | 440/2637 | 243/1590 | 81/529 | chr1 | 27623128 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:27612100 | T | G | 1 | a0002c0006t0007 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*814A>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 13/13 | 814 | chr1 | 27612100 | ||||||
| chr1:27612120 | G | A | 1 | a0001c0001t0006 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*794C>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 13/13 | 794 | chr1 | 27612120 | ||||||
| chr1:27612221 | C | T | 1 | a0001c0003t0008 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*693G>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 13/13 | 693 | chr1 | 27612221 | ||||||
| chr1:27612257 | C | A | 1 | a0002c0006t0007 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*657G>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 13/13 | 657 | chr1 | 27612257 | ||||||
| chr1:27612266 | T | G | 1 | a0002c0006t0007 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*648A>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 13/13 | 648 | chr1 | 27612266 | ||||||
| chr1:27612294 | T | G | 1 | a0002c0006t0007 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*620A>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 13/13 | 620 | chr1 | 27612294 | ||||||
| chr1:27612356 | A | T | 1 | a0002c0006t0007 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*558T>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 13/13 | 558 | chr1 | 27612356 | ||||||
| chr1:27612464 | A | G | 1 | a0001c0001t0005 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*450T>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 13/13 | 450 | chr1 | 27612464 | ||||||
| chr1:27612582 | G | T | 1 | a0002c0006t0007 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*332C>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 13/13 | 332 | chr1 | 27612582 | ||||||
| chr1:27612584 | G | T | 1 | a0002c0006t0007 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*330C>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 13/13 | 330 | chr1 | 27612584 | ||||||
| chr1:27612678 | G | T | 1 | a0001c0001t0003 | 2 | HG02922.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*236C>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 13/13 | 236 | chr1 | 27612678 | ||||||
| chr1:27612722 | A | C | 1 | a0002c0006t0007 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*192T>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 13/13 | 192 | chr1 | 27612722 | ||||||
| chr1:27612793 | C | G | 1 | a0002c0006t0007 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*121G>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 13/13 | 121 | chr1 | 27612793 | ||||||
| chr1:27612794 | G | A | 3 | a0001c0001t0002 a0001c0001t0003 a0001c0004t0002 |
6 | HG02258.hp1 HG02451.hp2 HG02922.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*120C>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 13/13 | 120 | chr1 | 27612794 | ||||||
| chr1:27612805 | T | G | 1 | a0002c0006t0007 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*109A>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 13/13 | 109 | chr1 | 27612805 | ||||||
| chr1:27625142 | G | A | 2 | a0001c0003t0008 a0001c0003t0009 |
2 | NA18906.hp2 NA21309.hp2 |
5_prime_UTR_variant | MODIFIER | c.-67C>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 2/13 | 1226 | chr1 | 27625142 | ||||||
| chr1:27635118 | C | T | 1 | a0001c0001t0004 | 1 | NA20805.hp1 | 5_prime_UTR_variant | MODIFIER | c.-130G>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/13 | 11202 | chr1 | 27635118 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:27613152 | G | A | 1 | a0001c0001t0006g0058 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1382-30C>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 12/12 | chr1 | 27613152 | |||||||
| chr1:27613177 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1381+42C>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 12/12 | chr1 | 27613177 | |||||||
| chr1:27613213 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG02647.hp1 | splice_region_variant&intron_variant | LOW | c.1381+6C>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 12/12 | chr1 | 27613213 | |||||||
| chr1:27613560 | G | T | 1 | a0002c0006t0007g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1250-210C>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 11/12 | chr1 | 27613560 | |||||||
| chr1:27613606 | G | A | 37 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(34): Show |
45 | HG00639.hp2 HG01069.hp2 HG01070.hp1 others(42): Show |
intron_variant | MODIFIER | c.1250-256C>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 11/12 | chr1 | 27613606 | |||||||
| chr1:27613637 | C | A | 1 | a0002c0006t0007g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1250-287G>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 11/12 | chr1 | 27613637 | |||||||
| chr1:27613639 | A | G | 1 | a0002c0006t0007g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1250-289T>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 11/12 | chr1 | 27613639 | |||||||
| chr1:27613694 | C | CA | 10 | a0001c0001t0001g0019 a0001c0001t0001g0084 a0001c0001t0001g0119 others(7): Show |
11 | HG01433.hp1 HG01884.hp2 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.1250-345dupT | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 11/12 | chr1 | 27613694 | |||||||
| chr1:27613694 | CA | C | 32 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0018 others(29): Show |
36 | HG00099.hp1 HG00323.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.1250-345delT | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 11/12 | chr1 | 27613694 | |||||||
| chr1:27613694 | CAA | C | 24 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0012 others(21): Show |
32 | HG00639.hp1 HG01069.hp2 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.1250-346_1250-345d others(4): Show |
FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 11/12 | chr1 | 27613694 | |||||||
| chr1:27613694 | CAAAAAAA others(1): Show |
C | 11 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0029 others(8): Show |
15 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(12): Show |
intron_variant | MODIFIER | c.1250-352_1250-345d others(10): Show |
FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 11/12 | chr1 | 27613694 | |||||||
| chr1:27613694 | CAAAAAAA others(3): Show |
C | 1 | a0001c0003t0009g0061 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1250-354_1250-345d others(12): Show |
FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 11/12 | chr1 | 27613694 | |||||||
| chr1:27613717 | A | G | 1 | a0001c0001t0001g0025 | 2 | HG00621.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.1250-367T>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 11/12 | chr1 | 27613717 | |||||||
| chr1:27613723 | C | G | 1 | a0001c0005t0001g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1250-373G>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 11/12 | chr1 | 27613723 | |||||||
| chr1:27613740 | C | A | 1 | a0002c0006t0007g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1250-390G>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 11/12 | chr1 | 27613740 | |||||||
| chr1:27613882 | A | T | 1 | a0002c0006t0007g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1250-532T>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 11/12 | chr1 | 27613882 | |||||||
| chr1:27613885 | G | A | 2 | a0001c0001t0001g0112 a0001c0001t0006g0058 |
2 | HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1250-535C>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 11/12 | chr1 | 27613885 | |||||||
| chr1:27613905 | T | G | 1 | a0002c0006t0007g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1249+525A>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 11/12 | chr1 | 27613905 | |||||||
| chr1:27613960 | C | A | 1 | a0002c0006t0007g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1249+470G>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 11/12 | chr1 | 27613960 | |||||||
| chr1:27613963 | C | T | 2 | a0001c0001t0001g0112 a0001c0001t0006g0058 |
2 | HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1249+467G>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 11/12 | chr1 | 27613963 | |||||||
| chr1:27613991 | T | A | 1 | a0002c0006t0007g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1249+439A>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 11/12 | chr1 | 27613991 | |||||||
| chr1:27614004 | A | C | 1 | a0002c0006t0007g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1249+426T>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 11/12 | chr1 | 27614004 | |||||||
| chr1:27614030 | A | C | 1 | a0002c0006t0007g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1249+400T>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 11/12 | chr1 | 27614030 | |||||||
| chr1:27614069 | A | T | 1 | a0002c0006t0007g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1249+361T>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 11/12 | chr1 | 27614069 | |||||||
| chr1:27614070 | T | G | 1 | a0002c0006t0007g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1249+360A>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 11/12 | chr1 | 27614070 | |||||||
| chr1:27614099 | A | G | 1 | a0001c0001t0001g0082 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1249+331T>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 11/12 | chr1 | 27614099 | |||||||
| chr1:27614220 | G | A | 1 | a0001c0001t0001g0049 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1249+210C>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 11/12 | chr1 | 27614220 | |||||||
| chr1:27614223 | A | T | 1 | a0002c0006t0007g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1249+207T>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 11/12 | chr1 | 27614223 | |||||||
| chr1:27614610 | G | C | 1 | a0001c0001t0001g0127 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1096-27C>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 10/12 | chr1 | 27614610 | |||||||
| chr1:27614618 | T | G | 1 | a0001c0001t0001g0172 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1096-35A>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 10/12 | chr1 | 27614618 | |||||||
| chr1:27614638 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1096-55C>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 10/12 | chr1 | 27614638 | |||||||
| chr1:27614642 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1096-59C>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 10/12 | chr1 | 27614642 | |||||||
| chr1:27614735 | A | C | 1 | a0002c0006t0007g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1095+115T>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 10/12 | chr1 | 27614735 | |||||||
| chr1:27614749 | C | A | 1 | a0001c0001t0001g0194 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1095+101G>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 10/12 | chr1 | 27614749 | |||||||
| chr1:27614750 | A | C | 1 | a0002c0006t0007g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1095+100T>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 10/12 | chr1 | 27614750 | |||||||
| chr1:27614781 | A | G | 1 | a0002c0006t0007g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1095+69T>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 10/12 | chr1 | 27614781 | |||||||
| chr1:27614782 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1095+68C>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 10/12 | chr1 | 27614782 | |||||||
| chr1:27614828 | T | A | 1 | a0002c0006t0007g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1095+22A>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 10/12 | chr1 | 27614828 | |||||||
| chr1:27614946 | T | A | 1 | a0002c0006t0007g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1019-20A>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 9/12 | chr1 | 27614946 | |||||||
| chr1:27614975 | G | C | 1 | a0002c0006t0007g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1019-49C>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 9/12 | chr1 | 27614975 | |||||||
| chr1:27614994 | G | T | 1 | a0002c0006t0007g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1019-68C>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 9/12 | chr1 | 27614994 | |||||||
| chr1:27615000 | G | C | 1 | a0002c0006t0007g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1019-74C>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 9/12 | chr1 | 27615000 | |||||||
| chr1:27615130 | T | G | 1 | a0002c0006t0007g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1019-204A>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 9/12 | chr1 | 27615130 | |||||||
| chr1:27615131 | G | T | 1 | a0002c0006t0007g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1019-205C>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 9/12 | chr1 | 27615131 | |||||||
| chr1:27615148 | C | A | 2 | a0001c0001t0001g0112 a0001c0001t0006g0058 |
2 | HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1019-222G>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 9/12 | chr1 | 27615148 | |||||||
| chr1:27615155 | G | C | 1 | a0001c0001t0001g0112 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1019-229C>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 9/12 | chr1 | 27615155 | |||||||
| chr1:27615183 | C | G | 2 | a0001c0003t0008g0091 a0001c0003t0009g0061 |
2 | NA18906.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1018+251G>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 9/12 | chr1 | 27615183 | |||||||
| chr1:27615278 | C | A | 1 | a0002c0006t0007g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1018+156G>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 9/12 | chr1 | 27615278 | |||||||
| chr1:27615279 | A | C | 1 | a0002c0006t0007g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1018+155T>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 9/12 | chr1 | 27615279 | |||||||
| chr1:27615281 | C | T | 1 | a0002c0006t0007g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1018+153G>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 9/12 | chr1 | 27615281 | |||||||
| chr1:27615346 | C | T | 1 | a0002c0006t0007g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1018+88G>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 9/12 | chr1 | 27615346 | |||||||
| chr1:27615421 | T | A | 3 | a0001c0001t0006g0058 a0001c0003t0008g0091 a0001c0003t0009g0061 |
3 | HG03540.hp1 NA18906.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1018+13A>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 9/12 | chr1 | 27615421 | |||||||
| chr1:27615644 | T | G | 3 | a0001c0001t0001g0029 a0001c0001t0001g0089 a0001c0001t0001g0192 |
4 | HG00642.hp1 HG00733.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.839-31A>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 8/12 | chr1 | 27615644 | |||||||
| chr1:27615665 | T | C | 55 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(52): Show |
67 | HG00639.hp1 HG00639.hp2 HG01069.hp2 others(64): Show |
intron_variant | MODIFIER | c.838+24A>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 8/12 | chr1 | 27615665 | |||||||
| chr1:27615675 | C | G | 1 | a0002c0006t0007g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.838+14G>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 8/12 | chr1 | 27615675 | |||||||
| chr1:27615890 | C | T | 2 | a0001c0001t0001g0099 a0001c0001t0001g0157 |
2 | HG01175.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.683-46G>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 7/12 | chr1 | 27615890 | |||||||
| chr1:27616037 | T | G | 1 | a0002c0006t0007g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.683-193A>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 7/12 | chr1 | 27616037 | |||||||
| chr1:27616078 | A | C | 1 | a0002c0006t0007g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.683-234T>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 7/12 | chr1 | 27616078 | |||||||
| chr1:27616145 | A | C | 27 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0016 others(24): Show |
31 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.683-301T>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 7/12 | chr1 | 27616145 | |||||||
| chr1:27616204 | G | A | 1 | a0001c0001t0001g0045 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.683-360C>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 7/12 | chr1 | 27616204 | |||||||
| chr1:27616452 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.682+405G>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 7/12 | chr1 | 27616452 | |||||||
| chr1:27616479 | A | C | 1 | a0002c0006t0007g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.682+378T>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 7/12 | chr1 | 27616479 | |||||||
| chr1:27616499 | C | A | 1 | a0002c0006t0007g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.682+358G>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 7/12 | chr1 | 27616499 | |||||||
| chr1:27616500 | A | C | 1 | a0002c0006t0007g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.682+357T>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 7/12 | chr1 | 27616500 | |||||||
| chr1:27616668 | T | C | 2 | a0001c0001t0001g0087 a0001c0001t0001g0203 |
2 | HG02257.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.682+189A>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 7/12 | chr1 | 27616668 | |||||||
| chr1:27616797 | T | C | 55 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(52): Show |
67 | HG00639.hp1 HG00639.hp2 HG01069.hp2 others(64): Show |
intron_variant | MODIFIER | c.682+60A>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 7/12 | chr1 | 27616797 | |||||||
| chr1:27617014 | G | C | 6 | a0001c0001t0001g0025 a0001c0001t0001g0128 a0001c0001t0001g0133 others(3): Show |
7 | HG00621.hp2 HG01928.hp1 HG02273.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.533-8C>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 6/12 | chr1 | 27617014 | |||||||
| chr1:27617130 | G | A | 2 | a0001c0003t0008g0091 a0001c0003t0009g0061 |
2 | NA18906.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.532+63C>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 6/12 | chr1 | 27617130 | |||||||
| chr1:27617177 | G | A | 6 | a0001c0001t0001g0004 a0001c0001t0001g0116 a0001c0001t0001g0120 others(3): Show |
11 | HG01081.hp1 HG01099.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.532+16C>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 6/12 | chr1 | 27617177 | |||||||
| chr1:27617325 | T | G | 1 | a0002c0006t0007g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.429-29A>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27617325 | |||||||
| chr1:27617340 | C | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0072 a0001c0001t0001g0073 others(2): Show |
9 | HG00639.hp1 HG02258.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.429-44G>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27617340 | |||||||
| chr1:27617365 | A | G | 1 | a0002c0006t0007g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.429-69T>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27617365 | |||||||
| chr1:27617378 | A | G | 1 | a0001c0003t0009g0061 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.429-82T>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27617378 | |||||||
| chr1:27617489 | T | A | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(196): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.429-193A>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27617489 | |||||||
| chr1:27617506 | C | T | 1 | a0002c0006t0007g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.429-210G>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27617506 | |||||||
| chr1:27617559 | T | G | 1 | a0002c0006t0007g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.429-263A>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27617559 | |||||||
| chr1:27617674 | C | T | 2 | a0001c0003t0008g0091 a0001c0003t0009g0061 |
2 | NA18906.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.429-378G>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27617674 | |||||||
| chr1:27617710 | T | G | 1 | a0002c0006t0007g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.429-414A>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27617710 | |||||||
| chr1:27617833 | C | T | 2 | a0001c0001t0001g0090 a0001c0001t0001g0097 |
2 | HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.429-537G>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27617833 | |||||||
| chr1:27617973 | A | G | 1 | a0001c0001t0001g0059 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.429-677T>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27617973 | |||||||
| chr1:27617993 | A | G | 1 | a0002c0006t0007g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.429-697T>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27617993 | |||||||
| chr1:27618049 | T | G | 1 | a0002c0006t0007g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.429-753A>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27618049 | |||||||
| chr1:27618073 | C | T | 2 | a0001c0003t0008g0091 a0001c0003t0009g0061 |
2 | NA18906.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.429-777G>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27618073 | |||||||
| chr1:27618170 | G | T | 5 | a0001c0001t0002g0075 a0001c0001t0003g0064 a0001c0001t0003g0066 others(2): Show |
5 | HG02258.hp1 HG02451.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.429-874C>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27618170 | |||||||
| chr1:27618204 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.429-908C>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27618204 | |||||||
| chr1:27618267 | G | C | 2 | a0001c0003t0008g0091 a0001c0003t0009g0061 |
2 | NA18906.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.429-971C>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27618267 | |||||||
| chr1:27618313 | T | A | 1 | a0002c0006t0007g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.429-1017A>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27618313 | |||||||
| chr1:27618533 | G | A | 3 | a0001c0001t0001g0093 a0001c0001t0001g0145 a0001c0001t0001g0196 |
3 | HG02145.hp2 HG02976.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.429-1237C>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27618533 | |||||||
| chr1:27618535 | G | T | 1 | a0001c0001t0001g0025 | 2 | HG00621.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.429-1239C>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27618535 | |||||||
| chr1:27618579 | A | T | 1 | a0002c0006t0007g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.429-1283T>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27618579 | |||||||
| chr1:27618615 | T | G | 1 | a0002c0006t0007g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.429-1319A>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27618615 | |||||||
| chr1:27618682 | G | A | 21 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0074 others(18): Show |
24 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.429-1386C>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27618682 | |||||||
| chr1:27618763 | C | A | 28 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0016 others(25): Show |
32 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.429-1467G>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27618763 | |||||||
| chr1:27618848 | A | G | 40 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(37): Show |
50 | HG00639.hp1 HG01175.hp1 HG01255.hp1 others(47): Show |
intron_variant | MODIFIER | c.429-1552T>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27618848 | |||||||
| chr1:27618924 | C | T | 2 | a0001c0003t0008g0091 a0001c0003t0009g0061 |
2 | NA18906.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.429-1628G>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27618924 | |||||||
| chr1:27619058 | C | T | 1 | a0001c0001t0001g0025 | 2 | HG00621.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.429-1762G>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27619058 | |||||||
| chr1:27619252 | T | G | 1 | a0002c0006t0007g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.429-1956A>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27619252 | |||||||
| chr1:27619357 | A | T | 1 | a0002c0006t0007g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.429-2061T>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27619357 | |||||||
| chr1:27619443 | G | A | 2 | a0001c0001t0001g0099 a0001c0001t0001g0157 |
2 | HG01175.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.428+2116C>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27619443 | |||||||
| chr1:27619446 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.428+2113G>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27619446 | |||||||
| chr1:27619468 | T | C | 2 | a0001c0001t0001g0074 a0001c0001t0001g0106 |
2 | HG02970.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.428+2091A>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27619468 | |||||||
| chr1:27619520 | T | C | 1 | a0002c0006t0007g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.428+2039A>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27619520 | |||||||
| chr1:27619943 | T | C | 1 | a0001c0001t0001g0079 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.428+1616A>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27619943 | |||||||
| chr1:27619969 | A | AT | 5 | a0001c0001t0001g0074 a0001c0001t0001g0090 a0001c0001t0001g0097 others(2): Show |
5 | HG02809.hp1 HG02970.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.428+1589dupA | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27619969 | |||||||
| chr1:27619974 | T | A | 1 | a0002c0006t0007g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.428+1585A>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27619974 | |||||||
| chr1:27620074 | T | C | 51 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(48): Show |
62 | HG00639.hp1 HG00639.hp2 HG01069.hp2 others(59): Show |
intron_variant | MODIFIER | c.428+1485A>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27620074 | |||||||
| chr1:27620175 | G | A | 1 | a0001c0001t0003g0064 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.428+1384C>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27620175 | |||||||
| chr1:27620538 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.428+1021C>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27620538 | |||||||
| chr1:27620638 | G | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0140 a0001c0001t0001g0198 |
4 | HG01978.hp1 HG02602.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.428+921C>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27620638 | |||||||
| chr1:27620647 | G | T | 1 | a0001c0001t0001g0125 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.428+912C>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27620647 | |||||||
| chr1:27620670 | G | C | 1 | a0001c0001t0001g0180 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.428+889C>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27620670 | |||||||
| chr1:27620735 | G | T | 4 | a0001c0001t0001g0054 a0001c0001t0001g0065 a0001c0001t0001g0162 others(1): Show |
4 | HG02738.hp1 HG03654.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.428+824C>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27620735 | |||||||
| chr1:27620750 | T | C | 2 | a0001c0003t0008g0091 a0001c0003t0009g0061 |
2 | NA18906.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.428+809A>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27620750 | |||||||
| chr1:27620786 | G | T | 7 | a0001c0001t0001g0006 a0001c0001t0001g0081 a0001c0001t0001g0092 others(4): Show |
10 | HG01255.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.428+773C>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27620786 | |||||||
| chr1:27620787 | A | T | 7 | a0001c0001t0001g0006 a0001c0001t0001g0081 a0001c0001t0001g0092 others(4): Show |
10 | HG01255.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.428+772T>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27620787 | |||||||
| chr1:27620871 | A | C | 35 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0013 others(32): Show |
42 | HG00639.hp1 HG01175.hp1 HG01257.hp2 others(39): Show |
intron_variant | MODIFIER | c.428+688T>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27620871 | |||||||
| chr1:27620874 | A | T | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | NA18993.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.428+685T>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27620874 | |||||||
| chr1:27620991 | C | CA | 24 | a0001c0001t0001g0024 a0001c0001t0001g0040 a0001c0001t0001g0041 others(21): Show |
25 | HG00438.hp1 HG00438.hp2 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.428+567dupT | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27620991 | |||||||
| chr1:27620991 | C | CAA | 12 | a0001c0001t0001g0008 a0001c0001t0001g0081 a0001c0001t0001g0092 others(9): Show |
14 | HG00609.hp1 HG02055.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.428+566_428+567dup others(2): Show |
FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27620991 | |||||||
| chr1:27620991 | C | CAAAAAAA others(9): Show |
6 | a0001c0001t0001g0016 a0001c0001t0001g0060 a0001c0001t0001g0104 others(3): Show |
7 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.428+552_428+567dup others(16): Show |
FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27620991 | |||||||
| chr1:27620991 | C | CAAAAAAA others(13): Show |
1 | a0001c0005t0001g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.428+548_428+567dup others(20): Show |
FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27620991 | |||||||
| chr1:27620991 | C | CAAAAAAA others(14): Show |
1 | a0001c0001t0001g0085 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.428+547_428+567dup others(21): Show |
FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27620991 | |||||||
| chr1:27620991 | CA | C | 18 | a0001c0001t0001g0043 a0001c0001t0001g0070 a0001c0001t0001g0076 others(15): Show |
18 | HG00099.hp1 HG00733.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.428+567delT | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27620991 | |||||||
| chr1:27620991 | CAAAA | C | 21 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0072 others(18): Show |
27 | HG00639.hp1 HG01175.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.428+564_428+567del others(4): Show |
FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27620991 | |||||||
| chr1:27620991 | CAAAAA | C | 9 | a0001c0001t0001g0013 a0001c0001t0001g0082 a0001c0001t0001g0093 others(6): Show |
10 | HG01891.hp2 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.428+563_428+567del others(5): Show |
FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27620991 | |||||||
| chr1:27621016 | A | G | 6 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0034 others(3): Show |
8 | HG02015.hp1 HG02132.hp2 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.428+543T>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27621016 | |||||||
| chr1:27621016 | AAAAG | A | 10 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0029 others(7): Show |
11 | HG00423.hp1 HG00642.hp1 HG00733.hp2 others(8): Show |
intron_variant | MODIFIER | c.428+539_428+542del others(4): Show |
FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27621016 | |||||||
| chr1:27621048 | CAAAAAG | C | 6 | a0001c0001t0001g0212 a0001c0001t0002g0075 a0001c0001t0003g0064 others(3): Show |
6 | HG02258.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.428+505_428+510del others(6): Show |
FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27621048 | |||||||
| chr1:27621054 | G | C | 28 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0013 others(25): Show |
35 | HG00639.hp1 HG01175.hp1 HG01257.hp2 others(32): Show |
intron_variant | MODIFIER | c.428+505C>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27621054 | |||||||
| chr1:27621060 | G | C | 34 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0013 others(31): Show |
41 | HG00639.hp1 HG01175.hp1 HG01257.hp2 others(38): Show |
intron_variant | MODIFIER | c.428+499C>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27621060 | |||||||
| chr1:27621301 | G | A | 42 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(39): Show |
52 | HG00639.hp1 HG01175.hp1 HG01255.hp1 others(49): Show |
intron_variant | MODIFIER | c.428+258C>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27621301 | |||||||
| chr1:27621329 | C | T | 2 | a0001c0001t0001g0099 a0001c0001t0001g0157 |
2 | HG01175.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.428+230G>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27621329 | |||||||
| chr1:27621359 | G | A | 1 | a0001c0001t0001g0006 | 4 | HG01255.hp1 HG02257.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.428+200C>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27621359 | |||||||
| chr1:27621410 | A | C | 8 | a0001c0001t0001g0006 a0001c0001t0001g0081 a0001c0001t0001g0092 others(5): Show |
11 | HG01255.hp1 HG02109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.428+149T>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 5/12 | chr1 | 27621410 | |||||||
| chr1:27621740 | C | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0116 a0001c0001t0001g0120 others(2): Show |
10 | HG01081.hp1 HG01261.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.330-83G>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 4/12 | chr1 | 27621740 | |||||||
| chr1:27621799 | C | T | 1 | a0001c0001t0001g0151 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.330-142G>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 4/12 | chr1 | 27621799 | |||||||
| chr1:27621865 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.330-208C>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 4/12 | chr1 | 27621865 | |||||||
| chr1:27621932 | A | T | 17 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0059 others(14): Show |
21 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.330-275T>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 4/12 | chr1 | 27621932 | |||||||
| chr1:27621933 | G | A | 2 | a0001c0001t0001g0051 a0001c0001t0001g0149 |
2 | HG02165.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.330-276C>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 4/12 | chr1 | 27621933 | |||||||
| chr1:27622288 | C | CA | 15 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0041 others(12): Show |
17 | HG01175.hp2 HG01261.hp2 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.330-632dupT | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 4/12 | chr1 | 27622288 | |||||||
| chr1:27622288 | C | CAA | 6 | a0001c0001t0001g0006 a0001c0001t0001g0081 a0001c0001t0001g0092 others(3): Show |
9 | HG01255.hp1 HG02109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.330-633_330-632dup others(2): Show |
FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 4/12 | chr1 | 27622288 | |||||||
| chr1:27622383 | C | T | 3 | a0001c0001t0001g0070 a0001c0001t0001g0078 a0001c0001t0001g0113 |
3 | HG02451.hp1 HG02559.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.329+659G>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 4/12 | chr1 | 27622383 | |||||||
| chr1:27622407 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.329+635A>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 4/12 | chr1 | 27622407 | |||||||
| chr1:27622423 | T | C | 3 | a0001c0001t0001g0090 a0001c0001t0001g0097 a0001c0001t0006g0058 |
3 | HG02809.hp1 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.329+619A>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 4/12 | chr1 | 27622423 | |||||||
| chr1:27622443 | C | T | 27 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0068 others(24): Show |
30 | HG01175.hp1 HG01257.hp2 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.329+599G>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 4/12 | chr1 | 27622443 | |||||||
| chr1:27622574 | C | G | 1 | a0001c0001t0001g0182 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.329+468G>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 4/12 | chr1 | 27622574 | |||||||
| chr1:27622615 | T | C | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(200): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.329+427A>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 4/12 | chr1 | 27622615 | |||||||
| chr1:27622777 | A | G | 34 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0013 others(31): Show |
41 | HG00639.hp1 HG01175.hp1 HG01257.hp2 others(38): Show |
intron_variant | MODIFIER | c.329+265T>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 4/12 | chr1 | 27622777 | |||||||
| chr1:27622802 | G | A | 7 | a0001c0001t0001g0006 a0001c0001t0001g0081 a0001c0001t0001g0092 others(4): Show |
10 | HG01255.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.329+240C>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 4/12 | chr1 | 27622802 | |||||||
| chr1:27622881 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.329+161G>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 4/12 | chr1 | 27622881 | |||||||
| chr1:27622887 | C | T | 2 | a0001c0001t0001g0210 a0001c0001t0001g0211 |
2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.329+155G>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 4/12 | chr1 | 27622887 | |||||||
| chr1:27623249 | C | T | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | NA18993.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.227-105G>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 3/12 | chr1 | 27623249 | |||||||
| chr1:27623262 | G | A | 5 | a0001c0001t0001g0027 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
6 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(3): Show |
intron_variant | MODIFIER | c.227-118C>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 3/12 | chr1 | 27623262 | |||||||
| chr1:27624102 | G | A | 2 | a0001c0001t0001g0099 a0001c0001t0001g0157 |
2 | HG01175.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.-13-173C>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 2/12 | chr1 | 27624102 | |||||||
| chr1:27624185 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-13-256G>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 2/12 | chr1 | 27624185 | |||||||
| chr1:27624189 | G | A | 3 | a0001c0001t0002g0075 a0001c0001t0003g0064 a0001c0001t0003g0066 |
3 | HG02258.hp1 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-13-260C>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 2/12 | chr1 | 27624189 | |||||||
| chr1:27624275 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-13-346C>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 2/12 | chr1 | 27624275 | |||||||
| chr1:27624372 | CTA | C | 36 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0013 others(33): Show |
42 | HG01175.hp1 HG01255.hp1 HG01257.hp2 others(39): Show |
intron_variant | MODIFIER | c.-13-445_-13-444del others(2): Show |
FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 2/12 | chr1 | 27624372 | |||||||
| chr1:27624471 | T | C | 1 | a0001c0001t0001g0021 | 2 | NA18969.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.-13-542A>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 2/12 | chr1 | 27624471 | |||||||
| chr1:27624616 | C | T | 200 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(197): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.-14+473G>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 2/12 | chr1 | 27624616 | |||||||
| chr1:27624879 | C | T | 6 | a0001c0001t0001g0212 a0001c0001t0002g0075 a0001c0001t0003g0064 others(3): Show |
6 | HG02258.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14+210G>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 2/12 | chr1 | 27624879 | |||||||
| chr1:27624995 | G | C | 1 | a0001c0001t0001g0112 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-14+94C>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 2/12 | chr1 | 27624995 | |||||||
| chr1:27625043 | C | G | 3 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0119 |
3 | HG02027.hp1 NA18950.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.-14+46G>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 2/12 | chr1 | 27625043 | |||||||
| chr1:27625447 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-76-296G>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27625447 | |||||||
| chr1:27625565 | A | T | 1 | a0001c0001t0001g0112 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-76-414T>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27625565 | |||||||
| chr1:27625669 | A | G | 53 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(50): Show |
64 | HG00639.hp1 HG00639.hp2 HG01069.hp2 others(61): Show |
intron_variant | MODIFIER | c.-76-518T>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27625669 | |||||||
| chr1:27625694 | A | G | 6 | a0001c0001t0001g0005 a0001c0001t0001g0072 a0001c0001t0001g0073 others(3): Show |
10 | HG00639.hp1 HG02258.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.-76-543T>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27625694 | |||||||
| chr1:27625846 | G | A | 3 | a0001c0001t0001g0103 a0001c0002t0001g0055 a0001c0002t0001g0057 |
3 | HG02698.hp1 HG02698.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-76-695C>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27625846 | |||||||
| chr1:27625893 | C | A | 1 | a0001c0001t0001g0182 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-76-742G>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27625893 | |||||||
| chr1:27625945 | A | C | 7 | a0001c0001t0001g0006 a0001c0001t0001g0081 a0001c0001t0001g0092 others(4): Show |
10 | HG01255.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-76-794T>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27625945 | |||||||
| chr1:27626133 | G | A | 8 | a0001c0001t0001g0006 a0001c0001t0001g0081 a0001c0001t0001g0082 others(5): Show |
11 | HG01255.hp1 HG02109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-76-982C>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27626133 | |||||||
| chr1:27626154 | C | T | 1 | a0001c0002t0001g0056 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-76-1003G>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27626154 | |||||||
| chr1:27626237 | A | G | 7 | a0001c0001t0001g0006 a0001c0001t0001g0081 a0001c0001t0001g0092 others(4): Show |
10 | HG01255.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-76-1086T>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27626237 | |||||||
| chr1:27626434 | T | A | 1 | a0001c0001t0001g0112 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-76-1283A>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27626434 | |||||||
| chr1:27626595 | A | G | 49 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(46): Show |
60 | HG00639.hp1 HG00639.hp2 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.-76-1444T>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27626595 | |||||||
| chr1:27626826 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-76-1675C>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27626826 | |||||||
| chr1:27626830 | G | C | 3 | a0001c0001t0001g0050 a0001c0001t0001g0151 a0001c0001t0001g0190 |
3 | HG00673.hp1 NA19009.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.-76-1679C>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27626830 | |||||||
| chr1:27626863 | G | T | 33 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0013 others(30): Show |
40 | HG00639.hp1 HG01175.hp1 HG01257.hp2 others(37): Show |
intron_variant | MODIFIER | c.-76-1712C>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27626863 | |||||||
| chr1:27627000 | C | A | 1 | a0001c0001t0001g0202 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-76-1849G>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27627000 | |||||||
| chr1:27627003 | T | TA | 36 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0013 others(33): Show |
43 | HG00639.hp1 HG01175.hp1 HG01257.hp2 others(40): Show |
intron_variant | MODIFIER | c.-76-1853dupT | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27627003 | |||||||
| chr1:27627097 | T | C | 27 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0068 others(24): Show |
30 | HG01175.hp1 HG01257.hp2 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.-76-1946A>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27627097 | |||||||
| chr1:27627105 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-76-1954G>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27627105 | |||||||
| chr1:27627132 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-76-1981C>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27627132 | |||||||
| chr1:27627447 | A | AAC | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0072 others(2): Show |
5 | HG00597.hp1 HG01884.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-76-2298_-76-2297d others(4): Show |
FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27627447 | |||||||
| chr1:27627447 | A | AACAC | 12 | a0001c0001t0001g0013 a0001c0001t0001g0074 a0001c0001t0001g0090 others(9): Show |
13 | HG01891.hp2 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-76-2300_-76-2297d others(6): Show |
FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27627447 | |||||||
| chr1:27627447 | A | AACACAC | 3 | a0001c0001t0002g0075 a0001c0001t0003g0066 a0001c0005t0001g0071 |
3 | HG02258.hp1 HG02486.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-76-2302_-76-2297d others(8): Show |
FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27627447 | |||||||
| chr1:27627447 | A | AACACACA others(1): Show |
6 | a0001c0001t0001g0016 a0001c0001t0001g0060 a0001c0001t0001g0085 others(3): Show |
7 | HG01069.hp2 HG01071.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.-76-2304_-76-2297d others(10): Show |
FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27627447 | |||||||
| chr1:27627447 | A | AACACACA others(3): Show |
1 | a0001c0001t0001g0111 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-76-2306_-76-2297d others(12): Show |
FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27627447 | |||||||
| chr1:27627447 | AAC | A | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.-76-2298_-76-2297d others(4): Show |
FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27627447 | |||||||
| chr1:27627447 | AACAC | A | 9 | a0001c0001t0001g0006 a0001c0001t0001g0081 a0001c0001t0001g0092 others(6): Show |
12 | HG01255.hp1 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-76-2300_-76-2297d others(6): Show |
FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27627447 | |||||||
| chr1:27627447 | AACACAC | A | 2 | a0001c0001t0001g0183 a0001c0001t0001g0184 |
2 | NA18993.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.-76-2302_-76-2297d others(8): Show |
FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27627447 | |||||||
| chr1:27627516 | G | A | 49 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(46): Show |
60 | HG00639.hp1 HG00639.hp2 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.-76-2365C>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27627516 | |||||||
| chr1:27627576 | A | T | 7 | a0001c0001t0001g0006 a0001c0001t0001g0081 a0001c0001t0001g0092 others(4): Show |
10 | HG01255.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-76-2425T>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27627576 | |||||||
| chr1:27627904 | T | C | 35 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0013 others(32): Show |
41 | HG01175.hp1 HG01255.hp1 HG01257.hp2 others(38): Show |
intron_variant | MODIFIER | c.-76-2753A>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27627904 | |||||||
| chr1:27628075 | C | G | 2 | a0001c0001t0001g0053 a0001c0001t0001g0118 |
2 | HG03017.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-76-2924G>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27628075 | |||||||
| chr1:27628099 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-76-2948G>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27628099 | |||||||
| chr1:27628116 | C | T | 4 | a0001c0001t0001g0033 a0001c0001t0001g0117 a0001c0001t0001g0135 others(1): Show |
4 | HG00423.hp1 HG02074.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.-76-2965G>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27628116 | |||||||
| chr1:27628129 | C | G | 1 | a0001c0001t0001g0112 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-76-2978G>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27628129 | |||||||
| chr1:27628171 | C | CA | 17 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0030 others(14): Show |
21 | HG01070.hp1 HG01071.hp2 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.-76-3021dupT | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27628171 | |||||||
| chr1:27628185 | A | C | 1 | a0001c0001t0001g0099 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-76-3034T>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27628185 | |||||||
| chr1:27628186 | C | A | 7 | a0001c0001t0001g0005 a0001c0001t0001g0072 a0001c0001t0001g0073 others(4): Show |
11 | HG00639.hp1 HG02258.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-76-3035G>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27628186 | |||||||
| chr1:27628186 | C | CA | 7 | a0001c0001t0001g0016 a0001c0001t0001g0060 a0001c0001t0001g0085 others(4): Show |
8 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.-76-3036dupT | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27628186 | |||||||
| chr1:27628195 | A | C | 32 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0013 others(29): Show |
38 | HG01175.hp1 HG01255.hp1 HG01257.hp2 others(35): Show |
intron_variant | MODIFIER | c.-76-3044T>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27628195 | |||||||
| chr1:27628196 | C | A | 2 | a0001c0001t0001g0014 a0001c0001t0001g0098 |
3 | HG00642.hp2 HG03654.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-76-3045G>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27628196 | |||||||
| chr1:27628197 | C | A | 3 | a0001c0001t0001g0076 a0001c0001t0001g0193 a0001c0001t0001g0194 |
3 | HG01099.hp2 HG01175.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-76-3046G>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27628197 | |||||||
| chr1:27628245 | G | A | 6 | a0001c0001t0001g0013 a0001c0001t0001g0074 a0001c0001t0001g0090 others(3): Show |
7 | HG01891.hp2 HG02809.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.-76-3094C>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27628245 | |||||||
| chr1:27628516 | T | TAC | 32 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0022 others(29): Show |
43 | HG00609.hp2 HG00621.hp1 HG01515.hp2 others(40): Show |
intron_variant | MODIFIER | c.-76-3367_-76-3366d others(4): Show |
FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27628516 | |||||||
| chr1:27628516 | T | TACAC | 19 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0048 others(16): Show |
23 | HG00423.hp2 HG00597.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.-76-3369_-76-3366d others(6): Show |
FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27628516 | |||||||
| chr1:27628516 | T | TACACAC | 6 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0072 others(3): Show |
12 | HG00639.hp1 HG02145.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.-76-3371_-76-3366d others(8): Show |
FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27628516 | |||||||
| chr1:27628516 | T | TACACACA others(1): Show |
5 | a0001c0001t0001g0079 a0001c0001t0001g0083 a0001c0001t0001g0151 others(2): Show |
5 | HG02055.hp2 HG02572.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-76-3373_-76-3366d others(10): Show |
FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27628516 | |||||||
| chr1:27628516 | TAC | T | 21 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0062 others(18): Show |
23 | HG00099.hp1 HG00438.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.-76-3367_-76-3366d others(4): Show |
FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27628516 | |||||||
| chr1:27628516 | TACAC | T | 15 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0053 others(12): Show |
17 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.-76-3369_-76-3366d others(6): Show |
FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27628516 | |||||||
| chr1:27628516 | TACACAC | T | 3 | a0001c0001t0001g0093 a0001c0001t0001g0145 a0001c0001t0001g0196 |
3 | HG02145.hp2 HG02976.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-76-3371_-76-3366d others(8): Show |
FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27628516 | |||||||
| chr1:27628516 | TACACACA others(7): Show |
T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0146 a0001c0001t0001g0147 others(1): Show |
6 | HG02055.hp1 HG02615.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-76-3379_-76-3366d others(16): Show |
FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27628516 | |||||||
| chr1:27628575 | C | T | 1 | a0001c0005t0001g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-76-3424G>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27628575 | |||||||
| chr1:27628816 | A | G | 31 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0013 others(28): Show |
39 | HG00639.hp1 HG01175.hp1 HG01255.hp1 others(36): Show |
intron_variant | MODIFIER | c.-76-3665T>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27628816 | |||||||
| chr1:27628933 | G | A | 21 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0068 others(18): Show |
26 | HG00639.hp1 HG01175.hp1 HG01257.hp2 others(23): Show |
intron_variant | MODIFIER | c.-76-3782C>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27628933 | |||||||
| chr1:27629499 | A | AAG | 10 | a0001c0001t0001g0016 a0001c0001t0001g0059 a0001c0001t0001g0060 others(7): Show |
11 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.-76-4350_-76-4349d others(4): Show |
FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27629499 | |||||||
| chr1:27629629 | T | C | 1 | a0001c0001t0001g0031 | 2 | HG00323.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.-76-4478A>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27629629 | |||||||
| chr1:27629775 | T | G | 7 | a0001c0001t0001g0006 a0001c0001t0001g0081 a0001c0001t0001g0092 others(4): Show |
10 | HG01255.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-76-4624A>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27629775 | |||||||
| chr1:27629852 | T | C | 1 | a0001c0001t0001g0033 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-76-4701A>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27629852 | |||||||
| chr1:27629907 | T | C | 2 | a0001c0001t0001g0006 a0001c0001t0001g0081 |
5 | HG01255.hp1 HG02257.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-76-4756A>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27629907 | |||||||
| chr1:27629935 | A | T | 1 | a0001c0001t0001g0059 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-76-4784T>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27629935 | |||||||
| chr1:27630050 | AT | A | 11 | a0001c0001t0001g0009 a0001c0001t0001g0092 a0001c0001t0001g0094 others(8): Show |
13 | HG01175.hp1 HG02055.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.-76-4900delA | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27630050 | |||||||
| chr1:27630057 | T | C | 2 | a0001c0001t0001g0141 a0001c0001t0001g0142 |
2 | HG01074.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.-76-4906A>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27630057 | |||||||
| chr1:27630197 | C | T | 1 | a0001c0001t0002g0075 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-77+4868G>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27630197 | |||||||
| chr1:27630199 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-77+4866G>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27630199 | |||||||
| chr1:27630211 | G | C | 1 | a0001c0001t0001g0196 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-77+4854C>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27630211 | |||||||
| chr1:27630288 | C | T | 1 | a0003c0008t0001g0166 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-77+4777G>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27630288 | |||||||
| chr1:27630300 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-77+4765C>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27630300 | |||||||
| chr1:27630342 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-77+4723A>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27630342 | |||||||
| chr1:27630345 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-77+4720T>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27630345 | |||||||
| chr1:27630525 | A | G | 1 | a0001c0005t0001g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-77+4540T>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27630525 | |||||||
| chr1:27630563 | G | T | 3 | a0001c0001t0001g0090 a0001c0001t0001g0097 a0001c0001t0006g0058 |
3 | HG02809.hp1 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-77+4502C>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27630563 | |||||||
| chr1:27630578 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-77+4487G>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27630578 | |||||||
| chr1:27630582 | GGA | G | 48 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(45): Show |
60 | HG00639.hp1 HG00639.hp2 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.-77+4481_-77+4482d others(4): Show |
FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27630582 | |||||||
| chr1:27630631 | C | T | 3 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 |
3 | HG00733.hp2 HG01099.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.-77+4434G>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27630631 | |||||||
| chr1:27630709 | A | G | 1 | a0001c0001t0001g0100 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-77+4356T>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27630709 | |||||||
| chr1:27630855 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-77+4210C>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27630855 | |||||||
| chr1:27630980 | A | G | 5 | a0001c0001t0001g0140 a0001c0001t0001g0145 a0001c0001t0001g0196 others(2): Show |
5 | HG01978.hp1 HG02145.hp2 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.-77+4085T>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27630980 | |||||||
| chr1:27631331 | C | T | 2 | a0001c0001t0001g0141 a0001c0001t0001g0142 |
2 | HG01074.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.-77+3734G>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27631331 | |||||||
| chr1:27631333 | C | T | 9 | a0001c0001t0001g0028 a0001c0001t0001g0065 a0001c0001t0001g0161 others(6): Show |
10 | HG00099.hp2 HG00741.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.-77+3732G>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27631333 | |||||||
| chr1:27631470 | G | C | 8 | a0001c0001t0001g0027 a0001c0001t0001g0109 a0001c0001t0001g0110 others(5): Show |
9 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(6): Show |
intron_variant | MODIFIER | c.-77+3595C>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27631470 | |||||||
| chr1:27631586 | A | G | 6 | a0001c0001t0001g0009 a0001c0001t0001g0204 a0001c0001t0001g0205 others(3): Show |
8 | HG01884.hp2 HG02055.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.-77+3479T>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27631586 | |||||||
| chr1:27631591 | C | G | 6 | a0001c0001t0001g0027 a0001c0001t0001g0109 a0001c0001t0001g0110 others(3): Show |
7 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(4): Show |
intron_variant | MODIFIER | c.-77+3474G>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27631591 | |||||||
| chr1:27631636 | A | G | 1 | a0001c0001t0001g0082 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-77+3429T>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27631636 | |||||||
| chr1:27631671 | T | C | 2 | a0001c0001t0001g0141 a0001c0001t0001g0142 |
2 | HG01074.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.-77+3394A>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27631671 | |||||||
| chr1:27631713 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-77+3352C>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27631713 | |||||||
| chr1:27631728 | G | T | 2 | a0001c0001t0001g0141 a0001c0001t0001g0142 |
2 | HG01074.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.-77+3337C>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27631728 | |||||||
| chr1:27631734 | A | G | 40 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0012 others(37): Show |
50 | HG00621.hp2 HG01070.hp1 HG01071.hp2 others(47): Show |
intron_variant | MODIFIER | c.-77+3331T>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27631734 | |||||||
| chr1:27631828 | C | T | 29 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0015 others(26): Show |
37 | HG00621.hp2 HG01074.hp2 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.-77+3237G>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27631828 | |||||||
| chr1:27631842 | G | T | 1 | a0001c0001t0001g0152 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-77+3223C>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27631842 | |||||||
| chr1:27631926 | C | G | 1 | a0001c0001t0001g0151 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-77+3139G>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27631926 | |||||||
| chr1:27631973 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-77+3092C>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27631973 | |||||||
| chr1:27632119 | G | GTTCTTC | 4 | a0001c0001t0001g0140 a0001c0001t0001g0198 a0001c0001t0001g0199 others(1): Show |
4 | HG01978.hp1 HG02602.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.-77+2940_-77+2945d others(8): Show |
FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27632119 | |||||||
| chr1:27632137 | C | CT | 13 | a0001c0001t0001g0009 a0001c0001t0001g0059 a0001c0001t0001g0092 others(10): Show |
15 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.-77+2927dupA | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27632137 | |||||||
| chr1:27632140 | C | T | 14 | a0001c0001t0001g0009 a0001c0001t0001g0059 a0001c0001t0001g0092 others(11): Show |
16 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.-77+2925G>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27632140 | |||||||
| chr1:27632140 | CT | C | 10 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0051 others(7): Show |
10 | HG01074.hp1 HG01099.hp1 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.-77+2924delA | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27632140 | |||||||
| chr1:27632140 | CTTT | C | 32 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(29): Show |
42 | HG00597.hp2 HG00609.hp2 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.-77+2922_-77+2924d others(5): Show |
FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27632140 | |||||||
| chr1:27632143 | T | C | 1 | a0001c0001t0001g0001 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-77+2922A>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27632143 | |||||||
| chr1:27632144 | T | C | 1 | a0001c0001t0001g0051 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-77+2921A>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27632144 | |||||||
| chr1:27632339 | T | C | 2 | a0001c0001t0001g0141 a0001c0001t0001g0142 |
2 | HG01074.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.-77+2726A>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27632339 | |||||||
| chr1:27632482 | C | T | 2 | a0001c0001t0001g0104 a0001c0001t0001g0105 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-77+2583G>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27632482 | |||||||
| chr1:27632845 | G | A | 2 | a0001c0001t0001g0143 a0001c0001t0001g0200 |
2 | HG02897.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-77+2220C>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27632845 | |||||||
| chr1:27632912 | T | C | 3 | a0001c0001t0001g0059 a0001c0001t0001g0081 a0001c0001t0001g0082 |
3 | HG02615.hp1 HG03041.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-77+2153A>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27632912 | |||||||
| chr1:27633174 | A | G | 1 | a0001c0003t0008g0091 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-77+1891T>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27633174 | |||||||
| chr1:27633235 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-77+1830C>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27633235 | |||||||
| chr1:27633241 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-77+1824G>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27633241 | |||||||
| chr1:27633500 | C | T | 36 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(33): Show |
51 | HG00597.hp2 HG00609.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.-77+1565G>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27633500 | |||||||
| chr1:27633739 | A | G | 17 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0059 others(14): Show |
22 | HG01255.hp1 HG01884.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.-77+1326T>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27633739 | |||||||
| chr1:27633743 | A | G | 95 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(92): Show |
123 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(120): Show |
intron_variant | MODIFIER | c.-77+1322T>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27633743 | |||||||
| chr1:27634144 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-77+921C>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27634144 | |||||||
| chr1:27634281 | G | A | 39 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(36): Show |
51 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.-77+784C>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27634281 | |||||||
| chr1:27634290 | C | T | 22 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0033 others(19): Show |
31 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.-77+775G>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27634290 | |||||||
| chr1:27634321 | C | G | 68 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(65): Show |
88 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.-77+744G>C | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27634321 | |||||||
| chr1:27634467 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-77+598G>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27634467 | |||||||
| chr1:27634600 | C | T | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(2): Show |
5 | HG01884.hp1 HG02451.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-77+465G>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27634600 | |||||||
| chr1:27634609 | G | C | 12 | a0001c0001t0001g0009 a0001c0001t0001g0202 a0001c0001t0001g0203 others(9): Show |
14 | HG01884.hp2 HG02055.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.-77+456C>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27634609 | |||||||
| chr1:27634625 | C | T | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(2): Show |
5 | HG01884.hp1 HG02451.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-77+440G>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27634625 | |||||||
| chr1:27634740 | T | C | 1 | a0001c0001t0001g0213 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-77+325A>G | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27634740 | |||||||
| chr1:27634751 | T | A | 1 | a0001c0001t0006g0058 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-77+314A>T | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27634751 | |||||||
| chr1:27634759 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-77+306G>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27634759 | |||||||
| chr1:27634826 | C | T | 8 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0059 others(5): Show |
12 | HG01070.hp1 HG01071.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.-77+239G>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27634826 | |||||||
| chr1:27634885 | G | T | 1 | a0001c0001t0006g0058 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-77+180C>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27634885 | |||||||
| chr1:27635001 | C | T | 28 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(25): Show |
38 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.-77+64G>A | FGR | ENSG00000000938.13 | transcript | ENST00000374005.8 | protein_coding | 1/12 | chr1 | 27635001 |