Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2149 |
| ensemblid | ENSG00000181104.7 |
| hgncid | 3537 |
| symbol | F2R |
| name | coagulation factor II thrombin receptor |
| refseq_nuc | NM_001992.5 |
| refseq_prot | NP_001983.2 |
| ensembl_nuc | ENST00000319211.5 |
| ensembl_prot | ENSP00000321326.4 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 76716126 |
| end | 76735770 |
| strand | + |
| ver | v1.2 |
| region | chr5:76716126-76735770 |
| region5000 | chr5:76711126-76740770 |
| regionname0 | F2R_chr5_76716126_76735770 |
| regionname5000 | F2R_chr5_76711126_76740770 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 425 | 421 | 91 | 82 | 182 | 16 | 48 | 140 | F2R_chr5_76711126_76740770 | F2R | MGPRR others(420): Show |
chr5 | 76711126 | 76740770 |
| a0002 | 0/0 | 425 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | MGPRR others(420): Show |
chr5 | 76711126 | 76740770 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1275 | 420 | 90 | 82 | 182 | 16 | 48 | F2R_chr5_76711126_76740770 | F2R | ATGGG others(1270): Show |
chr5 | 76711126 | 76740770 | ||
| a0001c0002 | 0/0 | 1275 | 1 | 1 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | ATGGG others(1270): Show |
chr5 | 76711126 | 76740770 | ||
| a0002c0003 | 0/0 | 1275 | 1 | 1 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | ATGGG others(1270): Show |
chr5 | 76711126 | 76740770 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3727 | 310 | 49 | 58 | 151 | 12 | 38 | F2R_chr5_76711126_76740770 | F2R | AACCG others(3722): Show |
chr5 | 76711126 | 76740770 |
| a0001c0001t0002 | 0/0 | 3727 | 42 | 4 | 13 | 16 | 2 | 7 | F2R_chr5_76711126_76740770 | F2R | AACCG others(3722): Show |
chr5 | 76711126 | 76740770 |
| a0001c0001t0003 | 0/0 | 3727 | 14 | 4 | 5 | 5 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | AACCG others(3722): Show |
chr5 | 76711126 | 76740770 |
| a0001c0001t0004 | 0/0 | 3727 | 11 | 10 | 1 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | AACCG others(3722): Show |
chr5 | 76711126 | 76740770 |
| a0001c0001t0005 | 0/0 | 3727 | 7 | 2 | 1 | 0 | 2 | 2 | F2R_chr5_76711126_76740770 | F2R | AACCG others(3722): Show |
chr5 | 76711126 | 76740770 |
| a0001c0001t0006 | 0/0 | 3727 | 5 | 5 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | AACCG others(3722): Show |
chr5 | 76711126 | 76740770 |
| a0001c0001t0007 | 0/0 | 3727 | 4 | 4 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | AACCG others(3722): Show |
chr5 | 76711126 | 76740770 |
| a0001c0001t0008 | 0/0 | 3727 | 3 | 3 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | AACCG others(3722): Show |
chr5 | 76711126 | 76740770 |
| a0001c0001t0009 | 0/0 | 3727 | 2 | 2 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | AACCG others(3722): Show |
chr5 | 76711126 | 76740770 |
| a0001c0001t0010 | 0/0 | 3727 | 3 | 0 | 0 | 3 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | AACCG others(3722): Show |
chr5 | 76711126 | 76740770 |
| a0001c0001t0011 | 0/0 | 3727 | 2 | 0 | 0 | 2 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | AACCA others(3722): Show |
chr5 | 76711126 | 76740770 |
| a0001c0001t0012 | 0/0 | 3727 | 2 | 2 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | AACCG others(3722): Show |
chr5 | 76711126 | 76740770 |
| a0001c0001t0013 | 0/0 | 3727 | 2 | 0 | 2 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | AACCG others(3722): Show |
chr5 | 76711126 | 76740770 |
| a0001c0001t0014 | 0/0 | 3727 | 1 | 1 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | AACCG others(3722): Show |
chr5 | 76711126 | 76740770 |
| a0001c0001t0015 | 0/0 | 3727 | 1 | 0 | 0 | 1 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | AACCG others(3722): Show |
chr5 | 76711126 | 76740770 |
| a0001c0001t0016 | 0/0 | 3727 | 1 | 1 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | AACCG others(3722): Show |
chr5 | 76711126 | 76740770 |
| a0001c0001t0017 | 0/0 | 3727 | 1 | 0 | 0 | 1 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | AACCG others(3722): Show |
chr5 | 76711126 | 76740770 |
| a0001c0001t0018 | 0/0 | 3727 | 1 | 0 | 1 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | AACCG others(3722): Show |
chr5 | 76711126 | 76740770 |
| a0001c0001t0019 | 0/0 | 3727 | 1 | 0 | 1 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | AACCG others(3722): Show |
chr5 | 76711126 | 76740770 |
| a0001c0001t0020 | 0/0 | 3727 | 1 | 0 | 0 | 1 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | AACCG others(3722): Show |
chr5 | 76711126 | 76740770 |
| a0001c0001t0021 | 0/0 | 3727 | 1 | 1 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | AACCG others(3722): Show |
chr5 | 76711126 | 76740770 |
| a0001c0001t0022 | 0/0 | 3727 | 1 | 1 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | AACCG others(3722): Show |
chr5 | 76711126 | 76740770 |
| a0001c0001t0023 | 0/0 | 3727 | 1 | 0 | 0 | 0 | 0 | 1 | F2R_chr5_76711126_76740770 | F2R | AACCG others(3722): Show |
chr5 | 76711126 | 76740770 |
| a0001c0001t0024 | 0/0 | 3727 | 1 | 1 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | AACCG others(3722): Show |
chr5 | 76711126 | 76740770 |
| a0001c0001t0025 | 0/0 | 3727 | 1 | 0 | 0 | 1 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | AACCG others(3722): Show |
chr5 | 76711126 | 76740770 |
| a0001c0001t0026 | 0/0 | 3727 | 1 | 0 | 0 | 1 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | AACCG others(3722): Show |
chr5 | 76711126 | 76740770 |
| a0001c0002t0009 | 0/0 | 3727 | 1 | 1 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | AACCG others(3722): Show |
chr5 | 76711126 | 76740770 |
| a0002c0003t0002 | 0/0 | 3727 | 1 | 1 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | AACCG others(3722): Show |
chr5 | 76711126 | 76740770 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 42 | 1 | 0 | 38 | 0 | 3 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0002 | 0/0 | 41 | 1 | 12 | 24 | 1 | 3 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0003 | 0/0 | 30 | 0 | 6 | 19 | 3 | 2 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0005 | 0/0 | 14 | 0 | 4 | 0 | 1 | 9 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0006 | 0/0 | 12 | 1 | 1 | 8 | 1 | 1 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0007 | 0/0 | 10 | 0 | 1 | 5 | 1 | 3 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0013 | 0/0 | 5 | 2 | 3 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0015 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0016 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0019 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0020 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0028 | 1/0 | 3 | 0 | 0 | 2 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0030 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0031 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0050 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0053 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0141 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0002g0004 | 0/0 | 20 | 1 | 6 | 7 | 0 | 6 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0002g0018 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0002g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0002g0026 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0002g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0003g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0003g0017 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0003g0021 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0003g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0004g0010 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0004g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0005g0012 | 0/0 | 5 | 2 | 0 | 0 | 1 | 2 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0005g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0005g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0006g0014 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0007g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0007g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0008g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0009g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0010g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0010g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0011g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0012g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0013g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0014g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0015g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0016g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0017g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0018g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0019g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0020g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0021g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0022g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0023g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0024g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0025g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0001t0026g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0001c0002t0009g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| a0002c0003t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0018 | EUR | GBR | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0030 | EUR | GBR | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | FIN | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG00280 | hp2 | a0001 | c0001 | t0005 | g0012 | EUR | FIN | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0156 | EUR | FIN | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0086 | EUR | FIN | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG00408 | hp1 | a0001 | c0001 | t0017 | g0004 | EAS | CHS | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | CHS | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | CHS | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG00639 | hp2 | a0001 | c0001 | t0019 | g0003 | AMR | PUR | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG00642 | hp1 | a0001 | c0001 | t0004 | g0139 | AMR | PUR | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0021 | AMR | PUR | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0017 | AMR | PUR | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0132 | AMR | PUR | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01175 | hp1 | a0001 | c0001 | t0005 | g0073 | AMR | PUR | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0017 | AMR | CLM | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0017 | AMR | CLM | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0157 | AMR | CLM | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | CLM | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01433 | hp1 | a0001 | c0001 | t0013 | g0027 | AMR | CLM | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01515 | hp1 | a0001 | c0001 | t0005 | g0072 | EUR | IBS | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0053 | EUR | IBS | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01891 | hp2 | a0001 | c0001 | t0014 | g0138 | AFR | ACB | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0017 | AMR | PEL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0026 | AMR | PEL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01943 | hp2 | a0001 | c0001 | t0013 | g0027 | AMR | PEL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01975 | hp1 | a0001 | c0001 | t0018 | g0104 | AMR | PEL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PEL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02055 | hp1 | a0001 | c0001 | t0008 | g0008 | AFR | ACB | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02074 | hp2 | a0001 | c0001 | t0011 | g0001 | EAS | KHV | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02083 | hp1 | a0001 | c0001 | t0011 | g0001 | EAS | KHV | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0012 | AFR | ACB | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0079 | AMR | PEL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | CDX | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02258 | hp2 | a0001 | c0001 | t0006 | g0014 | AFR | ACB | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02280 | hp2 | a0001 | c0001 | t0022 | g0147 | AFR | ACB | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02451 | hp1 | a0001 | c0001 | t0006 | g0014 | AFR | ACB | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02451 | hp2 | a0001 | c0002 | t0009 | g0095 | AFR | ACB | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0010 | AFR | GWD | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02615 | hp1 | a0002 | c0003 | t0002 | g0008 | AFR | GWD | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0014 | AFR | GWD | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0146 | AFR | GWD | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0010 | AFR | GWD | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0032 | AFR | GWD | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02647 | hp2 | a0001 | c0001 | t0024 | g0153 | AFR | GWD | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02717 | hp2 | a0001 | c0001 | t0009 | g0043 | AFR | GWD | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0081 | AFR | GWD | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0032 | AFR | GWD | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0150 | AFR | GWD | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0010 | AFR | GWD | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02922 | hp2 | a0001 | c0001 | t0006 | g0014 | AFR | ESN | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02970 | hp2 | a0001 | c0001 | t0007 | g0022 | AFR | ESN | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG03041 | hp2 | a0001 | c0001 | t0007 | g0022 | AFR | GWD | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ESN | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0010 | AFR | MSL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG03225 | hp1 | a0001 | c0001 | t0012 | g0038 | AFR | MSL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0076 | AFR | MSL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | MSL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG03486 | hp1 | a0001 | c0001 | t0008 | g0008 | AFR | MSL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0010 | AFR | MSL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG03540 | hp2 | a0001 | c0001 | t0012 | g0038 | AFR | GWD | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0151 | AFR | MSL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG03579 | hp2 | a0001 | c0001 | t0008 | g0008 | AFR | MSL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG03654 | hp1 | a0001 | c0001 | t0005 | g0012 | SAS | PJL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0078 | SAS | STU | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | STU | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG03704 | hp2 | a0001 | c0001 | t0005 | g0012 | SAS | PJL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | BEB | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | BEB | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | BEB | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | BEB | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | BEB | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | STU | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG04184 | hp1 | a0001 | c0001 | t0023 | g0131 | SAS | BEB | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | STU | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | STU | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | STU | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | STU | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | YRI | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | CHB | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | CHB | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18906 | hp1 | a0001 | c0001 | t0007 | g0054 | AFR | YRI | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | YRI | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18965 | hp1 | a0001 | c0001 | t0025 | g0023 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18969 | hp1 | a0001 | c0001 | t0010 | g0004 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18983 | hp2 | a0001 | c0001 | t0026 | g0002 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | LWK | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | LWK | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | LWK | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | LWK | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19065 | hp1 | a0001 | c0001 | t0015 | g0011 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19076 | hp1 | a0001 | c0001 | t0010 | g0004 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19081 | hp2 | a0001 | c0001 | t0020 | g0003 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19083 | hp2 | a0001 | c0001 | t0010 | g0089 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | YRI | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA20129 | hp1 | a0001 | c0001 | t0009 | g0043 | AFR | ASW | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0098 | EUR | TSI | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | TSI | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | TSI | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | GIH | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02109 | hp2 | a0001 | c0001 | t0016 | g0009 | AFR | ACB | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | ACB | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0010 | AFR | ACB | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ACB | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG03471 | hp1 | a0001 | c0001 | t0006 | g0014 | AFR | MSL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG03471 | hp2 | a0001 | c0001 | t0007 | g0022 | AFR | MSL | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG06807 | hp1 | a0001 | c0001 | t0005 | g0012 | AFR | USA | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0155 | AFR | USA | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | USA | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | USA | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA21309 | hp1 | a0001 | c0001 | t0021 | g0052 | AFR | LWK | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | LWK | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0141 | REF | REF | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0028 | REF | REF | F2R_chr5_76711126_76740770 | F2R | chr5 | 76711126 | 76740770 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:76733460 | C | A | 1 | a0002 | 1 | HG02615.hp1 | missense_variant | MODERATE | c.1235C>A | p.Ser412Tyr | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 2/2 | 1417/3727 | 1235/1278 | 412/425 | chr5 | 76733460 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:76732963 | G | A | 1 | a0001c0002 | 1 | HG02451.hp2 | synonymous_variant | LOW | c.738G>A | p.Val246Val | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 2/2 | 920/3727 | 738/1278 | 246/425 | chr5 | 76732963 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:76716130 | G | A | 1 | a0001c0001t0011 | 2 | HG02074.hp2 HG02083.hp1 |
5_prime_UTR_variant | MODIFIER | c.-178G>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/2 | 178 | chr5 | 76716130 | ||||||
| chr5:76716136 | G | A | 2 | a0001c0001t0006 a0001c0001t0014 |
6 | HG01891.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-172G>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/2 | 172 | chr5 | 76716136 | ||||||
| chr5:76716154 | G | A | 3 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0015 |
19 | HG00735.hp1 HG00741.hp2 HG01257.hp1 others(16): Show |
5_prime_UTR_variant | MODIFIER | c.-154G>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/2 | 154 | chr5 | 76716154 | ||||||
| chr5:76716174 | T | C | 3 | a0001c0001t0003 a0001c0001t0015 a0001c0001t0016 |
16 | HG00735.hp1 HG00741.hp2 HG01257.hp1 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-134T>C | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/2 | 134 | chr5 | 76716174 | ||||||
| chr5:76733547 | T | C | 2 | a0001c0001t0004 a0001c0001t0006 |
16 | HG00642.hp1 HG02258.hp2 HG02451.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*44T>C | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 2/2 | 44 | chr5 | 76733547 | ||||||
| chr5:76733588 | T | C | 1 | a0001c0001t0015 | 1 | NA19065.hp1 | 3_prime_UTR_variant | MODIFIER | c.*85T>C | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 2/2 | 85 | chr5 | 76733588 | ||||||
| chr5:76733926 | G | T | 1 | a0001c0001t0010 | 3 | NA18969.hp1 NA19076.hp1 NA19083.hp2 |
3_prime_UTR_variant | MODIFIER | c.*423G>T | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 2/2 | 423 | chr5 | 76733926 | ||||||
| chr5:76733950 | T | C | 1 | a0001c0001t0017 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*447T>C | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 2/2 | 447 | chr5 | 76733950 | ||||||
| chr5:76733954 | A | G | 1 | a0001c0001t0026 | 1 | NA18983.hp2 | 3_prime_UTR_variant | MODIFIER | c.*451A>G | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 2/2 | 451 | chr5 | 76733954 | ||||||
| chr5:76734282 | T | C | 1 | a0001c0001t0018 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*779T>C | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 2/2 | 779 | chr5 | 76734282 | ||||||
| chr5:76734498 | T | C | 1 | a0001c0001t0019 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*995T>C | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 2/2 | 995 | chr5 | 76734498 | ||||||
| chr5:76734542 | G | C | 1 | a0001c0001t0020 | 1 | NA19081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1039G>C | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 2/2 | 1039 | chr5 | 76734542 | ||||||
| chr5:76734776 | G | A | 1 | a0001c0001t0021 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1273G>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 2/2 | 1273 | chr5 | 76734776 | ||||||
| chr5:76734869 | A | C | 1 | a0001c0001t0007 | 4 | HG02970.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1366A>C | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 2/2 | 1366 | chr5 | 76734869 | ||||||
| chr5:76734970 | A | T | 1 | a0001c0001t0013 | 2 | HG01433.hp1 HG01943.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1467A>T | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 2/2 | 1467 | chr5 | 76734970 | ||||||
| chr5:76734971 | T | C | 7 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0008 others(4): Show |
59 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*1468T>C | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 2/2 | 1468 | chr5 | 76734971 | ||||||
| chr5:76735029 | A | G | 1 | a0001c0001t0008 | 3 | HG02055.hp1 HG03486.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1526A>G | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 2/2 | 1526 | chr5 | 76735029 | ||||||
| chr5:76735210 | A | C | 6 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0010 others(3): Show |
52 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*1707A>C | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 2/2 | 1707 | chr5 | 76735210 | ||||||
| chr5:76735211 | C | T | 1 | a0001c0001t0025 | 1 | NA18965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1708C>T | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 2/2 | 1708 | chr5 | 76735211 | ||||||
| chr5:76735244 | C | T | 2 | a0001c0001t0009 a0001c0002t0009 |
3 | HG02451.hp2 HG02717.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1741C>T | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 2/2 | 1741 | chr5 | 76735244 | ||||||
| chr5:76735343 | A | G | 2 | a0001c0001t0009 a0001c0002t0009 |
3 | HG02451.hp2 HG02717.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1840A>G | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 2/2 | 1840 | chr5 | 76735343 | ||||||
| chr5:76735400 | G | A | 1 | a0001c0001t0022 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1897G>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 2/2 | 1897 | chr5 | 76735400 | ||||||
| chr5:76735409 | C | G | 1 | a0001c0001t0024 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1906C>G | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 2/2 | 1906 | chr5 | 76735409 | ||||||
| chr5:76735429 | G | A | 1 | a0001c0001t0023 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1926G>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 2/2 | 1926 | chr5 | 76735429 | ||||||
| chr5:76735563 | G | A | 1 | a0001c0001t0012 | 2 | HG03225.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2060G>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 2/2 | 2060 | chr5 | 76735563 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:76716530 | G | A | 8 | a0001c0001t0003g0011 a0001c0001t0003g0017 a0001c0001t0003g0021 others(5): Show |
19 | HG00735.hp1 HG00741.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.88+135G>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76716530 | |||||||
| chr5:76716660 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.88+265G>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76716660 | |||||||
| chr5:76716920 | C | T | 5 | a0001c0001t0001g0016 a0001c0001t0001g0053 a0001c0001t0002g0155 others(2): Show |
10 | HG00323.hp1 HG00639.hp1 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.88+525C>T | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76716920 | |||||||
| chr5:76717018 | G | A | 66 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(63): Show |
196 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.88+623G>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76717018 | |||||||
| chr5:76717029 | G | T | 1 | a0001c0001t0001g0154 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.88+634G>T | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76717029 | |||||||
| chr5:76717088 | C | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(111): Show |
295 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.88+693C>T | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76717088 | |||||||
| chr5:76717098 | T | G | 2 | a0001c0001t0003g0021 a0001c0001t0003g0032 |
5 | HG00735.hp1 HG02486.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.88+703T>G | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76717098 | |||||||
| chr5:76717110 | G | T | 7 | a0001c0001t0001g0094 a0001c0001t0003g0011 a0001c0001t0003g0017 others(4): Show |
16 | HG00735.hp1 HG00741.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.88+715G>T | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76717110 | |||||||
| chr5:76717467 | A | T | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | HG00597.hp1 HG00673.hp2 |
intron_variant | MODIFIER | c.88+1072A>T | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76717467 | |||||||
| chr5:76717540 | G | T | 3 | a0001c0001t0001g0048 a0001c0001t0001g0123 a0001c0001t0001g0124 |
4 | NA18612.hp2 NA18747.hp2 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.88+1145G>T | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76717540 | |||||||
| chr5:76717639 | G | C | 48 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(45): Show |
99 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(96): Show |
intron_variant | MODIFIER | c.88+1244G>C | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76717639 | |||||||
| chr5:76717660 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.88+1265G>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76717660 | |||||||
| chr5:76717683 | C | T | 4 | a0001c0001t0001g0152 a0001c0001t0004g0010 a0001c0001t0004g0150 others(1): Show |
9 | HG02559.hp1 HG02572.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.88+1288C>T | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76717683 | |||||||
| chr5:76717696 | T | C | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 |
3 | HG01167.hp1 HG01169.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.88+1301T>C | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76717696 | |||||||
| chr5:76717741 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.88+1346G>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76717741 | |||||||
| chr5:76718106 | G | A | 117 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(114): Show |
302 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.88+1711G>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76718106 | |||||||
| chr5:76718175 | C | A | 114 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(111): Show |
296 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.88+1780C>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76718175 | |||||||
| chr5:76718196 | G | A | 2 | a0001c0001t0001g0053 a0001c0001t0002g0155 |
3 | HG01516.hp1 HG02698.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.88+1801G>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76718196 | |||||||
| chr5:76718265 | A | T | 8 | a0001c0001t0001g0015 a0001c0001t0001g0020 a0001c0001t0001g0031 others(5): Show |
17 | HG00733.hp1 HG01243.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.88+1870A>T | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76718265 | |||||||
| chr5:76718494 | G | A | 67 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(64): Show |
198 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.88+2099G>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76718494 | |||||||
| chr5:76718551 | G | A | 10 | a0001c0001t0001g0094 a0001c0001t0001g0097 a0001c0001t0003g0011 others(7): Show |
21 | HG00735.hp1 HG00741.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.88+2156G>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76718551 | |||||||
| chr5:76718597 | G | T | 1 | a0001c0001t0001g0143 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.88+2202G>T | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76718597 | |||||||
| chr5:76718619 | A | C | 1 | a0001c0001t0001g0091 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.88+2224A>C | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76718619 | |||||||
| chr5:76718679 | A | T | 1 | a0001c0001t0001g0142 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.88+2284A>T | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76718679 | |||||||
| chr5:76718775 | A | T | 7 | a0001c0001t0001g0009 a0001c0001t0001g0096 a0001c0001t0001g0152 others(4): Show |
16 | HG01884.hp2 HG02109.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.88+2380A>T | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76718775 | |||||||
| chr5:76719183 | C | T | 1 | a0001c0001t0001g0041 | 2 | HG01255.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.88+2788C>T | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76719183 | |||||||
| chr5:76719286 | G | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(111): Show |
297 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.88+2891G>T | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76719286 | |||||||
| chr5:76719317 | C | T | 5 | a0001c0001t0001g0015 a0001c0001t0001g0031 a0001c0001t0001g0148 others(2): Show |
11 | HG00733.hp1 HG01243.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.88+2922C>T | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76719317 | |||||||
| chr5:76719368 | T | C | 1 | a0001c0001t0024g0153 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.88+2973T>C | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76719368 | |||||||
| chr5:76719435 | C | A | 9 | a0001c0001t0001g0094 a0001c0001t0003g0011 a0001c0001t0003g0017 others(6): Show |
20 | HG00735.hp1 HG00741.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.88+3040C>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76719435 | |||||||
| chr5:76719538 | G | C | 1 | a0001c0001t0001g0098 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.88+3143G>C | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76719538 | |||||||
| chr5:76719587 | T | A | 1 | a0001c0001t0024g0153 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.88+3192T>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76719587 | |||||||
| chr5:76719588 | C | CA | 42 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(39): Show |
93 | HG00140.hp2 HG00280.hp1 HG00642.hp2 others(90): Show |
intron_variant | MODIFIER | c.88+3204dupA | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 76719588 | ||||||
| chr5:76719630 | G | A | 68 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(65): Show |
196 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.88+3235G>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76719630 | |||||||
| chr5:76719638 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.88+3243G>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76719638 | |||||||
| chr5:76719673 | G | A | 1 | a0001c0001t0001g0049 | 2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.88+3278G>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76719673 | |||||||
| chr5:76719738 | A | G | 2 | a0001c0001t0001g0056 a0001c0001t0001g0122 |
2 | HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.88+3343A>G | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76719738 | |||||||
| chr5:76719839 | G | A | 118 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(115): Show |
303 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.88+3444G>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76719839 | |||||||
| chr5:76719853 | G | C | 1 | a0001c0001t0024g0153 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.88+3458G>C | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76719853 | |||||||
| chr5:76719866 | C | A | 3 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0128 |
5 | HG01891.hp1 HG02572.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+3471C>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76719866 | |||||||
| chr5:76719904 | C | T | 1 | a0001c0002t0009g0095 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.88+3509C>T | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76719904 | |||||||
| chr5:76719907 | A | G | 1 | a0001c0001t0001g0142 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.88+3512A>G | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76719907 | |||||||
| chr5:76720022 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.88+3627A>G | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76720022 | |||||||
| chr5:76720081 | A | ACTAT | 2 | a0001c0001t0007g0022 a0001c0001t0007g0054 |
4 | HG02970.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+3703_88+3706dup others(4): Show |
F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 76720081 | ||||||
| chr5:76720127 | C | T | 2 | a0001c0001t0006g0014 a0001c0001t0014g0138 |
6 | HG01891.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+3732C>T | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76720127 | |||||||
| chr5:76720167 | G | T | 2 | a0001c0001t0006g0014 a0001c0001t0014g0138 |
6 | HG01891.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+3772G>T | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76720167 | |||||||
| chr5:76720213 | C | A | 1 | a0001c0001t0001g0059 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.88+3818C>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76720213 | |||||||
| chr5:76720230 | G | A | 1 | a0001c0001t0001g0060 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.88+3835G>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76720230 | |||||||
| chr5:76720248 | C | T | 1 | a0001c0001t0001g0152 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.88+3853C>T | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76720248 | |||||||
| chr5:76720429 | C | A | 6 | a0001c0001t0001g0013 a0001c0001t0001g0052 a0001c0001t0001g0140 others(3): Show |
10 | HG00642.hp1 HG00738.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.88+4034C>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76720429 | |||||||
| chr5:76720853 | G | C | 2 | a0001c0001t0007g0022 a0001c0001t0007g0054 |
4 | HG02970.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+4458G>C | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76720853 | |||||||
| chr5:76720999 | A | G | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(165): Show |
417 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(414): Show |
intron_variant | MODIFIER | c.88+4604A>G | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76720999 | |||||||
| chr5:76721051 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.88+4656C>T | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76721051 | |||||||
| chr5:76721120 | C | T | 1 | a0001c0001t0001g0013 | 5 | HG00738.hp2 HG01070.hp2 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+4725C>T | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76721120 | |||||||
| chr5:76721121 | G | A | 102 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(99): Show |
265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.88+4726G>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76721121 | |||||||
| chr5:76721149 | G | A | 1 | a0001c0001t0001g0100 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.88+4754G>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76721149 | |||||||
| chr5:76721150 | G | A | 71 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(68): Show |
199 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.88+4755G>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76721150 | |||||||
| chr5:76721496 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.88+5101C>T | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76721496 | |||||||
| chr5:76721786 | CCAAACAG others(41): Show |
C | 3 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0128 |
5 | HG01891.hp1 HG02572.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+5442_88+5489del others(48): Show |
F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 76721786 | ||||||
| chr5:76721922 | A | G | 1 | a0001c0001t0009g0043 | 2 | HG02717.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.88+5527A>G | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76721922 | |||||||
| chr5:76722039 | T | C | 4 | a0001c0001t0004g0010 a0001c0001t0004g0150 a0001c0001t0004g0151 others(1): Show |
13 | HG02258.hp2 HG02451.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.88+5644T>C | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76722039 | |||||||
| chr5:76722098 | G | T | 4 | a0001c0001t0004g0010 a0001c0001t0004g0150 a0001c0001t0004g0151 others(1): Show |
13 | HG02258.hp2 HG02451.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.88+5703G>T | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76722098 | |||||||
| chr5:76722201 | A | C | 1 | a0001c0001t0010g0089 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.88+5806A>C | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76722201 | |||||||
| chr5:76722202 | T | A | 1 | a0001c0001t0010g0089 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.88+5807T>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76722202 | |||||||
| chr5:76722203 | C | T | 1 | a0001c0001t0010g0089 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.88+5808C>T | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76722203 | |||||||
| chr5:76722496 | G | A | 1 | a0001c0001t0002g0157 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.88+6101G>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76722496 | |||||||
| chr5:76722499 | G | C | 1 | a0001c0001t0003g0032 | 2 | HG02647.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.88+6104G>C | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76722499 | |||||||
| chr5:76722503 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.88+6108A>G | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76722503 | |||||||
| chr5:76722516 | CT | C | 18 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0035 others(15): Show |
49 | HG00140.hp1 HG00558.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.88+6124delT | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 76722516 | ||||||
| chr5:76722628 | G | C | 1 | a0001c0001t0003g0032 | 2 | HG02647.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.88+6233G>C | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76722628 | |||||||
| chr5:76722855 | G | A | 1 | a0001c0001t0001g0144 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.88+6460G>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76722855 | |||||||
| chr5:76722950 | C | CA | 132 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(129): Show |
326 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(323): Show |
intron_variant | MODIFIER | c.88+6569dupA | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 76722950 | ||||||
| chr5:76722950 | C | CAA | 4 | a0001c0001t0001g0134 a0001c0001t0002g0024 a0001c0001t0002g0044 others(1): Show |
7 | HG01175.hp2 NA18943.hp1 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.88+6568_88+6569dup others(2): Show |
F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 76722950 | ||||||
| chr5:76723156 | C | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0140 |
6 | HG00738.hp2 HG01070.hp2 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.88+6761C>T | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76723156 | |||||||
| chr5:76723219 | C | T | 1 | a0001c0001t0001g0016 | 5 | HG00639.hp1 HG01069.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+6824C>T | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76723219 | |||||||
| chr5:76723264 | T | G | 1 | a0001c0001t0001g0031 | 3 | HG01884.hp1 HG02723.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.88+6869T>G | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76723264 | |||||||
| chr5:76723271 | C | A | 55 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(52): Show |
121 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(118): Show |
intron_variant | MODIFIER | c.88+6876C>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76723271 | |||||||
| chr5:76723339 | T | C | 1 | a0001c0001t0001g0108 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.88+6944T>C | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76723339 | |||||||
| chr5:76723434 | A | G | 1 | a0001c0001t0001g0152 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.88+7039A>G | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76723434 | |||||||
| chr5:76723491 | C | T | 45 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0033 others(42): Show |
133 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.88+7096C>T | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76723491 | |||||||
| chr5:76723516 | A | G | 2 | a0001c0001t0001g0105 a0001c0001t0001g0106 |
2 | HG01109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.88+7121A>G | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76723516 | |||||||
| chr5:76723570 | G | T | 1 | a0001c0001t0010g0089 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.88+7175G>T | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76723570 | |||||||
| chr5:76723644 | T | G | 1 | a0001c0001t0001g0074 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.88+7249T>G | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76723644 | |||||||
| chr5:76723680 | C | A | 1 | a0001c0001t0001g0088 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.88+7285C>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76723680 | |||||||
| chr5:76723900 | C | A | 1 | a0001c0001t0001g0075 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.88+7505C>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76723900 | |||||||
| chr5:76724076 | G | A | 2 | a0001c0001t0007g0022 a0001c0001t0007g0054 |
4 | HG02970.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+7681G>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76724076 | |||||||
| chr5:76724375 | A | G | 5 | a0001c0001t0001g0008 a0001c0001t0002g0008 a0001c0001t0002g0132 others(2): Show |
7 | HG01167.hp2 HG02055.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.89-7939A>G | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76724375 | |||||||
| chr5:76724422 | A | C | 1 | a0001c0001t0001g0087 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.89-7892A>C | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76724422 | |||||||
| chr5:76724531 | TTTATTTG others(30): Show |
T | 21 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0025 others(18): Show |
58 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.89-7750_89-7714del others(37): Show |
F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 76724531 | ||||||
| chr5:76724793 | A | T | 1 | a0001c0001t0002g0018 | 4 | HG00099.hp2 HG01074.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-7521A>T | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76724793 | |||||||
| chr5:76724867 | T | C | 1 | a0001c0001t0001g0030 | 3 | HG00140.hp2 HG00642.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.89-7447T>C | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76724867 | |||||||
| chr5:76724915 | C | CAGTAATG others(31): Show |
1 | a0001c0001t0010g0089 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.89-7382_89-7381ins others(38): Show |
F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 76724915 | ||||||
| chr5:76724929 | T | C | 3 | a0001c0001t0001g0009 a0001c0001t0001g0096 a0001c0001t0016g0009 |
7 | HG01884.hp2 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.89-7385T>C | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76724929 | |||||||
| chr5:76724952 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.89-7362T>C | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76724952 | |||||||
| chr5:76724983 | T | C | 2 | a0001c0001t0002g0076 a0001c0001t0012g0038 |
3 | HG03225.hp1 HG03225.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.89-7331T>C | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76724983 | |||||||
| chr5:76725225 | C | T | 1 | a0001c0001t0002g0076 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.89-7089C>T | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76725225 | |||||||
| chr5:76725242 | T | C | 2 | a0001c0001t0007g0022 a0001c0001t0007g0054 |
4 | HG02970.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.89-7072T>C | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76725242 | |||||||
| chr5:76725307 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.89-7007G>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76725307 | |||||||
| chr5:76725348 | T | C | 2 | a0001c0001t0001g0071 a0001c0001t0001g0077 |
2 | HG02015.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.89-6966T>C | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76725348 | |||||||
| chr5:76725622 | A | AT | 133 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(130): Show |
327 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.89-6686dupT | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 76725622 | ||||||
| chr5:76725646 | G | A | 2 | a0001c0001t0007g0022 a0001c0001t0007g0054 |
4 | HG02970.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.89-6668G>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76725646 | |||||||
| chr5:76725772 | C | A | 1 | a0001c0001t0002g0078 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.89-6542C>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76725772 | |||||||
| chr5:76725800 | C | T | 1 | a0001c0001t0001g0059 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.89-6514C>T | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76725800 | |||||||
| chr5:76725962 | TGTCA | T | 2 | a0001c0001t0003g0021 a0001c0001t0003g0032 |
5 | HG00735.hp1 HG02486.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-6348_89-6345del others(4): Show |
F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 76725962 | ||||||
| chr5:76726052 | A | C | 1 | a0001c0001t0002g0076 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.89-6262A>C | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76726052 | |||||||
| chr5:76726159 | G | A | 3 | a0001c0001t0001g0009 a0001c0001t0001g0096 a0001c0001t0016g0009 |
7 | HG01884.hp2 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.89-6155G>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76726159 | |||||||
| chr5:76726184 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.89-6130G>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76726184 | |||||||
| chr5:76726388 | G | A | 2 | a0001c0001t0003g0021 a0001c0001t0003g0032 |
5 | HG00735.hp1 HG02486.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-5926G>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76726388 | |||||||
| chr5:76726407 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.89-5907T>C | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76726407 | |||||||
| chr5:76726527 | A | C | 1 | a0001c0001t0001g0120 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.89-5787A>C | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76726527 | |||||||
| chr5:76726536 | CA | C | 4 | a0001c0001t0001g0015 a0001c0001t0001g0031 a0001c0001t0001g0070 others(1): Show |
10 | HG00733.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.89-5763delA | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 76726536 | ||||||
| chr5:76726794 | T | A | 1 | a0001c0001t0002g0079 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.89-5520T>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76726794 | |||||||
| chr5:76726856 | T | C | 1 | a0001c0001t0004g0139 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.89-5458T>C | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76726856 | |||||||
| chr5:76726902 | A | G | 4 | a0001c0001t0001g0035 a0001c0001t0001g0066 a0001c0001t0001g0102 others(1): Show |
5 | HG02132.hp2 NA18946.hp1 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-5412A>G | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76726902 | |||||||
| chr5:76727264 | T | C | 1 | a0001c0001t0001g0063 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.89-5050T>C | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76727264 | |||||||
| chr5:76727284 | G | C | 1 | a0001c0001t0001g0031 | 3 | HG01884.hp1 HG02723.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.89-5030G>C | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76727284 | |||||||
| chr5:76727391 | A | C | 1 | a0001c0001t0023g0131 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.89-4923A>C | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76727391 | |||||||
| chr5:76727636 | T | TATAG | 2 | a0001c0001t0003g0021 a0001c0001t0003g0032 |
5 | HG00735.hp1 HG02486.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-4677_89-4676ins others(4): Show |
F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 76727636 | ||||||
| chr5:76727669 | A | G | 1 | a0001c0001t0001g0016 | 5 | HG00639.hp1 HG01069.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.89-4645A>G | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76727669 | |||||||
| chr5:76727763 | C | CT | 6 | a0001c0001t0001g0046 a0001c0001t0001g0098 a0001c0001t0001g0119 others(3): Show |
7 | HG01069.hp2 HG01192.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.89-4536dupT | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 76727763 | ||||||
| chr5:76727764 | T | A | 1 | a0001c0001t0001g0105 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.89-4550T>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76727764 | |||||||
| chr5:76727844 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.89-4470G>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76727844 | |||||||
| chr5:76727854 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.89-4460C>T | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76727854 | |||||||
| chr5:76727886 | CT | C | 6 | a0001c0001t0001g0045 a0001c0001t0001g0059 a0001c0001t0001g0080 others(3): Show |
9 | HG01167.hp2 HG02970.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.89-4410delT | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 76727886 | ||||||
| chr5:76728010 | C | T | 1 | a0001c0001t0006g0014 | 5 | HG02258.hp2 HG02451.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.89-4304C>T | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76728010 | |||||||
| chr5:76728224 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.89-4090T>C | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76728224 | |||||||
| chr5:76728402 | A | G | 46 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0033 others(43): Show |
137 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.89-3912A>G | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76728402 | |||||||
| chr5:76728494 | G | A | 7 | a0001c0001t0004g0010 a0001c0001t0004g0081 a0001c0001t0004g0139 others(4): Show |
16 | HG00642.hp1 HG02258.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.89-3820G>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76728494 | |||||||
| chr5:76728629 | G | T | 1 | a0001c0001t0001g0086 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.89-3685G>T | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76728629 | |||||||
| chr5:76728685 | C | CT | 18 | a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0030 others(15): Show |
38 | HG00140.hp2 HG00642.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.89-3606dupT | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 76728685 | ||||||
| chr5:76728685 | C | CTT | 8 | a0001c0001t0001g0040 a0001c0001t0001g0042 a0001c0001t0001g0051 others(5): Show |
12 | HG01515.hp1 HG01978.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.89-3607_89-3606dup others(2): Show |
F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 76728685 | ||||||
| chr5:76728685 | C | CTTT | 35 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0001t0001g0034 others(32): Show |
115 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.89-3608_89-3606dup others(3): Show |
F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 76728685 | ||||||
| chr5:76728685 | C | CTTTT | 14 | a0001c0001t0001g0006 a0001c0001t0001g0041 a0001c0001t0001g0058 others(11): Show |
32 | HG00544.hp1 HG00597.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.89-3609_89-3606dup others(4): Show |
F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 76728685 | ||||||
| chr5:76728685 | CT | C | 6 | a0001c0001t0001g0009 a0001c0001t0001g0096 a0001c0001t0001g0102 others(3): Show |
10 | HG01257.hp2 HG01884.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.89-3606delT | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 76728685 | ||||||
| chr5:76728730 | G | A | 1 | a0001c0001t0007g0054 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.89-3584G>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76728730 | |||||||
| chr5:76728849 | C | A | 3 | a0001c0001t0001g0094 a0001c0001t0003g0017 a0001c0001t0018g0104 |
6 | HG00741.hp2 HG01123.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-3465C>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76728849 | |||||||
| chr5:76728862 | T | C | 1 | a0001c0001t0001g0083 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.89-3452T>C | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76728862 | |||||||
| chr5:76728882 | G | A | 7 | a0001c0001t0001g0036 a0001c0001t0001g0094 a0001c0001t0003g0011 others(4): Show |
14 | HG00741.hp2 HG01123.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.89-3432G>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76728882 | |||||||
| chr5:76728993 | C | T | 1 | a0001c0001t0001g0034 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.89-3321C>T | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76728993 | |||||||
| chr5:76728994 | A | G | 57 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0033 others(54): Show |
159 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.89-3320A>G | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76728994 | |||||||
| chr5:76729078 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.89-3236C>T | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76729078 | |||||||
| chr5:76729201 | C | A | 1 | a0001c0001t0001g0130 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.89-3113C>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76729201 | |||||||
| chr5:76729382 | G | A | 2 | a0001c0001t0001g0109 a0001c0001t0001g0112 |
2 | HG02683.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.89-2932G>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76729382 | |||||||
| chr5:76729419 | C | T | 5 | a0001c0001t0004g0010 a0001c0001t0004g0139 a0001c0001t0004g0146 others(2): Show |
14 | HG00642.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.89-2895C>T | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76729419 | |||||||
| chr5:76729491 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.89-2823A>G | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76729491 | |||||||
| chr5:76729785 | A | G | 1 | a0001c0001t0004g0081 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.89-2529A>G | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76729785 | |||||||
| chr5:76730023 | T | C | 2 | a0001c0001t0001g0056 a0001c0001t0001g0122 |
2 | HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.89-2291T>C | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76730023 | |||||||
| chr5:76730161 | A | T | 2 | a0001c0001t0003g0021 a0001c0001t0003g0032 |
5 | HG00735.hp1 HG02486.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-2153A>T | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76730161 | |||||||
| chr5:76730453 | T | G | 1 | a0001c0001t0004g0151 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.89-1861T>G | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76730453 | |||||||
| chr5:76730509 | T | C | 1 | a0001c0001t0024g0153 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.89-1805T>C | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76730509 | |||||||
| chr5:76730531 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0025g0023 |
3 | HG02129.hp2 HG03017.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.89-1783G>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76730531 | |||||||
| chr5:76730660 | T | G | 1 | a0001c0001t0001g0084 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.89-1654T>G | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76730660 | |||||||
| chr5:76730754 | A | G | 2 | a0001c0001t0007g0022 a0001c0001t0007g0054 |
4 | HG02970.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.89-1560A>G | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76730754 | |||||||
| chr5:76731187 | A | G | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | HG01099.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.89-1127A>G | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76731187 | |||||||
| chr5:76731207 | A | G | 7 | a0001c0001t0004g0010 a0001c0001t0004g0081 a0001c0001t0004g0139 others(4): Show |
16 | HG00642.hp1 HG02258.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.89-1107A>G | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76731207 | |||||||
| chr5:76731378 | G | A | 2 | a0001c0001t0003g0021 a0001c0001t0003g0032 |
5 | HG00735.hp1 HG02486.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-936G>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76731378 | |||||||
| chr5:76731400 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.89-914G>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76731400 | |||||||
| chr5:76731431 | G | A | 1 | a0001c0001t0001g0114 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.89-883G>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76731431 | |||||||
| chr5:76731460 | T | A | 2 | a0001c0001t0001g0109 a0001c0001t0001g0112 |
2 | HG02683.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.89-854T>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76731460 | |||||||
| chr5:76731508 | C | CT | 11 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0064 others(8): Show |
21 | HG00735.hp1 HG01884.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.89-791dupT | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 76731508 | ||||||
| chr5:76731508 | CT | C | 10 | a0001c0001t0001g0013 a0001c0001t0001g0058 a0001c0001t0001g0085 others(7): Show |
14 | HG00621.hp1 HG00738.hp2 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.89-791delT | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | 76731508 | ||||||
| chr5:76731553 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.89-761G>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76731553 | |||||||
| chr5:76731716 | G | A | 2 | a0001c0001t0001g0052 a0001c0001t0021g0052 |
2 | NA18522.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.89-598G>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76731716 | |||||||
| chr5:76731797 | G | A | 1 | a0001c0001t0002g0067 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.89-517G>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76731797 | |||||||
| chr5:76731805 | G | A | 3 | a0001c0001t0002g0024 a0001c0001t0002g0044 a0001c0001t0002g0067 |
6 | NA18943.hp1 NA18968.hp2 NA19056.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-509G>A | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76731805 | |||||||
| chr5:76731831 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.89-483A>G | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76731831 | |||||||
| chr5:76731837 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.89-477T>C | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76731837 | |||||||
| chr5:76731860 | C | T | 2 | a0001c0001t0007g0022 a0001c0001t0007g0054 |
4 | HG02970.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.89-454C>T | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76731860 | |||||||
| chr5:76731998 | A | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(127): Show |
323 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.89-316A>C | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76731998 | |||||||
| chr5:76732299 | A | T | 26 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0033 others(23): Show |
84 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.89-15A>T | F2R | ENSG00000181104.7 | transcript | ENST00000319211.5 | protein_coding | 1/1 | chr5 | 76732299 |