Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2356 |
| ensemblid | ENSG00000136877.15 |
| hgncid | 3824 |
| symbol | FPGS |
| name | folylpolyglutamate synthase |
| refseq_nuc | NM_004957.6 |
| refseq_prot | NP_004948.4 |
| ensembl_nuc | ENST00000373247.7 |
| ensembl_prot | ENSP00000362344.2 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 127802882 |
| end | 127814081 |
| strand | + |
| ver | v1.2 |
| region | chr9:127802882-127814081 |
| region5000 | chr9:127797882-127819081 |
| regionname0 | FPGS_chr9_127802882_127814081 |
| regionname5000 | FPGS_chr9_127797882_127819081 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 587 | 340 | 81 | 50 | 174 | 5 | 29 | 128 | FPGS_chr9_127797882_127819081 | FPGS | MSRAR others(582): Show |
chr9 | 127797882 | 127819081 |
| a0002 | 1/0 | 587 | 58 | 13 | 16 | 6 | 7 | 15 | 6 | FPGS_chr9_127797882_127819081 | FPGS | MSRAR others(582): Show |
chr9 | 127797882 | 127819081 |
| a0003 | 0/0 | 587 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | MSRAR others(582): Show |
chr9 | 127797882 | 127819081 |
| a0004 | 0/0 | 587 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | MSRAR others(582): Show |
chr9 | 127797882 | 127819081 |
| a0005 | 0/0 | 587 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | MSRAR others(582): Show |
chr9 | 127797882 | 127819081 |
| a0006 | 0/0 | 587 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | MSRAR others(582): Show |
chr9 | 127797882 | 127819081 |
| a0007 | 0/0 | 568 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | MSRAR others(563): Show |
chr9 | 127797882 | 127819081 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1761 | 306 | 57 | 50 | 170 | 5 | 23 | FPGS_chr9_127797882_127819081 | FPGS | ATGTC others(1756): Show |
chr9 | 127797882 | 127819081 | ||
| a0001c0003 | 0/0 | 1761 | 26 | 22 | 0 | 1 | 0 | 3 | FPGS_chr9_127797882_127819081 | FPGS | ATGTC others(1756): Show |
chr9 | 127797882 | 127819081 | ||
| a0001c0005 | 0/0 | 1761 | 2 | 0 | 0 | 0 | 0 | 2 | FPGS_chr9_127797882_127819081 | FPGS | ATGTC others(1756): Show |
chr9 | 127797882 | 127819081 | ||
| a0001c0008 | 0/0 | 1761 | 2 | 0 | 0 | 2 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | ATGTC others(1756): Show |
chr9 | 127797882 | 127819081 | ||
| a0001c0011 | 0/0 | 1761 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | ATGTC others(1756): Show |
chr9 | 127797882 | 127819081 | ||
| a0001c0012 | 0/0 | 1761 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | ATGTC others(1756): Show |
chr9 | 127797882 | 127819081 | ||
| a0001c0013 | 0/0 | 1761 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | ATGTC others(1756): Show |
chr9 | 127797882 | 127819081 | ||
| a0001c0014 | 0/0 | 1761 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | ATGTC others(1756): Show |
chr9 | 127797882 | 127819081 | ||
| a0002c0002 | 1/0 | 1761 | 58 | 13 | 16 | 6 | 7 | 15 | FPGS_chr9_127797882_127819081 | FPGS | ATGTC others(1756): Show |
chr9 | 127797882 | 127819081 | ||
| a0003c0007 | 0/0 | 1761 | 2 | 0 | 0 | 2 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | ATGTC others(1756): Show |
chr9 | 127797882 | 127819081 | ||
| a0004c0004 | 0/0 | 1761 | 2 | 0 | 2 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | ATGTC others(1756): Show |
chr9 | 127797882 | 127819081 | ||
| a0005c0006 | 0/0 | 1761 | 2 | 0 | 2 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | ATGTC others(1756): Show |
chr9 | 127797882 | 127819081 | ||
| a0006c0009 | 0/0 | 1761 | 1 | 0 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | ATGTC others(1756): Show |
chr9 | 127797882 | 127819081 | ||
| a0007c0010 | 0/0 | 1792 | 1 | 0 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | ATGTC others(1787): Show |
chr9 | 127797882 | 127819081 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2284 | 183 | 23 | 37 | 109 | 3 | 11 | FPGS_chr9_127797882_127819081 | FPGS | GTCTC others(2279): Show |
chr9 | 127797882 | 127819081 |
| a0001c0001t0002 | 0/1 | 2284 | 120 | 33 | 12 | 61 | 2 | 11 | FPGS_chr9_127797882_127819081 | FPGS | GTCTC others(2279): Show |
chr9 | 127797882 | 127819081 |
| a0001c0001t0003 | 0/0 | 2282 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | GTCTC others(2277): Show |
chr9 | 127797882 | 127819081 |
| a0001c0001t0004 | 0/0 | 2284 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | GTCTC others(2279): Show |
chr9 | 127797882 | 127819081 |
| a0001c0001t0006 | 0/0 | 2284 | 1 | 0 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | GTCTC others(2279): Show |
chr9 | 127797882 | 127819081 |
| a0001c0003t0001 | 0/0 | 2284 | 2 | 2 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | GTCTC others(2279): Show |
chr9 | 127797882 | 127819081 |
| a0001c0003t0003 | 0/0 | 2282 | 24 | 20 | 0 | 1 | 0 | 3 | FPGS_chr9_127797882_127819081 | FPGS | GTCTC others(2277): Show |
chr9 | 127797882 | 127819081 |
| a0001c0005t0002 | 0/0 | 2284 | 2 | 0 | 0 | 0 | 0 | 2 | FPGS_chr9_127797882_127819081 | FPGS | GTCTC others(2279): Show |
chr9 | 127797882 | 127819081 |
| a0001c0008t0001 | 0/0 | 2284 | 2 | 0 | 0 | 2 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | GTCTC others(2279): Show |
chr9 | 127797882 | 127819081 |
| a0001c0011t0002 | 0/0 | 2284 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | GTCTC others(2279): Show |
chr9 | 127797882 | 127819081 |
| a0001c0012t0002 | 0/0 | 2284 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | GTCTC others(2279): Show |
chr9 | 127797882 | 127819081 |
| a0001c0013t0001 | 0/0 | 2284 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | GTCTC others(2279): Show |
chr9 | 127797882 | 127819081 |
| a0001c0014t0002 | 0/0 | 2284 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | GTCTC others(2279): Show |
chr9 | 127797882 | 127819081 |
| a0002c0002t0001 | 0/0 | 2284 | 1 | 0 | 0 | 0 | 1 | 0 | FPGS_chr9_127797882_127819081 | FPGS | GTCTC others(2279): Show |
chr9 | 127797882 | 127819081 |
| a0002c0002t0002 | 1/0 | 2284 | 55 | 13 | 16 | 6 | 6 | 13 | FPGS_chr9_127797882_127819081 | FPGS | GTCTC others(2279): Show |
chr9 | 127797882 | 127819081 |
| a0002c0002t0005 | 0/0 | 2284 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | GTCTC others(2279): Show |
chr9 | 127797882 | 127819081 |
| a0002c0002t0007 | 0/0 | 2284 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | GTCTC others(2279): Show |
chr9 | 127797882 | 127819081 |
| a0003c0007t0001 | 0/0 | 2284 | 2 | 0 | 0 | 2 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | GTCTC others(2279): Show |
chr9 | 127797882 | 127819081 |
| a0004c0004t0002 | 0/0 | 2284 | 2 | 0 | 2 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | GTCTC others(2279): Show |
chr9 | 127797882 | 127819081 |
| a0005c0006t0001 | 0/0 | 2284 | 2 | 0 | 2 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | GTCTC others(2279): Show |
chr9 | 127797882 | 127819081 |
| a0006c0009t0002 | 0/0 | 2284 | 1 | 0 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | GTCTC others(2279): Show |
chr9 | 127797882 | 127819081 |
| a0007c0010t0001 | 0/0 | 2315 | 1 | 0 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | GTCTC others(2310): Show |
chr9 | 127797882 | 127819081 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 91 | 3 | 27 | 51 | 3 | 7 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0001g0004 | 0/0 | 13 | 0 | 0 | 13 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0001g0006 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0001g0010 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0001g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0001g0012 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0002g0002 | 0/1 | 74 | 14 | 10 | 40 | 1 | 8 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0002g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0002g0007 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0002g0009 | 0/0 | 5 | 1 | 0 | 4 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0002g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0002g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0004g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0001t0006g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0003t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0003t0003g0005 | 0/0 | 10 | 7 | 0 | 1 | 0 | 2 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0003t0003g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0003t0003g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0003t0003g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0003t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0003t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0003t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0003t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0003t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0003t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0003t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0005t0002g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0008t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0011t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0012t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0013t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0001c0014t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0002c0002t0002g0003 | 0/0 | 33 | 8 | 10 | 5 | 2 | 8 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0002c0002t0002g0018 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0002c0002t0002g0028 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0002c0002t0002g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0002c0002t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0002c0002t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0002c0002t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0002c0002t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0002c0002t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0002c0002t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0002c0002t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0002c0002t0005g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0002c0002t0007g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0003c0007t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0004c0004t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0005c0006t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0005c0006t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0006c0009t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| a0007c0010t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG00099 | hp2 | a0002 | c0002 | t0002 | g0028 | EUR | GBR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG00140 | hp1 | a0002 | c0002 | t0002 | g0089 | EUR | GBR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG00140 | hp2 | a0002 | c0002 | t0002 | g0094 | EUR | GBR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG00323 | hp2 | a0002 | c0002 | t0002 | g0003 | EUR | FIN | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG00408 | hp2 | a0003 | c0007 | t0001 | g0001 | EAS | CHS | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | CHS | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG00544 | hp1 | a0001 | c0008 | t0001 | g0025 | EAS | CHS | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | CHS | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG00639 | hp1 | a0002 | c0002 | t0002 | g0029 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG00642 | hp1 | a0006 | c0009 | t0002 | g0088 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG00738 | hp1 | a0007 | c0010 | t0001 | g0067 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG00738 | hp2 | a0002 | c0002 | t0002 | g0003 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01070 | hp1 | a0004 | c0004 | t0002 | g0003 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01071 | hp1 | a0004 | c0004 | t0002 | g0003 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01081 | hp2 | a0002 | c0002 | t0002 | g0095 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01106 | hp1 | a0002 | c0002 | t0002 | g0003 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0119 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01167 | hp2 | a0002 | c0002 | t0002 | g0090 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01169 | hp2 | a0002 | c0002 | t0002 | g0003 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01192 | hp1 | a0001 | c0001 | t0006 | g0001 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01243 | hp2 | a0002 | c0002 | t0002 | g0003 | AMR | PUR | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01255 | hp1 | a0005 | c0006 | t0001 | g0001 | AMR | CLM | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01256 | hp2 | a0002 | c0002 | t0002 | g0003 | AMR | CLM | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01346 | hp2 | a0002 | c0002 | t0002 | g0029 | AMR | CLM | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01433 | hp1 | a0002 | c0002 | t0002 | g0003 | AMR | CLM | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01433 | hp2 | a0002 | c0002 | t0002 | g0003 | AMR | CLM | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0033 | EUR | IBS | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01884 | hp1 | a0001 | c0013 | t0001 | g0050 | AFR | ACB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01884 | hp2 | a0002 | c0002 | t0002 | g0003 | AFR | ACB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01928 | hp1 | a0005 | c0006 | t0001 | g0017 | AMR | PEL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01952 | hp1 | a0002 | c0002 | t0002 | g0003 | AMR | PEL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01975 | hp1 | a0002 | c0002 | t0002 | g0003 | AMR | PEL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01993 | hp2 | a0002 | c0002 | t0002 | g0003 | AMR | PEL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | KHV | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02056 | hp2 | a0003 | c0007 | t0001 | g0001 | EAS | KHV | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02080 | hp2 | a0001 | c0003 | t0003 | g0005 | EAS | KHV | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02145 | hp1 | a0002 | c0002 | t0002 | g0003 | AFR | ACB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02148 | hp1 | a0002 | c0002 | t0002 | g0102 | AMR | PEL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CDX | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02257 | hp2 | a0002 | c0002 | t0002 | g0003 | AFR | ACB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02258 | hp1 | a0001 | c0003 | t0003 | g0044 | AFR | ACB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02258 | hp2 | a0001 | c0003 | t0003 | g0014 | AFR | ACB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02280 | hp1 | a0001 | c0003 | t0003 | g0005 | AFR | ACB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02280 | hp2 | a0001 | c0003 | t0003 | g0013 | AFR | ACB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02300 | hp1 | a0002 | c0002 | t0002 | g0099 | AMR | PEL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02451 | hp1 | a0002 | c0002 | t0002 | g0093 | AFR | ACB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02602 | hp1 | a0002 | c0002 | t0002 | g0003 | SAS | PJL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02615 | hp2 | a0001 | c0003 | t0003 | g0005 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02622 | hp1 | a0001 | c0003 | t0003 | g0005 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02622 | hp2 | a0002 | c0002 | t0002 | g0092 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02630 | hp1 | a0001 | c0003 | t0003 | g0045 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02647 | hp2 | a0002 | c0002 | t0002 | g0003 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02683 | hp1 | a0001 | c0003 | t0003 | g0041 | SAS | PJL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02683 | hp2 | a0002 | c0002 | t0002 | g0003 | SAS | PJL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02698 | hp1 | a0002 | c0002 | t0007 | g0003 | SAS | PJL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02723 | hp1 | a0001 | c0003 | t0003 | g0043 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0111 | SAS | PJL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02735 | hp2 | a0002 | c0002 | t0002 | g0096 | SAS | PJL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02809 | hp1 | a0001 | c0012 | t0002 | g0040 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0118 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0085 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02886 | hp1 | a0001 | c0003 | t0003 | g0013 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02895 | hp1 | a0002 | c0002 | t0002 | g0003 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0106 | AFR | ESN | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02965 | hp1 | a0001 | c0003 | t0001 | g0032 | AFR | ESN | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02965 | hp2 | a0001 | c0003 | t0003 | g0005 | AFR | ESN | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | ESN | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02976 | hp1 | a0002 | c0002 | t0002 | g0003 | AFR | ESN | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG03017 | hp1 | a0002 | c0002 | t0002 | g0103 | SAS | PJL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG03041 | hp1 | a0001 | c0003 | t0001 | g0032 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG03041 | hp2 | a0002 | c0002 | t0002 | g0097 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | MSL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | MSL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG03130 | hp2 | a0001 | c0003 | t0003 | g0014 | AFR | ESN | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG03139 | hp1 | a0001 | c0003 | t0003 | g0005 | AFR | ESN | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0114 | AFR | ESN | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ESN | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG03195 | hp2 | a0002 | c0002 | t0002 | g0003 | AFR | ESN | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG03209 | hp1 | a0001 | c0003 | t0003 | g0047 | AFR | MSL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | MSL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG03225 | hp2 | a0002 | c0002 | t0002 | g0018 | AFR | MSL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG03239 | hp1 | a0002 | c0002 | t0002 | g0003 | SAS | PJL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG03239 | hp2 | a0001 | c0003 | t0003 | g0005 | SAS | PJL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG03453 | hp1 | a0001 | c0003 | t0003 | g0046 | AFR | MSL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | MSL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | MSL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | MSL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0030 | SAS | PJL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ESN | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG03516 | hp2 | a0001 | c0003 | t0003 | g0042 | AFR | ESN | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG03540 | hp2 | a0001 | c0003 | t0003 | g0013 | AFR | GWD | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG03579 | hp1 | a0001 | c0003 | t0003 | g0005 | AFR | MSL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0060 | AFR | MSL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG03654 | hp1 | a0002 | c0002 | t0002 | g0003 | SAS | PJL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0001 | SAS | PJL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG03669 | hp2 | a0002 | c0002 | t0002 | g0028 | SAS | PJL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | STU | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | STU | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG03704 | hp1 | a0001 | c0003 | t0003 | g0005 | SAS | PJL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG03831 | hp1 | a0001 | c0005 | t0002 | g0002 | SAS | BEB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG03831 | hp2 | a0002 | c0002 | t0005 | g0003 | SAS | BEB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG03834 | hp2 | a0002 | c0002 | t0002 | g0100 | SAS | BEB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG03927 | hp1 | a0002 | c0002 | t0002 | g0003 | SAS | BEB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG03927 | hp2 | a0002 | c0002 | t0002 | g0003 | SAS | BEB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | STU | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | STU | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG04184 | hp1 | a0002 | c0002 | t0002 | g0003 | SAS | BEB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG04184 | hp2 | a0001 | c0011 | t0002 | g0116 | SAS | BEB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG04199 | hp1 | a0002 | c0002 | t0002 | g0104 | SAS | STU | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | STU | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0034 | SAS | STU | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG04228 | hp2 | a0001 | c0005 | t0002 | g0002 | SAS | STU | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | YRI | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | YRI | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | CHB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | CHB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | YRI | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18941 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18946 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18969 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18971 | hp1 | a0001 | c0008 | t0001 | g0025 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18983 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | LWK | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | LWK | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19043 | hp1 | a0001 | c0003 | t0003 | g0048 | AFR | LWK | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19043 | hp2 | a0001 | c0003 | t0003 | g0014 | AFR | LWK | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19057 | hp2 | a0001 | c0014 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19063 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19068 | hp1 | a0002 | c0002 | t0002 | g0101 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | YRI | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA19240 | hp2 | a0001 | c0003 | t0003 | g0005 | AFR | YRI | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0075 | AFR | ASW | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA20752 | hp2 | a0002 | c0002 | t0002 | g0091 | EUR | TSI | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA20805 | hp1 | a0002 | c0002 | t0002 | g0003 | EUR | TSI | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0098 | EUR | TSI | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA20905 | hp2 | a0002 | c0002 | t0002 | g0003 | SAS | GIH | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | ACB | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0076 | AFR | MSL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG03471 | hp2 | a0002 | c0002 | t0002 | g0018 | AFR | MSL | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG06807 | hp1 | a0002 | c0002 | t0002 | g0003 | AFR | USA | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | USA | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | USA | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | LWK | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | LWK | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0002 | REF | REF | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0002 | g0018 | REF | REF | FPGS_chr9_127797882_127819081 | FPGS | chr9 | 127797882 | 127819081 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:127802988 | A | G | 6 | a0001 a0003 a0004 others(3): Show |
347 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(344): Show |
missense_variant | MODERATE | c.64A>G | p.Ile22Val | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 1/15 | 107/2284 | 64/1764 | 22/587 | chr9 | 127802988 | |||
| chr9:127809767 | G | A | 1 | a0006 | 1 | HG00642.hp1 | missense_variant | MODERATE | c.1144G>A | p.Ala382Thr | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 12/15 | 1187/2284 | 1144/1764 | 382/587 | chr9 | 127809767 | |||
| chr9:127813236 | C | T | 1 | a0006 | 1 | HG00642.hp1 | missense_variant | MODERATE | c.1396C>T | p.Arg466Cys | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 15/15 | 1439/2284 | 1396/1764 | 466/587 | chr9 | 127813236 | |||
| chr9:127813306 | C | T | 1 | a0003 | 2 | HG00408.hp2 HG02056.hp2 |
missense_variant | MODERATE | c.1466C>T | p.Ala489Val | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 15/15 | 1509/2284 | 1466/1764 | 489/587 | chr9 | 127813306 | |||
| chr9:127813336 | C | T | 1 | a0005 | 2 | HG01255.hp1 HG01928.hp1 |
missense_variant | MODERATE | c.1496C>T | p.Ser499Phe | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 15/15 | 1539/2284 | 1496/1764 | 499/587 | chr9 | 127813336 | |||
| chr9:127813339 | T | C | 1 | a0004 | 2 | HG01070.hp1 HG01071.hp1 |
missense_variant | MODERATE | c.1499T>C | p.Leu500Pro | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 15/15 | 1542/2284 | 1499/1764 | 500/587 | chr9 | 127813339 | |||
| chr9:127813461 | C | CCAAAGGG others(24): Show |
1 | a0007 | 1 | HG00738.hp1 | frameshift_variant | HIGH | c.1624_1654dupAAGGGC others(25): Show |
p.Ser552fs | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 15/15 | 1698/2284 | 1655/1764 | 552/587 | INFO_REALIGN_3_PRIME | chr9 | 127813461 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:127803047 | G | A | 1 | a0001c0003 | 26 | HG02080.hp2 HG02258.hp1 HG02258.hp2 others(23): Show |
synonymous_variant | LOW | c.123G>A | p.Pro41Pro | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 1/15 | 166/2284 | 123/1764 | 41/587 | chr9 | 127803047 | |||
| chr9:127804290 | C | T | 1 | a0001c0014 | 1 | NA19057.hp2 | synonymous_variant | LOW | c.144C>T | p.Ala48Ala | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 2/15 | 187/2284 | 144/1764 | 48/587 | chr9 | 127804290 | |||
| chr9:127804389 | G | A | 1 | a0006c0009 | 1 | HG00642.hp1 | synonymous_variant | LOW | c.243G>A | p.Leu81Leu | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 2/15 | 286/2284 | 243/1764 | 81/587 | chr9 | 127804389 | |||
| chr9:127804516 | G | T | 1 | a0001c0013 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.285G>T | p.Arg95Arg | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 3/15 | 328/2284 | 285/1764 | 95/587 | chr9 | 127804516 | |||
| chr9:127804531 | C | T | 1 | a0001c0012 | 1 | HG02809.hp1 | synonymous_variant | LOW | c.300C>T | p.His100His | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 3/15 | 343/2284 | 300/1764 | 100/587 | chr9 | 127804531 | |||
| chr9:127808593 | C | T | 1 | a0001c0008 | 2 | HG00544.hp1 NA18971.hp1 |
synonymous_variant | LOW | c.858C>T | p.Leu286Leu | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 10/15 | 901/2284 | 858/1764 | 286/587 | chr9 | 127808593 | |||
| chr9:127808888 | C | T | 1 | a0001c0011 | 1 | HG04184.hp2 | splice_region_variant&synonymous_variant | LOW | c.1059C>T | p.Leu353Leu | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 11/15 | 1102/2284 | 1059/1764 | 353/587 | chr9 | 127808888 | |||
| chr9:127813338 | C | T | 1 | a0001c0005 | 2 | HG03831.hp1 HG04228.hp2 |
synonymous_variant | LOW | c.1498C>T | p.Leu500Leu | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 15/15 | 1541/2284 | 1498/1764 | 500/587 | chr9 | 127813338 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:127802888 | C | T | 1 | a0002c0002t0007 | 1 | HG02698.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-37C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 1/15 | chr9 | 127802888 | |||||||
| chr9:127813643 | G | T | 1 | a0001c0001t0006 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*39G>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 15/15 | 39 | chr9 | 127813643 | ||||||
| chr9:127813796 | T | C | 12 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(9): Show |
221 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(218): Show |
3_prime_UTR_variant | MODIFIER | c.*192T>C | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 15/15 | 192 | chr9 | 127813796 | ||||||
| chr9:127813840 | A | C | 1 | a0002c0002t0005 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*236A>C | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 15/15 | 236 | chr9 | 127813840 | ||||||
| chr9:127813941 | C | T | 1 | a0001c0001t0004 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*337C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 15/15 | 337 | chr9 | 127813941 | ||||||
| chr9:127814045 | CTT | C | 2 | a0001c0001t0003 a0001c0003t0003 |
25 | HG02080.hp2 HG02258.hp1 HG02258.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*443_*444delTT | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 15/15 | 443 | INFO_REALIGN_3_PRIME | chr9 | 127814045 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:127803090 | G | A | 2 | a0001c0001t0002g0033 a0001c0001t0002g0034 |
2 | HG01517.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.138+28G>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 1/14 | chr9 | 127803090 | |||||||
| chr9:127803168 | C | T | 1 | a0001c0001t0001g0012 | 4 | HG01099.hp2 HG03130.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.138+106C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 1/14 | chr9 | 127803168 | |||||||
| chr9:127803273 | A | G | 2 | a0001c0001t0002g0120 a0001c0001t0002g0121 |
2 | NA18993.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.138+211A>G | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 1/14 | chr9 | 127803273 | |||||||
| chr9:127803286 | C | G | 1 | a0001c0003t0001g0032 | 2 | HG02965.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.138+224C>G | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 1/14 | chr9 | 127803286 | |||||||
| chr9:127803360 | C | T | 1 | a0001c0001t0002g0119 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.138+298C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 1/14 | chr9 | 127803360 | |||||||
| chr9:127803396 | G | A | 1 | a0001c0001t0001g0035 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.138+334G>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 1/14 | chr9 | 127803396 | |||||||
| chr9:127803598 | C | T | 25 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0030 others(22): Show |
104 | HG00323.hp1 HG00423.hp1 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.138+536C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 1/14 | chr9 | 127803598 | |||||||
| chr9:127803676 | C | T | 1 | a0001c0001t0001g0035 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.139-609C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 1/14 | chr9 | 127803676 | |||||||
| chr9:127803746 | T | G | 1 | a0001c0001t0001g0036 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.139-539T>G | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 1/14 | chr9 | 127803746 | |||||||
| chr9:127803906 | G | A | 108 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(105): Show |
344 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(341): Show |
intron_variant | MODIFIER | c.139-379G>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 1/14 | chr9 | 127803906 | |||||||
| chr9:127803968 | G | A | 5 | a0001c0001t0002g0007 a0001c0001t0002g0037 a0001c0001t0002g0038 others(2): Show |
9 | HG02486.hp2 HG02572.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.139-317G>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 1/14 | chr9 | 127803968 | |||||||
| chr9:127803988 | G | A | 12 | a0001c0003t0001g0032 a0001c0003t0003g0005 a0001c0003t0003g0013 others(9): Show |
26 | HG02080.hp2 HG02258.hp1 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.139-297G>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 1/14 | chr9 | 127803988 | |||||||
| chr9:127804030 | G | A | 1 | a0001c0001t0002g0105 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.139-255G>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 1/14 | chr9 | 127804030 | |||||||
| chr9:127804179 | G | A | 1 | a0002c0002t0002g0089 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.139-106G>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 1/14 | chr9 | 127804179 | |||||||
| chr9:127804260 | A | G | 13 | a0001c0003t0001g0032 a0001c0003t0003g0005 a0001c0003t0003g0013 others(10): Show |
27 | HG00642.hp1 HG02080.hp2 HG02258.hp1 others(24): Show |
intron_variant | MODIFIER | c.139-25A>G | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 1/14 | chr9 | 127804260 | |||||||
| chr9:127804863 | A | G | 1 | a0001c0001t0002g0118 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.386+163A>G | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127804863 | |||||||
| chr9:127804890 | A | AT | 17 | a0001c0001t0001g0086 a0001c0001t0002g0026 a0001c0001t0002g0027 others(14): Show |
33 | HG02080.hp2 HG02258.hp1 HG02258.hp2 others(30): Show |
intron_variant | MODIFIER | c.386+206dupT | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr9 | 127804890 | ||||||
| chr9:127804890 | A | ATT | 3 | a0001c0001t0001g0011 a0001c0001t0001g0087 a0001c0003t0003g0048 |
6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.386+205_386+206dup others(2): Show |
FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr9 | 127804890 | ||||||
| chr9:127804890 | AT | A | 7 | a0001c0001t0001g0019 a0001c0001t0001g0051 a0001c0001t0002g0009 others(4): Show |
12 | HG01167.hp2 HG01884.hp1 HG02897.hp2 others(9): Show |
intron_variant | MODIFIER | c.386+206delT | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr9 | 127804890 | ||||||
| chr9:127804925 | A | G | 1 | a0001c0003t0003g0047 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.386+225A>G | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127804925 | |||||||
| chr9:127805108 | C | T | 12 | a0001c0003t0001g0032 a0001c0003t0003g0005 a0001c0003t0003g0013 others(9): Show |
26 | HG02080.hp2 HG02258.hp1 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.386+408C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127805108 | |||||||
| chr9:127805146 | C | T | 1 | a0002c0002t0002g0103 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.386+446C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127805146 | |||||||
| chr9:127805232 | T | A | 1 | a0001c0001t0001g0052 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.386+532T>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127805232 | |||||||
| chr9:127805328 | G | A | 1 | a0006c0009t0002g0088 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.386+628G>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127805328 | |||||||
| chr9:127805377 | A | T | 129 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(126): Show |
400 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(397): Show |
intron_variant | MODIFIER | c.386+677A>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127805377 | |||||||
| chr9:127805393 | G | A | 1 | a0001c0001t0002g0106 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.386+693G>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127805393 | |||||||
| chr9:127805409 | T | TA | 13 | a0001c0001t0001g0053 a0001c0003t0001g0032 a0001c0003t0003g0005 others(10): Show |
27 | HG01993.hp1 HG02080.hp2 HG02258.hp1 others(24): Show |
intron_variant | MODIFIER | c.386+721dupA | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr9 | 127805409 | ||||||
| chr9:127805476 | A | G | 1 | a0001c0001t0001g0084 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.386+776A>G | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127805476 | |||||||
| chr9:127805579 | C | T | 5 | a0001c0001t0002g0007 a0001c0001t0002g0037 a0001c0001t0002g0038 others(2): Show |
9 | HG02486.hp2 HG02572.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.386+879C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127805579 | |||||||
| chr9:127805658 | A | G | 2 | a0001c0001t0002g0033 a0001c0001t0002g0034 |
2 | HG01517.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.386+958A>G | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127805658 | |||||||
| chr9:127805697 | A | G | 2 | a0001c0001t0002g0120 a0001c0001t0002g0121 |
2 | NA18993.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.386+997A>G | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127805697 | |||||||
| chr9:127805823 | A | C | 12 | a0001c0003t0001g0032 a0001c0003t0003g0005 a0001c0003t0003g0013 others(9): Show |
26 | HG02080.hp2 HG02258.hp1 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.386+1123A>C | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127805823 | |||||||
| chr9:127805880 | C | T | 5 | a0001c0001t0001g0006 a0001c0001t0001g0081 a0001c0001t0001g0082 others(2): Show |
15 | HG00438.hp1 HG00544.hp1 HG02135.hp1 others(12): Show |
intron_variant | MODIFIER | c.387-1093C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127805880 | |||||||
| chr9:127805881 | C | T | 2 | a0001c0001t0001g0010 a0001c0001t0001g0080 |
5 | HG01167.hp1 HG02723.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.387-1092C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127805881 | |||||||
| chr9:127805912 | T | C | 6 | a0001c0001t0001g0004 a0001c0001t0001g0054 a0001c0001t0001g0056 others(3): Show |
18 | HG00408.hp1 HG00558.hp1 HG02132.hp2 others(15): Show |
intron_variant | MODIFIER | c.387-1061T>C | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127805912 | |||||||
| chr9:127805929 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.387-1044G>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127805929 | |||||||
| chr9:127806050 | C | T | 1 | a0001c0001t0001g0079 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.387-923C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127806050 | |||||||
| chr9:127806134 | C | T | 1 | a0001c0001t0002g0115 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.387-839C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127806134 | |||||||
| chr9:127806135 | G | A | 3 | a0001c0003t0003g0013 a0001c0003t0003g0042 a0001c0003t0003g0047 |
5 | HG02280.hp2 HG02886.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.387-838G>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127806135 | |||||||
| chr9:127806303 | C | G | 1 | a0001c0001t0001g0078 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.387-670C>G | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127806303 | |||||||
| chr9:127806366 | C | T | 1 | a0001c0003t0003g0042 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.387-607C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127806366 | |||||||
| chr9:127806379 | G | C | 1 | a0002c0002t0002g0094 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.387-594G>C | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127806379 | |||||||
| chr9:127806397 | T | G | 1 | a0001c0001t0001g0059 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.387-576T>G | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127806397 | |||||||
| chr9:127806403 | G | A | 3 | a0001c0003t0003g0013 a0001c0003t0003g0042 a0001c0003t0003g0047 |
5 | HG02280.hp2 HG02886.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.387-570G>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127806403 | |||||||
| chr9:127806407 | G | A | 10 | a0001c0003t0001g0032 a0001c0003t0003g0005 a0001c0003t0003g0013 others(7): Show |
22 | HG02080.hp2 HG02258.hp1 HG02280.hp1 others(19): Show |
intron_variant | MODIFIER | c.387-566G>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127806407 | |||||||
| chr9:127806420 | C | T | 1 | a0001c0001t0001g0012 | 4 | HG01099.hp2 HG03130.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.387-553C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127806420 | |||||||
| chr9:127806454 | C | T | 1 | a0006c0009t0002g0088 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.387-519C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127806454 | |||||||
| chr9:127806484 | C | T | 1 | a0001c0001t0001g0077 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.387-489C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127806484 | |||||||
| chr9:127806583 | G | A | 1 | a0001c0001t0002g0120 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.387-390G>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127806583 | |||||||
| chr9:127806719 | G | A | 1 | a0001c0001t0002g0060 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.387-254G>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127806719 | |||||||
| chr9:127806838 | G | T | 1 | a0001c0003t0003g0046 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.387-135G>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127806838 | |||||||
| chr9:127806882 | G | T | 1 | a0001c0001t0001g0058 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.387-91G>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127806882 | |||||||
| chr9:127806926 | C | T | 1 | a0002c0002t0002g0102 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.387-47C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 4/14 | chr9 | 127806926 | |||||||
| chr9:127807288 | T | C | 1 | a0002c0002t0002g0095 | 1 | HG01081.hp2 | splice_donor_variant&intron_variant | HIGH | c.579+2T>C | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 6/14 | chr9 | 127807288 | |||||||
| chr9:127807523 | C | T | 1 | a0001c0001t0002g0034 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.641+41C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 7/14 | chr9 | 127807523 | |||||||
| chr9:127807533 | C | T | 1 | a0001c0001t0001g0012 | 4 | HG01099.hp2 HG03130.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.641+51C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 7/14 | chr9 | 127807533 | |||||||
| chr9:127807554 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.642-32G>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 7/14 | chr9 | 127807554 | |||||||
| chr9:127807896 | C | T | 1 | a0001c0001t0001g0008 | 5 | HG02027.hp2 NA18963.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.744+208C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 8/14 | chr9 | 127807896 | |||||||
| chr9:127807935 | G | C | 1 | a0002c0002t0002g0028 | 2 | HG00099.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.744+247G>C | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 8/14 | chr9 | 127807935 | |||||||
| chr9:127807948 | A | C | 1 | a0001c0001t0002g0114 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.744+260A>C | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 8/14 | chr9 | 127807948 | |||||||
| chr9:127808024 | C | T | 13 | a0001c0001t0003g0076 a0001c0003t0001g0032 a0001c0003t0003g0005 others(10): Show |
27 | HG02080.hp2 HG02258.hp1 HG02258.hp2 others(24): Show |
intron_variant | MODIFIER | c.745-210C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 8/14 | chr9 | 127808024 | |||||||
| chr9:127808105 | C | A | 13 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0020 others(10): Show |
25 | HG01099.hp2 HG01884.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.745-129C>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 8/14 | chr9 | 127808105 | |||||||
| chr9:127808330 | G | A | 5 | a0001c0001t0001g0006 a0001c0001t0001g0081 a0001c0001t0001g0082 others(2): Show |
15 | HG00438.hp1 HG00544.hp1 HG02135.hp1 others(12): Show |
intron_variant | MODIFIER | c.822+19G>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 9/14 | chr9 | 127808330 | |||||||
| chr9:127808358 | T | C | 1 | a0001c0001t0001g0062 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.822+47T>C | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 9/14 | chr9 | 127808358 | |||||||
| chr9:127808359 | C | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0062 |
3 | HG01168.hp2 HG01169.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.822+48C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 9/14 | chr9 | 127808359 | |||||||
| chr9:127808432 | G | T | 1 | a0001c0001t0001g0052 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.822+121G>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 9/14 | chr9 | 127808432 | |||||||
| chr9:127808434 | C | T | 1 | a0001c0001t0001g0052 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.822+123C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 9/14 | chr9 | 127808434 | |||||||
| chr9:127808771 | G | A | 5 | a0001c0001t0002g0007 a0001c0001t0002g0037 a0001c0001t0002g0038 others(2): Show |
9 | HG02486.hp2 HG02572.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.971-29G>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 10/14 | chr9 | 127808771 | |||||||
| chr9:127808946 | A | AT | 26 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0017 others(23): Show |
52 | HG00438.hp1 HG00544.hp1 HG01928.hp1 others(49): Show |
intron_variant | MODIFIER | c.1060+77dupT | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr9 | 127808946 | ||||||
| chr9:127808946 | AT | A | 7 | a0001c0001t0001g0015 a0001c0001t0001g0054 a0001c0001t0002g0030 others(4): Show |
10 | HG00642.hp1 HG02735.hp2 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.1060+77delT | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr9 | 127808946 | ||||||
| chr9:127809010 | A | G | 1 | a0001c0001t0002g0112 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1060+121A>G | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 11/14 | chr9 | 127809010 | |||||||
| chr9:127809076 | T | C | 3 | a0001c0003t0003g0013 a0001c0003t0003g0042 a0001c0003t0003g0047 |
5 | HG02280.hp2 HG02886.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060+187T>C | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 11/14 | chr9 | 127809076 | |||||||
| chr9:127809078 | T | A | 3 | a0001c0003t0003g0013 a0001c0003t0003g0042 a0001c0003t0003g0047 |
5 | HG02280.hp2 HG02886.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060+189T>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 11/14 | chr9 | 127809078 | |||||||
| chr9:127809079 | T | A | 3 | a0001c0003t0003g0013 a0001c0003t0003g0042 a0001c0003t0003g0047 |
5 | HG02280.hp2 HG02886.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060+190T>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 11/14 | chr9 | 127809079 | |||||||
| chr9:127809080 | C | A | 3 | a0001c0003t0003g0013 a0001c0003t0003g0042 a0001c0003t0003g0047 |
5 | HG02280.hp2 HG02886.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060+191C>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 11/14 | chr9 | 127809080 | |||||||
| chr9:127809081 | T | G | 3 | a0001c0003t0003g0013 a0001c0003t0003g0042 a0001c0003t0003g0047 |
5 | HG02280.hp2 HG02886.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060+192T>G | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 11/14 | chr9 | 127809081 | |||||||
| chr9:127809082 | C | T | 3 | a0001c0003t0003g0013 a0001c0003t0003g0042 a0001c0003t0003g0047 |
5 | HG02280.hp2 HG02886.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060+193C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 11/14 | chr9 | 127809082 | |||||||
| chr9:127809084 | T | G | 3 | a0001c0003t0003g0013 a0001c0003t0003g0042 a0001c0003t0003g0047 |
5 | HG02280.hp2 HG02886.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060+195T>G | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 11/14 | chr9 | 127809084 | |||||||
| chr9:127809085 | C | A | 3 | a0001c0003t0003g0013 a0001c0003t0003g0042 a0001c0003t0003g0047 |
5 | HG02280.hp2 HG02886.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060+196C>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 11/14 | chr9 | 127809085 | |||||||
| chr9:127809137 | C | T | 1 | a0001c0001t0002g0111 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1060+248C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 11/14 | chr9 | 127809137 | |||||||
| chr9:127809279 | T | G | 1 | a0001c0001t0001g0063 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1060+390T>G | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 11/14 | chr9 | 127809279 | |||||||
| chr9:127809555 | G | C | 1 | a0001c0008t0001g0025 | 2 | HG00544.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1061-129G>C | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 11/14 | chr9 | 127809555 | |||||||
| chr9:127809594 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1061-90G>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 11/14 | chr9 | 127809594 | |||||||
| chr9:127809839 | G | A | 2 | a0001c0001t0002g0026 a0001c0001t0002g0085 |
3 | HG02647.hp1 HG02818.hp2 HG03098.hp1 |
splice_region_variant&intron_variant | LOW | c.1211+5G>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 12/14 | chr9 | 127809839 | |||||||
| chr9:127809844 | A | G | 69 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(66): Show |
219 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.1211+10A>G | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 12/14 | chr9 | 127809844 | |||||||
| chr9:127809898 | A | G | 2 | a0001c0001t0001g0020 a0001c0013t0001g0050 |
3 | HG01884.hp1 HG02572.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1211+64A>G | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 12/14 | chr9 | 127809898 | |||||||
| chr9:127809942 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1212-89G>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 12/14 | chr9 | 127809942 | |||||||
| chr9:127809975 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1212-56G>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 12/14 | chr9 | 127809975 | |||||||
| chr9:127810026 | C | G | 3 | a0001c0001t0002g0110 a0001c0001t0002g0120 a0001c0001t0002g0121 |
3 | NA18966.hp2 NA18993.hp2 NA19012.hp1 |
splice_region_variant&intron_variant | LOW | c.1212-5C>G | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 12/14 | chr9 | 127810026 | |||||||
| chr9:127810161 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0074 |
3 | HG00621.hp1 HG02056.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.1287+55C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 13/14 | chr9 | 127810161 | |||||||
| chr9:127810178 | G | T | 1 | a0001c0001t0001g0012 | 4 | HG01099.hp2 HG03130.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1287+72G>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 13/14 | chr9 | 127810178 | |||||||
| chr9:127810420 | A | G | 1 | a0002c0002t0002g0100 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1287+314A>G | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 13/14 | chr9 | 127810420 | |||||||
| chr9:127810427 | C | T | 1 | a0002c0002t0002g0092 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1287+321C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 13/14 | chr9 | 127810427 | |||||||
| chr9:127810744 | C | T | 1 | a0001c0003t0003g0045 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1288-201C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 13/14 | chr9 | 127810744 | |||||||
| chr9:127810830 | C | T | 1 | a0001c0001t0002g0075 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1288-115C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 13/14 | chr9 | 127810830 | |||||||
| chr9:127810871 | C | T | 1 | a0001c0001t0001g0077 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1288-74C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 13/14 | chr9 | 127810871 | |||||||
| chr9:127811069 | G | C | 1 | a0001c0001t0001g0080 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1354+58G>C | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127811069 | |||||||
| chr9:127811070 | G | T | 1 | a0001c0001t0001g0080 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1354+59G>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127811070 | |||||||
| chr9:127811092 | G | A | 1 | a0001c0001t0001g0020 | 2 | HG02572.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1354+81G>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127811092 | |||||||
| chr9:127811095 | GTAGGAAA others(24): Show |
G | 1 | a0007c0010t0001g0067 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1354+85_1354+115de others(32): Show |
FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127811095 | |||||||
| chr9:127811132 | T | C | 2 | a0001c0001t0003g0076 a0001c0003t0001g0032 |
3 | HG02965.hp1 HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1354+121T>C | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127811132 | |||||||
| chr9:127811134 | G | A | 1 | a0007c0010t0001g0067 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1354+123G>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127811134 | |||||||
| chr9:127811313 | CA | C | 4 | a0001c0001t0001g0011 a0001c0001t0001g0061 a0001c0001t0001g0086 others(1): Show |
7 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1354+312delA | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr9 | 127811313 | ||||||
| chr9:127811406 | C | T | 1 | a0001c0013t0001g0050 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1354+395C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127811406 | |||||||
| chr9:127811450 | C | T | 1 | a0001c0013t0001g0050 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1354+439C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127811450 | |||||||
| chr9:127811480 | C | CA | 14 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0016 others(11): Show |
29 | HG00438.hp1 HG00544.hp1 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.1354+483dupA | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr9 | 127811480 | ||||||
| chr9:127811480 | C | CAA | 38 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(35): Show |
156 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.1354+482_1354+483d others(4): Show |
FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr9 | 127811480 | ||||||
| chr9:127811617 | C | T | 28 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0027 others(25): Show |
105 | HG00323.hp1 HG00423.hp1 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.1354+606C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127811617 | |||||||
| chr9:127811619 | G | T | 1 | a0001c0001t0002g0113 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1354+608G>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127811619 | |||||||
| chr9:127811693 | C | T | 1 | a0001c0001t0001g0073 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1354+682C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127811693 | |||||||
| chr9:127811829 | C | T | 1 | a0001c0001t0001g0022 | 2 | NA19001.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1354+818C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127811829 | |||||||
| chr9:127811843 | C | A | 3 | a0001c0001t0001g0021 a0001c0001t0001g0053 a0001c0001t0001g0068 |
4 | HG01928.hp2 HG01981.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.1354+832C>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127811843 | |||||||
| chr9:127811888 | G | A | 1 | a0001c0001t0001g0052 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1354+877G>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127811888 | |||||||
| chr9:127812082 | T | TA | 13 | a0001c0001t0003g0076 a0001c0003t0001g0032 a0001c0003t0003g0005 others(10): Show |
27 | HG02080.hp2 HG02258.hp1 HG02258.hp2 others(24): Show |
intron_variant | MODIFIER | c.1354+1080dupA | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr9 | 127812082 | ||||||
| chr9:127812322 | A | AT | 32 | a0001c0001t0001g0011 a0001c0001t0001g0061 a0001c0001t0001g0072 others(29): Show |
74 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(71): Show |
intron_variant | MODIFIER | c.1355-857dupT | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr9 | 127812322 | ||||||
| chr9:127812322 | AT | A | 15 | a0001c0001t0001g0069 a0001c0001t0001g0084 a0001c0001t0002g0060 others(12): Show |
28 | HG02080.hp2 HG02258.hp1 HG02258.hp2 others(25): Show |
intron_variant | MODIFIER | c.1355-857delT | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr9 | 127812322 | ||||||
| chr9:127812348 | G | T | 1 | a0001c0001t0001g0083 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1355-847G>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127812348 | |||||||
| chr9:127812352 | C | G | 4 | a0001c0001t0001g0011 a0001c0001t0001g0061 a0001c0001t0001g0086 others(1): Show |
7 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1355-843C>G | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127812352 | |||||||
| chr9:127812403 | T | C | 4 | a0001c0001t0001g0021 a0001c0001t0001g0053 a0001c0001t0001g0068 others(1): Show |
5 | HG01928.hp2 HG01934.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.1355-792T>C | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127812403 | |||||||
| chr9:127812463 | C | T | 1 | a0002c0002t0002g0099 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1355-732C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127812463 | |||||||
| chr9:127812479 | C | T | 1 | a0001c0001t0002g0109 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1355-716C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127812479 | |||||||
| chr9:127812643 | A | G | 1 | a0001c0001t0002g0117 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1355-552A>G | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127812643 | |||||||
| chr9:127812648 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1355-547C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127812648 | |||||||
| chr9:127812699 | G | GT | 43 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(40): Show |
172 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.1355-495dupT | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr9 | 127812699 | ||||||
| chr9:127812700 | T | G | 13 | a0001c0001t0003g0076 a0001c0003t0001g0032 a0001c0003t0003g0005 others(10): Show |
27 | HG02080.hp2 HG02258.hp1 HG02258.hp2 others(24): Show |
intron_variant | MODIFIER | c.1355-495T>G | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127812700 | |||||||
| chr9:127812701 | G | T | 71 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(68): Show |
223 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.1355-494G>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127812701 | |||||||
| chr9:127812924 | G | T | 1 | a0002c0002t0002g0093 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1355-271G>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127812924 | |||||||
| chr9:127813006 | T | A | 2 | a0002c0002t0002g0029 a0002c0002t0002g0096 |
3 | HG00639.hp1 HG01346.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1355-189T>A | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127813006 | |||||||
| chr9:127813080 | A | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0061 a0001c0001t0001g0087 |
6 | HG02145.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1355-115A>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127813080 | |||||||
| chr9:127813120 | C | T | 1 | a0001c0003t0003g0044 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1355-75C>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127813120 | |||||||
| chr9:127813121 | A | T | 1 | a0006c0009t0002g0088 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1355-74A>T | FPGS | ENSG00000136877.15 | transcript | ENST00000373247.7 | protein_coding | 14/14 | chr9 | 127813121 |