Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 388646 |
| ensemblid | ENSG00000213512.3 |
| hgncid | 29606 |
| symbol | GBP7 |
| name | guanylate binding protein 7 |
| refseq_nuc | NM_207398.3 |
| refseq_prot | NP_997281.2 |
| ensembl_nuc | ENST00000294671.3 |
| ensembl_prot | ENSP00000294671.2 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 89131742 |
| end | 89176003 |
| strand | - |
| ver | v1.2 |
| region | chr1:89131742-89176003 |
| region5000 | chr1:89126742-89181003 |
| regionname0 | GBP7_chr1_89131742_89176003 |
| regionname5000 | GBP7_chr1_89126742_89181003 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 638 | 258 | 54 | 43 | 125 | 9 | 26 | 99 | GBP7_chr1_89126742_89181003 | GBP7 | MASEI others(633): Show |
chr1 | 89126742 | 89181003 |
| a0002 | 1/0 | 638 | 99 | 17 | 24 | 38 | 7 | 12 | 26 | GBP7_chr1_89126742_89181003 | GBP7 | MASEI others(633): Show |
chr1 | 89126742 | 89181003 |
| a0003 | 0/0 | 638 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | MASEI others(633): Show |
chr1 | 89126742 | 89181003 |
| a0004 | 0/0 | 638 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | MASEI others(633): Show |
chr1 | 89126742 | 89181003 |
| a0005 | 0/0 | 638 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | MASEI others(633): Show |
chr1 | 89126742 | 89181003 |
| a0006 | 0/0 | 638 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | MASEI others(633): Show |
chr1 | 89126742 | 89181003 |
| a0007 | 0/0 | 638 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | MASEI others(633): Show |
chr1 | 89126742 | 89181003 |
| a0008 | 0/0 | 638 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | MASEI others(633): Show |
chr1 | 89126742 | 89181003 |
| a0009 | 0/0 | 638 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GBP7_chr1_89126742_89181003 | GBP7 | MASEI others(633): Show |
chr1 | 89126742 | 89181003 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1914 | 254 | 54 | 43 | 122 | 9 | 25 | GBP7_chr1_89126742_89181003 | GBP7 | ATGGC others(1909): Show |
chr1 | 89126742 | 89181003 | ||
| a0001c0007 | 0/0 | 1914 | 3 | 0 | 0 | 3 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | ATGGC others(1909): Show |
chr1 | 89126742 | 89181003 | ||
| a0001c0014 | 0/0 | 1914 | 1 | 0 | 0 | 0 | 0 | 1 | GBP7_chr1_89126742_89181003 | GBP7 | ATGGC others(1909): Show |
chr1 | 89126742 | 89181003 | ||
| a0002c0002 | 1/0 | 1914 | 90 | 15 | 19 | 36 | 7 | 12 | GBP7_chr1_89126742_89181003 | GBP7 | ATGGC others(1909): Show |
chr1 | 89126742 | 89181003 | ||
| a0002c0003 | 0/0 | 1914 | 6 | 0 | 4 | 2 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | ATGGC others(1909): Show |
chr1 | 89126742 | 89181003 | ||
| a0002c0009 | 0/0 | 1914 | 2 | 2 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | ATGGC others(1909): Show |
chr1 | 89126742 | 89181003 | ||
| a0002c0010 | 0/0 | 1914 | 1 | 0 | 1 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | ATGGC others(1909): Show |
chr1 | 89126742 | 89181003 | ||
| a0003c0004 | 0/0 | 1914 | 6 | 6 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | ATGGC others(1909): Show |
chr1 | 89126742 | 89181003 | ||
| a0004c0005 | 0/0 | 1914 | 4 | 4 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | ATGGC others(1909): Show |
chr1 | 89126742 | 89181003 | ||
| a0005c0008 | 0/0 | 1914 | 3 | 2 | 1 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | ATGGC others(1909): Show |
chr1 | 89126742 | 89181003 | ||
| a0006c0006 | 0/0 | 1914 | 3 | 3 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | ATGGC others(1909): Show |
chr1 | 89126742 | 89181003 | ||
| a0007c0013 | 0/0 | 1914 | 1 | 1 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | ATGGC others(1909): Show |
chr1 | 89126742 | 89181003 | ||
| a0008c0012 | 0/0 | 1914 | 1 | 1 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | ATGGC others(1909): Show |
chr1 | 89126742 | 89181003 | ||
| a0009c0011 | 0/0 | 1914 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | ATGGC others(1909): Show |
chr1 | 89126742 | 89181003 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2426 | 227 | 32 | 42 | 122 | 8 | 22 | GBP7_chr1_89126742_89181003 | GBP7 | AGAAC others(2421): Show |
chr1 | 89126742 | 89181003 |
| a0001c0001t0002 | 0/0 | 2426 | 10 | 10 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | AGAAC others(2421): Show |
chr1 | 89126742 | 89181003 |
| a0001c0001t0003 | 0/0 | 2426 | 12 | 12 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | AGAAC others(2421): Show |
chr1 | 89126742 | 89181003 |
| a0001c0001t0004 | 0/0 | 2426 | 3 | 0 | 1 | 0 | 1 | 1 | GBP7_chr1_89126742_89181003 | GBP7 | AGAAC others(2421): Show |
chr1 | 89126742 | 89181003 |
| a0001c0001t0005 | 0/0 | 2426 | 1 | 0 | 0 | 0 | 0 | 1 | GBP7_chr1_89126742_89181003 | GBP7 | AGAAC others(2421): Show |
chr1 | 89126742 | 89181003 |
| a0001c0001t0006 | 0/0 | 2426 | 1 | 0 | 0 | 0 | 0 | 1 | GBP7_chr1_89126742_89181003 | GBP7 | AGAAC others(2421): Show |
chr1 | 89126742 | 89181003 |
| a0001c0007t0001 | 0/0 | 2426 | 3 | 0 | 0 | 3 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | AGAAC others(2421): Show |
chr1 | 89126742 | 89181003 |
| a0001c0014t0001 | 0/0 | 2426 | 1 | 0 | 0 | 0 | 0 | 1 | GBP7_chr1_89126742_89181003 | GBP7 | AGAAC others(2421): Show |
chr1 | 89126742 | 89181003 |
| a0002c0002t0001 | 0/0 | 2426 | 2 | 2 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | AGAAC others(2421): Show |
chr1 | 89126742 | 89181003 |
| a0002c0002t0002 | 1/0 | 2426 | 88 | 13 | 19 | 36 | 7 | 12 | GBP7_chr1_89126742_89181003 | GBP7 | AGAAC others(2421): Show |
chr1 | 89126742 | 89181003 |
| a0002c0003t0003 | 0/0 | 2426 | 6 | 0 | 4 | 2 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | AGAAC others(2421): Show |
chr1 | 89126742 | 89181003 |
| a0002c0009t0003 | 0/0 | 2426 | 2 | 2 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | AGAAC others(2421): Show |
chr1 | 89126742 | 89181003 |
| a0002c0010t0002 | 0/0 | 2426 | 1 | 0 | 1 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | AGAAC others(2421): Show |
chr1 | 89126742 | 89181003 |
| a0003c0004t0003 | 0/0 | 2426 | 6 | 6 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | AGAAC others(2421): Show |
chr1 | 89126742 | 89181003 |
| a0004c0005t0001 | 0/0 | 2426 | 4 | 4 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | AGAAC others(2421): Show |
chr1 | 89126742 | 89181003 |
| a0005c0008t0003 | 0/0 | 2426 | 3 | 2 | 1 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | AGAAC others(2421): Show |
chr1 | 89126742 | 89181003 |
| a0006c0006t0002 | 0/0 | 2426 | 3 | 3 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | AGAAC others(2421): Show |
chr1 | 89126742 | 89181003 |
| a0007c0013t0002 | 0/0 | 2426 | 1 | 1 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | AGAAC others(2421): Show |
chr1 | 89126742 | 89181003 |
| a0008c0012t0001 | 0/0 | 2426 | 1 | 1 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | AGAAC others(2421): Show |
chr1 | 89126742 | 89181003 |
| a0009c0011t0002 | 0/0 | 2426 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | AGAAC others(2421): Show |
chr1 | 89126742 | 89181003 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 16 | 0 | 2 | 11 | 0 | 3 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0002 | 0/0 | 15 | 0 | 0 | 15 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0005 | 0/0 | 10 | 0 | 4 | 0 | 2 | 4 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0006 | 0/0 | 10 | 0 | 2 | 8 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0007 | 0/0 | 9 | 1 | 3 | 4 | 0 | 1 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0009 | 0/0 | 7 | 2 | 0 | 5 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0010 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0011 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0013 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0017 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0043 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0058 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0059 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0083 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0002g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0003g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0003g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0003g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0004g0018 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0005g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0001t0006g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0007t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0007t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0001c0014t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0002t0002g0003 | 0/0 | 11 | 2 | 0 | 9 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0002t0002g0004 | 0/0 | 11 | 0 | 3 | 5 | 0 | 3 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0002t0002g0008 | 0/0 | 9 | 0 | 5 | 1 | 2 | 1 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0002t0002g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0002t0002g0025 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0002t0002g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0002t0002g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0002t0002g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0002t0002g0054 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0002t0002g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0002t0002g0056 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0002t0002g0057 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0002t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0002t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0002t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0002t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0002t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0002t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0002t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0002t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0002t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0002t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0002t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0002t0002g0175 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0002t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0002t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0002t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0002t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0002t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0002t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0002t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0002t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0002t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0003t0003g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0003t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0003t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0003t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0003t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0009t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0009t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0002c0010t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0003c0004t0003g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0003c0004t0003g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0003c0004t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0004c0005t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0004c0005t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0004c0005t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0005c0008t0003g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0005c0008t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0006c0006t0002g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0006c0006t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0007c0013t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0008c0012t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| a0009c0011t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0205 | EUR | GBR | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0104 | EUR | GBR | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0068 | EUR | GBR | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG00140 | hp2 | a0002 | c0002 | t0002 | g0008 | EUR | GBR | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0115 | EUR | FIN | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG00280 | hp2 | a0002 | c0002 | t0002 | g0008 | EUR | FIN | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG00323 | hp1 | a0002 | c0002 | t0002 | g0025 | EUR | FIN | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0032 | EUR | FIN | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG00408 | hp1 | a0002 | c0002 | t0002 | g0025 | EAS | CHS | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG00558 | hp1 | a0002 | c0002 | t0002 | g0024 | EAS | CHS | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG00597 | hp1 | a0002 | c0002 | t0002 | g0067 | EAS | CHS | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG00597 | hp2 | a0002 | c0002 | t0002 | g0158 | EAS | CHS | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG00609 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | CHS | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | CHS | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG00639 | hp2 | a0002 | c0002 | t0002 | g0164 | AMR | PUR | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG00642 | hp2 | a0002 | c0002 | t0002 | g0186 | AMR | PUR | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG00733 | hp2 | a0002 | c0002 | t0002 | g0185 | AMR | PUR | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG00735 | hp2 | a0002 | c0002 | t0002 | g0004 | AMR | PUR | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01069 | hp2 | a0002 | c0002 | t0002 | g0179 | AMR | PUR | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01070 | hp1 | a0002 | c0002 | t0002 | g0159 | AMR | PUR | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01071 | hp2 | a0002 | c0002 | t0002 | g0008 | AMR | PUR | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01074 | hp2 | a0002 | c0003 | t0003 | g0085 | AMR | PUR | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01099 | hp1 | a0002 | c0002 | t0002 | g0160 | AMR | PUR | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01109 | hp1 | a0002 | c0002 | t0002 | g0008 | AMR | PUR | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01109 | hp2 | a0005 | c0008 | t0003 | g0028 | AMR | PUR | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01169 | hp2 | a0002 | c0002 | t0002 | g0008 | AMR | PUR | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01192 | hp1 | a0002 | c0002 | t0002 | g0204 | AMR | PUR | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01243 | hp1 | a0002 | c0002 | t0002 | g0173 | AMR | PUR | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01255 | hp2 | a0002 | c0002 | t0002 | g0178 | AMR | CLM | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01256 | hp2 | a0002 | c0003 | t0003 | g0031 | AMR | CLM | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01258 | hp2 | a0002 | c0003 | t0003 | g0031 | AMR | CLM | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01261 | hp1 | a0002 | c0002 | t0002 | g0004 | AMR | CLM | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01361 | hp1 | a0002 | c0002 | t0002 | g0008 | AMR | CLM | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01496 | hp1 | a0002 | c0003 | t0003 | g0087 | AMR | CLM | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0021 | EUR | IBS | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01515 | hp2 | a0002 | c0002 | t0002 | g0056 | EUR | IBS | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01516 | hp2 | a0002 | c0002 | t0002 | g0167 | EUR | IBS | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01517 | hp2 | a0002 | c0002 | t0002 | g0056 | EUR | IBS | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01884 | hp1 | a0002 | c0002 | t0002 | g0181 | AFR | ACB | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01884 | hp2 | a0002 | c0002 | t0002 | g0203 | AFR | ACB | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01943 | hp1 | a0002 | c0002 | t0002 | g0004 | AMR | PEL | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01975 | hp2 | a0002 | c0002 | t0002 | g0157 | AMR | PEL | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG01993 | hp2 | a0001 | c0001 | t0004 | g0018 | AMR | PEL | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02056 | hp2 | a0001 | c0007 | t0001 | g0075 | EAS | KHV | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02071 | hp1 | a0002 | c0002 | t0002 | g0024 | EAS | KHV | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02074 | hp2 | a0002 | c0002 | t0002 | g0168 | EAS | KHV | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02080 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | KHV | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02135 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | KHV | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02145 | hp1 | a0003 | c0004 | t0003 | g0016 | AFR | ACB | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | CDX | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02165 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | CDX | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0149 | AFR | ACB | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02273 | hp2 | a0002 | c0002 | t0002 | g0170 | AMR | PEL | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02293 | hp2 | a0002 | c0010 | t0002 | g0171 | AMR | PEL | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02300 | hp1 | a0002 | c0002 | t0002 | g0008 | AMR | PEL | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02451 | hp2 | a0002 | c0002 | t0002 | g0176 | AFR | ACB | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02615 | hp1 | a0002 | c0002 | t0002 | g0003 | AFR | GWD | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02615 | hp2 | a0005 | c0008 | t0003 | g0028 | AFR | GWD | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0030 | AFR | GWD | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02630 | hp1 | a0007 | c0013 | t0002 | g0154 | AFR | GWD | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02630 | hp2 | a0002 | c0002 | t0002 | g0052 | AFR | GWD | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02647 | hp2 | a0002 | c0002 | t0002 | g0077 | AFR | GWD | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02683 | hp1 | a0002 | c0002 | t0002 | g0008 | SAS | PJL | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02683 | hp2 | a0001 | c0014 | t0001 | g0141 | SAS | PJL | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02717 | hp2 | a0006 | c0006 | t0002 | g0035 | AFR | GWD | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0150 | AFR | GWD | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02723 | hp2 | a0006 | c0006 | t0002 | g0035 | AFR | GWD | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02886 | hp1 | a0008 | c0012 | t0001 | g0098 | AFR | GWD | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02886 | hp2 | a0002 | c0002 | t0002 | g0052 | AFR | GWD | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0063 | AFR | GWD | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0060 | AFR | GWD | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0206 | AFR | GWD | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0207 | AFR | GWD | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02965 | hp1 | a0004 | c0005 | t0001 | g0190 | AFR | ESN | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0027 | AFR | ESN | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02976 | hp1 | a0002 | c0002 | t0002 | g0165 | AFR | ESN | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0201 | AFR | ESN | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG03017 | hp2 | a0002 | c0002 | t0002 | g0169 | SAS | PJL | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG03041 | hp1 | a0002 | c0002 | t0002 | g0182 | AFR | GWD | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0184 | AFR | GWD | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | MSL | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG03098 | hp2 | a0005 | c0008 | t0003 | g0064 | AFR | MSL | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | ESN | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0066 | AFR | ESN | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG03139 | hp1 | a0003 | c0004 | t0003 | g0029 | AFR | ESN | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG03139 | hp2 | a0003 | c0004 | t0003 | g0016 | AFR | ESN | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG03195 | hp2 | a0002 | c0002 | t0002 | g0163 | AFR | ESN | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0148 | AFR | MSL | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG03225 | hp1 | a0002 | c0009 | t0003 | g0092 | AFR | MSL | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG03225 | hp2 | a0006 | c0006 | t0002 | g0091 | AFR | MSL | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | MSL | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | MSL | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG03490 | hp1 | a0002 | c0002 | t0002 | g0054 | SAS | PJL | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0054 | SAS | PJL | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0202 | AFR | ESN | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG03516 | hp2 | a0004 | c0005 | t0001 | g0037 | AFR | ESN | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0061 | AFR | GWD | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0030 | AFR | GWD | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG03579 | hp1 | a0002 | c0002 | t0001 | g0183 | AFR | MSL | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG03669 | hp2 | a0002 | c0002 | t0002 | g0034 | SAS | PJL | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG03688 | hp1 | a0002 | c0002 | t0002 | g0188 | SAS | STU | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | STU | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG03831 | hp1 | a0002 | c0002 | t0002 | g0034 | SAS | BEB | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG03831 | hp2 | a0001 | c0001 | t0006 | g0209 | SAS | BEB | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG03834 | hp2 | a0002 | c0002 | t0002 | g0004 | SAS | BEB | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | STU | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | STU | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG04184 | hp2 | a0001 | c0001 | t0005 | g0078 | SAS | BEB | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG04199 | hp1 | a0002 | c0002 | t0002 | g0072 | SAS | STU | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | STU | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG04204 | hp1 | a0002 | c0002 | t0002 | g0004 | SAS | STU | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0018 | SAS | STU | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG04228 | hp1 | a0002 | c0002 | t0002 | g0004 | SAS | STU | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18522 | hp1 | a0004 | c0005 | t0001 | g0037 | AFR | YRI | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | CHB | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18612 | hp2 | a0001 | c0007 | t0001 | g0036 | EAS | CHB | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18747 | hp1 | a0002 | c0002 | t0002 | g0161 | EAS | CHB | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | CHB | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18906 | hp1 | a0003 | c0004 | t0003 | g0016 | AFR | YRI | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | YRI | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18940 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18943 | hp2 | a0002 | c0002 | t0002 | g0025 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18944 | hp1 | a0002 | c0002 | t0002 | g0189 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18946 | hp1 | a0002 | c0002 | t0002 | g0055 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18947 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18950 | hp1 | a0001 | c0007 | t0001 | g0036 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18959 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18962 | hp2 | a0002 | c0002 | t0002 | g0055 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18965 | hp2 | a0002 | c0002 | t0002 | g0166 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18968 | hp1 | a0002 | c0002 | t0002 | g0053 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18971 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18982 | hp1 | a0002 | c0002 | t0002 | g0053 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18988 | hp1 | a0002 | c0002 | t0002 | g0024 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18991 | hp1 | a0002 | c0002 | t0002 | g0057 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18993 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19001 | hp2 | a0002 | c0003 | t0003 | g0088 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19004 | hp2 | a0002 | c0002 | t0002 | g0057 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19006 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19030 | hp1 | a0002 | c0009 | t0003 | g0089 | AFR | LWK | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0062 | AFR | LWK | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19043 | hp1 | a0004 | c0005 | t0001 | g0093 | AFR | LWK | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19043 | hp2 | a0002 | c0002 | t0002 | g0003 | AFR | LWK | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19054 | hp1 | a0002 | c0002 | t0002 | g0177 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19062 | hp1 | a0009 | c0011 | t0002 | g0162 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19064 | hp1 | a0002 | c0002 | t0002 | g0187 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19075 | hp1 | a0002 | c0002 | t0002 | g0172 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19076 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19080 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19082 | hp2 | a0002 | c0003 | t0003 | g0086 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19084 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19085 | hp1 | a0002 | c0002 | t0002 | g0174 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19091 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0147 | AFR | YRI | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ASW | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0027 | AFR | ASW | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA20752 | hp1 | a0002 | c0002 | t0002 | g0180 | EUR | TSI | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0018 | EUR | TSI | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA20905 | hp2 | a0002 | c0002 | t0002 | g0071 | SAS | GIH | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0146 | AFR | MSL | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | MSL | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | USA | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| HG06807 | hp2 | a0002 | c0002 | t0002 | g0156 | AFR | USA | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA20300 | hp1 | a0003 | c0004 | t0003 | g0029 | AFR | USA | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | USA | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA21309 | hp1 | a0002 | c0002 | t0002 | g0090 | AFR | LWK | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| NA21309 | hp2 | a0003 | c0004 | t0003 | g0065 | AFR | LWK | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0083 | REF | REF | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0002 | g0175 | REF | REF | GBP7_chr1_89126742_89181003 | GBP7 | chr1 | 89126742 | 89181003 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:89132238 | C | T | 1 | a0007 | 1 | HG02630.hp1 | missense_variant | MODERATE | c.1828G>A | p.Gly610Arg | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 11/11 | 1930/2426 | 1828/1917 | 610/638 | chr1 | 89132238 | |||
| chr1:89149317 | C | G | 1 | a0007 | 1 | HG02630.hp1 | missense_variant | MODERATE | c.1127G>C | p.Ser376Thr | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 7/11 | 1229/2426 | 1127/1917 | 376/638 | chr1 | 89149317 | |||
| chr1:89149340 | C | G | 1 | a0003 | 6 | HG02145.hp1 HG03139.hp1 HG03139.hp2 others(3): Show |
missense_variant | MODERATE | c.1104G>C | p.Met368Ile | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 7/11 | 1206/2426 | 1104/1917 | 368/638 | chr1 | 89149340 | |||
| chr1:89150330 | G | A | 1 | a0005 | 3 | HG01109.hp2 HG02615.hp2 HG03098.hp2 |
missense_variant&splice_region_variant | MODERATE | c.871C>T | p.Arg291Trp | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 6/11 | 973/2426 | 871/1917 | 291/638 | chr1 | 89150330 | |||
| chr1:89150335 | C | G | 1 | a0008 | 1 | HG02886.hp1 | missense_variant | MODERATE | c.866G>C | p.Gly289Ala | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 6/11 | 968/2426 | 866/1917 | 289/638 | chr1 | 89150335 | |||
| chr1:89150509 | T | C | 2 | a0006 a0007 |
4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
missense_variant | MODERATE | c.692A>G | p.Gln231Arg | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 6/11 | 794/2426 | 692/1917 | 231/638 | chr1 | 89150509 | |||
| chr1:89152777 | T | G | 1 | a0009 | 1 | NA19062.hp1 | missense_variant&splice_region_variant | MODERATE | c.319A>C | p.Ser107Arg | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 4/11 | 421/2426 | 319/1917 | 107/638 | chr1 | 89152777 | |||
| chr1:89164792 | G | T | 1 | a0006 | 3 | HG02717.hp2 HG02723.hp2 HG03225.hp2 |
missense_variant | MODERATE | c.257C>A | p.Pro86His | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/11 | 359/2426 | 257/1917 | 86/638 | chr1 | 89164792 | |||
| chr1:89171802 | C | T | 1 | a0004 | 4 | HG02965.hp1 HG03516.hp2 NA18522.hp1 others(1): Show |
missense_variant | MODERATE | c.134G>A | p.Gly45Asp | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/11 | 236/2426 | 134/1917 | 45/638 | chr1 | 89171802 | |||
| chr1:89171821 | C | G | 1 | a0006 | 3 | HG02717.hp2 HG02723.hp2 HG03225.hp2 |
missense_variant | MODERATE | c.115G>C | p.Val39Leu | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/11 | 217/2426 | 115/1917 | 39/638 | chr1 | 89171821 | |||
| chr1:89171895 | G | A | 7 | a0001 a0003 a0004 others(4): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
missense_variant | MODERATE | c.41C>T | p.Thr14Ile | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/11 | 143/2426 | 41/1917 | 14/638 | chr1 | 89171895 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:89132320 | A | G | 1 | a0007c0013 | 1 | HG02630.hp1 | synonymous_variant | LOW | c.1746T>C | p.Ile582Ile | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 11/11 | 1848/2426 | 1746/1917 | 582/638 | chr1 | 89132320 | |||
| chr1:89133330 | G | T | 1 | a0002c0003 | 6 | HG01074.hp2 HG01256.hp2 HG01258.hp2 others(3): Show |
synonymous_variant | LOW | c.1590C>A | p.Leu530Leu | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 10/11 | 1692/2426 | 1590/1917 | 530/638 | chr1 | 89133330 | |||
| chr1:89147597 | G | A | 2 | a0002c0003 a0002c0009 |
8 | HG01074.hp2 HG01256.hp2 HG01258.hp2 others(5): Show |
synonymous_variant | LOW | c.1335C>T | p.Asp445Asp | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/11 | 1437/2426 | 1335/1917 | 445/638 | chr1 | 89147597 | |||
| chr1:89149520 | A | C | 1 | a0002c0010 | 1 | HG02293.hp2 | synonymous_variant | LOW | c.924T>G | p.Thr308Thr | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 7/11 | 1026/2426 | 924/1917 | 308/638 | chr1 | 89149520 | |||
| chr1:89152760 | G | A | 1 | a0001c0014 | 1 | HG02683.hp2 | synonymous_variant | LOW | c.336C>T | p.Asp112Asp | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 4/11 | 438/2426 | 336/1917 | 112/638 | chr1 | 89152760 | |||
| chr1:89171804 | C | G | 1 | a0001c0007 | 3 | HG02056.hp2 NA18612.hp2 NA18950.hp1 |
synonymous_variant | LOW | c.132G>C | p.Val44Val | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/11 | 234/2426 | 132/1917 | 44/638 | chr1 | 89171804 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:89131971 | G | A | 1 | a0001c0001t0004 | 3 | HG01993.hp2 HG04204.hp2 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*178C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 11/11 | 178 | chr1 | 89131971 | ||||||
| chr1:89132057 | T | G | 5 | a0001c0001t0003 a0002c0003t0003 a0002c0009t0003 others(2): Show |
29 | HG01074.hp2 HG01109.hp2 HG01256.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*92A>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 11/11 | 92 | chr1 | 89132057 | ||||||
| chr1:89132072 | T | C | 9 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(6): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
3_prime_UTR_variant | MODIFIER | c.*77A>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 11/11 | 77 | chr1 | 89132072 | ||||||
| chr1:89171948 | C | G | 1 | a0001c0001t0005 | 1 | HG04184.hp2 | 5_prime_UTR_variant | MODIFIER | c.-13G>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/11 | 13 | chr1 | 89171948 | ||||||
| chr1:89175924 | G | A | 1 | a0001c0001t0006 | 1 | HG03831.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-23C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 1/11 | chr1 | 89175924 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:89132450 | A | G | 2 | a0006c0006t0002g0035 a0006c0006t0002g0091 |
3 | HG02717.hp2 HG02723.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1663-47T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 10/10 | chr1 | 89132450 | |||||||
| chr1:89132458 | G | T | 3 | a0006c0006t0002g0035 a0006c0006t0002g0091 a0007c0013t0002g0154 |
4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1663-55C>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 10/10 | chr1 | 89132458 | |||||||
| chr1:89132547 | A | G | 1 | a0001c0001t0001g0045 | 2 | HG02165.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.1663-144T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 10/10 | chr1 | 89132547 | |||||||
| chr1:89132553 | G | A | 1 | a0001c0001t0001g0109 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1663-150C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 10/10 | chr1 | 89132553 | |||||||
| chr1:89132846 | A | G | 1 | a0002c0002t0002g0166 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1662+412T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 10/10 | chr1 | 89132846 | |||||||
| chr1:89132965 | G | A | 3 | a0006c0006t0002g0035 a0006c0006t0002g0091 a0007c0013t0002g0154 |
4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1662+293C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 10/10 | chr1 | 89132965 | |||||||
| chr1:89133060 | A | G | 8 | a0001c0001t0003g0027 a0001c0001t0003g0030 a0001c0001t0003g0062 others(5): Show |
11 | HG01109.hp2 HG02615.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1662+198T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 10/10 | chr1 | 89133060 | |||||||
| chr1:89133123 | T | C | 3 | a0006c0006t0002g0035 a0006c0006t0002g0091 a0007c0013t0002g0154 |
4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1662+135A>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 10/10 | chr1 | 89133123 | |||||||
| chr1:89133564 | G | A | 21 | a0001c0001t0003g0026 a0001c0001t0003g0027 a0001c0001t0003g0030 others(18): Show |
29 | HG01074.hp2 HG01109.hp2 HG01256.hp2 others(26): Show |
intron_variant | MODIFIER | c.1469-113C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89133564 | |||||||
| chr1:89133693 | G | C | 1 | a0002c0002t0002g0160 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1469-242C>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89133693 | |||||||
| chr1:89133741 | T | C | 1 | a0002c0009t0003g0092 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1469-290A>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89133741 | |||||||
| chr1:89133746 | C | T | 1 | a0002c0002t0002g0176 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1469-295G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89133746 | |||||||
| chr1:89133749 | A | G | 1 | a0001c0001t0001g0136 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1469-298T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89133749 | |||||||
| chr1:89133856 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1469-405T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89133856 | |||||||
| chr1:89133875 | G | A | 7 | a0002c0003t0003g0031 a0002c0003t0003g0085 a0002c0003t0003g0086 others(4): Show |
8 | HG01074.hp2 HG01256.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1469-424C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89133875 | |||||||
| chr1:89134011 | G | T | 1 | a0002c0009t0003g0092 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1469-560C>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89134011 | |||||||
| chr1:89134219 | A | G | 3 | a0006c0006t0002g0035 a0006c0006t0002g0091 a0007c0013t0002g0154 |
4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1469-768T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89134219 | |||||||
| chr1:89134393 | A | G | 3 | a0006c0006t0002g0035 a0006c0006t0002g0091 a0007c0013t0002g0154 |
4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1469-942T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89134393 | |||||||
| chr1:89134437 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1469-986C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89134437 | |||||||
| chr1:89134604 | GA | G | 48 | a0001c0001t0002g0047 a0001c0001t0002g0148 a0001c0001t0002g0150 others(45): Show |
88 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.1469-1154delT | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89134604 | |||||||
| chr1:89134604 | GAA | G | 15 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0041 others(12): Show |
30 | HG01243.hp1 HG01261.hp2 HG01346.hp2 others(27): Show |
intron_variant | MODIFIER | c.1469-1155_1469-115 others(6): Show |
GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89134604 | |||||||
| chr1:89134604 | GAAA | G | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(130): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1469-1156_1469-115 others(7): Show |
GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89134604 | |||||||
| chr1:89134624 | A | G | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(154): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.1469-1173T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89134624 | |||||||
| chr1:89134635 | C | T | 3 | a0004c0005t0001g0037 a0004c0005t0001g0093 a0004c0005t0001g0190 |
4 | HG02965.hp1 HG03516.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1469-1184G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89134635 | |||||||
| chr1:89134704 | C | T | 56 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(53): Show |
109 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.1469-1253G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89134704 | |||||||
| chr1:89134727 | A | C | 1 | a0002c0002t0002g0024 | 3 | HG00558.hp1 HG02071.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.1469-1276T>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89134727 | |||||||
| chr1:89134897 | G | T | 3 | a0001c0001t0003g0026 a0001c0001t0003g0060 a0001c0001t0003g0061 |
4 | HG02896.hp1 HG03098.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1469-1446C>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89134897 | |||||||
| chr1:89134908 | T | G | 1 | a0002c0002t0002g0180 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1469-1457A>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89134908 | |||||||
| chr1:89134992 | T | A | 9 | a0001c0001t0002g0047 a0001c0001t0002g0146 a0001c0001t0002g0147 others(6): Show |
10 | HG02257.hp2 HG02723.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.1469-1541A>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89134992 | |||||||
| chr1:89135060 | G | C | 1 | a0001c0001t0001g0042 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1469-1609C>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89135060 | |||||||
| chr1:89135129 | C | G | 3 | a0003c0004t0003g0016 a0003c0004t0003g0029 a0003c0004t0003g0065 |
6 | HG02145.hp1 HG03139.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1469-1678G>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89135129 | |||||||
| chr1:89135302 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1469-1851T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89135302 | |||||||
| chr1:89135332 | G | C | 9 | a0001c0001t0002g0047 a0001c0001t0002g0146 a0001c0001t0002g0147 others(6): Show |
10 | HG02257.hp2 HG02723.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.1469-1881C>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89135332 | |||||||
| chr1:89135534 | G | A | 3 | a0006c0006t0002g0035 a0006c0006t0002g0091 a0007c0013t0002g0154 |
4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1469-2083C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89135534 | |||||||
| chr1:89135646 | G | A | 21 | a0001c0001t0003g0026 a0001c0001t0003g0027 a0001c0001t0003g0030 others(18): Show |
29 | HG01074.hp2 HG01109.hp2 HG01256.hp2 others(26): Show |
intron_variant | MODIFIER | c.1469-2195C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89135646 | |||||||
| chr1:89135745 | C | G | 1 | a0002c0002t0002g0055 | 2 | NA18946.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.1469-2294G>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89135745 | |||||||
| chr1:89135792 | G | A | 3 | a0006c0006t0002g0035 a0006c0006t0002g0091 a0007c0013t0002g0154 |
4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1469-2341C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89135792 | |||||||
| chr1:89135811 | C | T | 21 | a0001c0001t0003g0026 a0001c0001t0003g0027 a0001c0001t0003g0030 others(18): Show |
29 | HG01074.hp2 HG01109.hp2 HG01256.hp2 others(26): Show |
intron_variant | MODIFIER | c.1469-2360G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89135811 | |||||||
| chr1:89135903 | G | T | 3 | a0006c0006t0002g0035 a0006c0006t0002g0091 a0007c0013t0002g0154 |
4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1469-2452C>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89135903 | |||||||
| chr1:89135947 | C | T | 3 | a0006c0006t0002g0035 a0006c0006t0002g0091 a0007c0013t0002g0154 |
4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1469-2496G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89135947 | |||||||
| chr1:89136146 | G | A | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(121): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1469-2695C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89136146 | |||||||
| chr1:89136271 | C | T | 3 | a0006c0006t0002g0035 a0006c0006t0002g0091 a0007c0013t0002g0154 |
4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1469-2820G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89136271 | |||||||
| chr1:89136272 | G | A | 1 | a0007c0013t0002g0154 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1469-2821C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89136272 | |||||||
| chr1:89136416 | A | C | 2 | a0001c0001t0001g0032 a0001c0001t0001g0033 |
4 | HG00323.hp2 NA18957.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.1469-2965T>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89136416 | |||||||
| chr1:89136433 | TAAAA | T | 8 | a0001c0001t0003g0027 a0001c0001t0003g0030 a0001c0001t0003g0062 others(5): Show |
11 | HG01109.hp2 HG02615.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1469-2986_1469-298 others(8): Show |
GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89136433 | |||||||
| chr1:89136460 | G | A | 1 | a0002c0002t0002g0181 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1469-3009C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89136460 | |||||||
| chr1:89136495 | A | G | 1 | a0001c0001t0001g0050 | 2 | NA18979.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1469-3044T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89136495 | |||||||
| chr1:89136693 | C | G | 7 | a0002c0003t0003g0031 a0002c0003t0003g0085 a0002c0003t0003g0086 others(4): Show |
8 | HG01074.hp2 HG01256.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1469-3242G>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89136693 | |||||||
| chr1:89136792 | G | T | 1 | a0002c0002t0002g0172 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1469-3341C>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89136792 | |||||||
| chr1:89136923 | A | C | 1 | a0007c0013t0002g0154 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1469-3472T>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89136923 | |||||||
| chr1:89136975 | T | G | 1 | a0002c0003t0003g0031 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1469-3524A>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89136975 | |||||||
| chr1:89137008 | G | C | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(145): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.1469-3557C>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89137008 | |||||||
| chr1:89137060 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1469-3609T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89137060 | |||||||
| chr1:89137201 | G | T | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(154): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.1469-3750C>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89137201 | |||||||
| chr1:89137215 | T | C | 3 | a0006c0006t0002g0035 a0006c0006t0002g0091 a0007c0013t0002g0154 |
4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1469-3764A>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89137215 | |||||||
| chr1:89137464 | A | G | 1 | a0002c0003t0003g0086 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1469-4013T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89137464 | |||||||
| chr1:89137559 | ATCT | A | 2 | a0006c0006t0002g0035 a0006c0006t0002g0091 |
3 | HG02717.hp2 HG02723.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1468+3984_1468+398 others(7): Show |
GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89137559 | |||||||
| chr1:89138027 | G | A | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(154): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.1468+3519C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89138027 | |||||||
| chr1:89138060 | A | G | 14 | a0001c0001t0003g0026 a0001c0001t0003g0027 a0001c0001t0003g0030 others(11): Show |
21 | HG01109.hp2 HG02145.hp1 HG02615.hp2 others(18): Show |
intron_variant | MODIFIER | c.1468+3486T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89138060 | |||||||
| chr1:89138079 | C | A | 1 | a0001c0001t0001g0044 | 2 | HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1468+3467G>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89138079 | |||||||
| chr1:89138324 | GAAC | G | 14 | a0001c0001t0003g0026 a0001c0001t0003g0027 a0001c0001t0003g0030 others(11): Show |
21 | HG01109.hp2 HG02145.hp1 HG02615.hp2 others(18): Show |
intron_variant | MODIFIER | c.1468+3219_1468+322 others(7): Show |
GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89138324 | |||||||
| chr1:89138336 | C | A | 1 | a0001c0001t0001g0126 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1468+3210G>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89138336 | |||||||
| chr1:89138499 | A | G | 4 | a0001c0001t0003g0027 a0001c0001t0003g0063 a0005c0008t0003g0028 others(1): Show |
6 | HG01109.hp2 HG02615.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1468+3047T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89138499 | |||||||
| chr1:89138815 | A | G | 3 | a0003c0004t0003g0016 a0003c0004t0003g0029 a0003c0004t0003g0065 |
6 | HG02145.hp1 HG03139.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1468+2731T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89138815 | |||||||
| chr1:89138946 | A | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(121): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1468+2600T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89138946 | |||||||
| chr1:89138966 | A | T | 3 | a0002c0003t0003g0031 a0002c0003t0003g0085 a0002c0003t0003g0087 |
4 | HG01074.hp2 HG01256.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1468+2580T>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89138966 | |||||||
| chr1:89138989 | C | G | 1 | a0002c0002t0002g0034 | 2 | HG03669.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1468+2557G>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89138989 | |||||||
| chr1:89139107 | A | G | 1 | a0002c0009t0003g0092 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1468+2439T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89139107 | |||||||
| chr1:89139128 | A | G | 3 | a0006c0006t0002g0035 a0006c0006t0002g0091 a0007c0013t0002g0154 |
4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1468+2418T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89139128 | |||||||
| chr1:89139206 | A | G | 1 | a0002c0002t0002g0166 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1468+2340T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89139206 | |||||||
| chr1:89139491 | C | T | 1 | a0002c0009t0003g0089 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1468+2055G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89139491 | |||||||
| chr1:89139588 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1468+1958G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89139588 | |||||||
| chr1:89139626 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1468+1920C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89139626 | |||||||
| chr1:89139649 | C | A | 1 | a0002c0002t0002g0157 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1468+1897G>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89139649 | |||||||
| chr1:89139793 | C | T | 9 | a0001c0001t0002g0047 a0001c0001t0002g0146 a0001c0001t0002g0147 others(6): Show |
10 | HG02257.hp2 HG02723.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.1468+1753G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89139793 | |||||||
| chr1:89139868 | G | A | 3 | a0006c0006t0002g0035 a0006c0006t0002g0091 a0007c0013t0002g0154 |
4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1468+1678C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89139868 | |||||||
| chr1:89139871 | G | T | 1 | a0001c0001t0001g0103 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1468+1675C>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89139871 | |||||||
| chr1:89139885 | G | A | 1 | a0007c0013t0002g0154 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1468+1661C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89139885 | |||||||
| chr1:89140006 | G | A | 2 | a0004c0005t0001g0037 a0004c0005t0001g0093 |
3 | HG03516.hp2 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1468+1540C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89140006 | |||||||
| chr1:89140012 | A | G | 9 | a0001c0001t0002g0047 a0001c0001t0002g0146 a0001c0001t0002g0147 others(6): Show |
10 | HG02257.hp2 HG02723.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.1468+1534T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89140012 | |||||||
| chr1:89140091 | A | G | 6 | a0002c0003t0003g0031 a0002c0003t0003g0085 a0002c0003t0003g0086 others(3): Show |
7 | HG01074.hp2 HG01256.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1468+1455T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89140091 | |||||||
| chr1:89140102 | C | T | 1 | a0001c0001t0003g0201 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1468+1444G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89140102 | |||||||
| chr1:89140147 | T | C | 2 | a0002c0002t0002g0056 a0002c0002t0002g0164 |
3 | HG00639.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1468+1399A>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89140147 | |||||||
| chr1:89140262 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1468+1284G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89140262 | |||||||
| chr1:89140263 | A | G | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(145): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.1468+1283T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89140263 | |||||||
| chr1:89140278 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1468+1268G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89140278 | |||||||
| chr1:89140304 | G | C | 1 | a0001c0001t0001g0049 | 2 | HG00558.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.1468+1242C>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89140304 | |||||||
| chr1:89140445 | A | G | 7 | a0001c0001t0001g0020 a0001c0001t0001g0039 a0001c0001t0001g0100 others(4): Show |
10 | HG00408.hp2 HG00673.hp2 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.1468+1101T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89140445 | |||||||
| chr1:89140460 | G | GA | 6 | a0001c0001t0003g0063 a0002c0002t0002g0177 a0002c0003t0003g0031 others(3): Show |
10 | HG01256.hp2 HG01258.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1468+1085dupT | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89140460 | |||||||
| chr1:89140460 | G | GAA | 20 | a0001c0001t0001g0118 a0001c0001t0001g0122 a0001c0001t0001g0135 others(17): Show |
24 | HG01074.hp2 HG01109.hp2 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.1468+1084_1468+108 others(6): Show |
GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89140460 | |||||||
| chr1:89140460 | G | GAAA | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(120): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1468+1083_1468+108 others(7): Show |
GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89140460 | |||||||
| chr1:89140545 | AT | A | 3 | a0006c0006t0002g0035 a0006c0006t0002g0091 a0007c0013t0002g0154 |
4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1468+1000delA | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89140545 | |||||||
| chr1:89140552 | A | G | 1 | a0002c0002t0002g0181 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1468+994T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89140552 | |||||||
| chr1:89140749 | G | A | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(121): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1468+797C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89140749 | |||||||
| chr1:89140772 | C | G | 3 | a0006c0006t0002g0035 a0006c0006t0002g0091 a0007c0013t0002g0154 |
4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1468+774G>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89140772 | |||||||
| chr1:89140900 | C | T | 1 | a0007c0013t0002g0154 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1468+646G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89140900 | |||||||
| chr1:89141087 | A | G | 1 | a0002c0002t0001g0183 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1468+459T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89141087 | |||||||
| chr1:89141103 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1468+443T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89141103 | |||||||
| chr1:89141208 | AG | A | 5 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0041 others(2): Show |
6 | HG02897.hp1 NA18948.hp1 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.1468+337delC | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89141208 | |||||||
| chr1:89141209 | G | A | 122 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(119): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.1468+337C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89141209 | |||||||
| chr1:89141402 | C | T | 2 | a0006c0006t0002g0035 a0006c0006t0002g0091 |
3 | HG02717.hp2 HG02723.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1468+144G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89141402 | |||||||
| chr1:89141539 | C | T | 3 | a0006c0006t0002g0035 a0006c0006t0002g0091 a0007c0013t0002g0154 |
4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.1468+7G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 9/10 | chr1 | 89141539 | |||||||
| chr1:89141786 | TC | T | 2 | a0006c0006t0002g0035 a0006c0006t0002g0091 |
3 | HG02717.hp2 HG02723.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1366-139delG | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89141786 | |||||||
| chr1:89141796 | G | T | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(121): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1366-148C>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89141796 | |||||||
| chr1:89141803 | T | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(154): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.1366-155A>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89141803 | |||||||
| chr1:89141907 | G | A | 2 | a0001c0001t0002g0206 a0001c0001t0002g0207 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1366-259C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89141907 | |||||||
| chr1:89141925 | T | C | 3 | a0001c0001t0001g0023 a0001c0001t0001g0138 a0001c0001t0001g0142 |
5 | NA18942.hp2 NA19056.hp2 NA19057.hp2 others(2): Show |
intron_variant | MODIFIER | c.1366-277A>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89141925 | |||||||
| chr1:89141933 | G | A | 3 | a0001c0001t0003g0026 a0001c0001t0003g0060 a0001c0001t0003g0061 |
4 | HG02896.hp1 HG03098.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1366-285C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89141933 | |||||||
| chr1:89141977 | T | A | 1 | a0001c0001t0001g0058 | 2 | HG00423.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.1366-329A>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89141977 | |||||||
| chr1:89142097 | T | C | 1 | a0002c0002t0002g0165 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1366-449A>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89142097 | |||||||
| chr1:89142195 | A | C | 1 | a0002c0009t0003g0092 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1366-547T>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89142195 | |||||||
| chr1:89142218 | T | TAC | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(154): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.1366-571_1366-570i others(4): Show |
GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89142218 | |||||||
| chr1:89142229 | G | A | 4 | a0002c0002t0002g0071 a0002c0002t0002g0072 a0002c0002t0002g0167 others(1): Show |
4 | HG01255.hp2 HG01516.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.1366-581C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89142229 | |||||||
| chr1:89142386 | A | G | 57 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(54): Show |
110 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.1366-738T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89142386 | |||||||
| chr1:89142397 | C | T | 5 | a0001c0001t0002g0146 a0001c0001t0002g0147 a0001c0001t0002g0202 others(2): Show |
5 | HG02896.hp2 HG02897.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1366-749G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89142397 | |||||||
| chr1:89142399 | A | G | 1 | a0007c0013t0002g0154 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1366-751T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89142399 | |||||||
| chr1:89142437 | A | G | 6 | a0001c0001t0001g0046 a0001c0001t0001g0074 a0001c0001t0001g0143 others(3): Show |
7 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1366-789T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89142437 | |||||||
| chr1:89142446 | C | T | 2 | a0004c0005t0001g0037 a0004c0005t0001g0093 |
3 | HG03516.hp2 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1366-798G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89142446 | |||||||
| chr1:89142516 | G | A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0094 |
4 | HG01515.hp1 HG03704.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.1366-868C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89142516 | |||||||
| chr1:89142789 | C | CA | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(202): Show |
372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.1366-1142dupT | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89142789 | |||||||
| chr1:89142810 | G | A | 1 | a0007c0013t0002g0154 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1366-1162C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89142810 | |||||||
| chr1:89142893 | C | T | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(154): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.1366-1245G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89142893 | |||||||
| chr1:89142935 | T | G | 2 | a0006c0006t0002g0035 a0006c0006t0002g0091 |
3 | HG02717.hp2 HG02723.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1366-1287A>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89142935 | |||||||
| chr1:89143553 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1366-1905C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89143553 | |||||||
| chr1:89143555 | A | T | 3 | a0006c0006t0002g0035 a0006c0006t0002g0091 a0007c0013t0002g0154 |
4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1366-1907T>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89143555 | |||||||
| chr1:89143847 | G | T | 2 | a0001c0001t0001g0128 a0001c0001t0001g0132 |
2 | NA18983.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.1366-2199C>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89143847 | |||||||
| chr1:89143908 | G | A | 3 | a0006c0006t0002g0035 a0006c0006t0002g0091 a0007c0013t0002g0154 |
4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1366-2260C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89143908 | |||||||
| chr1:89143934 | T | C | 2 | a0001c0001t0001g0046 a0001c0001t0001g0155 |
3 | HG01891.hp1 HG02451.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1366-2286A>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89143934 | |||||||
| chr1:89144366 | G | A | 2 | a0003c0004t0003g0029 a0003c0004t0003g0065 |
3 | HG03139.hp1 NA20300.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1366-2718C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89144366 | |||||||
| chr1:89144669 | A | G | 1 | a0002c0002t0002g0067 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1365+2898T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89144669 | |||||||
| chr1:89144730 | T | G | 5 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0006c0006t0002g0035 others(2): Show |
6 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1365+2837A>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89144730 | |||||||
| chr1:89144787 | A | C | 3 | a0006c0006t0002g0035 a0006c0006t0002g0091 a0007c0013t0002g0154 |
4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1365+2780T>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89144787 | |||||||
| chr1:89144851 | T | C | 3 | a0001c0001t0003g0026 a0001c0001t0003g0060 a0001c0001t0003g0061 |
4 | HG02896.hp1 HG03098.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1365+2716A>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89144851 | |||||||
| chr1:89144952 | CT | C | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(147): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.1365+2614delA | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89144952 | |||||||
| chr1:89144985 | G | A | 6 | a0001c0001t0003g0027 a0001c0001t0003g0062 a0001c0001t0003g0063 others(3): Show |
8 | HG01109.hp2 HG02615.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1365+2582C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89144985 | |||||||
| chr1:89145014 | G | A | 2 | a0002c0002t0002g0163 a0002c0002t0002g0181 |
2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1365+2553C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89145014 | |||||||
| chr1:89145021 | C | T | 3 | a0006c0006t0002g0035 a0006c0006t0002g0091 a0007c0013t0002g0154 |
4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1365+2546G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89145021 | |||||||
| chr1:89145101 | C | T | 33 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(30): Show |
65 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.1365+2466G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89145101 | |||||||
| chr1:89145120 | T | G | 1 | a0002c0002t0002g0090 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1365+2447A>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89145120 | |||||||
| chr1:89145238 | A | C | 2 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
2 | NA19006.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1365+2329T>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89145238 | |||||||
| chr1:89145351 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0205 |
11 | HG00099.hp1 HG01074.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.1365+2216G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89145351 | |||||||
| chr1:89145364 | G | A | 2 | a0001c0001t0001g0032 a0001c0001t0001g0033 |
4 | HG00323.hp2 NA18957.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.1365+2203C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89145364 | |||||||
| chr1:89145399 | T | C | 6 | a0001c0001t0001g0046 a0001c0001t0001g0074 a0001c0001t0001g0143 others(3): Show |
7 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1365+2168A>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89145399 | |||||||
| chr1:89145625 | C | T | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(154): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.1365+1942G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89145625 | |||||||
| chr1:89145648 | G | A | 1 | a0001c0001t0001g0137 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1365+1919C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89145648 | |||||||
| chr1:89145904 | AT | A | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(122): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1365+1662delA | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89145904 | |||||||
| chr1:89146185 | CAA | C | 1 | a0001c0001t0001g0010 | 6 | HG01074.hp1 HG01243.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.1365+1380_1365+138 others(6): Show |
GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89146185 | |||||||
| chr1:89146197 | A | G | 6 | a0001c0001t0001g0046 a0001c0001t0001g0074 a0001c0001t0001g0143 others(3): Show |
7 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1365+1370T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89146197 | |||||||
| chr1:89146564 | A | G | 6 | a0001c0001t0001g0046 a0001c0001t0001g0074 a0001c0001t0001g0143 others(3): Show |
7 | HG01891.hp1 HG02055.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1365+1003T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89146564 | |||||||
| chr1:89146696 | C | T | 2 | a0006c0006t0002g0035 a0006c0006t0002g0091 |
3 | HG02717.hp2 HG02723.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1365+871G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89146696 | |||||||
| chr1:89146849 | A | G | 1 | a0001c0001t0003g0030 | 2 | HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1365+718T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89146849 | |||||||
| chr1:89146906 | A | G | 1 | a0002c0003t0003g0085 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1365+661T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89146906 | |||||||
| chr1:89146927 | C | T | 7 | a0002c0003t0003g0031 a0002c0003t0003g0085 a0002c0003t0003g0086 others(4): Show |
8 | HG01074.hp2 HG01256.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1365+640G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89146927 | |||||||
| chr1:89146945 | A | T | 1 | a0001c0001t0001g0121 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1365+622T>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89146945 | |||||||
| chr1:89147008 | C | A | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(152): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.1365+559G>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89147008 | |||||||
| chr1:89147010 | C | T | 1 | a0001c0001t0002g0150 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1365+557G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89147010 | |||||||
| chr1:89147026 | A | G | 1 | a0001c0001t0001g0048 | 2 | NA18999.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1365+541T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89147026 | |||||||
| chr1:89147102 | C | G | 3 | a0006c0006t0002g0035 a0006c0006t0002g0091 a0007c0013t0002g0154 |
4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1365+465G>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89147102 | |||||||
| chr1:89147146 | C | A | 1 | a0001c0001t0001g0196 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1365+421G>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89147146 | |||||||
| chr1:89147247 | G | A | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(152): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.1365+320C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89147247 | |||||||
| chr1:89147330 | A | G | 55 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(52): Show |
108 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.1365+237T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89147330 | |||||||
| chr1:89147400 | G | A | 1 | a0001c0001t0001g0070 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1365+167C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89147400 | |||||||
| chr1:89147508 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1365+59C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 8/10 | chr1 | 89147508 | |||||||
| chr1:89147869 | G | A | 1 | a0007c0013t0002g0154 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1153-90C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 7/10 | chr1 | 89147869 | |||||||
| chr1:89147890 | C | T | 3 | a0006c0006t0002g0035 a0006c0006t0002g0091 a0007c0013t0002g0154 |
4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1153-111G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 7/10 | chr1 | 89147890 | |||||||
| chr1:89147997 | G | A | 1 | a0001c0001t0001g0019 | 3 | HG01069.hp1 HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1153-218C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 7/10 | chr1 | 89147997 | |||||||
| chr1:89148563 | C | A | 5 | a0002c0002t0001g0183 a0002c0002t0001g0184 a0002c0002t0002g0052 others(2): Show |
6 | HG01884.hp2 HG02630.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1152+729G>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 7/10 | chr1 | 89148563 | |||||||
| chr1:89148583 | T | G | 7 | a0002c0003t0003g0031 a0002c0003t0003g0085 a0002c0003t0003g0086 others(4): Show |
8 | HG01074.hp2 HG01256.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1152+709A>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 7/10 | chr1 | 89148583 | |||||||
| chr1:89148634 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1152+658G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 7/10 | chr1 | 89148634 | |||||||
| chr1:89148860 | T | C | 5 | a0002c0003t0003g0031 a0002c0003t0003g0085 a0002c0003t0003g0086 others(2): Show |
6 | HG01074.hp2 HG01256.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1152+432A>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 7/10 | chr1 | 89148860 | |||||||
| chr1:89148865 | T | A | 1 | a0001c0001t0002g0147 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1152+427A>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 7/10 | chr1 | 89148865 | |||||||
| chr1:89149129 | T | A | 1 | a0001c0001t0001g0129 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1152+163A>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 7/10 | chr1 | 89149129 | |||||||
| chr1:89149164 | C | T | 3 | a0006c0006t0002g0035 a0006c0006t0002g0091 a0007c0013t0002g0154 |
4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1152+128G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 7/10 | chr1 | 89149164 | |||||||
| chr1:89149196 | T | C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(152): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.1152+96A>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 7/10 | chr1 | 89149196 | |||||||
| chr1:89149215 | A | G | 1 | a0001c0001t0001g0084 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1152+77T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 7/10 | chr1 | 89149215 | |||||||
| chr1:89149218 | G | A | 1 | a0007c0013t0002g0154 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1152+74C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 7/10 | chr1 | 89149218 | |||||||
| chr1:89149628 | C | T | 1 | a0002c0002t0002g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.872-56G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 6/10 | chr1 | 89149628 | |||||||
| chr1:89149669 | C | T | 1 | a0001c0001t0005g0078 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.872-97G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 6/10 | chr1 | 89149669 | |||||||
| chr1:89149720 | A | G | 1 | a0001c0001t0001g0133 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.872-148T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 6/10 | chr1 | 89149720 | |||||||
| chr1:89149856 | GA | G | 16 | a0001c0001t0001g0040 a0002c0002t0002g0004 a0002c0002t0002g0025 others(13): Show |
31 | HG00323.hp1 HG00408.hp1 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.872-285delT | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 6/10 | chr1 | 89149856 | |||||||
| chr1:89150019 | A | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(152): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.871+311T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 6/10 | chr1 | 89150019 | |||||||
| chr1:89150253 | G | A | 2 | a0001c0001t0001g0140 a0001c0001t0005g0078 |
2 | HG04115.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.871+77C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 6/10 | chr1 | 89150253 | |||||||
| chr1:89150296 | C | T | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(142): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.871+34G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 6/10 | chr1 | 89150296 | |||||||
| chr1:89150576 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA18983.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.626-1G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 5/10 | chr1 | 89150576 | |||||||
| chr1:89150778 | A | G | 1 | a0002c0002t0002g0170 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.626-203T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 5/10 | chr1 | 89150778 | |||||||
| chr1:89150956 | C | T | 3 | a0006c0006t0002g0035 a0006c0006t0002g0091 a0007c0013t0002g0154 |
4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.626-381G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 5/10 | chr1 | 89150956 | |||||||
| chr1:89151117 | A | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0205 |
11 | HG00099.hp1 HG01074.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.626-542T>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 5/10 | chr1 | 89151117 | |||||||
| chr1:89151241 | A | G | 1 | a0001c0001t0001g0195 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.626-666T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 5/10 | chr1 | 89151241 | |||||||
| chr1:89151259 | T | G | 7 | a0002c0003t0003g0031 a0002c0003t0003g0085 a0002c0003t0003g0086 others(4): Show |
8 | HG01074.hp2 HG01256.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.626-684A>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 5/10 | chr1 | 89151259 | |||||||
| chr1:89151453 | C | T | 3 | a0006c0006t0002g0035 a0006c0006t0002g0091 a0007c0013t0002g0154 |
4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.625+815G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 5/10 | chr1 | 89151453 | |||||||
| chr1:89151454 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.625+814C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 5/10 | chr1 | 89151454 | |||||||
| chr1:89151743 | A | AT | 10 | a0002c0003t0003g0031 a0002c0003t0003g0085 a0002c0003t0003g0086 others(7): Show |
12 | HG01074.hp2 HG01256.hp2 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.625+524dupA | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 5/10 | chr1 | 89151743 | |||||||
| chr1:89151914 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.625+354A>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 5/10 | chr1 | 89151914 | |||||||
| chr1:89151936 | C | T | 3 | a0006c0006t0002g0035 a0006c0006t0002g0091 a0007c0013t0002g0154 |
4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.625+332G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 5/10 | chr1 | 89151936 | |||||||
| chr1:89152180 | T | A | 1 | a0002c0002t0002g0185 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.625+88A>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 5/10 | chr1 | 89152180 | |||||||
| chr1:89152205 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.625+63C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 5/10 | chr1 | 89152205 | |||||||
| chr1:89152789 | GA | G | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(138): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.319-13delT | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89152789 | |||||||
| chr1:89152789 | GAA | G | 15 | a0001c0001t0001g0023 a0001c0001t0001g0084 a0001c0001t0001g0105 others(12): Show |
20 | HG01109.hp2 HG02055.hp2 HG02615.hp2 others(17): Show |
intron_variant | MODIFIER | c.319-14_319-13delTT | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89152789 | |||||||
| chr1:89152859 | C | T | 1 | a0002c0002t0002g0169 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.319-82G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89152859 | |||||||
| chr1:89152980 | C | G | 15 | a0001c0001t0001g0046 a0001c0001t0001g0074 a0001c0001t0001g0143 others(12): Show |
17 | HG01891.hp1 HG02055.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.319-203G>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89152980 | |||||||
| chr1:89152988 | C | G | 15 | a0001c0001t0001g0046 a0001c0001t0001g0074 a0001c0001t0001g0143 others(12): Show |
17 | HG01891.hp1 HG02055.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.319-211G>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89152988 | |||||||
| chr1:89153033 | C | T | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(142): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.319-256G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89153033 | |||||||
| chr1:89153128 | C | G | 2 | a0001c0001t0001g0046 a0001c0001t0001g0155 |
3 | HG01891.hp1 HG02451.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.319-351G>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89153128 | |||||||
| chr1:89153484 | A | G | 1 | a0001c0001t0001g0123 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.319-707T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89153484 | |||||||
| chr1:89153572 | A | G | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(142): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.319-795T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89153572 | |||||||
| chr1:89153654 | A | G | 7 | a0002c0003t0003g0031 a0002c0003t0003g0085 a0002c0003t0003g0086 others(4): Show |
8 | HG01074.hp2 HG01256.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.319-877T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89153654 | |||||||
| chr1:89153905 | G | T | 6 | a0002c0003t0003g0031 a0002c0003t0003g0085 a0002c0003t0003g0086 others(3): Show |
7 | HG01074.hp2 HG01256.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.319-1128C>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89153905 | |||||||
| chr1:89154033 | A | C | 1 | a0001c0001t0001g0104 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.319-1256T>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89154033 | |||||||
| chr1:89154109 | A | G | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(138): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.319-1332T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89154109 | |||||||
| chr1:89154208 | A | C | 1 | a0002c0002t0002g0168 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.319-1431T>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89154208 | |||||||
| chr1:89154239 | G | A | 2 | a0002c0002t0002g0186 a0002c0002t0002g0188 |
2 | HG00642.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.319-1462C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89154239 | |||||||
| chr1:89154424 | A | G | 3 | a0006c0006t0002g0035 a0006c0006t0002g0091 a0007c0013t0002g0154 |
4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.319-1647T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89154424 | |||||||
| chr1:89154443 | T | A | 1 | a0007c0013t0002g0154 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.319-1666A>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89154443 | |||||||
| chr1:89154465 | G | T | 1 | a0002c0002t0002g0163 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.319-1688C>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89154465 | |||||||
| chr1:89154545 | C | A | 5 | a0001c0001t0002g0146 a0001c0001t0002g0147 a0001c0001t0002g0202 others(2): Show |
5 | HG02896.hp2 HG02897.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.319-1768G>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89154545 | |||||||
| chr1:89154563 | T | G | 2 | a0001c0001t0001g0019 a0001c0001t0001g0097 |
4 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.319-1786A>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89154563 | |||||||
| chr1:89154578 | C | T | 1 | a0007c0013t0002g0154 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.319-1801G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89154578 | |||||||
| chr1:89154633 | G | C | 3 | a0006c0006t0002g0035 a0006c0006t0002g0091 a0007c0013t0002g0154 |
4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.319-1856C>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89154633 | |||||||
| chr1:89154704 | TAAATAAA others(3): Show |
T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0113 |
6 | NA18940.hp2 NA18965.hp1 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.319-1937_319-1928d others(12): Show |
GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89154704 | |||||||
| chr1:89154788 | A | G | 1 | a0007c0013t0002g0154 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.319-2011T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89154788 | |||||||
| chr1:89154807 | A | AAAAAT | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(152): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.319-2035_319-2031d others(7): Show |
GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89154807 | |||||||
| chr1:89154847 | A | G | 13 | a0001c0001t0003g0026 a0001c0001t0003g0027 a0001c0001t0003g0030 others(10): Show |
20 | HG01109.hp2 HG02145.hp1 HG02615.hp2 others(17): Show |
intron_variant | MODIFIER | c.319-2070T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89154847 | |||||||
| chr1:89154848 | G | A | 1 | a0001c0001t0001g0020 | 3 | NA18957.hp2 NA18980.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.319-2071C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89154848 | |||||||
| chr1:89154886 | T | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(142): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.319-2109A>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89154886 | |||||||
| chr1:89155039 | T | C | 1 | a0002c0009t0003g0092 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.319-2262A>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89155039 | |||||||
| chr1:89155181 | C | A | 1 | a0002c0002t0002g0165 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.319-2404G>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89155181 | |||||||
| chr1:89155208 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.319-2431A>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89155208 | |||||||
| chr1:89155267 | T | A | 6 | a0001c0001t0001g0013 a0001c0001t0001g0023 a0001c0001t0001g0125 others(3): Show |
12 | HG01192.hp2 HG01975.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.319-2490A>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89155267 | |||||||
| chr1:89155291 | C | T | 1 | a0002c0002t0002g0167 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.319-2514G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89155291 | |||||||
| chr1:89155347 | A | G | 1 | a0002c0009t0003g0092 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.319-2570T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89155347 | |||||||
| chr1:89155378 | C | T | 1 | a0007c0013t0002g0154 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.319-2601G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89155378 | |||||||
| chr1:89155428 | G | A | 1 | a0002c0002t0002g0187 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.319-2651C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89155428 | |||||||
| chr1:89155471 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.319-2694G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89155471 | |||||||
| chr1:89155541 | C | T | 2 | a0006c0006t0002g0035 a0006c0006t0002g0091 |
3 | HG02717.hp2 HG02723.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.319-2764G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89155541 | |||||||
| chr1:89155624 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.319-2847C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89155624 | |||||||
| chr1:89155783 | T | G | 58 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(55): Show |
112 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.319-3006A>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89155783 | |||||||
| chr1:89156047 | A | C | 3 | a0006c0006t0002g0035 a0006c0006t0002g0091 a0007c0013t0002g0154 |
4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.319-3270T>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89156047 | |||||||
| chr1:89156133 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.319-3356G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89156133 | |||||||
| chr1:89156146 | C | T | 8 | a0001c0001t0001g0138 a0002c0003t0003g0031 a0002c0003t0003g0085 others(5): Show |
9 | HG01074.hp2 HG01256.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.319-3369G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89156146 | |||||||
| chr1:89156147 | G | A | 3 | a0006c0006t0002g0035 a0006c0006t0002g0091 a0007c0013t0002g0154 |
4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.319-3370C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89156147 | |||||||
| chr1:89156278 | G | A | 1 | a0001c0001t0002g0150 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.319-3501C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89156278 | |||||||
| chr1:89156290 | A | G | 1 | a0004c0005t0001g0093 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.319-3513T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89156290 | |||||||
| chr1:89156347 | A | G | 20 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0022 others(17): Show |
41 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.319-3570T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89156347 | |||||||
| chr1:89156365 | A | T | 3 | a0006c0006t0002g0035 a0006c0006t0002g0091 a0007c0013t0002g0154 |
4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.319-3588T>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89156365 | |||||||
| chr1:89156370 | A | G | 15 | a0001c0001t0001g0046 a0001c0001t0001g0074 a0001c0001t0001g0143 others(12): Show |
17 | HG01891.hp1 HG02055.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.319-3593T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89156370 | |||||||
| chr1:89156436 | A | T | 3 | a0003c0004t0003g0016 a0003c0004t0003g0029 a0003c0004t0003g0065 |
6 | HG02145.hp1 HG03139.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.319-3659T>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89156436 | |||||||
| chr1:89156459 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.319-3682T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89156459 | |||||||
| chr1:89156539 | A | G | 15 | a0001c0001t0001g0046 a0001c0001t0001g0074 a0001c0001t0001g0143 others(12): Show |
17 | HG01891.hp1 HG02055.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.319-3762T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89156539 | |||||||
| chr1:89156577 | C | T | 2 | a0002c0002t0002g0054 a0002c0002t0002g0160 |
3 | HG01099.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.319-3800G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89156577 | |||||||
| chr1:89156595 | T | C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(152): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.319-3818A>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89156595 | |||||||
| chr1:89156673 | T | C | 2 | a0006c0006t0002g0035 a0006c0006t0002g0091 |
3 | HG02717.hp2 HG02723.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.319-3896A>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89156673 | |||||||
| chr1:89156692 | C | T | 1 | a0007c0013t0002g0154 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.319-3915G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89156692 | |||||||
| chr1:89156814 | C | T | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(142): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.319-4037G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89156814 | |||||||
| chr1:89157000 | C | T | 2 | a0006c0006t0002g0035 a0006c0006t0002g0091 |
3 | HG02717.hp2 HG02723.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.319-4223G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89157000 | |||||||
| chr1:89157117 | C | T | 1 | a0007c0013t0002g0154 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.319-4340G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89157117 | |||||||
| chr1:89157401 | A | T | 1 | a0007c0013t0002g0154 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.319-4624T>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89157401 | |||||||
| chr1:89157405 | A | G | 2 | a0006c0006t0002g0035 a0006c0006t0002g0091 |
3 | HG02717.hp2 HG02723.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.319-4628T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89157405 | |||||||
| chr1:89157464 | C | A | 1 | a0007c0013t0002g0154 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.319-4687G>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89157464 | |||||||
| chr1:89157530 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.319-4753C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89157530 | |||||||
| chr1:89157568 | G | C | 3 | a0006c0006t0002g0035 a0006c0006t0002g0091 a0007c0013t0002g0154 |
4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.319-4791C>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89157568 | |||||||
| chr1:89157823 | G | A | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(152): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.319-5046C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89157823 | |||||||
| chr1:89157826 | G | A | 7 | a0002c0003t0003g0031 a0002c0003t0003g0085 a0002c0003t0003g0086 others(4): Show |
8 | HG01074.hp2 HG01256.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.319-5049C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89157826 | |||||||
| chr1:89157887 | C | T | 1 | a0002c0009t0003g0089 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.319-5110G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89157887 | |||||||
| chr1:89158075 | G | A | 1 | a0002c0002t0002g0164 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.319-5298C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89158075 | |||||||
| chr1:89158310 | T | TGCCCTC | 5 | a0002c0003t0003g0031 a0002c0003t0003g0085 a0002c0003t0003g0086 others(2): Show |
6 | HG01074.hp2 HG01256.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.319-5539_319-5534d others(8): Show |
GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89158310 | |||||||
| chr1:89158686 | A | G | 1 | a0001c0001t0002g0206 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.319-5909T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89158686 | |||||||
| chr1:89158803 | T | A | 1 | a0001c0001t0001g0113 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.318+5928A>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89158803 | |||||||
| chr1:89158806 | A | G | 2 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
2 | NA19006.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.318+5925T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89158806 | |||||||
| chr1:89158901 | C | G | 3 | a0006c0006t0002g0035 a0006c0006t0002g0091 a0007c0013t0002g0154 |
4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.318+5830G>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89158901 | |||||||
| chr1:89158908 | A | G | 13 | a0001c0001t0003g0026 a0001c0001t0003g0027 a0001c0001t0003g0030 others(10): Show |
20 | HG01109.hp2 HG02145.hp1 HG02615.hp2 others(17): Show |
intron_variant | MODIFIER | c.318+5823T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89158908 | |||||||
| chr1:89158949 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.318+5782G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89158949 | |||||||
| chr1:89158955 | C | G | 3 | a0001c0001t0001g0013 a0001c0001t0001g0125 a0001c0001t0001g0129 |
7 | HG01192.hp2 HG01975.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.318+5776G>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89158955 | |||||||
| chr1:89159020 | A | G | 3 | a0006c0006t0002g0035 a0006c0006t0002g0091 a0007c0013t0002g0154 |
4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.318+5711T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89159020 | |||||||
| chr1:89159212 | G | C | 3 | a0006c0006t0002g0035 a0006c0006t0002g0091 a0007c0013t0002g0154 |
4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.318+5519C>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89159212 | |||||||
| chr1:89159339 | A | G | 7 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0192 others(4): Show |
9 | HG00423.hp1 HG02004.hp2 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.318+5392T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89159339 | |||||||
| chr1:89159614 | A | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(152): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.318+5117T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89159614 | |||||||
| chr1:89159687 | G | A | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(129): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.318+5044C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89159687 | |||||||
| chr1:89159688 | C | G | 1 | a0002c0002t0002g0166 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.318+5043G>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89159688 | |||||||
| chr1:89159727 | G | A | 3 | a0006c0006t0002g0035 a0006c0006t0002g0091 a0007c0013t0002g0154 |
4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.318+5004C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89159727 | |||||||
| chr1:89159754 | A | C | 1 | a0002c0003t0003g0086 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.318+4977T>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89159754 | |||||||
| chr1:89159835 | A | G | 1 | a0002c0002t0002g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.318+4896T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89159835 | |||||||
| chr1:89160111 | T | A | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(152): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.318+4620A>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89160111 | |||||||
| chr1:89160226 | G | T | 1 | a0001c0001t0001g0128 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.318+4505C>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89160226 | |||||||
| chr1:89160299 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.318+4432C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89160299 | |||||||
| chr1:89160416 | G | A | 1 | a0002c0002t0002g0188 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.318+4315C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89160416 | |||||||
| chr1:89160480 | T | C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(152): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.318+4251A>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89160480 | |||||||
| chr1:89160525 | A | G | 1 | a0002c0003t0003g0085 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.318+4206T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89160525 | |||||||
| chr1:89161009 | C | T | 1 | a0007c0013t0002g0154 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.318+3722G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89161009 | |||||||
| chr1:89161243 | C | T | 1 | a0007c0013t0002g0154 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.318+3488G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89161243 | |||||||
| chr1:89161430 | C | T | 1 | a0002c0002t0002g0166 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.318+3301G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89161430 | |||||||
| chr1:89161459 | A | G | 1 | a0001c0001t0001g0127 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.318+3272T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89161459 | |||||||
| chr1:89161549 | A | G | 3 | a0001c0001t0001g0014 a0001c0001t0001g0123 a0001c0001t0001g0126 |
6 | HG00609.hp2 NA18968.hp2 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.318+3182T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89161549 | |||||||
| chr1:89161554 | T | G | 2 | a0006c0006t0002g0035 a0006c0006t0002g0091 |
3 | HG02717.hp2 HG02723.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.318+3177A>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89161554 | |||||||
| chr1:89161628 | G | T | 1 | a0001c0001t0001g0125 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.318+3103C>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89161628 | |||||||
| chr1:89161787 | C | T | 1 | a0002c0002t0002g0165 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.318+2944G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89161787 | |||||||
| chr1:89161830 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.318+2901C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89161830 | |||||||
| chr1:89161908 | A | G | 2 | a0006c0006t0002g0035 a0006c0006t0002g0091 |
3 | HG02717.hp2 HG02723.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.318+2823T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89161908 | |||||||
| chr1:89162042 | C | CT | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(137): Show |
263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.318+2688dupA | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89162042 | |||||||
| chr1:89162293 | T | C | 2 | a0001c0001t0001g0051 a0001c0001t0001g0153 |
3 | HG02145.hp2 HG02809.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.318+2438A>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89162293 | |||||||
| chr1:89162335 | G | C | 3 | a0006c0006t0002g0035 a0006c0006t0002g0091 a0007c0013t0002g0154 |
4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.318+2396C>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89162335 | |||||||
| chr1:89162474 | C | G | 1 | a0001c0001t0001g0048 | 2 | NA18999.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.318+2257G>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89162474 | |||||||
| chr1:89162839 | C | T | 1 | a0007c0013t0002g0154 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.318+1892G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89162839 | |||||||
| chr1:89162991 | A | G | 2 | a0001c0001t0001g0102 a0001c0001t0004g0018 |
4 | HG01993.hp2 HG02735.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.318+1740T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89162991 | |||||||
| chr1:89163230 | T | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(52): Show |
108 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.318+1501A>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89163230 | |||||||
| chr1:89163236 | T | A | 2 | a0006c0006t0002g0035 a0006c0006t0002g0091 |
3 | HG02717.hp2 HG02723.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.318+1495A>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89163236 | |||||||
| chr1:89163254 | G | T | 1 | a0007c0013t0002g0154 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.318+1477C>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89163254 | |||||||
| chr1:89163396 | C | CT | 5 | a0001c0001t0001g0102 a0002c0002t0002g0163 a0002c0002t0002g0164 others(2): Show |
6 | HG00639.hp2 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.318+1334dupA | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89163396 | |||||||
| chr1:89163597 | AC | A | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(152): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.318+1133delG | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89163597 | |||||||
| chr1:89163602 | C | A | 1 | a0007c0013t0002g0154 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.318+1129G>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89163602 | |||||||
| chr1:89163911 | T | C | 2 | a0004c0005t0001g0037 a0004c0005t0001g0093 |
3 | HG03516.hp2 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.318+820A>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89163911 | |||||||
| chr1:89163958 | T | C | 3 | a0006c0006t0002g0035 a0006c0006t0002g0091 a0007c0013t0002g0154 |
4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.318+773A>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89163958 | |||||||
| chr1:89164178 | C | T | 5 | a0001c0001t0002g0146 a0001c0001t0002g0147 a0001c0001t0002g0202 others(2): Show |
5 | HG02896.hp2 HG02897.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.318+553G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89164178 | |||||||
| chr1:89164248 | A | G | 3 | a0006c0006t0002g0035 a0006c0006t0002g0091 a0007c0013t0002g0154 |
4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.318+483T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89164248 | |||||||
| chr1:89164363 | C | A | 1 | a0007c0013t0002g0154 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.318+368G>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89164363 | |||||||
| chr1:89164456 | T | G | 2 | a0006c0006t0002g0035 a0006c0006t0002g0091 |
3 | HG02717.hp2 HG02723.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.318+275A>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89164456 | |||||||
| chr1:89164648 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.318+83G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89164648 | |||||||
| chr1:89164691 | A | T | 1 | a0001c0001t0001g0101 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.318+40T>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 3/10 | chr1 | 89164691 | |||||||
| chr1:89164860 | T | C | 1 | a0007c0013t0002g0154 | 1 | HG02630.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.191-2A>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89164860 | |||||||
| chr1:89164935 | A | G | 1 | a0002c0002t0002g0163 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.191-77T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89164935 | |||||||
| chr1:89165038 | G | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(52): Show |
108 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.191-180C>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89165038 | |||||||
| chr1:89165372 | C | T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0100 |
3 | HG00408.hp2 HG00673.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.191-514G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89165372 | |||||||
| chr1:89165405 | T | C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(152): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.191-547A>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89165405 | |||||||
| chr1:89165500 | C | CA | 11 | a0001c0001t0003g0026 a0001c0001t0003g0060 a0001c0001t0003g0061 others(8): Show |
13 | HG01074.hp2 HG01256.hp2 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.191-643dupT | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89165500 | |||||||
| chr1:89165500 | C | CAA | 8 | a0001c0001t0003g0027 a0001c0001t0003g0030 a0001c0001t0003g0062 others(5): Show |
13 | HG02145.hp1 HG02622.hp1 HG02895.hp1 others(10): Show |
intron_variant | MODIFIER | c.191-644_191-643dup others(2): Show |
GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89165500 | |||||||
| chr1:89165507 | A | AG | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(128): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.191-650_191-649ins others(1): Show |
GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89165507 | |||||||
| chr1:89165510 | G | A | 4 | a0005c0008t0003g0028 a0005c0008t0003g0064 a0006c0006t0002g0035 others(1): Show |
6 | HG01109.hp2 HG02615.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.191-652C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89165510 | |||||||
| chr1:89165510 | GA | G | 8 | a0002c0002t0002g0003 a0002c0002t0002g0053 a0002c0002t0002g0054 others(5): Show |
21 | HG00609.hp1 HG01099.hp1 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.191-653delT | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89165510 | |||||||
| chr1:89165513 | A | G | 9 | a0001c0001t0002g0047 a0001c0001t0002g0146 a0001c0001t0002g0147 others(6): Show |
10 | HG02257.hp2 HG02723.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.191-655T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89165513 | |||||||
| chr1:89165551 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.191-693G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89165551 | |||||||
| chr1:89165755 | A | G | 1 | a0007c0013t0002g0154 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.191-897T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89165755 | |||||||
| chr1:89165913 | C | T | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(153): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.191-1055G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89165913 | |||||||
| chr1:89165978 | C | A | 1 | a0001c0001t0001g0199 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.191-1120G>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89165978 | |||||||
| chr1:89166059 | C | T | 1 | a0002c0002t0002g0158 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.191-1201G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89166059 | |||||||
| chr1:89166317 | GA | G | 2 | a0004c0005t0001g0037 a0004c0005t0001g0093 |
3 | HG03516.hp2 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.191-1460delT | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89166317 | |||||||
| chr1:89166609 | A | C | 2 | a0006c0006t0002g0035 a0006c0006t0002g0091 |
3 | HG02717.hp2 HG02723.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.191-1751T>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89166609 | |||||||
| chr1:89166711 | T | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(152): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.191-1853A>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89166711 | |||||||
| chr1:89166894 | T | C | 1 | a0007c0013t0002g0154 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.191-2036A>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89166894 | |||||||
| chr1:89167044 | A | C | 1 | a0001c0001t0001g0099 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.191-2186T>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89167044 | |||||||
| chr1:89167171 | A | G | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(142): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.191-2313T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89167171 | |||||||
| chr1:89167179 | CT | C | 6 | a0002c0003t0003g0031 a0002c0003t0003g0085 a0002c0003t0003g0086 others(3): Show |
7 | HG01074.hp2 HG01256.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.191-2322delA | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89167179 | |||||||
| chr1:89167332 | G | A | 3 | a0004c0005t0001g0037 a0004c0005t0001g0093 a0004c0005t0001g0190 |
4 | HG02965.hp1 HG03516.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.191-2474C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89167332 | |||||||
| chr1:89167429 | T | TTTTGTTT others(1): Show |
3 | a0006c0006t0002g0035 a0006c0006t0002g0091 a0007c0013t0002g0154 |
4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.191-2579_191-2572d others(10): Show |
GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89167429 | |||||||
| chr1:89167524 | T | A | 1 | a0001c0001t0001g0144 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.191-2666A>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89167524 | |||||||
| chr1:89167527 | T | C | 1 | a0001c0001t0001g0144 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.191-2669A>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89167527 | |||||||
| chr1:89167529 | C | CCCAGAAG others(7): Show |
1 | a0001c0001t0001g0144 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.191-2672_191-2671i others(16): Show |
GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89167529 | |||||||
| chr1:89167534 | G | T | 1 | a0001c0001t0001g0144 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.191-2676C>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89167534 | |||||||
| chr1:89167536 | A | T | 1 | a0001c0001t0001g0144 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.191-2678T>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89167536 | |||||||
| chr1:89167538 | A | T | 1 | a0001c0001t0001g0144 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.191-2680T>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89167538 | |||||||
| chr1:89167544 | C | G | 1 | a0001c0001t0001g0144 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.191-2686G>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89167544 | |||||||
| chr1:89167548 | A | G | 1 | a0001c0001t0001g0144 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.191-2690T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89167548 | |||||||
| chr1:89167552 | A | G | 1 | a0001c0001t0001g0144 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.191-2694T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89167552 | |||||||
| chr1:89167553 | A | C | 1 | a0001c0001t0001g0144 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.191-2695T>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89167553 | |||||||
| chr1:89167556 | T | A | 1 | a0001c0001t0001g0144 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.191-2698A>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89167556 | |||||||
| chr1:89167568 | A | C | 1 | a0001c0001t0001g0144 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.191-2710T>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89167568 | |||||||
| chr1:89167569 | C | A | 1 | a0001c0001t0001g0144 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.191-2711G>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89167569 | |||||||
| chr1:89167580 | G | C | 3 | a0001c0001t0001g0144 a0006c0006t0002g0035 a0006c0006t0002g0091 |
4 | HG02717.hp2 HG02723.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.191-2722C>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89167580 | |||||||
| chr1:89167584 | A | T | 1 | a0001c0001t0001g0144 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.191-2726T>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89167584 | |||||||
| chr1:89167592 | A | T | 1 | a0001c0001t0001g0144 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.191-2734T>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89167592 | |||||||
| chr1:89167594 | A | G | 1 | a0001c0001t0001g0144 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.191-2736T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89167594 | |||||||
| chr1:89167597 | A | T | 1 | a0001c0001t0001g0144 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.191-2739T>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89167597 | |||||||
| chr1:89167599 | T | A | 1 | a0001c0001t0001g0144 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.191-2741A>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89167599 | |||||||
| chr1:89167600 | T | G | 1 | a0001c0001t0001g0144 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.191-2742A>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89167600 | |||||||
| chr1:89167603 | A | G | 1 | a0001c0001t0001g0144 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.191-2745T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89167603 | |||||||
| chr1:89167615 | A | T | 3 | a0001c0001t0001g0144 a0006c0006t0002g0035 a0006c0006t0002g0091 |
4 | HG02717.hp2 HG02723.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.191-2757T>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89167615 | |||||||
| chr1:89167619 | A | T | 1 | a0001c0001t0001g0144 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.191-2761T>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89167619 | |||||||
| chr1:89167628 | T | C | 1 | a0001c0001t0001g0144 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.191-2770A>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89167628 | |||||||
| chr1:89167630 | C | T | 15 | a0001c0001t0001g0046 a0001c0001t0001g0074 a0001c0001t0001g0143 others(12): Show |
17 | HG01891.hp1 HG02055.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.191-2772G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89167630 | |||||||
| chr1:89167634 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.191-2776G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89167634 | |||||||
| chr1:89167638 | G | C | 1 | a0001c0001t0001g0144 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.191-2780C>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89167638 | |||||||
| chr1:89167639 | A | C | 1 | a0001c0001t0001g0144 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.191-2781T>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89167639 | |||||||
| chr1:89167641 | G | A | 1 | a0001c0001t0001g0144 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.191-2783C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89167641 | |||||||
| chr1:89167648 | T | G | 1 | a0001c0001t0001g0144 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.191-2790A>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89167648 | |||||||
| chr1:89167652 | T | C | 1 | a0001c0001t0001g0144 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.191-2794A>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89167652 | |||||||
| chr1:89167654 | GTGTGAAG others(3): Show |
G | 1 | a0001c0001t0001g0144 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.191-2806_191-2797d others(12): Show |
GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89167654 | |||||||
| chr1:89167669 | G | A | 1 | a0001c0001t0001g0144 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.191-2811C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89167669 | |||||||
| chr1:89167671 | C | A | 1 | a0001c0001t0001g0144 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.191-2813G>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89167671 | |||||||
| chr1:89167674 | T | C | 1 | a0001c0001t0001g0144 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.191-2816A>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89167674 | |||||||
| chr1:89167675 | G | A | 1 | a0001c0001t0001g0144 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.191-2817C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89167675 | |||||||
| chr1:89167676 | G | A | 1 | a0001c0001t0001g0144 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.191-2818C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89167676 | |||||||
| chr1:89167682 | C | G | 1 | a0001c0001t0001g0144 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.191-2824G>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89167682 | |||||||
| chr1:89167683 | A | C | 1 | a0001c0001t0001g0144 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.191-2825T>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89167683 | |||||||
| chr1:89167685 | G | T | 1 | a0001c0001t0001g0144 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.191-2827C>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89167685 | |||||||
| chr1:89167693 | T | G | 1 | a0001c0001t0001g0144 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.191-2835A>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89167693 | |||||||
| chr1:89167694 | T | G | 1 | a0001c0001t0001g0144 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.191-2836A>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89167694 | |||||||
| chr1:89167711 | T | G | 1 | a0001c0001t0001g0144 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.191-2853A>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89167711 | |||||||
| chr1:89167750 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.191-2892C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89167750 | |||||||
| chr1:89167850 | A | G | 1 | a0001c0001t0001g0123 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.191-2992T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89167850 | |||||||
| chr1:89167974 | G | A | 2 | a0001c0001t0001g0200 a0001c0001t0003g0201 |
2 | HG02257.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.191-3116C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89167974 | |||||||
| chr1:89168019 | C | A | 3 | a0006c0006t0002g0035 a0006c0006t0002g0091 a0007c0013t0002g0154 |
4 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.191-3161G>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89168019 | |||||||
| chr1:89168019 | C | T | 1 | a0002c0002t0002g0157 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.191-3161G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89168019 | |||||||
| chr1:89168258 | A | G | 5 | a0002c0003t0003g0031 a0002c0003t0003g0085 a0002c0003t0003g0086 others(2): Show |
6 | HG01074.hp2 HG01256.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.191-3400T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89168258 | |||||||
| chr1:89168318 | G | C | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG00280.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.190+3428C>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89168318 | |||||||
| chr1:89168548 | C | A | 2 | a0002c0002t0002g0025 a0002c0002t0002g0189 |
4 | HG00323.hp1 HG00408.hp1 NA18943.hp2 others(1): Show |
intron_variant | MODIFIER | c.190+3198G>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89168548 | |||||||
| chr1:89168639 | C | T | 3 | a0001c0001t0003g0026 a0001c0001t0003g0060 a0001c0001t0003g0061 |
4 | HG02896.hp1 HG03098.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.190+3107G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89168639 | |||||||
| chr1:89168741 | C | A | 3 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0084 |
5 | HG00323.hp2 NA18957.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.190+3005G>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89168741 | |||||||
| chr1:89168781 | A | AAAC | 55 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(52): Show |
107 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.190+2962_190+2964d others(5): Show |
GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89168781 | |||||||
| chr1:89168781 | A | AAACAAC | 5 | a0001c0001t0001g0022 a0001c0001t0001g0122 a0001c0001t0003g0026 others(2): Show |
8 | HG02896.hp1 HG03098.hp1 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.190+2959_190+2964d others(8): Show |
GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89168781 | |||||||
| chr1:89168781 | AAAC | A | 12 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0045 others(9): Show |
29 | HG01515.hp1 HG02015.hp1 HG02056.hp1 others(26): Show |
intron_variant | MODIFIER | c.190+2962_190+2964d others(5): Show |
GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89168781 | |||||||
| chr1:89168971 | AGTT | A | 2 | a0006c0006t0002g0035 a0006c0006t0002g0091 |
3 | HG02717.hp2 HG02723.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.190+2772_190+2774d others(5): Show |
GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89168971 | |||||||
| chr1:89168974 | T | TAA | 6 | a0002c0003t0003g0031 a0002c0003t0003g0085 a0002c0003t0003g0086 others(3): Show |
7 | HG01074.hp2 HG01256.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.190+2770_190+2771d others(4): Show |
GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89168974 | |||||||
| chr1:89168981 | A | AAC | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(127): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.190+2764_190+2765i others(4): Show |
GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89168981 | |||||||
| chr1:89168981 | A | C | 2 | a0001c0001t0001g0046 a0001c0001t0001g0155 |
3 | HG01891.hp1 HG02451.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.190+2765T>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89168981 | |||||||
| chr1:89168985 | C | A | 16 | a0001c0001t0003g0026 a0001c0001t0003g0027 a0001c0001t0003g0030 others(13): Show |
24 | HG01109.hp2 HG02145.hp1 HG02615.hp2 others(21): Show |
intron_variant | MODIFIER | c.190+2761G>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89168985 | |||||||
| chr1:89168988 | A | AAAC | 8 | a0001c0001t0003g0026 a0001c0001t0003g0027 a0001c0001t0003g0030 others(5): Show |
12 | HG01109.hp2 HG02615.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.190+2757_190+2758i others(5): Show |
GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89168988 | |||||||
| chr1:89168988 | A | AAC | 3 | a0003c0004t0003g0016 a0003c0004t0003g0029 a0003c0004t0003g0065 |
6 | HG02145.hp1 HG03139.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.190+2757_190+2758i others(4): Show |
GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89168988 | |||||||
| chr1:89168988 | A | AC | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(129): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.190+2757_190+2758i others(3): Show |
GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89168988 | |||||||
| chr1:89168992 | C | A | 2 | a0006c0006t0002g0035 a0006c0006t0002g0091 |
3 | HG02717.hp2 HG02723.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.190+2754G>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89168992 | |||||||
| chr1:89169083 | A | C | 1 | a0001c0001t0002g0047 | 2 | HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.190+2663T>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89169083 | |||||||
| chr1:89169332 | C | T | 2 | a0006c0006t0002g0035 a0006c0006t0002g0091 |
3 | HG02717.hp2 HG02723.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.190+2414G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89169332 | |||||||
| chr1:89169455 | C | T | 3 | a0003c0004t0003g0016 a0003c0004t0003g0029 a0003c0004t0003g0065 |
6 | HG02145.hp1 HG03139.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.190+2291G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89169455 | |||||||
| chr1:89169687 | T | C | 1 | a0007c0013t0002g0154 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.190+2059A>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89169687 | |||||||
| chr1:89169758 | A | G | 1 | a0002c0009t0003g0092 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.190+1988T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89169758 | |||||||
| chr1:89169781 | G | A | 2 | a0001c0001t0001g0051 a0001c0001t0001g0153 |
3 | HG02145.hp2 HG02809.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.190+1965C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89169781 | |||||||
| chr1:89169851 | T | C | 1 | a0007c0013t0002g0154 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.190+1895A>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89169851 | |||||||
| chr1:89169908 | G | A | 1 | a0001c0001t0003g0026 | 2 | HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.190+1838C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89169908 | |||||||
| chr1:89169951 | G | A | 1 | a0001c0001t0001g0120 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.190+1795C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89169951 | |||||||
| chr1:89170103 | A | G | 2 | a0001c0001t0001g0038 a0008c0012t0001g0098 |
3 | HG01891.hp2 HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.190+1643T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89170103 | |||||||
| chr1:89170240 | G | T | 1 | a0001c0001t0001g0097 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.190+1506C>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89170240 | |||||||
| chr1:89170310 | C | A | 1 | a0006c0006t0002g0091 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.190+1436G>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89170310 | |||||||
| chr1:89170407 | G | GA | 3 | a0001c0001t0003g0026 a0001c0001t0003g0060 a0001c0001t0003g0061 |
4 | HG02896.hp1 HG03098.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.190+1338dupT | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89170407 | |||||||
| chr1:89170599 | C | G | 1 | a0001c0001t0001g0191 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.190+1147G>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89170599 | |||||||
| chr1:89170751 | T | C | 1 | a0001c0001t0001g0059 | 2 | NA19000.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.190+995A>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89170751 | |||||||
| chr1:89170841 | C | T | 2 | a0001c0001t0001g0046 a0001c0001t0001g0155 |
3 | HG01891.hp1 HG02451.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.190+905G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89170841 | |||||||
| chr1:89170852 | C | T | 13 | a0001c0001t0003g0026 a0001c0001t0003g0027 a0001c0001t0003g0030 others(10): Show |
20 | HG01109.hp2 HG02145.hp1 HG02615.hp2 others(17): Show |
intron_variant | MODIFIER | c.190+894G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89170852 | |||||||
| chr1:89170859 | C | T | 1 | a0003c0004t0003g0029 | 2 | HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.190+887G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89170859 | |||||||
| chr1:89170994 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.190+752C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89170994 | |||||||
| chr1:89171188 | C | T | 1 | a0002c0002t0002g0156 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.190+558G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89171188 | |||||||
| chr1:89171264 | C | T | 59 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(56): Show |
122 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.190+482G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89171264 | |||||||
| chr1:89171293 | C | G | 1 | a0002c0002t0002g0052 | 2 | HG02630.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.190+453G>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89171293 | |||||||
| chr1:89171298 | T | A | 1 | a0002c0002t0002g0057 | 2 | NA18991.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.190+448A>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89171298 | |||||||
| chr1:89171395 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.190+351T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89171395 | |||||||
| chr1:89171711 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.190+35T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89171711 | |||||||
| chr1:89171741 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG03710.hp2 | splice_region_variant&intron_variant | LOW | c.190+5G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 2/10 | chr1 | 89171741 | |||||||
| chr1:89172300 | A | G | 2 | a0006c0006t0002g0035 a0006c0006t0002g0091 |
3 | HG02717.hp2 HG02723.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-19-346T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 1/10 | chr1 | 89172300 | |||||||
| chr1:89172309 | T | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(152): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.-19-355A>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 1/10 | chr1 | 89172309 | |||||||
| chr1:89172414 | C | T | 1 | a0001c0001t0001g0017 | 3 | HG00639.hp1 HG02572.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-19-460G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 1/10 | chr1 | 89172414 | |||||||
| chr1:89172428 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-19-474G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 1/10 | chr1 | 89172428 | |||||||
| chr1:89172595 | A | G | 1 | a0002c0002t0002g0090 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-19-641T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 1/10 | chr1 | 89172595 | |||||||
| chr1:89172631 | C | G | 6 | a0002c0003t0003g0031 a0002c0003t0003g0085 a0002c0003t0003g0086 others(3): Show |
7 | HG01074.hp2 HG01256.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19-677G>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 1/10 | chr1 | 89172631 | |||||||
| chr1:89172682 | G | C | 1 | a0001c0001t0001g0155 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-19-728C>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 1/10 | chr1 | 89172682 | |||||||
| chr1:89172760 | C | CT | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(134): Show |
250 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.-19-807dupA | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 1/10 | chr1 | 89172760 | |||||||
| chr1:89172970 | G | A | 1 | a0002c0002t0002g0203 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-19-1016C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 1/10 | chr1 | 89172970 | |||||||
| chr1:89173016 | T | A | 1 | a0001c0007t0001g0075 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-19-1062A>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 1/10 | chr1 | 89173016 | |||||||
| chr1:89173091 | G | A | 1 | a0002c0002t0002g0204 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-19-1137C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 1/10 | chr1 | 89173091 | |||||||
| chr1:89173284 | A | G | 5 | a0002c0003t0003g0031 a0002c0003t0003g0085 a0002c0003t0003g0086 others(2): Show |
6 | HG01074.hp2 HG01256.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19-1330T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 1/10 | chr1 | 89173284 | |||||||
| chr1:89173334 | A | G | 1 | a0002c0002t0002g0034 | 2 | HG03669.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.-19-1380T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 1/10 | chr1 | 89173334 | |||||||
| chr1:89173679 | A | G | 11 | a0001c0001t0001g0005 a0001c0001t0001g0032 a0001c0001t0001g0033 others(8): Show |
22 | HG00323.hp2 HG00735.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.-19-1725T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 1/10 | chr1 | 89173679 | |||||||
| chr1:89173814 | C | A | 1 | a0001c0001t0001g0205 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-19-1860G>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 1/10 | chr1 | 89173814 | |||||||
| chr1:89173833 | C | T | 1 | a0002c0002t0002g0077 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-19-1879G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 1/10 | chr1 | 89173833 | |||||||
| chr1:89173911 | A | C | 4 | a0001c0001t0003g0027 a0001c0001t0003g0063 a0005c0008t0003g0028 others(1): Show |
6 | HG01109.hp2 HG02615.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19-1957T>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 1/10 | chr1 | 89173911 | |||||||
| chr1:89173915 | A | C | 1 | a0001c0001t0001g0076 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-19-1961T>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 1/10 | chr1 | 89173915 | |||||||
| chr1:89174216 | C | T | 1 | a0001c0007t0001g0075 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-20+1705G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 1/10 | chr1 | 89174216 | |||||||
| chr1:89174276 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-20+1645G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 1/10 | chr1 | 89174276 | |||||||
| chr1:89174466 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-20+1455G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 1/10 | chr1 | 89174466 | |||||||
| chr1:89174673 | A | G | 2 | a0002c0002t0002g0071 a0002c0002t0002g0072 |
2 | HG04199.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-20+1248T>C | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 1/10 | chr1 | 89174673 | |||||||
| chr1:89174717 | C | T | 1 | a0002c0003t0003g0031 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-20+1204G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 1/10 | chr1 | 89174717 | |||||||
| chr1:89174793 | C | A | 2 | a0001c0001t0002g0206 a0001c0001t0002g0207 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-20+1128G>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 1/10 | chr1 | 89174793 | |||||||
| chr1:89175011 | G | T | 1 | a0001c0001t0001g0070 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-20+910C>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 1/10 | chr1 | 89175011 | |||||||
| chr1:89175147 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-20+774C>T | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 1/10 | chr1 | 89175147 | |||||||
| chr1:89175296 | C | T | 1 | a0001c0001t0003g0062 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-20+625G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 1/10 | chr1 | 89175296 | |||||||
| chr1:89175412 | A | C | 3 | a0001c0001t0003g0026 a0001c0001t0003g0060 a0001c0001t0003g0061 |
4 | HG02896.hp1 HG03098.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+509T>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 1/10 | chr1 | 89175412 | |||||||
| chr1:89175488 | C | T | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG00140.hp1 HG00642.hp1 |
intron_variant | MODIFIER | c.-20+433G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 1/10 | chr1 | 89175488 | |||||||
| chr1:89175732 | C | T | 1 | a0002c0002t0002g0067 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-20+189G>A | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 1/10 | chr1 | 89175732 | |||||||
| chr1:89175867 | A | C | 13 | a0001c0001t0003g0026 a0001c0001t0003g0027 a0001c0001t0003g0030 others(10): Show |
20 | HG01109.hp2 HG02145.hp1 HG02615.hp2 others(17): Show |
intron_variant | MODIFIER | c.-20+54T>G | GBP7 | ENSG00000213512.3 | transcript | ENST00000294671.3 | protein_coding | 1/10 | chr1 | 89175867 |