Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10956 |
| ensemblid | ENSG00000135506.17 |
| hgncid | 16994 |
| symbol | OS9 |
| name | OS9 endoplasmic reticulum lectin |
| refseq_nuc | NM_006812.4 |
| refseq_prot | NP_006803.1 |
| ensembl_nuc | ENST00000315970.12 |
| ensembl_prot | ENSP00000318165.7 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 57694132 |
| end | 57721557 |
| strand | + |
| ver | v1.2 |
| region | chr12:57694132-57721557 |
| region5000 | chr12:57689132-57726557 |
| regionname0 | OS9_chr12_57694132_57721557 |
| regionname5000 | OS9_chr12_57689132_57726557 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 667 | 338 | 93 | 64 | 123 | 14 | 42 | 87 | OS9_chr12_57689132_57726557 | OS9 | MAAET others(662): Show |
chr12 | 57689132 | 57726557 |
| a0002 | 0/0 | 667 | 6 | 0 | 0 | 6 | 0 | 0 | 6 | OS9_chr12_57689132_57726557 | OS9 | MAAET others(662): Show |
chr12 | 57689132 | 57726557 |
| a0003 | 0/0 | 667 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | MAAET others(662): Show |
chr12 | 57689132 | 57726557 |
| a0004 | 0/0 | 667 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | MAAET others(662): Show |
chr12 | 57689132 | 57726557 |
| a0005 | 0/0 | 667 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | MAAET others(662): Show |
chr12 | 57689132 | 57726557 |
| a0006 | 0/0 | 667 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | MAAET others(662): Show |
chr12 | 57689132 | 57726557 |
| a0007 | 0/0 | 667 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | MAAER others(662): Show |
chr12 | 57689132 | 57726557 |
| a0008 | 0/0 | 598 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | MAAET others(593): Show |
chr12 | 57689132 | 57726557 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2001 | 228 | 57 | 46 | 91 | 9 | 24 | OS9_chr12_57689132_57726557 | OS9 | ATGGC others(1996): Show |
chr12 | 57689132 | 57726557 | ||
| a0001c0002 | 0/1 | 2001 | 97 | 26 | 17 | 32 | 5 | 16 | OS9_chr12_57689132_57726557 | OS9 | ATGGC others(1996): Show |
chr12 | 57689132 | 57726557 | ||
| a0001c0003 | 0/0 | 2001 | 9 | 8 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | ATGGC others(1996): Show |
chr12 | 57689132 | 57726557 | ||
| a0001c0006 | 0/0 | 2001 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | ATGGC others(1996): Show |
chr12 | 57689132 | 57726557 | ||
| a0001c0010 | 0/0 | 2001 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | ATGGC others(1996): Show |
chr12 | 57689132 | 57726557 | ||
| a0001c0011 | 0/0 | 2001 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | ATGGC others(1996): Show |
chr12 | 57689132 | 57726557 | ||
| a0001c0013 | 0/0 | 2001 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | ATGGC others(1996): Show |
chr12 | 57689132 | 57726557 | ||
| a0002c0004 | 0/0 | 2001 | 6 | 0 | 0 | 6 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | ATGGC others(1996): Show |
chr12 | 57689132 | 57726557 | ||
| a0003c0005 | 0/0 | 2001 | 3 | 2 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | ATGGC others(1996): Show |
chr12 | 57689132 | 57726557 | ||
| a0004c0009 | 0/0 | 2001 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | ATGGC others(1996): Show |
chr12 | 57689132 | 57726557 | ||
| a0005c0007 | 0/0 | 2001 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | ATGGC others(1996): Show |
chr12 | 57689132 | 57726557 | ||
| a0006c0012 | 0/0 | 2001 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | ATGGC others(1996): Show |
chr12 | 57689132 | 57726557 | ||
| a0007c0014 | 0/0 | 2001 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | ATGGC others(1996): Show |
chr12 | 57689132 | 57726557 | ||
| a0008c0008 | 0/0 | 1991 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | ATGGC others(1986): Show |
chr12 | 57689132 | 57726557 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2682 | 227 | 57 | 45 | 91 | 9 | 24 | OS9_chr12_57689132_57726557 | OS9 | AGATT others(2677): Show |
chr12 | 57689132 | 57726557 |
| a0001c0001t0005 | 0/0 | 2682 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | AGATT others(2677): Show |
chr12 | 57689132 | 57726557 |
| a0001c0002t0002 | 0/1 | 2682 | 93 | 22 | 17 | 32 | 5 | 16 | OS9_chr12_57689132_57726557 | OS9 | AGATT others(2677): Show |
chr12 | 57689132 | 57726557 |
| a0001c0002t0003 | 0/0 | 2682 | 4 | 4 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | AGATT others(2677): Show |
chr12 | 57689132 | 57726557 |
| a0001c0003t0002 | 0/0 | 2682 | 9 | 8 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | AGATT others(2677): Show |
chr12 | 57689132 | 57726557 |
| a0001c0006t0001 | 0/0 | 2682 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | AGATT others(2677): Show |
chr12 | 57689132 | 57726557 |
| a0001c0010t0001 | 0/0 | 2682 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | AGATT others(2677): Show |
chr12 | 57689132 | 57726557 |
| a0001c0011t0001 | 0/0 | 2682 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | AGATT others(2677): Show |
chr12 | 57689132 | 57726557 |
| a0001c0013t0001 | 0/0 | 2682 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | AGATT others(2677): Show |
chr12 | 57689132 | 57726557 |
| a0002c0004t0002 | 0/0 | 2682 | 6 | 0 | 0 | 6 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | AGATT others(2677): Show |
chr12 | 57689132 | 57726557 |
| a0003c0005t0002 | 0/0 | 2682 | 3 | 2 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | AGATT others(2677): Show |
chr12 | 57689132 | 57726557 |
| a0004c0009t0001 | 0/0 | 2682 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | AGATT others(2677): Show |
chr12 | 57689132 | 57726557 |
| a0005c0007t0002 | 0/0 | 2682 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | AGATT others(2677): Show |
chr12 | 57689132 | 57726557 |
| a0006c0012t0001 | 0/0 | 2682 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | AGATT others(2677): Show |
chr12 | 57689132 | 57726557 |
| a0007c0014t0004 | 0/0 | 2682 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | AGATT others(2677): Show |
chr12 | 57689132 | 57726557 |
| a0008c0008t0001 | 0/0 | 2672 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | AGATT others(2667): Show |
chr12 | 57689132 | 57726557 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 16 | 1 | 5 | 8 | 0 | 2 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0003 | 0/0 | 8 | 1 | 5 | 1 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0004 | 0/0 | 7 | 0 | 2 | 5 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0007 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0091 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0001t0005g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0002 | 0/0 | 6 | 0 | 2 | 1 | 1 | 2 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0015 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0018 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0035 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0211 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0002t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0003t0002g0040 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0003t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0003t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0003t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0003t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0003t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0003t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0003t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0006t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0010t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0011t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0001c0013t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0002c0004t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0002c0004t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0002c0004t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0002c0004t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0002c0004t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0003c0005t0002g0002 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0003c0005t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0004c0009t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0005c0007t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0006c0012t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0007c0014t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| a0008c0008t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0002 | g0002 | EUR | GBR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | GBR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0060 | EUR | GBR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00140 | hp2 | a0001 | c0002 | t0002 | g0174 | EUR | GBR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00280 | hp1 | a0001 | c0002 | t0002 | g0223 | EUR | FIN | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0243 | EUR | FIN | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0212 | EUR | FIN | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0059 | EUR | FIN | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00408 | hp2 | a0001 | c0002 | t0002 | g0237 | EAS | CHS | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00423 | hp1 | a0001 | c0002 | t0002 | g0035 | EAS | CHS | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00544 | hp1 | a0001 | c0002 | t0002 | g0209 | EAS | CHS | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00544 | hp2 | a0001 | c0002 | t0002 | g0143 | EAS | CHS | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00621 | hp1 | a0001 | c0002 | t0002 | g0221 | EAS | CHS | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00735 | hp1 | a0001 | c0002 | t0002 | g0032 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00741 | hp1 | a0001 | c0002 | t0002 | g0189 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01070 | hp2 | a0001 | c0002 | t0002 | g0226 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01074 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01081 | hp2 | a0001 | c0002 | t0002 | g0015 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01106 | hp2 | a0001 | c0002 | t0002 | g0032 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0213 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01109 | hp2 | a0001 | c0003 | t0002 | g0040 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01167 | hp2 | a0004 | c0009 | t0001 | g0012 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01168 | hp1 | a0001 | c0002 | t0002 | g0187 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01175 | hp2 | a0001 | c0002 | t0002 | g0184 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0222 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01243 | hp1 | a0001 | c0002 | t0002 | g0218 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01243 | hp2 | a0003 | c0005 | t0002 | g0002 | AMR | PUR | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01258 | hp2 | a0001 | c0002 | t0002 | g0228 | AMR | CLM | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01261 | hp2 | a0001 | c0002 | t0002 | g0180 | AMR | CLM | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0217 | AMR | CLM | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | CLM | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01361 | hp1 | a0005 | c0007 | t0002 | g0167 | AMR | CLM | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01433 | hp2 | a0001 | c0002 | t0002 | g0177 | AMR | CLM | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01496 | hp2 | a0001 | c0002 | t0002 | g0181 | AMR | CLM | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0038 | EUR | IBS | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0071 | EUR | IBS | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0038 | EUR | IBS | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01517 | hp2 | a0001 | c0002 | t0002 | g0018 | EUR | IBS | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01884 | hp1 | a0001 | c0003 | t0002 | g0239 | AFR | ACB | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01891 | hp1 | a0001 | c0010 | t0001 | g0109 | AFR | ACB | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01891 | hp2 | a0001 | c0002 | t0003 | g0248 | AFR | ACB | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01978 | hp2 | a0001 | c0002 | t0002 | g0015 | AMR | PEL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02027 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | KHV | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02027 | hp2 | a0001 | c0002 | t0002 | g0198 | EAS | KHV | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02056 | hp1 | a0001 | c0002 | t0002 | g0158 | EAS | KHV | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02074 | hp1 | a0001 | c0002 | t0002 | g0164 | EAS | KHV | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02080 | hp1 | a0001 | c0002 | t0002 | g0015 | EAS | KHV | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02129 | hp1 | a0001 | c0002 | t0002 | g0183 | EAS | KHV | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0185 | EAS | KHV | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02165 | hp1 | a0001 | c0002 | t0002 | g0034 | EAS | CDX | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02165 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | CDX | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02280 | hp1 | a0003 | c0005 | t0002 | g0018 | AFR | ACB | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02293 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02300 | hp1 | a0006 | c0012 | t0001 | g0010 | AMR | PEL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02451 | hp1 | a0001 | c0002 | t0002 | g0219 | AFR | ACB | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02523 | hp2 | a0001 | c0002 | t0002 | g0179 | EAS | KHV | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02572 | hp2 | a0007 | c0014 | t0004 | g0055 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02602 | hp1 | a0001 | c0002 | t0002 | g0172 | SAS | PJL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02615 | hp1 | a0001 | c0002 | t0002 | g0157 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0037 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02683 | hp1 | a0001 | c0002 | t0002 | g0030 | SAS | PJL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02683 | hp2 | a0001 | c0006 | t0001 | g0056 | SAS | PJL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02698 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02717 | hp2 | a0001 | c0002 | t0002 | g0014 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02723 | hp2 | a0001 | c0002 | t0002 | g0231 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02735 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02809 | hp1 | a0001 | c0003 | t0002 | g0238 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02895 | hp1 | a0001 | c0002 | t0002 | g0224 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02897 | hp2 | a0001 | c0002 | t0002 | g0225 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0017 | AFR | ESN | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ESN | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02965 | hp1 | a0001 | c0002 | t0003 | g0247 | AFR | ESN | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ESN | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ESN | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03041 | hp2 | a0001 | c0003 | t0002 | g0191 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | MSL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03098 | hp2 | a0001 | c0002 | t0002 | g0037 | AFR | MSL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ESN | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03130 | hp2 | a0001 | c0002 | t0002 | g0216 | AFR | ESN | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03139 | hp1 | a0001 | c0002 | t0003 | g0249 | AFR | ESN | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03139 | hp2 | a0001 | c0002 | t0002 | g0014 | AFR | ESN | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | MSL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03225 | hp1 | a0001 | c0003 | t0002 | g0040 | AFR | MSL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03239 | hp2 | a0001 | c0002 | t0002 | g0197 | SAS | PJL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | MSL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03453 | hp2 | a0001 | c0002 | t0002 | g0159 | AFR | MSL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03486 | hp1 | a0001 | c0002 | t0002 | g0160 | AFR | MSL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03486 | hp2 | a0001 | c0013 | t0001 | g0090 | AFR | MSL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0030 | SAS | PJL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ESN | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03540 | hp2 | a0003 | c0005 | t0002 | g0002 | AFR | GWD | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | MSL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03579 | hp2 | a0001 | c0003 | t0002 | g0200 | AFR | MSL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0144 | SAS | PJL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03654 | hp2 | a0001 | c0011 | t0001 | g0039 | SAS | PJL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03669 | hp1 | a0001 | c0002 | t0002 | g0018 | SAS | PJL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | STU | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0163 | SAS | STU | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03704 | hp1 | a0001 | c0002 | t0002 | g0178 | SAS | PJL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03704 | hp2 | a0001 | c0002 | t0002 | g0173 | SAS | PJL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03710 | hp1 | a0001 | c0002 | t0002 | g0199 | SAS | PJL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03831 | hp1 | a0001 | c0002 | t0002 | g0168 | SAS | BEB | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03927 | hp2 | a0001 | c0002 | t0002 | g0166 | SAS | BEB | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | STU | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | STU | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0195 | SAS | BEB | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | BEB | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | STU | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | STU | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG04204 | hp1 | a0001 | c0002 | t0002 | g0196 | SAS | STU | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | STU | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | STU | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | STU | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18522 | hp1 | a0001 | c0002 | t0002 | g0036 | AFR | YRI | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | YRI | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | YRI | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18906 | hp2 | a0001 | c0002 | t0002 | g0017 | AFR | YRI | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18940 | hp2 | a0002 | c0004 | t0002 | g0186 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18946 | hp2 | a0001 | c0002 | t0002 | g0033 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18947 | hp1 | a0002 | c0004 | t0002 | g0016 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18957 | hp2 | a0001 | c0002 | t0002 | g0169 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0044 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0033 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18967 | hp2 | a0001 | c0002 | t0002 | g0208 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18969 | hp1 | a0001 | c0002 | t0002 | g0171 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18970 | hp2 | a0002 | c0004 | t0002 | g0016 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18971 | hp2 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0182 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18980 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18983 | hp1 | a0001 | c0002 | t0002 | g0043 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18985 | hp2 | a0002 | c0004 | t0002 | g0227 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18997 | hp1 | a0002 | c0004 | t0002 | g0188 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA18997 | hp2 | a0008 | c0008 | t0001 | g0146 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19010 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19030 | hp1 | a0001 | c0003 | t0002 | g0229 | AFR | LWK | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | LWK | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19043 | hp1 | a0001 | c0002 | t0002 | g0201 | AFR | LWK | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | LWK | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19054 | hp1 | a0001 | c0002 | t0002 | g0176 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19055 | hp2 | a0002 | c0004 | t0002 | g0251 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19058 | hp2 | a0001 | c0002 | t0002 | g0175 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19065 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19070 | hp2 | a0001 | c0002 | t0002 | g0170 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19082 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19088 | hp1 | a0001 | c0002 | t0002 | g0034 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19240 | hp1 | a0001 | c0003 | t0002 | g0190 | AFR | YRI | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA19240 | hp2 | a0001 | c0002 | t0003 | g0250 | AFR | YRI | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0220 | AFR | ASW | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ASW | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0161 | EUR | TSI | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA20752 | hp2 | a0001 | c0002 | t0002 | g0165 | EUR | TSI | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | GIH | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | GIH | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02486 | hp1 | a0001 | c0002 | t0002 | g0017 | AFR | ACB | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02559 | hp1 | a0001 | c0002 | t0002 | g0014 | AFR | ACB | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG02559 | hp2 | a0001 | c0002 | t0002 | g0036 | AFR | ACB | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | MSL | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG06807 | hp1 | a0001 | c0003 | t0002 | g0230 | AFR | USA | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| HG06807 | hp2 | a0001 | c0002 | t0002 | g0215 | AFR | USA | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA20300 | hp1 | a0001 | c0002 | t0002 | g0035 | AFR | USA | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | USA | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | LWK | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | LWK | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0002 | g0211 | REF | REF | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0091 | REF | REF | OS9_chr12_57689132_57726557 | OS9 | chr12 | 57689132 | 57726557 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:57694175 | C | G | 1 | a0007 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.14C>G | p.Thr5Arg | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 1/15 | 44/2682 | 14/2004 | 5/667 | chr12 | 57694175 | |||
| chr12:57694900 | A | G | 1 | a0006 | 1 | HG02300.hp1 | missense_variant | MODERATE | c.313A>G | p.Met105Val | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 2/15 | 343/2682 | 313/2004 | 105/667 | chr12 | 57694900 | |||
| chr12:57716432 | G | A | 1 | a0002 | 6 | NA18940.hp2 NA18947.hp1 NA18970.hp2 others(3): Show |
missense_variant | MODERATE | c.913G>A | p.Asp305Asn | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 8/15 | 943/2682 | 913/2004 | 305/667 | chr12 | 57716432 | |||
| chr12:57718278 | G | A | 1 | a0005 | 1 | HG01361.hp1 | missense_variant | MODERATE | c.1267G>A | p.Glu423Lys | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 11/15 | 1297/2682 | 1267/2004 | 423/667 | chr12 | 57718278 | |||
| chr12:57718372 | C | T | 1 | a0003 | 3 | HG01243.hp2 HG02280.hp1 HG03540.hp2 |
missense_variant | MODERATE | c.1361C>T | p.Ser454Leu | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 11/15 | 1391/2682 | 1361/2004 | 454/667 | chr12 | 57718372 | |||
| chr12:57720435 | TGGGCTGA others(3): Show |
T | 1 | a0008 | 1 | NA18997.hp2 | frameshift_variant | HIGH | c.1797_1806delGGCTGA others(4): Show |
p.Trp599fs | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 14/15 | 1827/2682 | 1797/2004 | 599/667 | INFO_REALIGN_3_PRIME | chr12 | 57720435 | ||
| chr12:57720496 | A | G | 1 | a0008 | 1 | NA18997.hp2 | missense_variant | MODERATE | c.1856A>G | p.Lys619Arg | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 14/15 | 1886/2682 | 1856/2004 | 619/667 | chr12 | 57720496 | |||
| chr12:57720514 | T | G | 1 | a0008 | 1 | NA18997.hp2 | missense_variant | MODERATE | c.1874T>G | p.Ile625Ser | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 14/15 | 1904/2682 | 1874/2004 | 625/667 | chr12 | 57720514 | |||
| chr12:57720851 | G | A | 1 | a0004 | 1 | HG01167.hp2 | missense_variant | MODERATE | c.1946G>A | p.Arg649Gln | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 15/15 | 1976/2682 | 1946/2004 | 649/667 | chr12 | 57720851 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:57694207 | C | T | 1 | a0001c0013 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.46C>T | p.Leu16Leu | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 1/15 | 76/2682 | 46/2004 | 16/667 | chr12 | 57694207 | |||
| chr12:57694302 | G | A | 1 | a0001c0003 | 9 | HG01109.hp2 HG01884.hp1 HG02809.hp1 others(6): Show |
synonymous_variant | LOW | c.141G>A | p.Pro47Pro | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 1/15 | 171/2682 | 141/2004 | 47/667 | chr12 | 57694302 | |||
| chr12:57715924 | T | G | 1 | a0001c0006 | 1 | HG02683.hp2 | synonymous_variant | LOW | c.744T>G | p.Pro248Pro | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 6/15 | 774/2682 | 744/2004 | 248/667 | chr12 | 57715924 | |||
| chr12:57717883 | C | T | 1 | a0001c0011 | 1 | HG03654.hp2 | synonymous_variant | LOW | c.1059C>T | p.Asn353Asn | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 10/15 | 1089/2682 | 1059/2004 | 353/667 | chr12 | 57717883 | |||
| chr12:57718406 | A | G | 6 | a0001c0002 a0001c0003 a0002c0004 others(3): Show |
116 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(113): Show |
synonymous_variant | LOW | c.1395A>G | p.Glu465Glu | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 11/15 | 1425/2682 | 1395/2004 | 465/667 | chr12 | 57718406 | |||
| chr12:57719082 | C | T | 1 | a0001c0010 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.1500C>T | p.Leu500Leu | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 12/15 | 1530/2682 | 1500/2004 | 500/667 | chr12 | 57719082 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:57694143 | A | G | 1 | a0001c0001t0005 | 1 | HG01109.hp1 | 5_prime_UTR_variant | MODIFIER | c.-19A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 1/15 | 19 | chr12 | 57694143 | ||||||
| chr12:57721382 | C | T | 1 | a0007c0014t0004 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*473C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 15/15 | 473 | chr12 | 57721382 | ||||||
| chr12:57721426 | C | G | 1 | a0001c0002t0003 | 4 | HG01891.hp2 HG02965.hp1 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*517C>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 15/15 | 517 | chr12 | 57721426 | ||||||
| chr12:57721488 | T | C | 5 | a0001c0002t0002 a0001c0003t0002 a0002c0004t0002 others(2): Show |
111 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*579T>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 15/15 | 579 | chr12 | 57721488 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:57694554 | C | T | 2 | a0001c0001t0001g0257 a0001c0001t0001g0258 |
2 | NA18943.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.163-196C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 1/14 | chr12 | 57694554 | |||||||
| chr12:57694622 | T | C | 1 | a0001c0001t0001g0042 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.163-128T>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 1/14 | chr12 | 57694622 | |||||||
| chr12:57694728 | C | A | 2 | a0001c0002t0002g0043 a0001c0002t0002g0044 |
2 | NA18959.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.163-22C>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 1/14 | chr12 | 57694728 | |||||||
| chr12:57695048 | A | T | 1 | a0001c0001t0001g0256 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.339+122A>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 2/14 | chr12 | 57695048 | |||||||
| chr12:57695228 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.339+302C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 2/14 | chr12 | 57695228 | |||||||
| chr12:57695248 | T | G | 2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.339+322T>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 2/14 | chr12 | 57695248 | |||||||
| chr12:57695460 | T | G | 4 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(1): Show |
4 | HG02109.hp2 HG02145.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.340-320T>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 2/14 | chr12 | 57695460 | |||||||
| chr12:57695513 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.340-267C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 2/14 | chr12 | 57695513 | |||||||
| chr12:57695595 | A | G | 1 | a0001c0001t0001g0254 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.340-185A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 2/14 | chr12 | 57695595 | |||||||
| chr12:57695596 | G | A | 2 | a0001c0001t0001g0051 a0001c0001t0001g0052 |
2 | HG01168.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.340-184G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 2/14 | chr12 | 57695596 | |||||||
| chr12:57695630 | A | T | 125 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(122): Show |
165 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.340-150A>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 2/14 | chr12 | 57695630 | |||||||
| chr12:57695906 | C | T | 10 | a0001c0001t0001g0031 a0001c0001t0001g0148 a0001c0001t0001g0149 others(7): Show |
11 | HG02145.hp2 HG02622.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.404-56C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 3/14 | chr12 | 57695906 | |||||||
| chr12:57695921 | C | T | 3 | a0001c0001t0001g0013 a0001c0001t0001g0147 a0008c0008t0001g0146 |
5 | NA18983.hp2 NA18997.hp2 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.404-41C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 3/14 | chr12 | 57695921 | |||||||
| chr12:57695946 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.404-16G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 3/14 | chr12 | 57695946 | |||||||
| chr12:57696209 | G | C | 1 | a0001c0001t0001g0054 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.481-66G>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 4/14 | chr12 | 57696209 | |||||||
| chr12:57696268 | T | C | 5 | a0001c0002t0002g0014 a0001c0002t0002g0157 a0001c0002t0002g0158 others(2): Show |
7 | HG02056.hp1 HG02559.hp1 HG02615.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.481-7T>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 4/14 | chr12 | 57696268 | |||||||
| chr12:57696449 | AGTCGG | A | 66 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0161 others(63): Show |
89 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.579+78_579+82delTC others(3): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57696449 | ||||||
| chr12:57696451 | T | G | 59 | a0001c0001t0001g0003 a0001c0001t0001g0038 a0001c0001t0001g0039 others(56): Show |
76 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.579+78T>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57696451 | |||||||
| chr12:57696453 | GGGGC | G | 14 | a0001c0002t0002g0043 a0001c0002t0002g0044 a0001c0002t0002g0218 others(11): Show |
15 | HG00408.hp2 HG00621.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.579+84_579+87delCG others(2): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57696453 | ||||||
| chr12:57696456 | GCGGGGGC | G | 35 | a0001c0001t0001g0003 a0001c0001t0001g0038 a0001c0001t0001g0039 others(32): Show |
51 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.579+84_579+90delCG others(5): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57696456 | |||||||
| chr12:57696457 | C | G | 1 | a0001c0002t0003g0247 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.579+84C>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57696457 | |||||||
| chr12:57696462 | GC | G | 38 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0161 others(35): Show |
51 | HG00099.hp1 HG00140.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.579+90delC | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57696462 | |||||||
| chr12:57696463 | C | A | 2 | a0001c0002t0002g0222 a0003c0005t0002g0018 |
2 | HG01192.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.579+90C>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57696463 | |||||||
| chr12:57696463 | C | G | 53 | a0001c0001t0001g0006 a0001c0001t0001g0194 a0001c0001t0001g0202 others(50): Show |
57 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.579+90C>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57696463 | |||||||
| chr12:57696464 | G | A | 1 | a0007c0014t0004g0055 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.579+91G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57696464 | |||||||
| chr12:57696518 | G | A | 46 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(43): Show |
75 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.579+145G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57696518 | |||||||
| chr12:57696656 | C | T | 1 | a0001c0001t0001g0087 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.579+283C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57696656 | |||||||
| chr12:57696727 | C | T | 1 | a0001c0001t0001g0145 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.579+354C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57696727 | |||||||
| chr12:57696819 | C | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0156 |
3 | HG02622.hp1 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.579+446C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57696819 | |||||||
| chr12:57696939 | A | G | 233 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(230): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.579+566A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57696939 | |||||||
| chr12:57697256 | T | G | 3 | a0001c0001t0001g0161 a0001c0001t0001g0212 a0001c0001t0005g0213 |
3 | HG00323.hp1 HG01109.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.579+883T>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57697256 | |||||||
| chr12:57697333 | A | G | 3 | a0001c0002t0002g0030 a0001c0002t0002g0143 a0001c0002t0002g0144 |
4 | HG00544.hp2 HG02683.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.579+960A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57697333 | |||||||
| chr12:57697365 | A | C | 1 | a0007c0014t0004g0055 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.579+992A>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57697365 | |||||||
| chr12:57697489 | A | T | 1 | a0007c0014t0004g0055 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.579+1116A>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57697489 | |||||||
| chr12:57697612 | T | C | 1 | a0007c0014t0004g0055 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.579+1239T>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57697612 | |||||||
| chr12:57697627 | T | C | 2 | a0001c0001t0001g0162 a0001c0001t0001g0214 |
2 | HG02602.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.579+1254T>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57697627 | |||||||
| chr12:57697697 | A | G | 3 | a0001c0001t0001g0210 a0001c0001t0001g0252 a0001c0001t0001g0253 |
3 | NA18948.hp2 NA18965.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.579+1324A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57697697 | |||||||
| chr12:57697862 | A | AAC | 36 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0025 others(33): Show |
46 | HG00558.hp1 HG00597.hp1 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.579+1516_579+1517d others(4): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57697862 | ||||||
| chr12:57697862 | A | AACAC | 5 | a0001c0001t0001g0116 a0001c0002t0003g0247 a0001c0002t0003g0248 others(2): Show |
5 | HG00408.hp1 HG01891.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.579+1514_579+1517d others(6): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57697862 | ||||||
| chr12:57697862 | A | AACACAC | 22 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(19): Show |
37 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.579+1512_579+1517d others(8): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57697862 | ||||||
| chr12:57697862 | A | AACACACA others(1): Show |
5 | a0001c0001t0001g0115 a0001c0001t0001g0161 a0001c0001t0001g0202 others(2): Show |
5 | HG00323.hp1 HG01109.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.579+1510_579+1517d others(10): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57697862 | ||||||
| chr12:57697862 | A | AACACACA others(3): Show |
8 | a0001c0001t0001g0210 a0001c0001t0001g0252 a0001c0001t0001g0253 others(5): Show |
9 | HG01109.hp2 HG01884.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.579+1508_579+1517d others(12): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57697862 | ||||||
| chr12:57697862 | A | AACACACA others(5): Show |
25 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0162 others(22): Show |
26 | HG00408.hp2 HG00733.hp2 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.579+1506_579+1517d others(14): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57697862 | ||||||
| chr12:57697862 | A | AACACACA others(7): Show |
15 | a0001c0002t0002g0016 a0001c0002t0002g0043 a0001c0002t0002g0044 others(12): Show |
16 | HG00741.hp1 HG01070.hp2 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.579+1504_579+1517d others(16): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57697862 | ||||||
| chr12:57697862 | A | AACACACA others(9): Show |
36 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0014 others(33): Show |
52 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(49): Show |
intron_variant | MODIFIER | c.579+1502_579+1517d others(18): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57697862 | ||||||
| chr12:57697862 | A | AACACACA others(11): Show |
13 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(10): Show |
19 | HG01081.hp2 HG01346.hp2 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.579+1500_579+1517d others(20): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57697862 | ||||||
| chr12:57697862 | A | AACACACA others(13): Show |
4 | a0001c0001t0001g0047 a0001c0002t0002g0032 a0001c0002t0002g0163 others(1): Show |
5 | HG00735.hp1 HG01106.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.579+1498_579+1517d others(22): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57697862 | ||||||
| chr12:57697862 | A | ACACACAC others(8): Show |
1 | a0002c0004t0002g0251 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.579+1489_579+1490i others(17): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57697862 | |||||||
| chr12:57697862 | A | ACACACAC others(10): Show |
1 | a0001c0002t0002g0209 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.579+1489_579+1490i others(19): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57697862 | |||||||
| chr12:57697862 | A | ACACACAC others(12): Show |
1 | a0001c0001t0001g0142 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.579+1489_579+1490i others(21): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57697862 | |||||||
| chr12:57697889 | A | G | 1 | a0007c0014t0004g0055 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.579+1516A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57697889 | |||||||
| chr12:57697908 | A | C | 1 | a0001c0002t0002g0208 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.579+1535A>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57697908 | |||||||
| chr12:57697908 | AACACACA others(9): Show |
A | 8 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(5): Show |
8 | HG02055.hp1 HG02145.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.579+1551_579+1566d others(18): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57697908 | ||||||
| chr12:57697908 | AACACACA others(11): Show |
A | 12 | a0001c0001t0001g0162 a0001c0002t0002g0017 a0001c0002t0002g0037 others(9): Show |
15 | HG01243.hp1 HG01361.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.579+1551_579+1568d others(20): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57697908 | ||||||
| chr12:57697908 | AACACACA others(13): Show |
A | 33 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0115 others(30): Show |
38 | HG00621.hp1 HG00733.hp2 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.579+1551_579+1570d others(22): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57697908 | ||||||
| chr12:57697908 | AACACACA others(15): Show |
A | 76 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(73): Show |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.579+1551_579+1572d others(24): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57697908 | ||||||
| chr12:57697908 | AACACACA others(17): Show |
A | 1 | a0001c0002t0002g0185 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.579+1551_579+1574d others(26): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57697908 | ||||||
| chr12:57697910 | CACACACA others(7): Show |
C | 1 | a0001c0001t0001g0050 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.579+1551_579+1564d others(16): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57697910 | ||||||
| chr12:57697911 | ACACACAC others(14): Show |
A | 1 | a0001c0001t0001g0246 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.579+1539_579+1559d others(23): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57697911 | |||||||
| chr12:57697912 | C | A | 1 | a0007c0014t0004g0055 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.579+1539C>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57697912 | |||||||
| chr12:57697924 | T | C | 1 | a0001c0001t0001g0001 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.579+1551T>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57697924 | |||||||
| chr12:57697924 | T | TAC | 41 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(38): Show |
59 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.579+1592_579+1593d others(4): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57697924 | ||||||
| chr12:57697924 | T | TACAC | 27 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(24): Show |
30 | HG00099.hp2 HG00558.hp2 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.579+1590_579+1593d others(6): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57697924 | ||||||
| chr12:57697924 | T | TACACAC | 13 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0027 others(10): Show |
14 | HG00642.hp1 HG01934.hp2 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.579+1588_579+1593d others(8): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57697924 | ||||||
| chr12:57697924 | T | TACACACA others(1): Show |
7 | a0001c0001t0001g0020 a0001c0001t0001g0042 a0001c0001t0001g0045 others(4): Show |
7 | HG02257.hp1 HG02622.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.579+1586_579+1593d others(10): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57697924 | ||||||
| chr12:57697924 | T | TACACACA others(3): Show |
1 | a0001c0001t0001g0076 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.579+1584_579+1593d others(12): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57697924 | ||||||
| chr12:57697924 | TAC | T | 17 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(14): Show |
21 | HG00438.hp2 HG00558.hp1 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.579+1592_579+1593d others(4): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57697924 | ||||||
| chr12:57697924 | TACACACA others(3): Show |
T | 1 | a0001c0001t0001g0087 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.579+1584_579+1593d others(12): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57697924 | ||||||
| chr12:57697924 | TACACACA others(7): Show |
T | 11 | a0001c0001t0001g0023 a0001c0001t0001g0088 a0001c0001t0001g0089 others(8): Show |
13 | HG00544.hp2 HG01496.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.579+1580_579+1593d others(16): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57697924 | ||||||
| chr12:57697926 | C | A | 1 | a0001c0002t0002g0208 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.579+1553C>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57697926 | |||||||
| chr12:57697927 | A | G | 1 | a0001c0002t0002g0208 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.579+1554A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57697927 | |||||||
| chr12:57697928 | C | A | 3 | a0001c0003t0002g0190 a0001c0003t0002g0229 a0001c0003t0002g0238 |
3 | HG02809.hp1 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.579+1555C>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57697928 | |||||||
| chr12:57697930 | C | A | 12 | a0001c0001t0001g0162 a0001c0002t0002g0017 a0001c0002t0002g0208 others(9): Show |
14 | HG01243.hp1 HG01361.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.579+1557C>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57697930 | |||||||
| chr12:57697932 | C | A | 32 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0192 others(29): Show |
37 | HG00621.hp1 HG00733.hp2 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.579+1559C>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57697932 | |||||||
| chr12:57697934 | C | A | 77 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(74): Show |
109 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.579+1561C>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57697934 | |||||||
| chr12:57697936 | C | A | 1 | a0001c0002t0002g0185 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.579+1563C>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57697936 | |||||||
| chr12:57698071 | A | C | 2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.579+1698A>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57698071 | |||||||
| chr12:57698175 | T | C | 2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.579+1802T>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57698175 | |||||||
| chr12:57698216 | C | A | 1 | a0001c0001t0001g0142 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.579+1843C>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57698216 | |||||||
| chr12:57698230 | C | A | 1 | a0001c0002t0002g0208 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.579+1857C>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57698230 | |||||||
| chr12:57698233 | G | A | 3 | a0001c0001t0001g0053 a0001c0001t0001g0059 a0001c0001t0001g0060 |
3 | HG00140.hp1 HG00323.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.579+1860G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57698233 | |||||||
| chr12:57698305 | C | CACTT | 137 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(134): Show |
178 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.579+1933_579+1936d others(6): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57698305 | ||||||
| chr12:57698363 | T | A | 1 | a0001c0002t0002g0216 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.579+1990T>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57698363 | |||||||
| chr12:57698673 | C | T | 3 | a0001c0002t0002g0030 a0001c0002t0002g0143 a0001c0002t0002g0144 |
4 | HG00544.hp2 HG02683.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.579+2300C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57698673 | |||||||
| chr12:57698734 | G | T | 1 | a0001c0002t0002g0158 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.579+2361G>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57698734 | |||||||
| chr12:57698771 | A | G | 126 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(123): Show |
166 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.579+2398A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57698771 | |||||||
| chr12:57699168 | A | T | 2 | a0001c0001t0001g0140 a0001c0001t0001g0141 |
2 | HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.579+2795A>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57699168 | |||||||
| chr12:57699317 | T | G | 1 | a0001c0001t0001g0117 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.579+2944T>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57699317 | |||||||
| chr12:57699365 | C | A | 1 | a0001c0001t0001g0011 | 3 | HG03490.hp1 HG03492.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.579+2992C>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57699365 | |||||||
| chr12:57699393 | G | C | 1 | a0001c0001t0001g0088 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.579+3020G>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57699393 | |||||||
| chr12:57699710 | T | G | 1 | a0001c0001t0001g0061 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.579+3337T>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57699710 | |||||||
| chr12:57699824 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.579+3451G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57699824 | |||||||
| chr12:57699952 | G | A | 128 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(125): Show |
168 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.579+3579G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57699952 | |||||||
| chr12:57700026 | C | T | 1 | a0001c0001t0001g0214 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.579+3653C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57700026 | |||||||
| chr12:57700034 | G | A | 4 | a0001c0002t0002g0014 a0001c0002t0002g0157 a0001c0002t0002g0159 others(1): Show |
6 | HG02559.hp1 HG02615.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.579+3661G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57700034 | |||||||
| chr12:57700037 | G | A | 2 | a0001c0001t0001g0140 a0001c0001t0001g0141 |
2 | HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.579+3664G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57700037 | |||||||
| chr12:57700052 | A | G | 137 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(134): Show |
178 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.579+3679A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57700052 | |||||||
| chr12:57700279 | A | G | 2 | a0001c0001t0001g0114 a0001c0001t0001g0142 |
2 | HG02055.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.579+3906A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57700279 | |||||||
| chr12:57700315 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.579+3942A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57700315 | |||||||
| chr12:57700491 | G | A | 3 | a0001c0001t0001g0203 a0001c0001t0001g0241 a0001c0002t0002g0231 |
3 | HG01167.hp1 HG01175.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.579+4118G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57700491 | |||||||
| chr12:57700714 | C | T | 13 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0162 others(10): Show |
14 | HG00733.hp2 HG01070.hp1 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.579+4341C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57700714 | |||||||
| chr12:57700939 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.579+4566C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57700939 | |||||||
| chr12:57701026 | T | A | 3 | a0001c0002t0002g0224 a0001c0002t0002g0225 a0001c0002t0002g0231 |
3 | HG02723.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.579+4653T>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57701026 | |||||||
| chr12:57701081 | C | CT | 254 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(251): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.579+4708_579+4709i others(3): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57701081 | |||||||
| chr12:57701245 | G | T | 7 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(4): Show |
7 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.579+4872G>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57701245 | |||||||
| chr12:57701262 | A | AT | 10 | a0001c0001t0001g0024 a0001c0001t0001g0086 a0001c0001t0001g0093 others(7): Show |
11 | HG00621.hp2 HG00738.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.579+4920dupT | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57701262 | ||||||
| chr12:57701262 | AT | A | 33 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0026 others(30): Show |
42 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.579+4920delT | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57701262 | ||||||
| chr12:57701262 | ATT | A | 52 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(49): Show |
87 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.579+4919_579+4920d others(4): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57701262 | ||||||
| chr12:57701262 | ATTT | A | 9 | a0001c0001t0001g0045 a0001c0001t0001g0051 a0001c0001t0001g0062 others(6): Show |
9 | HG01168.hp2 HG02055.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.579+4918_579+4920d others(5): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57701262 | ||||||
| chr12:57701262 | ATTTTTTT | A | 27 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0162 others(24): Show |
30 | HG00423.hp1 HG00621.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.579+4914_579+4920d others(9): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57701262 | ||||||
| chr12:57701262 | ATTTTTTT others(1): Show |
A | 95 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(92): Show |
132 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.579+4913_579+4920d others(10): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57701262 | ||||||
| chr12:57701303 | T | C | 7 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(4): Show |
7 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.579+4930T>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57701303 | |||||||
| chr12:57701432 | C | T | 1 | a0001c0002t0002g0215 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.579+5059C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57701432 | |||||||
| chr12:57701439 | T | C | 11 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(8): Show |
12 | HG00544.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.579+5066T>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57701439 | |||||||
| chr12:57701468 | G | A | 2 | a0001c0001t0001g0140 a0001c0001t0001g0141 |
2 | HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.579+5095G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57701468 | |||||||
| chr12:57701627 | T | G | 1 | a0001c0001t0001g0064 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.579+5254T>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57701627 | |||||||
| chr12:57701658 | C | A | 11 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(8): Show |
12 | HG00544.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.579+5285C>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57701658 | |||||||
| chr12:57701788 | G | GTTTGT | 126 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(123): Show |
166 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.579+5434_579+5438d others(7): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57701788 | ||||||
| chr12:57701793 | T | TTTTGC | 8 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0028 others(5): Show |
14 | HG00609.hp2 HG00642.hp1 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.579+5424_579+5425i others(7): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57701793 | ||||||
| chr12:57701817 | A | G | 1 | a0001c0002t0002g0044 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.579+5444A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57701817 | |||||||
| chr12:57701986 | G | A | 3 | a0001c0002t0002g0030 a0001c0002t0002g0143 a0001c0002t0002g0144 |
4 | HG00544.hp2 HG02683.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.579+5613G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57701986 | |||||||
| chr12:57702028 | A | G | 11 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(8): Show |
12 | HG00544.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.579+5655A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57702028 | |||||||
| chr12:57702038 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.579+5665G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57702038 | |||||||
| chr12:57702134 | AG | A | 3 | a0001c0002t0002g0030 a0001c0002t0002g0143 a0001c0002t0002g0144 |
4 | HG00544.hp2 HG02683.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.579+5762delG | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57702134 | |||||||
| chr12:57702206 | T | C | 73 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0014 others(70): Show |
97 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.579+5833T>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57702206 | |||||||
| chr12:57702210 | C | T | 8 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(5): Show |
8 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.579+5837C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57702210 | |||||||
| chr12:57702270 | G | T | 1 | a0001c0002t0002g0216 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.579+5897G>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57702270 | |||||||
| chr12:57702302 | C | G | 1 | a0001c0002t0002g0181 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.579+5929C>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57702302 | |||||||
| chr12:57702364 | T | C | 1 | a0001c0002t0002g0172 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.579+5991T>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57702364 | |||||||
| chr12:57702606 | G | C | 8 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(5): Show |
8 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.579+6233G>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57702606 | |||||||
| chr12:57703741 | A | T | 1 | a0001c0001t0001g0255 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.579+7368A>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57703741 | |||||||
| chr12:57703762 | AT | A | 116 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(113): Show |
155 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.579+7400delT | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57703762 | ||||||
| chr12:57703762 | ATT | A | 17 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0162 others(14): Show |
18 | HG00733.hp2 HG01070.hp1 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.579+7399_579+7400d others(4): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57703762 | ||||||
| chr12:57703832 | C | T | 1 | a0007c0014t0004g0055 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.579+7459C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57703832 | |||||||
| chr12:57703903 | G | A | 3 | a0001c0002t0002g0195 a0001c0002t0002g0196 a0001c0002t0002g0199 |
3 | HG03710.hp1 HG04184.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.579+7530G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57703903 | |||||||
| chr12:57703967 | A | G | 21 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0026 others(18): Show |
29 | HG00408.hp1 HG00558.hp1 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.579+7594A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57703967 | |||||||
| chr12:57704079 | T | C | 101 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0162 others(98): Show |
128 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.579+7706T>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57704079 | |||||||
| chr12:57704100 | A | G | 3 | a0001c0001t0001g0053 a0001c0001t0001g0059 a0001c0001t0001g0060 |
3 | HG00140.hp1 HG00323.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.579+7727A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57704100 | |||||||
| chr12:57704334 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.579+7961C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57704334 | |||||||
| chr12:57704406 | G | A | 16 | a0001c0001t0001g0024 a0001c0001t0001g0096 a0001c0001t0001g0097 others(13): Show |
17 | HG01261.hp1 HG01884.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.579+8033G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57704406 | |||||||
| chr12:57704429 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.579+8056C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57704429 | |||||||
| chr12:57704437 | C | T | 136 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(133): Show |
177 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.579+8064C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57704437 | |||||||
| chr12:57704537 | C | CA | 72 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0014 others(69): Show |
96 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.579+8175dupA | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57704537 | ||||||
| chr12:57704619 | A | C | 3 | a0001c0001t0001g0210 a0001c0001t0001g0252 a0001c0001t0001g0253 |
3 | NA18948.hp2 NA18965.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.579+8246A>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57704619 | |||||||
| chr12:57704620 | G | C | 3 | a0001c0001t0001g0210 a0001c0001t0001g0252 a0001c0001t0001g0253 |
3 | NA18948.hp2 NA18965.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.579+8247G>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57704620 | |||||||
| chr12:57704631 | T | C | 4 | a0001c0002t0002g0014 a0001c0002t0002g0157 a0001c0002t0002g0159 others(1): Show |
6 | HG02559.hp1 HG02615.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.579+8258T>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57704631 | |||||||
| chr12:57704642 | A | C | 125 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(122): Show |
165 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.579+8269A>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57704642 | |||||||
| chr12:57704643 | G | A | 1 | a0001c0002t0002g0173 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.579+8270G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57704643 | |||||||
| chr12:57704643 | G | T | 1 | a0001c0002t0002g0158 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.579+8270G>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57704643 | |||||||
| chr12:57704963 | C | T | 27 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(24): Show |
41 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.579+8590C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57704963 | |||||||
| chr12:57705315 | C | T | 3 | a0001c0002t0002g0030 a0001c0002t0002g0143 a0001c0002t0002g0144 |
4 | HG00544.hp2 HG02683.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.579+8942C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57705315 | |||||||
| chr12:57705445 | CTT | C | 7 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(4): Show |
7 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.579+9073_579+9074d others(4): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57705445 | |||||||
| chr12:57705581 | C | G | 2 | a0001c0002t0002g0036 a0001c0002t0002g0219 |
3 | HG02451.hp1 HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.579+9208C>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57705581 | |||||||
| chr12:57705600 | C | T | 1 | a0001c0002t0002g0180 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.579+9227C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57705600 | |||||||
| chr12:57705617 | C | T | 1 | a0001c0002t0002g0201 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.579+9244C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57705617 | |||||||
| chr12:57705673 | G | A | 11 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(8): Show |
12 | HG00544.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.579+9300G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57705673 | |||||||
| chr12:57705878 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.579+9505T>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57705878 | |||||||
| chr12:57705926 | T | C | 8 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(5): Show |
8 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.579+9553T>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57705926 | |||||||
| chr12:57705953 | G | A | 73 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0014 others(70): Show |
97 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.579+9580G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57705953 | |||||||
| chr12:57706028 | C | A | 1 | a0001c0001t0001g0097 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.579+9655C>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57706028 | |||||||
| chr12:57706057 | A | G | 11 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(8): Show |
12 | HG00544.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.579+9684A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57706057 | |||||||
| chr12:57706193 | G | A | 8 | a0001c0003t0002g0040 a0001c0003t0002g0190 a0001c0003t0002g0191 others(5): Show |
9 | HG01109.hp2 HG01884.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.580-9567G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57706193 | |||||||
| chr12:57706275 | T | A | 126 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(123): Show |
166 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.580-9485T>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57706275 | |||||||
| chr12:57706528 | G | A | 4 | a0001c0002t0002g0165 a0001c0002t0002g0174 a0001c0002t0002g0181 others(1): Show |
4 | HG00140.hp2 HG01070.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.580-9232G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57706528 | |||||||
| chr12:57706720 | A | G | 1 | a0007c0014t0004g0055 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.580-9040A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57706720 | |||||||
| chr12:57706737 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.580-9023T>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57706737 | |||||||
| chr12:57706768 | T | G | 136 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(133): Show |
177 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.580-8992T>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57706768 | |||||||
| chr12:57706846 | G | GA | 83 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(80): Show |
113 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.580-8891dupA | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57706846 | ||||||
| chr12:57706846 | G | GAA | 84 | a0001c0001t0001g0046 a0001c0001t0001g0134 a0001c0001t0001g0149 others(81): Show |
109 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.580-8892_580-8891d others(4): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57706846 | ||||||
| chr12:57706846 | G | GAAAAAAA others(9): Show |
2 | a0001c0002t0002g0030 a0001c0002t0002g0144 |
3 | HG02683.hp1 HG03492.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.580-8906_580-8891d others(18): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57706846 | ||||||
| chr12:57706846 | G | GAAAAAAA others(10): Show |
1 | a0001c0002t0002g0143 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.580-8907_580-8891d others(19): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57706846 | ||||||
| chr12:57706846 | GA | G | 12 | a0001c0001t0001g0012 a0001c0001t0001g0072 a0001c0001t0001g0084 others(9): Show |
13 | HG01167.hp2 HG02615.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.580-8891delA | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57706846 | ||||||
| chr12:57706864 | AAAAAAG | A | 7 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(4): Show |
7 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.580-8895_580-8890d others(8): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57706864 | |||||||
| chr12:57706870 | G | A | 4 | a0001c0002t0002g0030 a0001c0002t0002g0143 a0001c0002t0002g0144 others(1): Show |
5 | HG00544.hp2 HG02572.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.580-8890G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57706870 | |||||||
| chr12:57706900 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.580-8860A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57706900 | |||||||
| chr12:57707074 | A | G | 249 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(246): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.580-8686A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57707074 | |||||||
| chr12:57707186 | G | C | 11 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(8): Show |
12 | HG00544.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.580-8574G>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57707186 | |||||||
| chr12:57707516 | C | T | 1 | a0001c0002t0002g0198 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.580-8244C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57707516 | |||||||
| chr12:57707527 | C | T | 7 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(4): Show |
7 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.580-8233C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57707527 | |||||||
| chr12:57707571 | T | G | 11 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(8): Show |
12 | HG00544.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.580-8189T>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57707571 | |||||||
| chr12:57707638 | A | G | 1 | a0001c0002t0002g0143 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.580-8122A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57707638 | |||||||
| chr12:57707689 | G | A | 11 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0001g0117 others(8): Show |
15 | HG01358.hp2 HG01928.hp1 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.580-8071G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57707689 | |||||||
| chr12:57707783 | A | AT | 7 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(4): Show |
7 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.580-7969dupT | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57707783 | ||||||
| chr12:57707802 | A | C | 12 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0162 others(9): Show |
13 | HG00733.hp2 HG01070.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.580-7958A>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57707802 | |||||||
| chr12:57707929 | G | GA | 69 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(66): Show |
106 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.580-7817dupA | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57707929 | ||||||
| chr12:57707936 | A | G | 1 | a0001c0002t0002g0178 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.580-7824A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57707936 | |||||||
| chr12:57707944 | T | A | 1 | a0001c0002t0002g0175 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.580-7816T>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57707944 | |||||||
| chr12:57707964 | G | A | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | NA19007.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.580-7796G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57707964 | |||||||
| chr12:57708009 | C | G | 1 | a0001c0001t0001g0206 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.580-7751C>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57708009 | |||||||
| chr12:57708031 | T | A | 2 | a0001c0001t0001g0089 a0001c0001t0001g0093 |
2 | NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.580-7729T>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57708031 | |||||||
| chr12:57708049 | C | T | 1 | a0007c0014t0004g0055 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.580-7711C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57708049 | |||||||
| chr12:57708060 | T | G | 1 | a0001c0001t0001g0104 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.580-7700T>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57708060 | |||||||
| chr12:57708083 | C | T | 8 | a0001c0001t0001g0121 a0001c0001t0001g0127 a0001c0001t0001g0134 others(5): Show |
8 | HG01255.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.580-7677C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57708083 | |||||||
| chr12:57708090 | T | A | 1 | a0001c0002t0002g0032 | 2 | HG00735.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.580-7670T>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57708090 | |||||||
| chr12:57708276 | A | AT | 125 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(122): Show |
165 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.580-7477dupT | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57708276 | ||||||
| chr12:57708283 | T | A | 1 | a0001c0002t0002g0144 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.580-7477T>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57708283 | |||||||
| chr12:57708625 | CA | C | 7 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(4): Show |
7 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.580-7120delA | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57708625 | ||||||
| chr12:57708767 | C | T | 1 | a0001c0002t0002g0201 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.580-6993C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57708767 | |||||||
| chr12:57708956 | T | C | 11 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(8): Show |
12 | HG00544.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.580-6804T>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57708956 | |||||||
| chr12:57709264 | T | G | 4 | a0001c0001t0001g0038 a0001c0001t0001g0234 a0001c0001t0001g0235 others(1): Show |
5 | HG00733.hp2 HG01070.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.580-6496T>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57709264 | |||||||
| chr12:57709352 | T | C | 1 | a0007c0014t0004g0055 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.580-6408T>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57709352 | |||||||
| chr12:57709541 | A | T | 1 | a0001c0002t0002g0160 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.580-6219A>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57709541 | |||||||
| chr12:57709574 | T | C | 2 | a0001c0003t0002g0190 a0001c0003t0002g0229 |
2 | NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.580-6186T>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57709574 | |||||||
| chr12:57709640 | G | C | 1 | a0001c0001t0001g0105 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.580-6120G>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57709640 | |||||||
| chr12:57709809 | A | G | 136 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(133): Show |
177 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.580-5951A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57709809 | |||||||
| chr12:57709861 | C | CT | 8 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(5): Show |
8 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.580-5890dupT | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57709861 | ||||||
| chr12:57709906 | G | A | 8 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(5): Show |
8 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.580-5854G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57709906 | |||||||
| chr12:57710015 | G | C | 8 | a0001c0003t0002g0040 a0001c0003t0002g0190 a0001c0003t0002g0191 others(5): Show |
9 | HG01109.hp2 HG01884.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.580-5745G>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57710015 | |||||||
| chr12:57710031 | C | T | 11 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(8): Show |
12 | HG00544.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.580-5729C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57710031 | |||||||
| chr12:57710133 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.580-5627G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57710133 | |||||||
| chr12:57710237 | T | TA | 7 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0028 others(4): Show |
13 | HG00609.hp2 HG00642.hp1 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.580-5521dupA | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57710237 | ||||||
| chr12:57710311 | T | C | 2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.580-5449T>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57710311 | |||||||
| chr12:57710321 | C | A | 125 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(122): Show |
165 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.580-5439C>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57710321 | |||||||
| chr12:57710374 | G | C | 1 | a0001c0002t0002g0189 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.580-5386G>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57710374 | |||||||
| chr12:57710694 | A | G | 20 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0028 others(17): Show |
27 | HG00609.hp2 HG00642.hp1 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.580-5066A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57710694 | |||||||
| chr12:57710715 | C | A | 8 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(5): Show |
8 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.580-5045C>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57710715 | |||||||
| chr12:57710853 | C | A | 136 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(133): Show |
177 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.580-4907C>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57710853 | |||||||
| chr12:57710996 | A | G | 11 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(8): Show |
12 | HG00544.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.580-4764A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57710996 | |||||||
| chr12:57711038 | C | CA | 66 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(63): Show |
103 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.580-4699dupA | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57711038 | ||||||
| chr12:57711038 | C | CAA | 9 | a0001c0001t0001g0052 a0001c0001t0001g0067 a0001c0001t0001g0068 others(6): Show |
9 | HG01433.hp1 HG02074.hp2 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.580-4700_580-4699d others(4): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57711038 | ||||||
| chr12:57711038 | CA | C | 8 | a0001c0001t0001g0045 a0001c0001t0001g0204 a0001c0001t0001g0207 others(5): Show |
8 | HG00597.hp2 HG02723.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.580-4699delA | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57711038 | ||||||
| chr12:57711038 | CAA | C | 120 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(117): Show |
160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.580-4700_580-4699d others(4): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57711038 | ||||||
| chr12:57711038 | CAAA | C | 9 | a0001c0001t0001g0115 a0001c0001t0001g0241 a0001c0002t0002g0030 others(6): Show |
10 | HG00544.hp2 HG01167.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.580-4701_580-4699d others(5): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57711038 | ||||||
| chr12:57711101 | C | A | 13 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0162 others(10): Show |
14 | HG00733.hp2 HG01070.hp1 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.580-4659C>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57711101 | |||||||
| chr12:57711208 | G | A | 4 | a0001c0002t0003g0247 a0001c0002t0003g0248 a0001c0002t0003g0249 others(1): Show |
4 | HG01891.hp2 HG02965.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-4552G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57711208 | |||||||
| chr12:57711292 | T | A | 3 | a0001c0002t0002g0030 a0001c0002t0002g0143 a0001c0002t0002g0144 |
4 | HG00544.hp2 HG02683.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-4468T>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57711292 | |||||||
| chr12:57711311 | TAG | T | 136 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(133): Show |
177 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.580-4443_580-4442d others(4): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57711311 | ||||||
| chr12:57711338 | C | CT | 8 | a0001c0001t0001g0088 a0001c0001t0001g0134 a0001c0001t0001g0135 others(5): Show |
9 | HG01255.hp1 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.580-4396dupT | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57711338 | ||||||
| chr12:57711338 | CT | C | 99 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(96): Show |
140 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.580-4396delT | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57711338 | ||||||
| chr12:57711338 | CTTT | C | 10 | a0001c0001t0001g0233 a0001c0001t0001g0245 a0001c0002t0002g0174 others(7): Show |
10 | HG00140.hp2 HG01192.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.580-4398_580-4396d others(5): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57711338 | ||||||
| chr12:57711338 | CTTTT | C | 114 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(111): Show |
154 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.580-4399_580-4396d others(6): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57711338 | ||||||
| chr12:57711408 | G | A | 2 | a0001c0001t0001g0098 a0001c0001t0001g0110 |
2 | HG02109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.580-4352G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57711408 | |||||||
| chr12:57711439 | C | T | 1 | a0001c0002t0002g0185 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.580-4321C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57711439 | |||||||
| chr12:57711472 | G | A | 3 | a0001c0002t0002g0224 a0001c0002t0002g0225 a0001c0002t0002g0231 |
3 | HG02723.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.580-4288G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57711472 | |||||||
| chr12:57711481 | G | GGACT | 4 | a0001c0001t0001g0012 a0001c0001t0001g0106 a0001c0001t0001g0107 others(1): Show |
5 | HG01167.hp2 HG02615.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.580-4278_580-4275d others(6): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57711481 | ||||||
| chr12:57711512 | A | G | 4 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(1): Show |
4 | HG02109.hp2 HG02145.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-4248A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57711512 | |||||||
| chr12:57711592 | T | A | 3 | a0001c0002t0002g0030 a0001c0002t0002g0143 a0001c0002t0002g0144 |
4 | HG00544.hp2 HG02683.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-4168T>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57711592 | |||||||
| chr12:57711592 | T | G | 230 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(227): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.580-4168T>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57711592 | |||||||
| chr12:57711665 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.580-4095C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57711665 | |||||||
| chr12:57711804 | T | TTGGGCTG others(7): Show |
1 | a0001c0001t0001g0082 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.580-3952_580-3939d others(16): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57711804 | ||||||
| chr12:57711916 | C | G | 1 | a0007c0014t0004g0055 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.580-3844C>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57711916 | |||||||
| chr12:57711917 | T | G | 1 | a0007c0014t0004g0055 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.580-3843T>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57711917 | |||||||
| chr12:57711974 | G | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0152 |
2 | HG02622.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.580-3786G>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57711974 | |||||||
| chr12:57712066 | G | C | 1 | a0001c0001t0001g0121 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.580-3694G>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57712066 | |||||||
| chr12:57712286 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.580-3474C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57712286 | |||||||
| chr12:57712333 | G | A | 4 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(1): Show |
4 | HG02109.hp2 HG02145.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-3427G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57712333 | |||||||
| chr12:57712430 | T | G | 1 | a0001c0002t0002g0195 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.580-3330T>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57712430 | |||||||
| chr12:57712495 | TC | T | 121 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(118): Show |
160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.580-3264delC | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57712495 | |||||||
| chr12:57712607 | TATGTTTC others(18): Show |
T | 1 | a0001c0001t0001g0048 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.580-3142_580-3118d others(27): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57712607 | ||||||
| chr12:57712710 | C | T | 2 | a0001c0001t0001g0140 a0001c0001t0001g0141 |
2 | HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.580-3050C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57712710 | |||||||
| chr12:57712768 | T | C | 4 | a0001c0002t0003g0247 a0001c0002t0003g0248 a0001c0002t0003g0249 others(1): Show |
4 | HG01891.hp2 HG02965.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-2992T>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57712768 | |||||||
| chr12:57712851 | G | A | 11 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(8): Show |
12 | HG00544.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.580-2909G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57712851 | |||||||
| chr12:57712976 | G | A | 4 | a0001c0002t0003g0247 a0001c0002t0003g0248 a0001c0002t0003g0249 others(1): Show |
4 | HG01891.hp2 HG02965.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-2784G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57712976 | |||||||
| chr12:57713027 | G | T | 1 | a0001c0001t0001g0126 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.580-2733G>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57713027 | |||||||
| chr12:57713053 | A | G | 132 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(129): Show |
172 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.580-2707A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57713053 | |||||||
| chr12:57713275 | C | T | 11 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(8): Show |
12 | HG00544.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.580-2485C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57713275 | |||||||
| chr12:57713287 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.580-2473C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57713287 | |||||||
| chr12:57713441 | T | A | 6 | a0001c0001t0001g0023 a0001c0001t0001g0088 a0001c0001t0001g0092 others(3): Show |
7 | HG01496.hp1 HG02486.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.580-2319T>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57713441 | |||||||
| chr12:57713493 | C | T | 1 | a0007c0014t0004g0055 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.580-2267C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57713493 | |||||||
| chr12:57713526 | CCT | C | 11 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(8): Show |
12 | HG00544.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.580-2231_580-2230d others(4): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57713526 | ||||||
| chr12:57713698 | C | CT | 22 | a0001c0001t0001g0006 a0001c0001t0001g0045 a0001c0001t0001g0046 others(19): Show |
26 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(23): Show |
intron_variant | MODIFIER | c.580-2043dupT | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57713698 | ||||||
| chr12:57713698 | CT | C | 9 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0059 others(6): Show |
11 | HG00099.hp2 HG00323.hp2 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.580-2043delT | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57713698 | ||||||
| chr12:57713706 | T | TC | 3 | a0001c0002t0002g0030 a0001c0002t0002g0143 a0001c0002t0002g0144 |
4 | HG00544.hp2 HG02683.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-2054_580-2053i others(3): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57713706 | |||||||
| chr12:57713817 | C | A | 1 | a0001c0001t0001g0115 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.580-1943C>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57713817 | |||||||
| chr12:57713942 | AC | A | 7 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(4): Show |
7 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.580-1817delC | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57713942 | |||||||
| chr12:57714269 | C | T | 121 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(118): Show |
160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.580-1491C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57714269 | |||||||
| chr12:57714270 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.580-1490G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57714270 | |||||||
| chr12:57714311 | A | G | 7 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(4): Show |
7 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.580-1449A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57714311 | |||||||
| chr12:57714419 | T | G | 132 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(129): Show |
172 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.580-1341T>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57714419 | |||||||
| chr12:57714636 | C | T | 11 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(8): Show |
12 | HG00544.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.580-1124C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57714636 | |||||||
| chr12:57714660 | A | T | 1 | a0007c0014t0004g0055 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.580-1100A>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57714660 | |||||||
| chr12:57714736 | C | T | 27 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(24): Show |
41 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.580-1024C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57714736 | |||||||
| chr12:57714757 | C | T | 8 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0028 others(5): Show |
14 | HG00609.hp2 HG00642.hp1 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.580-1003C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57714757 | |||||||
| chr12:57714828 | A | G | 1 | a0007c0014t0004g0055 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.580-932A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57714828 | |||||||
| chr12:57715018 | A | G | 1 | a0001c0002t0002g0170 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.580-742A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57715018 | |||||||
| chr12:57715069 | TA | T | 3 | a0001c0002t0002g0030 a0001c0002t0002g0143 a0001c0002t0002g0144 |
4 | HG00544.hp2 HG02683.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-683delA | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr12 | 57715069 | ||||||
| chr12:57715252 | C | T | 11 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(8): Show |
12 | HG00544.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.580-508C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57715252 | |||||||
| chr12:57715269 | C | T | 7 | a0001c0002t0002g0201 a0001c0003t0002g0040 a0001c0003t0002g0190 others(4): Show |
8 | HG01109.hp2 HG01884.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.580-491C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57715269 | |||||||
| chr12:57715596 | A | G | 3 | a0001c0001t0001g0053 a0001c0001t0001g0059 a0001c0001t0001g0060 |
3 | HG00140.hp1 HG00323.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.580-164A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57715596 | |||||||
| chr12:57715654 | C | T | 7 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(4): Show |
7 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.580-106C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 5/14 | chr12 | 57715654 | |||||||
| chr12:57716019 | G | C | 7 | a0001c0002t0002g0005 a0001c0002t0002g0166 a0001c0002t0002g0179 others(4): Show |
11 | HG00408.hp2 HG00544.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.790+49G>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 6/14 | chr12 | 57716019 | |||||||
| chr12:57716020 | G | T | 8 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(5): Show |
8 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.790+50G>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 6/14 | chr12 | 57716020 | |||||||
| chr12:57716279 | T | TG | 99 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0047 others(96): Show |
129 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.892+95dupG | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 57716279 | ||||||
| chr12:57716279 | T | TGG | 20 | a0001c0001t0001g0006 a0001c0001t0001g0041 a0001c0001t0001g0205 others(17): Show |
26 | HG00438.hp1 HG00738.hp1 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.892+94_892+95dupGG | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr12 | 57716279 | ||||||
| chr12:57716281 | G | GC | 4 | a0001c0002t0002g0017 a0001c0002t0002g0036 a0001c0002t0002g0037 others(1): Show |
8 | HG02451.hp1 HG02486.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.892+88_892+89insC | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 7/14 | chr12 | 57716281 | |||||||
| chr12:57716284 | G | C | 1 | a0001c0001t0001g0154 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.892+91G>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 7/14 | chr12 | 57716284 | |||||||
| chr12:57716315 | C | T | 1 | a0001c0001t0001g0243 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.893-97C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 7/14 | chr12 | 57716315 | |||||||
| chr12:57717018 | A | G | 1 | a0001c0002t0002g0183 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1045+274A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 9/14 | chr12 | 57717018 | |||||||
| chr12:57717432 | T | C | 1 | a0007c0014t0004g0055 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1046-438T>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 9/14 | chr12 | 57717432 | |||||||
| chr12:57717602 | G | A | 13 | a0001c0002t0002g0201 a0001c0002t0003g0247 a0001c0002t0003g0248 others(10): Show |
14 | HG01109.hp2 HG01884.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1046-268G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 9/14 | chr12 | 57717602 | |||||||
| chr12:57717638 | C | T | 8 | a0001c0003t0002g0040 a0001c0003t0002g0190 a0001c0003t0002g0191 others(5): Show |
9 | HG01109.hp2 HG01884.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1046-232C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 9/14 | chr12 | 57717638 | |||||||
| chr12:57717792 | C | CA | 106 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(103): Show |
153 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.1046-51dupA | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 57717792 | ||||||
| chr12:57717792 | C | CAA | 13 | a0001c0001t0001g0020 a0001c0001t0001g0028 a0001c0001t0001g0068 others(10): Show |
15 | HG01358.hp1 HG01358.hp2 HG01952.hp2 others(12): Show |
intron_variant | MODIFIER | c.1046-52_1046-51dup others(2): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 57717792 | ||||||
| chr12:57717792 | CAAA | C | 24 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(21): Show |
38 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.1046-53_1046-51del others(3): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 57717792 | ||||||
| chr12:57717792 | CAAAAAA | C | 7 | a0001c0002t0002g0169 a0001c0002t0002g0187 a0001c0002t0002g0189 others(4): Show |
7 | HG00741.hp1 HG01168.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.1046-56_1046-51del others(6): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 57717792 | ||||||
| chr12:57717792 | CAAAAAAA | C | 76 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0014 others(73): Show |
101 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.1046-57_1046-51del others(7): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | 57717792 | ||||||
| chr12:57717988 | AC | A | 3 | a0001c0001t0001g0101 a0001c0001t0001g0111 a0001c0010t0001g0109 |
3 | HG01891.hp1 HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1134+33delC | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr12 | 57717988 | ||||||
| chr12:57718088 | G | C | 2 | a0001c0001t0001g0140 a0001c0001t0001g0141 |
2 | HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1135-58G>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 10/14 | chr12 | 57718088 | |||||||
| chr12:57718510 | C | A | 3 | a0001c0001t0001g0054 a0001c0001t0001g0085 a0001c0001t0001g0087 |
3 | HG00558.hp2 HG02523.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.1410+89C>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 11/14 | chr12 | 57718510 | |||||||
| chr12:57718654 | C | A | 29 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(26): Show |
43 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.1410+233C>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 11/14 | chr12 | 57718654 | |||||||
| chr12:57718794 | CTTTGGAA others(25): Show |
C | 2 | a0001c0001t0001g0098 a0001c0001t0001g0110 |
2 | HG02109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1411-198_1411-167d others(34): Show |
OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 11/14 | chr12 | 57718794 | |||||||
| chr12:57718820 | G | A | 2 | a0001c0002t0002g0224 a0001c0002t0002g0225 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1411-173G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 11/14 | chr12 | 57718820 | |||||||
| chr12:57718935 | C | T | 2 | a0001c0001t0001g0140 a0001c0001t0001g0141 |
2 | HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1411-58C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 11/14 | chr12 | 57718935 | |||||||
| chr12:57719342 | A | G | 255 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(252): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.1600+160A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 12/14 | chr12 | 57719342 | |||||||
| chr12:57719375 | C | T | 85 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0014 others(82): Show |
107 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.1600+193C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 12/14 | chr12 | 57719375 | |||||||
| chr12:57719484 | T | C | 1 | a0001c0002t0002g0216 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1600+302T>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 12/14 | chr12 | 57719484 | |||||||
| chr12:57719633 | C | A | 73 | a0001c0002t0002g0002 a0001c0002t0002g0005 a0001c0002t0002g0014 others(70): Show |
93 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.1600+451C>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 12/14 | chr12 | 57719633 | |||||||
| chr12:57719776 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0152 |
2 | HG02622.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1601-323C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 12/14 | chr12 | 57719776 | |||||||
| chr12:57719847 | T | C | 3 | a0001c0002t0002g0030 a0001c0002t0002g0143 a0001c0002t0002g0144 |
4 | HG00544.hp2 HG02683.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.1601-252T>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 12/14 | chr12 | 57719847 | |||||||
| chr12:57719886 | C | T | 1 | a0007c0014t0004g0055 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1601-213C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 12/14 | chr12 | 57719886 | |||||||
| chr12:57720050 | T | C | 1 | a0007c0014t0004g0055 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1601-49T>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 12/14 | chr12 | 57720050 | |||||||
| chr12:57720092 | C | G | 1 | a0001c0001t0001g0053 | 1 | HG00741.hp2 | splice_region_variant&intron_variant | LOW | c.1601-7C>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 12/14 | chr12 | 57720092 | |||||||
| chr12:57720349 | G | A | 1 | a0001c0001t0005g0213 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1766-57G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 13/14 | chr12 | 57720349 | |||||||
| chr12:57720522 | A | G | 1 | a0008c0008t0001g0146 | 1 | NA18997.hp2 | splice_region_variant&intron_variant | LOW | c.1878+4A>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 14/14 | chr12 | 57720522 | |||||||
| chr12:57720531 | T | G | 1 | a0008c0008t0001g0146 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1878+13T>G | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 14/14 | chr12 | 57720531 | |||||||
| chr12:57720532 | A | C | 1 | a0008c0008t0001g0146 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1878+14A>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 14/14 | chr12 | 57720532 | |||||||
| chr12:57720537 | C | T | 1 | a0008c0008t0001g0146 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1878+19C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 14/14 | chr12 | 57720537 | |||||||
| chr12:57720539 | A | C | 1 | a0008c0008t0001g0146 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1878+21A>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 14/14 | chr12 | 57720539 | |||||||
| chr12:57720540 | G | C | 1 | a0008c0008t0001g0146 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1878+22G>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 14/14 | chr12 | 57720540 | |||||||
| chr12:57720541 | T | C | 1 | a0008c0008t0001g0146 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1878+23T>C | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 14/14 | chr12 | 57720541 | |||||||
| chr12:57720547 | C | T | 1 | a0008c0008t0001g0146 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1878+29C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 14/14 | chr12 | 57720547 | |||||||
| chr12:57720570 | G | A | 3 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0142 |
3 | HG02055.hp1 HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1878+52G>A | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 14/14 | chr12 | 57720570 | |||||||
| chr12:57720582 | C | T | 1 | a0001c0002t0002g0159 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1878+64C>T | OS9 | ENSG00000135506.17 | transcript | ENST00000315970.12 | protein_coding | 14/14 | chr12 | 57720582 |