Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 654346 |
| ensemblid | ENSG00000171916.17 |
| hgncid | 33874 |
| symbol | LGALS9C |
| name | galectin 9C |
| refseq_nuc | NM_001040078.3 |
| refseq_prot | NP_001035167.2 |
| ensembl_nuc | ENST00000328114.11 |
| ensembl_prot | ENSP00000329932.6 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 18476789 |
| end | 18494945 |
| strand | + |
| ver | v1.2 |
| region | chr17:18476789-18494945 |
| region5000 | chr17:18471789-18499945 |
| regionname0 | LGALS9C_chr17_18476789_18494945 |
| regionname5000 | LGALS9C_chr17_18471789_18499945 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 356 | 196 | 27 | 28 | 122 | 3 | 15 | 90 | LGALS9C_chr17_18471789_18499945 | LGALS9C | MAFSG others(351): Show |
chr17 | 18471789 | 18499945 |
| a0002 | 0/0 | 356 | 71 | 11 | 15 | 36 | 2 | 7 | 32 | LGALS9C_chr17_18471789_18499945 | LGALS9C | MAFSG others(351): Show |
chr17 | 18471789 | 18499945 |
| a0003 | 0/0 | 356 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | MAFSG others(351): Show |
chr17 | 18471789 | 18499945 |
| a0004 | 0/0 | 356 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | MAFSG others(351): Show |
chr17 | 18471789 | 18499945 |
| a0005 | 0/0 | 356 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | MAFSG others(351): Show |
chr17 | 18471789 | 18499945 |
| a0006 | 0/0 | 356 | 2 | 0 | 0 | 0 | 1 | 1 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | MAFSG others(351): Show |
chr17 | 18471789 | 18499945 |
| a0007 | 0/0 | 356 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | MAFSG others(351): Show |
chr17 | 18471789 | 18499945 |
| a0008 | 0/0 | 356 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | MAFSG others(351): Show |
chr17 | 18471789 | 18499945 |
| a0009 | 0/0 | 356 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | MAFSG others(351): Show |
chr17 | 18471789 | 18499945 |
| a0010 | 0/0 | 356 | 2 | 0 | 0 | 1 | 0 | 1 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C | MAFSG others(351): Show |
chr17 | 18471789 | 18499945 |
| a0011 | 0/0 | 356 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | MAFSG others(351): Show |
chr17 | 18471789 | 18499945 |
| a0012 | 0/0 | 356 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C | MAFSG others(351): Show |
chr17 | 18471789 | 18499945 |
| a0013 | 0/0 | 356 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | MAFSG others(351): Show |
chr17 | 18471789 | 18499945 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1068 | 194 | 26 | 27 | 122 | 3 | 15 | LGALS9C_chr17_18471789_18499945 | LGALS9C | ATGGC others(1063): Show |
chr17 | 18471789 | 18499945 | ||
| a0001c0011 | 0/0 | 1068 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | ATGGC others(1063): Show |
chr17 | 18471789 | 18499945 | ||
| a0001c0015 | 0/0 | 1068 | 1 | 0 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | ATGGC others(1063): Show |
chr17 | 18471789 | 18499945 | ||
| a0002c0002 | 0/0 | 1068 | 71 | 11 | 15 | 36 | 2 | 7 | LGALS9C_chr17_18471789_18499945 | LGALS9C | ATGGC others(1063): Show |
chr17 | 18471789 | 18499945 | ||
| a0003c0004 | 0/0 | 1068 | 4 | 3 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | ATGGC others(1063): Show |
chr17 | 18471789 | 18499945 | ||
| a0004c0003 | 0/0 | 1068 | 4 | 4 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | ATGGC others(1063): Show |
chr17 | 18471789 | 18499945 | ||
| a0005c0005 | 0/0 | 1068 | 3 | 3 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | ATGGC others(1063): Show |
chr17 | 18471789 | 18499945 | ||
| a0006c0008 | 0/0 | 1068 | 2 | 0 | 0 | 0 | 1 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C | ATGGC others(1063): Show |
chr17 | 18471789 | 18499945 | ||
| a0007c0013 | 0/0 | 1068 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | ATGGC others(1063): Show |
chr17 | 18471789 | 18499945 | ||
| a0007c0014 | 0/0 | 1068 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | ATGGC others(1063): Show |
chr17 | 18471789 | 18499945 | ||
| a0008c0009 | 0/0 | 1068 | 2 | 0 | 0 | 0 | 0 | 2 | LGALS9C_chr17_18471789_18499945 | LGALS9C | ATGGC others(1063): Show |
chr17 | 18471789 | 18499945 | ||
| a0009c0007 | 0/0 | 1068 | 2 | 0 | 0 | 0 | 0 | 2 | LGALS9C_chr17_18471789_18499945 | LGALS9C | ATGGC others(1063): Show |
chr17 | 18471789 | 18499945 | ||
| a0010c0006 | 0/0 | 1068 | 2 | 0 | 0 | 1 | 0 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C | ATGGC others(1063): Show |
chr17 | 18471789 | 18499945 | ||
| a0011c0010 | 0/0 | 1068 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | ATGGC others(1063): Show |
chr17 | 18471789 | 18499945 | ||
| a0012c0016 | 0/0 | 1068 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | ATGGC others(1063): Show |
chr17 | 18471789 | 18499945 | ||
| a0013c0012 | 0/0 | 1068 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | ATGGC others(1063): Show |
chr17 | 18471789 | 18499945 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1715 | 187 | 24 | 24 | 120 | 3 | 15 | LGALS9C_chr17_18471789_18499945 | LGALS9C | ATTCC others(1710): Show |
chr17 | 18471789 | 18499945 |
| a0001c0001t0002 | 0/0 | 1715 | 4 | 0 | 3 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | ATTCC others(1710): Show |
chr17 | 18471789 | 18499945 |
| a0001c0001t0004 | 0/0 | 1715 | 2 | 2 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | ATTCC others(1710): Show |
chr17 | 18471789 | 18499945 |
| a0001c0001t0006 | 0/0 | 1715 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | ATTCC others(1710): Show |
chr17 | 18471789 | 18499945 |
| a0001c0011t0002 | 0/0 | 1715 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | ATTCC others(1710): Show |
chr17 | 18471789 | 18499945 |
| a0001c0015t0001 | 0/0 | 1715 | 1 | 0 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | ATTCC others(1710): Show |
chr17 | 18471789 | 18499945 |
| a0002c0002t0002 | 0/0 | 1715 | 71 | 11 | 15 | 36 | 2 | 7 | LGALS9C_chr17_18471789_18499945 | LGALS9C | ATTCC others(1710): Show |
chr17 | 18471789 | 18499945 |
| a0003c0004t0001 | 0/0 | 1715 | 4 | 3 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | ATTCC others(1710): Show |
chr17 | 18471789 | 18499945 |
| a0004c0003t0001 | 0/0 | 1715 | 4 | 4 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | ATTCC others(1710): Show |
chr17 | 18471789 | 18499945 |
| a0005c0005t0001 | 0/0 | 1715 | 3 | 3 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | ATTCC others(1710): Show |
chr17 | 18471789 | 18499945 |
| a0006c0008t0001 | 0/0 | 1715 | 2 | 0 | 0 | 0 | 1 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C | ATTCC others(1710): Show |
chr17 | 18471789 | 18499945 |
| a0007c0013t0005 | 0/0 | 1715 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | ATTCC others(1710): Show |
chr17 | 18471789 | 18499945 |
| a0007c0014t0003 | 0/0 | 1715 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | ATTCC others(1710): Show |
chr17 | 18471789 | 18499945 |
| a0008c0009t0002 | 0/0 | 1715 | 2 | 0 | 0 | 0 | 0 | 2 | LGALS9C_chr17_18471789_18499945 | LGALS9C | ATTCC others(1710): Show |
chr17 | 18471789 | 18499945 |
| a0009c0007t0001 | 0/0 | 1715 | 2 | 0 | 0 | 0 | 0 | 2 | LGALS9C_chr17_18471789_18499945 | LGALS9C | ATTCC others(1710): Show |
chr17 | 18471789 | 18499945 |
| a0010c0006t0001 | 0/0 | 1715 | 2 | 0 | 0 | 1 | 0 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C | ATTCC others(1710): Show |
chr17 | 18471789 | 18499945 |
| a0011c0010t0001 | 0/0 | 1715 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | ATTCC others(1710): Show |
chr17 | 18471789 | 18499945 |
| a0012c0016t0001 | 0/0 | 1715 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | ATTCC others(1710): Show |
chr17 | 18471789 | 18499945 |
| a0013c0012t0003 | 0/0 | 1715 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | ATTCC others(1710): Show |
chr17 | 18471789 | 18499945 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 23 | 1 | 3 | 19 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0003 | 0/0 | 18 | 0 | 4 | 14 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0004 | 0/0 | 13 | 1 | 3 | 4 | 0 | 5 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0006 | 1/0 | 6 | 0 | 1 | 2 | 0 | 2 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0004g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0001t0006g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0011t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0001c0015t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0002c0002t0002g0002 | 0/0 | 21 | 0 | 6 | 13 | 0 | 2 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0002c0002t0002g0005 | 0/0 | 11 | 2 | 1 | 6 | 1 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0002c0002t0002g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0002c0002t0002g0014 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0002c0002t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0002c0002t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0002c0002t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0002c0002t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0002c0002t0002g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0002c0002t0002g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0002c0002t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0002c0002t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0002c0002t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0002c0002t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0002c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0002c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0002c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0002c0002t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0002c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0002c0002t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0002c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0002c0002t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0002c0002t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0002c0002t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0003c0004t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0003c0004t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0003c0004t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0003c0004t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0004c0003t0001g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0004c0003t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0005c0005t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0005c0005t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0005c0005t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0006c0008t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0007c0013t0005g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0007c0014t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0008c0009t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0008c0009t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0009c0007t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0010c0006t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0010c0006t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0011c0010t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0012c0016t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| a0013c0012t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0002 | g0014 | EUR | GBR | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG00099 | hp2 | a0002 | c0002 | t0002 | g0005 | EUR | GBR | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0147 | EUR | GBR | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | GBR | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | FIN | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG00323 | hp2 | a0006 | c0008 | t0001 | g0024 | EUR | FIN | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | CHS | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG00639 | hp2 | a0002 | c0002 | t0002 | g0014 | AMR | PUR | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG00673 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | CHS | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG00733 | hp1 | a0002 | c0002 | t0002 | g0014 | AMR | PUR | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG00735 | hp1 | a0002 | c0002 | t0002 | g0061 | AMR | PUR | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG00741 | hp1 | a0003 | c0004 | t0001 | g0084 | AMR | PUR | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG01069 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG01070 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0151 | AMR | PUR | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG01071 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG01099 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG01106 | hp1 | a0001 | c0015 | t0001 | g0142 | AMR | PUR | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG01109 | hp1 | a0002 | c0002 | t0002 | g0036 | AMR | PUR | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG01192 | hp1 | a0002 | c0002 | t0002 | g0005 | AMR | PUR | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG01358 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG01891 | hp1 | a0005 | c0005 | t0001 | g0041 | AFR | ACB | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | ACB | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG01928 | hp1 | a0002 | c0002 | t0002 | g0037 | AMR | PEL | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02004 | hp2 | a0002 | c0002 | t0002 | g0123 | AMR | PEL | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0060 | EAS | KHV | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02055 | hp2 | a0002 | c0002 | t0002 | g0119 | AFR | ACB | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02074 | hp2 | a0002 | c0002 | t0002 | g0058 | EAS | KHV | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02129 | hp1 | a0002 | c0002 | t0002 | g0062 | EAS | KHV | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CDX | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | CDX | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02257 | hp2 | a0005 | c0005 | t0001 | g0042 | AFR | ACB | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02273 | hp2 | a0002 | c0002 | t0002 | g0122 | AMR | PEL | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02280 | hp1 | a0011 | c0010 | t0001 | g0031 | AFR | ACB | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02280 | hp2 | a0002 | c0002 | t0002 | g0036 | AFR | ACB | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02293 | hp1 | a0002 | c0002 | t0002 | g0037 | AMR | PEL | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02451 | hp2 | a0003 | c0004 | t0001 | g0127 | AFR | ACB | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02572 | hp1 | a0007 | c0014 | t0003 | g0150 | AFR | GWD | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02602 | hp1 | a0008 | c0009 | t0002 | g0126 | SAS | PJL | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02622 | hp1 | a0002 | c0002 | t0002 | g0005 | AFR | GWD | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02630 | hp1 | a0002 | c0002 | t0002 | g0013 | AFR | GWD | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02630 | hp2 | a0001 | c0011 | t0002 | g0087 | AFR | GWD | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02735 | hp2 | a0008 | c0009 | t0002 | g0125 | SAS | PJL | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02895 | hp1 | a0005 | c0005 | t0001 | g0078 | AFR | GWD | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02895 | hp2 | a0002 | c0002 | t0002 | g0005 | AFR | GWD | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02922 | hp2 | a0003 | c0004 | t0001 | g0129 | AFR | ESN | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02970 | hp1 | a0004 | c0003 | t0001 | g0043 | AFR | ESN | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG03017 | hp1 | a0009 | c0007 | t0001 | g0006 | SAS | PJL | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG03017 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG03130 | hp2 | a0003 | c0004 | t0001 | g0128 | AFR | ESN | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG03139 | hp1 | a0002 | c0002 | t0002 | g0124 | AFR | ESN | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ESN | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG03195 | hp2 | a0002 | c0002 | t0002 | g0013 | AFR | ESN | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG03239 | hp1 | a0009 | c0007 | t0001 | g0006 | SAS | PJL | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG03239 | hp2 | a0006 | c0008 | t0001 | g0024 | SAS | PJL | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG03453 | hp1 | a0002 | c0002 | t0002 | g0053 | AFR | MSL | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | MSL | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG03491 | hp2 | a0002 | c0002 | t0002 | g0064 | SAS | PJL | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG03516 | hp1 | a0002 | c0002 | t0002 | g0054 | AFR | ESN | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG03540 | hp1 | a0004 | c0003 | t0001 | g0011 | AFR | GWD | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG03654 | hp2 | a0002 | c0002 | t0002 | g0005 | SAS | PJL | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG03704 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG03831 | hp1 | a0002 | c0002 | t0002 | g0057 | SAS | BEB | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG03831 | hp2 | a0010 | c0006 | t0001 | g0137 | SAS | BEB | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG03927 | hp1 | a0002 | c0002 | t0002 | g0059 | SAS | BEB | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | BEB | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | BEB | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | BEB | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG04115 | hp2 | a0002 | c0002 | t0002 | g0121 | SAS | STU | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18522 | hp1 | a0002 | c0002 | t0002 | g0013 | AFR | YRI | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | YRI | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18747 | hp1 | a0001 | c0001 | t0006 | g0111 | EAS | CHB | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CHB | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | YRI | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | YRI | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18941 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18944 | hp1 | a0002 | c0002 | t0002 | g0040 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18949 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18952 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18953 | hp1 | a0002 | c0002 | t0002 | g0021 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18957 | hp2 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18960 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18961 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18966 | hp1 | a0002 | c0002 | t0002 | g0040 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18967 | hp1 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18969 | hp2 | a0002 | c0002 | t0002 | g0063 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18971 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18972 | hp1 | a0002 | c0002 | t0002 | g0056 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18978 | hp1 | a0002 | c0002 | t0002 | g0066 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18980 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18984 | hp2 | a0002 | c0002 | t0002 | g0065 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18986 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18990 | hp1 | a0012 | c0016 | t0001 | g0075 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18991 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18999 | hp2 | a0010 | c0006 | t0001 | g0091 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA19005 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA19010 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA19011 | hp1 | a0002 | c0002 | t0002 | g0021 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA19030 | hp1 | a0004 | c0003 | t0001 | g0011 | AFR | LWK | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA19030 | hp2 | a0002 | c0002 | t0002 | g0055 | AFR | LWK | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA19043 | hp1 | a0013 | c0012 | t0003 | g0149 | AFR | LWK | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | LWK | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA19054 | hp2 | a0002 | c0002 | t0002 | g0035 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA19062 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA19063 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA19065 | hp2 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA19067 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA19075 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA19081 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA19084 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA19086 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA19087 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA19088 | hp1 | a0002 | c0002 | t0002 | g0035 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG01123 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02109 | hp2 | a0004 | c0003 | t0001 | g0011 | AFR | ACB | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| HG02559 | hp2 | a0007 | c0013 | t0005 | g0045 | AFR | ACB | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | USA | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | USA | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0006 | REF | REF | LGALS9C_chr17_18471789_18499945 | LGALS9C | chr17 | 18471789 | 18499945 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:18476871 | G | C | 1 | a0011 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.17G>C | p.Cys6Ser | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/11 | 83/1715 | 17/1071 | 6/356 | chr17 | 18476871 | |||
| chr17:18483878 | G | A | 1 | a0004 | 4 | HG02109.hp2 HG02970.hp1 HG03540.hp1 others(1): Show |
missense_variant | MODERATE | c.43G>A | p.Val15Ile | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/11 | 109/1715 | 43/1071 | 15/356 | chr17 | 18483878 | |||
| chr17:18483954 | G | C | 3 | a0005 a0007 a0013 |
6 | HG01891.hp1 HG02257.hp2 HG02559.hp2 others(3): Show |
missense_variant | MODERATE | c.119G>C | p.Cys40Ser | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/11 | 185/1715 | 119/1071 | 40/356 | chr17 | 18483954 | |||
| chr17:18485971 | G | A | 1 | a0005 | 3 | HG01891.hp1 HG02257.hp2 HG02895.hp1 |
missense_variant | MODERATE | c.169G>A | p.Asp57Asn | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/11 | 235/1715 | 169/1071 | 57/356 | chr17 | 18485971 | |||
| chr17:18486044 | C | G | 4 | a0002 a0003 a0004 others(1): Show |
82 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(79): Show |
missense_variant | MODERATE | c.242C>G | p.Thr81Arg | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/11 | 308/1715 | 242/1071 | 81/356 | chr17 | 18486044 | |||
| chr17:18486050 | G | C | 1 | a0010 | 2 | HG03831.hp2 NA18999.hp2 |
missense_variant | MODERATE | c.248G>C | p.Gly83Ala | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/11 | 314/1715 | 248/1071 | 83/356 | chr17 | 18486050 | |||
| chr17:18487689 | G | A | 3 | a0002 a0004 a0008 |
77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
missense_variant | MODERATE | c.376G>A | p.Val126Met | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 4/11 | 442/1715 | 376/1071 | 126/356 | chr17 | 18487689 | |||
| chr17:18488950 | G | A | 1 | a0003 | 4 | HG00741.hp1 HG02451.hp2 HG02922.hp2 others(1): Show |
missense_variant | MODERATE | c.454G>A | p.Ala152Thr | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/11 | 520/1715 | 454/1071 | 152/356 | chr17 | 18488950 | |||
| chr17:18488990 | C | A | 1 | a0009 | 2 | HG03017.hp1 HG03239.hp1 |
missense_variant | MODERATE | c.494C>A | p.Ser165Tyr | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/11 | 560/1715 | 494/1071 | 165/356 | chr17 | 18488990 | |||
| chr17:18490742 | G | A | 2 | a0003 a0013 |
5 | HG00741.hp1 HG02451.hp2 HG02922.hp2 others(2): Show |
missense_variant | MODERATE | c.550G>A | p.Val184Met | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 6/11 | 616/1715 | 550/1071 | 184/356 | chr17 | 18490742 | |||
| chr17:18491954 | G | C | 1 | a0006 | 2 | HG00323.hp2 HG03239.hp2 |
missense_variant | MODERATE | c.637G>C | p.Ala213Pro | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 8/11 | 703/1715 | 637/1071 | 213/356 | chr17 | 18491954 | |||
| chr17:18494240 | C | G | 1 | a0012 | 1 | NA18990.hp1 | missense_variant | MODERATE | c.944C>G | p.Ala315Gly | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 11/11 | 1010/1715 | 944/1071 | 315/356 | chr17 | 18494240 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:18483931 | T | C | 1 | a0001c0011 | 1 | HG02630.hp2 | synonymous_variant | LOW | c.96T>C | p.Thr32Thr | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/11 | 162/1715 | 96/1071 | 32/356 | chr17 | 18483931 | |||
| chr17:18487679 | C | T | 3 | a0002c0002 a0004c0003 a0008c0009 |
77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
synonymous_variant | LOW | c.366C>T | p.Tyr122Tyr | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 4/11 | 432/1715 | 366/1071 | 122/356 | chr17 | 18487679 | |||
| chr17:18488958 | C | A | 1 | a0005c0005 | 3 | HG01891.hp1 HG02257.hp2 HG02895.hp1 |
synonymous_variant | LOW | c.462C>A | p.Pro154Pro | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/11 | 528/1715 | 462/1071 | 154/356 | chr17 | 18488958 | |||
| chr17:18491302 | T | C | 5 | a0002c0002 a0003c0004 a0004c0003 others(2): Show |
82 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(79): Show |
synonymous_variant | LOW | c.606T>C | p.Ser202Ser | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 7/11 | 672/1715 | 606/1071 | 202/356 | chr17 | 18491302 | |||
| chr17:18492817 | T | C | 1 | a0001c0015 | 1 | HG01106.hp1 | synonymous_variant | LOW | c.882T>C | p.Ser294Ser | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 10/11 | 948/1715 | 882/1071 | 294/356 | chr17 | 18492817 | |||
| chr17:18492838 | C | T | 1 | a0007c0013 | 1 | HG02559.hp2 | synonymous_variant | LOW | c.903C>T | p.Phe301Phe | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 10/11 | 969/1715 | 903/1071 | 301/356 | chr17 | 18492838 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:18476821 | C | G | 1 | a0001c0001t0006 | 1 | NA18747.hp1 | 5_prime_UTR_variant | MODIFIER | c.-34C>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/11 | 34 | chr17 | 18476821 | ||||||
| chr17:18476830 | T | C | 1 | a0001c0001t0006 | 1 | NA18747.hp1 | 5_prime_UTR_variant | MODIFIER | c.-25T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/11 | 25 | chr17 | 18476830 | ||||||
| chr17:18494413 | T | G | 4 | a0001c0001t0002 a0001c0011t0002 a0002c0002t0002 others(1): Show |
78 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*46T>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 11/11 | 46 | chr17 | 18494413 | ||||||
| chr17:18494415 | G | A | 1 | a0007c0013t0005 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*48G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 11/11 | 48 | chr17 | 18494415 | ||||||
| chr17:18494771 | C | T | 1 | a0001c0001t0004 | 2 | HG01891.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*404C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 11/11 | 404 | chr17 | 18494771 | ||||||
| chr17:18494778 | C | A | 1 | a0001c0001t0004 | 2 | HG01891.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*411C>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 11/11 | 411 | chr17 | 18494778 | ||||||
| chr17:18494913 | A | G | 2 | a0007c0014t0003 a0013c0012t0003 |
2 | HG02572.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*546A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 11/11 | 546 | chr17 | 18494913 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:18476982 | G | A | 2 | a0005c0005t0001g0041 a0005c0005t0001g0042 |
2 | HG01891.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.39+89G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18476982 | |||||||
| chr17:18477052 | G | A | 2 | a0004c0003t0001g0011 a0004c0003t0001g0043 |
4 | HG02109.hp2 HG02970.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.39+159G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18477052 | |||||||
| chr17:18477085 | A | G | 2 | a0001c0001t0001g0152 a0001c0001t0002g0151 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.39+192A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18477085 | |||||||
| chr17:18477102 | G | A | 2 | a0001c0001t0001g0152 a0001c0001t0002g0151 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.39+209G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18477102 | |||||||
| chr17:18477176 | A | G | 2 | a0007c0014t0003g0150 a0013c0012t0003g0149 |
2 | HG02572.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.39+283A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18477176 | |||||||
| chr17:18477348 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.39+455C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18477348 | |||||||
| chr17:18477463 | T | G | 2 | a0001c0001t0001g0012 a0001c0001t0001g0044 |
4 | HG00140.hp2 HG00323.hp1 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.39+570T>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18477463 | |||||||
| chr17:18477568 | G | T | 1 | a0002c0002t0002g0040 | 2 | NA18944.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.39+675G>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18477568 | |||||||
| chr17:18477573 | G | A | 3 | a0007c0013t0005g0045 a0007c0014t0003g0150 a0013c0012t0003g0149 |
3 | HG02559.hp2 HG02572.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.39+680G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18477573 | |||||||
| chr17:18477576 | G | A | 3 | a0007c0013t0005g0045 a0007c0014t0003g0150 a0013c0012t0003g0149 |
3 | HG02559.hp2 HG02572.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.39+683G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18477576 | |||||||
| chr17:18477662 | C | T | 1 | a0007c0014t0003g0150 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.39+769C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18477662 | |||||||
| chr17:18477774 | C | T | 25 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(22): Show |
58 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.39+881C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18477774 | |||||||
| chr17:18477836 | T | C | 1 | a0001c0001t0001g0046 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.39+943T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18477836 | |||||||
| chr17:18477843 | C | A | 1 | a0013c0012t0003g0149 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.39+950C>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18477843 | |||||||
| chr17:18477861 | G | A | 1 | a0007c0013t0005g0045 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.39+968G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18477861 | |||||||
| chr17:18477940 | T | C | 35 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0047 others(32): Show |
67 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.39+1047T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18477940 | |||||||
| chr17:18477954 | C | T | 3 | a0003c0004t0001g0127 a0003c0004t0001g0128 a0003c0004t0001g0129 |
3 | HG02451.hp2 HG02922.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.39+1061C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18477954 | |||||||
| chr17:18478029 | A | C | 47 | a0001c0001t0001g0010 a0001c0001t0001g0052 a0001c0001t0001g0115 others(44): Show |
94 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.39+1136A>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18478029 | |||||||
| chr17:18478035 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.39+1142G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18478035 | |||||||
| chr17:18478107 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.39+1214C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18478107 | |||||||
| chr17:18478148 | T | C | 4 | a0001c0001t0001g0023 a0001c0001t0001g0068 a0001c0001t0001g0069 others(1): Show |
5 | HG02055.hp1 HG02486.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.39+1255T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18478148 | |||||||
| chr17:18478150 | G | C | 1 | a0001c0001t0001g0131 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.39+1257G>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18478150 | |||||||
| chr17:18478156 | C | G | 1 | a0001c0001t0001g0113 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.39+1263C>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18478156 | |||||||
| chr17:18478156 | C | T | 10 | a0002c0002t0002g0005 a0002c0002t0002g0035 a0002c0002t0002g0036 others(7): Show |
23 | HG00099.hp2 HG01109.hp1 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.39+1263C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18478156 | |||||||
| chr17:18478208 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.39+1315C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18478208 | |||||||
| chr17:18478209 | A | G | 4 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0112 others(1): Show |
4 | HG01978.hp1 HG02129.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.39+1316A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18478209 | |||||||
| chr17:18478233 | G | T | 2 | a0001c0001t0001g0120 a0001c0001t0002g0022 |
3 | HG01069.hp1 HG01099.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.39+1340G>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18478233 | |||||||
| chr17:18478252 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.39+1359A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18478252 | |||||||
| chr17:18478492 | T | C | 45 | a0001c0001t0001g0010 a0001c0001t0001g0052 a0001c0001t0001g0115 others(42): Show |
91 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.39+1599T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18478492 | |||||||
| chr17:18478497 | C | T | 1 | a0013c0012t0003g0149 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.39+1604C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18478497 | |||||||
| chr17:18478517 | T | G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0071 |
4 | HG02572.hp2 HG02622.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.39+1624T>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18478517 | |||||||
| chr17:18478621 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.39+1728A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18478621 | |||||||
| chr17:18478646 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.39+1753G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18478646 | |||||||
| chr17:18478697 | A | C | 1 | a0007c0013t0005g0045 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.39+1804A>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18478697 | |||||||
| chr17:18478782 | C | T | 2 | a0001c0001t0001g0120 a0001c0001t0002g0022 |
3 | HG01069.hp1 HG01099.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.39+1889C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18478782 | |||||||
| chr17:18478783 | G | A | 13 | a0001c0001t0001g0010 a0001c0001t0001g0115 a0001c0001t0001g0116 others(10): Show |
29 | HG00099.hp2 HG01109.hp1 HG01192.hp1 others(26): Show |
intron_variant | MODIFIER | c.39+1890G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18478783 | |||||||
| chr17:18478860 | T | A | 1 | a0001c0001t0001g0120 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.39+1967T>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18478860 | |||||||
| chr17:18478914 | G | C | 5 | a0005c0005t0001g0041 a0005c0005t0001g0042 a0007c0013t0005g0045 others(2): Show |
5 | HG01891.hp1 HG02257.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.39+2021G>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18478914 | |||||||
| chr17:18479040 | G | C | 1 | a0001c0001t0001g0072 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.39+2147G>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18479040 | |||||||
| chr17:18479070 | C | T | 2 | a0004c0003t0001g0011 a0004c0003t0001g0043 |
4 | HG02109.hp2 HG02970.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.39+2177C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18479070 | |||||||
| chr17:18479098 | C | T | 1 | a0002c0002t0002g0037 | 2 | HG01928.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.39+2205C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18479098 | |||||||
| chr17:18479119 | C | T | 2 | a0004c0003t0001g0011 a0004c0003t0001g0043 |
4 | HG02109.hp2 HG02970.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.39+2226C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18479119 | |||||||
| chr17:18479244 | C | T | 1 | a0001c0001t0006g0111 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.39+2351C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18479244 | |||||||
| chr17:18479274 | T | C | 1 | a0001c0001t0001g0046 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.39+2381T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18479274 | |||||||
| chr17:18479317 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.39+2424A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18479317 | |||||||
| chr17:18479366 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.39+2473G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18479366 | |||||||
| chr17:18479386 | G | A | 4 | a0002c0002t0002g0013 a0002c0002t0002g0053 a0002c0002t0002g0054 others(1): Show |
6 | HG02630.hp1 HG03195.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.39+2493G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18479386 | |||||||
| chr17:18479439 | C | T | 2 | a0001c0001t0001g0120 a0001c0001t0002g0022 |
3 | HG01069.hp1 HG01099.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.39+2546C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18479439 | |||||||
| chr17:18479472 | T | C | 44 | a0001c0001t0001g0010 a0001c0001t0001g0115 a0001c0001t0001g0116 others(41): Show |
90 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.39+2579T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18479472 | |||||||
| chr17:18479533 | T | C | 2 | a0005c0005t0001g0041 a0005c0005t0001g0042 |
2 | HG01891.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.39+2640T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18479533 | |||||||
| chr17:18479555 | A | T | 4 | a0002c0002t0002g0013 a0002c0002t0002g0053 a0002c0002t0002g0054 others(1): Show |
6 | HG02630.hp1 HG03195.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.39+2662A>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18479555 | |||||||
| chr17:18479655 | C | T | 1 | a0001c0001t0006g0111 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.39+2762C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18479655 | |||||||
| chr17:18479867 | G | GCTGC | 15 | a0001c0001t0001g0010 a0001c0001t0001g0115 a0001c0001t0001g0116 others(12): Show |
31 | HG00099.hp2 HG01109.hp1 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.39+2985_39+2988dup others(4): Show |
LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 18479867 | ||||||
| chr17:18479879 | C | A | 1 | a0001c0001t0002g0130 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.39+2986C>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18479879 | |||||||
| chr17:18479880 | C | T | 17 | a0002c0002t0002g0002 a0002c0002t0002g0014 a0002c0002t0002g0019 others(14): Show |
43 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.39+2987C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18479880 | |||||||
| chr17:18479969 | G | A | 1 | a0006c0008t0001g0024 | 2 | HG00323.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.39+3076G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18479969 | |||||||
| chr17:18480112 | G | A | 1 | a0013c0012t0003g0149 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.39+3219G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18480112 | |||||||
| chr17:18480156 | T | C | 1 | a0007c0013t0005g0045 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.39+3263T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18480156 | |||||||
| chr17:18480178 | C | T | 1 | a0002c0002t0002g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.39+3285C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18480178 | |||||||
| chr17:18480208 | C | CA | 13 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0073 others(10): Show |
19 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(16): Show |
intron_variant | MODIFIER | c.39+3333dupA | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 18480208 | ||||||
| chr17:18480208 | CA | C | 6 | a0001c0001t0001g0069 a0001c0001t0001g0106 a0001c0001t0001g0107 others(3): Show |
7 | HG01069.hp1 HG01099.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.39+3333delA | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 18480208 | ||||||
| chr17:18480219 | A | C | 18 | a0001c0001t0001g0010 a0001c0001t0001g0116 a0001c0001t0001g0117 others(15): Show |
36 | HG00099.hp2 HG01109.hp1 HG01192.hp1 others(33): Show |
intron_variant | MODIFIER | c.39+3326A>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18480219 | |||||||
| chr17:18480220 | A | AC | 14 | a0002c0002t0002g0002 a0002c0002t0002g0014 a0002c0002t0002g0019 others(11): Show |
40 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.39+3327_39+3328ins others(1): Show |
LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18480220 | |||||||
| chr17:18480226 | A | C | 1 | a0001c0001t0001g0034 | 2 | NA18955.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.39+3333A>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18480226 | |||||||
| chr17:18480322 | G | A | 21 | a0001c0001t0001g0010 a0001c0001t0001g0115 a0001c0001t0001g0116 others(18): Show |
39 | HG00099.hp2 HG01109.hp1 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.39+3429G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18480322 | |||||||
| chr17:18480554 | C | G | 2 | a0001c0001t0001g0039 a0001c0001t0001g0146 |
3 | HG01109.hp2 HG02647.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.40-3321C>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18480554 | |||||||
| chr17:18480620 | T | C | 2 | a0001c0001t0001g0080 a0001c0001t0001g0081 |
2 | HG00735.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.40-3255T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18480620 | |||||||
| chr17:18480685 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.40-3190A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18480685 | |||||||
| chr17:18480812 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.40-3063C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18480812 | |||||||
| chr17:18481012 | T | A | 1 | a0002c0002t0002g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.40-2863T>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18481012 | |||||||
| chr17:18481091 | A | G | 1 | a0007c0013t0005g0045 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.40-2784A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18481091 | |||||||
| chr17:18481117 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.40-2758G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18481117 | |||||||
| chr17:18481227 | G | A | 2 | a0005c0005t0001g0041 a0005c0005t0001g0042 |
2 | HG01891.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.40-2648G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18481227 | |||||||
| chr17:18481366 | G | A | 34 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0013 others(31): Show |
77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.40-2509G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18481366 | |||||||
| chr17:18481383 | C | T | 1 | a0001c0001t0001g0046 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.40-2492C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18481383 | |||||||
| chr17:18481384 | G | A | 8 | a0002c0002t0002g0005 a0002c0002t0002g0035 a0002c0002t0002g0036 others(5): Show |
21 | HG00099.hp2 HG01109.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.40-2491G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18481384 | |||||||
| chr17:18481485 | A | G | 12 | a0002c0002t0002g0005 a0002c0002t0002g0013 a0002c0002t0002g0035 others(9): Show |
27 | HG00099.hp2 HG01109.hp1 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.40-2390A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18481485 | |||||||
| chr17:18481513 | C | T | 1 | a0001c0001t0001g0103 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.40-2362C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18481513 | |||||||
| chr17:18481515 | C | T | 1 | a0007c0013t0005g0045 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.40-2360C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18481515 | |||||||
| chr17:18481658 | G | A | 1 | a0001c0001t0001g0134 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.40-2217G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18481658 | |||||||
| chr17:18481666 | AAGTATTT others(24): Show |
A | 1 | a0001c0001t0001g0070 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.40-2208_40-2178del others(31): Show |
LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18481666 | |||||||
| chr17:18481759 | C | T | 19 | a0002c0002t0002g0002 a0002c0002t0002g0014 a0002c0002t0002g0019 others(16): Show |
47 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.40-2116C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18481759 | |||||||
| chr17:18481782 | G | T | 1 | a0001c0001t0001g0107 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.40-2093G>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18481782 | |||||||
| chr17:18481828 | G | C | 1 | a0001c0001t0001g0120 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.40-2047G>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18481828 | |||||||
| chr17:18481925 | T | C | 37 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0013 others(34): Show |
80 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.40-1950T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18481925 | |||||||
| chr17:18482035 | A | T | 1 | a0001c0001t0001g0070 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.40-1840A>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482035 | |||||||
| chr17:18482081 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.40-1794C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482081 | |||||||
| chr17:18482140 | G | A | 14 | a0002c0002t0002g0005 a0002c0002t0002g0013 a0002c0002t0002g0035 others(11): Show |
29 | HG00099.hp2 HG01109.hp1 HG01192.hp1 others(26): Show |
intron_variant | MODIFIER | c.40-1735G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482140 | |||||||
| chr17:18482158 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.40-1717T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482158 | |||||||
| chr17:18482159 | C | A | 1 | a0002c0002t0002g0054 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.40-1716C>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482159 | |||||||
| chr17:18482159 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.40-1716C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482159 | |||||||
| chr17:18482197 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.40-1678G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482197 | |||||||
| chr17:18482197 | G | C | 1 | a0001c0001t0001g0080 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.40-1678G>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482197 | |||||||
| chr17:18482204 | G | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0044 a0001c0001t0001g0114 |
5 | HG02109.hp1 HG02451.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.40-1671G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482204 | |||||||
| chr17:18482213 | G | A | 1 | a0007c0013t0005g0045 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.40-1662G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482213 | |||||||
| chr17:18482266 | C | T | 14 | a0002c0002t0002g0005 a0002c0002t0002g0013 a0002c0002t0002g0035 others(11): Show |
29 | HG00099.hp2 HG01109.hp1 HG01192.hp1 others(26): Show |
intron_variant | MODIFIER | c.40-1609C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482266 | |||||||
| chr17:18482295 | A | C | 1 | a0001c0001t0001g0070 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.40-1580A>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482295 | |||||||
| chr17:18482418 | A | C | 1 | a0001c0001t0001g0070 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.40-1457A>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482418 | |||||||
| chr17:18482478 | G | A | 16 | a0002c0002t0002g0005 a0002c0002t0002g0013 a0002c0002t0002g0035 others(13): Show |
31 | HG00099.hp2 HG01109.hp1 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.40-1397G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482478 | |||||||
| chr17:18482484 | C | T | 18 | a0002c0002t0002g0002 a0002c0002t0002g0014 a0002c0002t0002g0019 others(15): Show |
45 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.40-1391C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482484 | |||||||
| chr17:18482507 | C | CA | 14 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0027 others(11): Show |
22 | HG00733.hp2 HG00741.hp2 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.40-1350dupA | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 18482507 | ||||||
| chr17:18482507 | C | CAA | 16 | a0001c0001t0001g0135 a0002c0002t0002g0002 a0002c0002t0002g0014 others(13): Show |
41 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.40-1351_40-1350dup others(2): Show |
LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 18482507 | ||||||
| chr17:18482507 | CA | C | 13 | a0001c0001t0001g0033 a0001c0001t0001g0068 a0001c0001t0001g0079 others(10): Show |
14 | HG00438.hp1 HG00558.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.40-1350delA | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 18482507 | ||||||
| chr17:18482507 | CAA | C | 8 | a0002c0002t0002g0005 a0002c0002t0002g0035 a0002c0002t0002g0036 others(5): Show |
21 | HG00099.hp2 HG01109.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.40-1351_40-1350del others(2): Show |
LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 18482507 | ||||||
| chr17:18482530 | G | A | 1 | a0002c0002t0002g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.40-1345G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482530 | |||||||
| chr17:18482531 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.40-1344G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482531 | |||||||
| chr17:18482568 | A | C | 2 | a0004c0003t0001g0011 a0004c0003t0001g0043 |
4 | HG02109.hp2 HG02970.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.40-1307A>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482568 | |||||||
| chr17:18482582 | C | T | 1 | a0002c0002t0002g0054 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.40-1293C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482582 | |||||||
| chr17:18482606 | A | T | 13 | a0002c0002t0002g0005 a0002c0002t0002g0013 a0002c0002t0002g0035 others(10): Show |
28 | HG00099.hp2 HG01109.hp1 HG01192.hp1 others(25): Show |
intron_variant | MODIFIER | c.40-1269A>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482606 | |||||||
| chr17:18482628 | G | A | 10 | a0002c0002t0002g0005 a0002c0002t0002g0035 a0002c0002t0002g0036 others(7): Show |
23 | HG00099.hp2 HG01109.hp1 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.40-1247G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482628 | |||||||
| chr17:18482673 | G | A | 2 | a0005c0005t0001g0041 a0005c0005t0001g0042 |
2 | HG01891.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.40-1202G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482673 | |||||||
| chr17:18482679 | C | A | 1 | a0001c0001t0001g0070 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.40-1196C>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482679 | |||||||
| chr17:18482853 | G | A | 1 | a0007c0014t0003g0150 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.40-1022G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482853 | |||||||
| chr17:18482868 | A | G | 15 | a0002c0002t0002g0005 a0002c0002t0002g0013 a0002c0002t0002g0035 others(12): Show |
30 | HG00099.hp2 HG01109.hp1 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.40-1007A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482868 | |||||||
| chr17:18482898 | C | G | 1 | a0002c0002t0002g0064 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.40-977C>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482898 | |||||||
| chr17:18482912 | TG | T | 21 | a0002c0002t0002g0002 a0002c0002t0002g0014 a0002c0002t0002g0019 others(18): Show |
49 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.40-957delG | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 18482912 | ||||||
| chr17:18482946 | T | C | 1 | a0007c0013t0005g0045 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.40-929T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482946 | |||||||
| chr17:18483118 | G | C | 15 | a0002c0002t0002g0005 a0002c0002t0002g0013 a0002c0002t0002g0035 others(12): Show |
30 | HG00099.hp2 HG01109.hp1 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.40-757G>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18483118 | |||||||
| chr17:18483175 | G | A | 2 | a0005c0005t0001g0041 a0005c0005t0001g0042 |
2 | HG01891.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.40-700G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18483175 | |||||||
| chr17:18483179 | AAG | A | 20 | a0002c0002t0002g0002 a0002c0002t0002g0014 a0002c0002t0002g0019 others(17): Show |
48 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.40-690_40-689delGA | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 18483179 | ||||||
| chr17:18483204 | C | T | 16 | a0002c0002t0002g0002 a0002c0002t0002g0014 a0002c0002t0002g0020 others(13): Show |
41 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.40-671C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18483204 | |||||||
| chr17:18483228 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.40-647G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18483228 | |||||||
| chr17:18483243 | C | A | 1 | a0001c0001t0001g0070 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.40-632C>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18483243 | |||||||
| chr17:18483397 | C | T | 3 | a0001c0001t0001g0025 a0001c0001t0001g0097 a0001c0001t0001g0104 |
4 | HG02027.hp1 HG02071.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.40-478C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18483397 | |||||||
| chr17:18483404 | G | A | 18 | a0002c0002t0002g0002 a0002c0002t0002g0014 a0002c0002t0002g0019 others(15): Show |
44 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.40-471G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18483404 | |||||||
| chr17:18483407 | C | T | 38 | a0001c0001t0001g0051 a0001c0001t0001g0107 a0002c0002t0002g0002 others(35): Show |
81 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.40-468C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18483407 | |||||||
| chr17:18483424 | G | A | 20 | a0002c0002t0002g0002 a0002c0002t0002g0014 a0002c0002t0002g0019 others(17): Show |
48 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.40-451G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18483424 | |||||||
| chr17:18483452 | G | A | 1 | a0004c0003t0001g0043 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.40-423G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18483452 | |||||||
| chr17:18483562 | G | T | 4 | a0002c0002t0002g0013 a0002c0002t0002g0053 a0002c0002t0002g0054 others(1): Show |
6 | HG02630.hp1 HG03195.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.40-313G>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18483562 | |||||||
| chr17:18483571 | G | A | 1 | a0010c0006t0001g0137 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.40-304G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18483571 | |||||||
| chr17:18483686 | T | C | 20 | a0002c0002t0002g0002 a0002c0002t0002g0014 a0002c0002t0002g0019 others(17): Show |
48 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.40-189T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18483686 | |||||||
| chr17:18483709 | C | T | 2 | a0007c0014t0003g0150 a0013c0012t0003g0149 |
2 | HG02572.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.40-166C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18483709 | |||||||
| chr17:18483777 | A | T | 1 | a0001c0001t0001g0070 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.40-98A>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18483777 | |||||||
| chr17:18483815 | C | T | 38 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0013 others(35): Show |
82 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.40-60C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18483815 | |||||||
| chr17:18483817 | A | G | 17 | a0002c0002t0002g0005 a0002c0002t0002g0013 a0002c0002t0002g0035 others(14): Show |
32 | HG00099.hp2 HG01109.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.40-58A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18483817 | |||||||
| chr17:18483854 | C | T | 10 | a0002c0002t0002g0005 a0002c0002t0002g0035 a0002c0002t0002g0036 others(7): Show |
23 | HG00099.hp2 HG01109.hp1 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.40-21C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18483854 | |||||||
| chr17:18483977 | A | G | 1 | a0007c0013t0005g0045 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.131+11A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18483977 | |||||||
| chr17:18484041 | C | T | 37 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0013 others(34): Show |
80 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.131+75C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18484041 | |||||||
| chr17:18484079 | G | T | 19 | a0002c0002t0002g0002 a0002c0002t0002g0014 a0002c0002t0002g0019 others(16): Show |
47 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.131+113G>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18484079 | |||||||
| chr17:18484152 | T | G | 1 | a0001c0001t0001g0070 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.131+186T>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18484152 | |||||||
| chr17:18484164 | G | A | 1 | a0003c0004t0001g0127 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.131+198G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18484164 | |||||||
| chr17:18484208 | A | G | 37 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0013 others(34): Show |
80 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.131+242A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18484208 | |||||||
| chr17:18484302 | CA | C | 34 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0013 others(31): Show |
77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.131+337delA | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18484302 | |||||||
| chr17:18484312 | C | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0072 |
5 | HG00558.hp2 HG00597.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.131+346C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18484312 | |||||||
| chr17:18484456 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.131+490C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18484456 | |||||||
| chr17:18484509 | C | A | 1 | a0001c0001t0001g0120 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.131+543C>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18484509 | |||||||
| chr17:18484538 | C | T | 1 | a0002c0002t0002g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.131+572C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18484538 | |||||||
| chr17:18484599 | G | GTGCAGCT others(13): Show |
1 | a0001c0001t0001g0096 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.131+634_131+653dup others(20): Show |
LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 18484599 | ||||||
| chr17:18484650 | G | T | 19 | a0002c0002t0002g0002 a0002c0002t0002g0014 a0002c0002t0002g0019 others(16): Show |
46 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.131+684G>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18484650 | |||||||
| chr17:18484775 | C | G | 32 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0013 others(29): Show |
75 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.131+809C>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18484775 | |||||||
| chr17:18484799 | C | T | 34 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0013 others(31): Show |
77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.131+833C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18484799 | |||||||
| chr17:18484803 | C | T | 1 | a0007c0013t0005g0045 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.131+837C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18484803 | |||||||
| chr17:18484868 | C | T | 3 | a0005c0005t0001g0041 a0005c0005t0001g0042 a0005c0005t0001g0078 |
3 | HG01891.hp1 HG02257.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.131+902C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18484868 | |||||||
| chr17:18484885 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.131+919C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18484885 | |||||||
| chr17:18484958 | T | C | 34 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0013 others(31): Show |
77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.132-976T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18484958 | |||||||
| chr17:18484959 | G | T | 11 | a0002c0002t0002g0005 a0002c0002t0002g0020 a0002c0002t0002g0035 others(8): Show |
25 | HG00099.hp2 HG01109.hp1 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.132-975G>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18484959 | |||||||
| chr17:18484980 | C | A | 1 | a0001c0001t0001g0071 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.132-954C>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18484980 | |||||||
| chr17:18485012 | G | A | 20 | a0001c0001t0001g0026 a0002c0002t0002g0002 a0002c0002t0002g0014 others(17): Show |
48 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.132-922G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18485012 | |||||||
| chr17:18485323 | G | A | 38 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0013 others(35): Show |
81 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.132-611G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18485323 | |||||||
| chr17:18485354 | A | AAT | 27 | a0002c0002t0002g0002 a0002c0002t0002g0013 a0002c0002t0002g0014 others(24): Show |
56 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.132-567_132-566dup others(2): Show |
LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 18485354 | ||||||
| chr17:18485354 | A | AATAT | 11 | a0002c0002t0002g0005 a0002c0002t0002g0020 a0002c0002t0002g0035 others(8): Show |
25 | HG00099.hp2 HG01109.hp1 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.132-569_132-566dup others(4): Show |
LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 18485354 | ||||||
| chr17:18485360 | T | A | 1 | a0001c0001t0001g0070 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.132-574T>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18485360 | |||||||
| chr17:18485439 | G | A | 15 | a0002c0002t0002g0005 a0002c0002t0002g0013 a0002c0002t0002g0020 others(12): Show |
31 | HG00099.hp2 HG01109.hp1 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.132-495G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18485439 | |||||||
| chr17:18485562 | G | T | 34 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0013 others(31): Show |
77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.132-372G>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18485562 | |||||||
| chr17:18485604 | T | C | 2 | a0007c0014t0003g0150 a0013c0012t0003g0149 |
2 | HG02572.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.132-330T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18485604 | |||||||
| chr17:18485752 | C | T | 39 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0013 others(36): Show |
82 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.132-182C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18485752 | |||||||
| chr17:18485792 | G | C | 4 | a0003c0004t0001g0084 a0003c0004t0001g0127 a0003c0004t0001g0128 others(1): Show |
4 | HG00741.hp1 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.132-142G>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18485792 | |||||||
| chr17:18485863 | C | T | 4 | a0003c0004t0001g0084 a0003c0004t0001g0127 a0003c0004t0001g0128 others(1): Show |
4 | HG00741.hp1 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.132-71C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18485863 | |||||||
| chr17:18486138 | A | G | 34 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0013 others(31): Show |
77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
splice_region_variant&intron_variant | LOW | c.333+3A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18486138 | |||||||
| chr17:18486203 | G | C | 1 | a0001c0001t0001g0070 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.333+68G>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18486203 | |||||||
| chr17:18486245 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.333+110C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18486245 | |||||||
| chr17:18486461 | A | G | 2 | a0002c0002t0002g0122 a0002c0002t0002g0123 |
2 | HG02004.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.333+326A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18486461 | |||||||
| chr17:18486504 | C | T | 38 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0013 others(35): Show |
81 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.333+369C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18486504 | |||||||
| chr17:18486520 | T | C | 1 | a0001c0001t0001g0098 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.333+385T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18486520 | |||||||
| chr17:18486539 | G | A | 2 | a0007c0014t0003g0150 a0013c0012t0003g0149 |
2 | HG02572.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.333+404G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18486539 | |||||||
| chr17:18486554 | C | T | 3 | a0005c0005t0001g0041 a0005c0005t0001g0042 a0005c0005t0001g0078 |
3 | HG01891.hp1 HG02257.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.333+419C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18486554 | |||||||
| chr17:18486645 | T | A | 1 | a0001c0001t0001g0070 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.333+510T>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18486645 | |||||||
| chr17:18486651 | A | T | 34 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0013 others(31): Show |
77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.333+516A>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18486651 | |||||||
| chr17:18486705 | A | G | 2 | a0001c0001t0001g0009 a0001c0001t0001g0072 |
5 | HG00558.hp2 HG00597.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.333+570A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18486705 | |||||||
| chr17:18486734 | A | G | 1 | a0001c0001t0001g0050 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.333+599A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18486734 | |||||||
| chr17:18486747 | C | A | 1 | a0001c0001t0001g0070 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.333+612C>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18486747 | |||||||
| chr17:18486765 | G | T | 1 | a0001c0001t0001g0096 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.333+630G>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18486765 | |||||||
| chr17:18486778 | G | A | 1 | a0005c0005t0001g0041 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.333+643G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18486778 | |||||||
| chr17:18486807 | A | T | 34 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0013 others(31): Show |
77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.333+672A>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18486807 | |||||||
| chr17:18486839 | A | G | 3 | a0002c0002t0002g0054 a0007c0014t0003g0150 a0013c0012t0003g0149 |
3 | HG02572.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.333+704A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18486839 | |||||||
| chr17:18486857 | C | A | 1 | a0002c0002t0002g0021 | 2 | NA18953.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.333+722C>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18486857 | |||||||
| chr17:18486857 | C | T | 6 | a0002c0002t0002g0053 a0003c0004t0001g0084 a0003c0004t0001g0127 others(3): Show |
6 | HG00741.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.333+722C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18486857 | |||||||
| chr17:18486858 | G | A | 4 | a0002c0002t0002g0055 a0005c0005t0001g0041 a0005c0005t0001g0042 others(1): Show |
4 | HG01891.hp1 HG02257.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.333+723G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18486858 | |||||||
| chr17:18486887 | G | A | 5 | a0002c0002t0002g0013 a0005c0005t0001g0041 a0005c0005t0001g0042 others(2): Show |
7 | HG01891.hp1 HG02257.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.333+752G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18486887 | |||||||
| chr17:18486887 | G | C | 7 | a0002c0002t0002g0054 a0003c0004t0001g0084 a0003c0004t0001g0127 others(4): Show |
7 | HG00741.hp1 HG02451.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.333+752G>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18486887 | |||||||
| chr17:18486953 | T | C | 24 | a0002c0002t0002g0002 a0002c0002t0002g0014 a0002c0002t0002g0019 others(21): Show |
51 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.334-694T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18486953 | |||||||
| chr17:18486970 | T | C | 46 | a0001c0001t0001g0025 a0001c0001t0001g0029 a0001c0001t0001g0074 others(43): Show |
91 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.334-677T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18486970 | |||||||
| chr17:18487007 | C | A | 1 | a0007c0014t0003g0150 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.334-640C>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18487007 | |||||||
| chr17:18487019 | C | A | 31 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0013 others(28): Show |
74 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.334-628C>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18487019 | |||||||
| chr17:18487023 | G | T | 16 | a0002c0002t0002g0002 a0002c0002t0002g0014 a0002c0002t0002g0019 others(13): Show |
41 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.334-624G>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18487023 | |||||||
| chr17:18487100 | G | A | 34 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0013 others(31): Show |
77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.334-547G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18487100 | |||||||
| chr17:18487108 | G | C | 32 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0013 others(29): Show |
73 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.334-539G>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18487108 | |||||||
| chr17:18487145 | A | G | 1 | a0007c0013t0005g0045 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.334-502A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18487145 | |||||||
| chr17:18487211 | C | T | 16 | a0002c0002t0002g0002 a0002c0002t0002g0014 a0002c0002t0002g0019 others(13): Show |
41 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.334-436C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18487211 | |||||||
| chr17:18487292 | CA | C | 29 | a0001c0001t0001g0018 a0001c0001t0001g0032 a0001c0001t0001g0046 others(26): Show |
45 | HG00099.hp2 HG01109.hp1 HG01192.hp1 others(42): Show |
intron_variant | MODIFIER | c.334-338delA | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 18487292 | ||||||
| chr17:18487292 | CAA | C | 5 | a0001c0001t0001g0007 a0001c0001t0001g0095 a0004c0003t0001g0011 others(2): Show |
12 | HG00438.hp2 HG00597.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.334-339_334-338del others(2): Show |
LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 18487292 | ||||||
| chr17:18487319 | A | AAAAT | 34 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0013 others(31): Show |
77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.334-325_334-322dup others(4): Show |
LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 18487319 | ||||||
| chr17:18487435 | A | C | 34 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0013 others(31): Show |
77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.334-212A>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18487435 | |||||||
| chr17:18487463 | C | T | 1 | a0002c0002t0002g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.334-184C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18487463 | |||||||
| chr17:18487488 | G | T | 34 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0013 others(31): Show |
77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.334-159G>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18487488 | |||||||
| chr17:18487500 | C | T | 1 | a0002c0002t0002g0054 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.334-147C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18487500 | |||||||
| chr17:18487509 | C | A | 1 | a0001c0001t0001g0086 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.334-138C>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18487509 | |||||||
| chr17:18487527 | G | A | 4 | a0003c0004t0001g0084 a0003c0004t0001g0127 a0003c0004t0001g0128 others(1): Show |
4 | HG00741.hp1 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.334-120G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18487527 | |||||||
| chr17:18487563 | T | C | 34 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0013 others(31): Show |
77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.334-84T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18487563 | |||||||
| chr17:18487614 | A | G | 33 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0014 others(30): Show |
74 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.334-33A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18487614 | |||||||
| chr17:18487616 | C | T | 29 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0025 others(26): Show |
56 | HG00609.hp2 HG00673.hp2 HG01106.hp2 others(53): Show |
intron_variant | MODIFIER | c.334-31C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18487616 | |||||||
| chr17:18487621 | C | T | 4 | a0005c0005t0001g0041 a0005c0005t0001g0042 a0005c0005t0001g0078 others(1): Show |
4 | HG01891.hp1 HG02257.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.334-26C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18487621 | |||||||
| chr17:18487630 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.334-17G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18487630 | |||||||
| chr17:18487771 | C | T | 1 | a0007c0013t0005g0045 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.444+14C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 4/10 | chr17 | 18487771 | |||||||
| chr17:18487801 | GGGCCCAG others(14): Show |
G | 4 | a0003c0004t0001g0084 a0003c0004t0001g0127 a0003c0004t0001g0128 others(1): Show |
4 | HG00741.hp1 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.444+53_444+73delGT others(19): Show |
LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 18487801 | ||||||
| chr17:18487830 | C | T | 34 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0013 others(31): Show |
77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.444+73C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 4/10 | chr17 | 18487830 | |||||||
| chr17:18487993 | G | T | 34 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0013 others(31): Show |
77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.444+236G>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 4/10 | chr17 | 18487993 | |||||||
| chr17:18488011 | G | A | 1 | a0002c0002t0002g0053 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.444+254G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 4/10 | chr17 | 18488011 | |||||||
| chr17:18488160 | T | C | 14 | a0001c0001t0001g0120 a0001c0001t0002g0022 a0001c0001t0002g0151 others(11): Show |
15 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.444+403T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 4/10 | chr17 | 18488160 | |||||||
| chr17:18488193 | C | G | 4 | a0003c0004t0001g0084 a0003c0004t0001g0127 a0003c0004t0001g0128 others(1): Show |
4 | HG00741.hp1 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.444+436C>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 4/10 | chr17 | 18488193 | |||||||
| chr17:18488239 | G | T | 1 | a0001c0011t0002g0087 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.444+482G>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 4/10 | chr17 | 18488239 | |||||||
| chr17:18488435 | T | A | 34 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0013 others(31): Show |
77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.445-506T>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 4/10 | chr17 | 18488435 | |||||||
| chr17:18488493 | C | A | 1 | a0001c0001t0001g0070 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.445-448C>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 4/10 | chr17 | 18488493 | |||||||
| chr17:18488494 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.445-447T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 4/10 | chr17 | 18488494 | |||||||
| chr17:18488495 | A | T | 1 | a0001c0001t0001g0070 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.445-446A>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 4/10 | chr17 | 18488495 | |||||||
| chr17:18488502 | G | A | 1 | a0002c0002t0002g0013 | 3 | HG02630.hp1 HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.445-439G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 4/10 | chr17 | 18488502 | |||||||
| chr17:18488517 | C | T | 32 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0014 others(29): Show |
73 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.445-424C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 4/10 | chr17 | 18488517 | |||||||
| chr17:18488614 | A | G | 38 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0013 others(35): Show |
81 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.445-327A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 4/10 | chr17 | 18488614 | |||||||
| chr17:18488615 | A | G | 18 | a0002c0002t0002g0002 a0002c0002t0002g0014 a0002c0002t0002g0019 others(15): Show |
45 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.445-326A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 4/10 | chr17 | 18488615 | |||||||
| chr17:18488631 | T | C | 1 | a0001c0001t0001g0088 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.445-310T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 4/10 | chr17 | 18488631 | |||||||
| chr17:18488680 | T | C | 7 | a0001c0001t0001g0007 a0001c0001t0001g0032 a0001c0001t0001g0051 others(4): Show |
13 | HG00438.hp2 HG00597.hp1 HG00609.hp1 others(10): Show |
intron_variant | MODIFIER | c.445-261T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 4/10 | chr17 | 18488680 | |||||||
| chr17:18488756 | A | G | 1 | a0002c0002t0002g0058 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.445-185A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 4/10 | chr17 | 18488756 | |||||||
| chr17:18488790 | C | T | 1 | a0001c0001t0001g0100 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.445-151C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 4/10 | chr17 | 18488790 | |||||||
| chr17:18488796 | G | T | 1 | a0002c0002t0002g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.445-145G>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 4/10 | chr17 | 18488796 | |||||||
| chr17:18488800 | C | T | 27 | a0001c0001t0001g0068 a0001c0001t0001g0113 a0001c0001t0001g0115 others(24): Show |
54 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.445-141C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 4/10 | chr17 | 18488800 | |||||||
| chr17:18489049 | C | A | 16 | a0002c0002t0002g0002 a0002c0002t0002g0014 a0002c0002t0002g0019 others(13): Show |
41 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.540+13C>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18489049 | |||||||
| chr17:18489063 | G | A | 29 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0014 others(26): Show |
68 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.540+27G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18489063 | |||||||
| chr17:18489106 | C | T | 1 | a0001c0001t0001g0069 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.540+70C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18489106 | |||||||
| chr17:18489224 | A | C | 34 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0013 others(31): Show |
77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.540+188A>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18489224 | |||||||
| chr17:18489226 | C | G | 34 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0013 others(31): Show |
77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.540+190C>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18489226 | |||||||
| chr17:18489228 | T | C | 34 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0013 others(31): Show |
77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.540+192T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18489228 | |||||||
| chr17:18489339 | C | CA | 34 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0013 others(31): Show |
77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.540+304dupA | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr17 | 18489339 | ||||||
| chr17:18489349 | C | T | 1 | a0001c0001t0001g0069 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.540+313C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18489349 | |||||||
| chr17:18489358 | A | G | 2 | a0004c0003t0001g0011 a0004c0003t0001g0043 |
4 | HG02109.hp2 HG02970.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.540+322A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18489358 | |||||||
| chr17:18489429 | T | C | 44 | a0001c0001t0001g0140 a0001c0011t0002g0087 a0002c0002t0002g0002 others(41): Show |
87 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.540+393T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18489429 | |||||||
| chr17:18489509 | A | C | 37 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0013 others(34): Show |
80 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.540+473A>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18489509 | |||||||
| chr17:18489512 | C | A | 1 | a0001c0001t0001g0146 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.540+476C>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18489512 | |||||||
| chr17:18489577 | T | C | 1 | a0001c0011t0002g0087 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.540+541T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18489577 | |||||||
| chr17:18489618 | T | C | 34 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0013 others(31): Show |
77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.540+582T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18489618 | |||||||
| chr17:18489619 | C | G | 3 | a0002c0002t0002g0013 a0002c0002t0002g0053 a0002c0002t0002g0054 |
5 | HG02630.hp1 HG03195.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.540+583C>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18489619 | |||||||
| chr17:18489661 | G | T | 34 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0013 others(31): Show |
77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.540+625G>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18489661 | |||||||
| chr17:18489683 | C | T | 1 | a0002c0002t0002g0013 | 3 | HG02630.hp1 HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.540+647C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18489683 | |||||||
| chr17:18489729 | A | G | 1 | a0002c0002t0002g0123 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.540+693A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18489729 | |||||||
| chr17:18489763 | T | C | 1 | a0001c0001t0001g0141 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.540+727T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18489763 | |||||||
| chr17:18489875 | CT | C | 45 | a0001c0011t0002g0087 a0002c0002t0002g0002 a0002c0002t0002g0005 others(42): Show |
88 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.540+841delT | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr17 | 18489875 | ||||||
| chr17:18490142 | C | T | 34 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0013 others(31): Show |
77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.541-591C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18490142 | |||||||
| chr17:18490216 | A | G | 4 | a0003c0004t0001g0084 a0003c0004t0001g0127 a0003c0004t0001g0128 others(1): Show |
4 | HG00741.hp1 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.541-517A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18490216 | |||||||
| chr17:18490290 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.541-443C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18490290 | |||||||
| chr17:18490370 | C | T | 4 | a0003c0004t0001g0084 a0003c0004t0001g0127 a0003c0004t0001g0128 others(1): Show |
4 | HG00741.hp1 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.541-363C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18490370 | |||||||
| chr17:18490379 | A | G | 34 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0013 others(31): Show |
77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.541-354A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18490379 | |||||||
| chr17:18490382 | G | A | 2 | a0001c0001t0001g0074 a0001c0001t0001g0085 |
2 | HG02027.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.541-351G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18490382 | |||||||
| chr17:18490398 | C | T | 3 | a0002c0002t0002g0013 a0002c0002t0002g0053 a0002c0002t0002g0054 |
5 | HG02630.hp1 HG03195.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.541-335C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18490398 | |||||||
| chr17:18490430 | G | A | 3 | a0005c0005t0001g0041 a0005c0005t0001g0042 a0005c0005t0001g0078 |
3 | HG01891.hp1 HG02257.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.541-303G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18490430 | |||||||
| chr17:18490566 | A | G | 42 | a0001c0001t0001g0033 a0001c0001t0001g0079 a0001c0001t0001g0098 others(39): Show |
86 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.541-167A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18490566 | |||||||
| chr17:18490695 | C | T | 1 | a0002c0002t0002g0121 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.541-38C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18490695 | |||||||
| chr17:18490696 | G | A | 6 | a0003c0004t0001g0084 a0003c0004t0001g0127 a0003c0004t0001g0128 others(3): Show |
6 | HG00741.hp1 HG02451.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.541-37G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18490696 | |||||||
| chr17:18490787 | T | C | 1 | a0002c0002t0002g0059 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.576+19T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 6/10 | chr17 | 18490787 | |||||||
| chr17:18490893 | G | A | 4 | a0003c0004t0001g0084 a0003c0004t0001g0127 a0003c0004t0001g0128 others(1): Show |
4 | HG00741.hp1 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.576+125G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 6/10 | chr17 | 18490893 | |||||||
| chr17:18490943 | C | T | 2 | a0001c0001t0001g0031 a0011c0010t0001g0031 |
2 | HG02280.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.576+175C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 6/10 | chr17 | 18490943 | |||||||
| chr17:18491011 | C | T | 1 | a0001c0011t0002g0087 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.576+243C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 6/10 | chr17 | 18491011 | |||||||
| chr17:18491042 | C | T | 1 | a0013c0012t0003g0149 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.577-231C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 6/10 | chr17 | 18491042 | |||||||
| chr17:18491087 | T | C | 2 | a0001c0001t0001g0097 a0001c0001t0001g0104 |
2 | NA18973.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.577-186T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 6/10 | chr17 | 18491087 | |||||||
| chr17:18491104 | C | T | 38 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0013 others(35): Show |
81 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.577-169C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 6/10 | chr17 | 18491104 | |||||||
| chr17:18491117 | T | C | 34 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0013 others(31): Show |
77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.577-156T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 6/10 | chr17 | 18491117 | |||||||
| chr17:18491125 | G | A | 3 | a0005c0005t0001g0041 a0005c0005t0001g0042 a0005c0005t0001g0078 |
3 | HG01891.hp1 HG02257.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.577-148G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 6/10 | chr17 | 18491125 | |||||||
| chr17:18491143 | C | T | 1 | a0001c0001t0001g0032 | 2 | NA18985.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.577-130C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 6/10 | chr17 | 18491143 | |||||||
| chr17:18491249 | T | A | 1 | a0001c0001t0001g0117 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.577-24T>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 6/10 | chr17 | 18491249 | |||||||
| chr17:18491270 | C | T | 1 | a0001c0001t0001g0038 | 2 | HG03491.hp1 HG03492.hp2 |
splice_region_variant&intron_variant | LOW | c.577-3C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 6/10 | chr17 | 18491270 | |||||||
| chr17:18491416 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0070 |
3 | HG02055.hp1 HG02486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.627+93C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 7/10 | chr17 | 18491416 | |||||||
| chr17:18491600 | A | G | 34 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0013 others(31): Show |
77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.627+277A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 7/10 | chr17 | 18491600 | |||||||
| chr17:18491704 | T | A | 1 | a0001c0001t0001g0012 | 3 | HG00140.hp2 HG00323.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.628-241T>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 7/10 | chr17 | 18491704 | |||||||
| chr17:18491713 | T | C | 1 | a0002c0002t0002g0035 | 2 | NA19054.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.628-232T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 7/10 | chr17 | 18491713 | |||||||
| chr17:18491759 | T | G | 2 | a0001c0001t0001g0030 a0001c0001t0001g0148 |
3 | HG00408.hp1 HG02155.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.628-186T>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 7/10 | chr17 | 18491759 | |||||||
| chr17:18492084 | T | C | 1 | a0002c0002t0002g0060 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.672+95T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 8/10 | chr17 | 18492084 | |||||||
| chr17:18492131 | G | A | 4 | a0005c0005t0001g0041 a0005c0005t0001g0042 a0005c0005t0001g0078 others(1): Show |
4 | HG01891.hp1 HG02257.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.672+142G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 8/10 | chr17 | 18492131 | |||||||
| chr17:18492333 | G | T | 37 | a0001c0001t0001g0052 a0002c0002t0002g0002 a0002c0002t0002g0005 others(34): Show |
80 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.673-124G>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 8/10 | chr17 | 18492333 | |||||||
| chr17:18492382 | C | A | 4 | a0003c0004t0001g0084 a0003c0004t0001g0127 a0003c0004t0001g0128 others(1): Show |
4 | HG00741.hp1 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.673-75C>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 8/10 | chr17 | 18492382 | |||||||
| chr17:18492420 | A | G | 4 | a0003c0004t0001g0084 a0003c0004t0001g0127 a0003c0004t0001g0128 others(1): Show |
4 | HG00741.hp1 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.673-37A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 8/10 | chr17 | 18492420 | |||||||
| chr17:18492630 | G | C | 33 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0013 others(30): Show |
76 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.762-67G>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 9/10 | chr17 | 18492630 | |||||||
| chr17:18492678 | G | A | 23 | a0002c0002t0002g0002 a0002c0002t0002g0013 a0002c0002t0002g0014 others(20): Show |
52 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.762-19G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 9/10 | chr17 | 18492678 | |||||||
| chr17:18492693 | C | G | 1 | a0001c0015t0001g0142 | 1 | HG01106.hp1 | splice_region_variant&intron_variant | LOW | c.762-4C>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 9/10 | chr17 | 18492693 | |||||||
| chr17:18492905 | C | CAG | 17 | a0001c0001t0001g0102 a0001c0001t0001g0133 a0001c0015t0001g0142 others(14): Show |
30 | HG00099.hp2 HG01106.hp1 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.924+46_924+47insAG | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 10/10 | chr17 | 18492905 | |||||||
| chr17:18492932 | T | C | 43 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0017 others(40): Show |
85 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.924+73T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 10/10 | chr17 | 18492932 | |||||||
| chr17:18492949 | G | A | 8 | a0001c0001t0001g0003 a0001c0001t0001g0134 a0001c0001t0001g0140 others(5): Show |
25 | HG00408.hp2 HG01975.hp1 HG01978.hp2 others(22): Show |
intron_variant | MODIFIER | c.924+90G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 10/10 | chr17 | 18492949 | |||||||
| chr17:18492997 | A | G | 31 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0013 others(28): Show |
72 | HG00099.hp2 HG00673.hp1 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.924+138A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 10/10 | chr17 | 18492997 | |||||||
| chr17:18493011 | T | C | 31 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0013 others(28): Show |
72 | HG00099.hp2 HG00673.hp1 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.924+152T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 10/10 | chr17 | 18493011 | |||||||
| chr17:18493020 | T | G | 31 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0013 others(28): Show |
72 | HG00099.hp2 HG00673.hp1 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.924+161T>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 10/10 | chr17 | 18493020 | |||||||
| chr17:18493078 | A | G | 32 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0013 others(29): Show |
75 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.924+219A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 10/10 | chr17 | 18493078 | |||||||
| chr17:18493097 | T | C | 32 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0013 others(29): Show |
75 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.924+238T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 10/10 | chr17 | 18493097 | |||||||
| chr17:18493104 | C | T | 32 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0013 others(29): Show |
75 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.924+245C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 10/10 | chr17 | 18493104 | |||||||
| chr17:18493176 | A | G | 12 | a0002c0002t0002g0005 a0002c0002t0002g0020 a0002c0002t0002g0035 others(9): Show |
26 | HG00099.hp2 HG01109.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.924+317A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 10/10 | chr17 | 18493176 | |||||||
| chr17:18493218 | A | G | 35 | a0001c0001t0001g0099 a0002c0002t0002g0002 a0002c0002t0002g0005 others(32): Show |
76 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.924+359A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 10/10 | chr17 | 18493218 | |||||||
| chr17:18493247 | C | G | 31 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0014 others(28): Show |
72 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.924+388C>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 10/10 | chr17 | 18493247 | |||||||
| chr17:18493248 | G | A | 40 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0013 others(37): Show |
83 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.924+389G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 10/10 | chr17 | 18493248 | |||||||
| chr17:18493260 | C | A | 1 | a0007c0014t0003g0150 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.924+401C>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 10/10 | chr17 | 18493260 | |||||||
| chr17:18493415 | T | C | 43 | a0001c0001t0001g0023 a0001c0001t0001g0070 a0001c0001t0001g0071 others(40): Show |
87 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.924+556T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 10/10 | chr17 | 18493415 | |||||||
| chr17:18493431 | A | G | 33 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0013 others(30): Show |
76 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.924+572A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 10/10 | chr17 | 18493431 | |||||||
| chr17:18493454 | G | A | 1 | a0002c0002t0002g0062 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.924+595G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 10/10 | chr17 | 18493454 | |||||||
| chr17:18493547 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.925-674C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 10/10 | chr17 | 18493547 | |||||||
| chr17:18493809 | C | T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0146 |
3 | HG01109.hp2 HG02647.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.925-412C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 10/10 | chr17 | 18493809 | |||||||
| chr17:18494014 | C | T | 1 | a0001c0001t0001g0092 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.925-207C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 10/10 | chr17 | 18494014 | |||||||
| chr17:18494032 | C | G | 34 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0013 others(31): Show |
77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.925-189C>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 10/10 | chr17 | 18494032 | |||||||
| chr17:18494118 | G | T | 1 | a0002c0002t0002g0055 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.925-103G>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 10/10 | chr17 | 18494118 |