Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 166012 |
| ensemblid | ENSG00000180767.11 |
| hgncid | 21755 |
| symbol | CHST13 |
| name | carbohydrate sulfotransferase 13 |
| refseq_nuc | NM_152889.3 |
| refseq_prot | NP_690849.1 |
| ensembl_nuc | ENST00000319340.7 |
| ensembl_prot | ENSP00000317404.2 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 126524155 |
| end | 126543291 |
| strand | + |
| ver | v1.2 |
| region | chr3:126524155-126543291 |
| region5000 | chr3:126519155-126548291 |
| regionname0 | CHST13_chr3_126524155_126543291 |
| regionname5000 | CHST13_chr3_126519155_126548291 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 341 | 185 | 36 | 43 | 76 | 8 | 21 | 62 | CHST13_chr3_126519155_126548291 | CHST13 | MGRRC others(336): Show |
chr3 | 126519155 | 126548291 |
| a0002 | 0/1 | 341 | 73 | 3 | 17 | 45 | 5 | 2 | 37 | CHST13_chr3_126519155_126548291 | CHST13 | MGRRC others(336): Show |
chr3 | 126519155 | 126548291 |
| a0003 | 0/0 | 341 | 56 | 38 | 11 | 0 | 1 | 6 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | MGRRC others(336): Show |
chr3 | 126519155 | 126548291 |
| a0004 | 0/0 | 341 | 30 | 5 | 3 | 16 | 2 | 4 | 13 | CHST13_chr3_126519155_126548291 | CHST13 | MGRRC others(336): Show |
chr3 | 126519155 | 126548291 |
| a0005 | 0/0 | 341 | 8 | 7 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | MGRRC others(336): Show |
chr3 | 126519155 | 126548291 |
| a0006 | 0/0 | 341 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | MGRRC others(336): Show |
chr3 | 126519155 | 126548291 |
| a0007 | 0/0 | 341 | 4 | 0 | 3 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | MGRRC others(336): Show |
chr3 | 126519155 | 126548291 |
| a0008 | 0/0 | 341 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | MGRRC others(336): Show |
chr3 | 126519155 | 126548291 |
| a0009 | 0/0 | 341 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | MGRRC others(336): Show |
chr3 | 126519155 | 126548291 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1023 | 185 | 36 | 43 | 76 | 8 | 21 | CHST13_chr3_126519155_126548291 | CHST13 | ATGGG others(1018): Show |
chr3 | 126519155 | 126548291 | ||
| a0002c0002 | 0/1 | 1023 | 73 | 3 | 17 | 45 | 5 | 2 | CHST13_chr3_126519155_126548291 | CHST13 | ATGGG others(1018): Show |
chr3 | 126519155 | 126548291 | ||
| a0003c0004 | 0/0 | 1023 | 27 | 20 | 7 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | ATGGG others(1018): Show |
chr3 | 126519155 | 126548291 | ||
| a0003c0005 | 0/0 | 1023 | 21 | 12 | 3 | 0 | 0 | 6 | CHST13_chr3_126519155_126548291 | CHST13 | ATGGG others(1018): Show |
chr3 | 126519155 | 126548291 | ||
| a0003c0007 | 0/0 | 1023 | 7 | 5 | 1 | 0 | 1 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | ATGGG others(1018): Show |
chr3 | 126519155 | 126548291 | ||
| a0003c0010 | 0/0 | 1023 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | ATGGG others(1018): Show |
chr3 | 126519155 | 126548291 | ||
| a0004c0003 | 0/0 | 1023 | 30 | 5 | 3 | 16 | 2 | 4 | CHST13_chr3_126519155_126548291 | CHST13 | ATGGG others(1018): Show |
chr3 | 126519155 | 126548291 | ||
| a0005c0006 | 0/0 | 1023 | 8 | 7 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | ATGGG others(1018): Show |
chr3 | 126519155 | 126548291 | ||
| a0006c0008 | 0/0 | 1023 | 6 | 6 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | ATGGG others(1018): Show |
chr3 | 126519155 | 126548291 | ||
| a0007c0009 | 0/0 | 1023 | 4 | 0 | 3 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | ATGGG others(1018): Show |
chr3 | 126519155 | 126548291 | ||
| a0008c0012 | 0/0 | 1023 | 1 | 0 | 0 | 0 | 0 | 1 | CHST13_chr3_126519155_126548291 | CHST13 | ATGGG others(1018): Show |
chr3 | 126519155 | 126548291 | ||
| a0009c0011 | 0/0 | 1023 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | ATGGG others(1018): Show |
chr3 | 126519155 | 126548291 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1917 | 183 | 36 | 42 | 75 | 8 | 21 | CHST13_chr3_126519155_126548291 | CHST13 | AGTCC others(1912): Show |
chr3 | 126519155 | 126548291 |
| a0001c0001t0003 | 0/0 | 1917 | 1 | 0 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | AGTCC others(1912): Show |
chr3 | 126519155 | 126548291 |
| a0001c0001t0005 | 0/0 | 1917 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | AGTCC others(1912): Show |
chr3 | 126519155 | 126548291 |
| a0002c0002t0001 | 0/1 | 1917 | 73 | 3 | 17 | 45 | 5 | 2 | CHST13_chr3_126519155_126548291 | CHST13 | AGTCC others(1912): Show |
chr3 | 126519155 | 126548291 |
| a0003c0004t0001 | 0/0 | 1917 | 27 | 20 | 7 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | AGTCC others(1912): Show |
chr3 | 126519155 | 126548291 |
| a0003c0005t0001 | 0/0 | 1917 | 21 | 12 | 3 | 0 | 0 | 6 | CHST13_chr3_126519155_126548291 | CHST13 | AGTCC others(1912): Show |
chr3 | 126519155 | 126548291 |
| a0003c0007t0001 | 0/0 | 1917 | 6 | 5 | 0 | 0 | 1 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | AGTCC others(1912): Show |
chr3 | 126519155 | 126548291 |
| a0003c0007t0006 | 0/0 | 1917 | 1 | 0 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | AGTCC others(1912): Show |
chr3 | 126519155 | 126548291 |
| a0003c0010t0001 | 0/0 | 1917 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | AGTCC others(1912): Show |
chr3 | 126519155 | 126548291 |
| a0004c0003t0002 | 0/0 | 1917 | 30 | 5 | 3 | 16 | 2 | 4 | CHST13_chr3_126519155_126548291 | CHST13 | AGTCC others(1912): Show |
chr3 | 126519155 | 126548291 |
| a0005c0006t0001 | 0/0 | 1917 | 8 | 7 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | AGTCC others(1912): Show |
chr3 | 126519155 | 126548291 |
| a0006c0008t0001 | 0/0 | 1917 | 6 | 6 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | AGTCC others(1912): Show |
chr3 | 126519155 | 126548291 |
| a0007c0009t0002 | 0/0 | 1917 | 4 | 0 | 3 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | AGTCC others(1912): Show |
chr3 | 126519155 | 126548291 |
| a0008c0012t0001 | 0/0 | 1917 | 1 | 0 | 0 | 0 | 0 | 1 | CHST13_chr3_126519155_126548291 | CHST13 | AGTCC others(1912): Show |
chr3 | 126519155 | 126548291 |
| a0009c0011t0004 | 0/0 | 1917 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | AGTCC others(1912): Show |
chr3 | 126519155 | 126548291 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 63 | 3 | 11 | 38 | 2 | 9 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0004 | 0/0 | 19 | 12 | 0 | 3 | 0 | 4 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0005 | 0/0 | 9 | 0 | 6 | 0 | 2 | 1 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0007 | 0/0 | 8 | 0 | 3 | 0 | 1 | 4 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0010 | 0/0 | 6 | 1 | 4 | 0 | 1 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0019 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0025 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0044 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0001c0001t0005g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0002c0002t0001g0002 | 0/0 | 32 | 0 | 3 | 27 | 1 | 1 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0002c0002t0001g0008 | 0/0 | 8 | 0 | 8 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0002c0002t0001g0009 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0002c0002t0001g0014 | 0/0 | 5 | 2 | 2 | 0 | 0 | 1 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0002c0002t0001g0021 | 0/0 | 4 | 0 | 1 | 0 | 3 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0002c0002t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0002c0002t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0002c0002t0001g0119 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0002c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0003c0004t0001g0011 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0003c0004t0001g0012 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0003c0004t0001g0016 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0003c0004t0001g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0003c0004t0001g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0003c0004t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0003c0004t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0003c0004t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0003c0004t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0003c0004t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0003c0004t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0003c0004t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0003c0004t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0003c0005t0001g0018 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0003c0005t0001g0020 | 0/0 | 4 | 0 | 1 | 0 | 0 | 3 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0003c0005t0001g0023 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0003c0005t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0003c0005t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0003c0005t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0003c0005t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0003c0005t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0003c0005t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0003c0005t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0003c0005t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0003c0005t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0003c0007t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0003c0007t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0003c0007t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0003c0007t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0003c0007t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0003c0007t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0003c0007t0006g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0003c0010t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0004c0003t0002g0003 | 0/0 | 20 | 1 | 0 | 14 | 2 | 3 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0004c0003t0002g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0004c0003t0002g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0004c0003t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0004c0003t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0004c0003t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0004c0003t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0004c0003t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0004c0003t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0005c0006t0001g0006 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0006c0008t0001g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0006c0008t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0007c0009t0002g0003 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0007c0009t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0007c0009t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0008c0012t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| a0009c0011t0004g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0096 | EUR | GBR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0068 | EUR | FIN | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | FIN | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG00323 | hp1 | a0003 | c0007 | t0001 | g0092 | EUR | FIN | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG00323 | hp2 | a0004 | c0003 | t0002 | g0003 | EUR | FIN | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG00639 | hp2 | a0005 | c0006 | t0001 | g0006 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG00733 | hp2 | a0003 | c0004 | t0001 | g0011 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG00735 | hp1 | a0003 | c0005 | t0001 | g0023 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0037 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01099 | hp1 | a0003 | c0007 | t0006 | g0107 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0037 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01109 | hp1 | a0003 | c0004 | t0001 | g0016 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01109 | hp2 | a0003 | c0004 | t0001 | g0112 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01167 | hp2 | a0004 | c0003 | t0002 | g0034 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01169 | hp2 | a0004 | c0003 | t0002 | g0034 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01175 | hp1 | a0003 | c0004 | t0001 | g0011 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0021 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01243 | hp2 | a0003 | c0004 | t0001 | g0016 | AMR | PUR | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01255 | hp2 | a0003 | c0004 | t0001 | g0036 | AMR | CLM | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01256 | hp2 | a0002 | c0002 | t0001 | g0014 | AMR | CLM | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0014 | AMR | CLM | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01261 | hp1 | a0004 | c0003 | t0002 | g0126 | AMR | CLM | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0008 | AMR | CLM | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01346 | hp2 | a0003 | c0004 | t0001 | g0081 | AMR | CLM | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01358 | hp1 | a0003 | c0005 | t0001 | g0023 | AMR | CLM | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01358 | hp2 | a0003 | c0005 | t0001 | g0020 | AMR | CLM | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0008 | AMR | CLM | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0008 | AMR | CLM | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01516 | hp1 | a0004 | c0003 | t0002 | g0003 | EUR | IBS | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0021 | EUR | IBS | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0021 | EUR | IBS | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01884 | hp2 | a0004 | c0003 | t0002 | g0003 | AFR | ACB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01891 | hp1 | a0002 | c0002 | t0001 | g0014 | AFR | ACB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01891 | hp2 | a0003 | c0004 | t0001 | g0095 | AFR | ACB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01928 | hp1 | a0007 | c0009 | t0002 | g0003 | AMR | PEL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0008 | AMR | PEL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0061 | AMR | PEL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0008 | AMR | PEL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01952 | hp2 | a0002 | c0002 | t0001 | g0127 | AMR | PEL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01975 | hp1 | a0007 | c0009 | t0002 | g0098 | AMR | PEL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01981 | hp1 | a0007 | c0009 | t0002 | g0097 | AMR | PEL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0008 | AMR | PEL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0008 | AMR | PEL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0118 | EAS | KHV | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02055 | hp1 | a0004 | c0003 | t0002 | g0086 | AFR | ACB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02055 | hp2 | a0003 | c0007 | t0001 | g0087 | AFR | ACB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02056 | hp1 | a0004 | c0003 | t0002 | g0093 | EAS | KHV | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02071 | hp2 | a0002 | c0002 | t0001 | g0038 | EAS | KHV | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02083 | hp1 | a0004 | c0003 | t0002 | g0003 | EAS | KHV | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02132 | hp1 | a0007 | c0009 | t0002 | g0003 | EAS | KHV | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02135 | hp1 | a0004 | c0003 | t0002 | g0100 | EAS | KHV | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02145 | hp1 | a0003 | c0004 | t0001 | g0011 | AFR | ACB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02258 | hp1 | a0003 | c0005 | t0001 | g0106 | AFR | ACB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02273 | hp1 | a0002 | c0002 | t0001 | g0008 | AMR | PEL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02280 | hp2 | a0003 | c0004 | t0001 | g0117 | AFR | ACB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02572 | hp1 | a0003 | c0007 | t0001 | g0108 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02602 | hp1 | a0003 | c0005 | t0001 | g0020 | SAS | PJL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02622 | hp1 | a0003 | c0004 | t0001 | g0082 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02647 | hp1 | a0003 | c0005 | t0001 | g0103 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02647 | hp2 | a0003 | c0004 | t0001 | g0012 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02683 | hp1 | a0003 | c0005 | t0001 | g0020 | SAS | PJL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02698 | hp1 | a0008 | c0012 | t0001 | g0072 | SAS | PJL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02698 | hp2 | a0003 | c0005 | t0001 | g0020 | SAS | PJL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02723 | hp1 | a0003 | c0004 | t0001 | g0026 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02723 | hp2 | a0003 | c0004 | t0001 | g0036 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02818 | hp1 | a0003 | c0004 | t0001 | g0116 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02818 | hp2 | a0006 | c0008 | t0001 | g0032 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02886 | hp1 | a0003 | c0004 | t0001 | g0113 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02886 | hp2 | a0005 | c0006 | t0001 | g0006 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02895 | hp1 | a0006 | c0008 | t0001 | g0032 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02895 | hp2 | a0003 | c0005 | t0001 | g0018 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02896 | hp1 | a0003 | c0004 | t0001 | g0011 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02896 | hp2 | a0003 | c0005 | t0001 | g0076 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02897 | hp1 | a0003 | c0005 | t0001 | g0018 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02897 | hp2 | a0003 | c0005 | t0001 | g0073 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02922 | hp2 | a0003 | c0004 | t0001 | g0011 | AFR | ESN | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02965 | hp1 | a0003 | c0004 | t0001 | g0012 | AFR | ESN | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02965 | hp2 | a0003 | c0010 | t0001 | g0084 | AFR | ESN | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ESN | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02970 | hp2 | a0006 | c0008 | t0001 | g0017 | AFR | ESN | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02976 | hp1 | a0005 | c0006 | t0001 | g0006 | AFR | ESN | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG03098 | hp1 | a0005 | c0006 | t0001 | g0006 | AFR | MSL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG03098 | hp2 | a0003 | c0004 | t0001 | g0026 | AFR | MSL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG03139 | hp1 | a0003 | c0004 | t0001 | g0012 | AFR | ESN | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG03195 | hp1 | a0005 | c0006 | t0001 | g0006 | AFR | ESN | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG03195 | hp2 | a0003 | c0004 | t0001 | g0012 | AFR | ESN | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG03209 | hp1 | a0004 | c0003 | t0002 | g0033 | AFR | MSL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG03209 | hp2 | a0003 | c0005 | t0001 | g0035 | AFR | MSL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG03225 | hp1 | a0003 | c0005 | t0001 | g0018 | AFR | MSL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG03225 | hp2 | a0003 | c0007 | t0001 | g0041 | AFR | MSL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0014 | AFR | MSL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG03490 | hp1 | a0003 | c0005 | t0001 | g0023 | SAS | PJL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG03516 | hp1 | a0003 | c0004 | t0001 | g0114 | AFR | ESN | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG03516 | hp2 | a0004 | c0003 | t0002 | g0099 | AFR | ESN | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG03540 | hp1 | a0003 | c0007 | t0001 | g0109 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0124 | AFR | GWD | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG03579 | hp1 | a0003 | c0004 | t0001 | g0016 | AFR | MSL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG03579 | hp2 | a0006 | c0008 | t0001 | g0017 | AFR | MSL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG03654 | hp1 | a0004 | c0003 | t0002 | g0003 | SAS | PJL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG03654 | hp2 | a0003 | c0005 | t0001 | g0077 | SAS | PJL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0014 | SAS | STU | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG03688 | hp2 | a0004 | c0003 | t0002 | g0003 | SAS | STU | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG03942 | hp2 | a0003 | c0005 | t0001 | g0104 | SAS | BEB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | STU | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG04228 | hp2 | a0004 | c0003 | t0002 | g0003 | SAS | STU | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18522 | hp1 | a0003 | c0005 | t0001 | g0035 | AFR | YRI | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18522 | hp2 | a0005 | c0006 | t0001 | g0006 | AFR | YRI | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | CHB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18906 | hp1 | a0006 | c0008 | t0001 | g0017 | AFR | YRI | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18906 | hp2 | a0005 | c0006 | t0001 | g0006 | AFR | YRI | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18947 | hp2 | a0004 | c0003 | t0002 | g0003 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18949 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0120 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18953 | hp2 | a0002 | c0002 | t0001 | g0130 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18954 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18957 | hp2 | a0004 | c0003 | t0002 | g0003 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18959 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18968 | hp1 | a0004 | c0003 | t0002 | g0003 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0038 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18969 | hp2 | a0004 | c0003 | t0002 | g0003 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0121 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0123 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18982 | hp2 | a0002 | c0002 | t0001 | g0129 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18983 | hp1 | a0001 | c0001 | t0005 | g0075 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0125 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18992 | hp1 | a0004 | c0003 | t0002 | g0003 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18993 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18997 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA18999 | hp2 | a0004 | c0003 | t0002 | g0003 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19005 | hp2 | a0004 | c0003 | t0002 | g0003 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19007 | hp1 | a0004 | c0003 | t0002 | g0003 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | LWK | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | LWK | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19043 | hp1 | a0004 | c0003 | t0002 | g0033 | AFR | LWK | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19043 | hp2 | a0003 | c0005 | t0001 | g0110 | AFR | LWK | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19059 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19062 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19063 | hp2 | a0004 | c0003 | t0002 | g0003 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0074 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19074 | hp2 | a0004 | c0003 | t0002 | g0003 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19079 | hp2 | a0004 | c0003 | t0002 | g0003 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19083 | hp1 | a0004 | c0003 | t0002 | g0003 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19089 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA19091 | hp2 | a0004 | c0003 | t0002 | g0003 | EAS | JPT | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ASW | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA20129 | hp2 | a0005 | c0006 | t0001 | g0006 | AFR | ASW | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0002 | EUR | TSI | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0046 | EUR | TSI | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0021 | EUR | TSI | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | GIH | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA20905 | hp2 | a0004 | c0003 | t0002 | g0088 | SAS | GIH | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02109 | hp1 | a0003 | c0007 | t0001 | g0101 | AFR | ACB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02486 | hp2 | a0003 | c0005 | t0001 | g0105 | AFR | ACB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02559 | hp1 | a0003 | c0005 | t0001 | g0018 | AFR | ACB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG02559 | hp2 | a0003 | c0004 | t0001 | g0016 | AFR | ACB | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | MSL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG06807 | hp1 | a0003 | c0004 | t0001 | g0012 | AFR | USA | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| HG06807 | hp2 | a0003 | c0004 | t0001 | g0026 | AFR | USA | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA20300 | hp2 | a0006 | c0008 | t0001 | g0017 | AFR | USA | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA21309 | hp1 | a0009 | c0011 | t0004 | g0079 | AFR | LWK | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0119 | REF | REF | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0044 | REF | REF | CHST13_chr3_126519155_126548291 | CHST13 | chr3 | 126519155 | 126548291 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:126536303 | C | T | 1 | a0008 | 1 | HG02698.hp1 | missense_variant | MODERATE | c.130C>T | p.Leu44Phe | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/3 | 308/1917 | 130/1026 | 44/341 | chr3 | 126536303 | |||
| chr3:126536323 | C | G | 1 | a0009 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.150C>G | p.Ser50Arg | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/3 | 328/1917 | 150/1026 | 50/341 | chr3 | 126536323 | |||
| chr3:126541787 | A | G | 2 | a0004 a0007 |
34 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(31): Show |
missense_variant | MODERATE | c.235A>G | p.Ser79Gly | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 3/3 | 413/1917 | 235/1026 | 79/341 | chr3 | 126541787 | |||
| chr3:126541929 | C | T | 1 | a0005 | 8 | HG00639.hp2 HG02886.hp2 HG02976.hp1 others(5): Show |
missense_variant | MODERATE | c.377C>T | p.Ala126Val | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 3/3 | 555/1917 | 377/1026 | 126/341 | chr3 | 126541929 | |||
| chr3:126541988 | C | T | 1 | a0006 | 6 | HG02818.hp2 HG02895.hp1 HG02970.hp2 others(3): Show |
missense_variant | MODERATE | c.436C>T | p.Pro146Ser | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 3/3 | 614/1917 | 436/1026 | 146/341 | chr3 | 126541988 | |||
| chr3:126542048 | G | A | 1 | a0007 | 4 | HG01928.hp1 HG01975.hp1 HG01981.hp1 others(1): Show |
missense_variant | MODERATE | c.496G>A | p.Ala166Thr | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 3/3 | 674/1917 | 496/1026 | 166/341 | chr3 | 126542048 | |||
| chr3:126542364 | C | T | 2 | a0002 a0008 |
73 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(70): Show |
missense_variant | MODERATE | c.812C>T | p.Ala271Val | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 3/3 | 990/1917 | 812/1026 | 271/341 | chr3 | 126542364 | |||
| chr3:126542502 | G | A | 4 | a0002 a0003 a0008 others(1): Show |
130 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(127): Show |
missense_variant | MODERATE | c.950G>A | p.Arg317Gln | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 3/3 | 1128/1917 | 950/1026 | 317/341 | chr3 | 126542502 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:126541765 | G | T | 3 | a0002c0002 a0003c0004 a0008c0012 |
100 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(97): Show |
synonymous_variant | LOW | c.213G>T | p.Arg71Arg | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 3/3 | 391/1917 | 213/1026 | 71/341 | chr3 | 126541765 | |||
| chr3:126542014 | C | T | 1 | a0006c0008 | 6 | HG02818.hp2 HG02895.hp1 HG02970.hp2 others(3): Show |
synonymous_variant | LOW | c.462C>T | p.Asp154Asp | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 3/3 | 640/1917 | 462/1026 | 154/341 | chr3 | 126542014 | |||
| chr3:126542152 | C | T | 1 | a0003c0005 | 21 | HG00735.hp1 HG01358.hp1 HG01358.hp2 others(18): Show |
synonymous_variant | LOW | c.600C>T | p.Tyr200Tyr | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 3/3 | 778/1917 | 600/1026 | 200/341 | chr3 | 126542152 | |||
| chr3:126542359 | G | A | 6 | a0002c0002 a0003c0004 a0003c0005 others(3): Show |
129 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(126): Show |
synonymous_variant | LOW | c.807G>A | p.Thr269Thr | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 3/3 | 985/1917 | 807/1026 | 269/341 | chr3 | 126542359 | |||
| chr3:126542383 | G | A | 1 | a0003c0010 | 1 | HG02965.hp2 | synonymous_variant | LOW | c.831G>A | p.Val277Val | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 3/3 | 1009/1917 | 831/1026 | 277/341 | chr3 | 126542383 | |||
| chr3:126542470 | C | T | 1 | a0006c0008 | 6 | HG02818.hp2 HG02895.hp1 HG02970.hp2 others(3): Show |
synonymous_variant | LOW | c.918C>T | p.Arg306Arg | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 3/3 | 1096/1917 | 918/1026 | 306/341 | chr3 | 126542470 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:126542702 | C | T | 1 | a0003c0007t0006 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*124C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 3/3 | 124 | chr3 | 126542702 | ||||||
| chr3:126542747 | C | A | 1 | a0001c0001t0003 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*169C>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 3/3 | 169 | chr3 | 126542747 | ||||||
| chr3:126542810 | C | T | 1 | a0001c0001t0005 | 1 | NA18983.hp1 | 3_prime_UTR_variant | MODIFIER | c.*232C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 3/3 | 232 | chr3 | 126542810 | ||||||
| chr3:126543249 | G | C | 2 | a0004c0003t0002 a0007c0009t0002 |
34 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*671G>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 3/3 | 671 | chr3 | 126543249 | ||||||
| chr3:126543250 | G | A | 1 | a0009c0011t0004 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*672G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 3/3 | 672 | chr3 | 126543250 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:126524576 | A | C | 88 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0019 others(85): Show |
223 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.97+147A>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126524576 | |||||||
| chr3:126524774 | A | T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0131 |
3 | HG02300.hp1 HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.97+345A>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126524774 | |||||||
| chr3:126524836 | C | A | 1 | a0003c0005t0001g0073 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.97+407C>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126524836 | |||||||
| chr3:126524837 | A | C | 1 | a0003c0005t0001g0073 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.97+408A>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126524837 | |||||||
| chr3:126524846 | G | A | 1 | a0001c0001t0001g0040 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.97+417G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126524846 | |||||||
| chr3:126524982 | G | A | 1 | a0002c0002t0001g0074 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.97+553G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126524982 | |||||||
| chr3:126525012 | G | A | 1 | a0001c0001t0005g0075 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.97+583G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126525012 | |||||||
| chr3:126525208 | T | C | 2 | a0003c0005t0001g0073 a0003c0005t0001g0076 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.97+779T>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126525208 | |||||||
| chr3:126525491 | G | T | 20 | a0001c0001t0001g0122 a0001c0001t0001g0128 a0002c0002t0001g0002 others(17): Show |
74 | HG00408.hp2 HG00558.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.97+1062G>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126525491 | |||||||
| chr3:126525633 | G | A | 1 | a0002c0002t0001g0118 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.97+1204G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126525633 | |||||||
| chr3:126525748 | G | A | 22 | a0001c0001t0001g0122 a0001c0001t0001g0128 a0002c0002t0001g0002 others(19): Show |
78 | HG00408.hp2 HG00558.hp1 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.97+1319G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126525748 | |||||||
| chr3:126525969 | C | T | 1 | a0003c0005t0001g0073 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.97+1540C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126525969 | |||||||
| chr3:126526007 | T | C | 90 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0019 others(87): Show |
232 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.97+1578T>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126526007 | |||||||
| chr3:126526086 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.97+1657G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126526086 | |||||||
| chr3:126526233 | T | G | 2 | a0001c0001t0001g0030 a0009c0011t0004g0079 |
3 | HG01081.hp1 HG01496.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.97+1804T>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126526233 | |||||||
| chr3:126526311 | G | A | 1 | a0001c0001t0001g0080 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.97+1882G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126526311 | |||||||
| chr3:126526349 | G | A | 2 | a0001c0001t0001g0039 a0001c0001t0001g0131 |
3 | HG02300.hp1 HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.97+1920G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126526349 | |||||||
| chr3:126526404 | C | A | 4 | a0003c0004t0001g0011 a0003c0004t0001g0012 a0003c0004t0001g0081 others(1): Show |
12 | HG00733.hp2 HG01175.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.97+1975C>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126526404 | |||||||
| chr3:126526664 | C | A | 1 | a0001c0001t0001g0083 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.97+2235C>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126526664 | |||||||
| chr3:126526902 | C | T | 14 | a0001c0001t0001g0030 a0001c0001t0001g0115 a0003c0004t0001g0011 others(11): Show |
26 | HG00733.hp2 HG01081.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.97+2473C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126526902 | |||||||
| chr3:126527068 | C | G | 1 | a0003c0005t0001g0073 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.97+2639C>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126527068 | |||||||
| chr3:126527071 | G | C | 1 | a0003c0005t0001g0073 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.97+2642G>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126527071 | |||||||
| chr3:126527072 | A | T | 1 | a0002c0002t0001g0130 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.97+2643A>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126527072 | |||||||
| chr3:126527113 | C | T | 72 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0019 others(69): Show |
192 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.97+2684C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126527113 | |||||||
| chr3:126527257 | C | T | 2 | a0001c0001t0001g0030 a0009c0011t0004g0079 |
3 | HG01081.hp1 HG01496.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.97+2828C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126527257 | |||||||
| chr3:126527407 | T | A | 1 | a0004c0003t0002g0086 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.97+2978T>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126527407 | |||||||
| chr3:126527470 | C | T | 1 | a0002c0002t0001g0129 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.97+3041C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126527470 | |||||||
| chr3:126527527 | G | A | 20 | a0001c0001t0001g0122 a0002c0002t0001g0002 a0002c0002t0001g0008 others(17): Show |
74 | HG00408.hp2 HG00558.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.97+3098G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126527527 | |||||||
| chr3:126527531 | G | A | 2 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
2 | NA19009.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.97+3102G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126527531 | |||||||
| chr3:126527561 | C | T | 16 | a0001c0001t0001g0030 a0001c0001t0001g0115 a0003c0004t0001g0011 others(13): Show |
35 | HG00639.hp2 HG00733.hp2 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.97+3132C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126527561 | |||||||
| chr3:126527640 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.97+3211C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126527640 | |||||||
| chr3:126527646 | G | A | 2 | a0003c0007t0001g0041 a0005c0006t0001g0006 |
9 | HG00639.hp2 HG02886.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.97+3217G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126527646 | |||||||
| chr3:126527650 | C | A | 1 | a0003c0007t0001g0087 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.97+3221C>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126527650 | |||||||
| chr3:126527680 | G | A | 1 | a0004c0003t0002g0088 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.97+3251G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126527680 | |||||||
| chr3:126527684 | G | C | 74 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0019 others(71): Show |
197 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.97+3255G>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126527684 | |||||||
| chr3:126527735 | AAATTGGT others(15): Show |
A | 1 | a0001c0001t0001g0071 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.97+3307_97+3328del others(22): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126527735 | |||||||
| chr3:126527752 | C | G | 2 | a0001c0001t0001g0085 a0003c0010t0001g0084 |
2 | HG01884.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.97+3323C>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126527752 | |||||||
| chr3:126527792 | G | A | 70 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0019 others(67): Show |
193 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.97+3363G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126527792 | |||||||
| chr3:126528324 | C | G | 14 | a0003c0005t0001g0020 a0003c0005t0001g0023 a0003c0005t0001g0035 others(11): Show |
20 | HG00735.hp1 HG01099.hp1 HG01358.hp1 others(17): Show |
intron_variant | MODIFIER | c.97+3895C>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126528324 | |||||||
| chr3:126528352 | A | G | 1 | a0001c0001t0001g0019 | 4 | HG00735.hp2 HG01074.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.97+3923A>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126528352 | |||||||
| chr3:126528355 | T | A | 76 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0019 others(73): Show |
205 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.97+3926T>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126528355 | |||||||
| chr3:126528472 | G | C | 4 | a0001c0001t0001g0030 a0003c0007t0001g0041 a0005c0006t0001g0006 others(1): Show |
12 | HG00639.hp2 HG01081.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.97+4043G>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126528472 | |||||||
| chr3:126528615 | G | A | 48 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0019 others(45): Show |
145 | HG00408.hp2 HG00558.hp1 HG00597.hp1 others(142): Show |
intron_variant | MODIFIER | c.97+4186G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126528615 | |||||||
| chr3:126528621 | G | A | 1 | a0003c0007t0001g0092 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.97+4192G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126528621 | |||||||
| chr3:126528626 | T | G | 2 | a0002c0002t0001g0008 a0002c0002t0001g0127 |
9 | HG01346.hp1 HG01361.hp1 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.97+4197T>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126528626 | |||||||
| chr3:126528675 | G | A | 1 | a0004c0003t0002g0093 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.97+4246G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126528675 | |||||||
| chr3:126528767 | C | T | 1 | a0001c0001t0001g0070 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.97+4338C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126528767 | |||||||
| chr3:126528772 | A | C | 1 | a0004c0003t0002g0126 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.97+4343A>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126528772 | |||||||
| chr3:126528952 | C | T | 43 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(40): Show |
136 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.97+4523C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126528952 | |||||||
| chr3:126528954 | C | G | 1 | a0002c0002t0001g0125 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.97+4525C>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126528954 | |||||||
| chr3:126528979 | G | A | 1 | a0003c0004t0001g0016 | 4 | HG01109.hp1 HG01243.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+4550G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126528979 | |||||||
| chr3:126529005 | C | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(52): Show |
157 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.97+4576C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126529005 | |||||||
| chr3:126529130 | ACCCTGCA others(11): Show |
A | 20 | a0002c0002t0001g0096 a0003c0007t0001g0041 a0003c0007t0001g0087 others(17): Show |
49 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.97+4708_97+4725del others(18): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 126529130 | ||||||
| chr3:126529142 | GCGCGAGC others(11): Show |
G | 4 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0006c0008t0001g0017 others(1): Show |
8 | HG02630.hp1 HG02818.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.97+4714_97+4731del others(18): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126529142 | |||||||
| chr3:126529165 | G | A | 12 | a0002c0002t0001g0096 a0004c0003t0002g0003 a0004c0003t0002g0033 others(9): Show |
34 | HG00099.hp2 HG00323.hp2 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.97+4736G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126529165 | |||||||
| chr3:126529384 | G | A | 2 | a0003c0004t0001g0026 a0003c0004t0001g0112 |
4 | HG01109.hp2 HG02723.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+4955G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126529384 | |||||||
| chr3:126529464 | G | A | 2 | a0001c0001t0001g0078 a0001c0001t0001g0094 |
2 | HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.97+5035G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126529464 | |||||||
| chr3:126529673 | C | T | 12 | a0003c0005t0001g0018 a0003c0005t0001g0020 a0003c0005t0001g0023 others(9): Show |
21 | HG00735.hp1 HG01358.hp1 HG01358.hp2 others(18): Show |
intron_variant | MODIFIER | c.97+5244C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126529673 | |||||||
| chr3:126529760 | C | T | 1 | a0003c0010t0001g0084 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.97+5331C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126529760 | |||||||
| chr3:126529782 | C | G | 22 | a0002c0002t0001g0096 a0003c0007t0001g0041 a0003c0007t0001g0087 others(19): Show |
51 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.97+5353C>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126529782 | |||||||
| chr3:126529930 | C | T | 4 | a0003c0007t0001g0041 a0003c0007t0001g0087 a0003c0007t0001g0092 others(1): Show |
4 | HG00323.hp1 HG02055.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.97+5501C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126529930 | |||||||
| chr3:126530061 | C | T | 1 | a0009c0011t0004g0079 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.97+5632C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126530061 | |||||||
| chr3:126530079 | A | C | 12 | a0002c0002t0001g0096 a0004c0003t0002g0003 a0004c0003t0002g0033 others(9): Show |
34 | HG00099.hp2 HG00323.hp2 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.97+5650A>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126530079 | |||||||
| chr3:126530107 | C | A | 1 | a0003c0005t0001g0077 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.97+5678C>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126530107 | |||||||
| chr3:126530172 | G | T | 33 | a0001c0001t0001g0115 a0001c0001t0001g0122 a0002c0002t0001g0002 others(30): Show |
101 | HG00408.hp2 HG00558.hp1 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.97+5743G>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126530172 | |||||||
| chr3:126530187 | G | T | 1 | a0003c0004t0001g0012 | 5 | HG02647.hp2 HG02965.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.97+5758G>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126530187 | |||||||
| chr3:126530377 | C | T | 5 | a0003c0007t0001g0041 a0003c0007t0001g0087 a0003c0007t0001g0092 others(2): Show |
12 | HG00323.hp1 HG00639.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.98-5894C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126530377 | |||||||
| chr3:126530383 | C | T | 1 | a0002c0002t0001g0124 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.98-5888C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126530383 | |||||||
| chr3:126530422 | G | A | 50 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0001g0115 others(47): Show |
144 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.98-5849G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126530422 | |||||||
| chr3:126530438 | C | T | 1 | a0002c0002t0001g0127 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.98-5833C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126530438 | |||||||
| chr3:126530439 | G | A | 1 | a0002c0002t0001g0037 | 2 | HG01074.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.98-5832G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126530439 | |||||||
| chr3:126530464 | C | T | 3 | a0003c0007t0001g0108 a0003c0007t0001g0109 a0003c0007t0006g0107 |
3 | HG01099.hp1 HG02572.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.98-5807C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126530464 | |||||||
| chr3:126530467 | C | A | 2 | a0003c0007t0001g0041 a0003c0007t0001g0087 |
2 | HG02055.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.98-5804C>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126530467 | |||||||
| chr3:126530566 | G | A | 1 | a0003c0004t0001g0016 | 4 | HG01109.hp1 HG01243.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.98-5705G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126530566 | |||||||
| chr3:126530594 | G | T | 1 | a0001c0001t0001g0069 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.98-5677G>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126530594 | |||||||
| chr3:126530601 | C | T | 1 | a0001c0001t0001g0080 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.98-5670C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126530601 | |||||||
| chr3:126530745 | G | A | 1 | a0002c0002t0001g0021 | 4 | HG01175.hp2 HG01516.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-5526G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126530745 | |||||||
| chr3:126530837 | T | G | 4 | a0003c0007t0001g0041 a0003c0007t0001g0087 a0003c0007t0001g0092 others(1): Show |
4 | HG00323.hp1 HG02055.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-5434T>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126530837 | |||||||
| chr3:126530838 | G | A | 1 | a0008c0012t0001g0072 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.98-5433G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126530838 | |||||||
| chr3:126530925 | G | A | 1 | a0001c0001t0001g0046 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.98-5346G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126530925 | |||||||
| chr3:126530944 | G | A | 4 | a0003c0004t0001g0026 a0003c0004t0001g0036 a0003c0004t0001g0112 others(1): Show |
7 | HG01109.hp2 HG01255.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-5327G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126530944 | |||||||
| chr3:126530981 | T | G | 129 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(126): Show |
361 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.98-5290T>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126530981 | |||||||
| chr3:126531034 | A | C | 37 | a0001c0001t0001g0115 a0001c0001t0001g0122 a0002c0002t0001g0002 others(34): Show |
105 | HG00408.hp2 HG00558.hp1 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.98-5237A>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126531034 | |||||||
| chr3:126531035 | A | G | 1 | a0001c0001t0001g0068 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.98-5236A>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126531035 | |||||||
| chr3:126531037 | G | T | 5 | a0003c0007t0001g0041 a0003c0007t0001g0087 a0003c0007t0001g0092 others(2): Show |
12 | HG00323.hp1 HG00639.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.98-5234G>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126531037 | |||||||
| chr3:126531193 | C | T | 19 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0019 others(16): Show |
52 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.98-5078C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126531193 | |||||||
| chr3:126531244 | C | A | 20 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0019 others(17): Show |
53 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.98-5027C>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126531244 | |||||||
| chr3:126531261 | A | G | 1 | a0001c0001t0001g0067 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.98-5010A>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126531261 | |||||||
| chr3:126531292 | G | A | 20 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0019 others(17): Show |
53 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.98-4979G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126531292 | |||||||
| chr3:126531596 | T | G | 3 | a0001c0001t0001g0005 a0001c0001t0001g0046 a0001c0001t0001g0047 |
11 | HG00642.hp1 HG01069.hp1 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.98-4675T>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126531596 | |||||||
| chr3:126531604 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.98-4667C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126531604 | |||||||
| chr3:126531625 | C | T | 1 | a0009c0011t0004g0079 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.98-4646C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126531625 | |||||||
| chr3:126531744 | G | T | 1 | a0009c0011t0004g0079 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.98-4527G>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126531744 | |||||||
| chr3:126531775 | G | C | 1 | a0001c0001t0001g0048 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.98-4496G>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126531775 | |||||||
| chr3:126531878 | A | G | 129 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(126): Show |
361 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.98-4393A>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126531878 | |||||||
| chr3:126531926 | A | G | 3 | a0003c0004t0001g0016 a0003c0004t0001g0116 a0003c0004t0001g0117 |
6 | HG01109.hp1 HG01243.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.98-4345A>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126531926 | |||||||
| chr3:126531955 | C | A | 6 | a0003c0004t0001g0011 a0003c0004t0001g0012 a0003c0004t0001g0081 others(3): Show |
14 | HG00733.hp2 HG01175.hp1 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.98-4316C>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126531955 | |||||||
| chr3:126532032 | G | A | 4 | a0003c0004t0001g0026 a0003c0004t0001g0036 a0003c0004t0001g0112 others(1): Show |
7 | HG01109.hp2 HG01255.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-4239G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126532032 | |||||||
| chr3:126532055 | T | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(126): Show |
361 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.98-4216T>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126532055 | |||||||
| chr3:126532151 | G | A | 2 | a0001c0001t0001g0078 a0001c0001t0001g0094 |
2 | HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.98-4120G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126532151 | |||||||
| chr3:126532292 | T | A | 1 | a0001c0001t0001g0049 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.98-3979T>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126532292 | |||||||
| chr3:126532370 | G | A | 9 | a0003c0005t0001g0020 a0003c0005t0001g0023 a0003c0005t0001g0073 others(6): Show |
14 | HG00735.hp1 HG01358.hp1 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.98-3901G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126532370 | |||||||
| chr3:126532442 | T | TGTATGTG | 12 | a0003c0005t0001g0018 a0003c0005t0001g0020 a0003c0005t0001g0023 others(9): Show |
21 | HG00735.hp1 HG01358.hp1 HG01358.hp2 others(18): Show |
intron_variant | MODIFIER | c.98-3823_98-3817dup others(7): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 126532442 | ||||||
| chr3:126532562 | A | G | 1 | a0001c0001t0001g0048 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.98-3709A>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126532562 | |||||||
| chr3:126532606 | C | G | 3 | a0002c0002t0001g0008 a0002c0002t0001g0014 a0002c0002t0001g0127 |
14 | HG01256.hp2 HG01258.hp2 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.98-3665C>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126532606 | |||||||
| chr3:126532637 | C | T | 1 | a0001c0001t0001g0065 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.98-3634C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126532637 | |||||||
| chr3:126532649 | A | G | 1 | a0009c0011t0004g0079 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.98-3622A>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126532649 | |||||||
| chr3:126532664 | T | C | 2 | a0006c0008t0001g0017 a0006c0008t0001g0032 |
6 | HG02818.hp2 HG02895.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.98-3607T>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126532664 | |||||||
| chr3:126532975 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.98-3296T>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126532975 | |||||||
| chr3:126533038 | A | T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(70): Show |
221 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.98-3233A>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126533038 | |||||||
| chr3:126533160 | G | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0090 |
4 | HG02280.hp1 HG02622.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-3111G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126533160 | |||||||
| chr3:126533355 | G | A | 1 | a0001c0001t0001g0102 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.98-2916G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126533355 | |||||||
| chr3:126533532 | T | TTTGTGTA others(16): Show |
1 | a0008c0012t0001g0072 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.98-2738_98-2716dup others(23): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 126533532 | ||||||
| chr3:126533582 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.98-2689C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126533582 | |||||||
| chr3:126533662 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.98-2609G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126533662 | |||||||
| chr3:126533663 | G | T | 20 | a0001c0001t0001g0122 a0002c0002t0001g0002 a0002c0002t0001g0008 others(17): Show |
74 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.98-2608G>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126533663 | |||||||
| chr3:126533684 | T | C | 18 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0019 others(15): Show |
51 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.98-2587T>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126533684 | |||||||
| chr3:126533804 | T | G | 6 | a0003c0004t0001g0011 a0003c0004t0001g0012 a0003c0004t0001g0081 others(3): Show |
14 | HG00733.hp2 HG01175.hp1 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.98-2467T>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126533804 | |||||||
| chr3:126533867 | T | A | 125 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(122): Show |
357 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(354): Show |
intron_variant | MODIFIER | c.98-2404T>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126533867 | |||||||
| chr3:126533868 | T | A | 4 | a0003c0007t0001g0041 a0003c0007t0001g0087 a0003c0007t0001g0092 others(1): Show |
4 | HG00323.hp1 HG02055.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-2403T>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126533868 | |||||||
| chr3:126533909 | T | A | 1 | a0001c0001t0001g0051 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.98-2362T>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126533909 | |||||||
| chr3:126534032 | T | A | 2 | a0001c0001t0001g0027 a0001c0001t0001g0051 |
3 | HG00741.hp1 HG02135.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.98-2239T>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126534032 | |||||||
| chr3:126534041 | G | A | 12 | a0003c0005t0001g0018 a0003c0005t0001g0020 a0003c0005t0001g0023 others(9): Show |
21 | HG00735.hp1 HG01358.hp1 HG01358.hp2 others(18): Show |
intron_variant | MODIFIER | c.98-2230G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126534041 | |||||||
| chr3:126534262 | C | T | 12 | a0003c0005t0001g0018 a0003c0005t0001g0020 a0003c0005t0001g0023 others(9): Show |
21 | HG00735.hp1 HG01358.hp1 HG01358.hp2 others(18): Show |
intron_variant | MODIFIER | c.98-2009C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126534262 | |||||||
| chr3:126534279 | A | T | 2 | a0003c0004t0001g0012 a0003c0004t0001g0095 |
6 | HG01891.hp2 HG02647.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.98-1992A>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126534279 | |||||||
| chr3:126534330 | T | C | 128 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(125): Show |
353 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.98-1941T>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126534330 | |||||||
| chr3:126534342 | C | T | 1 | a0005c0006t0001g0006 | 8 | HG00639.hp2 HG02886.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.98-1929C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126534342 | |||||||
| chr3:126534354 | T | C | 7 | a0003c0007t0001g0041 a0003c0007t0001g0087 a0003c0007t0001g0092 others(4): Show |
7 | HG00323.hp1 HG01099.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.98-1917T>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126534354 | |||||||
| chr3:126534390 | GAGAC | G | 18 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0019 others(15): Show |
51 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.98-1862_98-1859del others(4): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 126534390 | ||||||
| chr3:126534475 | A | G | 1 | a0001c0001t0001g0013 | 5 | NA18942.hp1 NA18963.hp2 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.98-1796A>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126534475 | |||||||
| chr3:126534644 | G | A | 1 | a0005c0006t0001g0006 | 8 | HG00639.hp2 HG02886.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.98-1627G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126534644 | |||||||
| chr3:126534914 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.98-1357C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126534914 | |||||||
| chr3:126534961 | G | A | 18 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0019 others(15): Show |
51 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.98-1310G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126534961 | |||||||
| chr3:126535061 | C | CACACAGA others(23): Show |
32 | a0001c0001t0001g0115 a0001c0001t0001g0122 a0002c0002t0001g0002 others(29): Show |
100 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.98-1209_98-1208ins others(30): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 126535061 | ||||||
| chr3:126535063 | G | C | 2 | a0002c0002t0001g0123 a0002c0002t0001g0130 |
2 | NA18953.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.98-1208G>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535063 | |||||||
| chr3:126535083 | C | CCAGCCGG others(23): Show |
93 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(90): Show |
249 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.98-1173_98-1172ins others(30): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 126535083 | ||||||
| chr3:126535083 | C | T | 32 | a0001c0001t0001g0115 a0001c0001t0001g0122 a0002c0002t0001g0002 others(29): Show |
100 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.98-1188C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535083 | |||||||
| chr3:126535088 | C | CGGGAGAC others(23): Show |
2 | a0002c0002t0001g0123 a0002c0002t0001g0130 |
2 | NA18953.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.98-1173_98-1172ins others(30): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 126535088 | ||||||
| chr3:126535091 | GAGACAGA others(293): Show |
G | 1 | a0001c0001t0001g0031 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.98-1172_98-873del | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 126535091 | ||||||
| chr3:126535123 | G | A | 1 | a0001c0001t0001g0019 | 4 | HG00735.hp2 HG01074.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-1148G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535123 | |||||||
| chr3:126535158 | G | GAGACAGA others(27): Show |
1 | a0001c0001t0001g0019 | 4 | HG00735.hp2 HG01074.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-1098_98-1065dup others(34): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 126535158 | ||||||
| chr3:126535186 | G | A | 1 | a0009c0011t0004g0079 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.98-1085G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535186 | |||||||
| chr3:126535207 | G | A | 12 | a0003c0005t0001g0018 a0003c0005t0001g0020 a0003c0005t0001g0023 others(9): Show |
21 | HG00735.hp1 HG01358.hp1 HG01358.hp2 others(18): Show |
intron_variant | MODIFIER | c.98-1064G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535207 | |||||||
| chr3:126535219 | C | T | 2 | a0002c0002t0001g0123 a0002c0002t0001g0130 |
2 | NA18953.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.98-1052C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535219 | |||||||
| chr3:126535319 | G | GAGACAGA others(61): Show |
1 | a0003c0007t0001g0108 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.98-923_98-856dupGC others(66): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 126535319 | ||||||
| chr3:126535351 | G | A | 1 | a0009c0011t0004g0079 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.98-920G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535351 | |||||||
| chr3:126535416 | A | G | 1 | a0001c0001t0001g0031 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.98-855A>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535416 | |||||||
| chr3:126535421 | GAGAC | G | 17 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0019 others(14): Show |
49 | HG00735.hp2 HG01074.hp2 HG01496.hp1 others(46): Show |
intron_variant | MODIFIER | c.98-839_98-836delAC others(2): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 126535421 | ||||||
| chr3:126535436 | C | T | 1 | a0001c0001t0001g0031 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.98-835C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535436 | |||||||
| chr3:126535440 | C | G | 1 | a0001c0001t0001g0031 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.98-831C>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535440 | |||||||
| chr3:126535461 | G | C | 1 | a0001c0001t0001g0031 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.98-810G>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535461 | |||||||
| chr3:126535470 | T | C | 1 | a0001c0001t0001g0031 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.98-801T>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535470 | |||||||
| chr3:126535473 | C | T | 2 | a0002c0002t0001g0009 a0002c0002t0001g0129 |
9 | NA18949.hp1 NA18959.hp2 NA18968.hp2 others(6): Show |
intron_variant | MODIFIER | c.98-798C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535473 | |||||||
| chr3:126535477 | G | T | 1 | a0001c0001t0001g0031 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.98-794G>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535477 | |||||||
| chr3:126535487 | G | A | 1 | a0001c0001t0001g0031 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.98-784G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535487 | |||||||
| chr3:126535504 | T | C | 19 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0019 others(16): Show |
52 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.98-767T>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535504 | |||||||
| chr3:126535508 | G | C | 1 | a0001c0001t0001g0031 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.98-763G>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535508 | |||||||
| chr3:126535511 | G | T | 17 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0019 others(14): Show |
49 | HG00735.hp2 HG01074.hp2 HG01496.hp1 others(46): Show |
intron_variant | MODIFIER | c.98-760G>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535511 | |||||||
| chr3:126535521 | G | A | 17 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0019 others(14): Show |
49 | HG00735.hp2 HG01074.hp2 HG01496.hp1 others(46): Show |
intron_variant | MODIFIER | c.98-750G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535521 | |||||||
| chr3:126535525 | GAC | G | 17 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0019 others(14): Show |
49 | HG00735.hp2 HG01074.hp2 HG01496.hp1 others(46): Show |
intron_variant | MODIFIER | c.98-740_98-739delCA | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 126535525 | ||||||
| chr3:126535529 | C | G | 1 | a0001c0001t0001g0031 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.98-742C>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535529 | |||||||
| chr3:126535531 | C | T | 1 | a0001c0001t0001g0031 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.98-740C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535531 | |||||||
| chr3:126535542 | C | G | 1 | a0001c0001t0001g0031 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.98-729C>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535542 | |||||||
| chr3:126535545 | G | GTCCCCAG others(523): Show |
1 | a0003c0010t0001g0084 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.98-723_98-722insCC others(528): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 126535545 | ||||||
| chr3:126535545 | G | T | 1 | a0001c0001t0001g0031 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.98-726G>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535545 | |||||||
| chr3:126535551 | A | AGCAGGGA others(27): Show |
1 | a0003c0004t0001g0113 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.98-718_98-717insAG others(32): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 126535551 | ||||||
| chr3:126535551 | A | AGCCGGGA others(27): Show |
108 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(105): Show |
307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.98-700_98-699insCA others(32): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 126535551 | ||||||
| chr3:126535551 | A | AGCCGGGA others(27): Show |
17 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0019 others(14): Show |
49 | HG00735.hp2 HG01074.hp2 HG01496.hp1 others(46): Show |
intron_variant | MODIFIER | c.98-707_98-706insTA others(32): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr3 | 126535551 | ||||||
| chr3:126535551 | A | G | 2 | a0001c0001t0001g0031 a0003c0010t0001g0084 |
3 | HG01070.hp2 HG01071.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.98-720A>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535551 | |||||||
| chr3:126535580 | A | G | 1 | a0002c0002t0001g0120 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.98-691A>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535580 | |||||||
| chr3:126535589 | A | G | 1 | a0002c0002t0001g0120 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.98-682A>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535589 | |||||||
| chr3:126535591 | T | C | 1 | a0002c0002t0001g0120 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.98-680T>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535591 | |||||||
| chr3:126535602 | C | A | 1 | a0002c0002t0001g0120 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.98-669C>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535602 | |||||||
| chr3:126535604 | G | A | 1 | a0002c0002t0001g0120 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.98-667G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535604 | |||||||
| chr3:126535619 | T | C | 1 | a0002c0002t0001g0120 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.98-652T>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535619 | |||||||
| chr3:126535625 | C | T | 1 | a0002c0002t0001g0120 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.98-646C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535625 | |||||||
| chr3:126535627 | A | G | 1 | a0002c0002t0001g0120 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.98-644A>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535627 | |||||||
| chr3:126535636 | A | C | 1 | a0002c0002t0001g0120 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.98-635A>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535636 | |||||||
| chr3:126535638 | A | G | 1 | a0002c0002t0001g0120 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.98-633A>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535638 | |||||||
| chr3:126535648 | A | G | 1 | a0005c0006t0001g0006 | 8 | HG00639.hp2 HG02886.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.98-623A>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535648 | |||||||
| chr3:126535651 | G | T | 1 | a0002c0002t0001g0120 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.98-620G>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535651 | |||||||
| chr3:126535653 | C | T | 1 | a0002c0002t0001g0120 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.98-618C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535653 | |||||||
| chr3:126535670 | C | G | 1 | a0002c0002t0001g0120 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.98-601C>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535670 | |||||||
| chr3:126535720 | G | T | 1 | a0009c0011t0004g0079 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.98-551G>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535720 | |||||||
| chr3:126535724 | C | T | 55 | a0001c0001t0001g0115 a0001c0001t0001g0122 a0002c0002t0001g0002 others(52): Show |
132 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.98-547C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535724 | |||||||
| chr3:126535849 | G | A | 34 | a0001c0001t0001g0115 a0001c0001t0001g0122 a0002c0002t0001g0002 others(31): Show |
102 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.98-422G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535849 | |||||||
| chr3:126535852 | T | C | 2 | a0003c0004t0001g0012 a0003c0004t0001g0095 |
6 | HG01891.hp2 HG02647.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.98-419T>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535852 | |||||||
| chr3:126535897 | G | C | 1 | a0001c0001t0001g0019 | 4 | HG00735.hp2 HG01074.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-374G>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126535897 | |||||||
| chr3:126536029 | C | T | 2 | a0001c0001t0001g0043 a0001c0001t0001g0080 |
2 | NA19067.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.98-242C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126536029 | |||||||
| chr3:126536046 | G | A | 18 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0019 others(15): Show |
51 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.98-225G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126536046 | |||||||
| chr3:126536252 | T | G | 1 | a0001c0001t0001g0028 | 2 | NA18997.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.98-19T>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 1/2 | chr3 | 126536252 | |||||||
| chr3:126536526 | T | G | 6 | a0003c0004t0001g0011 a0003c0004t0001g0012 a0003c0004t0001g0081 others(3): Show |
14 | HG00733.hp2 HG01175.hp1 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.180+173T>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126536526 | |||||||
| chr3:126536601 | G | C | 1 | a0007c0009t0002g0097 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.180+248G>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126536601 | |||||||
| chr3:126536710 | G | C | 1 | a0001c0001t0001g0102 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.180+357G>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126536710 | |||||||
| chr3:126536786 | G | A | 1 | a0001c0001t0001g0019 | 4 | HG00735.hp2 HG01074.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.180+433G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126536786 | |||||||
| chr3:126536790 | G | C | 1 | a0003c0004t0001g0112 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.180+437G>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126536790 | |||||||
| chr3:126536863 | GCT | G | 54 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(51): Show |
169 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.180+523_180+524del others(2): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126536863 | ||||||
| chr3:126536882 | C | CACACACA others(3): Show |
1 | a0003c0005t0001g0106 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.180+538_180+539ins others(10): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126536882 | ||||||
| chr3:126536895 | AAACACAC others(6): Show |
A | 1 | a0004c0003t0002g0003 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.180+544_180+556del others(13): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126536895 | ||||||
| chr3:126536896 | A | AAC | 26 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(23): Show |
80 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.180+570_180+571dup others(2): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126536896 | ||||||
| chr3:126536896 | A | AACAC | 9 | a0002c0002t0001g0002 a0002c0002t0001g0120 a0003c0004t0001g0011 others(6): Show |
16 | HG00733.hp2 HG01109.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.180+568_180+571dup others(4): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126536896 | ||||||
| chr3:126536896 | A | AACACAC | 5 | a0001c0001t0001g0115 a0003c0004t0001g0011 a0003c0004t0001g0012 others(2): Show |
11 | HG01346.hp2 HG01891.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.180+566_180+571dup others(6): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126536896 | ||||||
| chr3:126536896 | A | AACACACA others(1): Show |
2 | a0003c0005t0001g0018 a0003c0005t0001g0023 |
5 | HG02559.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.180+564_180+571dup others(8): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126536896 | ||||||
| chr3:126536896 | A | AACACACA others(3): Show |
8 | a0003c0005t0001g0020 a0003c0005t0001g0023 a0003c0005t0001g0035 others(5): Show |
13 | HG00735.hp1 HG01358.hp1 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.180+562_180+571dup others(10): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126536896 | ||||||
| chr3:126536896 | A | AACACACA others(5): Show |
1 | a0003c0005t0001g0110 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.180+560_180+571dup others(12): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126536896 | ||||||
| chr3:126536896 | A | C | 1 | a0003c0005t0001g0106 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.180+543A>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126536896 | |||||||
| chr3:126536896 | AAC | A | 19 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0019 others(16): Show |
56 | HG00639.hp2 HG00735.hp2 HG01070.hp2 others(53): Show |
intron_variant | MODIFIER | c.180+570_180+571del others(2): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126536896 | ||||||
| chr3:126536896 | AACACAC | A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0010 |
8 | HG00738.hp2 HG01168.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.180+566_180+571del others(6): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126536896 | ||||||
| chr3:126536921 | A | C | 1 | a0005c0006t0001g0006 | 8 | HG00639.hp2 HG02886.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.180+568A>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126536921 | |||||||
| chr3:126536923 | A | C | 2 | a0003c0007t0001g0092 a0003c0007t0001g0109 |
2 | HG00323.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.180+570A>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126536923 | |||||||
| chr3:126536924 | C | CACACACA others(4): Show |
1 | a0003c0005t0001g0103 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.180+571_180+572ins others(11): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126536924 | |||||||
| chr3:126536928 | A | C | 1 | a0003c0007t0001g0108 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.180+575A>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126536928 | |||||||
| chr3:126537017 | G | A | 1 | a0002c0002t0001g0021 | 4 | HG01175.hp2 HG01516.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.180+664G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126537017 | |||||||
| chr3:126537035 | C | G | 55 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(52): Show |
170 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.180+682C>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126537035 | |||||||
| chr3:126537041 | G | T | 18 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0019 others(15): Show |
51 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.180+688G>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126537041 | |||||||
| chr3:126537110 | C | G | 1 | a0009c0011t0004g0079 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.180+757C>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126537110 | |||||||
| chr3:126537149 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.180+796A>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126537149 | |||||||
| chr3:126537289 | G | A | 1 | a0001c0001t0001g0029 | 2 | NA18945.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.180+936G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126537289 | |||||||
| chr3:126537297 | G | A | 2 | a0001c0001t0001g0078 a0001c0001t0001g0094 |
2 | HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.180+944G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126537297 | |||||||
| chr3:126537373 | G | A | 32 | a0001c0001t0001g0115 a0002c0002t0001g0002 a0002c0002t0001g0008 others(29): Show |
99 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.180+1020G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126537373 | |||||||
| chr3:126537459 | A | G | 1 | a0009c0011t0004g0079 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.180+1106A>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126537459 | |||||||
| chr3:126537568 | G | A | 1 | a0005c0006t0001g0006 | 8 | HG00639.hp2 HG02886.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.180+1215G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126537568 | |||||||
| chr3:126537705 | G | A | 18 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0019 others(15): Show |
51 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.180+1352G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126537705 | |||||||
| chr3:126537755 | CAT | C | 18 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0019 others(15): Show |
51 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.180+1404_180+1405d others(4): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126537755 | ||||||
| chr3:126537812 | G | A | 1 | a0001c0001t0001g0053 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.180+1459G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126537812 | |||||||
| chr3:126537826 | T | G | 72 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0019 others(69): Show |
182 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.180+1473T>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126537826 | |||||||
| chr3:126537932 | A | G | 129 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(126): Show |
361 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.180+1579A>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126537932 | |||||||
| chr3:126538138 | G | A | 19 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0019 others(16): Show |
52 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.180+1785G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126538138 | |||||||
| chr3:126538168 | A | G | 1 | a0001c0001t0001g0022 | 3 | HG01258.hp1 HG01361.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.180+1815A>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126538168 | |||||||
| chr3:126538172 | A | G | 1 | a0003c0007t0001g0101 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.180+1819A>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126538172 | |||||||
| chr3:126538205 | C | A | 6 | a0003c0004t0001g0011 a0003c0004t0001g0012 a0003c0004t0001g0081 others(3): Show |
14 | HG00733.hp2 HG01175.hp1 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.180+1852C>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126538205 | |||||||
| chr3:126538236 | C | T | 33 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0009 others(30): Show |
101 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.180+1883C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126538236 | |||||||
| chr3:126538323 | C | T | 20 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0019 others(17): Show |
53 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.180+1970C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126538323 | |||||||
| chr3:126538362 | G | C | 1 | a0001c0001t0001g0091 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.180+2009G>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126538362 | |||||||
| chr3:126538383 | T | G | 1 | a0003c0005t0001g0104 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.180+2030T>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126538383 | |||||||
| chr3:126538393 | G | A | 52 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0009 others(49): Show |
129 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.180+2040G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126538393 | |||||||
| chr3:126538435 | G | A | 1 | a0002c0002t0001g0127 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.180+2082G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126538435 | |||||||
| chr3:126538513 | A | C | 20 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0019 others(17): Show |
53 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.180+2160A>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126538513 | |||||||
| chr3:126538528 | TGGGCTCA others(15): Show |
T | 1 | a0001c0001t0005g0075 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.180+2179_180+2200d others(24): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126538528 | ||||||
| chr3:126538592 | G | A | 1 | a0009c0011t0004g0079 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.180+2239G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126538592 | |||||||
| chr3:126538668 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.180+2315C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126538668 | |||||||
| chr3:126538725 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.180+2372C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126538725 | |||||||
| chr3:126538738 | G | A | 7 | a0003c0007t0001g0041 a0003c0007t0001g0087 a0003c0007t0001g0092 others(4): Show |
7 | HG00323.hp1 HG01099.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.180+2385G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126538738 | |||||||
| chr3:126538764 | T | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(126): Show |
361 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.180+2411T>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126538764 | |||||||
| chr3:126538765 | G | A | 1 | a0002c0002t0001g0121 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.180+2412G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126538765 | |||||||
| chr3:126538903 | T | C | 3 | a0001c0001t0001g0078 a0001c0001t0001g0094 a0001c0001t0001g0115 |
3 | HG02630.hp1 HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.180+2550T>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126538903 | |||||||
| chr3:126538948 | C | T | 1 | a0002c0002t0001g0096 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.180+2595C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126538948 | |||||||
| chr3:126539009 | C | T | 7 | a0003c0007t0001g0041 a0003c0007t0001g0087 a0003c0007t0001g0092 others(4): Show |
7 | HG00323.hp1 HG01099.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.180+2656C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126539009 | |||||||
| chr3:126539010 | G | A | 2 | a0006c0008t0001g0017 a0006c0008t0001g0032 |
6 | HG02818.hp2 HG02895.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.180+2657G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126539010 | |||||||
| chr3:126539029 | C | G | 55 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(52): Show |
170 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.180+2676C>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126539029 | |||||||
| chr3:126539034 | C | A | 2 | a0006c0008t0001g0017 a0006c0008t0001g0032 |
6 | HG02818.hp2 HG02895.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.180+2681C>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126539034 | |||||||
| chr3:126539037 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.180+2684T>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126539037 | |||||||
| chr3:126539073 | G | A | 20 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0019 others(17): Show |
53 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.181-2660G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126539073 | |||||||
| chr3:126539183 | C | T | 20 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0019 others(17): Show |
53 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.181-2550C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126539183 | |||||||
| chr3:126539202 | C | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(52): Show |
170 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.181-2531C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126539202 | |||||||
| chr3:126539442 | C | A | 19 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0009 others(16): Show |
73 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.181-2291C>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126539442 | |||||||
| chr3:126539486 | CAT | C | 3 | a0001c0001t0001g0007 a0001c0001t0001g0048 a0005c0006t0001g0006 |
17 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.181-2244_181-2243d others(4): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126539486 | ||||||
| chr3:126539512 | C | A | 1 | a0008c0012t0001g0072 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.181-2221C>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126539512 | |||||||
| chr3:126539520 | C | A | 1 | a0008c0012t0001g0072 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.181-2213C>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126539520 | |||||||
| chr3:126539541 | A | C | 1 | a0008c0012t0001g0072 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.181-2192A>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126539541 | |||||||
| chr3:126539569 | A | C | 1 | a0008c0012t0001g0072 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.181-2164A>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126539569 | |||||||
| chr3:126539598 | C | A | 1 | a0008c0012t0001g0072 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.181-2135C>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126539598 | |||||||
| chr3:126539602 | A | T | 1 | a0008c0012t0001g0072 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.181-2131A>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126539602 | |||||||
| chr3:126539722 | C | A | 2 | a0001c0001t0001g0078 a0001c0001t0001g0094 |
2 | HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.181-2011C>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126539722 | |||||||
| chr3:126539748 | C | CCACA | 20 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0019 others(17): Show |
53 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.181-1981_181-1978d others(6): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126539748 | ||||||
| chr3:126539777 | A | ACACACAC | 18 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0019 others(15): Show |
49 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(46): Show |
intron_variant | MODIFIER | c.181-1944_181-1938d others(9): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126539777 | ||||||
| chr3:126539797 | ACAC | A | 32 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0009 others(29): Show |
100 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.181-1932_181-1930d others(5): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126539797 | ||||||
| chr3:126539810 | C | T | 2 | a0003c0004t0001g0026 a0003c0004t0001g0112 |
4 | HG01109.hp2 HG02723.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.181-1923C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126539810 | |||||||
| chr3:126539829 | ACACACAC others(2): Show |
A | 3 | a0001c0001t0001g0078 a0001c0001t0001g0131 a0006c0008t0001g0017 |
6 | HG02451.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.181-1895_181-1887d others(11): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126539829 | ||||||
| chr3:126539838 | C | T | 17 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0019 others(14): Show |
47 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.181-1895C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126539838 | |||||||
| chr3:126539842 | A | ACACACAC others(4): Show |
17 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0019 others(14): Show |
47 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.181-1887_181-1886i others(13): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126539842 | ||||||
| chr3:126539847 | T | C | 17 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0019 others(14): Show |
47 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.181-1886T>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126539847 | |||||||
| chr3:126539862 | C | CCAAACCA others(427): Show |
5 | a0001c0001t0001g0039 a0001c0001t0001g0085 a0001c0001t0001g0094 others(2): Show |
7 | HG01884.hp1 HG02300.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.181-1869_181-1868i others(436): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126539862 | ||||||
| chr3:126539862 | C | CCAAACCA others(427): Show |
12 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0019 others(9): Show |
40 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.181-1869_181-1868i others(436): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126539862 | ||||||
| chr3:126539868 | C | A | 17 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0019 others(14): Show |
47 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.181-1865C>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126539868 | |||||||
| chr3:126539874 | C | CACACACC others(445): Show |
1 | a0001c0001t0001g0056 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.181-1853_181-1852i others(454): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126539874 | ||||||
| chr3:126539875 | A | AC | 17 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0019 others(14): Show |
47 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.181-1857dupC | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126539875 | ||||||
| chr3:126539875 | A | ACACACCC others(451): Show |
1 | a0001c0001t0001g0055 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.181-1853_181-1852i others(460): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126539875 | ||||||
| chr3:126539875 | A | ACACACCC others(447): Show |
1 | a0003c0005t0001g0110 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.181-1853_181-1852i others(456): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126539875 | ||||||
| chr3:126539875 | A | ACACACCC others(448): Show |
3 | a0001c0001t0001g0078 a0001c0001t0001g0131 a0006c0008t0001g0017 |
6 | HG02451.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.181-1853_181-1852i others(457): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126539875 | ||||||
| chr3:126539875 | A | ACACACCC others(452): Show |
1 | a0009c0011t0004g0079 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.181-1853_181-1852i others(461): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126539875 | ||||||
| chr3:126539875 | A | ACACACCC others(452): Show |
58 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(55): Show |
180 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.181-1853_181-1852i others(461): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126539875 | ||||||
| chr3:126539875 | A | ACACACCC others(450): Show |
1 | a0001c0001t0001g0045 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.181-1853_181-1852i others(459): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126539875 | ||||||
| chr3:126539875 | A | ACACACCC others(450): Show |
1 | a0003c0007t0001g0109 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.181-1853_181-1852i others(459): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126539875 | ||||||
| chr3:126539875 | A | ACACACCC others(452): Show |
1 | a0001c0001t0001g0060 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.181-1853_181-1852i others(461): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126539875 | ||||||
| chr3:126539875 | A | ACACACCC others(450): Show |
11 | a0003c0005t0001g0018 a0003c0005t0001g0020 a0003c0005t0001g0023 others(8): Show |
20 | HG00735.hp1 HG01358.hp1 HG01358.hp2 others(17): Show |
intron_variant | MODIFIER | c.181-1853_181-1852i others(459): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126539875 | ||||||
| chr3:126539875 | A | ACACACCC others(443): Show |
33 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0009 others(30): Show |
101 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.181-1853_181-1852i others(452): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126539875 | ||||||
| chr3:126539875 | A | ACACACCC others(452): Show |
1 | a0001c0001t0003g0061 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.181-1853_181-1852i others(461): Show |
CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | 126539875 | ||||||
| chr3:126539896 | A | C | 108 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(105): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.181-1837A>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126539896 | |||||||
| chr3:126539972 | A | G | 5 | a0003c0004t0001g0011 a0003c0004t0001g0012 a0003c0004t0001g0082 others(2): Show |
13 | HG00733.hp2 HG01175.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.181-1761A>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126539972 | |||||||
| chr3:126539989 | A | C | 1 | a0003c0004t0001g0082 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.181-1744A>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126539989 | |||||||
| chr3:126540028 | C | T | 20 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0019 others(17): Show |
53 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.181-1705C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126540028 | |||||||
| chr3:126540080 | G | A | 1 | a0001c0001t0001g0010 | 6 | HG00738.hp2 HG01168.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.181-1653G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126540080 | |||||||
| chr3:126540100 | G | C | 128 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(125): Show |
353 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.181-1633G>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126540100 | |||||||
| chr3:126540177 | G | A | 1 | a0001c0001t0001g0015 | 4 | NA18944.hp2 NA18974.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.181-1556G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126540177 | |||||||
| chr3:126540355 | A | T | 20 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0019 others(17): Show |
53 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.181-1378A>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126540355 | |||||||
| chr3:126540422 | G | C | 1 | a0007c0009t0002g0098 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.181-1311G>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126540422 | |||||||
| chr3:126540526 | G | A | 53 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0009 others(50): Show |
130 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.181-1207G>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126540526 | |||||||
| chr3:126540548 | G | T | 20 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0019 others(17): Show |
53 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.181-1185G>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126540548 | |||||||
| chr3:126540589 | T | C | 1 | a0003c0010t0001g0084 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.181-1144T>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126540589 | |||||||
| chr3:126540615 | C | T | 6 | a0003c0004t0001g0011 a0003c0004t0001g0012 a0003c0004t0001g0081 others(3): Show |
14 | HG00733.hp2 HG01175.hp1 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.181-1118C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126540615 | |||||||
| chr3:126540642 | G | C | 2 | a0003c0007t0001g0041 a0003c0007t0001g0087 |
2 | HG02055.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.181-1091G>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126540642 | |||||||
| chr3:126540760 | T | C | 2 | a0004c0003t0002g0033 a0004c0003t0002g0099 |
3 | HG03209.hp1 HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.181-973T>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126540760 | |||||||
| chr3:126540862 | C | G | 1 | a0001c0001t0001g0059 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.181-871C>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126540862 | |||||||
| chr3:126540957 | A | G | 5 | a0003c0005t0001g0073 a0003c0005t0001g0076 a0003c0005t0001g0103 others(2): Show |
5 | HG02486.hp2 HG02647.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.181-776A>G | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126540957 | |||||||
| chr3:126540968 | G | T | 1 | a0003c0007t0001g0108 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.181-765G>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126540968 | |||||||
| chr3:126541057 | C | A | 1 | a0004c0003t0002g0034 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.181-676C>A | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126541057 | |||||||
| chr3:126541064 | T | C | 12 | a0003c0005t0001g0018 a0003c0005t0001g0020 a0003c0005t0001g0023 others(9): Show |
21 | HG00735.hp1 HG01358.hp1 HG01358.hp2 others(18): Show |
intron_variant | MODIFIER | c.181-669T>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126541064 | |||||||
| chr3:126541320 | C | T | 33 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0009 others(30): Show |
101 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.181-413C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126541320 | |||||||
| chr3:126541340 | T | C | 4 | a0003c0004t0001g0026 a0003c0004t0001g0036 a0003c0004t0001g0112 others(1): Show |
7 | HG01109.hp2 HG01255.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.181-393T>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126541340 | |||||||
| chr3:126541354 | A | C | 1 | a0001c0001t0001g0058 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.181-379A>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126541354 | |||||||
| chr3:126541417 | C | T | 1 | a0001c0001t0001g0057 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.181-316C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126541417 | |||||||
| chr3:126541602 | G | C | 1 | a0001c0001t0001g0090 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.181-131G>C | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126541602 | |||||||
| chr3:126541686 | C | T | 1 | a0004c0003t0002g0093 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.181-47C>T | CHST13 | ENSG00000180767.11 | transcript | ENST00000319340.7 | protein_coding | 2/2 | chr3 | 126541686 |