Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1075 |
| ensemblid | ENSG00000109861.17 |
| hgncid | 2528 |
| symbol | CTSC |
| name | cathepsin C |
| refseq_nuc | NM_001814.6 |
| refseq_prot | NP_001805.4 |
| ensembl_nuc | ENST00000227266.10 |
| ensembl_prot | ENSP00000227266.4 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 88293592 |
| end | 88337736 |
| strand | - |
| ver | v1.2 |
| region | chr11:88293592-88337736 |
| region5000 | chr11:88288592-88342736 |
| regionname0 | CTSC_chr11_88293592_88337736 |
| regionname5000 | CTSC_chr11_88288592_88342736 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 463 | 367 | 80 | 60 | 177 | 11 | 38 | 134 | CTSC_chr11_88288592_88342736 | CTSC | MGAGP others(458): Show |
chr11 | 88288592 | 88342736 |
| a0002 | 0/0 | 463 | 47 | 11 | 8 | 25 | 1 | 2 | 22 | CTSC_chr11_88288592_88342736 | CTSC | MGAGP others(458): Show |
chr11 | 88288592 | 88342736 |
| a0003 | 1/0 | 463 | 18 | 4 | 8 | 0 | 4 | 1 | 0 | CTSC_chr11_88288592_88342736 | CTSC | MGAGP others(458): Show |
chr11 | 88288592 | 88342736 |
| a0004 | 0/0 | 463 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CTSC_chr11_88288592_88342736 | CTSC | MGAGP others(458): Show |
chr11 | 88288592 | 88342736 |
| a0005 | 0/0 | 463 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | MGAGP others(458): Show |
chr11 | 88288592 | 88342736 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1389 | 365 | 79 | 60 | 176 | 11 | 38 | CTSC_chr11_88288592_88342736 | CTSC | ATGGG others(1384): Show |
chr11 | 88288592 | 88342736 | ||
| a0001c0004 | 0/0 | 1389 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | ATGGG others(1384): Show |
chr11 | 88288592 | 88342736 | ||
| a0001c0006 | 0/0 | 1389 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | ATGGG others(1384): Show |
chr11 | 88288592 | 88342736 | ||
| a0002c0002 | 0/0 | 1389 | 47 | 11 | 8 | 25 | 1 | 2 | CTSC_chr11_88288592_88342736 | CTSC | ATGGG others(1384): Show |
chr11 | 88288592 | 88342736 | ||
| a0003c0003 | 1/0 | 1389 | 18 | 4 | 8 | 0 | 4 | 1 | CTSC_chr11_88288592_88342736 | CTSC | ATGGG others(1384): Show |
chr11 | 88288592 | 88342736 | ||
| a0004c0005 | 0/0 | 1389 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | ATGGG others(1384): Show |
chr11 | 88288592 | 88342736 | ||
| a0005c0007 | 0/0 | 1389 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | ATGGG others(1384): Show |
chr11 | 88288592 | 88342736 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1870 | 343 | 72 | 51 | 175 | 8 | 36 | CTSC_chr11_88288592_88342736 | CTSC | ACCGC others(1865): Show |
chr11 | 88288592 | 88342736 |
| a0001c0001t0002 | 0/0 | 1870 | 15 | 4 | 7 | 0 | 3 | 1 | CTSC_chr11_88288592_88342736 | CTSC | ACCGC others(1865): Show |
chr11 | 88288592 | 88342736 |
| a0001c0001t0003 | 0/0 | 1870 | 3 | 0 | 2 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | ACCGC others(1865): Show |
chr11 | 88288592 | 88342736 |
| a0001c0001t0004 | 0/0 | 1870 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | ACCGC others(1865): Show |
chr11 | 88288592 | 88342736 |
| a0001c0001t0005 | 0/0 | 1969 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | ACCGC others(1964): Show |
chr11 | 88288592 | 88342736 |
| a0001c0001t0006 | 0/0 | 1870 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | ACCGC others(1865): Show |
chr11 | 88288592 | 88342736 |
| a0001c0001t0007 | 0/0 | 1870 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | ACCGC others(1865): Show |
chr11 | 88288592 | 88342736 |
| a0001c0004t0001 | 0/0 | 1870 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | ACCGC others(1865): Show |
chr11 | 88288592 | 88342736 |
| a0001c0006t0001 | 0/0 | 1870 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | ACCGC others(1865): Show |
chr11 | 88288592 | 88342736 |
| a0002c0002t0001 | 0/0 | 1870 | 47 | 11 | 8 | 25 | 1 | 2 | CTSC_chr11_88288592_88342736 | CTSC | ACCGC others(1865): Show |
chr11 | 88288592 | 88342736 |
| a0003c0003t0001 | 1/0 | 1870 | 18 | 4 | 8 | 0 | 4 | 1 | CTSC_chr11_88288592_88342736 | CTSC | ACCGC others(1865): Show |
chr11 | 88288592 | 88342736 |
| a0004c0005t0001 | 0/0 | 1870 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | ACCGC others(1865): Show |
chr11 | 88288592 | 88342736 |
| a0005c0007t0001 | 0/0 | 1870 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | ACCGC others(1865): Show |
chr11 | 88288592 | 88342736 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 17 | 0 | 1 | 14 | 0 | 2 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0002 | 0/0 | 15 | 1 | 7 | 6 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0003 | 0/0 | 12 | 0 | 0 | 11 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0005 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0006 | 0/0 | 7 | 1 | 0 | 5 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0015 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0170 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0002g0008 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0003g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0003g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0003g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0006g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0001t0007g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0004t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0001c0006t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0002c0002t0001g0004 | 0/0 | 8 | 0 | 2 | 6 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0002c0002t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0002c0002t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0002c0002t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0002c0002t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0002c0002t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0002c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0002c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0002c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0002c0002t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0002c0002t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0002c0002t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0003c0003t0001g0010 | 1/0 | 5 | 0 | 2 | 0 | 2 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0003c0003t0001g0020 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0003c0003t0001g0050 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0003c0003t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0003c0003t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0003c0003t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0003c0003t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0003c0003t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0003c0003t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0003c0003t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0003c0003t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0004c0005t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| a0005c0007t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0076 | EUR | GBR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | GBR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0104 | EUR | GBR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0046 | EUR | GBR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0213 | EUR | FIN | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0234 | EUR | FIN | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0133 | EUR | FIN | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG00323 | hp2 | a0003 | c0003 | t0001 | g0020 | EUR | FIN | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | CHS | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0107 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0057 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG00738 | hp1 | a0003 | c0003 | t0001 | g0010 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG00741 | hp1 | a0003 | c0003 | t0001 | g0020 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0297 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01109 | hp2 | a0003 | c0003 | t0001 | g0050 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01168 | hp2 | a0003 | c0003 | t0001 | g0020 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01169 | hp1 | a0003 | c0003 | t0001 | g0169 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0295 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01192 | hp2 | a0003 | c0003 | t0001 | g0010 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01243 | hp2 | a0003 | c0003 | t0001 | g0287 | AMR | PUR | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0058 | AMR | CLM | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01346 | hp1 | a0003 | c0003 | t0001 | g0286 | AMR | CLM | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0056 | EUR | IBS | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01516 | hp2 | a0003 | c0003 | t0001 | g0010 | EUR | IBS | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0008 | EUR | IBS | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01517 | hp2 | a0003 | c0003 | t0001 | g0010 | EUR | IBS | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0053 | AFR | ACB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0061 | AFR | ACB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01978 | hp1 | a0002 | c0002 | t0001 | g0108 | AMR | PEL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0114 | AMR | PEL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PEL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0103 | AMR | PEL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | ACB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0292 | AFR | ACB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | KHV | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0113 | EAS | KHV | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | KHV | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | ACB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | CDX | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | CDX | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | ACB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02257 | hp2 | a0001 | c0006 | t0001 | g0093 | AFR | ACB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0112 | AFR | ACB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02273 | hp1 | a0002 | c0002 | t0001 | g0105 | AMR | PEL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0060 | AMR | PEL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | ACB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02717 | hp2 | a0001 | c0001 | t0005 | g0062 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02738 | hp2 | a0004 | c0005 | t0001 | g0236 | SAS | PJL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02809 | hp1 | a0003 | c0003 | t0001 | g0050 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0017 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0293 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02895 | hp2 | a0003 | c0003 | t0001 | g0283 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02897 | hp1 | a0003 | c0003 | t0001 | g0284 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ESN | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | ESN | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | ESN | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | ESN | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ESN | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0111 | AFR | ESN | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG03041 | hp1 | a0003 | c0003 | t0001 | g0119 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0017 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | MSL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | ESN | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0063 | AFR | ESN | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | MSL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | MSL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | MSL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG03453 | hp1 | a0002 | c0002 | t0001 | g0021 | AFR | MSL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | MSL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0054 | AFR | ESN | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0017 | AFR | MSL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0296 | SAS | PJL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | STU | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | STU | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0055 | SAS | PJL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0116 | SAS | BEB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | BEB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG04115 | hp1 | a0003 | c0003 | t0001 | g0285 | SAS | STU | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | STU | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | BEB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | STU | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0245 | SAS | STU | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0117 | SAS | STU | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | STU | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0276 | SAS | STU | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | STU | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | YRI | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | YRI | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | CHB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | CHB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | CHB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18747 | hp2 | a0001 | c0004 | t0001 | g0098 | EAS | CHB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | YRI | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | YRI | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18940 | hp2 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0118 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18953 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18959 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0101 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18986 | hp1 | a0001 | c0001 | t0006 | g0177 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18993 | hp1 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0218 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0106 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19003 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19006 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | LWK | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | LWK | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19043 | hp1 | a0002 | c0002 | t0001 | g0021 | AFR | LWK | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0278 | AFR | LWK | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19055 | hp2 | a0002 | c0002 | t0001 | g0109 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0110 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0102 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19072 | hp2 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19079 | hp1 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19083 | hp2 | a0002 | c0002 | t0001 | g0115 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19086 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA19240 | hp2 | a0001 | c0001 | t0007 | g0298 | AFR | YRI | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ASW | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ASW | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0215 | EUR | TSI | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0059 | EUR | TSI | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0220 | EUR | TSI | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA20805 | hp2 | a0003 | c0003 | t0001 | g0282 | EUR | TSI | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0096 | AMR | CLM | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0021 | AFR | ACB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | ACB | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG03471 | hp1 | a0005 | c0007 | t0001 | g0294 | AFR | MSL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | MSL | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | USA | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0064 | AFR | USA | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | USA | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | USA | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | LWK | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | LWK | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0170 | REF | REF | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| homoSapiens | grch38p0 | a0003 | c0003 | t0001 | g0010 | REF | REF | CTSC_chr11_88288592_88342736 | CTSC | chr11 | 88288592 | 88342736 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:88294041 | T | C | 1 | a0002 | 47 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(44): Show |
missense_variant | MODERATE | c.1357A>G | p.Ile453Val | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 7/7 | 1421/1870 | 1357/1392 | 453/463 | chr11 | 88294041 | |||
| chr11:88294395 | C | G | 1 | a0004 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.1003G>C | p.Glu335Gln | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 7/7 | 1067/1870 | 1003/1392 | 335/463 | chr11 | 88294395 | |||
| chr11:88312415 | A | G | 4 | a0001 a0002 a0004 others(1): Show |
415 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(412): Show |
missense_variant | MODERATE | c.458T>C | p.Ile153Thr | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/7 | 522/1870 | 458/1392 | 153/463 | chr11 | 88312415 | |||
| chr11:88337611 | G | A | 1 | a0005 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.62C>T | p.Ala21Val | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/7 | 126/1870 | 62/1392 | 21/463 | chr11 | 88337611 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:88294225 | A | C | 1 | a0002c0002 | 47 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(44): Show |
synonymous_variant | LOW | c.1173T>G | p.Thr391Thr | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 7/7 | 1237/1870 | 1173/1392 | 391/463 | chr11 | 88294225 | |||
| chr11:88296197 | G | A | 1 | a0001c0006 | 1 | HG02257.hp2 | synonymous_variant | LOW | c.825C>T | p.Thr275Thr | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 6/7 | 889/1870 | 825/1392 | 275/463 | chr11 | 88296197 | |||
| chr11:88312429 | A | G | 1 | a0001c0004 | 1 | NA18747.hp2 | synonymous_variant | LOW | c.444T>C | p.Asn148Asn | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/7 | 508/1870 | 444/1392 | 148/463 | chr11 | 88312429 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:88293751 | T | G | 1 | a0001c0001t0006 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*255A>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 7/7 | 255 | chr11 | 88293751 | ||||||
| chr11:88293785 | T | C | 1 | a0001c0001t0005 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*221A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 7/7 | 221 | chr11 | 88293785 | ||||||
| chr11:88293814 | T | TAGAAAAA others(92): Show |
1 | a0001c0001t0005 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*191_*192insTTTTTT others(93): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 7/7 | 191 | chr11 | 88293814 | ||||||
| chr11:88337690 | A | G | 3 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0007 |
17 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
5_prime_UTR_variant | MODIFIER | c.-18T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/7 | 18 | chr11 | 88337690 | ||||||
| chr11:88337707 | C | G | 1 | a0001c0001t0004 | 1 | HG01884.hp1 | 5_prime_UTR_variant | MODIFIER | c.-35G>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/7 | 35 | chr11 | 88337707 | ||||||
| chr11:88337717 | G | C | 1 | a0001c0001t0003 | 3 | HG01081.hp2 HG01192.hp1 HG03654.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-45C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/7 | chr11 | 88337717 | |||||||
| chr11:88337726 | G | A | 1 | a0001c0001t0007 | 1 | NA19240.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-54C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/7 | chr11 | 88337726 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:88294672 | T | G | 4 | a0001c0001t0001g0014 a0001c0001t0001g0048 a0001c0001t0001g0266 others(1): Show |
8 | NA18943.hp1 NA18944.hp1 NA18947.hp1 others(5): Show |
intron_variant | MODIFIER | c.890-164A>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 6/6 | chr11 | 88294672 | |||||||
| chr11:88294811 | G | A | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | NA18612.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.890-303C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 6/6 | chr11 | 88294811 | |||||||
| chr11:88295288 | A | G | 2 | a0001c0001t0001g0256 a0001c0001t0001g0257 |
2 | HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.890-780T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 6/6 | chr11 | 88295288 | |||||||
| chr11:88295291 | A | C | 3 | a0002c0002t0001g0021 a0002c0002t0001g0292 a0002c0002t0001g0293 |
5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.890-783T>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 6/6 | chr11 | 88295291 | |||||||
| chr11:88295301 | T | C | 1 | a0001c0001t0001g0133 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.890-793A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 6/6 | chr11 | 88295301 | |||||||
| chr11:88295325 | T | C | 1 | a0001c0001t0001g0258 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.889+808A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 6/6 | chr11 | 88295325 | |||||||
| chr11:88295358 | G | T | 129 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0011 others(126): Show |
181 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.889+775C>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 6/6 | chr11 | 88295358 | |||||||
| chr11:88295424 | G | C | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0258 |
3 | HG01243.hp1 HG02451.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.889+709C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 6/6 | chr11 | 88295424 | |||||||
| chr11:88295672 | T | C | 185 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0011 others(182): Show |
258 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.889+461A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 6/6 | chr11 | 88295672 | |||||||
| chr11:88295673 | G | A | 1 | a0005c0007t0001g0294 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.889+460C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 6/6 | chr11 | 88295673 | |||||||
| chr11:88295767 | G | C | 2 | a0002c0002t0001g0116 a0002c0002t0001g0117 |
2 | HG03831.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.889+366C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 6/6 | chr11 | 88295767 | |||||||
| chr11:88295936 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.889+197A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 6/6 | chr11 | 88295936 | |||||||
| chr11:88296027 | T | C | 2 | a0001c0001t0001g0052 a0001c0001t0001g0066 |
3 | HG02818.hp2 HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.889+106A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 6/6 | chr11 | 88296027 | |||||||
| chr11:88296097 | A | C | 3 | a0001c0001t0001g0175 a0001c0001t0001g0183 a0001c0001t0001g0192 |
3 | HG00673.hp2 HG02027.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.889+36T>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 6/6 | chr11 | 88296097 | |||||||
| chr11:88296319 | A | C | 3 | a0002c0002t0001g0021 a0002c0002t0001g0292 a0002c0002t0001g0293 |
5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.758-55T>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88296319 | |||||||
| chr11:88296417 | T | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0011 others(126): Show |
181 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.758-153A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88296417 | |||||||
| chr11:88296449 | T | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0011 others(126): Show |
181 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.758-185A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88296449 | |||||||
| chr11:88296725 | T | A | 101 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(98): Show |
157 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.758-461A>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88296725 | |||||||
| chr11:88296825 | T | C | 36 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0038 others(33): Show |
63 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.758-561A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88296825 | |||||||
| chr11:88296833 | A | G | 34 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0038 others(31): Show |
60 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.758-569T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88296833 | |||||||
| chr11:88296989 | A | T | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(282): Show |
414 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(411): Show |
intron_variant | MODIFIER | c.758-725T>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88296989 | |||||||
| chr11:88297041 | C | T | 1 | a0001c0001t0007g0298 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.758-777G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88297041 | |||||||
| chr11:88297168 | A | T | 1 | a0001c0001t0001g0066 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.758-904T>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88297168 | |||||||
| chr11:88297198 | C | T | 2 | a0001c0001t0001g0235 a0001c0001t0001g0253 |
2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.758-934G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88297198 | |||||||
| chr11:88297289 | C | T | 286 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(283): Show |
415 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(412): Show |
intron_variant | MODIFIER | c.758-1025G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88297289 | |||||||
| chr11:88297305 | A | G | 1 | a0001c0001t0001g0120 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.758-1041T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88297305 | |||||||
| chr11:88297521 | A | G | 98 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(95): Show |
141 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.758-1257T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88297521 | |||||||
| chr11:88297587 | T | C | 1 | a0001c0001t0001g0083 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.758-1323A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88297587 | |||||||
| chr11:88297617 | G | A | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(125): Show |
205 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.758-1353C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88297617 | |||||||
| chr11:88297731 | G | C | 1 | a0001c0001t0001g0189 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.758-1467C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88297731 | |||||||
| chr11:88297763 | G | A | 93 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(90): Show |
134 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.758-1499C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88297763 | |||||||
| chr11:88298044 | G | C | 1 | a0001c0001t0001g0082 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.758-1780C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88298044 | |||||||
| chr11:88298050 | T | C | 45 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0015 others(42): Show |
80 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.758-1786A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88298050 | |||||||
| chr11:88298060 | G | A | 3 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 |
3 | HG02647.hp2 HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.758-1796C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88298060 | |||||||
| chr11:88298064 | C | T | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(229): Show |
345 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(342): Show |
intron_variant | MODIFIER | c.758-1800G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88298064 | |||||||
| chr11:88298124 | T | C | 2 | a0001c0001t0001g0165 a0001c0001t0001g0273 |
2 | HG01993.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.758-1860A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88298124 | |||||||
| chr11:88298263 | A | G | 3 | a0002c0002t0001g0021 a0002c0002t0001g0292 a0002c0002t0001g0293 |
5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.758-1999T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88298263 | |||||||
| chr11:88298413 | A | C | 1 | a0001c0001t0001g0120 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.757+2117T>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88298413 | |||||||
| chr11:88298462 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.757+2068G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88298462 | |||||||
| chr11:88298548 | G | A | 3 | a0002c0002t0001g0021 a0002c0002t0001g0292 a0002c0002t0001g0293 |
5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.757+1982C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88298548 | |||||||
| chr11:88298595 | T | C | 2 | a0001c0001t0001g0139 a0001c0001t0001g0168 |
2 | HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.757+1935A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88298595 | |||||||
| chr11:88298625 | A | G | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG01243.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.757+1905T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88298625 | |||||||
| chr11:88298633 | A | G | 1 | a0001c0001t0001g0210 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.757+1897T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88298633 | |||||||
| chr11:88298697 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.757+1833G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88298697 | |||||||
| chr11:88298713 | A | T | 1 | a0003c0003t0001g0119 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.757+1817T>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88298713 | |||||||
| chr11:88298794 | G | C | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG01243.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.757+1736C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88298794 | |||||||
| chr11:88298893 | A | C | 1 | a0001c0001t0001g0226 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.757+1637T>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88298893 | |||||||
| chr11:88298958 | G | A | 2 | a0001c0001t0001g0195 a0001c0001t0001g0196 |
2 | HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.757+1572C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88298958 | |||||||
| chr11:88299056 | G | A | 141 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(138): Show |
200 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.757+1474C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88299056 | |||||||
| chr11:88299110 | T | A | 1 | a0001c0001t0001g0182 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.757+1420A>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88299110 | |||||||
| chr11:88299153 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.757+1377G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88299153 | |||||||
| chr11:88299251 | A | G | 39 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0016 others(36): Show |
71 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.757+1279T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88299251 | |||||||
| chr11:88299278 | A | G | 1 | a0002c0002t0001g0112 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.757+1252T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88299278 | |||||||
| chr11:88299393 | T | G | 1 | a0001c0001t0001g0082 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.757+1137A>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88299393 | |||||||
| chr11:88299394 | A | T | 1 | a0001c0001t0001g0082 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.757+1136T>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88299394 | |||||||
| chr11:88299467 | C | T | 1 | a0001c0001t0001g0281 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.757+1063G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88299467 | |||||||
| chr11:88299531 | G | T | 1 | a0001c0001t0001g0203 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.757+999C>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88299531 | |||||||
| chr11:88299683 | C | T | 1 | a0001c0001t0001g0229 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.757+847G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88299683 | |||||||
| chr11:88299806 | G | C | 1 | a0001c0001t0001g0165 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.757+724C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88299806 | |||||||
| chr11:88299901 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.757+629G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88299901 | |||||||
| chr11:88299966 | G | C | 1 | a0001c0001t0001g0276 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.757+564C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88299966 | |||||||
| chr11:88300344 | A | T | 64 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(61): Show |
86 | HG00280.hp1 HG00423.hp1 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.757+186T>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88300344 | |||||||
| chr11:88300353 | T | C | 287 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(284): Show |
416 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(413): Show |
intron_variant | MODIFIER | c.757+177A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88300353 | |||||||
| chr11:88300431 | C | A | 1 | a0002c0002t0001g0278 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.757+99G>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88300431 | |||||||
| chr11:88300440 | T | C | 1 | a0001c0001t0001g0224 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.757+90A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88300440 | |||||||
| chr11:88300493 | A | G | 286 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(283): Show |
415 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(412): Show |
intron_variant | MODIFIER | c.757+37T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88300493 | |||||||
| chr11:88300506 | A | G | 1 | a0001c0001t0001g0034 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.757+24T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 5/6 | chr11 | 88300506 | |||||||
| chr11:88300836 | G | A | 4 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0005g0062 others(1): Show |
4 | HG02486.hp1 HG02717.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.642-191C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88300836 | |||||||
| chr11:88300839 | GTTTC | G | 51 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(48): Show |
66 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.642-198_642-195del others(4): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88300839 | |||||||
| chr11:88300924 | T | G | 3 | a0002c0002t0001g0021 a0002c0002t0001g0292 a0002c0002t0001g0293 |
5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.642-279A>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88300924 | |||||||
| chr11:88300995 | A | G | 3 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 |
3 | HG01243.hp1 HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.642-350T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88300995 | |||||||
| chr11:88301377 | G | A | 1 | a0001c0001t0001g0046 | 2 | HG00140.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.642-732C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88301377 | |||||||
| chr11:88301461 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.642-816C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88301461 | |||||||
| chr11:88301712 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.642-1067G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88301712 | |||||||
| chr11:88301742 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.642-1097G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88301742 | |||||||
| chr11:88301799 | AAC | A | 39 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0016 others(36): Show |
71 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.642-1156_642-1155d others(4): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88301799 | |||||||
| chr11:88301804 | ACG | A | 10 | a0001c0001t0001g0052 a0001c0001t0001g0124 a0001c0001t0001g0125 others(7): Show |
11 | HG01891.hp1 HG02280.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.642-1161_642-1160d others(4): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88301804 | |||||||
| chr11:88301804 | ACGCG | A | 4 | a0001c0001t0001g0030 a0001c0001t0001g0144 a0001c0001t0001g0150 others(1): Show |
5 | HG00639.hp1 HG01069.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.642-1163_642-1160d others(6): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88301804 | |||||||
| chr11:88301806 | G | GCA | 4 | a0001c0001t0001g0019 a0001c0001t0001g0045 a0001c0001t0001g0238 others(1): Show |
7 | HG01884.hp2 HG01952.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.642-1162_642-1161i others(4): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88301806 | |||||||
| chr11:88301806 | GCGCGCA | G | 47 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(44): Show |
61 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.642-1167_642-1162d others(8): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88301806 | |||||||
| chr11:88301807 | C | T | 2 | a0003c0003t0001g0283 a0003c0003t0001g0284 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.642-1162G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88301807 | |||||||
| chr11:88301808 | G | A | 7 | a0001c0001t0001g0019 a0001c0001t0001g0045 a0001c0001t0001g0238 others(4): Show |
12 | HG01884.hp2 HG01952.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.642-1163C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88301808 | |||||||
| chr11:88301808 | G | GCA | 92 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(89): Show |
126 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.642-1164_642-1163i others(4): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88301808 | |||||||
| chr11:88301808 | G | GCACA | 20 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0033 others(17): Show |
23 | HG00323.hp1 HG00597.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.642-1164_642-1163i others(6): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88301808 | |||||||
| chr11:88301808 | G | GCACACAC others(1): Show |
4 | a0001c0001t0001g0009 a0001c0001t0001g0181 a0001c0001t0001g0188 others(1): Show |
7 | NA18953.hp2 NA18955.hp2 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.642-1164_642-1163i others(10): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88301808 | |||||||
| chr11:88301808 | G | GCACACAC others(3): Show |
7 | a0001c0001t0001g0009 a0001c0001t0001g0180 a0001c0001t0001g0182 others(4): Show |
8 | HG02602.hp2 NA18948.hp2 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.642-1164_642-1163i others(12): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88301808 | |||||||
| chr11:88301808 | G | GCACACAC others(5): Show |
1 | a0001c0001t0001g0212 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.642-1164_642-1163i others(14): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88301808 | |||||||
| chr11:88301810 | G | A | 221 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(218): Show |
327 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.642-1165C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88301810 | |||||||
| chr11:88301810 | G | GCA | 3 | a0001c0001t0001g0001 a0001c0001t0001g0042 a0001c0001t0001g0051 |
3 | HG00423.hp2 NA18967.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.642-1167_642-1166d others(4): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88301810 | |||||||
| chr11:88301835 | C | CACAG | 3 | a0002c0002t0001g0021 a0002c0002t0001g0292 a0002c0002t0001g0293 |
5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.642-1191_642-1190i others(6): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88301835 | |||||||
| chr11:88301835 | C | G | 45 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0015 others(42): Show |
80 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.642-1190G>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88301835 | |||||||
| chr11:88301837 | G | C | 57 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(54): Show |
75 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.642-1192C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88301837 | |||||||
| chr11:88301839 | G | C | 49 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(46): Show |
64 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.642-1194C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88301839 | |||||||
| chr11:88301861 | C | T | 143 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(140): Show |
202 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.642-1216G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88301861 | |||||||
| chr11:88302203 | G | A | 1 | a0002c0002t0001g0278 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.642-1558C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88302203 | |||||||
| chr11:88302418 | T | C | 8 | a0001c0001t0002g0008 a0001c0001t0002g0055 a0001c0001t0002g0056 others(5): Show |
12 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.642-1773A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88302418 | |||||||
| chr11:88302424 | C | T | 1 | a0001c0001t0002g0059 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.642-1779G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88302424 | |||||||
| chr11:88302583 | A | G | 2 | a0001c0001t0001g0033 a0001c0001t0001g0194 |
3 | HG02135.hp1 HG02165.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.642-1938T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88302583 | |||||||
| chr11:88302585 | C | T | 4 | a0002c0002t0001g0027 a0002c0002t0001g0101 a0002c0002t0001g0102 others(1): Show |
5 | NA18940.hp2 NA18968.hp2 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.642-1940G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88302585 | |||||||
| chr11:88302620 | C | T | 44 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0015 others(41): Show |
79 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.642-1975G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88302620 | |||||||
| chr11:88302625 | CA | C | 42 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(39): Show |
57 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.642-1981delT | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88302625 | |||||||
| chr11:88302625 | CAA | C | 8 | a0001c0001t0001g0137 a0001c0001t0001g0273 a0001c0001t0002g0008 others(5): Show |
12 | HG01069.hp2 HG01071.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.642-1982_642-1981d others(4): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88302625 | |||||||
| chr11:88302625 | CAAA | C | 6 | a0001c0001t0001g0052 a0001c0001t0002g0061 a0002c0002t0001g0100 others(3): Show |
7 | HG00733.hp2 HG01891.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.642-1983_642-1981d others(5): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88302625 | |||||||
| chr11:88302625 | CAAAA | C | 45 | a0001c0001t0001g0039 a0001c0001t0001g0042 a0001c0001t0001g0043 others(42): Show |
61 | HG00140.hp1 HG00642.hp1 HG01109.hp1 others(58): Show |
intron_variant | MODIFIER | c.642-1984_642-1981d others(6): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88302625 | |||||||
| chr11:88302625 | CAAAAA | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
259 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.642-1985_642-1981d others(7): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88302625 | |||||||
| chr11:88302625 | CAAAAAAA others(4): Show |
C | 6 | a0001c0001t0001g0037 a0001c0001t0001g0133 a0001c0001t0001g0221 others(3): Show |
7 | HG00280.hp2 HG00323.hp1 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.642-1991_642-1981d others(13): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88302625 | |||||||
| chr11:88302816 | T | C | 1 | a0001c0001t0001g0275 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.642-2171A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88302816 | |||||||
| chr11:88302914 | C | T | 1 | a0001c0001t0001g0094 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.642-2269G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88302914 | |||||||
| chr11:88302929 | T | C | 1 | a0001c0001t0001g0239 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.642-2284A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88302929 | |||||||
| chr11:88303041 | A | G | 1 | a0001c0001t0001g0094 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.642-2396T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88303041 | |||||||
| chr11:88303326 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.642-2681G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88303326 | |||||||
| chr11:88303329 | C | T | 1 | a0001c0001t0001g0052 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.642-2684G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88303329 | |||||||
| chr11:88303333 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.642-2688G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88303333 | |||||||
| chr11:88303352 | T | C | 44 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0015 others(41): Show |
79 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.642-2707A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88303352 | |||||||
| chr11:88303388 | G | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
198 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.642-2743C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88303388 | |||||||
| chr11:88303421 | C | T | 72 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(69): Show |
109 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.642-2776G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88303421 | |||||||
| chr11:88303641 | T | G | 29 | a0001c0001t0001g0123 a0002c0002t0001g0004 a0002c0002t0001g0017 others(26): Show |
42 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.642-2996A>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88303641 | |||||||
| chr11:88303671 | T | C | 187 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(184): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.642-3026A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88303671 | |||||||
| chr11:88303903 | C | T | 1 | a0001c0001t0001g0052 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.642-3258G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88303903 | |||||||
| chr11:88303914 | C | CAG | 1 | a0001c0001t0001g0019 | 3 | HG03130.hp1 HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.642-3271_642-3270d others(4): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88303914 | |||||||
| chr11:88303962 | G | A | 4 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 others(1): Show |
4 | HG02647.hp2 HG02896.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.642-3317C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88303962 | |||||||
| chr11:88303980 | G | A | 3 | a0002c0002t0001g0021 a0002c0002t0001g0292 a0002c0002t0001g0293 |
5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.642-3335C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88303980 | |||||||
| chr11:88304054 | G | C | 2 | a0001c0001t0001g0246 a0001c0001t0001g0248 |
2 | HG02055.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.642-3409C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88304054 | |||||||
| chr11:88304296 | G | A | 1 | a0002c0002t0001g0293 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.642-3651C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88304296 | |||||||
| chr11:88304400 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.642-3755G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88304400 | |||||||
| chr11:88304733 | C | A | 4 | a0001c0001t0001g0028 a0001c0001t0001g0132 a0001c0001t0001g0135 others(1): Show |
5 | HG02922.hp2 HG03130.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.642-4088G>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88304733 | |||||||
| chr11:88304747 | G | A | 1 | a0001c0001t0001g0256 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.642-4102C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88304747 | |||||||
| chr11:88304833 | C | A | 8 | a0001c0001t0002g0008 a0001c0001t0002g0055 a0001c0001t0002g0056 others(5): Show |
12 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.642-4188G>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88304833 | |||||||
| chr11:88305054 | C | T | 2 | a0001c0001t0001g0156 a0001c0001t0001g0167 |
2 | HG01358.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.641+4109G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88305054 | |||||||
| chr11:88305059 | C | G | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG01243.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.641+4104G>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88305059 | |||||||
| chr11:88305095 | C | CA | 182 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(179): Show |
263 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.641+4067dupT | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88305095 | |||||||
| chr11:88305095 | C | CAA | 44 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0038 others(41): Show |
74 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.641+4066_641+4067d others(4): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88305095 | |||||||
| chr11:88305141 | A | G | 1 | a0001c0001t0001g0138 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.641+4022T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88305141 | |||||||
| chr11:88305476 | C | G | 5 | a0001c0001t0001g0019 a0001c0001t0001g0045 a0001c0001t0001g0242 others(2): Show |
8 | HG01884.hp2 HG02451.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.641+3687G>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88305476 | |||||||
| chr11:88305583 | C | T | 141 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(138): Show |
200 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.641+3580G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88305583 | |||||||
| chr11:88305608 | A | G | 8 | a0001c0001t0002g0008 a0001c0001t0002g0055 a0001c0001t0002g0056 others(5): Show |
12 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.641+3555T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88305608 | |||||||
| chr11:88305621 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.641+3542G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88305621 | |||||||
| chr11:88305655 | A | T | 230 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(227): Show |
343 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(340): Show |
intron_variant | MODIFIER | c.641+3508T>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88305655 | |||||||
| chr11:88305871 | C | G | 1 | a0001c0001t0001g0066 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.641+3292G>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88305871 | |||||||
| chr11:88305874 | G | A | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG01243.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.641+3289C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88305874 | |||||||
| chr11:88305882 | A | G | 1 | a0001c0001t0007g0298 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.641+3281T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88305882 | |||||||
| chr11:88305895 | G | T | 3 | a0002c0002t0001g0021 a0002c0002t0001g0292 a0002c0002t0001g0293 |
5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.641+3268C>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88305895 | |||||||
| chr11:88305980 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.641+3183C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88305980 | |||||||
| chr11:88306121 | T | C | 230 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(227): Show |
343 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(340): Show |
intron_variant | MODIFIER | c.641+3042A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88306121 | |||||||
| chr11:88306156 | C | A | 29 | a0001c0001t0001g0123 a0002c0002t0001g0004 a0002c0002t0001g0017 others(26): Show |
42 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.641+3007G>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88306156 | |||||||
| chr11:88306197 | T | C | 1 | a0001c0001t0001g0046 | 2 | HG00140.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.641+2966A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88306197 | |||||||
| chr11:88306276 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.641+2887A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88306276 | |||||||
| chr11:88306314 | G | T | 1 | a0001c0001t0003g0296 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.641+2849C>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88306314 | |||||||
| chr11:88306404 | C | T | 3 | a0002c0002t0001g0021 a0002c0002t0001g0292 a0002c0002t0001g0293 |
5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.641+2759G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88306404 | |||||||
| chr11:88306429 | C | A | 1 | a0001c0001t0002g0057 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.641+2734G>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88306429 | |||||||
| chr11:88306503 | G | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
198 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.641+2660C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88306503 | |||||||
| chr11:88306519 | C | T | 1 | a0001c0001t0001g0152 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.641+2644G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88306519 | |||||||
| chr11:88306522 | C | G | 2 | a0001c0001t0001g0077 a0001c0001t0001g0079 |
2 | HG03491.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.641+2641G>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88306522 | |||||||
| chr11:88306577 | T | C | 286 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(283): Show |
415 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(412): Show |
intron_variant | MODIFIER | c.641+2586A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88306577 | |||||||
| chr11:88306669 | A | T | 1 | a0001c0001t0001g0052 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.641+2494T>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88306669 | |||||||
| chr11:88306936 | AC | A | 7 | a0001c0001t0001g0175 a0001c0001t0001g0183 a0001c0001t0001g0184 others(4): Show |
7 | HG00423.hp1 HG00609.hp2 HG00673.hp2 others(4): Show |
intron_variant | MODIFIER | c.641+2226delG | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88306936 | |||||||
| chr11:88306977 | C | A | 44 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0015 others(41): Show |
79 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.641+2186G>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88306977 | |||||||
| chr11:88307028 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.641+2135G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88307028 | |||||||
| chr11:88307158 | G | A | 46 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(43): Show |
61 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.641+2005C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88307158 | |||||||
| chr11:88307173 | T | C | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG01243.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.641+1990A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88307173 | |||||||
| chr11:88307175 | TTC | T | 29 | a0001c0001t0001g0123 a0002c0002t0001g0004 a0002c0002t0001g0017 others(26): Show |
42 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.641+1986_641+1987d others(4): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88307175 | |||||||
| chr11:88307230 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.641+1933A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88307230 | |||||||
| chr11:88307255 | C | A | 1 | a0002c0002t0001g0109 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.641+1908G>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88307255 | |||||||
| chr11:88307331 | C | T | 29 | a0001c0001t0001g0123 a0002c0002t0001g0004 a0002c0002t0001g0017 others(26): Show |
42 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.641+1832G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88307331 | |||||||
| chr11:88307357 | A | G | 8 | a0001c0001t0002g0008 a0001c0001t0002g0055 a0001c0001t0002g0056 others(5): Show |
12 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.641+1806T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88307357 | |||||||
| chr11:88307407 | T | C | 2 | a0001c0001t0003g0295 a0001c0001t0003g0297 |
2 | HG01081.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.641+1756A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88307407 | |||||||
| chr11:88307489 | C | A | 3 | a0002c0002t0001g0021 a0002c0002t0001g0292 a0002c0002t0001g0293 |
5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.641+1674G>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88307489 | |||||||
| chr11:88307556 | C | CT | 45 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(42): Show |
60 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.641+1606dupA | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88307556 | |||||||
| chr11:88307556 | C | CTT | 12 | a0001c0001t0001g0138 a0001c0001t0001g0145 a0001c0001t0001g0146 others(9): Show |
14 | HG00733.hp1 HG01192.hp1 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.641+1605_641+1606d others(4): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88307556 | |||||||
| chr11:88307556 | CT | C | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(202): Show |
312 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(309): Show |
intron_variant | MODIFIER | c.641+1606delA | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88307556 | |||||||
| chr11:88307845 | C | T | 4 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 others(1): Show |
4 | HG02647.hp2 HG02896.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.641+1318G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88307845 | |||||||
| chr11:88307908 | T | C | 1 | a0003c0003t0001g0286 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.641+1255A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88307908 | |||||||
| chr11:88307929 | G | A | 3 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 |
3 | HG02647.hp2 HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.641+1234C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88307929 | |||||||
| chr11:88307965 | T | G | 52 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(49): Show |
68 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.641+1198A>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88307965 | |||||||
| chr11:88307992 | G | C | 2 | a0001c0001t0001g0173 a0001c0001t0001g0176 |
2 | NA18612.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.641+1171C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88307992 | |||||||
| chr11:88308035 | A | T | 2 | a0001c0001t0005g0062 a0001c0001t0007g0298 |
2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.641+1128T>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88308035 | |||||||
| chr11:88308084 | G | A | 2 | a0001c0001t0005g0062 a0001c0001t0007g0298 |
2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.641+1079C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88308084 | |||||||
| chr11:88308347 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.641+816C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88308347 | |||||||
| chr11:88308433 | G | A | 29 | a0001c0001t0001g0123 a0002c0002t0001g0004 a0002c0002t0001g0017 others(26): Show |
42 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.641+730C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88308433 | |||||||
| chr11:88308472 | A | ATTATT | 29 | a0001c0001t0001g0123 a0002c0002t0001g0004 a0002c0002t0001g0017 others(26): Show |
42 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.641+686_641+690dup others(5): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88308472 | |||||||
| chr11:88308472 | ATTATT | A | 144 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(141): Show |
205 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.641+686_641+690del others(5): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88308472 | |||||||
| chr11:88308545 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.641+618G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88308545 | |||||||
| chr11:88308568 | A | G | 29 | a0001c0001t0001g0123 a0002c0002t0001g0004 a0002c0002t0001g0017 others(26): Show |
42 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.641+595T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88308568 | |||||||
| chr11:88308769 | C | T | 34 | a0001c0001t0001g0066 a0001c0001t0001g0123 a0001c0001t0002g0054 others(31): Show |
49 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.641+394G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88308769 | |||||||
| chr11:88308810 | C | A | 32 | a0001c0001t0001g0123 a0002c0002t0001g0004 a0002c0002t0001g0017 others(29): Show |
47 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.641+353G>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88308810 | |||||||
| chr11:88309102 | G | A | 2 | a0001c0001t0001g0156 a0001c0001t0001g0167 |
2 | HG01358.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.641+61C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88309102 | |||||||
| chr11:88309129 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.641+34T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 4/6 | chr11 | 88309129 | |||||||
| chr11:88309406 | G | C | 1 | a0001c0001t0001g0268 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.486-88C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88309406 | |||||||
| chr11:88309461 | A | G | 1 | a0001c0001t0001g0176 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.486-143T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88309461 | |||||||
| chr11:88309606 | A | G | 2 | a0001c0001t0001g0165 a0001c0001t0001g0273 |
2 | HG01993.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.486-288T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88309606 | |||||||
| chr11:88309680 | T | C | 38 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0016 others(35): Show |
69 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.486-362A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88309680 | |||||||
| chr11:88309774 | T | C | 1 | a0001c0001t0001g0220 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.486-456A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88309774 | |||||||
| chr11:88309809 | TGC | T | 19 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0047 others(16): Show |
26 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.486-493_486-492del others(2): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88309809 | |||||||
| chr11:88309810 | GCGCGCAC others(3): Show |
G | 3 | a0002c0002t0001g0021 a0002c0002t0001g0292 a0002c0002t0001g0293 |
5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.486-502_486-493del others(10): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88309810 | |||||||
| chr11:88309812 | G | GCA | 11 | a0001c0001t0001g0048 a0001c0001t0001g0051 a0001c0001t0001g0134 others(8): Show |
13 | HG02486.hp1 HG02572.hp2 HG02602.hp2 others(10): Show |
intron_variant | MODIFIER | c.486-495_486-494ins others(2): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88309812 | |||||||
| chr11:88309812 | G | GCACA | 7 | a0001c0001t0001g0034 a0001c0001t0001g0172 a0001c0001t0001g0186 others(4): Show |
8 | HG02602.hp1 HG02698.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.486-495_486-494ins others(4): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88309812 | |||||||
| chr11:88309812 | GCGCA | G | 57 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0019 others(54): Show |
87 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.486-498_486-495del others(4): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88309812 | |||||||
| chr11:88309812 | GCGCACA | G | 27 | a0001c0001t0001g0171 a0001c0001t0001g0217 a0001c0001t0001g0258 others(24): Show |
39 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.486-500_486-495del others(6): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88309812 | |||||||
| chr11:88309812 | GCGCACAC others(1): Show |
G | 3 | a0002c0002t0001g0027 a0002c0002t0001g0099 a0002c0002t0001g0101 |
4 | NA18940.hp2 NA18968.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.486-502_486-495del others(8): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88309812 | |||||||
| chr11:88309812 | GCGCACAC others(5): Show |
G | 3 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 |
3 | HG02647.hp2 HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.486-506_486-495del others(12): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88309812 | |||||||
| chr11:88309814 | G | A | 73 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(70): Show |
100 | HG00280.hp1 HG00544.hp1 HG00673.hp2 others(97): Show |
intron_variant | MODIFIER | c.486-496C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88309814 | |||||||
| chr11:88309814 | G | GCA | 3 | a0001c0001t0001g0007 a0001c0001t0001g0032 a0003c0003t0001g0050 |
4 | HG00597.hp1 HG02809.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.486-498_486-497dup others(2): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88309814 | |||||||
| chr11:88309814 | GCA | G | 6 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0138 others(3): Show |
6 | HG01243.hp1 HG02451.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.486-498_486-497del others(2): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88309814 | |||||||
| chr11:88309814 | GCACA | G | 9 | a0001c0001t0001g0015 a0001c0001t0001g0025 a0001c0001t0001g0082 others(6): Show |
12 | HG01074.hp2 HG01978.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.486-500_486-497del others(4): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88309814 | |||||||
| chr11:88309814 | GCACACA | G | 38 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0016 others(35): Show |
69 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.486-502_486-497del others(6): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88309814 | |||||||
| chr11:88309818 | A | G | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0005g0062 others(1): Show |
4 | HG01243.hp1 HG02451.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.486-500T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88309818 | |||||||
| chr11:88309824 | A | G | 1 | a0001c0001t0002g0054 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.486-506T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88309824 | |||||||
| chr11:88310048 | A | T | 1 | a0001c0001t0001g0052 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.486-730T>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88310048 | |||||||
| chr11:88310180 | C | CT | 161 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(158): Show |
233 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.486-863dupA | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88310180 | |||||||
| chr11:88310180 | C | CTT | 6 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 others(3): Show |
6 | HG02074.hp2 HG02148.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.486-864_486-863dup others(2): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88310180 | |||||||
| chr11:88310180 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.486-862G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88310180 | |||||||
| chr11:88310180 | CT | C | 86 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(83): Show |
136 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.486-863delA | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88310180 | |||||||
| chr11:88310180 | CTT | C | 9 | a0001c0001t0001g0068 a0001c0001t0001g0094 a0001c0001t0001g0137 others(6): Show |
9 | HG01255.hp1 HG01975.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.486-864_486-863del others(2): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88310180 | |||||||
| chr11:88310340 | T | C | 3 | a0002c0002t0001g0021 a0002c0002t0001g0292 a0002c0002t0001g0293 |
5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.486-1022A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88310340 | |||||||
| chr11:88310449 | ACTAT | A | 8 | a0001c0001t0002g0008 a0001c0001t0002g0055 a0001c0001t0002g0056 others(5): Show |
12 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.486-1135_486-1132d others(6): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88310449 | |||||||
| chr11:88310453 | T | C | 43 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0015 others(40): Show |
78 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.486-1135A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88310453 | |||||||
| chr11:88310512 | T | A | 1 | a0001c0001t0001g0037 | 2 | HG03688.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.486-1194A>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88310512 | |||||||
| chr11:88310556 | T | C | 55 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(52): Show |
70 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.486-1238A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88310556 | |||||||
| chr11:88310557 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.486-1239C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88310557 | |||||||
| chr11:88310579 | G | A | 1 | a0001c0001t0001g0220 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.486-1261C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88310579 | |||||||
| chr11:88310704 | T | C | 1 | a0001c0001t0001g0201 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.486-1386A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88310704 | |||||||
| chr11:88310727 | TATC | T | 3 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 |
3 | HG02647.hp2 HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.486-1412_486-1410d others(5): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88310727 | |||||||
| chr11:88310898 | G | GCT | 286 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(283): Show |
415 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(412): Show |
intron_variant | MODIFIER | c.485+1488_485+1489d others(4): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88310898 | |||||||
| chr11:88310913 | T | C | 8 | a0001c0001t0002g0008 a0001c0001t0002g0055 a0001c0001t0002g0056 others(5): Show |
12 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.485+1475A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88310913 | |||||||
| chr11:88311183 | A | T | 3 | a0002c0002t0001g0021 a0002c0002t0001g0292 a0002c0002t0001g0293 |
5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+1205T>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88311183 | |||||||
| chr11:88311276 | C | A | 55 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(52): Show |
70 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.485+1112G>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88311276 | |||||||
| chr11:88311336 | G | C | 3 | a0002c0002t0001g0021 a0002c0002t0001g0292 a0002c0002t0001g0293 |
5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+1052C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88311336 | |||||||
| chr11:88311378 | T | A | 3 | a0002c0002t0001g0021 a0002c0002t0001g0292 a0002c0002t0001g0293 |
5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+1010A>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88311378 | |||||||
| chr11:88311418 | C | A | 3 | a0002c0002t0001g0021 a0002c0002t0001g0292 a0002c0002t0001g0293 |
5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.485+970G>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88311418 | |||||||
| chr11:88311445 | C | T | 1 | a0001c0001t0001g0052 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.485+943G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88311445 | |||||||
| chr11:88311598 | T | C | 3 | a0001c0001t0001g0015 a0001c0001t0001g0274 a0001c0001t0001g0275 |
6 | HG01074.hp2 HG02257.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.485+790A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88311598 | |||||||
| chr11:88311720 | T | A | 8 | a0001c0001t0002g0008 a0001c0001t0002g0055 a0001c0001t0002g0056 others(5): Show |
12 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.485+668A>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88311720 | |||||||
| chr11:88311853 | C | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0164 a0001c0001t0001g0270 |
6 | HG00408.hp1 NA18945.hp1 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.485+535G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88311853 | |||||||
| chr11:88311925 | C | T | 2 | a0001c0001t0001g0139 a0001c0001t0001g0168 |
2 | HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.485+463G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88311925 | |||||||
| chr11:88311957 | C | T | 43 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0015 others(40): Show |
78 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.485+431G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88311957 | |||||||
| chr11:88312096 | T | G | 47 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(44): Show |
62 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.485+292A>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88312096 | |||||||
| chr11:88312108 | A | C | 49 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(46): Show |
64 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.485+280T>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88312108 | |||||||
| chr11:88312116 | T | A | 1 | a0001c0001t0001g0081 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.485+272A>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88312116 | |||||||
| chr11:88312268 | C | T | 1 | a0002c0002t0001g0278 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.485+120G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 3/6 | chr11 | 88312268 | |||||||
| chr11:88312647 | C | CT | 286 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(283): Show |
415 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(412): Show |
intron_variant | MODIFIER | c.319-94dupA | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88312647 | |||||||
| chr11:88312726 | T | C | 2 | a0001c0001t0005g0062 a0001c0001t0007g0298 |
2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.319-172A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88312726 | |||||||
| chr11:88312911 | T | C | 6 | a0001c0001t0001g0019 a0001c0001t0001g0045 a0001c0001t0001g0242 others(3): Show |
9 | HG01884.hp2 HG02451.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.319-357A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88312911 | |||||||
| chr11:88312980 | G | T | 284 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(281): Show |
413 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(410): Show |
intron_variant | MODIFIER | c.319-426C>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88312980 | |||||||
| chr11:88313060 | A | C | 5 | a0001c0001t0001g0130 a0001c0001t0001g0223 a0001c0001t0001g0224 others(2): Show |
5 | HG02109.hp1 HG02886.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.319-506T>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88313060 | |||||||
| chr11:88313071 | T | C | 2 | a0001c0001t0001g0216 a0001c0001t0001g0262 |
2 | HG03239.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.319-517A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88313071 | |||||||
| chr11:88313108 | T | C | 286 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(283): Show |
415 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(412): Show |
intron_variant | MODIFIER | c.319-554A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88313108 | |||||||
| chr11:88313109 | G | A | 44 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0015 others(41): Show |
79 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.319-555C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88313109 | |||||||
| chr11:88313222 | A | C | 9 | a0001c0001t0001g0009 a0001c0001t0001g0180 a0001c0001t0001g0181 others(6): Show |
13 | HG02602.hp2 NA18948.hp2 NA18953.hp2 others(10): Show |
intron_variant | MODIFIER | c.319-668T>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88313222 | |||||||
| chr11:88313226 | C | T | 30 | a0001c0001t0001g0123 a0001c0001t0001g0127 a0002c0002t0001g0004 others(27): Show |
43 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.319-672G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88313226 | |||||||
| chr11:88313333 | G | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0174 a0001c0001t0001g0179 others(2): Show |
12 | HG02027.hp2 HG02080.hp2 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.319-779C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88313333 | |||||||
| chr11:88313471 | A | G | 1 | a0001c0001t0001g0138 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.319-917T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88313471 | |||||||
| chr11:88313567 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.319-1013G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88313567 | |||||||
| chr11:88313706 | C | A | 1 | a0001c0001t0001g0189 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.319-1152G>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88313706 | |||||||
| chr11:88313799 | G | GA | 5 | a0001c0001t0001g0085 a0002c0002t0001g0021 a0002c0002t0001g0100 others(2): Show |
7 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.319-1246dupT | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88313799 | |||||||
| chr11:88313960 | C | T | 1 | a0001c0001t0001g0135 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.319-1406G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88313960 | |||||||
| chr11:88313962 | T | A | 2 | a0002c0002t0001g0110 a0002c0002t0001g0115 |
2 | NA19057.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.319-1408A>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88313962 | |||||||
| chr11:88314021 | G | A | 100 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(97): Show |
153 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.319-1467C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88314021 | |||||||
| chr11:88314119 | G | C | 3 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 |
3 | HG02647.hp2 HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.319-1565C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88314119 | |||||||
| chr11:88314198 | C | T | 3 | a0002c0002t0001g0021 a0002c0002t0001g0292 a0002c0002t0001g0293 |
5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.319-1644G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88314198 | |||||||
| chr11:88314556 | C | T | 1 | a0001c0001t0002g0063 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.319-2002G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88314556 | |||||||
| chr11:88314573 | G | A | 1 | a0001c0001t0002g0064 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.319-2019C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88314573 | |||||||
| chr11:88314604 | T | C | 2 | a0001c0001t0001g0066 a0001c0001t0002g0054 |
2 | HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.319-2050A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88314604 | |||||||
| chr11:88314718 | G | A | 1 | a0001c0001t0001g0188 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.319-2164C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88314718 | |||||||
| chr11:88314738 | G | A | 1 | a0001c0001t0001g0086 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.319-2184C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88314738 | |||||||
| chr11:88314954 | C | CA | 3 | a0001c0001t0001g0012 a0001c0001t0001g0158 a0001c0001t0001g0159 |
6 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(3): Show |
intron_variant | MODIFIER | c.319-2401dupT | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88314954 | |||||||
| chr11:88314959 | A | G | 3 | a0002c0002t0001g0021 a0002c0002t0001g0292 a0002c0002t0001g0293 |
5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.319-2405T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88314959 | |||||||
| chr11:88314961 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.319-2407G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88314961 | |||||||
| chr11:88315088 | T | C | 3 | a0002c0002t0001g0021 a0002c0002t0001g0292 a0002c0002t0001g0293 |
5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.319-2534A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88315088 | |||||||
| chr11:88315105 | T | C | 3 | a0002c0002t0001g0021 a0002c0002t0001g0292 a0002c0002t0001g0293 |
5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.319-2551A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88315105 | |||||||
| chr11:88315117 | T | C | 2 | a0001c0001t0001g0243 a0001c0001t0001g0244 |
2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.319-2563A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88315117 | |||||||
| chr11:88315168 | G | C | 144 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(141): Show |
203 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.319-2614C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88315168 | |||||||
| chr11:88315365 | T | A | 1 | a0001c0001t0001g0210 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.319-2811A>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88315365 | |||||||
| chr11:88315594 | T | A | 8 | a0001c0001t0002g0008 a0001c0001t0002g0055 a0001c0001t0002g0056 others(5): Show |
12 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.319-3040A>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88315594 | |||||||
| chr11:88315606 | AAAT | A | 3 | a0002c0002t0001g0021 a0002c0002t0001g0292 a0002c0002t0001g0293 |
5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.319-3055_319-3053d others(5): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88315606 | |||||||
| chr11:88315773 | CAG | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(137): Show |
199 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.319-3221_319-3220d others(4): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88315773 | |||||||
| chr11:88315805 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.319-3251C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88315805 | |||||||
| chr11:88315821 | T | C | 1 | a0001c0001t0001g0079 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.319-3267A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88315821 | |||||||
| chr11:88315966 | G | C | 3 | a0002c0002t0001g0021 a0002c0002t0001g0292 a0002c0002t0001g0293 |
5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.319-3412C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88315966 | |||||||
| chr11:88316025 | G | T | 1 | a0001c0001t0001g0189 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.319-3471C>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88316025 | |||||||
| chr11:88316375 | G | A | 140 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(137): Show |
199 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.319-3821C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88316375 | |||||||
| chr11:88316446 | G | A | 3 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 |
3 | HG02647.hp2 HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.319-3892C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88316446 | |||||||
| chr11:88316475 | C | CTAAA | 42 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0015 others(39): Show |
77 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.319-3925_319-3922d others(6): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88316475 | |||||||
| chr11:88316475 | C | CTAAATAA others(1): Show |
7 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0120 others(4): Show |
7 | HG02280.hp2 HG02647.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.319-3929_319-3922d others(10): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88316475 | |||||||
| chr11:88316475 | C | CTAAATAA others(5): Show |
133 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0011 others(130): Show |
195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.319-3933_319-3922d others(14): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88316475 | |||||||
| chr11:88316475 | C | CTAAATAA others(9): Show |
65 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(62): Show |
89 | HG00280.hp1 HG00323.hp1 HG00673.hp2 others(86): Show |
intron_variant | MODIFIER | c.319-3937_319-3922d others(18): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88316475 | |||||||
| chr11:88316475 | C | CTAAATAA others(13): Show |
19 | a0001c0001t0001g0033 a0001c0001t0001g0051 a0001c0001t0001g0129 others(16): Show |
21 | HG00609.hp2 HG01261.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.319-3941_319-3922d others(22): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88316475 | |||||||
| chr11:88316475 | C | CTAAATAA others(17): Show |
1 | a0001c0001t0002g0064 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.319-3945_319-3922d others(26): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88316475 | |||||||
| chr11:88316500 | T | TAAATAAA others(5): Show |
8 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0068 others(5): Show |
10 | HG00639.hp1 HG01069.hp1 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.319-3947_319-3946i others(14): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88316500 | |||||||
| chr11:88316501 | A | AAATAAAT others(17): Show |
1 | a0001c0001t0001g0143 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.319-3948_319-3947i others(26): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88316501 | |||||||
| chr11:88316548 | T | C | 3 | a0001c0001t0001g0034 a0001c0001t0001g0172 a0001c0001t0001g0197 |
4 | HG02602.hp1 HG03017.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.319-3994A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88316548 | |||||||
| chr11:88316584 | C | A | 1 | a0001c0001t0001g0168 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.319-4030G>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88316584 | |||||||
| chr11:88316610 | CAT | C | 144 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(141): Show |
203 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.319-4058_319-4057d others(4): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88316610 | |||||||
| chr11:88316655 | C | T | 3 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0092 |
3 | HG00735.hp1 HG02683.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.319-4101G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88316655 | |||||||
| chr11:88316656 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.319-4102A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88316656 | |||||||
| chr11:88316680 | C | T | 3 | a0002c0002t0001g0021 a0002c0002t0001g0292 a0002c0002t0001g0293 |
5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.319-4126G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88316680 | |||||||
| chr11:88316728 | T | C | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG01243.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.319-4174A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88316728 | |||||||
| chr11:88316812 | A | G | 1 | a0001c0001t0001g0136 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.319-4258T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88316812 | |||||||
| chr11:88316814 | A | C | 4 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 others(1): Show |
4 | HG02647.hp2 HG02896.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.319-4260T>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88316814 | |||||||
| chr11:88316849 | A | C | 3 | a0002c0002t0001g0021 a0002c0002t0001g0292 a0002c0002t0001g0293 |
5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.319-4295T>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88316849 | |||||||
| chr11:88316885 | T | C | 3 | a0002c0002t0001g0021 a0002c0002t0001g0292 a0002c0002t0001g0293 |
5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.319-4331A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88316885 | |||||||
| chr11:88316891 | T | A | 3 | a0002c0002t0001g0021 a0002c0002t0001g0292 a0002c0002t0001g0293 |
5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.319-4337A>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88316891 | |||||||
| chr11:88317029 | C | T | 2 | a0001c0001t0001g0174 a0001c0001t0001g0179 |
2 | HG02080.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.319-4475G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88317029 | |||||||
| chr11:88317087 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.319-4533G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88317087 | |||||||
| chr11:88317116 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.319-4562C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88317116 | |||||||
| chr11:88317141 | A | G | 1 | a0001c0001t0001g0219 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.319-4587T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88317141 | |||||||
| chr11:88317210 | G | A | 3 | a0002c0002t0001g0021 a0002c0002t0001g0292 a0002c0002t0001g0293 |
5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.319-4656C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88317210 | |||||||
| chr11:88317246 | C | G | 2 | a0003c0003t0001g0283 a0003c0003t0001g0284 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.319-4692G>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88317246 | |||||||
| chr11:88317434 | T | TTAGTCTT others(1): Show |
3 | a0002c0002t0001g0021 a0002c0002t0001g0292 a0002c0002t0001g0293 |
5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.319-4881_319-4880i others(10): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88317434 | |||||||
| chr11:88317599 | G | T | 1 | a0001c0001t0001g0052 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.319-5045C>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88317599 | |||||||
| chr11:88317623 | G | A | 1 | a0003c0003t0001g0119 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.319-5069C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88317623 | |||||||
| chr11:88317665 | T | C | 10 | a0001c0001t0001g0003 a0001c0001t0001g0072 a0001c0001t0001g0073 others(7): Show |
21 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(18): Show |
intron_variant | MODIFIER | c.319-5111A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88317665 | |||||||
| chr11:88317671 | G | A | 1 | a0002c0002t0001g0278 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.319-5117C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88317671 | |||||||
| chr11:88317697 | G | A | 3 | a0002c0002t0001g0021 a0002c0002t0001g0292 a0002c0002t0001g0293 |
5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.319-5143C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88317697 | |||||||
| chr11:88317712 | T | C | 1 | a0001c0001t0001g0138 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.319-5158A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88317712 | |||||||
| chr11:88317864 | A | G | 2 | a0003c0003t0001g0020 a0003c0003t0001g0169 |
4 | HG00323.hp2 HG00741.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.319-5310T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88317864 | |||||||
| chr11:88318125 | T | A | 30 | a0001c0001t0001g0123 a0001c0001t0001g0127 a0002c0002t0001g0004 others(27): Show |
43 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.319-5571A>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88318125 | |||||||
| chr11:88318298 | C | T | 1 | a0001c0001t0001g0211 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.319-5744G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88318298 | |||||||
| chr11:88318340 | C | T | 1 | a0001c0001t0001g0178 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.319-5786G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88318340 | |||||||
| chr11:88318437 | T | C | 1 | a0001c0001t0006g0177 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.319-5883A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88318437 | |||||||
| chr11:88318563 | C | T | 1 | a0002c0002t0001g0278 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.319-6009G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88318563 | |||||||
| chr11:88318622 | T | C | 1 | a0002c0002t0001g0100 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.319-6068A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88318622 | |||||||
| chr11:88318631 | C | G | 75 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(72): Show |
112 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.319-6077G>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88318631 | |||||||
| chr11:88318708 | G | C | 128 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(125): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.319-6154C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88318708 | |||||||
| chr11:88318716 | A | G | 132 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(129): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.319-6162T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88318716 | |||||||
| chr11:88318751 | C | T | 1 | a0002c0002t0001g0278 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.319-6197G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88318751 | |||||||
| chr11:88318769 | A | G | 3 | a0002c0002t0001g0021 a0002c0002t0001g0292 a0002c0002t0001g0293 |
5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.319-6215T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88318769 | |||||||
| chr11:88318797 | T | A | 1 | a0002c0002t0001g0095 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.319-6243A>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88318797 | |||||||
| chr11:88318862 | T | C | 1 | a0001c0001t0001g0210 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.319-6308A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88318862 | |||||||
| chr11:88318904 | G | A | 48 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(45): Show |
63 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.319-6350C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88318904 | |||||||
| chr11:88318971 | T | C | 1 | a0001c0001t0001g0087 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.319-6417A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88318971 | |||||||
| chr11:88319075 | C | T | 37 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0016 others(34): Show |
69 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.319-6521G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88319075 | |||||||
| chr11:88319210 | A | G | 1 | a0001c0001t0001g0068 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.319-6656T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88319210 | |||||||
| chr11:88319318 | T | C | 37 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0016 others(34): Show |
69 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.319-6764A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88319318 | |||||||
| chr11:88319350 | T | C | 5 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0198 others(2): Show |
5 | HG01346.hp2 HG01934.hp1 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.319-6796A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88319350 | |||||||
| chr11:88319465 | C | G | 2 | a0002c0002t0001g0104 a0002c0002t0001g0107 |
2 | HG00140.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.319-6911G>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88319465 | |||||||
| chr11:88319672 | A | G | 3 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 |
3 | HG02647.hp2 HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.319-7118T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88319672 | |||||||
| chr11:88320003 | T | C | 2 | a0001c0001t0001g0066 a0001c0001t0002g0054 |
2 | HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.319-7449A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88320003 | |||||||
| chr11:88320742 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.319-8188G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88320742 | |||||||
| chr11:88320811 | T | C | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(362): Show |
intron_variant | MODIFIER | c.319-8257A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88320811 | |||||||
| chr11:88320823 | C | T | 3 | a0002c0002t0001g0021 a0002c0002t0001g0292 a0002c0002t0001g0293 |
5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.319-8269G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88320823 | |||||||
| chr11:88320888 | G | C | 3 | a0002c0002t0001g0021 a0002c0002t0001g0292 a0002c0002t0001g0293 |
5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.319-8334C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88320888 | |||||||
| chr11:88320924 | C | T | 2 | a0002c0002t0001g0116 a0002c0002t0001g0117 |
2 | HG03831.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.319-8370G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88320924 | |||||||
| chr11:88321178 | G | C | 270 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(267): Show |
393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
intron_variant | MODIFIER | c.319-8624C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88321178 | |||||||
| chr11:88321178 | G | T | 1 | a0001c0001t0001g0143 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.319-8624C>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88321178 | |||||||
| chr11:88321284 | T | C | 3 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 |
3 | HG02647.hp2 HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.319-8730A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88321284 | |||||||
| chr11:88321403 | G | A | 37 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0016 others(34): Show |
69 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.319-8849C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88321403 | |||||||
| chr11:88321439 | C | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG02523.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.319-8885G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88321439 | |||||||
| chr11:88321550 | G | A | 2 | a0001c0001t0001g0031 a0001c0001t0001g0136 |
3 | NA19063.hp2 NA19088.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.319-8996C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88321550 | |||||||
| chr11:88321602 | G | A | 1 | a0001c0001t0006g0177 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.319-9048C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88321602 | |||||||
| chr11:88321643 | T | C | 1 | a0002c0002t0001g0278 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.319-9089A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88321643 | |||||||
| chr11:88321744 | C | T | 1 | a0002c0002t0001g0105 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.319-9190G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88321744 | |||||||
| chr11:88321768 | A | G | 1 | a0001c0001t0001g0138 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.319-9214T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88321768 | |||||||
| chr11:88321842 | T | C | 3 | a0002c0002t0001g0021 a0002c0002t0001g0292 a0002c0002t0001g0293 |
5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.319-9288A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88321842 | |||||||
| chr11:88321852 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.319-9298T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88321852 | |||||||
| chr11:88321894 | G | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0274 a0001c0001t0001g0275 |
6 | HG01074.hp2 HG02257.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.319-9340C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88321894 | |||||||
| chr11:88321921 | C | T | 286 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(283): Show |
415 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(412): Show |
intron_variant | MODIFIER | c.319-9367G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88321921 | |||||||
| chr11:88322002 | G | A | 93 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(90): Show |
143 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.319-9448C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88322002 | |||||||
| chr11:88322032 | A | T | 1 | a0001c0001t0001g0073 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.319-9478T>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88322032 | |||||||
| chr11:88322123 | T | C | 40 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0015 others(37): Show |
75 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.319-9569A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88322123 | |||||||
| chr11:88322161 | G | C | 1 | a0001c0001t0001g0272 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.319-9607C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88322161 | |||||||
| chr11:88322199 | C | T | 1 | a0001c0001t0006g0177 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.319-9645G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88322199 | |||||||
| chr11:88322367 | T | C | 3 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 |
3 | HG02647.hp2 HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.319-9813A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88322367 | |||||||
| chr11:88322490 | T | G | 1 | a0001c0001t0001g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.319-9936A>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88322490 | |||||||
| chr11:88322525 | G | A | 8 | a0001c0001t0002g0008 a0001c0001t0002g0055 a0001c0001t0002g0056 others(5): Show |
12 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.319-9971C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88322525 | |||||||
| chr11:88322605 | G | A | 1 | a0002c0002t0001g0106 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.319-10051C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88322605 | |||||||
| chr11:88322606 | A | T | 1 | a0002c0002t0001g0106 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.319-10052T>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88322606 | |||||||
| chr11:88322621 | A | T | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(268): Show |
394 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(391): Show |
intron_variant | MODIFIER | c.319-10067T>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88322621 | |||||||
| chr11:88322626 | A | G | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(268): Show |
394 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(391): Show |
intron_variant | MODIFIER | c.319-10072T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88322626 | |||||||
| chr11:88322962 | A | G | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(238): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(348): Show |
intron_variant | MODIFIER | c.319-10408T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88322962 | |||||||
| chr11:88323007 | C | T | 3 | a0001c0001t0001g0072 a0001c0001t0001g0173 a0001c0001t0001g0176 |
3 | NA18612.hp1 NA18944.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.319-10453G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88323007 | |||||||
| chr11:88323108 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.319-10554C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88323108 | |||||||
| chr11:88323121 | C | T | 1 | a0002c0002t0001g0105 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.319-10567G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88323121 | |||||||
| chr11:88323228 | T | G | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(238): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(348): Show |
intron_variant | MODIFIER | c.319-10674A>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88323228 | |||||||
| chr11:88323415 | GC | G | 30 | a0001c0001t0001g0123 a0001c0001t0001g0127 a0002c0002t0001g0004 others(27): Show |
43 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.319-10862delG | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88323415 | |||||||
| chr11:88323461 | G | A | 1 | a0001c0001t0001g0135 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.319-10907C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88323461 | |||||||
| chr11:88323614 | T | C | 3 | a0002c0002t0001g0021 a0002c0002t0001g0292 a0002c0002t0001g0293 |
5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.319-11060A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88323614 | |||||||
| chr11:88323696 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.319-11142T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88323696 | |||||||
| chr11:88323698 | G | A | 1 | a0001c0001t0001g0164 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.319-11144C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88323698 | |||||||
| chr11:88323774 | G | A | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(277): Show |
409 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(406): Show |
intron_variant | MODIFIER | c.318+11163C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88323774 | |||||||
| chr11:88323790 | C | T | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | NA19066.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.318+11147G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88323790 | |||||||
| chr11:88324021 | C | A | 2 | a0001c0001t0005g0062 a0001c0001t0007g0298 |
2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.318+10916G>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88324021 | |||||||
| chr11:88324087 | C | G | 143 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(140): Show |
202 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.318+10850G>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88324087 | |||||||
| chr11:88324326 | T | C | 1 | a0001c0001t0001g0024 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.318+10611A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88324326 | |||||||
| chr11:88324552 | G | GA | 143 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(140): Show |
202 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.318+10384dupT | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88324552 | |||||||
| chr11:88324633 | C | T | 1 | a0001c0001t0001g0229 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.318+10304G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88324633 | |||||||
| chr11:88324714 | G | A | 3 | a0002c0002t0001g0017 a0002c0002t0001g0111 a0002c0002t0001g0112 |
5 | HG02258.hp2 HG02809.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.318+10223C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88324714 | |||||||
| chr11:88324988 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.318+9949C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88324988 | |||||||
| chr11:88325088 | AAAG | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(72): Show |
111 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.318+9846_318+9848d others(5): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88325088 | |||||||
| chr11:88325177 | T | C | 1 | a0002c0002t0001g0278 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.318+9760A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88325177 | |||||||
| chr11:88325262 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.318+9675A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88325262 | |||||||
| chr11:88325635 | A | T | 1 | a0001c0001t0001g0065 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.318+9302T>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88325635 | |||||||
| chr11:88325756 | G | C | 1 | a0001c0001t0001g0134 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.318+9181C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88325756 | |||||||
| chr11:88325921 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.318+9016A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88325921 | |||||||
| chr11:88326122 | G | C | 1 | a0001c0001t0001g0202 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.318+8815C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88326122 | |||||||
| chr11:88326326 | C | G | 1 | a0001c0001t0001g0175 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.318+8611G>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88326326 | |||||||
| chr11:88326367 | GCT | G | 3 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 |
3 | HG02647.hp2 HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.318+8568_318+8569d others(4): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88326367 | |||||||
| chr11:88326487 | T | C | 1 | a0001c0001t0001g0248 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.318+8450A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88326487 | |||||||
| chr11:88326515 | G | A | 268 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(265): Show |
391 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(388): Show |
intron_variant | MODIFIER | c.318+8422C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88326515 | |||||||
| chr11:88326519 | C | A | 1 | a0001c0001t0001g0143 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.318+8418G>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88326519 | |||||||
| chr11:88326525 | G | C | 1 | a0001c0001t0001g0203 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.318+8412C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88326525 | |||||||
| chr11:88326526 | T | TA | 128 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(125): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.318+8410dupT | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88326526 | |||||||
| chr11:88326526 | T | TAA | 137 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(134): Show |
196 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.318+8409_318+8410d others(4): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88326526 | |||||||
| chr11:88326571 | T | C | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(266): Show |
392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.318+8366A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88326571 | |||||||
| chr11:88326572 | A | T | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(266): Show |
392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.318+8365T>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88326572 | |||||||
| chr11:88326576 | T | C | 1 | a0001c0001t0001g0249 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.318+8361A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88326576 | |||||||
| chr11:88326648 | T | A | 1 | a0001c0001t0001g0204 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.318+8289A>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88326648 | |||||||
| chr11:88326706 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.318+8231C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88326706 | |||||||
| chr11:88326713 | T | A | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(266): Show |
392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.318+8224A>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88326713 | |||||||
| chr11:88326714 | T | C | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(266): Show |
392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.318+8223A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88326714 | |||||||
| chr11:88326726 | C | T | 2 | a0001c0001t0005g0062 a0001c0001t0007g0298 |
2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.318+8211G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88326726 | |||||||
| chr11:88326760 | C | A | 1 | a0003c0003t0001g0119 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.318+8177G>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88326760 | |||||||
| chr11:88326968 | G | A | 30 | a0001c0001t0001g0123 a0001c0001t0001g0127 a0002c0002t0001g0004 others(27): Show |
43 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.318+7969C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88326968 | |||||||
| chr11:88326969 | T | G | 4 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 others(1): Show |
4 | HG02647.hp2 HG02896.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.318+7968A>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88326969 | |||||||
| chr11:88327032 | C | T | 143 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(140): Show |
202 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.318+7905G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88327032 | |||||||
| chr11:88327331 | T | C | 274 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(271): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.318+7606A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88327331 | |||||||
| chr11:88327401 | A | AGAATATT others(22): Show |
2 | a0001c0001t0001g0124 a0001c0001t0001g0126 |
2 | HG02647.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.318+7507_318+7535d others(31): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88327401 | |||||||
| chr11:88327458 | C | T | 1 | a0002c0002t0001g0104 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.318+7479G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88327458 | |||||||
| chr11:88327475 | A | G | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG01243.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.318+7462T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88327475 | |||||||
| chr11:88327526 | C | T | 2 | a0001c0001t0001g0066 a0001c0001t0002g0054 |
2 | HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.318+7411G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88327526 | |||||||
| chr11:88327569 | C | T | 140 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(137): Show |
199 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.318+7368G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88327569 | |||||||
| chr11:88327674 | C | A | 4 | a0001c0001t0001g0051 a0001c0001t0001g0205 a0001c0001t0001g0289 others(1): Show |
5 | HG02698.hp1 NA18975.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.318+7263G>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88327674 | |||||||
| chr11:88327678 | C | T | 4 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0005g0062 others(1): Show |
4 | HG01243.hp1 HG02451.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.318+7259G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88327678 | |||||||
| chr11:88327845 | G | A | 1 | a0001c0001t0001g0028 | 2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.318+7092C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88327845 | |||||||
| chr11:88327930 | T | C | 3 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 |
3 | HG02647.hp2 HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.318+7007A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88327930 | |||||||
| chr11:88328113 | C | T | 1 | a0001c0001t0001g0022 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.318+6824G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88328113 | |||||||
| chr11:88328237 | A | C | 95 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(92): Show |
146 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.318+6700T>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88328237 | |||||||
| chr11:88328488 | A | G | 8 | a0001c0001t0002g0008 a0001c0001t0002g0055 a0001c0001t0002g0056 others(5): Show |
12 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.318+6449T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88328488 | |||||||
| chr11:88328502 | T | C | 5 | a0001c0001t0001g0014 a0001c0001t0001g0048 a0001c0001t0001g0222 others(2): Show |
9 | HG00544.hp1 NA18943.hp1 NA18944.hp1 others(6): Show |
intron_variant | MODIFIER | c.318+6435A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88328502 | |||||||
| chr11:88328524 | C | T | 274 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(271): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.318+6413G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88328524 | |||||||
| chr11:88328693 | T | C | 1 | a0001c0001t0001g0052 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.318+6244A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88328693 | |||||||
| chr11:88328721 | G | A | 29 | a0001c0001t0001g0123 a0002c0002t0001g0004 a0002c0002t0001g0017 others(26): Show |
42 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.318+6216C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88328721 | |||||||
| chr11:88328741 | C | T | 12 | a0001c0001t0001g0171 a0001c0001t0001g0217 a0001c0001t0002g0008 others(9): Show |
16 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.318+6196G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88328741 | |||||||
| chr11:88328831 | T | G | 5 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0207 others(2): Show |
7 | HG01496.hp1 HG01943.hp1 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.318+6106A>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88328831 | |||||||
| chr11:88329112 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.318+5825G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88329112 | |||||||
| chr11:88329180 | T | TAGA | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(266): Show |
392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.318+5756_318+5757i others(5): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88329180 | |||||||
| chr11:88329253 | G | A | 3 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 |
3 | HG01243.hp1 HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.318+5684C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88329253 | |||||||
| chr11:88329256 | C | T | 2 | a0001c0001t0001g0071 a0001c0001t0001g0265 |
2 | HG01099.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.318+5681G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88329256 | |||||||
| chr11:88329327 | C | G | 93 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(90): Show |
144 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.318+5610G>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88329327 | |||||||
| chr11:88329343 | G | A | 1 | a0001c0001t0001g0046 | 2 | HG00140.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.318+5594C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88329343 | |||||||
| chr11:88329411 | G | A | 2 | a0001c0001t0001g0165 a0001c0001t0001g0273 |
2 | HG01993.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.318+5526C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88329411 | |||||||
| chr11:88329455 | C | CA | 8 | a0001c0001t0002g0008 a0001c0001t0002g0055 a0001c0001t0002g0056 others(5): Show |
12 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.318+5481dupT | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88329455 | |||||||
| chr11:88329455 | C | CAAA | 6 | a0001c0001t0001g0171 a0001c0001t0001g0217 a0001c0001t0002g0054 others(3): Show |
6 | HG01891.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.318+5479_318+5481d others(5): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88329455 | |||||||
| chr11:88329455 | CAA | C | 29 | a0001c0001t0001g0123 a0001c0001t0001g0127 a0002c0002t0001g0004 others(26): Show |
44 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.318+5480_318+5481d others(4): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88329455 | |||||||
| chr11:88329455 | CAAA | C | 13 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0128 others(10): Show |
13 | HG00423.hp1 HG00621.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.318+5479_318+5481d others(5): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88329455 | |||||||
| chr11:88329455 | CAAAA | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(174): Show |
252 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.318+5478_318+5481d others(6): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88329455 | |||||||
| chr11:88329455 | CAAAAA | C | 44 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0016 others(41): Show |
76 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.318+5477_318+5481d others(7): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88329455 | |||||||
| chr11:88329455 | CAAAAAAA others(4): Show |
C | 1 | a0003c0003t0001g0282 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.318+5471_318+5481d others(13): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88329455 | |||||||
| chr11:88329455 | CAAAAAAA others(11): Show |
C | 3 | a0001c0001t0001g0015 a0001c0001t0001g0274 a0001c0001t0001g0275 |
6 | HG01074.hp2 HG02257.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.318+5464_318+5481d others(20): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88329455 | |||||||
| chr11:88329489 | T | C | 1 | a0001c0001t0002g0054 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.318+5448A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88329489 | |||||||
| chr11:88329716 | T | TTG | 4 | a0001c0001t0001g0171 a0001c0001t0001g0217 a0001c0001t0002g0063 others(1): Show |
4 | HG02965.hp2 HG02976.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.318+5219_318+5220d others(4): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88329716 | |||||||
| chr11:88329771 | G | A | 5 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0207 others(2): Show |
7 | HG01496.hp1 HG01943.hp1 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.318+5166C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88329771 | |||||||
| chr11:88329815 | C | A | 1 | a0001c0001t0001g0210 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.318+5122G>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88329815 | |||||||
| chr11:88329878 | T | C | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(266): Show |
392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.318+5059A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88329878 | |||||||
| chr11:88329899 | G | A | 1 | a0001c0001t0001g0135 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.318+5038C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88329899 | |||||||
| chr11:88330057 | G | C | 1 | a0001c0001t0001g0052 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.318+4880C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88330057 | |||||||
| chr11:88330173 | T | C | 1 | a0001c0001t0001g0121 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.318+4764A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88330173 | |||||||
| chr11:88330264 | C | A | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(234): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(344): Show |
intron_variant | MODIFIER | c.318+4673G>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88330264 | |||||||
| chr11:88330425 | T | A | 1 | a0001c0001t0001g0211 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.318+4512A>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88330425 | |||||||
| chr11:88330468 | C | A | 2 | a0002c0002t0001g0116 a0002c0002t0001g0117 |
2 | HG03831.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.318+4469G>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88330468 | |||||||
| chr11:88330537 | C | G | 1 | a0001c0001t0001g0173 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.318+4400G>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88330537 | |||||||
| chr11:88330573 | G | T | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(234): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(344): Show |
intron_variant | MODIFIER | c.318+4364C>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88330573 | |||||||
| chr11:88330591 | G | A | 1 | a0001c0001t0001g0212 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.318+4346C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88330591 | |||||||
| chr11:88330597 | C | G | 1 | a0001c0001t0001g0070 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.318+4340G>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88330597 | |||||||
| chr11:88330755 | G | A | 3 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 |
3 | HG02647.hp2 HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.318+4182C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88330755 | |||||||
| chr11:88330776 | C | T | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(89): Show |
142 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.318+4161G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88330776 | |||||||
| chr11:88330780 | A | G | 236 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(233): Show |
345 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.318+4157T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88330780 | |||||||
| chr11:88330795 | C | T | 12 | a0001c0001t0001g0171 a0001c0001t0001g0217 a0001c0001t0002g0008 others(9): Show |
16 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.318+4142G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88330795 | |||||||
| chr11:88330831 | G | A | 1 | a0001c0001t0001g0032 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.318+4106C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88330831 | |||||||
| chr11:88330834 | T | G | 1 | a0001c0001t0001g0212 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.318+4103A>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88330834 | |||||||
| chr11:88330858 | T | C | 1 | a0001c0001t0001g0213 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.318+4079A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88330858 | |||||||
| chr11:88330922 | G | A | 1 | a0002c0002t0001g0018 | 3 | NA18953.hp1 NA19006.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.318+4015C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88330922 | |||||||
| chr11:88330924 | T | C | 1 | a0001c0001t0001g0253 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.318+4013A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88330924 | |||||||
| chr11:88330973 | G | C | 1 | a0001c0001t0001g0254 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.318+3964C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88330973 | |||||||
| chr11:88331063 | C | T | 12 | a0001c0001t0001g0171 a0001c0001t0001g0217 a0001c0001t0002g0008 others(9): Show |
16 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.318+3874G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88331063 | |||||||
| chr11:88331219 | C | G | 1 | a0001c0001t0001g0226 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.318+3718G>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88331219 | |||||||
| chr11:88331280 | T | G | 1 | a0001c0001t0001g0123 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.318+3657A>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88331280 | |||||||
| chr11:88331307 | C | T | 3 | a0002c0002t0001g0027 a0002c0002t0001g0101 a0002c0002t0001g0102 |
4 | NA18940.hp2 NA18968.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.318+3630G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88331307 | |||||||
| chr11:88331433 | G | C | 3 | a0002c0002t0001g0021 a0002c0002t0001g0292 a0002c0002t0001g0293 |
5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.318+3504C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88331433 | |||||||
| chr11:88331438 | G | A | 2 | a0001c0001t0005g0062 a0001c0001t0007g0298 |
2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.318+3499C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88331438 | |||||||
| chr11:88331466 | T | C | 5 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(2): Show |
5 | HG02717.hp1 HG02723.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.318+3471A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88331466 | |||||||
| chr11:88331518 | G | A | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(89): Show |
142 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.318+3419C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88331518 | |||||||
| chr11:88331582 | A | G | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(234): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(344): Show |
intron_variant | MODIFIER | c.318+3355T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88331582 | |||||||
| chr11:88331652 | A | G | 1 | a0001c0001t0002g0055 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.318+3285T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88331652 | |||||||
| chr11:88331742 | T | G | 1 | a0001c0001t0001g0122 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.318+3195A>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88331742 | |||||||
| chr11:88331814 | A | C | 286 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(283): Show |
415 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(412): Show |
intron_variant | MODIFIER | c.318+3123T>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88331814 | |||||||
| chr11:88331962 | C | A | 4 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 others(1): Show |
4 | HG00741.hp2 HG01099.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.318+2975G>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88331962 | |||||||
| chr11:88331997 | C | T | 1 | a0002c0002t0001g0278 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.318+2940G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88331997 | |||||||
| chr11:88332135 | C | T | 1 | a0003c0003t0001g0119 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.318+2802G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88332135 | |||||||
| chr11:88332150 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.318+2787T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88332150 | |||||||
| chr11:88332259 | T | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(137): Show |
199 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.318+2678A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88332259 | |||||||
| chr11:88332326 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.318+2611A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88332326 | |||||||
| chr11:88332416 | T | C | 1 | a0002c0002t0001g0118 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.318+2521A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88332416 | |||||||
| chr11:88332990 | G | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0274 a0001c0001t0001g0275 |
6 | HG01074.hp2 HG02257.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.318+1947C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88332990 | |||||||
| chr11:88333086 | C | T | 2 | a0003c0003t0001g0050 a0003c0003t0001g0282 |
3 | HG01109.hp2 HG02809.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.318+1851G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88333086 | |||||||
| chr11:88333210 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.318+1727G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88333210 | |||||||
| chr11:88333276 | A | G | 1 | a0002c0002t0001g0278 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.318+1661T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88333276 | |||||||
| chr11:88333320 | T | C | 40 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0015 others(37): Show |
75 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.318+1617A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88333320 | |||||||
| chr11:88333471 | G | C | 3 | a0002c0002t0001g0021 a0002c0002t0001g0292 a0002c0002t0001g0293 |
5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.318+1466C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88333471 | |||||||
| chr11:88333546 | A | C | 12 | a0001c0001t0001g0171 a0001c0001t0001g0217 a0001c0001t0002g0008 others(9): Show |
16 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.318+1391T>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88333546 | |||||||
| chr11:88333569 | G | A | 93 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(90): Show |
144 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.318+1368C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88333569 | |||||||
| chr11:88333669 | T | G | 1 | a0001c0001t0001g0047 | 2 | NA18950.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.318+1268A>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88333669 | |||||||
| chr11:88333685 | G | T | 1 | a0001c0001t0001g0172 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.318+1252C>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88333685 | |||||||
| chr11:88333701 | CA | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(137): Show |
199 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.318+1235delT | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88333701 | |||||||
| chr11:88333763 | G | A | 3 | a0002c0002t0001g0021 a0002c0002t0001g0292 a0002c0002t0001g0293 |
5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.318+1174C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88333763 | |||||||
| chr11:88333887 | C | CT | 37 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0016 others(34): Show |
69 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.318+1049dupA | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88333887 | |||||||
| chr11:88334008 | A | G | 1 | a0001c0001t0001g0136 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.318+929T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88334008 | |||||||
| chr11:88334068 | T | G | 4 | a0001c0001t0001g0037 a0001c0001t0001g0219 a0001c0001t0001g0220 others(1): Show |
5 | HG03017.hp1 HG03654.hp2 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.318+869A>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88334068 | |||||||
| chr11:88334168 | T | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0048 a0001c0001t0001g0266 others(1): Show |
8 | NA18943.hp1 NA18944.hp1 NA18947.hp1 others(5): Show |
intron_variant | MODIFIER | c.318+769A>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88334168 | |||||||
| chr11:88334179 | G | A | 4 | a0001c0001t0001g0091 a0001c0001t0001g0124 a0001c0001t0001g0125 others(1): Show |
4 | HG02015.hp2 HG02647.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.318+758C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88334179 | |||||||
| chr11:88334226 | T | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(74): Show |
114 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.318+711A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88334226 | |||||||
| chr11:88334323 | A | G | 2 | a0001c0001t0001g0066 a0001c0001t0002g0054 |
2 | HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.318+614T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88334323 | |||||||
| chr11:88334347 | T | C | 20 | a0001c0001t0001g0014 a0001c0001t0001g0037 a0001c0001t0001g0046 others(17): Show |
27 | HG00140.hp2 HG00544.hp1 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.318+590A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88334347 | |||||||
| chr11:88334484 | A | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(142): Show |
205 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.318+453T>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88334484 | |||||||
| chr11:88334586 | C | G | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(266): Show |
392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.318+351G>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88334586 | |||||||
| chr11:88334596 | T | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(137): Show |
199 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.318+341A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88334596 | |||||||
| chr11:88334658 | G | T | 287 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(284): Show |
416 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(413): Show |
intron_variant | MODIFIER | c.318+279C>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88334658 | |||||||
| chr11:88334681 | C | T | 29 | a0001c0001t0001g0123 a0002c0002t0001g0004 a0002c0002t0001g0017 others(26): Show |
42 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.318+256G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88334681 | |||||||
| chr11:88334830 | C | T | 2 | a0001c0001t0001g0038 a0001c0001t0001g0039 |
4 | NA18964.hp2 NA18974.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.318+107G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88334830 | |||||||
| chr11:88334836 | T | A | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(266): Show |
392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.318+101A>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88334836 | |||||||
| chr11:88334884 | G | T | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(266): Show |
392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.318+53C>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 2/6 | chr11 | 88334884 | |||||||
| chr11:88335088 | GA | G | 31 | a0001c0001t0001g0123 a0001c0001t0001g0127 a0001c0001t0001g0222 others(28): Show |
44 | HG00140.hp1 HG00544.hp1 HG00642.hp1 others(41): Show |
splice_region_variant&intron_variant | LOW | c.173-7delT | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88335088 | |||||||
| chr11:88335136 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.173-54C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88335136 | |||||||
| chr11:88335161 | T | A | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(266): Show |
392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.173-79A>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88335161 | |||||||
| chr11:88335199 | GCA | G | 3 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 |
3 | HG02647.hp2 HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.173-119_173-118del others(2): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88335199 | |||||||
| chr11:88335293 | T | C | 8 | a0001c0001t0002g0008 a0001c0001t0002g0055 a0001c0001t0002g0056 others(5): Show |
12 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.173-211A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88335293 | |||||||
| chr11:88335375 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.173-293C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88335375 | |||||||
| chr11:88335428 | G | T | 269 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(266): Show |
392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.173-346C>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88335428 | |||||||
| chr11:88335585 | A | G | 4 | a0001c0001t0001g0171 a0001c0001t0001g0217 a0001c0001t0002g0063 others(1): Show |
4 | HG02965.hp2 HG02976.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.173-503T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88335585 | |||||||
| chr11:88335597 | C | T | 50 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(47): Show |
66 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.173-515G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88335597 | |||||||
| chr11:88335677 | C | G | 4 | a0001c0001t0001g0037 a0001c0001t0001g0219 a0001c0001t0001g0220 others(1): Show |
5 | HG03017.hp1 HG03654.hp2 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.173-595G>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88335677 | |||||||
| chr11:88335678 | T | C | 40 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0015 others(37): Show |
75 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.173-596A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88335678 | |||||||
| chr11:88335833 | C | T | 29 | a0001c0001t0001g0123 a0002c0002t0001g0004 a0002c0002t0001g0017 others(26): Show |
42 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.173-751G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88335833 | |||||||
| chr11:88335837 | G | A | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(89): Show |
142 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.173-755C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88335837 | |||||||
| chr11:88335948 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.173-866C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88335948 | |||||||
| chr11:88336014 | T | C | 37 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0016 others(34): Show |
69 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.173-932A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88336014 | |||||||
| chr11:88336077 | A | G | 3 | a0002c0002t0001g0026 a0002c0002t0001g0099 a0002c0002t0001g0100 |
4 | NA18966.hp1 NA19003.hp1 NA19072.hp2 others(1): Show |
intron_variant | MODIFIER | c.173-995T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88336077 | |||||||
| chr11:88336082 | G | C | 1 | a0001c0001t0001g0277 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.173-1000C>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88336082 | |||||||
| chr11:88336145 | A | G | 63 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(60): Show |
85 | HG00280.hp1 HG00423.hp1 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.173-1063T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88336145 | |||||||
| chr11:88336155 | G | T | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(268): Show |
394 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(391): Show |
intron_variant | MODIFIER | c.173-1073C>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88336155 | |||||||
| chr11:88336237 | TTA | T | 4 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 others(1): Show |
4 | HG00741.hp2 HG01099.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.173-1157_173-1156d others(4): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88336237 | |||||||
| chr11:88336238 | TAA | T | 261 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(258): Show |
381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.173-1158_173-1157d others(4): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88336238 | |||||||
| chr11:88336238 | TAAA | T | 6 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0034 others(3): Show |
6 | HG02015.hp1 HG02083.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.173-1159_173-1157d others(5): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88336238 | |||||||
| chr11:88336289 | C | T | 286 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(283): Show |
415 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(412): Show |
intron_variant | MODIFIER | c.173-1207G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88336289 | |||||||
| chr11:88336306 | C | G | 8 | a0001c0001t0002g0008 a0001c0001t0002g0055 a0001c0001t0002g0056 others(5): Show |
12 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.172+1195G>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88336306 | |||||||
| chr11:88336307 | G | A | 1 | a0002c0002t0001g0278 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.172+1194C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88336307 | |||||||
| chr11:88336395 | C | A | 4 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 others(1): Show |
4 | HG00741.hp2 HG01099.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.172+1106G>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88336395 | |||||||
| chr11:88336419 | ATCCTAGC others(3): Show |
A | 3 | a0002c0002t0001g0021 a0002c0002t0001g0292 a0002c0002t0001g0293 |
5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.172+1072_172+1081d others(12): Show |
CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88336419 | |||||||
| chr11:88336438 | C | T | 287 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(284): Show |
416 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(413): Show |
intron_variant | MODIFIER | c.172+1063G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88336438 | |||||||
| chr11:88336539 | C | CA | 7 | a0001c0001t0001g0051 a0001c0001t0001g0092 a0001c0001t0001g0094 others(4): Show |
8 | HG02257.hp2 HG04199.hp1 NA18953.hp2 others(5): Show |
intron_variant | MODIFIER | c.172+961dupT | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88336539 | |||||||
| chr11:88336539 | CA | C | 92 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(89): Show |
122 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.172+961delT | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88336539 | |||||||
| chr11:88336554 | A | G | 1 | a0002c0002t0001g0096 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.172+947T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88336554 | |||||||
| chr11:88336557 | A | T | 1 | a0001c0001t0001g0067 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.172+944T>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88336557 | |||||||
| chr11:88336643 | T | G | 1 | a0001c0001t0001g0291 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.172+858A>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88336643 | |||||||
| chr11:88336703 | G | T | 1 | a0001c0001t0001g0120 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.172+798C>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88336703 | |||||||
| chr11:88336733 | A | G | 1 | a0002c0002t0001g0095 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.172+768T>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88336733 | |||||||
| chr11:88336921 | T | C | 4 | a0001c0001t0002g0063 a0001c0001t0002g0064 a0001c0001t0005g0062 others(1): Show |
4 | HG02717.hp2 HG03195.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.172+580A>G | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88336921 | |||||||
| chr11:88336942 | A | T | 8 | a0001c0001t0002g0008 a0001c0001t0002g0055 a0001c0001t0002g0056 others(5): Show |
12 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.172+559T>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88336942 | |||||||
| chr11:88336995 | G | A | 3 | a0002c0002t0001g0021 a0002c0002t0001g0292 a0002c0002t0001g0293 |
5 | HG02055.hp2 HG02109.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.172+506C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88336995 | |||||||
| chr11:88337042 | G | GA | 47 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0016 others(44): Show |
82 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.172+458dupT | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88337042 | |||||||
| chr11:88337066 | C | G | 1 | a0003c0003t0001g0119 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.172+435G>C | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88337066 | |||||||
| chr11:88337167 | C | T | 29 | a0001c0001t0001g0097 a0001c0004t0001g0098 a0002c0002t0001g0004 others(26): Show |
42 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.172+334G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88337167 | |||||||
| chr11:88337244 | G | A | 1 | a0001c0001t0001g0052 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.172+257C>T | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88337244 | |||||||
| chr11:88337395 | C | T | 50 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0016 others(47): Show |
85 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.172+106G>A | CTSC | ENSG00000109861.17 | transcript | ENST00000227266.10 | protein_coding | 1/6 | chr11 | 88337395 |