Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1509 |
| ensemblid | ENSG00000117984.15 |
| hgncid | 2529 |
| symbol | CTSD |
| name | cathepsin D |
| refseq_nuc | NM_001909.5 |
| refseq_prot | NP_001900.1 |
| ensembl_nuc | ENST00000236671.7 |
| ensembl_prot | ENSP00000236671.2 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 1752755 |
| end | 1763927 |
| strand | - |
| ver | v1.2 |
| region | chr11:1752755-1763927 |
| region5000 | chr11:1747755-1768927 |
| regionname0 | CTSD_chr11_1752755_1763927 |
| regionname5000 | CTSD_chr11_1747755_1768927 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 412 | 367 | 89 | 64 | 157 | 14 | 41 | 117 | CTSD_chr11_1747755_1768927 | CTSD | MQPSS others(407): Show |
chr11 | 1747755 | 1768927 |
| a0002 | 0/0 | 412 | 17 | 3 | 8 | 1 | 0 | 5 | 0 | CTSD_chr11_1747755_1768927 | CTSD | MQPSS others(407): Show |
chr11 | 1747755 | 1768927 |
| a0003 | 0/0 | 412 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | MQPSS others(407): Show |
chr11 | 1747755 | 1768927 |
| a0004 | 0/0 | 412 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | MQPST others(407): Show |
chr11 | 1747755 | 1768927 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1236 | 338 | 82 | 61 | 139 | 14 | 40 | CTSD_chr11_1747755_1768927 | CTSD | ATGCA others(1231): Show |
chr11 | 1747755 | 1768927 | ||
| a0001c0002 | 0/0 | 1236 | 18 | 0 | 0 | 18 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | ATGCA others(1231): Show |
chr11 | 1747755 | 1768927 | ||
| a0001c0004 | 0/0 | 1236 | 7 | 6 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | ATGCA others(1231): Show |
chr11 | 1747755 | 1768927 | ||
| a0001c0005 | 0/0 | 1236 | 2 | 1 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | ATGCA others(1231): Show |
chr11 | 1747755 | 1768927 | ||
| a0001c0006 | 0/0 | 1236 | 2 | 0 | 2 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | ATGCA others(1231): Show |
chr11 | 1747755 | 1768927 | ||
| a0002c0003 | 0/0 | 1236 | 17 | 3 | 8 | 1 | 0 | 5 | CTSD_chr11_1747755_1768927 | CTSD | ATGCA others(1231): Show |
chr11 | 1747755 | 1768927 | ||
| a0003c0008 | 0/0 | 1236 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | ATGCA others(1231): Show |
chr11 | 1747755 | 1768927 | ||
| a0004c0007 | 0/0 | 1236 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | ATGCA others(1231): Show |
chr11 | 1747755 | 1768927 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2055 | 286 | 73 | 49 | 115 | 12 | 36 | CTSD_chr11_1747755_1768927 | CTSD | AACTG others(2050): Show |
chr11 | 1747755 | 1768927 |
| a0001c0001t0002 | 0/1 | 2055 | 23 | 2 | 3 | 14 | 1 | 2 | CTSD_chr11_1747755_1768927 | CTSD | AACTG others(2050): Show |
chr11 | 1747755 | 1768927 |
| a0001c0001t0003 | 0/0 | 2055 | 8 | 0 | 5 | 1 | 1 | 1 | CTSD_chr11_1747755_1768927 | CTSD | AACTG others(2050): Show |
chr11 | 1747755 | 1768927 |
| a0001c0001t0004 | 0/0 | 2055 | 5 | 5 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | AACTG others(2050): Show |
chr11 | 1747755 | 1768927 |
| a0001c0001t0005 | 0/0 | 2053 | 4 | 0 | 3 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | AACTG others(2048): Show |
chr11 | 1747755 | 1768927 |
| a0001c0001t0006 | 0/0 | 2055 | 4 | 0 | 0 | 4 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | AACTG others(2050): Show |
chr11 | 1747755 | 1768927 |
| a0001c0001t0007 | 0/0 | 2055 | 2 | 0 | 0 | 2 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | AACTG others(2050): Show |
chr11 | 1747755 | 1768927 |
| a0001c0001t0008 | 0/0 | 2055 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | AACTG others(2050): Show |
chr11 | 1747755 | 1768927 |
| a0001c0001t0009 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | AACTG others(2050): Show |
chr11 | 1747755 | 1768927 |
| a0001c0001t0011 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | AACTG others(2050): Show |
chr11 | 1747755 | 1768927 |
| a0001c0001t0012 | 0/0 | 2055 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | AACTG others(2050): Show |
chr11 | 1747755 | 1768927 |
| a0001c0001t0013 | 0/0 | 2055 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | AACTG others(2050): Show |
chr11 | 1747755 | 1768927 |
| a0001c0001t0015 | 0/0 | 2055 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | AACTG others(2050): Show |
chr11 | 1747755 | 1768927 |
| a0001c0002t0001 | 0/0 | 2055 | 16 | 0 | 0 | 16 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | AACTG others(2050): Show |
chr11 | 1747755 | 1768927 |
| a0001c0002t0010 | 0/0 | 2055 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | AACTG others(2050): Show |
chr11 | 1747755 | 1768927 |
| a0001c0002t0016 | 0/0 | 2055 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | AACTG others(2050): Show |
chr11 | 1747755 | 1768927 |
| a0001c0004t0002 | 0/0 | 2055 | 7 | 6 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | AACTG others(2050): Show |
chr11 | 1747755 | 1768927 |
| a0001c0005t0002 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | AACTG others(2050): Show |
chr11 | 1747755 | 1768927 |
| a0001c0005t0014 | 0/0 | 2055 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | AACTG others(2050): Show |
chr11 | 1747755 | 1768927 |
| a0001c0006t0001 | 0/0 | 2055 | 2 | 0 | 2 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | AACTG others(2050): Show |
chr11 | 1747755 | 1768927 |
| a0002c0003t0002 | 0/0 | 2055 | 14 | 1 | 8 | 1 | 0 | 4 | CTSD_chr11_1747755_1768927 | CTSD | AACTG others(2050): Show |
chr11 | 1747755 | 1768927 |
| a0002c0003t0003 | 0/0 | 2055 | 2 | 2 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | AACTG others(2050): Show |
chr11 | 1747755 | 1768927 |
| a0002c0003t0017 | 0/0 | 2055 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | AACTG others(2050): Show |
chr11 | 1747755 | 1768927 |
| a0003c0008t0001 | 0/0 | 2055 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | AACTG others(2050): Show |
chr11 | 1747755 | 1768927 |
| a0004c0007t0001 | 0/0 | 2055 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | AACTG others(2050): Show |
chr11 | 1747755 | 1768927 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 30 | 0 | 9 | 18 | 0 | 3 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0002 | 0/0 | 28 | 1 | 1 | 13 | 4 | 9 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0003 | 1/0 | 22 | 12 | 5 | 1 | 0 | 3 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0004 | 0/0 | 13 | 0 | 5 | 5 | 0 | 3 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0005 | 0/0 | 11 | 11 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0007 | 0/0 | 8 | 0 | 1 | 6 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0009 | 0/0 | 7 | 0 | 2 | 0 | 3 | 2 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0010 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0012 | 0/0 | 6 | 0 | 4 | 2 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0013 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0014 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0016 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0017 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0018 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0020 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0024 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0026 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0029 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0031 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0033 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0038 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0052 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0002g0006 | 0/0 | 9 | 0 | 1 | 7 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0002g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0002g0040 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0002g0053 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0002g0079 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0003g0019 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0004g0030 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0005g0025 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0005g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0006g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0006g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0007g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0007g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0008g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0009g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0011g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0012g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0013g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0001t0015g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0002t0001g0008 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0002t0001g0032 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0002t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0002t0010g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0002t0016g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0004t0002g0011 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0005t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0005t0014g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0001c0006t0001g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0002c0003t0002g0015 | 0/0 | 5 | 1 | 2 | 1 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0002c0003t0002g0021 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0002c0003t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0002c0003t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0002c0003t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0002c0003t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0002c0003t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0002c0003t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0002c0003t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0002c0003t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0002c0003t0017g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0003c0008t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| a0004c0007t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | GBR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0102 | EUR | FIN | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0053 | EUR | FIN | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0114 | EUR | FIN | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG00408 | hp2 | a0001 | c0002 | t0010 | g0143 | EAS | CHS | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0072 | EAS | CHS | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG00609 | hp2 | a0001 | c0001 | t0013 | g0117 | EAS | CHS | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG00733 | hp2 | a0001 | c0001 | t0012 | g0088 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0067 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG00741 | hp2 | a0002 | c0003 | t0002 | g0021 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0019 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01070 | hp2 | a0002 | c0003 | t0002 | g0015 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01071 | hp1 | a0002 | c0003 | t0002 | g0015 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0019 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01074 | hp1 | a0001 | c0001 | t0005 | g0101 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01074 | hp2 | a0001 | c0001 | t0005 | g0025 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01081 | hp1 | a0002 | c0003 | t0002 | g0021 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01168 | hp2 | a0001 | c0006 | t0001 | g0051 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0019 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01169 | hp2 | a0001 | c0006 | t0001 | g0051 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01175 | hp2 | a0002 | c0003 | t0002 | g0060 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01261 | hp1 | a0002 | c0003 | t0002 | g0058 | AMR | CLM | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01346 | hp2 | a0001 | c0004 | t0002 | g0011 | AMR | CLM | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01361 | hp1 | a0002 | c0003 | t0002 | g0063 | AMR | CLM | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0019 | AMR | CLM | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01433 | hp1 | a0002 | c0003 | t0002 | g0059 | AMR | CLM | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0082 | EUR | IBS | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0078 | EUR | IBS | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0100 | AMR | PEL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02027 | hp1 | a0002 | c0003 | t0002 | g0015 | EAS | KHV | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | KHV | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | KHV | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02083 | hp2 | a0003 | c0008 | t0001 | g0141 | EAS | KHV | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02132 | hp1 | a0001 | c0001 | t0008 | g0085 | EAS | KHV | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | KHV | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | KHV | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CDX | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CDX | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0030 | AFR | ACB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0030 | AFR | ACB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02273 | hp1 | a0001 | c0001 | t0005 | g0025 | AMR | PEL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02280 | hp1 | a0002 | c0003 | t0003 | g0064 | AFR | ACB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | KHV | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02683 | hp1 | a0001 | c0001 | t0005 | g0025 | SAS | PJL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02683 | hp2 | a0002 | c0003 | t0002 | g0021 | SAS | PJL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02809 | hp2 | a0001 | c0004 | t0002 | g0011 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0030 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02886 | hp2 | a0001 | c0004 | t0002 | g0011 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02965 | hp1 | a0001 | c0005 | t0002 | g0056 | AFR | ESN | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02970 | hp1 | a0001 | c0004 | t0002 | g0011 | AFR | ESN | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ESN | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02976 | hp2 | a0002 | c0003 | t0003 | g0065 | AFR | ESN | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG03041 | hp1 | a0001 | c0004 | t0002 | g0011 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | MSL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ESN | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0138 | AFR | MSL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | MSL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | MSL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG03239 | hp1 | a0001 | c0005 | t0014 | g0160 | SAS | PJL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0139 | AFR | MSL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0106 | SAS | PJL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG03516 | hp1 | a0001 | c0004 | t0002 | g0011 | AFR | ESN | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | STU | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG03704 | hp1 | a0002 | c0003 | t0017 | g0166 | SAS | PJL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | BEB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | BEB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG03927 | hp1 | a0002 | c0003 | t0002 | g0062 | SAS | BEB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | BEB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG03942 | hp2 | a0002 | c0003 | t0002 | g0015 | SAS | BEB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | BEB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | BEB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | STU | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0077 | SAS | STU | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG04204 | hp2 | a0002 | c0003 | t0002 | g0061 | SAS | STU | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | STU | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | STU | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | YRI | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | YRI | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CHB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18747 | hp1 | a0001 | c0002 | t0016 | g0165 | EAS | CHB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | CHB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | YRI | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18950 | hp1 | a0001 | c0001 | t0006 | g0090 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18953 | hp1 | a0004 | c0007 | t0001 | g0054 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18967 | hp2 | a0001 | c0001 | t0015 | g0164 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18977 | hp2 | a0001 | c0001 | t0006 | g0022 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18978 | hp2 | a0001 | c0001 | t0007 | g0091 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18983 | hp2 | a0001 | c0001 | t0006 | g0022 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA19005 | hp2 | a0001 | c0001 | t0006 | g0022 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | LWK | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | LWK | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA19043 | hp2 | a0001 | c0001 | t0011 | g0108 | AFR | LWK | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA19058 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA19082 | hp2 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA19084 | hp2 | a0001 | c0001 | t0007 | g0086 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA20129 | hp1 | a0001 | c0001 | t0009 | g0057 | AFR | ASW | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ASW | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0099 | EUR | TSI | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0097 | EUR | TSI | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | GIH | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02559 | hp1 | a0001 | c0004 | t0002 | g0011 | AFR | ACB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0116 | AFR | ACB | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | USA | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| HG06807 | hp2 | a0002 | c0003 | t0002 | g0015 | AFR | USA | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | USA | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | USA | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | LWK | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | LWK | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0079 | REF | REF | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0003 | REF | REF | CTSD_chr11_1747755_1768927 | CTSD | chr11 | 1747755 | 1768927 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:1754040 | C | T | 1 | a0003 | 1 | HG02083.hp2 | missense_variant | MODERATE | c.926G>A | p.Arg309His | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 7/9 | 994/2055 | 926/1239 | 309/412 | chr11 | 1754040 | |||
| chr11:1761364 | G | A | 1 | a0002 | 17 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(14): Show |
missense_variant | MODERATE | c.173C>T | p.Ala58Val | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 2/9 | 241/2055 | 173/1239 | 58/412 | chr11 | 1761364 | |||
| chr11:1763846 | C | G | 1 | a0004 | 1 | NA18953.hp1 | missense_variant | MODERATE | c.14G>C | p.Ser5Thr | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/9 | 82/2055 | 14/1239 | 5/412 | chr11 | 1763846 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:1753527 | G | T | 1 | a0001c0006 | 2 | HG01168.hp2 HG01169.hp2 |
synonymous_variant | LOW | c.1215C>A | p.Gly405Gly | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 9/9 | 1283/2055 | 1215/1239 | 405/412 | chr11 | 1753527 | |||
| chr11:1754015 | G | A | 1 | a0001c0002 | 18 | HG00408.hp2 HG02056.hp1 HG02135.hp1 others(15): Show |
synonymous_variant | LOW | c.951C>T | p.Ala317Ala | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 7/9 | 1019/2055 | 951/1239 | 317/412 | chr11 | 1754015 | |||
| chr11:1758975 | A | G | 3 | a0001c0004 a0001c0005 a0002c0003 |
26 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(23): Show |
synonymous_variant | LOW | c.465T>C | p.Thr155Thr | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 4/9 | 533/2055 | 465/1239 | 155/412 | chr11 | 1758975 | |||
| chr11:1759637 | G | A | 1 | a0002c0003 | 17 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(14): Show |
splice_region_variant&synonymous_variant | LOW | c.231C>T | p.Ala77Ala | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 3/9 | 299/2055 | 231/1239 | 77/412 | chr11 | 1759637 | |||
| chr11:1761348 | G | A | 1 | a0001c0004 | 7 | HG01346.hp2 HG02559.hp1 HG02809.hp2 others(4): Show |
synonymous_variant | LOW | c.189C>T | p.Thr63Thr | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 2/9 | 257/2055 | 189/1239 | 63/412 | chr11 | 1761348 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:1752849 | G | A | 1 | a0001c0001t0006 | 4 | NA18950.hp1 NA18977.hp2 NA18983.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*654C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 9/9 | 654 | chr11 | 1752849 | ||||||
| chr11:1752906 | T | G | 8 | a0001c0001t0002 a0001c0001t0012 a0001c0001t0013 others(5): Show |
48 | HG00323.hp1 HG00609.hp2 HG00733.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*597A>C | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 9/9 | 597 | chr11 | 1752906 | ||||||
| chr11:1753100 | G | A | 1 | a0001c0001t0007 | 2 | NA18978.hp2 NA19084.hp2 |
3_prime_UTR_variant | MODIFIER | c.*403C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 9/9 | 403 | chr11 | 1753100 | ||||||
| chr11:1753203 | C | T | 1 | a0001c0001t0004 | 5 | HG02257.hp2 HG02258.hp2 HG02818.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*300G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 9/9 | 300 | chr11 | 1753203 | ||||||
| chr11:1753209 | C | G | 1 | a0001c0001t0011 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*294G>C | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 9/9 | 294 | chr11 | 1753209 | ||||||
| chr11:1753227 | G | A | 1 | a0001c0001t0013 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*276C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 9/9 | 276 | chr11 | 1753227 | ||||||
| chr11:1753290 | GGA | G | 1 | a0001c0001t0005 | 4 | HG01074.hp1 HG01074.hp2 HG02273.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*211_*212delTC | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 9/9 | 211 | chr11 | 1753290 | ||||||
| chr11:1753293 | G | C | 1 | a0001c0005t0014 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*210C>G | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 9/9 | 210 | chr11 | 1753293 | ||||||
| chr11:1753359 | C | T | 1 | a0001c0002t0010 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*144G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 9/9 | 144 | chr11 | 1753359 | ||||||
| chr11:1753436 | T | C | 9 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0013 others(6): Show |
57 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*67A>G | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 9/9 | 67 | chr11 | 1753436 | ||||||
| chr11:1753484 | C | T | 1 | a0001c0001t0009 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*19G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 9/9 | 19 | chr11 | 1753484 | ||||||
| chr11:1753492 | C | T | 1 | a0001c0001t0008 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 9/9 | 11 | chr11 | 1753492 | ||||||
| chr11:1763862 | C | A | 1 | a0001c0001t0015 | 1 | NA18967.hp2 | 5_prime_UTR_variant | MODIFIER | c.-3G>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/9 | 3 | chr11 | 1763862 | ||||||
| chr11:1763891 | G | A | 1 | a0001c0002t0016 | 1 | NA18747.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-32C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/9 | chr11 | 1763891 | |||||||
| chr11:1763912 | G | A | 1 | a0002c0003t0017 | 1 | HG03704.hp1 | 5_prime_UTR_variant | MODIFIER | c.-53C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/9 | 53 | chr11 | 1763912 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:1753677 | C | T | 1 | a0001c0001t0002g0053 | 2 | HG00323.hp1 HG01069.hp2 |
splice_region_variant&intron_variant | LOW | c.1072-7G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 8/8 | chr11 | 1753677 | |||||||
| chr11:1753704 | A | G | 14 | a0001c0001t0002g0053 a0001c0004t0002g0011 a0001c0005t0002g0056 others(11): Show |
27 | HG00323.hp1 HG00741.hp2 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.1072-34T>C | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 8/8 | chr11 | 1753704 | |||||||
| chr11:1753711 | C | G | 1 | a0001c0001t0001g0045 | 2 | NA18949.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1072-41G>C | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 8/8 | chr11 | 1753711 | |||||||
| chr11:1753714 | G | GC | 12 | a0001c0001t0001g0034 a0001c0001t0001g0071 a0001c0001t0001g0094 others(9): Show |
14 | HG00558.hp2 HG01109.hp1 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.1072-45dupG | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 8/8 | chr11 | 1753714 | |||||||
| chr11:1753796 | C | T | 1 | a0001c0001t0002g0100 | 1 | HG01993.hp2 | splice_region_variant&intron_variant | LOW | c.1071+7G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 8/8 | chr11 | 1753796 | |||||||
| chr11:1754155 | C | T | 12 | a0001c0001t0001g0146 a0001c0001t0002g0053 a0001c0001t0005g0101 others(9): Show |
19 | HG00323.hp1 HG00741.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.828-17G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754155 | |||||||
| chr11:1754212 | A | C | 1 | a0001c0001t0001g0122 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.828-74T>G | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754212 | |||||||
| chr11:1754348 | T | TGAGGGGC others(64): Show |
1 | a0001c0001t0001g0050 | 2 | NA18949.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.828-281_828-211dup others(71): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754348 | |||||||
| chr11:1754348 | T | TGAGGGGC others(161): Show |
1 | a0001c0001t0001g0093 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.828-211_828-210ins others(168): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754348 | |||||||
| chr11:1754348 | T | TGAGGGGC others(74): Show |
1 | a0001c0001t0001g0126 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.828-211_828-210ins others(81): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754348 | |||||||
| chr11:1754348 | T | TGAGGGGC others(91): Show |
16 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0047 others(13): Show |
34 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.828-211_828-210ins others(98): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754348 | |||||||
| chr11:1754348 | T | TGAGGGGC others(162): Show |
1 | a0001c0001t0001g0161 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.828-211_828-210ins others(169): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754348 | |||||||
| chr11:1754358 | G | GGAGGGAT others(20): Show |
2 | a0001c0001t0001g0052 a0001c0001t0002g0100 |
3 | HG01993.hp2 HG02300.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.828-247_828-221dup others(27): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754358 | |||||||
| chr11:1754358 | G | GGAGGGAT others(47): Show |
1 | a0001c0001t0001g0151 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.828-221_828-220ins others(54): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754358 | |||||||
| chr11:1754358 | GGAGGGAT others(20): Show |
G | 1 | a0001c0001t0003g0106 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.828-247_828-221del others(27): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754358 | |||||||
| chr11:1754380 | G | C | 1 | a0001c0001t0004g0139 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.828-242C>G | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754380 | |||||||
| chr11:1754382 | C | CATGGAGG others(78): Show |
1 | a0001c0001t0002g0116 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.828-245_828-244ins others(85): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754382 | |||||||
| chr11:1754385 | A | G | 1 | a0001c0001t0002g0116 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.828-247T>C | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754385 | |||||||
| chr11:1754396 | G | GGGGATGG others(11): Show |
1 | a0002c0003t0002g0058 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.828-259_828-258ins others(18): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754396 | |||||||
| chr11:1754405 | G | GGGGCATA others(126): Show |
1 | a0001c0001t0001g0041 | 2 | HG02071.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.828-268_828-267ins others(133): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754405 | |||||||
| chr11:1754405 | G | GGGGCATA others(251): Show |
4 | a0001c0001t0001g0013 a0001c0001t0001g0128 a0001c0001t0001g0142 others(1): Show |
9 | HG02129.hp2 HG02165.hp2 NA18940.hp2 others(6): Show |
intron_variant | MODIFIER | c.828-268_828-267ins others(258): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754405 | |||||||
| chr11:1754410 | T | TG | 5 | a0001c0001t0001g0013 a0001c0001t0001g0041 a0001c0001t0001g0128 others(2): Show |
11 | HG02071.hp2 HG02129.hp2 HG02165.hp2 others(8): Show |
intron_variant | MODIFIER | c.828-273dupC | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754410 | |||||||
| chr11:1754412 | AAGGGATG others(19): Show |
A | 2 | a0001c0001t0001g0107 a0001c0001t0001g0109 |
2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.828-300_828-275del others(26): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754412 | |||||||
| chr11:1754426 | C | CATGGAGG others(335): Show |
1 | a0002c0003t0002g0060 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.828-289_828-288ins others(342): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754426 | |||||||
| chr11:1754431 | A | AGGGATGG others(137): Show |
1 | a0001c0001t0001g0002 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.828-294_828-293ins others(144): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754431 | |||||||
| chr11:1754441 | G | GGATGGAG others(146): Show |
1 | a0001c0001t0007g0091 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.828-304_828-303ins others(153): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754441 | |||||||
| chr11:1754481 | G | GAGAGTCA others(138): Show |
1 | a0001c0001t0001g0073 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.828-344_828-343ins others(145): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754481 | |||||||
| chr11:1754490 | A | AGAGGGAT others(9): Show |
1 | a0001c0001t0001g0105 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.828-368_828-353dup others(16): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754490 | |||||||
| chr11:1754490 | A | AGAGGGAT others(17): Show |
1 | a0001c0001t0001g0148 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.828-376_828-353dup others(24): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754490 | |||||||
| chr11:1754492 | A | AGGGATGT others(26): Show |
2 | a0001c0001t0001g0023 a0001c0001t0001g0104 |
4 | HG03654.hp2 NA18962.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.827+381_828-355dup others(33): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754492 | |||||||
| chr11:1754499 | T | A | 1 | a0001c0001t0001g0087 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.828-361A>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754499 | |||||||
| chr11:1754499 | T | TGGGGATG others(18): Show |
3 | a0001c0001t0001g0038 a0001c0001t0001g0128 a0001c0001t0011g0108 |
4 | HG01943.hp2 NA18522.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.827+382_828-362dup others(25): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754499 | |||||||
| chr11:1754499 | T | TGGGGATG others(172): Show |
1 | a0001c0001t0001g0095 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.828-362_828-361ins others(179): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754499 | |||||||
| chr11:1754499 | T | TGGGGATG others(626): Show |
1 | a0001c0001t0001g0152 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.828-362_828-361ins others(633): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754499 | |||||||
| chr11:1754500 | G | GGGGATGG others(347): Show |
1 | a0001c0001t0001g0123 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.828-363_828-362ins others(354): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754500 | |||||||
| chr11:1754507 | G | T | 1 | a0001c0005t0014g0160 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.828-369C>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754507 | |||||||
| chr11:1754508 | A | AGGGATGG others(18): Show |
3 | a0001c0001t0001g0003 a0001c0001t0001g0111 a0001c0001t0009g0057 |
3 | HG01884.hp1 HG02572.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.828-371_828-370ins others(25): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754508 | |||||||
| chr11:1754508 | A | AGGGATGG others(122): Show |
1 | a0001c0001t0001g0003 | 2 | HG01109.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.828-371_828-370ins others(129): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754508 | |||||||
| chr11:1754508 | A | G | 1 | a0001c0005t0014g0160 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.828-370T>C | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754508 | |||||||
| chr11:1754516 | A | AGGGATGG others(122): Show |
1 | a0001c0001t0001g0070 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.828-379_828-378ins others(129): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754516 | |||||||
| chr11:1754524 | AG | A | 8 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0034 others(5): Show |
15 | HG00323.hp2 HG01106.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.827+381delC | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754524 | |||||||
| chr11:1754525 | G | GGGATGGA others(17): Show |
1 | a0001c0001t0001g0005 | 3 | HG01891.hp2 HG02965.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.827+380_827+381ins others(24): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754525 | |||||||
| chr11:1754525 | G | GGGATGGA others(148): Show |
2 | a0001c0001t0002g0006 a0001c0001t0002g0039 |
5 | HG02135.hp2 NA18952.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.827+380_827+381ins others(155): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754525 | |||||||
| chr11:1754525 | G | GGGATGGA others(224): Show |
1 | a0001c0001t0001g0009 | 2 | HG00741.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.827+380_827+381ins others(231): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754525 | |||||||
| chr11:1754525 | G | GGGGATGG others(26): Show |
1 | a0001c0001t0001g0004 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.827+348_827+380dup others(33): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754525 | |||||||
| chr11:1754525 | G | GGGGATGG others(232): Show |
1 | a0001c0001t0001g0137 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.827+380_827+381ins others(239): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754525 | |||||||
| chr11:1754525 | G | GGGGATGT others(9): Show |
3 | a0001c0001t0001g0003 a0001c0001t0001g0089 a0001c0001t0003g0102 |
3 | HG00280.hp2 HG00642.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.827+380_827+381ins others(16): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754525 | |||||||
| chr11:1754525 | G | GGGGATGT others(17): Show |
44 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(41): Show |
126 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.827+380_827+381ins others(24): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754525 | |||||||
| chr11:1754525 | G | GGGGATGT others(25): Show |
1 | a0001c0001t0002g0116 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.827+380_827+381ins others(32): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754525 | |||||||
| chr11:1754525 | G | GGGGATGT others(33): Show |
1 | a0001c0001t0001g0002 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.827+380_827+381ins others(40): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754525 | |||||||
| chr11:1754525 | G | GGGGATGT others(34): Show |
3 | a0001c0001t0001g0007 a0001c0001t0001g0071 a0001c0001t0001g0075 |
4 | NA18612.hp1 NA18997.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.827+380_827+381ins others(41): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754525 | |||||||
| chr11:1754525 | G | GGGGATGT others(59): Show |
1 | a0001c0001t0001g0016 | 5 | NA18612.hp2 NA18945.hp1 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.827+380_827+381ins others(66): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754525 | |||||||
| chr11:1754525 | G | GGGGATGT others(141): Show |
1 | a0001c0001t0001g0005 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.827+380_827+381ins others(148): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754525 | |||||||
| chr11:1754525 | G | GGGGATGT others(137): Show |
1 | a0001c0001t0001g0001 | 2 | NA19079.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.827+380_827+381ins others(144): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754525 | |||||||
| chr11:1754525 | G | GGGGATGT others(190): Show |
1 | a0001c0001t0001g0133 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.827+380_827+381ins others(197): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754525 | |||||||
| chr11:1754525 | G | GGGGATGT others(145): Show |
1 | a0001c0001t0001g0018 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.827+380_827+381ins others(152): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754525 | |||||||
| chr11:1754525 | G | GGGGATGT others(178): Show |
1 | a0002c0003t0002g0021 | 3 | HG00741.hp2 HG01081.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.827+380_827+381ins others(185): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754525 | |||||||
| chr11:1754525 | G | GGGGATGT others(121): Show |
2 | a0001c0001t0001g0007 a0001c0001t0001g0163 |
5 | HG01496.hp1 HG04199.hp1 NA18942.hp2 others(2): Show |
intron_variant | MODIFIER | c.827+380_827+381ins others(128): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754525 | |||||||
| chr11:1754525 | G | GGGGATGT others(303): Show |
1 | a0001c0001t0001g0007 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.827+380_827+381ins others(310): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754525 | |||||||
| chr11:1754525 | G | GGGGATGT others(67): Show |
1 | a0001c0001t0001g0119 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.827+380_827+381ins others(74): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754525 | |||||||
| chr11:1754525 | G | GGGGATGT others(50): Show |
1 | a0001c0001t0001g0158 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.827+380_827+381ins others(57): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754525 | |||||||
| chr11:1754525 | G | GGGGATGT others(92): Show |
1 | a0001c0001t0001g0080 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.827+380_827+381ins others(99): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754525 | |||||||
| chr11:1754525 | G | GGGGATGT others(51): Show |
1 | a0001c0001t0001g0157 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.827+380_827+381ins others(58): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754525 | |||||||
| chr11:1754525 | G | GGGGATGT others(52): Show |
1 | a0001c0001t0001g0156 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.827+380_827+381ins others(59): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754525 | |||||||
| chr11:1754525 | GGGGATGG others(1): Show |
G | 5 | a0001c0001t0001g0036 a0001c0001t0002g0040 a0001c0002t0001g0032 others(2): Show |
8 | HG02056.hp1 HG02074.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.827+373_827+380del others(8): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754525 | |||||||
| chr11:1754532 | G | T | 5 | a0001c0001t0001g0017 a0001c0001t0001g0093 a0001c0001t0001g0140 others(2): Show |
10 | HG01243.hp1 HG03490.hp1 HG03492.hp2 others(7): Show |
intron_variant | MODIFIER | c.827+374C>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754532 | |||||||
| chr11:1754533 | A | AG | 59 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(56): Show |
176 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.827+372dupC | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754533 | |||||||
| chr11:1754533 | A | AGGGATGG others(10): Show |
2 | a0001c0001t0001g0089 a0001c0001t0001g0121 |
2 | HG02886.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.827+356_827+372dup others(17): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754533 | |||||||
| chr11:1754533 | A | AGGGATGG others(85): Show |
4 | a0001c0001t0001g0012 a0001c0001t0001g0076 a0001c0001t0001g0112 others(1): Show |
9 | HG00408.hp1 HG01346.hp1 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.827+372_827+373ins others(92): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754533 | |||||||
| chr11:1754533 | A | AGGGATGG others(129): Show |
1 | a0002c0003t0002g0058 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.827+372_827+373ins others(136): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754533 | |||||||
| chr11:1754533 | A | AGGGATGG others(104): Show |
1 | a0002c0003t0002g0061 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.827+372_827+373ins others(111): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754533 | |||||||
| chr11:1754533 | A | AGGGATGG others(88): Show |
1 | a0001c0001t0004g0138 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.827+372_827+373ins others(95): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754533 | |||||||
| chr11:1754533 | A | AGGGATGG others(122): Show |
1 | a0001c0001t0001g0130 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.827+372_827+373ins others(129): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754533 | |||||||
| chr11:1754533 | A | AGGGATGG others(35): Show |
1 | a0001c0001t0001g0126 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.827+372_827+373ins others(42): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754533 | |||||||
| chr11:1754533 | A | AGGGATGG others(138): Show |
1 | a0001c0001t0012g0088 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.827+372_827+373ins others(145): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754533 | |||||||
| chr11:1754533 | A | AGGGATGG others(134): Show |
1 | a0001c0001t0001g0154 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.827+372_827+373ins others(141): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754533 | |||||||
| chr11:1754533 | A | AGGGATGG others(139): Show |
1 | a0002c0003t0003g0064 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.827+372_827+373ins others(146): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754533 | |||||||
| chr11:1754533 | A | AGGGATGG others(146): Show |
5 | a0001c0001t0002g0053 a0002c0003t0002g0015 a0002c0003t0002g0059 others(2): Show |
10 | HG00323.hp1 HG01069.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.827+372_827+373ins others(153): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754533 | |||||||
| chr11:1754533 | A | AGGGATGG others(114): Show |
1 | a0001c0001t0003g0072 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.827+372_827+373ins others(121): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754533 | |||||||
| chr11:1754533 | A | AGGGATGG others(225): Show |
1 | a0001c0001t0001g0134 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.827+372_827+373ins others(232): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754533 | |||||||
| chr11:1754533 | A | AGGGATGG others(130): Show |
4 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0103 others(1): Show |
6 | HG02109.hp1 HG02630.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.827+372_827+373ins others(137): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754533 | |||||||
| chr11:1754533 | A | AGGGATGG others(138): Show |
1 | a0001c0001t0001g0136 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.827+372_827+373ins others(145): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754533 | |||||||
| chr11:1754533 | A | AGGGATGG others(155): Show |
1 | a0001c0001t0001g0120 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.827+372_827+373ins others(162): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754533 | |||||||
| chr11:1754533 | A | AGGGATGG others(336): Show |
1 | a0001c0001t0001g0135 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.827+372_827+373ins others(343): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754533 | |||||||
| chr11:1754533 | A | G | 5 | a0001c0001t0001g0017 a0001c0001t0001g0093 a0001c0001t0001g0140 others(2): Show |
10 | HG01243.hp1 HG03490.hp1 HG03492.hp2 others(7): Show |
intron_variant | MODIFIER | c.827+373T>C | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754533 | |||||||
| chr11:1754541 | A | AGGGATGG others(2): Show |
3 | a0001c0001t0001g0055 a0001c0001t0001g0147 a0001c0001t0001g0153 |
3 | NA18953.hp2 NA18954.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.827+356_827+364dup others(9): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754541 | |||||||
| chr11:1754544 | GATGGAGG others(18): Show |
G | 1 | a0001c0005t0002g0056 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.827+337_827+361del others(25): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754544 | |||||||
| chr11:1754549 | A | AGGGGATG others(27): Show |
1 | a0001c0001t0001g0004 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.827+356_827+357ins others(34): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754549 | |||||||
| chr11:1754550 | G | GGGATGGA others(153): Show |
1 | a0002c0003t0017g0166 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.827+355_827+356ins others(160): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754550 | |||||||
| chr11:1754550 | G | GGGGATGG others(18): Show |
1 | a0001c0001t0001g0029 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.827+355_827+356ins others(25): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754550 | |||||||
| chr11:1754552 | G | GATGGAGG others(18): Show |
1 | a0001c0002t0001g0046 | 2 | NA18947.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.827+353_827+354ins others(25): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754552 | |||||||
| chr11:1754552 | G | GATGGAGG others(35): Show |
2 | a0001c0001t0001g0017 a0001c0001t0001g0093 |
4 | NA19011.hp1 NA19082.hp1 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.827+353_827+354ins others(42): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754552 | |||||||
| chr11:1754559 | GGGATGGA others(29): Show |
G | 1 | a0001c0001t0001g0140 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.827+311_827+346del others(36): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754559 | |||||||
| chr11:1754561 | G | A | 1 | a0001c0005t0014g0160 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.827+345C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754561 | |||||||
| chr11:1754561 | G | GATGGAGG others(34): Show |
1 | a0001c0001t0001g0003 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.827+344_827+345ins others(41): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754561 | |||||||
| chr11:1754561 | G | GATGGAGG others(118): Show |
1 | a0001c0004t0002g0011 | 6 | HG01346.hp2 HG02559.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.827+344_827+345ins others(125): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754561 | |||||||
| chr11:1754561 | G | GATGGAGG others(176): Show |
1 | a0001c0004t0002g0011 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.827+344_827+345ins others(183): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754561 | |||||||
| chr11:1754597 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.827+309C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754597 | |||||||
| chr11:1754602 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.827+304T>C | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754602 | |||||||
| chr11:1754603 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.827+303C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754603 | |||||||
| chr11:1754612 | GGGGATGG others(10): Show |
G | 2 | a0001c0001t0001g0035 a0004c0007t0001g0054 |
3 | HG00438.hp2 NA18953.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.827+277_827+293del others(17): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754612 | |||||||
| chr11:1754621 | G | C | 1 | a0001c0005t0014g0160 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.827+285C>G | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754621 | |||||||
| chr11:1754638 | C | T | 1 | a0001c0001t0002g0115 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.827+268G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754638 | |||||||
| chr11:1754736 | TGGAGGGG others(3): Show |
T | 1 | a0001c0001t0001g0129 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.827+160_827+169del others(10): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754736 | |||||||
| chr11:1754855 | C | T | 1 | a0001c0001t0005g0101 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.827+51G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754855 | |||||||
| chr11:1754858 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.827+48G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754858 | |||||||
| chr11:1754859 | G | A | 1 | a0002c0003t0002g0063 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.827+47C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754859 | |||||||
| chr11:1754859 | G | GC | 6 | a0001c0001t0001g0092 a0001c0001t0001g0096 a0001c0001t0001g0124 others(3): Show |
6 | HG03098.hp2 HG03654.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.827+46dupG | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754859 | |||||||
| chr11:1754865 | G | A | 13 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0110 others(10): Show |
17 | HG02109.hp1 HG02257.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.827+41C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754865 | |||||||
| chr11:1754882 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.827+24C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 6/8 | chr11 | 1754882 | |||||||
| chr11:1755049 | T | A | 1 | a0001c0001t0002g0027 | 3 | NA18983.hp1 NA19011.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.705-21A>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1755049 | |||||||
| chr11:1755102 | G | A | 22 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(19): Show |
61 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.705-74C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1755102 | |||||||
| chr11:1755417 | G | C | 29 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0020 others(26): Show |
58 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.705-389C>G | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1755417 | |||||||
| chr11:1755510 | G | A | 7 | a0001c0001t0001g0007 a0001c0001t0001g0070 a0001c0001t0001g0071 others(4): Show |
14 | HG00558.hp1 HG01496.hp1 HG03927.hp2 others(11): Show |
intron_variant | MODIFIER | c.705-482C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1755510 | |||||||
| chr11:1755609 | T | G | 1 | a0001c0005t0002g0056 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.705-581A>C | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1755609 | |||||||
| chr11:1755703 | C | T | 1 | a0001c0001t0001g0024 | 3 | HG00639.hp2 HG01891.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.705-675G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1755703 | |||||||
| chr11:1755715 | C | A | 1 | a0001c0005t0014g0160 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.705-687G>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1755715 | |||||||
| chr11:1755806 | T | C | 3 | a0001c0001t0001g0097 a0001c0001t0001g0154 a0001c0001t0001g0155 |
3 | HG00438.hp1 HG04184.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.705-778A>G | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1755806 | |||||||
| chr11:1755807 | T | C | 12 | a0001c0005t0014g0160 a0002c0003t0002g0015 a0002c0003t0002g0021 others(9): Show |
18 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.705-779A>G | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1755807 | |||||||
| chr11:1755890 | C | T | 1 | a0003c0008t0001g0141 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.705-862G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1755890 | |||||||
| chr11:1755978 | G | A | 12 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0132 others(9): Show |
16 | HG02109.hp1 HG02257.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.705-950C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1755978 | |||||||
| chr11:1756082 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.705-1054A>G | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1756082 | |||||||
| chr11:1756109 | C | CGTGTGCC others(25): Show |
1 | a0001c0001t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.705-1113_705-1082d others(34): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1756109 | |||||||
| chr11:1756124 | C | G | 2 | a0002c0003t0003g0064 a0002c0003t0003g0065 |
2 | HG02280.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.705-1096G>C | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1756124 | |||||||
| chr11:1756139 | G | GCTGTGTG others(26): Show |
1 | a0001c0001t0001g0114 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.705-1144_705-1112d others(35): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1756139 | |||||||
| chr11:1756196 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.704+1128C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1756196 | |||||||
| chr11:1756277 | G | A | 1 | a0001c0001t0001g0037 | 2 | NA18981.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.704+1047C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1756277 | |||||||
| chr11:1756285 | C | T | 1 | a0001c0004t0002g0011 | 7 | HG01346.hp2 HG02559.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.704+1039G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1756285 | |||||||
| chr11:1756587 | G | A | 28 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0033 others(25): Show |
54 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.704+737C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1756587 | |||||||
| chr11:1756636 | T | C | 74 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0013 others(71): Show |
139 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(136): Show |
intron_variant | MODIFIER | c.704+688A>G | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1756636 | |||||||
| chr11:1756728 | A | T | 2 | a0001c0005t0002g0056 a0001c0005t0014g0160 |
2 | HG02965.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.704+596T>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1756728 | |||||||
| chr11:1756739 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.704+585G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1756739 | |||||||
| chr11:1756740 | G | A | 1 | a0001c0005t0014g0160 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.704+584C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1756740 | |||||||
| chr11:1756745 | C | T | 2 | a0002c0003t0002g0059 a0002c0003t0002g0060 |
2 | HG01175.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.704+579G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1756745 | |||||||
| chr11:1756807 | G | C | 1 | a0001c0005t0014g0160 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.704+517C>G | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1756807 | |||||||
| chr11:1756861 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.704+463G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1756861 | |||||||
| chr11:1756874 | G | A | 11 | a0002c0003t0002g0015 a0002c0003t0002g0021 a0002c0003t0002g0058 others(8): Show |
17 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.704+450C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1756874 | |||||||
| chr11:1756917 | C | A | 1 | a0001c0004t0002g0011 | 7 | HG01346.hp2 HG02559.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.704+407G>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1756917 | |||||||
| chr11:1756946 | G | A | 11 | a0002c0003t0002g0015 a0002c0003t0002g0021 a0002c0003t0002g0058 others(8): Show |
17 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.704+378C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1756946 | |||||||
| chr11:1757056 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.704+268G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1757056 | |||||||
| chr11:1757091 | C | T | 39 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0013 others(36): Show |
74 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.704+233G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1757091 | |||||||
| chr11:1757141 | C | T | 2 | a0001c0004t0002g0011 a0001c0005t0002g0056 |
8 | HG01346.hp2 HG02559.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.704+183G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1757141 | |||||||
| chr11:1757244 | A | G | 1 | a0001c0001t0001g0146 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.704+80T>C | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1757244 | |||||||
| chr11:1757266 | C | T | 11 | a0002c0003t0002g0015 a0002c0003t0002g0021 a0002c0003t0002g0058 others(8): Show |
17 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.704+58G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 5/8 | chr11 | 1757266 | |||||||
| chr11:1757583 | C | A | 1 | a0001c0001t0009g0057 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.472-27G>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 4/8 | chr11 | 1757583 | |||||||
| chr11:1757589 | A | G | 1 | a0001c0001t0002g0100 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.472-33T>C | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 4/8 | chr11 | 1757589 | |||||||
| chr11:1757655 | C | T | 14 | a0001c0004t0002g0011 a0001c0005t0002g0056 a0001c0005t0014g0160 others(11): Show |
26 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.472-99G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 4/8 | chr11 | 1757655 | |||||||
| chr11:1757717 | C | A | 11 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0044 others(8): Show |
20 | HG02055.hp1 HG02258.hp1 HG02615.hp2 others(17): Show |
intron_variant | MODIFIER | c.472-161G>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 4/8 | chr11 | 1757717 | |||||||
| chr11:1757755 | G | A | 11 | a0002c0003t0002g0015 a0002c0003t0002g0021 a0002c0003t0002g0058 others(8): Show |
17 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.472-199C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 4/8 | chr11 | 1757755 | |||||||
| chr11:1757783 | G | A | 1 | a0001c0001t0001g0099 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.472-227C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 4/8 | chr11 | 1757783 | |||||||
| chr11:1757802 | A | C | 1 | a0001c0005t0014g0160 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.472-246T>G | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 4/8 | chr11 | 1757802 | |||||||
| chr11:1757893 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.472-337C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 4/8 | chr11 | 1757893 | |||||||
| chr11:1757908 | C | T | 56 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(53): Show |
155 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.472-352G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 4/8 | chr11 | 1757908 | |||||||
| chr11:1757975 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.472-419G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 4/8 | chr11 | 1757975 | |||||||
| chr11:1758025 | C | T | 1 | a0001c0001t0001g0080 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.472-469G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 4/8 | chr11 | 1758025 | |||||||
| chr11:1758038 | C | T | 1 | a0001c0001t0001g0042 | 2 | HG02109.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.472-482G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 4/8 | chr11 | 1758038 | |||||||
| chr11:1758344 | C | T | 1 | a0001c0005t0014g0160 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.471+625G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 4/8 | chr11 | 1758344 | |||||||
| chr11:1758503 | G | C | 1 | a0001c0001t0001g0118 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.471+466C>G | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 4/8 | chr11 | 1758503 | |||||||
| chr11:1758534 | C | T | 6 | a0001c0001t0001g0010 a0001c0001t0001g0120 a0001c0001t0001g0121 others(3): Show |
12 | HG02258.hp1 HG02615.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.471+435G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 4/8 | chr11 | 1758534 | |||||||
| chr11:1758538 | C | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0119 |
8 | HG00140.hp1 HG00741.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.471+431G>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 4/8 | chr11 | 1758538 | |||||||
| chr11:1758572 | T | A | 3 | a0001c0001t0004g0030 a0001c0001t0004g0138 a0001c0001t0004g0139 |
5 | HG02257.hp2 HG02258.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.471+397A>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 4/8 | chr11 | 1758572 | |||||||
| chr11:1758588 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.471+381G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 4/8 | chr11 | 1758588 | |||||||
| chr11:1758702 | G | A | 1 | a0001c0005t0014g0160 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.471+267C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 4/8 | chr11 | 1758702 | |||||||
| chr11:1758831 | C | T | 1 | a0001c0001t0001g0033 | 3 | HG02622.hp2 HG02735.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.471+138G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 4/8 | chr11 | 1758831 | |||||||
| chr11:1759104 | G | A | 12 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0132 others(9): Show |
16 | HG02109.hp1 HG02257.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.353-17C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 3/8 | chr11 | 1759104 | |||||||
| chr11:1759464 | G | A | 1 | a0001c0001t0001g0028 | 3 | HG02818.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.352+52C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 3/8 | chr11 | 1759464 | |||||||
| chr11:1759468 | T | C | 2 | a0001c0001t0003g0067 a0001c0005t0014g0160 |
2 | HG00738.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.352+48A>G | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 3/8 | chr11 | 1759468 | |||||||
| chr11:1759474 | A | G | 1 | a0001c0001t0001g0018 | 4 | HG00733.hp1 HG00738.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.352+42T>C | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 3/8 | chr11 | 1759474 | |||||||
| chr11:1759725 | C | CAAGCCCT others(1): Show |
14 | a0001c0004t0002g0011 a0001c0005t0002g0056 a0001c0005t0014g0160 others(11): Show |
26 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.229-87_229-86insCA others(6): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 2/8 | chr11 | 1759725 | |||||||
| chr11:1759785 | C | A | 1 | a0001c0005t0014g0160 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.229-146G>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 2/8 | chr11 | 1759785 | |||||||
| chr11:1759908 | G | C | 1 | a0001c0005t0002g0056 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.229-269C>G | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 2/8 | chr11 | 1759908 | |||||||
| chr11:1760253 | G | A | 1 | a0001c0001t0001g0044 | 2 | HG02647.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.229-614C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 2/8 | chr11 | 1760253 | |||||||
| chr11:1760330 | C | T | 2 | a0001c0001t0001g0163 a0001c0001t0002g0077 |
2 | HG04199.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.229-691G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 2/8 | chr11 | 1760330 | |||||||
| chr11:1760530 | AG | A | 2 | a0001c0004t0002g0011 a0001c0005t0014g0160 |
8 | HG01346.hp2 HG02559.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.228+778delC | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 2/8 | chr11 | 1760530 | |||||||
| chr11:1760534 | G | A | 1 | a0001c0001t0001g0074 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.228+775C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 2/8 | chr11 | 1760534 | |||||||
| chr11:1760560 | T | C | 65 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0013 others(62): Show |
116 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(113): Show |
intron_variant | MODIFIER | c.228+749A>G | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 2/8 | chr11 | 1760560 | |||||||
| chr11:1760578 | T | C | 11 | a0002c0003t0002g0015 a0002c0003t0002g0021 a0002c0003t0002g0058 others(8): Show |
17 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.228+731A>G | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 2/8 | chr11 | 1760578 | |||||||
| chr11:1760651 | T | C | 1 | a0001c0001t0001g0075 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.228+658A>G | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 2/8 | chr11 | 1760651 | |||||||
| chr11:1761066 | G | A | 1 | a0001c0001t0001g0045 | 2 | NA18949.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.228+243C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 2/8 | chr11 | 1761066 | |||||||
| chr11:1761176 | G | C | 14 | a0001c0004t0002g0011 a0001c0005t0002g0056 a0001c0005t0014g0160 others(11): Show |
26 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.228+133C>G | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 2/8 | chr11 | 1761176 | |||||||
| chr11:1761213 | G | A | 2 | a0002c0003t0003g0064 a0002c0003t0003g0065 |
2 | HG02280.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.228+96C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 2/8 | chr11 | 1761213 | |||||||
| chr11:1761278 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.228+31C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 2/8 | chr11 | 1761278 | |||||||
| chr11:1761521 | A | G | 1 | a0001c0005t0002g0056 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.69-53T>C | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1761521 | |||||||
| chr11:1761523 | G | T | 1 | a0002c0003t0002g0058 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.69-55C>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1761523 | |||||||
| chr11:1761531 | T | C | 13 | a0001c0004t0002g0011 a0001c0005t0014g0160 a0002c0003t0002g0015 others(10): Show |
25 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.69-63A>G | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1761531 | |||||||
| chr11:1761649 | C | A | 1 | a0001c0001t0001g0048 | 2 | NA18940.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.69-181G>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1761649 | |||||||
| chr11:1761701 | G | A | 1 | a0003c0008t0001g0141 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.69-233C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1761701 | |||||||
| chr11:1761714 | G | A | 1 | a0001c0001t0001g0142 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.69-246C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1761714 | |||||||
| chr11:1761745 | C | T | 1 | a0001c0004t0002g0011 | 7 | HG01346.hp2 HG02559.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.69-277G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1761745 | |||||||
| chr11:1761822 | T | G | 1 | a0001c0001t0001g0157 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.69-354A>C | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1761822 | |||||||
| chr11:1761869 | G | A | 9 | a0001c0001t0001g0031 a0001c0001t0001g0144 a0001c0002t0001g0008 others(6): Show |
21 | HG00408.hp2 HG02040.hp1 HG02056.hp1 others(18): Show |
intron_variant | MODIFIER | c.69-401C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1761869 | |||||||
| chr11:1761959 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.69-491G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1761959 | |||||||
| chr11:1762030 | C | G | 2 | a0001c0001t0003g0067 a0001c0005t0014g0160 |
2 | HG00738.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.69-562G>C | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1762030 | |||||||
| chr11:1762048 | C | G | 8 | a0001c0001t0001g0007 a0001c0001t0001g0070 a0001c0001t0001g0071 others(5): Show |
15 | HG00558.hp1 HG01496.hp1 HG03927.hp2 others(12): Show |
intron_variant | MODIFIER | c.69-580G>C | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1762048 | |||||||
| chr11:1762186 | G | C | 1 | a0001c0001t0001g0146 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.69-718C>G | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1762186 | |||||||
| chr11:1762208 | C | G | 2 | a0001c0001t0001g0069 a0001c0001t0015g0164 |
2 | HG02132.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.69-740G>C | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1762208 | |||||||
| chr11:1762298 | C | G | 2 | a0001c0001t0001g0047 a0001c0001t0001g0048 |
4 | NA18940.hp1 NA18986.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.69-830G>C | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1762298 | |||||||
| chr11:1762420 | A | AGGAAGCT others(7): Show |
1 | a0001c0002t0001g0068 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.69-966_69-953dupCC others(12): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1762420 | |||||||
| chr11:1762422 | G | A | 1 | a0001c0005t0002g0056 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.69-954C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1762422 | |||||||
| chr11:1762527 | A | G | 14 | a0001c0001t0003g0067 a0001c0004t0002g0011 a0001c0005t0014g0160 others(11): Show |
26 | HG00738.hp2 HG00741.hp2 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.69-1059T>C | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1762527 | |||||||
| chr11:1762529 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.69-1061G>A | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1762529 | |||||||
| chr11:1762562 | G | A | 20 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0047 others(17): Show |
40 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.69-1094C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1762562 | |||||||
| chr11:1762565 | C | G | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | HG02523.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.69-1097G>C | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1762565 | |||||||
| chr11:1762566 | T | G | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | HG02523.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.69-1098A>C | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1762566 | |||||||
| chr11:1762858 | G | C | 1 | a0001c0004t0002g0011 | 7 | HG01346.hp2 HG02559.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.68+934C>G | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1762858 | |||||||
| chr11:1762903 | G | A | 3 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0002g0053 |
4 | HG00323.hp1 HG01069.hp2 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.68+889C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1762903 | |||||||
| chr11:1763070 | A | G | 14 | a0001c0004t0002g0011 a0001c0005t0002g0056 a0001c0005t0014g0160 others(11): Show |
26 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.68+722T>C | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1763070 | |||||||
| chr11:1763207 | C | G | 1 | a0001c0001t0009g0057 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.68+585G>C | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1763207 | |||||||
| chr11:1763217 | G | A | 2 | a0001c0004t0002g0011 a0001c0005t0014g0160 |
8 | HG01346.hp2 HG02559.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.68+575C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1763217 | |||||||
| chr11:1763354 | A | G | 1 | a0001c0001t0001g0014 | 5 | HG01934.hp2 HG01975.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.68+438T>C | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1763354 | |||||||
| chr11:1763364 | G | C | 1 | a0001c0005t0002g0056 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.68+428C>G | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1763364 | |||||||
| chr11:1763541 | C | G | 1 | a0001c0005t0002g0056 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.68+251G>C | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1763541 | |||||||
| chr11:1763646 | C | CGCGCAGG others(3): Show |
1 | a0001c0001t0001g0055 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.68+136_68+145dupCG others(8): Show |
CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1763646 | |||||||
| chr11:1763709 | G | A | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | NA18952.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.68+83C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1763709 | |||||||
| chr11:1763735 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.68+57C>T | CTSD | ENSG00000117984.15 | transcript | ENST00000236671.7 | protein_coding | 1/8 | chr11 | 1763735 |