Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1519 |
| ensemblid | ENSG00000256043.5 |
| hgncid | 2542 |
| symbol | CTSO |
| name | cathepsin O |
| refseq_nuc | NM_001334.3 |
| refseq_prot | NP_001325.1 |
| ensembl_nuc | ENST00000433477.4 |
| ensembl_prot | ENSP00000414904.3 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 155924118 |
| end | 155953866 |
| strand | - |
| ver | v1.2 |
| region | chr4:155924118-155953866 |
| region5000 | chr4:155919118-155958866 |
| regionname0 | CTSO_chr4_155924118_155953866 |
| regionname5000 | CTSO_chr4_155919118_155958866 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 321 | 347 | 79 | 68 | 144 | 10 | 46 | 120 | CTSO_chr4_155919118_155958866 | CTSO | MDVRA others(316): Show |
chr4 | 155919118 | 155958866 |
| a0002 | 0/0 | 321 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | MDVRA others(316): Show |
chr4 | 155919118 | 155958866 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 963 | 341 | 74 | 68 | 143 | 10 | 46 | CTSO_chr4_155919118_155958866 | CTSO | ATGGA others(958): Show |
chr4 | 155919118 | 155958866 | ||
| a0001c0002 | 0/0 | 963 | 3 | 3 | 0 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | ATGGA others(958): Show |
chr4 | 155919118 | 155958866 | ||
| a0001c0003 | 0/0 | 963 | 2 | 2 | 0 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | ATGGA others(958): Show |
chr4 | 155919118 | 155958866 | ||
| a0001c0005 | 0/0 | 963 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | ATGGA others(958): Show |
chr4 | 155919118 | 155958866 | ||
| a0002c0004 | 0/0 | 963 | 1 | 1 | 0 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | ATGGA others(958): Show |
chr4 | 155919118 | 155958866 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2902 | 153 | 13 | 40 | 84 | 4 | 12 | CTSO_chr4_155919118_155958866 | CTSO | AGAGG others(2897): Show |
chr4 | 155919118 | 155958866 |
| a0001c0001t0002 | 0/0 | 2902 | 86 | 11 | 17 | 35 | 3 | 20 | CTSO_chr4_155919118_155958866 | CTSO | AGAGG others(2897): Show |
chr4 | 155919118 | 155958866 |
| a0001c0001t0003 | 0/0 | 2903 | 37 | 27 | 2 | 3 | 1 | 4 | CTSO_chr4_155919118_155958866 | CTSO | AGAGG others(2898): Show |
chr4 | 155919118 | 155958866 |
| a0001c0001t0004 | 0/0 | 2903 | 23 | 14 | 3 | 4 | 0 | 2 | CTSO_chr4_155919118_155958866 | CTSO | AGAGG others(2898): Show |
chr4 | 155919118 | 155958866 |
| a0001c0001t0005 | 0/0 | 2902 | 17 | 1 | 3 | 8 | 1 | 4 | CTSO_chr4_155919118_155958866 | CTSO | AGAGG others(2897): Show |
chr4 | 155919118 | 155958866 |
| a0001c0001t0006 | 0/0 | 2903 | 4 | 4 | 0 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | AGAGG others(2898): Show |
chr4 | 155919118 | 155958866 |
| a0001c0001t0007 | 0/0 | 2902 | 3 | 0 | 1 | 0 | 1 | 1 | CTSO_chr4_155919118_155958866 | CTSO | AGAGG others(2897): Show |
chr4 | 155919118 | 155958866 |
| a0001c0001t0008 | 0/0 | 2902 | 3 | 3 | 0 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | AGAGG others(2897): Show |
chr4 | 155919118 | 155958866 |
| a0001c0001t0009 | 0/0 | 2903 | 3 | 0 | 0 | 3 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | AGAGG others(2898): Show |
chr4 | 155919118 | 155958866 |
| a0001c0001t0010 | 0/0 | 2902 | 2 | 0 | 0 | 2 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | AGAGG others(2897): Show |
chr4 | 155919118 | 155958866 |
| a0001c0001t0011 | 0/0 | 2902 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | AGAGG others(2897): Show |
chr4 | 155919118 | 155958866 |
| a0001c0001t0012 | 0/0 | 2902 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | AGAGG others(2897): Show |
chr4 | 155919118 | 155958866 |
| a0001c0001t0013 | 0/0 | 2902 | 1 | 0 | 0 | 0 | 0 | 1 | CTSO_chr4_155919118_155958866 | CTSO | AGAGG others(2897): Show |
chr4 | 155919118 | 155958866 |
| a0001c0001t0014 | 0/0 | 2902 | 1 | 0 | 1 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | AGAGG others(2897): Show |
chr4 | 155919118 | 155958866 |
| a0001c0001t0015 | 0/0 | 2902 | 1 | 0 | 1 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | AGAGG others(2897): Show |
chr4 | 155919118 | 155958866 |
| a0001c0001t0016 | 0/0 | 2902 | 1 | 0 | 0 | 0 | 0 | 1 | CTSO_chr4_155919118_155958866 | CTSO | AGAGG others(2897): Show |
chr4 | 155919118 | 155958866 |
| a0001c0001t0017 | 0/0 | 2902 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | AGAGG others(2897): Show |
chr4 | 155919118 | 155958866 |
| a0001c0001t0018 | 0/0 | 2902 | 1 | 0 | 0 | 0 | 0 | 1 | CTSO_chr4_155919118_155958866 | CTSO | AGAGG others(2897): Show |
chr4 | 155919118 | 155958866 |
| a0001c0001t0019 | 0/0 | 2902 | 1 | 1 | 0 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | AGAGG others(2897): Show |
chr4 | 155919118 | 155958866 |
| a0001c0001t0020 | 0/0 | 2902 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | AGAGG others(2897): Show |
chr4 | 155919118 | 155958866 |
| a0001c0002t0006 | 0/0 | 2903 | 3 | 3 | 0 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | AGAGG others(2898): Show |
chr4 | 155919118 | 155958866 |
| a0001c0003t0003 | 0/0 | 2903 | 1 | 1 | 0 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | AGAGG others(2898): Show |
chr4 | 155919118 | 155958866 |
| a0001c0003t0004 | 0/0 | 2903 | 1 | 1 | 0 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | AGAGG others(2898): Show |
chr4 | 155919118 | 155958866 |
| a0001c0005t0004 | 0/0 | 2903 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | AGAGG others(2898): Show |
chr4 | 155919118 | 155958866 |
| a0002c0004t0004 | 0/0 | 2903 | 1 | 1 | 0 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | AGAGG others(2898): Show |
chr4 | 155919118 | 155958866 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 37 | 0 | 10 | 24 | 1 | 2 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0004 | 0/0 | 8 | 0 | 4 | 2 | 1 | 1 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0008 | 0/0 | 6 | 0 | 4 | 2 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0011 | 0/0 | 5 | 4 | 0 | 0 | 1 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0002g0002 | 0/0 | 17 | 0 | 1 | 14 | 1 | 1 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0002g0007 | 0/0 | 6 | 1 | 0 | 0 | 0 | 5 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0002g0010 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0002g0015 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0002g0016 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0002g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0002g0023 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0002g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0002g0043 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0002g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0002g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0003g0003 | 0/0 | 9 | 8 | 0 | 0 | 1 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0003g0005 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0003g0013 | 0/0 | 4 | 0 | 1 | 1 | 0 | 2 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0003g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0003g0047 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0003g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0003g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0004g0006 | 0/0 | 7 | 5 | 0 | 2 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0004g0021 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0004g0052 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0004g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0004g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0004g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0004g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0005g0009 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0005g0012 | 0/0 | 5 | 1 | 2 | 0 | 0 | 2 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0005g0014 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0005g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0005g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0006g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0006g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0006g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0006g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0007g0026 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0007g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0008g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0008g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0009g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0010g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0011g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0012g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0013g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0014g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0015g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0016g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0017g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0018g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0019g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0001t0020g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0002t0006g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0003t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0003t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0001c0005t0004g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| a0002c0004t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | GBR | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | GBR | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG00280 | hp2 | a0001 | c0001 | t0007 | g0026 | EUR | FIN | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | CHS | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG00423 | hp2 | a0001 | c0001 | t0012 | g0061 | EAS | CHS | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG00639 | hp1 | a0001 | c0001 | t0015 | g0140 | AMR | PUR | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG00735 | hp2 | a0001 | c0001 | t0007 | g0065 | AMR | PUR | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0135 | AMR | PUR | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0029 | AMR | PUR | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | PUR | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0068 | AMR | PUR | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0056 | AMR | PUR | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0013 | AMR | PUR | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0133 | AMR | PUR | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0155 | AMR | PUR | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01167 | hp2 | a0001 | c0001 | t0005 | g0012 | AMR | PUR | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01168 | hp2 | a0001 | c0001 | t0005 | g0152 | AMR | PUR | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01169 | hp2 | a0001 | c0001 | t0005 | g0012 | AMR | PUR | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | CLM | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | CLM | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0163 | AMR | CLM | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0148 | AMR | CLM | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01358 | hp1 | a0001 | c0001 | t0014 | g0121 | AMR | CLM | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0131 | EUR | IBS | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01515 | hp2 | a0001 | c0001 | t0005 | g0014 | EUR | IBS | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0082 | AMR | PEL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01981 | hp1 | a0001 | c0001 | t0004 | g0157 | AMR | PEL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | ACB | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0169 | AFR | ACB | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | KHV | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | KHV | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | KHV | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | ACB | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0184 | AFR | ACB | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0164 | AMR | PEL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | CDX | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02155 | hp2 | a0001 | c0005 | t0004 | g0174 | EAS | CDX | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CDX | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | ACB | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | ACB | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | ACB | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0171 | AFR | ACB | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0052 | AFR | ACB | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0049 | AFR | GWD | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0179 | AFR | GWD | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0042 | SAS | PJL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02615 | hp1 | a0001 | c0002 | t0006 | g0025 | AFR | GWD | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0093 | AFR | GWD | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0053 | AFR | GWD | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | GWD | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02647 | hp1 | a0001 | c0003 | t0003 | g0181 | AFR | GWD | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0142 | AFR | GWD | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0067 | SAS | PJL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0078 | SAS | PJL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0021 | AFR | GWD | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02717 | hp2 | a0001 | c0002 | t0006 | g0025 | AFR | GWD | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0048 | AFR | GWD | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0085 | AFR | GWD | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0083 | SAS | PJL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0013 | SAS | PJL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02738 | hp1 | a0001 | c0001 | t0013 | g0117 | SAS | PJL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02738 | hp2 | a0001 | c0001 | t0004 | g0052 | SAS | PJL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0146 | AFR | GWD | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | GWD | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02896 | hp1 | a0001 | c0001 | t0008 | g0087 | AFR | GWD | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0053 | AFR | GWD | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ESN | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0156 | AFR | ESN | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0176 | AFR | ESN | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | ESN | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02970 | hp2 | a0001 | c0001 | t0006 | g0092 | AFR | ESN | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0145 | AFR | ESN | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | ESN | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0043 | SAS | PJL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | GWD | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | MSL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0090 | AFR | MSL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | ESN | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ESN | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ESN | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0180 | AFR | ESN | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | MSL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0147 | AFR | MSL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG03225 | hp1 | a0001 | c0003 | t0004 | g0182 | AFR | MSL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0086 | AFR | MSL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG03239 | hp1 | a0001 | c0001 | t0005 | g0014 | SAS | PJL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0023 | SAS | PJL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | MSL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG03453 | hp2 | a0001 | c0001 | t0019 | g0100 | AFR | MSL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0183 | AFR | MSL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0047 | SAS | PJL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0016 | SAS | PJL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0047 | SAS | PJL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG03516 | hp1 | a0001 | c0001 | t0006 | g0091 | AFR | ESN | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0021 | AFR | GWD | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | GWD | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG03579 | hp1 | a0001 | c0001 | t0008 | g0045 | AFR | MSL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | MSL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG03669 | hp1 | a0001 | c0001 | t0005 | g0014 | SAS | PJL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0076 | SAS | PJL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0154 | SAS | STU | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG03688 | hp2 | a0001 | c0001 | t0016 | g0132 | SAS | STU | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG03710 | hp1 | a0001 | c0001 | t0018 | g0168 | SAS | PJL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0042 | SAS | PJL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | BEB | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | BEB | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG03834 | hp1 | a0001 | c0001 | t0005 | g0012 | SAS | BEB | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0057 | SAS | BEB | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | BEB | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0089 | SAS | BEB | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0013 | SAS | BEB | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | STU | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | STU | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0136 | SAS | STU | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG04199 | hp2 | a0001 | c0001 | t0007 | g0026 | SAS | STU | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0178 | SAS | STU | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG04204 | hp2 | a0001 | c0001 | t0005 | g0012 | SAS | STU | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | STU | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0023 | SAS | STU | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | YRI | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | YRI | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0158 | AFR | YRI | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | YRI | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18940 | hp1 | a0001 | c0001 | t0005 | g0009 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18942 | hp2 | a0001 | c0001 | t0005 | g0009 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18947 | hp1 | a0001 | c0001 | t0004 | g0170 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18956 | hp2 | a0001 | c0001 | t0005 | g0041 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18957 | hp1 | a0001 | c0001 | t0009 | g0024 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18959 | hp1 | a0001 | c0001 | t0005 | g0009 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18962 | hp1 | a0001 | c0001 | t0005 | g0009 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18964 | hp2 | a0001 | c0001 | t0020 | g0108 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18981 | hp1 | a0001 | c0001 | t0010 | g0036 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18985 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18990 | hp1 | a0001 | c0001 | t0005 | g0041 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18990 | hp2 | a0001 | c0001 | t0017 | g0161 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18995 | hp2 | a0001 | c0001 | t0005 | g0009 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18997 | hp1 | a0001 | c0001 | t0009 | g0024 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA19000 | hp1 | a0001 | c0001 | t0011 | g0129 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA19001 | hp1 | a0001 | c0001 | t0010 | g0036 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA19007 | hp1 | a0001 | c0001 | t0005 | g0009 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | LWK | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA19063 | hp2 | a0001 | c0001 | t0009 | g0024 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA19076 | hp2 | a0001 | c0001 | t0004 | g0177 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0173 | AFR | YRI | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA19240 | hp2 | a0001 | c0002 | t0006 | g0025 | AFR | YRI | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | ASW | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ASW | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | TSI | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0134 | EUR | TSI | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0064 | EUR | TSI | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | GIH | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0021 | AMR | CLM | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0144 | AFR | ACB | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02486 | hp1 | a0001 | c0001 | t0006 | g0153 | AFR | ACB | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG02559 | hp2 | a0001 | c0001 | t0008 | g0045 | AFR | ACB | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0151 | AFR | MSL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| HG03471 | hp2 | a0002 | c0004 | t0004 | g0175 | AFR | MSL | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0012 | AFR | USA | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0048 | AFR | USA | CTSO_chr4_155919118_155958866 | CTSO | chr4 | 155919118 | 155958866 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:155928404 | C | T | 1 | a0002 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.863G>A | p.Arg288Gln | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 7/8 | 882/2903 | 863/966 | 288/321 | chr4 | 155928404 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:155929618 | C | A | 1 | a0001c0005 | 1 | HG02155.hp2 | synonymous_variant | LOW | c.762G>T | p.Leu254Leu | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 6/8 | 781/2903 | 762/966 | 254/321 | chr4 | 155929618 | |||
| chr4:155939515 | G | A | 1 | a0001c0003 | 2 | HG02647.hp1 HG03225.hp1 |
synonymous_variant | LOW | c.408C>T | p.Ser136Ser | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 4/8 | 427/2903 | 408/966 | 136/321 | chr4 | 155939515 | |||
| chr4:155953773 | G | A | 1 | a0001c0002 | 3 | HG02615.hp1 HG02717.hp2 NA19240.hp2 |
synonymous_variant | LOW | c.75C>T | p.Ser25Ser | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/8 | 94/2903 | 75/966 | 25/321 | chr4 | 155953773 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:155924223 | G | C | 1 | a0001c0001t0009 | 3 | NA18957.hp1 NA18997.hp1 NA19063.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1813C>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 8/8 | 1813 | chr4 | 155924223 | ||||||
| chr4:155924243 | C | A | 1 | a0001c0001t0014 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1793G>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 8/8 | 1793 | chr4 | 155924243 | ||||||
| chr4:155924488 | A | G | 1 | a0001c0001t0013 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1548T>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 8/8 | 1548 | chr4 | 155924488 | ||||||
| chr4:155924617 | T | C | 2 | a0001c0001t0006 a0001c0002t0006 |
7 | HG02486.hp1 HG02615.hp1 HG02615.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1419A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 8/8 | 1419 | chr4 | 155924617 | ||||||
| chr4:155924901 | G | A | 1 | a0001c0001t0008 | 3 | HG02559.hp2 HG02896.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1135C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 8/8 | 1135 | chr4 | 155924901 | ||||||
| chr4:155924902 | A | G | 1 | a0001c0001t0008 | 3 | HG02559.hp2 HG02896.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1134T>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 8/8 | 1134 | chr4 | 155924902 | ||||||
| chr4:155924913 | G | A | 1 | a0001c0001t0015 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1123C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 8/8 | 1123 | chr4 | 155924913 | ||||||
| chr4:155924935 | G | A | 9 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0010 others(6): Show |
164 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(161): Show |
3_prime_UTR_variant | MODIFIER | c.*1101C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 8/8 | 1101 | chr4 | 155924935 | ||||||
| chr4:155925109 | A | C | 1 | a0001c0001t0012 | 1 | HG00423.hp2 | 3_prime_UTR_variant | MODIFIER | c.*927T>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 8/8 | 927 | chr4 | 155925109 | ||||||
| chr4:155925199 | TA | T | 16 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(13): Show |
274 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(271): Show |
3_prime_UTR_variant | MODIFIER | c.*836delT | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 8/8 | 836 | chr4 | 155925199 | ||||||
| chr4:155925312 | T | G | 1 | a0001c0001t0016 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*724A>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 8/8 | 724 | chr4 | 155925312 | ||||||
| chr4:155925338 | T | C | 1 | a0001c0001t0017 | 1 | NA18990.hp2 | 3_prime_UTR_variant | MODIFIER | c.*698A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 8/8 | 698 | chr4 | 155925338 | ||||||
| chr4:155925419 | T | C | 1 | a0001c0001t0018 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*617A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 8/8 | 617 | chr4 | 155925419 | ||||||
| chr4:155925443 | T | C | 1 | a0001c0001t0019 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*593A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 8/8 | 593 | chr4 | 155925443 | ||||||
| chr4:155925446 | T | C | 1 | a0001c0001t0005 | 17 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*590A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 8/8 | 590 | chr4 | 155925446 | ||||||
| chr4:155925456 | G | A | 5 | a0001c0001t0004 a0001c0001t0009 a0001c0003t0004 others(2): Show |
29 | HG01123.hp2 HG01167.hp1 HG01981.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*580C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 8/8 | 580 | chr4 | 155925456 | ||||||
| chr4:155925495 | C | T | 1 | a0001c0001t0007 | 3 | HG00280.hp2 HG00735.hp2 HG04199.hp2 |
3_prime_UTR_variant | MODIFIER | c.*541G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 8/8 | 541 | chr4 | 155925495 | ||||||
| chr4:155925526 | C | A | 1 | a0001c0001t0020 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*510G>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 8/8 | 510 | chr4 | 155925526 | ||||||
| chr4:155925663 | G | T | 1 | a0001c0001t0010 | 2 | NA18981.hp1 NA19001.hp1 |
3_prime_UTR_variant | MODIFIER | c.*373C>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 8/8 | 373 | chr4 | 155925663 | ||||||
| chr4:155926032 | C | T | 1 | a0001c0001t0011 | 1 | NA19000.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 8/8 | 4 | chr4 | 155926032 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:155926078 | A | G | 135 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(132): Show |
250 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(247): Show |
splice_region_variant&intron_variant | LOW | c.932-8T>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 7/7 | chr4 | 155926078 | |||||||
| chr4:155926085 | AG | A | 135 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(132): Show |
250 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.932-16delC | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 7/7 | chr4 | 155926085 | |||||||
| chr4:155926236 | A | T | 1 | a0001c0001t0003g0053 | 2 | HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.932-166T>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 7/7 | chr4 | 155926236 | |||||||
| chr4:155926446 | C | A | 1 | a0001c0001t0002g0089 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.932-376G>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 7/7 | chr4 | 155926446 | |||||||
| chr4:155926485 | G | A | 1 | a0001c0003t0003g0181 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.932-415C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 7/7 | chr4 | 155926485 | |||||||
| chr4:155926505 | A | G | 1 | a0001c0001t0002g0127 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.932-435T>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 7/7 | chr4 | 155926505 | |||||||
| chr4:155926530 | A | C | 1 | a0001c0001t0003g0179 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.932-460T>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 7/7 | chr4 | 155926530 | |||||||
| chr4:155926797 | G | C | 1 | a0001c0001t0003g0053 | 2 | HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.932-727C>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 7/7 | chr4 | 155926797 | |||||||
| chr4:155927096 | C | T | 1 | a0001c0001t0001g0064 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.932-1026G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 7/7 | chr4 | 155927096 | |||||||
| chr4:155927096 | CT | C | 2 | a0001c0001t0001g0037 a0001c0001t0001g0118 |
3 | HG01981.hp2 HG02004.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.932-1027delA | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 7/7 | chr4 | 155927096 | |||||||
| chr4:155927497 | T | C | 1 | a0001c0001t0001g0119 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.931+839A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 7/7 | chr4 | 155927497 | |||||||
| chr4:155927558 | A | C | 1 | a0001c0003t0003g0181 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.931+778T>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 7/7 | chr4 | 155927558 | |||||||
| chr4:155927635 | T | C | 1 | a0001c0001t0002g0136 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.931+701A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 7/7 | chr4 | 155927635 | |||||||
| chr4:155927699 | C | T | 3 | a0001c0001t0006g0093 a0001c0001t0006g0153 a0001c0002t0006g0025 |
5 | HG02486.hp1 HG02615.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.931+637G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 7/7 | chr4 | 155927699 | |||||||
| chr4:155927706 | C | T | 5 | a0001c0001t0003g0048 a0001c0001t0003g0142 a0001c0001t0003g0156 others(2): Show |
6 | HG02647.hp2 HG02723.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.931+630G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 7/7 | chr4 | 155927706 | |||||||
| chr4:155927724 | G | A | 5 | a0001c0001t0005g0009 a0001c0001t0005g0012 a0001c0001t0005g0014 others(2): Show |
17 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.931+612C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 7/7 | chr4 | 155927724 | |||||||
| chr4:155927836 | T | C | 8 | a0001c0001t0003g0013 a0001c0001t0003g0047 a0001c0001t0003g0148 others(5): Show |
24 | HG01109.hp1 HG01167.hp2 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.931+500A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 7/7 | chr4 | 155927836 | |||||||
| chr4:155927876 | G | A | 1 | a0001c0001t0002g0086 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.931+460C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 7/7 | chr4 | 155927876 | |||||||
| chr4:155927946 | A | C | 69 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(66): Show |
134 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.931+390T>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 7/7 | chr4 | 155927946 | |||||||
| chr4:155928113 | T | G | 1 | a0001c0001t0004g0147 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.931+223A>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 7/7 | chr4 | 155928113 | |||||||
| chr4:155928177 | T | A | 2 | a0001c0001t0001g0039 a0001c0001t0001g0079 |
3 | NA18941.hp1 NA18972.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.931+159A>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 7/7 | chr4 | 155928177 | |||||||
| chr4:155928201 | C | CT | 155 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(152): Show |
288 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(285): Show |
intron_variant | MODIFIER | c.931+134dupA | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 7/7 | chr4 | 155928201 | |||||||
| chr4:155928611 | G | A | 19 | a0001c0001t0003g0031 a0001c0001t0004g0006 a0001c0001t0004g0021 others(16): Show |
31 | HG01123.hp2 HG01167.hp1 HG01981.hp1 others(28): Show |
intron_variant | MODIFIER | c.839-183C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 6/7 | chr4 | 155928611 | |||||||
| chr4:155928709 | A | T | 1 | a0001c0001t0001g0103 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.839-281T>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 6/7 | chr4 | 155928709 | |||||||
| chr4:155928743 | A | G | 2 | a0001c0001t0003g0005 a0001c0001t0003g0090 |
8 | HG02258.hp1 HG02630.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.839-315T>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 6/7 | chr4 | 155928743 | |||||||
| chr4:155928760 | C | T | 1 | a0001c0001t0003g0090 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.839-332G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 6/7 | chr4 | 155928760 | |||||||
| chr4:155928829 | C | G | 1 | a0001c0001t0002g0169 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.839-401G>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 6/7 | chr4 | 155928829 | |||||||
| chr4:155928902 | G | A | 3 | a0001c0001t0006g0093 a0001c0001t0006g0153 a0001c0002t0006g0025 |
5 | HG02486.hp1 HG02615.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.839-474C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 6/7 | chr4 | 155928902 | |||||||
| chr4:155928977 | G | A | 2 | a0001c0001t0002g0049 a0001c0001t0002g0183 |
3 | HG02572.hp1 HG03041.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.839-549C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 6/7 | chr4 | 155928977 | |||||||
| chr4:155928978 | C | T | 4 | a0001c0001t0001g0018 a0001c0001t0001g0071 a0001c0001t0001g0107 others(1): Show |
6 | HG01175.hp1 HG01361.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.839-550G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 6/7 | chr4 | 155928978 | |||||||
| chr4:155929004 | C | T | 1 | a0001c0001t0016g0132 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.838+538G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 6/7 | chr4 | 155929004 | |||||||
| chr4:155929005 | G | A | 3 | a0001c0001t0006g0093 a0001c0001t0006g0153 a0001c0002t0006g0025 |
5 | HG02486.hp1 HG02615.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.838+537C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 6/7 | chr4 | 155929005 | |||||||
| chr4:155929026 | T | C | 19 | a0001c0001t0003g0031 a0001c0001t0004g0006 a0001c0001t0004g0021 others(16): Show |
31 | HG01123.hp2 HG01167.hp1 HG01981.hp1 others(28): Show |
intron_variant | MODIFIER | c.838+516A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 6/7 | chr4 | 155929026 | |||||||
| chr4:155929089 | A | G | 2 | a0001c0001t0001g0111 a0001c0001t0001g0114 |
2 | HG00558.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.838+453T>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 6/7 | chr4 | 155929089 | |||||||
| chr4:155929150 | T | C | 1 | a0001c0001t0003g0179 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.838+392A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 6/7 | chr4 | 155929150 | |||||||
| chr4:155929185 | T | C | 3 | a0001c0001t0001g0027 a0001c0001t0001g0058 a0001c0001t0001g0072 |
4 | HG02074.hp2 NA18965.hp1 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.838+357A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 6/7 | chr4 | 155929185 | |||||||
| chr4:155929212 | A | G | 1 | a0001c0001t0002g0085 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.838+330T>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 6/7 | chr4 | 155929212 | |||||||
| chr4:155929261 | C | T | 2 | a0001c0001t0002g0133 a0001c0001t0016g0132 |
2 | HG01109.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.838+281G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 6/7 | chr4 | 155929261 | |||||||
| chr4:155929262 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.838+280C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 6/7 | chr4 | 155929262 | |||||||
| chr4:155929352 | G | A | 1 | a0001c0001t0001g0062 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.838+190C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 6/7 | chr4 | 155929352 | |||||||
| chr4:155929363 | G | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(146): Show |
283 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.838+179C>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 6/7 | chr4 | 155929363 | |||||||
| chr4:155929933 | A | G | 1 | a0001c0001t0001g0102 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.675-228T>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155929933 | |||||||
| chr4:155930050 | C | A | 1 | a0001c0001t0001g0130 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.675-345G>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155930050 | |||||||
| chr4:155930159 | C | A | 1 | a0001c0001t0006g0153 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.675-454G>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155930159 | |||||||
| chr4:155930160 | T | C | 65 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(62): Show |
130 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.675-455A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155930160 | |||||||
| chr4:155930228 | G | A | 2 | a0001c0001t0008g0045 a0001c0001t0008g0087 |
3 | HG02559.hp2 HG02896.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.675-523C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155930228 | |||||||
| chr4:155930398 | G | A | 1 | a0001c0001t0001g0104 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.675-693C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155930398 | |||||||
| chr4:155930454 | C | T | 1 | a0001c0001t0003g0047 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.675-749G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155930454 | |||||||
| chr4:155930702 | C | G | 1 | a0001c0001t0001g0120 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.675-997G>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155930702 | |||||||
| chr4:155930774 | A | G | 3 | a0001c0001t0003g0013 a0001c0001t0003g0047 a0001c0001t0003g0148 |
7 | HG01109.hp1 HG01346.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.675-1069T>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155930774 | |||||||
| chr4:155930812 | G | T | 1 | a0001c0001t0002g0162 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.675-1107C>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155930812 | |||||||
| chr4:155931378 | G | A | 1 | a0001c0001t0003g0053 | 2 | HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.675-1673C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155931378 | |||||||
| chr4:155931523 | A | C | 1 | a0001c0001t0001g0112 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.675-1818T>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155931523 | |||||||
| chr4:155931534 | A | C | 4 | a0001c0001t0003g0048 a0001c0001t0003g0142 a0001c0001t0003g0156 others(1): Show |
5 | HG02647.hp2 HG02723.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.675-1829T>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155931534 | |||||||
| chr4:155931580 | C | T | 1 | a0001c0001t0004g0155 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.675-1875G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155931580 | |||||||
| chr4:155931647 | T | C | 1 | a0001c0001t0003g0179 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.675-1942A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155931647 | |||||||
| chr4:155931796 | G | A | 17 | a0001c0001t0004g0006 a0001c0001t0004g0021 a0001c0001t0004g0052 others(14): Show |
28 | HG01123.hp2 HG01167.hp1 HG01981.hp1 others(25): Show |
intron_variant | MODIFIER | c.675-2091C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155931796 | |||||||
| chr4:155931923 | C | T | 1 | a0001c0001t0002g0164 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.675-2218G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155931923 | |||||||
| chr4:155931924 | G | A | 37 | a0001c0001t0002g0049 a0001c0001t0002g0183 a0001c0001t0003g0048 others(34): Show |
65 | HG01123.hp2 HG01167.hp1 HG01167.hp2 others(62): Show |
intron_variant | MODIFIER | c.675-2219C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155931924 | |||||||
| chr4:155931930 | G | A | 1 | a0001c0001t0002g0029 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.675-2225C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155931930 | |||||||
| chr4:155931955 | T | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(175): Show |
326 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(323): Show |
intron_variant | MODIFIER | c.675-2250A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155931955 | |||||||
| chr4:155932039 | T | G | 52 | a0001c0001t0001g0081 a0001c0001t0001g0125 a0001c0001t0001g0143 others(49): Show |
91 | HG00140.hp1 HG00408.hp1 HG00738.hp2 others(88): Show |
intron_variant | MODIFIER | c.675-2334A>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155932039 | |||||||
| chr4:155932087 | T | A | 8 | a0001c0001t0003g0013 a0001c0001t0003g0047 a0001c0001t0003g0148 others(5): Show |
24 | HG01109.hp1 HG01167.hp2 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.675-2382A>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155932087 | |||||||
| chr4:155932089 | G | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(175): Show |
326 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(323): Show |
intron_variant | MODIFIER | c.675-2384C>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155932089 | |||||||
| chr4:155932091 | A | G | 1 | a0001c0001t0001g0074 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.675-2386T>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155932091 | |||||||
| chr4:155932200 | G | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(135): Show |
254 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.675-2495C>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155932200 | |||||||
| chr4:155932253 | G | A | 4 | a0001c0001t0003g0048 a0001c0001t0003g0142 a0001c0001t0003g0156 others(1): Show |
5 | HG02647.hp2 HG02723.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.675-2548C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155932253 | |||||||
| chr4:155932495 | C | T | 1 | a0001c0001t0002g0163 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.675-2790G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155932495 | |||||||
| chr4:155932652 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.675-2947G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155932652 | |||||||
| chr4:155932687 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.675-2982G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155932687 | |||||||
| chr4:155932785 | C | T | 1 | a0001c0001t0002g0089 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.675-3080G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155932785 | |||||||
| chr4:155932916 | G | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(133): Show |
251 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.675-3211C>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155932916 | |||||||
| chr4:155932971 | A | G | 95 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(92): Show |
174 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.675-3266T>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155932971 | |||||||
| chr4:155933053 | T | C | 1 | a0001c0001t0003g0156 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.675-3348A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155933053 | |||||||
| chr4:155933107 | T | A | 4 | a0001c0001t0003g0048 a0001c0001t0003g0142 a0001c0001t0003g0156 others(1): Show |
5 | HG02647.hp2 HG02723.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.675-3402A>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155933107 | |||||||
| chr4:155933172 | G | A | 4 | a0001c0001t0001g0040 a0001c0001t0001g0098 a0001c0001t0001g0105 others(1): Show |
5 | NA18947.hp2 NA19000.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.675-3467C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155933172 | |||||||
| chr4:155933193 | G | T | 2 | a0001c0001t0003g0048 a0001c0001t0003g0142 |
3 | HG02647.hp2 HG02723.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.675-3488C>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155933193 | |||||||
| chr4:155933199 | A | G | 1 | a0001c0001t0004g0178 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.675-3494T>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155933199 | |||||||
| chr4:155933253 | T | C | 2 | a0001c0001t0005g0009 a0001c0001t0005g0152 |
7 | HG01168.hp2 NA18940.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.675-3548A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155933253 | |||||||
| chr4:155933297 | G | A | 1 | a0001c0001t0005g0152 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.675-3592C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155933297 | |||||||
| chr4:155933298 | C | T | 1 | a0001c0001t0005g0152 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.675-3593G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155933298 | |||||||
| chr4:155933299 | C | A | 1 | a0001c0001t0005g0152 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.675-3594G>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155933299 | |||||||
| chr4:155933302 | C | T | 1 | a0001c0001t0005g0152 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.675-3597G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155933302 | |||||||
| chr4:155933303 | A | G | 1 | a0001c0001t0005g0152 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.675-3598T>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155933303 | |||||||
| chr4:155933324 | T | A | 27 | a0001c0001t0001g0125 a0001c0001t0001g0165 a0001c0001t0001g0166 others(24): Show |
56 | HG00140.hp1 HG01069.hp1 HG01071.hp2 others(53): Show |
intron_variant | MODIFIER | c.675-3619A>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155933324 | |||||||
| chr4:155933330 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.675-3625G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155933330 | |||||||
| chr4:155933374 | CA | C | 2 | a0001c0001t0008g0045 a0001c0001t0008g0087 |
3 | HG02559.hp2 HG02896.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.675-3670delT | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155933374 | |||||||
| chr4:155933427 | A | G | 21 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(18): Show |
34 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.675-3722T>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155933427 | |||||||
| chr4:155933434 | T | A | 4 | a0001c0001t0006g0091 a0001c0001t0006g0092 a0001c0001t0006g0093 others(1): Show |
6 | HG02615.hp1 HG02615.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.675-3729A>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155933434 | |||||||
| chr4:155933624 | G | C | 1 | a0001c0001t0004g0170 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.674+3738C>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155933624 | |||||||
| chr4:155933682 | T | C | 1 | a0001c0001t0001g0030 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.674+3680A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155933682 | |||||||
| chr4:155933760 | T | C | 1 | a0001c0001t0006g0153 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.674+3602A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155933760 | |||||||
| chr4:155933803 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.674+3559G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155933803 | |||||||
| chr4:155933862 | T | C | 16 | a0001c0001t0001g0051 a0001c0001t0001g0172 a0001c0001t0004g0006 others(13): Show |
26 | HG02155.hp2 HG02258.hp2 HG02451.hp2 others(23): Show |
intron_variant | MODIFIER | c.674+3500A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155933862 | |||||||
| chr4:155933876 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.674+3486C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155933876 | |||||||
| chr4:155933980 | G | A | 123 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(120): Show |
242 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.674+3382C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155933980 | |||||||
| chr4:155934028 | G | A | 4 | a0001c0001t0002g0015 a0001c0001t0002g0085 a0001c0001t0002g0086 others(1): Show |
6 | HG01081.hp2 HG02630.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.674+3334C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155934028 | |||||||
| chr4:155934079 | C | T | 101 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(98): Show |
208 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(205): Show |
intron_variant | MODIFIER | c.674+3283G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155934079 | |||||||
| chr4:155934281 | G | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(93): Show |
194 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(191): Show |
intron_variant | MODIFIER | c.674+3081C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155934281 | |||||||
| chr4:155934472 | G | A | 68 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(65): Show |
136 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.674+2890C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155934472 | |||||||
| chr4:155934597 | A | C | 1 | a0001c0001t0001g0088 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.674+2765T>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155934597 | |||||||
| chr4:155934617 | T | C | 69 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(66): Show |
138 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.674+2745A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155934617 | |||||||
| chr4:155934869 | T | C | 1 | a0001c0001t0004g0176 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.674+2493A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155934869 | |||||||
| chr4:155934870 | G | A | 16 | a0001c0001t0001g0051 a0001c0001t0001g0172 a0001c0001t0004g0006 others(13): Show |
26 | HG02155.hp2 HG02258.hp2 HG02451.hp2 others(23): Show |
intron_variant | MODIFIER | c.674+2492C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155934870 | |||||||
| chr4:155935041 | C | A | 22 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(19): Show |
34 | HG00280.hp2 HG00423.hp2 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.674+2321G>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155935041 | |||||||
| chr4:155935181 | T | G | 2 | a0001c0001t0003g0179 a0001c0001t0006g0153 |
2 | HG02486.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.674+2181A>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155935181 | |||||||
| chr4:155935246 | C | T | 10 | a0001c0001t0001g0081 a0001c0001t0002g0042 a0001c0001t0002g0078 others(7): Show |
12 | HG00738.hp2 HG01109.hp2 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.674+2116G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155935246 | |||||||
| chr4:155935291 | C | T | 1 | a0001c0001t0008g0045 | 2 | HG02559.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.674+2071G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155935291 | |||||||
| chr4:155935334 | G | A | 1 | a0001c0001t0008g0087 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.674+2028C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155935334 | |||||||
| chr4:155935507 | G | A | 5 | a0001c0001t0003g0013 a0001c0001t0003g0047 a0001c0001t0003g0148 others(2): Show |
14 | HG01109.hp1 HG01168.hp2 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.674+1855C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155935507 | |||||||
| chr4:155935661 | T | C | 180 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(177): Show |
335 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(332): Show |
intron_variant | MODIFIER | c.674+1701A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155935661 | |||||||
| chr4:155935675 | T | C | 1 | a0001c0001t0002g0135 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.674+1687A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155935675 | |||||||
| chr4:155935731 | T | C | 1 | a0001c0001t0001g0128 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.674+1631A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155935731 | |||||||
| chr4:155935877 | T | G | 169 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(166): Show |
313 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(310): Show |
intron_variant | MODIFIER | c.674+1485A>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155935877 | |||||||
| chr4:155935923 | A | G | 88 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(85): Show |
167 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.674+1439T>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155935923 | |||||||
| chr4:155935930 | C | T | 68 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(65): Show |
137 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.674+1432G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155935930 | |||||||
| chr4:155935934 | A | G | 1 | a0001c0001t0001g0074 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.674+1428T>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155935934 | |||||||
| chr4:155936215 | G | A | 60 | a0001c0001t0001g0051 a0001c0001t0001g0081 a0001c0001t0001g0084 others(57): Show |
111 | HG00140.hp1 HG00738.hp2 HG01081.hp2 others(108): Show |
intron_variant | MODIFIER | c.674+1147C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155936215 | |||||||
| chr4:155936280 | G | GT | 25 | a0001c0001t0001g0143 a0001c0001t0001g0165 a0001c0001t0001g0166 others(22): Show |
54 | HG00140.hp1 HG01255.hp1 HG01256.hp2 others(51): Show |
intron_variant | MODIFIER | c.674+1081dupA | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155936280 | |||||||
| chr4:155936290 | G | A | 141 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(138): Show |
263 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.674+1072C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155936290 | |||||||
| chr4:155936497 | C | G | 1 | a0001c0001t0001g0063 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.674+865G>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155936497 | |||||||
| chr4:155936666 | T | C | 24 | a0001c0001t0001g0143 a0001c0001t0001g0165 a0001c0001t0001g0166 others(21): Show |
53 | HG00140.hp1 HG01255.hp1 HG01256.hp2 others(50): Show |
intron_variant | MODIFIER | c.674+696A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155936666 | |||||||
| chr4:155936755 | A | G | 1 | a0001c0001t0001g0035 | 2 | NA18949.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.674+607T>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155936755 | |||||||
| chr4:155936922 | T | C | 1 | a0001c0001t0003g0031 | 2 | NA18944.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.674+440A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155936922 | |||||||
| chr4:155937132 | C | A | 2 | a0001c0001t0004g0177 a0001c0001t0009g0024 |
4 | NA18957.hp1 NA18997.hp1 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.674+230G>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155937132 | |||||||
| chr4:155937202 | C | A | 1 | a0001c0001t0001g0099 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.674+160G>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155937202 | |||||||
| chr4:155937289 | C | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0111 a0001c0001t0001g0114 |
5 | HG00558.hp1 NA18944.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.674+73G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 5/7 | chr4 | 155937289 | |||||||
| chr4:155937508 | T | A | 13 | a0001c0001t0001g0008 a0001c0001t0001g0038 a0001c0001t0001g0039 others(10): Show |
21 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(18): Show |
intron_variant | MODIFIER | c.553-25A>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 4/7 | chr4 | 155937508 | |||||||
| chr4:155937556 | G | A | 1 | a0001c0001t0019g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.553-73C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 4/7 | chr4 | 155937556 | |||||||
| chr4:155937566 | G | T | 1 | a0001c0001t0003g0179 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.553-83C>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 4/7 | chr4 | 155937566 | |||||||
| chr4:155937695 | A | G | 1 | a0001c0001t0001g0107 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.553-212T>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 4/7 | chr4 | 155937695 | |||||||
| chr4:155937745 | G | T | 1 | a0001c0001t0004g0173 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.553-262C>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 4/7 | chr4 | 155937745 | |||||||
| chr4:155937818 | G | A | 62 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(59): Show |
97 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.553-335C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 4/7 | chr4 | 155937818 | |||||||
| chr4:155937865 | C | T | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | NA18973.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.553-382G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 4/7 | chr4 | 155937865 | |||||||
| chr4:155937945 | A | G | 16 | a0001c0001t0001g0051 a0001c0001t0001g0172 a0001c0001t0003g0179 others(13): Show |
26 | HG02155.hp2 HG02258.hp2 HG02451.hp2 others(23): Show |
intron_variant | MODIFIER | c.553-462T>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 4/7 | chr4 | 155937945 | |||||||
| chr4:155938004 | C | T | 1 | a0001c0001t0001g0037 | 2 | HG02004.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.553-521G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 4/7 | chr4 | 155938004 | |||||||
| chr4:155938038 | T | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(74): Show |
155 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.553-555A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 4/7 | chr4 | 155938038 | |||||||
| chr4:155938180 | T | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(136): Show |
252 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(249): Show |
intron_variant | MODIFIER | c.553-697A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 4/7 | chr4 | 155938180 | |||||||
| chr4:155938328 | A | G | 8 | a0001c0001t0002g0049 a0001c0001t0003g0048 a0001c0001t0003g0142 others(5): Show |
12 | HG01123.hp2 HG01167.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.553-845T>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 4/7 | chr4 | 155938328 | |||||||
| chr4:155938503 | C | T | 24 | a0001c0001t0001g0143 a0001c0001t0001g0165 a0001c0001t0001g0166 others(21): Show |
53 | HG00140.hp1 HG01255.hp1 HG01256.hp2 others(50): Show |
intron_variant | MODIFIER | c.552+868G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 4/7 | chr4 | 155938503 | |||||||
| chr4:155938772 | A | G | 5 | a0001c0001t0003g0013 a0001c0001t0003g0047 a0001c0001t0003g0148 others(2): Show |
14 | HG01109.hp1 HG01168.hp2 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.552+599T>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 4/7 | chr4 | 155938772 | |||||||
| chr4:155939064 | C | T | 1 | a0001c0001t0002g0059 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.552+307G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 4/7 | chr4 | 155939064 | |||||||
| chr4:155939065 | G | A | 3 | a0001c0001t0003g0013 a0001c0001t0003g0047 a0001c0001t0003g0148 |
7 | HG01109.hp1 HG01346.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.552+306C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 4/7 | chr4 | 155939065 | |||||||
| chr4:155939099 | C | T | 24 | a0001c0001t0001g0143 a0001c0001t0001g0165 a0001c0001t0001g0166 others(21): Show |
53 | HG00140.hp1 HG01255.hp1 HG01256.hp2 others(50): Show |
intron_variant | MODIFIER | c.552+272G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 4/7 | chr4 | 155939099 | |||||||
| chr4:155939239 | T | C | 71 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(68): Show |
138 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.552+132A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 4/7 | chr4 | 155939239 | |||||||
| chr4:155939341 | A | T | 1 | a0001c0001t0002g0160 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.552+30T>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 4/7 | chr4 | 155939341 | |||||||
| chr4:155939649 | C | G | 1 | a0001c0001t0001g0111 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.385-111G>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 3/7 | chr4 | 155939649 | |||||||
| chr4:155939696 | G | A | 2 | a0001c0001t0001g0122 a0001c0001t0002g0123 |
2 | NA18991.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.385-158C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 3/7 | chr4 | 155939696 | |||||||
| chr4:155939806 | G | A | 20 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0001g0088 others(17): Show |
30 | HG00738.hp2 HG01081.hp2 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.385-268C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 3/7 | chr4 | 155939806 | |||||||
| chr4:155939894 | T | C | 1 | a0001c0001t0019g0100 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.385-356A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 3/7 | chr4 | 155939894 | |||||||
| chr4:155939908 | C | T | 1 | a0001c0001t0008g0045 | 2 | HG02559.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.385-370G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 3/7 | chr4 | 155939908 | |||||||
| chr4:155939922 | A | G | 3 | a0001c0001t0003g0013 a0001c0001t0003g0047 a0001c0001t0003g0148 |
7 | HG01109.hp1 HG01346.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.385-384T>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 3/7 | chr4 | 155939922 | |||||||
| chr4:155939953 | C | T | 16 | a0001c0001t0001g0051 a0001c0001t0001g0172 a0001c0001t0003g0179 others(13): Show |
26 | HG02155.hp2 HG02258.hp2 HG02451.hp2 others(23): Show |
intron_variant | MODIFIER | c.385-415G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 3/7 | chr4 | 155939953 | |||||||
| chr4:155940217 | T | G | 25 | a0001c0001t0001g0143 a0001c0001t0001g0165 a0001c0001t0001g0166 others(22): Show |
54 | HG00140.hp1 HG01255.hp1 HG01256.hp2 others(51): Show |
intron_variant | MODIFIER | c.385-679A>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 3/7 | chr4 | 155940217 | |||||||
| chr4:155940284 | T | C | 2 | a0001c0001t0005g0009 a0001c0001t0005g0152 |
7 | HG01168.hp2 NA18940.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.385-746A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 3/7 | chr4 | 155940284 | |||||||
| chr4:155940395 | C | CA | 73 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(70): Show |
145 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.385-858dupT | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 3/7 | chr4 | 155940395 | |||||||
| chr4:155940419 | G | A | 2 | a0001c0001t0001g0124 a0001c0001t0002g0150 |
2 | HG00408.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.385-881C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 3/7 | chr4 | 155940419 | |||||||
| chr4:155940499 | C | T | 8 | a0001c0001t0001g0084 a0001c0001t0001g0088 a0001c0001t0002g0007 others(5): Show |
15 | HG01081.hp2 HG02559.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.385-961G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 3/7 | chr4 | 155940499 | |||||||
| chr4:155940627 | G | A | 1 | a0001c0001t0008g0045 | 2 | HG02559.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.385-1089C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 3/7 | chr4 | 155940627 | |||||||
| chr4:155940797 | C | T | 1 | a0001c0001t0004g0157 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.385-1259G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 3/7 | chr4 | 155940797 | |||||||
| chr4:155940842 | C | CA | 68 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(65): Show |
107 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.385-1305dupT | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 3/7 | chr4 | 155940842 | |||||||
| chr4:155940927 | TA | T | 92 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(89): Show |
176 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.384+1389delT | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 3/7 | chr4 | 155940927 | |||||||
| chr4:155940952 | C | T | 71 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(68): Show |
143 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.384+1365G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 3/7 | chr4 | 155940952 | |||||||
| chr4:155941025 | G | A | 3 | a0001c0001t0003g0013 a0001c0001t0003g0047 a0001c0001t0003g0148 |
7 | HG01109.hp1 HG01346.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.384+1292C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 3/7 | chr4 | 155941025 | |||||||
| chr4:155941072 | A | G | 1 | a0001c0001t0001g0019 | 3 | NA18944.hp1 NA18978.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.384+1245T>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 3/7 | chr4 | 155941072 | |||||||
| chr4:155941095 | G | A | 1 | a0001c0001t0002g0022 | 3 | NA18943.hp1 NA18986.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.384+1222C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 3/7 | chr4 | 155941095 | |||||||
| chr4:155941286 | A | T | 69 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(66): Show |
136 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.384+1031T>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 3/7 | chr4 | 155941286 | |||||||
| chr4:155941309 | C | T | 2 | a0001c0001t0002g0133 a0001c0001t0016g0132 |
2 | HG01109.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.384+1008G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 3/7 | chr4 | 155941309 | |||||||
| chr4:155941404 | T | G | 29 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(26): Show |
44 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.384+913A>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 3/7 | chr4 | 155941404 | |||||||
| chr4:155941446 | T | A | 16 | a0001c0001t0001g0051 a0001c0001t0001g0172 a0001c0001t0003g0179 others(13): Show |
26 | HG02155.hp2 HG02258.hp2 HG02451.hp2 others(23): Show |
intron_variant | MODIFIER | c.384+871A>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 3/7 | chr4 | 155941446 | |||||||
| chr4:155941563 | T | C | 1 | a0001c0001t0002g0135 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.384+754A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 3/7 | chr4 | 155941563 | |||||||
| chr4:155941670 | C | A | 1 | a0001c0001t0001g0125 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.384+647G>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 3/7 | chr4 | 155941670 | |||||||
| chr4:155941781 | C | T | 28 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(25): Show |
42 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.384+536G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 3/7 | chr4 | 155941781 | |||||||
| chr4:155941884 | AATGT | A | 3 | a0001c0001t0003g0013 a0001c0001t0003g0047 a0001c0001t0003g0148 |
7 | HG01109.hp1 HG01346.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.384+429_384+432del others(4): Show |
CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 3/7 | chr4 | 155941884 | |||||||
| chr4:155941912 | A | G | 1 | a0001c0001t0006g0153 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.384+405T>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 3/7 | chr4 | 155941912 | |||||||
| chr4:155941917 | T | C | 7 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(4): Show |
14 | HG01255.hp1 HG01346.hp1 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.384+400A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 3/7 | chr4 | 155941917 | |||||||
| chr4:155941975 | C | G | 1 | a0001c0001t0001g0110 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.384+342G>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 3/7 | chr4 | 155941975 | |||||||
| chr4:155942094 | T | C | 4 | a0001c0001t0001g0054 a0001c0001t0001g0185 a0001c0001t0002g0184 others(1): Show |
6 | HG02145.hp2 HG02451.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.384+223A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 3/7 | chr4 | 155942094 | |||||||
| chr4:155942100 | T | C | 20 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0001g0088 others(17): Show |
32 | HG00738.hp2 HG01081.hp2 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.384+217A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 3/7 | chr4 | 155942100 | |||||||
| chr4:155942236 | A | G | 4 | a0001c0001t0002g0049 a0001c0001t0003g0048 a0001c0001t0003g0142 others(1): Show |
6 | HG02572.hp1 HG02647.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.384+81T>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 3/7 | chr4 | 155942236 | |||||||
| chr4:155942271 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.384+46G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 3/7 | chr4 | 155942271 | |||||||
| chr4:155942304 | G | C | 1 | a0001c0001t0006g0153 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.384+13C>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 3/7 | chr4 | 155942304 | |||||||
| chr4:155942509 | A | G | 1 | a0001c0001t0001g0058 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.245-53T>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 2/7 | chr4 | 155942509 | |||||||
| chr4:155942520 | A | G | 1 | a0001c0001t0004g0173 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.245-64T>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 2/7 | chr4 | 155942520 | |||||||
| chr4:155942697 | G | A | 24 | a0001c0001t0001g0143 a0001c0001t0001g0165 a0001c0001t0001g0166 others(21): Show |
53 | HG00140.hp1 HG01255.hp1 HG01256.hp2 others(50): Show |
intron_variant | MODIFIER | c.245-241C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 2/7 | chr4 | 155942697 | |||||||
| chr4:155942724 | C | A | 3 | a0001c0001t0001g0081 a0001c0001t0002g0080 a0001c0001t0005g0041 |
4 | NA18956.hp2 NA18990.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.245-268G>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 2/7 | chr4 | 155942724 | |||||||
| chr4:155942872 | G | A | 2 | a0001c0001t0001g0081 a0001c0001t0002g0080 |
2 | NA19002.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.244+284C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 2/7 | chr4 | 155942872 | |||||||
| chr4:155943013 | A | G | 4 | a0001c0001t0001g0018 a0001c0001t0001g0071 a0001c0001t0001g0107 others(1): Show |
6 | HG01175.hp1 HG01361.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.244+143T>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 2/7 | chr4 | 155943013 | |||||||
| chr4:155943135 | A | G | 6 | a0001c0001t0001g0054 a0001c0001t0001g0185 a0001c0001t0002g0183 others(3): Show |
8 | HG02145.hp2 HG02451.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.244+21T>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 2/7 | chr4 | 155943135 | |||||||
| chr4:155943422 | T | C | 1 | a0001c0001t0001g0063 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.136-158A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155943422 | |||||||
| chr4:155943519 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.136-255C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155943519 | |||||||
| chr4:155943599 | C | A | 25 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(22): Show |
39 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(36): Show |
intron_variant | MODIFIER | c.136-335G>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155943599 | |||||||
| chr4:155944024 | C | T | 24 | a0001c0001t0001g0143 a0001c0001t0001g0165 a0001c0001t0001g0166 others(21): Show |
53 | HG00140.hp1 HG01255.hp1 HG01256.hp2 others(50): Show |
intron_variant | MODIFIER | c.136-760G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155944024 | |||||||
| chr4:155944050 | T | C | 28 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(25): Show |
42 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.136-786A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155944050 | |||||||
| chr4:155944180 | T | C | 1 | a0001c0001t0006g0153 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.136-916A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155944180 | |||||||
| chr4:155944202 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.136-938T>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155944202 | |||||||
| chr4:155944334 | A | C | 45 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(42): Show |
70 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.136-1070T>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155944334 | |||||||
| chr4:155944343 | A | T | 13 | a0001c0001t0001g0017 a0001c0001t0001g0035 a0001c0001t0001g0040 others(10): Show |
18 | NA18943.hp2 NA18947.hp2 NA18949.hp1 others(15): Show |
intron_variant | MODIFIER | c.136-1079T>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155944343 | |||||||
| chr4:155944356 | T | C | 1 | a0001c0001t0006g0153 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.136-1092A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155944356 | |||||||
| chr4:155944462 | G | A | 3 | a0001c0001t0001g0055 a0001c0001t0001g0064 a0001c0001t0007g0065 |
3 | HG00735.hp2 HG01069.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.136-1198C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155944462 | |||||||
| chr4:155944484 | T | G | 1 | a0001c0001t0001g0166 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.136-1220A>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155944484 | |||||||
| chr4:155944505 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.136-1241T>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155944505 | |||||||
| chr4:155944509 | G | A | 2 | a0001c0001t0005g0009 a0001c0001t0005g0152 |
7 | HG01168.hp2 NA18940.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.136-1245C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155944509 | |||||||
| chr4:155944576 | T | C | 3 | a0001c0001t0002g0042 a0001c0001t0002g0078 a0001c0001t0002g0135 |
4 | HG00738.hp2 HG02602.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-1312A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155944576 | |||||||
| chr4:155944809 | G | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(137): Show |
266 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.136-1545C>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155944809 | |||||||
| chr4:155944836 | A | G | 122 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(119): Show |
233 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.136-1572T>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155944836 | |||||||
| chr4:155944955 | T | TA | 85 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0017 others(82): Show |
162 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.136-1692dupT | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155944955 | |||||||
| chr4:155944955 | TA | T | 33 | a0001c0001t0001g0130 a0001c0001t0001g0143 a0001c0001t0001g0165 others(30): Show |
75 | HG00140.hp1 HG01123.hp2 HG01167.hp1 others(72): Show |
intron_variant | MODIFIER | c.136-1692delT | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155944955 | |||||||
| chr4:155944974 | A | C | 4 | a0001c0001t0001g0054 a0001c0001t0001g0185 a0001c0001t0002g0183 others(1): Show |
6 | HG02451.hp1 HG02486.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.136-1710T>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155944974 | |||||||
| chr4:155944992 | C | A | 1 | a0001c0001t0004g0178 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.136-1728G>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155944992 | |||||||
| chr4:155945022 | T | C | 169 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(166): Show |
313 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(310): Show |
intron_variant | MODIFIER | c.136-1758A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155945022 | |||||||
| chr4:155945114 | G | A | 1 | a0001c0001t0002g0154 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.136-1850C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155945114 | |||||||
| chr4:155945206 | G | C | 70 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(67): Show |
137 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.136-1942C>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155945206 | |||||||
| chr4:155945236 | G | A | 1 | a0001c0001t0004g0170 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.136-1972C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155945236 | |||||||
| chr4:155945243 | C | G | 1 | a0001c0001t0002g0089 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.136-1979G>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155945243 | |||||||
| chr4:155945515 | G | C | 2 | a0001c0001t0005g0009 a0001c0001t0005g0152 |
7 | HG01168.hp2 NA18940.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.136-2251C>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155945515 | |||||||
| chr4:155945613 | G | A | 21 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0001g0088 others(18): Show |
34 | HG00738.hp2 HG01081.hp2 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.136-2349C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155945613 | |||||||
| chr4:155945792 | G | A | 3 | a0001c0001t0003g0013 a0001c0001t0003g0047 a0001c0001t0003g0148 |
7 | HG01109.hp1 HG01346.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.136-2528C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155945792 | |||||||
| chr4:155945828 | A | G | 1 | a0001c0001t0001g0098 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.136-2564T>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155945828 | |||||||
| chr4:155945875 | C | A | 1 | a0001c0001t0002g0127 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.136-2611G>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155945875 | |||||||
| chr4:155945904 | C | T | 1 | a0001c0001t0004g0155 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.136-2640G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155945904 | |||||||
| chr4:155945948 | C | T | 25 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(22): Show |
39 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(36): Show |
intron_variant | MODIFIER | c.136-2684G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155945948 | |||||||
| chr4:155945975 | C | T | 3 | a0001c0001t0001g0084 a0001c0001t0002g0007 a0001c0001t0002g0083 |
8 | HG02559.hp1 HG02698.hp1 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.136-2711G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155945975 | |||||||
| chr4:155946088 | G | A | 2 | a0001c0001t0005g0009 a0001c0001t0005g0152 |
7 | HG01168.hp2 NA18940.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.136-2824C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155946088 | |||||||
| chr4:155946172 | T | G | 8 | a0001c0001t0002g0049 a0001c0001t0003g0048 a0001c0001t0003g0142 others(5): Show |
12 | HG01123.hp2 HG01167.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.136-2908A>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155946172 | |||||||
| chr4:155946218 | A | G | 1 | a0001c0001t0001g0097 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.136-2954T>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155946218 | |||||||
| chr4:155946237 | T | C | 21 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0001g0088 others(18): Show |
33 | HG00738.hp2 HG01081.hp2 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.136-2973A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155946237 | |||||||
| chr4:155946288 | C | T | 24 | a0001c0001t0001g0143 a0001c0001t0001g0165 a0001c0001t0001g0166 others(21): Show |
53 | HG00140.hp1 HG01255.hp1 HG01256.hp2 others(50): Show |
intron_variant | MODIFIER | c.136-3024G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155946288 | |||||||
| chr4:155946328 | C | T | 96 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(93): Show |
165 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.136-3064G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155946328 | |||||||
| chr4:155946465 | G | A | 1 | a0001c0001t0001g0128 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.136-3201C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155946465 | |||||||
| chr4:155946612 | G | T | 1 | a0001c0001t0001g0172 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.136-3348C>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155946612 | |||||||
| chr4:155946632 | G | C | 36 | a0001c0001t0001g0051 a0001c0001t0001g0081 a0001c0001t0001g0084 others(33): Show |
58 | HG00738.hp2 HG01081.hp2 HG01109.hp2 others(55): Show |
intron_variant | MODIFIER | c.136-3368C>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155946632 | |||||||
| chr4:155946735 | C | A | 1 | a0001c0001t0001g0069 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.136-3471G>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155946735 | |||||||
| chr4:155946850 | G | A | 172 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(169): Show |
318 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(315): Show |
intron_variant | MODIFIER | c.136-3586C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155946850 | |||||||
| chr4:155946861 | A | T | 172 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(169): Show |
318 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(315): Show |
intron_variant | MODIFIER | c.136-3597T>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155946861 | |||||||
| chr4:155946879 | G | A | 101 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(98): Show |
179 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.136-3615C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155946879 | |||||||
| chr4:155947016 | C | T | 101 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(98): Show |
179 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.136-3752G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155947016 | |||||||
| chr4:155947048 | G | T | 6 | a0001c0001t0003g0013 a0001c0001t0003g0047 a0001c0001t0003g0148 others(3): Show |
15 | HG01109.hp1 HG01168.hp2 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.136-3784C>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155947048 | |||||||
| chr4:155947076 | G | A | 27 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(24): Show |
41 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.136-3812C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155947076 | |||||||
| chr4:155947099 | G | A | 172 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(169): Show |
318 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(315): Show |
intron_variant | MODIFIER | c.136-3835C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155947099 | |||||||
| chr4:155947280 | T | G | 2 | a0001c0001t0001g0030 a0001c0001t0001g0070 |
3 | HG01070.hp1 HG01071.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.136-4016A>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155947280 | |||||||
| chr4:155947473 | G | A | 1 | a0001c0001t0008g0045 | 2 | HG02559.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.136-4209C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155947473 | |||||||
| chr4:155947548 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.136-4284A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155947548 | |||||||
| chr4:155947584 | A | G | 2 | a0001c0003t0003g0181 a0001c0003t0004g0182 |
2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.136-4320T>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155947584 | |||||||
| chr4:155947711 | T | G | 1 | a0001c0001t0006g0153 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.136-4447A>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155947711 | |||||||
| chr4:155947717 | G | T | 1 | a0001c0001t0002g0149 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.136-4453C>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155947717 | |||||||
| chr4:155947778 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.136-4514C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155947778 | |||||||
| chr4:155947816 | G | C | 8 | a0001c0001t0002g0049 a0001c0001t0003g0048 a0001c0001t0003g0142 others(5): Show |
12 | HG01123.hp2 HG01167.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.136-4552C>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155947816 | |||||||
| chr4:155947924 | T | C | 2 | a0001c0001t0001g0040 a0001c0001t0011g0129 |
3 | NA18947.hp2 NA19000.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.136-4660A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155947924 | |||||||
| chr4:155947937 | G | C | 22 | a0001c0001t0001g0143 a0001c0001t0001g0165 a0001c0001t0001g0166 others(19): Show |
50 | HG00140.hp1 HG01255.hp1 HG01256.hp2 others(47): Show |
intron_variant | MODIFIER | c.136-4673C>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155947937 | |||||||
| chr4:155947950 | T | C | 1 | a0001c0001t0001g0130 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.136-4686A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155947950 | |||||||
| chr4:155948038 | G | T | 1 | a0001c0001t0001g0096 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.136-4774C>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155948038 | |||||||
| chr4:155948065 | C | CT | 98 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(95): Show |
188 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.136-4802dupA | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155948065 | |||||||
| chr4:155948071 | T | TG | 75 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(72): Show |
131 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.136-4808_136-4807i others(3): Show |
CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155948071 | |||||||
| chr4:155948106 | G | A | 1 | a0001c0001t0002g0043 | 2 | HG01175.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.136-4842C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155948106 | |||||||
| chr4:155948153 | C | G | 1 | a0001c0001t0006g0091 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-4889G>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155948153 | |||||||
| chr4:155948155 | C | T | 1 | a0001c0001t0002g0057 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.136-4891G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155948155 | |||||||
| chr4:155948220 | G | A | 1 | a0001c0001t0018g0168 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.136-4956C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155948220 | |||||||
| chr4:155948352 | T | C | 1 | a0001c0001t0003g0179 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.136-5088A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155948352 | |||||||
| chr4:155948373 | T | TTG | 2 | a0001c0001t0002g0184 a0001c0001t0003g0053 |
3 | HG02145.hp2 HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.136-5111_136-5110d others(4): Show |
CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155948373 | |||||||
| chr4:155948373 | T | TTGTG | 2 | a0001c0001t0001g0054 a0001c0001t0001g0185 |
3 | HG02451.hp1 HG02486.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.136-5113_136-5110d others(6): Show |
CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155948373 | |||||||
| chr4:155948373 | TTGTG | T | 3 | a0001c0001t0002g0023 a0001c0003t0003g0181 a0001c0003t0004g0182 |
5 | HG02257.hp2 HG02647.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.136-5113_136-5110d others(6): Show |
CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155948373 | |||||||
| chr4:155948373 | TTGTGTG | T | 101 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(98): Show |
178 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.136-5115_136-5110d others(8): Show |
CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155948373 | |||||||
| chr4:155948373 | TTGTGTGT others(1): Show |
T | 68 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(65): Show |
135 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.136-5117_136-5110d others(10): Show |
CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155948373 | |||||||
| chr4:155948615 | A | G | 1 | a0001c0001t0002g0056 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.135+5098T>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155948615 | |||||||
| chr4:155948627 | T | C | 25 | a0001c0001t0001g0143 a0001c0001t0001g0165 a0001c0001t0001g0166 others(22): Show |
54 | HG00140.hp1 HG01255.hp1 HG01256.hp2 others(51): Show |
intron_variant | MODIFIER | c.135+5086A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155948627 | |||||||
| chr4:155948727 | C | T | 1 | a0001c0001t0004g0171 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.135+4986G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155948727 | |||||||
| chr4:155948767 | G | C | 1 | a0001c0001t0001g0137 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.135+4946C>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155948767 | |||||||
| chr4:155948857 | A | C | 172 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(169): Show |
318 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(315): Show |
intron_variant | MODIFIER | c.135+4856T>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155948857 | |||||||
| chr4:155948866 | A | G | 172 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(169): Show |
318 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(315): Show |
intron_variant | MODIFIER | c.135+4847T>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155948866 | |||||||
| chr4:155948890 | C | T | 16 | a0001c0001t0001g0051 a0001c0001t0001g0172 a0001c0001t0003g0179 others(13): Show |
26 | HG02155.hp2 HG02258.hp2 HG02451.hp2 others(23): Show |
intron_variant | MODIFIER | c.135+4823G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155948890 | |||||||
| chr4:155948979 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.135+4734G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155948979 | |||||||
| chr4:155949087 | T | C | 1 | a0001c0001t0006g0153 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.135+4626A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155949087 | |||||||
| chr4:155949187 | G | C | 172 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(169): Show |
318 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(315): Show |
intron_variant | MODIFIER | c.135+4526C>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155949187 | |||||||
| chr4:155949188 | C | T | 1 | a0001c0001t0005g0152 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.135+4525G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155949188 | |||||||
| chr4:155949247 | A | T | 1 | a0001c0001t0003g0144 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.135+4466T>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155949247 | |||||||
| chr4:155949250 | A | T | 2 | a0001c0001t0005g0009 a0001c0001t0005g0152 |
7 | HG01168.hp2 NA18940.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.135+4463T>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155949250 | |||||||
| chr4:155949293 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.135+4420A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155949293 | |||||||
| chr4:155949307 | A | C | 1 | a0001c0001t0002g0159 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.135+4406T>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155949307 | |||||||
| chr4:155949313 | T | C | 1 | a0001c0001t0001g0044 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.135+4400A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155949313 | |||||||
| chr4:155949429 | C | T | 2 | a0001c0001t0001g0046 a0001c0001t0003g0005 |
9 | HG02258.hp1 HG02630.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.135+4284G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155949429 | |||||||
| chr4:155949630 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.135+4083G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155949630 | |||||||
| chr4:155949631 | A | G | 173 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(170): Show |
319 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(316): Show |
intron_variant | MODIFIER | c.135+4082T>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155949631 | |||||||
| chr4:155949685 | G | C | 1 | a0001c0001t0002g0169 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.135+4028C>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155949685 | |||||||
| chr4:155949758 | T | C | 5 | a0001c0001t0001g0054 a0001c0001t0001g0185 a0001c0001t0002g0183 others(2): Show |
7 | HG02145.hp2 HG02451.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.135+3955A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155949758 | |||||||
| chr4:155949815 | T | A | 11 | a0001c0001t0001g0084 a0001c0001t0001g0088 a0001c0001t0002g0007 others(8): Show |
20 | HG01081.hp2 HG01256.hp2 HG01258.hp2 others(17): Show |
intron_variant | MODIFIER | c.135+3898A>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155949815 | |||||||
| chr4:155949994 | A | T | 1 | a0001c0001t0004g0170 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.135+3719T>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155949994 | |||||||
| chr4:155950006 | T | TA | 146 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(143): Show |
278 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(275): Show |
intron_variant | MODIFIER | c.135+3706dupT | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155950006 | |||||||
| chr4:155950103 | A | G | 1 | a0001c0001t0001g0073 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.135+3610T>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155950103 | |||||||
| chr4:155950121 | A | G | 28 | a0001c0001t0001g0143 a0001c0001t0001g0165 a0001c0001t0001g0166 others(25): Show |
58 | HG00140.hp1 HG01123.hp2 HG01167.hp1 others(55): Show |
intron_variant | MODIFIER | c.135+3592T>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155950121 | |||||||
| chr4:155950140 | G | T | 173 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(170): Show |
319 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(316): Show |
intron_variant | MODIFIER | c.135+3573C>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155950140 | |||||||
| chr4:155950185 | T | A | 146 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(143): Show |
278 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(275): Show |
intron_variant | MODIFIER | c.135+3528A>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155950185 | |||||||
| chr4:155950389 | G | A | 173 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(170): Show |
319 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(316): Show |
intron_variant | MODIFIER | c.135+3324C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155950389 | |||||||
| chr4:155950479 | A | C | 84 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(81): Show |
155 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.135+3234T>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155950479 | |||||||
| chr4:155950506 | GAA | G | 27 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(24): Show |
41 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.135+3205_135+3206d others(4): Show |
CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155950506 | |||||||
| chr4:155950550 | T | A | 151 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(148): Show |
285 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(282): Show |
intron_variant | MODIFIER | c.135+3163A>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155950550 | |||||||
| chr4:155950561 | A | G | 17 | a0001c0001t0001g0051 a0001c0001t0001g0172 a0001c0001t0003g0179 others(14): Show |
29 | HG02155.hp2 HG02258.hp2 HG02451.hp2 others(26): Show |
intron_variant | MODIFIER | c.135+3152T>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155950561 | |||||||
| chr4:155950584 | A | C | 11 | a0001c0001t0001g0084 a0001c0001t0001g0088 a0001c0001t0002g0007 others(8): Show |
20 | HG01081.hp2 HG01256.hp2 HG01258.hp2 others(17): Show |
intron_variant | MODIFIER | c.135+3129T>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155950584 | |||||||
| chr4:155950625 | C | T | 8 | a0001c0001t0002g0049 a0001c0001t0003g0048 a0001c0001t0003g0142 others(5): Show |
12 | HG01123.hp2 HG01167.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.135+3088G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155950625 | |||||||
| chr4:155950649 | G | T | 4 | a0001c0001t0003g0090 a0001c0001t0006g0091 a0001c0001t0006g0092 others(1): Show |
4 | HG02615.hp2 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+3064C>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155950649 | |||||||
| chr4:155950746 | G | A | 1 | a0001c0001t0004g0180 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.135+2967C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155950746 | |||||||
| chr4:155950852 | AC | A | 146 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(143): Show |
278 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(275): Show |
intron_variant | MODIFIER | c.135+2860delG | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155950852 | |||||||
| chr4:155950855 | C | G | 146 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(143): Show |
278 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(275): Show |
intron_variant | MODIFIER | c.135+2858G>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155950855 | |||||||
| chr4:155950857 | C | G | 146 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(143): Show |
278 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(275): Show |
intron_variant | MODIFIER | c.135+2856G>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155950857 | |||||||
| chr4:155950881 | G | C | 1 | a0001c0001t0002g0154 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.135+2832C>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155950881 | |||||||
| chr4:155950886 | C | T | 1 | a0001c0001t0002g0154 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.135+2827G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155950886 | |||||||
| chr4:155950896 | A | T | 11 | a0001c0001t0001g0084 a0001c0001t0001g0088 a0001c0001t0002g0007 others(8): Show |
20 | HG01081.hp2 HG01256.hp2 HG01258.hp2 others(17): Show |
intron_variant | MODIFIER | c.135+2817T>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155950896 | |||||||
| chr4:155950921 | G | A | 146 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(143): Show |
278 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(275): Show |
intron_variant | MODIFIER | c.135+2792C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155950921 | |||||||
| chr4:155950944 | T | A | 146 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(143): Show |
278 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(275): Show |
intron_variant | MODIFIER | c.135+2769A>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155950944 | |||||||
| chr4:155950955 | C | A | 1 | a0001c0001t0008g0045 | 2 | HG02559.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.135+2758G>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155950955 | |||||||
| chr4:155951109 | A | G | 2 | a0001c0001t0005g0009 a0001c0001t0005g0152 |
7 | HG01168.hp2 NA18940.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.135+2604T>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155951109 | |||||||
| chr4:155951138 | C | T | 2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
4 | HG00735.hp1 HG02602.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+2575G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155951138 | |||||||
| chr4:155951481 | G | A | 1 | a0001c0001t0005g0009 | 6 | NA18940.hp1 NA18942.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.135+2232C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155951481 | |||||||
| chr4:155951678 | C | T | 6 | a0001c0001t0003g0013 a0001c0001t0003g0047 a0001c0001t0003g0148 others(3): Show |
15 | HG01109.hp1 HG01168.hp2 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.135+2035G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155951678 | |||||||
| chr4:155951679 | C | T | 51 | a0001c0001t0001g0051 a0001c0001t0001g0143 a0001c0001t0001g0165 others(48): Show |
102 | HG00140.hp1 HG01109.hp1 HG01123.hp2 others(99): Show |
intron_variant | MODIFIER | c.135+2034G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155951679 | |||||||
| chr4:155951683 | T | C | 1 | a0001c0001t0001g0139 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.135+2030A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155951683 | |||||||
| chr4:155951741 | A | T | 95 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(92): Show |
176 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.135+1972T>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155951741 | |||||||
| chr4:155951759 | A | C | 1 | a0001c0001t0002g0082 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.135+1954T>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155951759 | |||||||
| chr4:155951806 | C | T | 5 | a0001c0001t0003g0013 a0001c0001t0003g0047 a0001c0001t0003g0148 others(2): Show |
14 | HG01109.hp1 HG01168.hp2 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.135+1907G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155951806 | |||||||
| chr4:155951846 | A | T | 34 | a0001c0001t0001g0143 a0001c0001t0001g0165 a0001c0001t0001g0166 others(31): Show |
73 | HG00140.hp1 HG01109.hp1 HG01123.hp2 others(70): Show |
intron_variant | MODIFIER | c.135+1867T>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155951846 | |||||||
| chr4:155951849 | C | T | 2 | a0001c0001t0001g0081 a0001c0001t0002g0080 |
2 | NA19002.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.135+1864G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155951849 | |||||||
| chr4:155951908 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.135+1805G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155951908 | |||||||
| chr4:155952195 | C | T | 1 | a0001c0001t0001g0079 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.135+1518G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155952195 | |||||||
| chr4:155952267 | G | C | 1 | a0001c0001t0001g0054 | 2 | HG02451.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.135+1446C>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155952267 | |||||||
| chr4:155952329 | A | G | 24 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(21): Show |
38 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.135+1384T>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155952329 | |||||||
| chr4:155952494 | C | T | 5 | a0001c0001t0003g0013 a0001c0001t0003g0047 a0001c0001t0003g0148 others(2): Show |
14 | HG01109.hp1 HG01168.hp2 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.135+1219G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155952494 | |||||||
| chr4:155952505 | C | G | 178 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(175): Show |
326 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(323): Show |
intron_variant | MODIFIER | c.135+1208G>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155952505 | |||||||
| chr4:155952535 | G | A | 1 | a0001c0001t0008g0045 | 2 | HG02559.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.135+1178C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155952535 | |||||||
| chr4:155952633 | A | G | 1 | a0001c0001t0004g0151 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.135+1080T>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155952633 | |||||||
| chr4:155952641 | A | G | 1 | a0001c0001t0002g0078 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.135+1072T>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155952641 | |||||||
| chr4:155952682 | A | G | 1 | a0001c0001t0001g0077 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.135+1031T>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155952682 | |||||||
| chr4:155952876 | T | C | 96 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(93): Show |
177 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.135+837A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155952876 | |||||||
| chr4:155952923 | A | C | 1 | a0001c0001t0002g0150 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.135+790T>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155952923 | |||||||
| chr4:155952933 | T | C | 1 | a0001c0001t0001g0072 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.135+780A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155952933 | |||||||
| chr4:155953050 | T | C | 1 | a0001c0001t0001g0141 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.135+663A>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155953050 | |||||||
| chr4:155953072 | A | T | 96 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(93): Show |
177 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.135+641T>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155953072 | |||||||
| chr4:155953171 | A | G | 178 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(175): Show |
326 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(323): Show |
intron_variant | MODIFIER | c.135+542T>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155953171 | |||||||
| chr4:155953376 | A | C | 180 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(177): Show |
335 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(332): Show |
intron_variant | MODIFIER | c.135+337T>G | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155953376 | |||||||
| chr4:155953412 | A | G | 1 | a0001c0001t0003g0148 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.135+301T>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155953412 | |||||||
| chr4:155953525 | C | T | 1 | a0001c0001t0002g0076 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.135+188G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155953525 | |||||||
| chr4:155953529 | A | G | 25 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(22): Show |
39 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(36): Show |
intron_variant | MODIFIER | c.135+184T>C | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155953529 | |||||||
| chr4:155953681 | G | A | 81 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(78): Show |
148 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.135+32C>T | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155953681 | |||||||
| chr4:155953690 | C | T | 5 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0002g0032 others(2): Show |
7 | NA18944.hp2 NA18972.hp1 NA18991.hp2 others(4): Show |
intron_variant | MODIFIER | c.135+23G>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155953690 | |||||||
| chr4:155953697 | G | T | 25 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(22): Show |
39 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(36): Show |
intron_variant | MODIFIER | c.135+16C>A | CTSO | ENSG00000256043.5 | transcript | ENST00000433477.4 | protein_coding | 1/7 | chr4 | 155953697 |