Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51380 |
| ensemblid | ENSG00000139631.20 |
| hgncid | 18966 |
| symbol | CSAD |
| name | cysteine sulfinic acid decarboxylase |
| refseq_nuc | NM_001244705.2 |
| refseq_prot | NP_001231634.1 |
| ensembl_nuc | ENST00000444623.6 |
| ensembl_prot | ENSP00000415485.1 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 53157663 |
| end | 53180925 |
| strand | - |
| ver | v1.2 |
| region | chr12:53157663-53180925 |
| region5000 | chr12:53152663-53185925 |
| regionname0 | CSAD_chr12_53157663_53180925 |
| regionname5000 | CSAD_chr12_53152663_53185925 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 493 | 328 | 89 | 41 | 148 | 6 | 42 | 115 | CSAD_chr12_53152663_53185925 | CSAD | MADSE others(488): Show |
chr12 | 53152663 | 53185925 |
| a0002 | 0/0 | 493 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | MADSE others(488): Show |
chr12 | 53152663 | 53185925 |
| a0003 | 0/0 | 493 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | MADSE others(488): Show |
chr12 | 53152663 | 53185925 |
| a0004 | 0/0 | 493 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | MADSE others(488): Show |
chr12 | 53152663 | 53185925 |
| a0005 | 0/0 | 493 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | MADSE others(488): Show |
chr12 | 53152663 | 53185925 |
| a0006 | 0/0 | 493 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | MADSE others(488): Show |
chr12 | 53152663 | 53185925 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1479 | 278 | 82 | 39 | 109 | 5 | 41 | CSAD_chr12_53152663_53185925 | CSAD | ATGGC others(1474): Show |
chr12 | 53152663 | 53185925 | ||
| a0001c0002 | 0/0 | 1479 | 41 | 1 | 1 | 38 | 1 | 0 | CSAD_chr12_53152663_53185925 | CSAD | ATGGC others(1474): Show |
chr12 | 53152663 | 53185925 | ||
| a0001c0003 | 0/0 | 1479 | 6 | 5 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | ATGGC others(1474): Show |
chr12 | 53152663 | 53185925 | ||
| a0001c0004 | 0/0 | 1479 | 2 | 1 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | ATGGC others(1474): Show |
chr12 | 53152663 | 53185925 | ||
| a0001c0008 | 0/0 | 1479 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | ATGGC others(1474): Show |
chr12 | 53152663 | 53185925 | ||
| a0002c0009 | 0/0 | 1479 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | ATGGC others(1474): Show |
chr12 | 53152663 | 53185925 | ||
| a0002c0010 | 0/0 | 1479 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | ATGGC others(1474): Show |
chr12 | 53152663 | 53185925 | ||
| a0003c0006 | 0/0 | 1479 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | ATGGC others(1474): Show |
chr12 | 53152663 | 53185925 | ||
| a0004c0011 | 0/0 | 1479 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | ATGGC others(1474): Show |
chr12 | 53152663 | 53185925 | ||
| a0005c0007 | 0/0 | 1479 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | ATGGC others(1474): Show |
chr12 | 53152663 | 53185925 | ||
| a0006c0005 | 0/0 | 1479 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | ATGGC others(1474): Show |
chr12 | 53152663 | 53185925 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2614 | 212 | 42 | 35 | 99 | 5 | 29 | CSAD_chr12_53152663_53185925 | CSAD | CTTCC others(2609): Show |
chr12 | 53152663 | 53185925 |
| a0001c0001t0002 | 0/0 | 2614 | 39 | 21 | 4 | 2 | 0 | 12 | CSAD_chr12_53152663_53185925 | CSAD | CTTCC others(2609): Show |
chr12 | 53152663 | 53185925 |
| a0001c0001t0003 | 0/0 | 2614 | 13 | 13 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | CTTCC others(2609): Show |
chr12 | 53152663 | 53185925 |
| a0001c0001t0004 | 0/0 | 2614 | 6 | 0 | 0 | 6 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | CTTCC others(2609): Show |
chr12 | 53152663 | 53185925 |
| a0001c0001t0007 | 0/0 | 2614 | 2 | 2 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | CTTCC others(2609): Show |
chr12 | 53152663 | 53185925 |
| a0001c0001t0008 | 0/0 | 2614 | 2 | 2 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | CTTCC others(2609): Show |
chr12 | 53152663 | 53185925 |
| a0001c0001t0009 | 0/0 | 2614 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | CTTCC others(2609): Show |
chr12 | 53152663 | 53185925 |
| a0001c0001t0010 | 0/0 | 2614 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | CTTCC others(2609): Show |
chr12 | 53152663 | 53185925 |
| a0001c0001t0012 | 0/0 | 2614 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | CTTCC others(2609): Show |
chr12 | 53152663 | 53185925 |
| a0001c0001t0013 | 0/0 | 2614 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | CTTCC others(2609): Show |
chr12 | 53152663 | 53185925 |
| a0001c0002t0002 | 0/0 | 2614 | 35 | 1 | 1 | 33 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | CTTCC others(2609): Show |
chr12 | 53152663 | 53185925 |
| a0001c0002t0006 | 0/0 | 2614 | 5 | 0 | 0 | 5 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | CTTCC others(2609): Show |
chr12 | 53152663 | 53185925 |
| a0001c0002t0011 | 0/0 | 2614 | 1 | 0 | 0 | 0 | 1 | 0 | CSAD_chr12_53152663_53185925 | CSAD | CTTCC others(2609): Show |
chr12 | 53152663 | 53185925 |
| a0001c0003t0005 | 0/0 | 2614 | 6 | 5 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | CTTCC others(2609): Show |
chr12 | 53152663 | 53185925 |
| a0001c0004t0002 | 0/0 | 2614 | 2 | 1 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | CTTCC others(2609): Show |
chr12 | 53152663 | 53185925 |
| a0001c0008t0014 | 0/0 | 2614 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | CTTCC others(2609): Show |
chr12 | 53152663 | 53185925 |
| a0002c0009t0001 | 0/0 | 2614 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | CTTCC others(2609): Show |
chr12 | 53152663 | 53185925 |
| a0002c0010t0002 | 0/0 | 2614 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | CTTCC others(2609): Show |
chr12 | 53152663 | 53185925 |
| a0003c0006t0001 | 0/0 | 2614 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | CTTCC others(2609): Show |
chr12 | 53152663 | 53185925 |
| a0004c0011t0001 | 0/0 | 2614 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | CTTCC others(2609): Show |
chr12 | 53152663 | 53185925 |
| a0005c0007t0001 | 0/0 | 2614 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | CTTCC others(2609): Show |
chr12 | 53152663 | 53185925 |
| a0006c0005t0001 | 0/0 | 2614 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | CTTCC others(2609): Show |
chr12 | 53152663 | 53185925 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 57 | 5 | 11 | 33 | 1 | 7 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0002 | 0/0 | 38 | 1 | 8 | 24 | 0 | 5 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 1 | 0 | 1 | 3 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0010 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0012 | 1/0 | 4 | 1 | 2 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0013 | 0/0 | 4 | 1 | 2 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0100 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0002g0004 | 0/0 | 8 | 2 | 1 | 1 | 0 | 4 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0002g0006 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0002g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0002g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0002g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0003g0005 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0003g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0003g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0004g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0007g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0008g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0009g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0010g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0012g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0001t0013g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0002t0002g0003 | 0/0 | 18 | 1 | 0 | 17 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0002t0002g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0002t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0002t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0002t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0002t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0002t0006g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0002t0006g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0002t0006g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0002t0011g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0003t0005g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0003t0005g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0003t0005g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0003t0005g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0003t0005g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0004t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0004t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0001c0008t0014g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0002c0009t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0002c0010t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0003c0006t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0004c0011t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0005c0007t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| a0006c0005t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | GBR | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0089 | EUR | GBR | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | FIN | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG00323 | hp2 | a0001 | c0002 | t0011 | g0044 | EUR | FIN | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG00423 | hp2 | a0001 | c0002 | t0002 | g0022 | EAS | CHS | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG00438 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | CHS | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG00544 | hp1 | a0001 | c0002 | t0002 | g0045 | EAS | CHS | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG00544 | hp2 | a0001 | c0002 | t0002 | g0023 | EAS | CHS | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG00558 | hp2 | a0001 | c0002 | t0002 | g0048 | EAS | CHS | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG01255 | hp1 | a0001 | c0003 | t0005 | g0114 | AMR | CLM | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0047 | AMR | CLM | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG01346 | hp1 | a0002 | c0010 | t0002 | g0046 | AMR | CLM | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG01433 | hp2 | a0003 | c0006 | t0001 | g0086 | AMR | CLM | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG01884 | hp1 | a0001 | c0003 | t0005 | g0113 | AFR | ACB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0051 | AFR | ACB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG01891 | hp2 | a0001 | c0001 | t0008 | g0028 | AFR | ACB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG01981 | hp1 | a0002 | c0009 | t0001 | g0119 | AMR | PEL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02056 | hp2 | a0001 | c0002 | t0002 | g0043 | EAS | KHV | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02071 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | KHV | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02071 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | KHV | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02135 | hp1 | a0001 | c0001 | t0012 | g0095 | EAS | KHV | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02145 | hp1 | a0001 | c0001 | t0010 | g0071 | AFR | ACB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | ACB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | CDX | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | ACB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | ACB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | ACB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02523 | hp1 | a0004 | c0011 | t0001 | g0117 | EAS | KHV | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0064 | SAS | PJL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02622 | hp2 | a0001 | c0003 | t0005 | g0035 | AFR | GWD | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02630 | hp2 | a0001 | c0003 | t0005 | g0035 | AFR | GWD | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0061 | SAS | PJL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | GWD | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ESN | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02922 | hp2 | a0001 | c0001 | t0009 | g0057 | AFR | ESN | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0054 | AFR | ESN | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ESN | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | ESN | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | ESN | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0058 | SAS | PJL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | MSL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | ESN | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG03139 | hp1 | a0001 | c0002 | t0002 | g0003 | AFR | ESN | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | ESN | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG03195 | hp1 | a0001 | c0001 | t0008 | g0028 | AFR | ESN | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | ESN | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | MSL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG03209 | hp2 | a0001 | c0001 | t0007 | g0029 | AFR | MSL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | MSL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0063 | SAS | PJL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG03453 | hp1 | a0001 | c0004 | t0002 | g0056 | AFR | MSL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG03453 | hp2 | a0001 | c0003 | t0005 | g0116 | AFR | MSL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | MSL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | MSL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0053 | AFR | GWD | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0070 | AFR | GWD | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG03579 | hp2 | a0001 | c0001 | t0007 | g0029 | AFR | MSL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0062 | SAS | PJL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG03688 | hp2 | a0001 | c0004 | t0002 | g0066 | SAS | STU | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | BEB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | BEB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | BEB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0060 | SAS | BEB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | STU | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | BEB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | BEB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0055 | SAS | STU | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | STU | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0059 | SAS | STU | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | YRI | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | CHB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CHB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CHB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18906 | hp1 | a0001 | c0003 | t0005 | g0115 | AFR | YRI | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | YRI | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18944 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18946 | hp2 | a0001 | c0002 | t0006 | g0072 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18948 | hp1 | a0001 | c0008 | t0014 | g0132 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18948 | hp2 | a0005 | c0007 | t0001 | g0088 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18950 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18952 | hp1 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18952 | hp2 | a0001 | c0002 | t0002 | g0022 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18954 | hp1 | a0001 | c0001 | t0013 | g0091 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18964 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18965 | hp2 | a0001 | c0002 | t0006 | g0016 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18967 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18973 | hp2 | a0001 | c0002 | t0002 | g0023 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18975 | hp1 | a0001 | c0002 | t0006 | g0016 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18985 | hp2 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18988 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18994 | hp2 | a0001 | c0002 | t0002 | g0041 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18995 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18997 | hp2 | a0001 | c0002 | t0002 | g0042 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18998 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19005 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19011 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0069 | AFR | LWK | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0068 | AFR | LWK | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | LWK | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | LWK | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19056 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19058 | hp1 | a0001 | c0002 | t0006 | g0073 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19060 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19062 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19064 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19070 | hp2 | a0001 | c0002 | t0006 | g0016 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19077 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19077 | hp2 | a0001 | c0001 | t0004 | g0102 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19082 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19083 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19084 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19085 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19085 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19087 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19089 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19091 | hp2 | a0001 | c0002 | t0002 | g0050 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19240 | hp1 | a0006 | c0005 | t0001 | g0144 | AFR | YRI | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | YRI | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | ASW | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0150 | EUR | TSI | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | ACB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | ACB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | ACB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0052 | AFR | ACB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | MSL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | MSL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | USA | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | USA | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA18955 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | LWK | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | LWK | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0100 | REF | REF | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0012 | REF | REF | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:53160142 | C | T | 1 | a0002 | 2 | HG01346.hp1 HG01981.hp1 |
missense_variant | MODERATE | c.1144G>A | p.Asp382Asn | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 14/17 | 1428/2614 | 1144/1482 | 382/493 | chr12 | 53160142 | |||
| chr12:53171972 | C | T | 1 | a0005 | 1 | NA18948.hp2 | missense_variant | MODERATE | c.361G>A | p.Ala121Thr | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 7/17 | 645/2614 | 361/1482 | 121/493 | chr12 | 53171972 | |||
| chr12:53172390 | A | T | 1 | a0003 | 1 | HG01433.hp2 | missense_variant | MODERATE | c.300T>A | p.His100Gln | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 6/17 | 584/2614 | 300/1482 | 100/493 | chr12 | 53172390 | |||
| chr12:53172428 | G | A | 1 | a0004 | 1 | HG02523.hp1 | missense_variant | MODERATE | c.262C>T | p.Arg88Trp | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 6/17 | 546/2614 | 262/1482 | 88/493 | chr12 | 53172428 | |||
| chr12:53173451 | A | T | 1 | a0006 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.20T>A | p.Leu7His | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 4/17 | 304/2614 | 20/1482 | 7/493 | chr12 | 53173451 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:53170081 | G | A | 2 | a0001c0002 a0002c0010 |
42 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(39): Show |
synonymous_variant | LOW | c.693C>T | p.Ala231Ala | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/17 | 977/2614 | 693/1482 | 231/493 | chr12 | 53170081 | |||
| chr12:53170473 | C | T | 1 | a0001c0003 | 6 | HG01255.hp1 HG01884.hp1 HG02622.hp2 others(3): Show |
synonymous_variant | LOW | c.597G>A | p.Ala199Ala | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 9/17 | 881/2614 | 597/1482 | 199/493 | chr12 | 53170473 | |||
| chr12:53171353 | C | T | 1 | a0001c0008 | 1 | NA18948.hp1 | synonymous_variant | LOW | c.540G>A | p.Pro180Pro | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 8/17 | 824/2614 | 540/1482 | 180/493 | chr12 | 53171353 | |||
| chr12:53172381 | G | A | 1 | a0001c0003 | 6 | HG01255.hp1 HG01884.hp1 HG02622.hp2 others(3): Show |
synonymous_variant | LOW | c.309C>T | p.Ala103Ala | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 6/17 | 593/2614 | 309/1482 | 103/493 | chr12 | 53172381 | |||
| chr12:53172625 | C | T | 1 | a0001c0004 | 2 | HG03453.hp1 HG03688.hp2 |
synonymous_variant | LOW | c.150G>A | p.Glu50Glu | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 5/17 | 434/2614 | 150/1482 | 50/493 | chr12 | 53172625 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:53157773 | G | T | 2 | a0001c0001t0001 a0001c0001t0008 |
3 | HG01891.hp2 HG03195.hp1 NA18983.hp1 |
3_prime_UTR_variant | MODIFIER | c.*738C>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 17/17 | 738 | chr12 | 53157773 | ||||||
| chr12:53157814 | A | G | 1 | a0001c0001t0010 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*697T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 17/17 | 697 | chr12 | 53157814 | ||||||
| chr12:53157940 | A | G | 1 | a0001c0001t0004 | 6 | HG02071.hp1 NA18998.hp2 NA19077.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*571T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 17/17 | 571 | chr12 | 53157940 | ||||||
| chr12:53157986 | T | C | 1 | a0001c0001t0008 | 2 | HG01891.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*525A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 17/17 | 525 | chr12 | 53157986 | ||||||
| chr12:53158046 | A | G | 1 | a0001c0001t0007 | 2 | HG03209.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*465T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 17/17 | 465 | chr12 | 53158046 | ||||||
| chr12:53158076 | G | C | 1 | a0001c0002t0011 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*435C>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 17/17 | 435 | chr12 | 53158076 | ||||||
| chr12:53158208 | G | A | 1 | a0001c0003t0005 | 6 | HG01255.hp1 HG01884.hp1 HG02622.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*303C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 17/17 | 303 | chr12 | 53158208 | ||||||
| chr12:53158264 | T | C | 1 | a0001c0001t0012 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*247A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 17/17 | 247 | chr12 | 53158264 | ||||||
| chr12:53158333 | A | C | 1 | a0001c0001t0010 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*178T>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 17/17 | 178 | chr12 | 53158333 | ||||||
| chr12:53158356 | G | A | 1 | a0001c0001t0003 | 13 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*155C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 17/17 | 155 | chr12 | 53158356 | ||||||
| chr12:53158415 | C | T | 1 | a0001c0001t0009 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*96G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 17/17 | 96 | chr12 | 53158415 | ||||||
| chr12:53158467 | C | A | 1 | a0001c0001t0013 | 1 | NA18954.hp1 | 3_prime_UTR_variant | MODIFIER | c.*44G>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 17/17 | 44 | chr12 | 53158467 | ||||||
| chr12:53158509 | G | A | 1 | a0001c0008t0014 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 17/17 | 2 | chr12 | 53158509 | ||||||
| chr12:53180823 | G | C | 1 | a0001c0002t0006 | 5 | NA18946.hp2 NA18965.hp2 NA18975.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-182C>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/17 | 7353 | chr12 | 53180823 | ||||||
| chr12:53180847 | A | C | 11 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0007 others(8): Show |
102 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(99): Show |
5_prime_UTR_variant | MODIFIER | c.-206T>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/17 | 7377 | chr12 | 53180847 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:53158691 | A | G | 24 | a0001c0001t0002g0049 a0001c0001t0003g0005 a0001c0001t0003g0024 others(21): Show |
58 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(55): Show |
splice_region_variant&intron_variant | LOW | c.1309-7T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 16/16 | chr12 | 53158691 | |||||||
| chr12:53158877 | G | T | 77 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0013 others(74): Show |
179 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.1309-193C>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 16/16 | chr12 | 53158877 | |||||||
| chr12:53159128 | A | C | 1 | a0001c0001t0003g0025 | 2 | HG03139.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1309-444T>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 16/16 | chr12 | 53159128 | |||||||
| chr12:53159448 | T | C | 18 | a0001c0001t0002g0049 a0001c0002t0002g0003 a0001c0002t0002g0009 others(15): Show |
43 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.1308+175A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 16/16 | chr12 | 53159448 | |||||||
| chr12:53159469 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1308+154G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 16/16 | chr12 | 53159469 | |||||||
| chr12:53159600 | A | G | 3 | a0001c0001t0002g0014 a0001c0001t0002g0051 a0001c0001t0002g0065 |
5 | HG01884.hp2 HG02145.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1308+23T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 16/16 | chr12 | 53159600 | |||||||
| chr12:53159615 | A | T | 1 | a0001c0001t0010g0071 | 1 | HG02145.hp1 | splice_region_variant&intron_variant | LOW | c.1308+8T>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 16/16 | chr12 | 53159615 | |||||||
| chr12:53159734 | A | G | 1 | a0001c0001t0010g0071 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1219-22T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 15/16 | chr12 | 53159734 | |||||||
| chr12:53159736 | G | A | 1 | a0001c0001t0007g0029 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1219-24C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 15/16 | chr12 | 53159736 | |||||||
| chr12:53159811 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1218+76T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 15/16 | chr12 | 53159811 | |||||||
| chr12:53160045 | C | T | 5 | a0001c0001t0003g0005 a0001c0001t0003g0024 a0001c0001t0003g0025 others(2): Show |
13 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1166+75G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 14/16 | chr12 | 53160045 | |||||||
| chr12:53160342 | T | C | 5 | a0001c0001t0003g0005 a0001c0001t0003g0024 a0001c0001t0003g0025 others(2): Show |
13 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.967-23A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 13/16 | chr12 | 53160342 | |||||||
| chr12:53160386 | T | G | 1 | a0001c0001t0007g0029 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.967-67A>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 13/16 | chr12 | 53160386 | |||||||
| chr12:53160412 | T | C | 1 | a0001c0001t0010g0071 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.967-93A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 13/16 | chr12 | 53160412 | |||||||
| chr12:53160499 | G | A | 17 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0013 others(14): Show |
65 | HG00140.hp1 HG00438.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.967-180C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 13/16 | chr12 | 53160499 | |||||||
| chr12:53160568 | C | A | 1 | a0001c0001t0001g0082 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.966+195G>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 13/16 | chr12 | 53160568 | |||||||
| chr12:53160578 | T | TTC | 5 | a0001c0001t0003g0005 a0001c0001t0003g0024 a0001c0001t0003g0025 others(2): Show |
13 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.966+183_966+184dup others(2): Show |
CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 13/16 | chr12 | 53160578 | |||||||
| chr12:53160599 | G | C | 5 | a0001c0001t0003g0005 a0001c0001t0003g0024 a0001c0001t0003g0025 others(2): Show |
13 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.966+164C>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 13/16 | chr12 | 53160599 | |||||||
| chr12:53160613 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.966+150G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 13/16 | chr12 | 53160613 | |||||||
| chr12:53161256 | G | C | 1 | a0001c0001t0001g0077 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.819+17C>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 11/16 | chr12 | 53161256 | |||||||
| chr12:53161450 | G | C | 1 | a0001c0001t0001g0150 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.703-61C>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53161450 | |||||||
| chr12:53161591 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.703-202G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53161591 | |||||||
| chr12:53161674 | A | T | 24 | a0001c0001t0002g0049 a0001c0001t0003g0005 a0001c0001t0003g0024 others(21): Show |
58 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.703-285T>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53161674 | |||||||
| chr12:53161999 | C | A | 19 | a0001c0001t0002g0049 a0001c0001t0007g0029 a0001c0002t0002g0003 others(16): Show |
45 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.703-610G>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53161999 | |||||||
| chr12:53162018 | G | A | 5 | a0001c0001t0003g0005 a0001c0001t0003g0024 a0001c0001t0003g0025 others(2): Show |
13 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.703-629C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53162018 | |||||||
| chr12:53162089 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.703-700C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53162089 | |||||||
| chr12:53162168 | G | C | 1 | a0001c0001t0001g0096 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.703-779C>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53162168 | |||||||
| chr12:53162198 | G | A | 2 | a0001c0003t0005g0113 a0001c0003t0005g0115 |
2 | HG01884.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.703-809C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53162198 | |||||||
| chr12:53162218 | A | C | 1 | a0001c0002t0002g0045 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.703-829T>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53162218 | |||||||
| chr12:53162286 | T | C | 1 | a0001c0001t0002g0061 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.703-897A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53162286 | |||||||
| chr12:53162338 | C | T | 2 | a0001c0004t0002g0056 a0001c0004t0002g0066 |
2 | HG03453.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.703-949G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53162338 | |||||||
| chr12:53162503 | G | A | 5 | a0001c0001t0003g0005 a0001c0001t0003g0024 a0001c0001t0003g0025 others(2): Show |
13 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.703-1114C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53162503 | |||||||
| chr12:53162568 | T | G | 1 | a0001c0002t0002g0047 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.703-1179A>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53162568 | |||||||
| chr12:53162629 | T | C | 1 | a0001c0002t0002g0050 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.703-1240A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53162629 | |||||||
| chr12:53162701 | T | C | 1 | a0001c0001t0001g0039 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.703-1312A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53162701 | |||||||
| chr12:53162764 | G | GA | 5 | a0001c0001t0003g0005 a0001c0001t0003g0024 a0001c0001t0003g0025 others(2): Show |
13 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.703-1376dupT | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53162764 | |||||||
| chr12:53162787 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.703-1398G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53162787 | |||||||
| chr12:53162813 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.703-1424C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53162813 | |||||||
| chr12:53162881 | G | C | 1 | a0001c0001t0003g0024 | 2 | HG02615.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.703-1492C>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53162881 | |||||||
| chr12:53162966 | C | A | 1 | a0001c0003t0005g0114 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.703-1577G>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53162966 | |||||||
| chr12:53162991 | G | A | 18 | a0001c0001t0002g0049 a0001c0002t0002g0003 a0001c0002t0002g0009 others(15): Show |
43 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.703-1602C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53162991 | |||||||
| chr12:53163017 | C | T | 1 | a0001c0001t0003g0025 | 2 | HG03139.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.703-1628G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53163017 | |||||||
| chr12:53163061 | CA | C | 5 | a0001c0001t0003g0005 a0001c0001t0003g0024 a0001c0001t0003g0025 others(2): Show |
13 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.703-1673delT | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53163061 | |||||||
| chr12:53163093 | T | C | 1 | a0001c0001t0001g0001 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.703-1704A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53163093 | |||||||
| chr12:53163330 | C | G | 4 | a0001c0001t0002g0006 a0001c0001t0002g0015 a0001c0001t0002g0068 others(1): Show |
10 | HG01109.hp1 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.703-1941G>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53163330 | |||||||
| chr12:53163505 | T | C | 1 | a0001c0001t0001g0098 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.703-2116A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53163505 | |||||||
| chr12:53163681 | AAT | A | 4 | a0001c0001t0001g0010 a0001c0001t0001g0089 a0001c0001t0001g0101 others(1): Show |
7 | HG00140.hp2 HG00323.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.703-2294_703-2293d others(4): Show |
CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53163681 | |||||||
| chr12:53163751 | C | A | 3 | a0001c0001t0001g0019 a0001c0001t0001g0080 a0001c0001t0001g0112 |
5 | NA18939.hp2 NA18962.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.703-2362G>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53163751 | |||||||
| chr12:53163903 | T | G | 1 | a0001c0001t0003g0025 | 2 | HG03139.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.703-2514A>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53163903 | |||||||
| chr12:53163984 | G | GTTGTAAG others(9): Show |
1 | a0001c0002t0006g0073 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.703-2596_703-2595i others(18): Show |
CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53163984 | |||||||
| chr12:53163985 | C | T | 1 | a0001c0002t0006g0073 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.703-2596G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53163985 | |||||||
| chr12:53163986 | C | A | 1 | a0001c0002t0006g0073 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.703-2597G>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53163986 | |||||||
| chr12:53164305 | C | A | 1 | a0001c0001t0001g0129 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.703-2916G>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53164305 | |||||||
| chr12:53164394 | T | G | 1 | a0001c0001t0002g0067 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.703-3005A>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53164394 | |||||||
| chr12:53164536 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.703-3147T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53164536 | |||||||
| chr12:53164591 | G | A | 1 | a0001c0008t0014g0132 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.703-3202C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53164591 | |||||||
| chr12:53164722 | C | T | 5 | a0001c0001t0003g0005 a0001c0001t0003g0024 a0001c0001t0003g0025 others(2): Show |
13 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.703-3333G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53164722 | |||||||
| chr12:53164759 | G | C | 5 | a0001c0001t0003g0005 a0001c0001t0003g0024 a0001c0001t0003g0025 others(2): Show |
13 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.703-3370C>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53164759 | |||||||
| chr12:53164909 | A | T | 5 | a0001c0001t0003g0005 a0001c0001t0003g0024 a0001c0001t0003g0025 others(2): Show |
13 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.703-3520T>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53164909 | |||||||
| chr12:53165040 | G | C | 1 | a0001c0001t0001g0099 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.703-3651C>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53165040 | |||||||
| chr12:53165202 | G | T | 5 | a0001c0001t0003g0005 a0001c0001t0003g0024 a0001c0001t0003g0025 others(2): Show |
13 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.703-3813C>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53165202 | |||||||
| chr12:53165245 | A | G | 77 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0013 others(74): Show |
179 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.703-3856T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53165245 | |||||||
| chr12:53165266 | A | G | 1 | a0001c0001t0007g0029 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.703-3877T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53165266 | |||||||
| chr12:53165287 | A | T | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.703-3898T>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53165287 | |||||||
| chr12:53165340 | C | CA | 8 | a0001c0001t0001g0136 a0001c0001t0003g0005 a0001c0001t0003g0024 others(5): Show |
17 | HG00673.hp2 HG01255.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.703-3952dupT | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53165340 | |||||||
| chr12:53165387 | G | A | 1 | a0001c0001t0002g0027 | 2 | HG02723.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.703-3998C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53165387 | |||||||
| chr12:53165400 | C | G | 5 | a0001c0001t0003g0005 a0001c0001t0003g0024 a0001c0001t0003g0025 others(2): Show |
13 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.703-4011G>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53165400 | |||||||
| chr12:53165404 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.703-4015A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53165404 | |||||||
| chr12:53165444 | A | G | 1 | a0001c0001t0008g0028 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.703-4055T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53165444 | |||||||
| chr12:53165456 | C | G | 1 | a0001c0001t0003g0053 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.703-4067G>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53165456 | |||||||
| chr12:53165524 | G | T | 1 | a0001c0001t0002g0060 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.703-4135C>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53165524 | |||||||
| chr12:53165555 | C | A | 2 | a0001c0004t0002g0056 a0001c0004t0002g0066 |
2 | HG03453.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.703-4166G>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53165555 | |||||||
| chr12:53165620 | G | C | 1 | a0001c0001t0001g0101 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.703-4231C>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53165620 | |||||||
| chr12:53165662 | C | CA | 10 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0093 others(7): Show |
13 | HG02109.hp1 HG02145.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.703-4274dupT | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53165662 | |||||||
| chr12:53165662 | CA | C | 10 | a0001c0001t0001g0033 a0001c0001t0001g0037 a0001c0001t0001g0074 others(7): Show |
12 | HG00323.hp2 HG01081.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.703-4274delT | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53165662 | |||||||
| chr12:53165703 | C | A | 2 | a0001c0001t0001g0145 a0006c0005t0001g0144 |
2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.703-4314G>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53165703 | |||||||
| chr12:53165820 | T | C | 1 | a0001c0001t0001g0011 | 4 | HG01891.hp1 HG03098.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.702+4252A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53165820 | |||||||
| chr12:53165909 | T | C | 1 | a0001c0001t0002g0062 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.702+4163A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53165909 | |||||||
| chr12:53165929 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.702+4143A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53165929 | |||||||
| chr12:53165974 | T | C | 1 | a0001c0001t0002g0014 | 3 | HG02145.hp2 HG02572.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.702+4098A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53165974 | |||||||
| chr12:53165989 | C | T | 1 | a0001c0002t0002g0048 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.702+4083G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53165989 | |||||||
| chr12:53166118 | T | C | 5 | a0001c0001t0003g0005 a0001c0001t0003g0024 a0001c0001t0003g0025 others(2): Show |
13 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.702+3954A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53166118 | |||||||
| chr12:53166120 | A | AG | 24 | a0001c0001t0002g0049 a0001c0001t0003g0005 a0001c0001t0003g0024 others(21): Show |
58 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.702+3951dupC | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53166120 | |||||||
| chr12:53166131 | C | T | 1 | a0001c0001t0001g0033 | 2 | HG03017.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.702+3941G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53166131 | |||||||
| chr12:53166200 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.702+3872G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53166200 | |||||||
| chr12:53166202 | C | G | 1 | a0001c0001t0001g0092 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.702+3870G>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53166202 | |||||||
| chr12:53166243 | C | T | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(143): Show |
327 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(324): Show |
intron_variant | MODIFIER | c.702+3829G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53166243 | |||||||
| chr12:53166331 | G | A | 1 | a0001c0001t0007g0029 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.702+3741C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53166331 | |||||||
| chr12:53166659 | G | C | 1 | a0001c0003t0005g0115 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.702+3413C>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53166659 | |||||||
| chr12:53166711 | G | A | 2 | a0001c0001t0002g0049 a0001c0002t0002g0022 |
3 | HG00423.hp2 NA18949.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.702+3361C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53166711 | |||||||
| chr12:53166798 | AAAAACAA others(3): Show |
A | 1 | a0001c0001t0001g0122 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.702+3264_702+3273d others(12): Show |
CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53166798 | |||||||
| chr12:53166862 | A | G | 1 | a0001c0001t0007g0029 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.702+3210T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53166862 | |||||||
| chr12:53166896 | T | A | 1 | a0001c0001t0001g0104 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.702+3176A>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53166896 | |||||||
| chr12:53166936 | C | A | 1 | a0001c0001t0001g0076 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.702+3136G>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53166936 | |||||||
| chr12:53166936 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.702+3136G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53166936 | |||||||
| chr12:53167201 | T | C | 1 | a0001c0001t0002g0069 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.702+2871A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53167201 | |||||||
| chr12:53167267 | A | G | 2 | a0001c0001t0001g0039 a0001c0002t0011g0044 |
3 | HG00323.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.702+2805T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53167267 | |||||||
| chr12:53167578 | T | C | 1 | a0001c0002t0006g0073 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.702+2494A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53167578 | |||||||
| chr12:53167874 | G | A | 1 | a0001c0001t0007g0029 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.702+2198C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53167874 | |||||||
| chr12:53168069 | C | T | 2 | a0001c0001t0001g0082 a0001c0001t0003g0025 |
3 | HG03139.hp2 NA19043.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.702+2003G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53168069 | |||||||
| chr12:53168394 | T | C | 1 | a0001c0001t0001g0105 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.702+1678A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53168394 | |||||||
| chr12:53168402 | A | C | 1 | a0001c0001t0013g0091 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.702+1670T>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53168402 | |||||||
| chr12:53168418 | A | C | 1 | a0001c0001t0002g0055 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.702+1654T>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53168418 | |||||||
| chr12:53168516 | A | G | 3 | a0001c0001t0001g0019 a0001c0001t0001g0080 a0001c0001t0001g0112 |
5 | NA18939.hp2 NA18962.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.702+1556T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53168516 | |||||||
| chr12:53168539 | C | G | 1 | a0001c0001t0001g0106 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.702+1533G>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53168539 | |||||||
| chr12:53168578 | T | C | 1 | a0001c0001t0001g0106 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.702+1494A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53168578 | |||||||
| chr12:53168932 | C | A | 2 | a0001c0004t0002g0056 a0001c0004t0002g0066 |
2 | HG03453.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.702+1140G>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53168932 | |||||||
| chr12:53169050 | C | A | 2 | a0001c0001t0001g0020 a0001c0001t0001g0142 |
4 | NA18999.hp2 NA19068.hp2 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.702+1022G>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53169050 | |||||||
| chr12:53169063 | C | T | 2 | a0001c0001t0002g0006 a0001c0001t0002g0068 |
6 | HG01109.hp1 HG02109.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.702+1009G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53169063 | |||||||
| chr12:53169105 | G | A | 3 | a0001c0001t0001g0019 a0001c0001t0001g0080 a0001c0001t0001g0112 |
5 | NA18939.hp2 NA18962.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.702+967C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53169105 | |||||||
| chr12:53169128 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.702+944G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53169128 | |||||||
| chr12:53169147 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.702+925A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53169147 | |||||||
| chr12:53169209 | A | G | 27 | a0001c0001t0001g0135 a0001c0001t0002g0049 a0001c0001t0003g0005 others(24): Show |
62 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.702+863T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53169209 | |||||||
| chr12:53169440 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.702+632A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53169440 | |||||||
| chr12:53169479 | CA | C | 33 | a0001c0001t0001g0032 a0001c0001t0001g0078 a0001c0001t0002g0004 others(30): Show |
70 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.702+592delT | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53169479 | |||||||
| chr12:53169495 | A | T | 1 | a0001c0001t0001g0134 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.702+577T>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53169495 | |||||||
| chr12:53169669 | C | A | 1 | a0001c0003t0005g0116 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.702+403G>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53169669 | |||||||
| chr12:53169686 | G | C | 1 | a0001c0001t0007g0029 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.702+386C>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53169686 | |||||||
| chr12:53169784 | CCTTCCAC others(50): Show |
C | 1 | a0001c0001t0001g0108 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.702+231_702+287del others(57): Show |
CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53169784 | |||||||
| chr12:53170008 | G | A | 1 | a0001c0001t0007g0029 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.702+64C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53170008 | |||||||
| chr12:53170044 | A | C | 1 | a0001c0001t0007g0029 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.702+28T>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53170044 | |||||||
| chr12:53170144 | G | A | 2 | a0001c0001t0002g0054 a0001c0001t0009g0057 |
2 | HG02922.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.648-18C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 9/16 | chr12 | 53170144 | |||||||
| chr12:53170150 | A | G | 1 | a0001c0002t0002g0021 | 2 | NA18952.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.648-24T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 9/16 | chr12 | 53170150 | |||||||
| chr12:53170373 | T | G | 5 | a0001c0001t0003g0005 a0001c0001t0003g0024 a0001c0001t0003g0025 others(2): Show |
13 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.647+50A>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 9/16 | chr12 | 53170373 | |||||||
| chr12:53170722 | G | GT | 5 | a0001c0001t0001g0031 a0001c0001t0001g0089 a0001c0001t0001g0127 others(2): Show |
6 | HG00140.hp2 HG03831.hp1 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.568-221dupA | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 8/16 | chr12 | 53170722 | |||||||
| chr12:53170722 | GT | G | 22 | a0001c0001t0001g0109 a0001c0001t0002g0049 a0001c0001t0003g0005 others(19): Show |
55 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.568-221delA | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 8/16 | chr12 | 53170722 | |||||||
| chr12:53170807 | G | A | 18 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0015 others(15): Show |
32 | HG01109.hp1 HG01256.hp2 HG02080.hp1 others(29): Show |
intron_variant | MODIFIER | c.568-305C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 8/16 | chr12 | 53170807 | |||||||
| chr12:53171001 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.567+325C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 8/16 | chr12 | 53171001 | |||||||
| chr12:53171124 | C | A | 1 | a0001c0002t0002g0048 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.567+202G>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 8/16 | chr12 | 53171124 | |||||||
| chr12:53171296 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.567+30G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 8/16 | chr12 | 53171296 | |||||||
| chr12:53171449 | A | G | 1 | a0001c0001t0002g0070 | 1 | HG03540.hp2 | splice_region_variant&intron_variant | LOW | c.452-8T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 7/16 | chr12 | 53171449 | |||||||
| chr12:53171459 | C | T | 1 | a0001c0001t0003g0025 | 2 | HG03139.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.452-18G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 7/16 | chr12 | 53171459 | |||||||
| chr12:53171673 | T | C | 78 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0013 others(75): Show |
180 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.451+209A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 7/16 | chr12 | 53171673 | |||||||
| chr12:53171849 | G | C | 1 | a0001c0001t0001g0111 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.451+33C>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 7/16 | chr12 | 53171849 | |||||||
| chr12:53172034 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.345-46C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 6/16 | chr12 | 53172034 | |||||||
| chr12:53172171 | C | G | 2 | a0001c0001t0001g0087 a0001c0001t0001g0123 |
2 | HG02135.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.344+175G>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 6/16 | chr12 | 53172171 | |||||||
| chr12:53172243 | C | G | 1 | a0001c0001t0001g0131 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.344+103G>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 6/16 | chr12 | 53172243 | |||||||
| chr12:53172293 | T | C | 3 | a0001c0001t0001g0019 a0001c0001t0001g0080 a0001c0001t0001g0112 |
5 | NA18939.hp2 NA18962.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.344+53A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 6/16 | chr12 | 53172293 | |||||||
| chr12:53172707 | C | T | 24 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0014 others(21): Show |
41 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(38): Show |
intron_variant | MODIFIER | c.127-59G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 4/16 | chr12 | 53172707 | |||||||
| chr12:53172730 | C | T | 2 | a0001c0001t0001g0145 a0006c0005t0001g0144 |
2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.127-82G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 4/16 | chr12 | 53172730 | |||||||
| chr12:53172930 | A | T | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0006c0005t0001g0144 |
3 | HG02809.hp1 HG02896.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.127-282T>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 4/16 | chr12 | 53172930 | |||||||
| chr12:53172934 | G | A | 5 | a0001c0001t0003g0005 a0001c0001t0003g0024 a0001c0001t0003g0025 others(2): Show |
13 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.127-286C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 4/16 | chr12 | 53172934 | |||||||
| chr12:53173006 | G | A | 6 | a0001c0001t0001g0008 a0001c0001t0003g0005 a0001c0001t0003g0024 others(3): Show |
18 | HG00140.hp1 HG01168.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.126+339C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 4/16 | chr12 | 53173006 | |||||||
| chr12:53173065 | G | A | 1 | a0001c0001t0010g0071 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.126+280C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 4/16 | chr12 | 53173065 | |||||||
| chr12:53173069 | G | A | 1 | a0001c0001t0007g0029 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.126+276C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 4/16 | chr12 | 53173069 | |||||||
| chr12:53173224 | G | C | 1 | a0001c0001t0001g0146 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.126+121C>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 4/16 | chr12 | 53173224 | |||||||
| chr12:53173244 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.126+101C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 4/16 | chr12 | 53173244 | |||||||
| chr12:53173254 | AG | A | 35 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0137 others(32): Show |
72 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.126+90delC | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 4/16 | chr12 | 53173254 | |||||||
| chr12:53173263 | G | T | 1 | a0001c0001t0010g0071 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.126+82C>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 4/16 | chr12 | 53173263 | |||||||
| chr12:53173278 | GGAAAAAA others(5): Show |
G | 1 | a0001c0001t0010g0071 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.126+55_126+66delTT others(10): Show |
CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 4/16 | chr12 | 53173278 | |||||||
| chr12:53173822 | A | G | 1 | a0001c0001t0008g0028 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-49-52T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53173822 | |||||||
| chr12:53173863 | A | G | 2 | a0001c0001t0001g0030 a0001c0001t0001g0085 |
3 | HG02630.hp1 HG03041.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-49-93T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53173863 | |||||||
| chr12:53173899 | C | CA | 5 | a0001c0001t0001g0080 a0001c0001t0002g0049 a0001c0001t0002g0064 others(2): Show |
5 | HG01981.hp1 HG02602.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49-130dupT | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53173899 | |||||||
| chr12:53174070 | C | G | 4 | a0001c0001t0002g0006 a0001c0001t0002g0015 a0001c0001t0002g0068 others(1): Show |
10 | HG01109.hp1 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.-49-300G>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53174070 | |||||||
| chr12:53174087 | G | A | 1 | a0001c0001t0002g0065 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-49-317C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53174087 | |||||||
| chr12:53174188 | CAGCT | C | 5 | a0001c0001t0003g0005 a0001c0001t0003g0024 a0001c0001t0003g0025 others(2): Show |
13 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.-49-422_-49-419del others(4): Show |
CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53174188 | |||||||
| chr12:53174307 | CA | C | 75 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0013 others(72): Show |
175 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.-49-538delT | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53174307 | |||||||
| chr12:53174371 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-49-601A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53174371 | |||||||
| chr12:53174426 | A | G | 1 | a0001c0001t0002g0058 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-49-656T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53174426 | |||||||
| chr12:53174737 | A | G | 1 | a0001c0001t0007g0029 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-49-967T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53174737 | |||||||
| chr12:53174797 | T | A | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0006c0005t0001g0144 |
3 | HG02809.hp1 HG02896.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-49-1027A>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53174797 | |||||||
| chr12:53175003 | A | T | 1 | a0001c0001t0001g0080 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-49-1233T>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53175003 | |||||||
| chr12:53175013 | T | C | 5 | a0001c0001t0003g0005 a0001c0001t0003g0024 a0001c0001t0003g0025 others(2): Show |
13 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.-49-1243A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53175013 | |||||||
| chr12:53175072 | C | G | 2 | a0001c0004t0002g0056 a0001c0004t0002g0066 |
2 | HG03453.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.-49-1302G>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53175072 | |||||||
| chr12:53175280 | G | A | 3 | a0001c0001t0001g0020 a0001c0001t0001g0141 a0001c0001t0001g0142 |
5 | NA18999.hp2 NA19058.hp2 NA19068.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49-1510C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53175280 | |||||||
| chr12:53175515 | T | C | 1 | a0001c0001t0001g0121 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-49-1745A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53175515 | |||||||
| chr12:53175605 | G | A | 1 | a0001c0001t0007g0029 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-49-1835C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53175605 | |||||||
| chr12:53175703 | A | G | 1 | a0001c0001t0009g0057 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-49-1933T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53175703 | |||||||
| chr12:53175759 | A | C | 1 | a0001c0002t0002g0041 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-49-1989T>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53175759 | |||||||
| chr12:53175955 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-49-2185C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53175955 | |||||||
| chr12:53175999 | C | A | 1 | a0001c0001t0002g0070 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-49-2229G>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53175999 | |||||||
| chr12:53176069 | G | A | 1 | a0001c0001t0003g0025 | 2 | HG03139.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-49-2299C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53176069 | |||||||
| chr12:53176124 | G | T | 1 | a0001c0001t0001g0080 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-49-2354C>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53176124 | |||||||
| chr12:53176238 | C | T | 50 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0014 others(47): Show |
102 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.-49-2468G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53176238 | |||||||
| chr12:53176422 | C | A | 2 | a0001c0001t0008g0028 a0001c0001t0010g0071 |
3 | HG01891.hp2 HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-49-2652G>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53176422 | |||||||
| chr12:53176438 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-50+2664C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53176438 | |||||||
| chr12:53176502 | G | A | 1 | a0001c0001t0001g0036 | 2 | NA18983.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.-50+2600C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53176502 | |||||||
| chr12:53176577 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-50+2525C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53176577 | |||||||
| chr12:53176668 | G | A | 1 | a0001c0002t0002g0050 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-50+2434C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53176668 | |||||||
| chr12:53176731 | A | T | 1 | a0001c0001t0002g0067 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-50+2371T>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53176731 | |||||||
| chr12:53176733 | T | A | 4 | a0001c0001t0003g0005 a0001c0001t0003g0024 a0001c0001t0003g0052 others(1): Show |
11 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.-50+2369A>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53176733 | |||||||
| chr12:53176875 | G | C | 18 | a0001c0001t0002g0049 a0001c0002t0002g0003 a0001c0002t0002g0009 others(15): Show |
43 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.-50+2227C>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53176875 | |||||||
| chr12:53177015 | G | A | 22 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0014 others(19): Show |
39 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(36): Show |
intron_variant | MODIFIER | c.-50+2087C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53177015 | |||||||
| chr12:53177084 | G | T | 1 | a0001c0001t0001g0080 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-50+2018C>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53177084 | |||||||
| chr12:53177584 | T | C | 1 | a0001c0001t0001g0143 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-50+1518A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53177584 | |||||||
| chr12:53177605 | C | T | 4 | a0001c0001t0003g0005 a0001c0001t0003g0024 a0001c0001t0003g0052 others(1): Show |
11 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.-50+1497G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53177605 | |||||||
| chr12:53177615 | A | C | 1 | a0001c0001t0001g0082 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-50+1487T>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53177615 | |||||||
| chr12:53177621 | A | G | 1 | a0001c0001t0008g0028 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-50+1481T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53177621 | |||||||
| chr12:53177623 | C | CTATT | 19 | a0001c0001t0001g0018 a0001c0001t0002g0049 a0001c0002t0002g0003 others(16): Show |
46 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.-50+1475_-50+1478d others(6): Show |
CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53177623 | |||||||
| chr12:53177669 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-50+1433C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53177669 | |||||||
| chr12:53177904 | T | C | 8 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0003g0005 others(5): Show |
16 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.-50+1198A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53177904 | |||||||
| chr12:53177919 | C | T | 1 | a0001c0001t0002g0055 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-50+1183G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53177919 | |||||||
| chr12:53177924 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-50+1178C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53177924 | |||||||
| chr12:53178049 | G | A | 1 | a0001c0001t0008g0028 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-50+1053C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53178049 | |||||||
| chr12:53178076 | A | C | 18 | a0001c0001t0002g0049 a0001c0002t0002g0003 a0001c0002t0002g0009 others(15): Show |
43 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.-50+1026T>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53178076 | |||||||
| chr12:53178270 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-50+832G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53178270 | |||||||
| chr12:53178316 | C | A | 1 | a0001c0001t0001g0080 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-50+786G>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53178316 | |||||||
| chr12:53178317 | A | C | 1 | a0001c0001t0001g0080 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-50+785T>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53178317 | |||||||
| chr12:53178340 | A | G | 1 | a0001c0001t0002g0026 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-50+762T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53178340 | |||||||
| chr12:53178346 | T | G | 24 | a0001c0001t0002g0049 a0001c0001t0003g0005 a0001c0001t0003g0024 others(21): Show |
58 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.-50+756A>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53178346 | |||||||
| chr12:53178401 | A | G | 1 | a0001c0001t0007g0029 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-50+701T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53178401 | |||||||
| chr12:53178513 | C | T | 1 | a0001c0001t0007g0029 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-50+589G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53178513 | |||||||
| chr12:53178758 | C | G | 1 | a0001c0001t0002g0026 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-50+344G>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53178758 | |||||||
| chr12:53178784 | CA | C | 18 | a0001c0001t0002g0049 a0001c0002t0002g0003 a0001c0002t0002g0009 others(15): Show |
43 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.-50+317delT | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53178784 | |||||||
| chr12:53178788 | AAAAAAT | A | 5 | a0001c0001t0003g0005 a0001c0001t0003g0024 a0001c0001t0003g0025 others(2): Show |
13 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.-50+308_-50+313del others(6): Show |
CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53178788 | |||||||
| chr12:53178876 | T | G | 1 | a0001c0001t0001g0125 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-50+226A>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53178876 | |||||||
| chr12:53178940 | G | A | 1 | a0001c0004t0002g0066 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-50+162C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53178940 | |||||||
| chr12:53179160 | A | G | 3 | a0001c0001t0001g0017 a0001c0001t0001g0078 a0001c0001t0001g0079 |
5 | HG01934.hp2 HG01975.hp2 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.-90-18T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/16 | chr12 | 53179160 | |||||||
| chr12:53179216 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-90-74G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/16 | chr12 | 53179216 | |||||||
| chr12:53179246 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-90-104G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/16 | chr12 | 53179246 | |||||||
| chr12:53179322 | G | A | 1 | a0001c0001t0002g0067 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-90-180C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/16 | chr12 | 53179322 | |||||||
| chr12:53179360 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-90-218A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/16 | chr12 | 53179360 | |||||||
| chr12:53179390 | C | T | 1 | a0001c0001t0002g0054 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-90-248G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/16 | chr12 | 53179390 | |||||||
| chr12:53179447 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-90-305C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/16 | chr12 | 53179447 | |||||||
| chr12:53179555 | T | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0149 |
5 | HG01074.hp2 HG01081.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-90-413A>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/16 | chr12 | 53179555 | |||||||
| chr12:53179621 | TTTCAATG | T | 5 | a0001c0001t0003g0005 a0001c0001t0003g0024 a0001c0001t0003g0025 others(2): Show |
13 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.-90-486_-90-480del others(7): Show |
CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/16 | chr12 | 53179621 | |||||||
| chr12:53179653 | G | A | 1 | a0001c0001t0007g0029 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-90-511C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/16 | chr12 | 53179653 | |||||||
| chr12:53179670 | C | CA | 5 | a0001c0001t0002g0006 a0001c0001t0002g0015 a0001c0001t0002g0068 others(2): Show |
11 | HG01109.hp1 HG02109.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-90-529dupT | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/16 | chr12 | 53179670 | |||||||
| chr12:53179715 | G | GT | 77 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0013 others(74): Show |
176 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.-90-574dupA | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/16 | chr12 | 53179715 | |||||||
| chr12:53179842 | T | C | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | HG03492.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.-90-700A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/16 | chr12 | 53179842 | |||||||
| chr12:53179851 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-90-709G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/16 | chr12 | 53179851 | |||||||
| chr12:53180032 | G | A | 1 | a0001c0001t0001g0150 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-91+700C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/16 | chr12 | 53180032 | |||||||
| chr12:53180119 | A | C | 18 | a0001c0001t0002g0049 a0001c0002t0002g0003 a0001c0002t0002g0009 others(15): Show |
43 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.-91+613T>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/16 | chr12 | 53180119 | |||||||
| chr12:53180185 | C | A | 1 | a0001c0001t0010g0071 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-91+547G>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/16 | chr12 | 53180185 | |||||||
| chr12:53180260 | G | C | 18 | a0001c0001t0002g0049 a0001c0002t0002g0003 a0001c0002t0002g0009 others(15): Show |
43 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.-91+472C>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/16 | chr12 | 53180260 | |||||||
| chr12:53180261 | A | C | 18 | a0001c0001t0002g0049 a0001c0002t0002g0003 a0001c0002t0002g0009 others(15): Show |
43 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.-91+471T>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/16 | chr12 | 53180261 | |||||||
| chr12:53180455 | A | G | 1 | a0001c0001t0002g0051 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-91+277T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/16 | chr12 | 53180455 | |||||||
| chr12:53180503 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-91+229C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/16 | chr12 | 53180503 | |||||||
| chr12:53180549 | A | C | 1 | a0001c0001t0001g0074 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-91+183T>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/16 | chr12 | 53180549 | |||||||
| chr12:53180554 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-91+178C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/16 | chr12 | 53180554 | |||||||
| chr12:53180582 | C | T | 18 | a0001c0001t0002g0049 a0001c0002t0002g0003 a0001c0002t0002g0009 others(15): Show |
43 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.-91+150G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/16 | chr12 | 53180582 | |||||||
| chr12:53180706 | G | A | 28 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0013 others(25): Show |
78 | HG00140.hp1 HG00438.hp1 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.-91+26C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/16 | chr12 | 53180706 | |||||||
| chr12:53180708 | C | A | 3 | a0001c0002t0006g0016 a0001c0002t0006g0072 a0001c0002t0006g0073 |
5 | NA18946.hp2 NA18965.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.-91+24G>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/16 | chr12 | 53180708 |