Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 377677 |
| ensemblid | ENSG00000185015.8 |
| hgncid | 14914 |
| symbol | CA13 |
| name | carbonic anhydrase 13 |
| refseq_nuc | NM_198584.3 |
| refseq_prot | NP_940986.1 |
| ensembl_nuc | ENST00000321764.4 |
| ensembl_prot | ENSP00000318912.3 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 85245458 |
| end | 85284073 |
| strand | + |
| ver | v1.2 |
| region | chr8:85245458-85284073 |
| region5000 | chr8:85240458-85289073 |
| regionname0 | CA13_chr8_85245458_85284073 |
| regionname5000 | CA13_chr8_85240458_85289073 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 262 | 346 | 91 | 62 | 146 | 8 | 37 | 110 | CA13_chr8_85240458_85289073 | CA13 | MSRLS others(257): Show |
chr8 | 85240458 | 85289073 |
| a0002 | 0/0 | 262 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | CA13_chr8_85240458_85289073 | CA13 | MSRLS others(257): Show |
chr8 | 85240458 | 85289073 |
| a0003 | 0/0 | 262 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | MSRLS others(257): Show |
chr8 | 85240458 | 85289073 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 786 | 346 | 91 | 62 | 146 | 8 | 37 | CA13_chr8_85240458_85289073 | CA13 | ATGTC others(781): Show |
chr8 | 85240458 | 85289073 | ||
| a0002c0002 | 0/0 | 786 | 3 | 0 | 2 | 0 | 0 | 1 | CA13_chr8_85240458_85289073 | CA13 | ATGTC others(781): Show |
chr8 | 85240458 | 85289073 | ||
| a0003c0003 | 0/0 | 786 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | ATGTC others(781): Show |
chr8 | 85240458 | 85289073 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3884 | 138 | 25 | 20 | 73 | 3 | 16 | CA13_chr8_85240458_85289073 | CA13 | ATTCA others(3879): Show |
chr8 | 85240458 | 85289073 |
| a0001c0001t0002 | 0/0 | 3884 | 124 | 34 | 31 | 42 | 2 | 15 | CA13_chr8_85240458_85289073 | CA13 | ATTCA others(3879): Show |
chr8 | 85240458 | 85289073 |
| a0001c0001t0003 | 0/0 | 3884 | 14 | 1 | 1 | 11 | 0 | 1 | CA13_chr8_85240458_85289073 | CA13 | ATTCA others(3879): Show |
chr8 | 85240458 | 85289073 |
| a0001c0001t0004 | 0/0 | 3885 | 13 | 5 | 4 | 0 | 1 | 3 | CA13_chr8_85240458_85289073 | CA13 | ATTCA others(3880): Show |
chr8 | 85240458 | 85289073 |
| a0001c0001t0005 | 0/0 | 3884 | 9 | 7 | 2 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | ATTCA others(3879): Show |
chr8 | 85240458 | 85289073 |
| a0001c0001t0006 | 0/0 | 3884 | 8 | 0 | 0 | 8 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | ATTCA others(3879): Show |
chr8 | 85240458 | 85289073 |
| a0001c0001t0007 | 0/0 | 3884 | 6 | 5 | 1 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | ATTCA others(3879): Show |
chr8 | 85240458 | 85289073 |
| a0001c0001t0008 | 0/0 | 3884 | 6 | 0 | 0 | 6 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | ATTCA others(3879): Show |
chr8 | 85240458 | 85289073 |
| a0001c0001t0009 | 0/0 | 3884 | 4 | 4 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | ATTCA others(3879): Show |
chr8 | 85240458 | 85289073 |
| a0001c0001t0011 | 0/0 | 3884 | 3 | 3 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | ATTCA others(3879): Show |
chr8 | 85240458 | 85289073 |
| a0001c0001t0012 | 0/0 | 3884 | 2 | 0 | 0 | 0 | 0 | 2 | CA13_chr8_85240458_85289073 | CA13 | ATTCA others(3879): Show |
chr8 | 85240458 | 85289073 |
| a0001c0001t0013 | 0/0 | 3884 | 2 | 2 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | ATTCA others(3879): Show |
chr8 | 85240458 | 85289073 |
| a0001c0001t0014 | 0/0 | 3884 | 2 | 0 | 1 | 0 | 1 | 0 | CA13_chr8_85240458_85289073 | CA13 | ATTCA others(3879): Show |
chr8 | 85240458 | 85289073 |
| a0001c0001t0015 | 0/0 | 3884 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | ATTCA others(3879): Show |
chr8 | 85240458 | 85289073 |
| a0001c0001t0016 | 0/0 | 3884 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | ATTCA others(3879): Show |
chr8 | 85240458 | 85289073 |
| a0001c0001t0017 | 0/0 | 3873 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | ATTCA others(3868): Show |
chr8 | 85240458 | 85289073 |
| a0001c0001t0018 | 0/1 | 3883 | 1 | 0 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | ATTCA others(3878): Show |
chr8 | 85240458 | 85289073 |
| a0001c0001t0019 | 0/0 | 3884 | 1 | 0 | 1 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | ATTCA others(3879): Show |
chr8 | 85240458 | 85289073 |
| a0001c0001t0020 | 0/0 | 3884 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | ATTCA others(3879): Show |
chr8 | 85240458 | 85289073 |
| a0001c0001t0021 | 0/0 | 3884 | 1 | 0 | 0 | 0 | 1 | 0 | CA13_chr8_85240458_85289073 | CA13 | ATTCA others(3879): Show |
chr8 | 85240458 | 85289073 |
| a0001c0001t0022 | 0/0 | 3884 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | ATTCA others(3879): Show |
chr8 | 85240458 | 85289073 |
| a0001c0001t0023 | 0/0 | 3884 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | ATTCA others(3879): Show |
chr8 | 85240458 | 85289073 |
| a0001c0001t0024 | 0/0 | 3891 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | ATTCA others(3886): Show |
chr8 | 85240458 | 85289073 |
| a0001c0001t0025 | 0/0 | 3884 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | ATTCA others(3879): Show |
chr8 | 85240458 | 85289073 |
| a0001c0001t0026 | 0/0 | 3884 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | ATTCA others(3879): Show |
chr8 | 85240458 | 85289073 |
| a0001c0001t0027 | 0/0 | 3884 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | ATTCA others(3879): Show |
chr8 | 85240458 | 85289073 |
| a0001c0001t0028 | 0/0 | 3884 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | ATTCA others(3879): Show |
chr8 | 85240458 | 85289073 |
| a0001c0001t0029 | 0/0 | 3884 | 1 | 0 | 1 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | ATTCA others(3879): Show |
chr8 | 85240458 | 85289073 |
| a0002c0002t0010 | 0/0 | 3884 | 3 | 0 | 2 | 0 | 0 | 1 | CA13_chr8_85240458_85289073 | CA13 | ATTCA others(3879): Show |
chr8 | 85240458 | 85289073 |
| a0003c0003t0002 | 0/0 | 3884 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | ATTCA others(3879): Show |
chr8 | 85240458 | 85289073 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0003 | 1/0 | 6 | 0 | 1 | 1 | 0 | 3 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0006 | 0/0 | 6 | 0 | 4 | 2 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0001 | 0/0 | 22 | 1 | 4 | 14 | 0 | 3 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0007 | 0/0 | 5 | 0 | 2 | 2 | 0 | 1 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0010 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0017 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0019 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0020 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0003g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0003g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0004g0009 | 0/0 | 4 | 1 | 1 | 0 | 1 | 1 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0004g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0004g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0004g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0004g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0005g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0005g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0005g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0005g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0005g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0005g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0005g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0006g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0006g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0006g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0007g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0007g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0007g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0007g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0007g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0008g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0008g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0008g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0009g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0009g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0009g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0011g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0011g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0011g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0012g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0012g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0013g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0013g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0014g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0015g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0016g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0017g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0018g0169 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0019g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0020g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0021g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0022g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0023g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0024g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0025g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0026g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0027g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0028g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0001c0001t0029g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0002c0002t0010g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0002c0002t0010g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| a0003c0003t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0020 | EUR | GBR | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0117 | EUR | GBR | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0029 | EUR | GBR | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0009 | EUR | GBR | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG00280 | hp1 | a0001 | c0001 | t0021 | g0239 | EUR | FIN | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG00280 | hp2 | a0001 | c0001 | t0014 | g0003 | EUR | FIN | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | CHS | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | CHS | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0059 | EAS | CHS | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | CHS | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | CHS | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0066 | EAS | CHS | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG00621 | hp2 | a0001 | c0001 | t0027 | g0114 | EAS | CHS | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0164 | AMR | PUR | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0182 | AMR | PUR | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01070 | hp1 | a0001 | c0001 | t0005 | g0049 | AMR | PUR | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01070 | hp2 | a0001 | c0001 | t0004 | g0147 | AMR | PUR | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0030 | AMR | PUR | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0030 | AMR | PUR | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01081 | hp2 | a0001 | c0001 | t0007 | g0188 | AMR | PUR | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0056 | AMR | PUR | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0217 | AMR | PUR | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0186 | AMR | PUR | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0034 | AMR | CLM | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01256 | hp2 | a0002 | c0002 | t0010 | g0043 | AMR | CLM | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01258 | hp1 | a0001 | c0001 | t0029 | g0034 | AMR | CLM | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01258 | hp2 | a0002 | c0002 | t0010 | g0043 | AMR | CLM | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0192 | AMR | CLM | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01261 | hp2 | a0001 | c0001 | t0005 | g0053 | AMR | CLM | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0201 | AMR | CLM | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0203 | AMR | CLM | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0009 | AMR | CLM | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | CLM | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | ACB | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | ACB | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | ACB | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0181 | AMR | PEL | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | PEL | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0185 | AMR | PEL | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PEL | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0180 | AMR | PEL | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | PEL | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0190 | AMR | PEL | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0050 | AFR | ACB | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | KHV | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | KHV | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | KHV | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0062 | EAS | KHV | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0063 | EAS | KHV | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | KHV | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02145 | hp2 | a0001 | c0001 | t0009 | g0036 | AFR | ACB | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CDX | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02273 | hp1 | a0001 | c0001 | t0019 | g0197 | AMR | PEL | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | PEL | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0170 | AFR | ACB | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0146 | AFR | ACB | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0055 | AFR | GWD | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02622 | hp2 | a0001 | c0001 | t0013 | g0223 | AFR | GWD | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0051 | AFR | GWD | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02630 | hp2 | a0001 | c0001 | t0007 | g0179 | AFR | GWD | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02647 | hp1 | a0001 | c0001 | t0011 | g0200 | AFR | GWD | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0222 | AFR | GWD | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02683 | hp1 | a0001 | c0001 | t0012 | g0001 | SAS | PJL | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0234 | SAS | PJL | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0054 | AFR | GWD | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0207 | AFR | GWD | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0165 | AFR | GWD | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02735 | hp2 | a0001 | c0001 | t0004 | g0009 | SAS | PJL | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0199 | AFR | GWD | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0206 | AFR | GWD | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0215 | AFR | GWD | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02886 | hp1 | a0003 | c0003 | t0002 | g0195 | AFR | GWD | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0221 | AFR | GWD | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02895 | hp1 | a0001 | c0001 | t0026 | g0145 | AFR | GWD | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02895 | hp2 | a0001 | c0001 | t0011 | g0155 | AFR | GWD | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | GWD | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02897 | hp1 | a0001 | c0001 | t0011 | g0154 | AFR | GWD | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | GWD | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02922 | hp2 | a0001 | c0001 | t0017 | g0177 | AFR | ESN | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0166 | AFR | ESN | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ESN | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02970 | hp1 | a0001 | c0001 | t0015 | g0022 | AFR | ESN | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02970 | hp2 | a0001 | c0001 | t0009 | g0036 | AFR | ESN | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0220 | AFR | ESN | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG03017 | hp2 | a0002 | c0002 | t0010 | g0231 | SAS | PJL | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG03041 | hp2 | a0001 | c0001 | t0023 | g0156 | AFR | GWD | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0212 | AFR | MSL | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0057 | AFR | MSL | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | ESN | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0052 | AFR | ESN | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | ESN | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0226 | AFR | ESN | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG03195 | hp1 | a0001 | c0001 | t0009 | g0230 | AFR | ESN | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0022 | AFR | ESN | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0216 | AFR | MSL | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | MSL | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | MSL | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0048 | AFR | MSL | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0218 | AFR | MSL | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG03453 | hp2 | a0001 | c0001 | t0007 | g0037 | AFR | MSL | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0163 | AFR | MSL | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0150 | AFR | MSL | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0174 | SAS | PJL | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0196 | SAS | PJL | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0219 | AFR | ESN | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0184 | AFR | GWD | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG03540 | hp2 | a0001 | c0001 | t0007 | g0187 | AFR | GWD | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | MSL | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | MSL | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0189 | SAS | STU | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | STU | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0035 | SAS | PJL | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | BEB | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0058 | SAS | BEB | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0204 | SAS | BEB | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | BEB | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | BEB | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG03942 | hp2 | a0001 | c0001 | t0004 | g0144 | SAS | BEB | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0227 | SAS | STU | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0176 | SAS | STU | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG04184 | hp1 | a0001 | c0001 | t0004 | g0149 | SAS | BEB | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG04184 | hp2 | a0001 | c0001 | t0012 | g0232 | SAS | BEB | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0228 | SAS | STU | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0159 | SAS | STU | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0229 | SAS | STU | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | STU | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | STU | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | STU | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18522 | hp1 | a0001 | c0001 | t0013 | g0224 | AFR | YRI | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | YRI | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | CHB | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHB | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18939 | hp2 | a0001 | c0001 | t0006 | g0011 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18941 | hp1 | a0001 | c0001 | t0008 | g0004 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18943 | hp2 | a0001 | c0001 | t0006 | g0011 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18948 | hp1 | a0001 | c0001 | t0020 | g0211 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18965 | hp1 | a0001 | c0001 | t0008 | g0002 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18966 | hp2 | a0001 | c0001 | t0006 | g0015 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18967 | hp2 | a0001 | c0001 | t0024 | g0071 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18971 | hp1 | a0001 | c0001 | t0006 | g0011 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18978 | hp2 | a0001 | c0001 | t0022 | g0183 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18979 | hp1 | a0001 | c0001 | t0008 | g0002 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18989 | hp1 | a0001 | c0001 | t0008 | g0004 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18993 | hp1 | a0001 | c0001 | t0006 | g0015 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA19002 | hp1 | a0001 | c0001 | t0008 | g0120 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA19005 | hp2 | a0001 | c0001 | t0028 | g0214 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA19011 | hp1 | a0001 | c0001 | t0008 | g0002 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA19012 | hp2 | a0001 | c0001 | t0006 | g0168 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0148 | AFR | LWK | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0160 | AFR | LWK | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA19043 | hp1 | a0001 | c0001 | t0007 | g0171 | AFR | LWK | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA19043 | hp2 | a0001 | c0001 | t0009 | g0167 | AFR | LWK | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA19055 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA19055 | hp2 | a0001 | c0001 | t0025 | g0123 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA19090 | hp1 | a0001 | c0001 | t0006 | g0015 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA19091 | hp1 | a0001 | c0001 | t0006 | g0011 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA19240 | hp1 | a0001 | c0001 | t0007 | g0037 | AFR | YRI | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA19240 | hp2 | a0001 | c0001 | t0016 | g0209 | AFR | YRI | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ASW | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | ASW | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0039 | EUR | TSI | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | TSI | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | GIH | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | GIH | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG01123 | hp2 | a0001 | c0001 | t0014 | g0003 | AMR | CLM | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0225 | AFR | ACB | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0041 | AFR | ACB | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0194 | AFR | ACB | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | MSL | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | MSL | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0233 | AFR | USA | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | USA | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | g0143 | AFR | LWK | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | LWK | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0018 | g0169 | REF | REF | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0003 | REF | REF | CA13_chr8_85240458_85289073 | CA13 | chr8 | 85240458 | 85289073 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:85259481 | G | T | 1 | a0003 | 1 | HG02886.hp1 | missense_variant | MODERATE | c.296G>T | p.Gly99Val | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 3/7 | 667/3884 | 296/789 | 99/262 | chr8 | 85259481 | |||
| chr8:85268490 | A | G | 1 | a0002 | 3 | HG01256.hp2 HG01258.hp2 HG03017.hp2 |
missense_variant | MODERATE | c.532A>G | p.Thr178Ala | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/7 | 903/3884 | 532/789 | 178/262 | chr8 | 85268490 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:85245482 | G | T | 1 | a0001c0001t0029 | 1 | HG01258.hp1 | 5_prime_UTR_variant | MODIFIER | c.-347G>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 1/7 | 347 | chr8 | 85245482 | ||||||
| chr8:85245533 | C | T | 2 | a0001c0001t0006 a0001c0001t0028 |
9 | NA18939.hp2 NA18943.hp2 NA18966.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-296C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 1/7 | 296 | chr8 | 85245533 | ||||||
| chr8:85245692 | C | T | 1 | a0001c0001t0027 | 1 | HG00621.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-137C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 1/7 | chr8 | 85245692 | |||||||
| chr8:85245743 | G | T | 1 | a0001c0001t0008 | 6 | NA18941.hp1 NA18965.hp1 NA18979.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-86G>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 1/7 | 86 | chr8 | 85245743 | ||||||
| chr8:85281577 | G | A | 18 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(15): Show |
168 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*228G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 7/7 | 228 | chr8 | 85281577 | ||||||
| chr8:85281611 | C | T | 1 | a0001c0001t0028 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*262C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 7/7 | 262 | chr8 | 85281611 | ||||||
| chr8:85281687 | A | AT | 1 | a0001c0001t0004 | 13 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*350dupT | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 7/7 | 351 | INFO_REALIGN_3_PRIME | chr8 | 85281687 | |||||
| chr8:85281705 | A | G | 1 | a0002c0002t0010 | 3 | HG01256.hp2 HG01258.hp2 HG03017.hp2 |
3_prime_UTR_variant | MODIFIER | c.*356A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 7/7 | 356 | chr8 | 85281705 | ||||||
| chr8:85282132 | A | C | 16 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0007 others(13): Show |
158 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*783A>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 7/7 | 783 | chr8 | 85282132 | ||||||
| chr8:85282155 | T | A | 1 | a0001c0001t0023 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*806T>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 7/7 | 806 | chr8 | 85282155 | ||||||
| chr8:85282258 | A | C | 2 | a0001c0001t0004 a0001c0001t0026 |
14 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*909A>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 7/7 | 909 | chr8 | 85282258 | ||||||
| chr8:85282272 | G | C | 1 | a0001c0001t0016 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*923G>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 7/7 | 923 | chr8 | 85282272 | ||||||
| chr8:85282285 | A | G | 1 | a0001c0001t0015 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*936A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 7/7 | 936 | chr8 | 85282285 | ||||||
| chr8:85282311 | A | G | 2 | a0001c0001t0005 a0001c0001t0015 |
10 | HG01070.hp1 HG01261.hp2 HG02055.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*962A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 7/7 | 962 | chr8 | 85282311 | ||||||
| chr8:85282732 | T | C | 1 | a0001c0001t0007 | 6 | HG01081.hp2 HG02630.hp2 HG03453.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1383T>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 7/7 | 1383 | chr8 | 85282732 | ||||||
| chr8:85282816 | C | T | 1 | a0001c0001t0013 | 2 | HG02622.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1467C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 7/7 | 1467 | chr8 | 85282816 | ||||||
| chr8:85282852 | T | G | 2 | a0001c0001t0011 a0001c0001t0023 |
4 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1503T>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 7/7 | 1503 | chr8 | 85282852 | ||||||
| chr8:85282917 | GTTTTTTT others(4): Show |
G | 1 | a0001c0001t0017 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1584_*1594delTTTT others(7): Show |
CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 7/7 | 1584 | INFO_REALIGN_3_PRIME | chr8 | 85282917 | |||||
| chr8:85282927 | GT | G | 15 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0007 others(12): Show |
154 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(151): Show |
3_prime_UTR_variant | MODIFIER | c.*1588delT | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 7/7 | 1588 | INFO_REALIGN_3_PRIME | chr8 | 85282927 | |||||
| chr8:85283065 | C | T | 1 | a0001c0001t0003 | 14 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1716C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 7/7 | 1716 | chr8 | 85283065 | ||||||
| chr8:85283088 | C | G | 1 | a0001c0001t0022 | 1 | NA18978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1739C>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 7/7 | 1739 | chr8 | 85283088 | ||||||
| chr8:85283258 | C | T | 1 | a0001c0001t0012 | 2 | HG02683.hp1 HG04184.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1909C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 7/7 | 1909 | chr8 | 85283258 | ||||||
| chr8:85283278 | A | G | 1 | a0001c0001t0021 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1929A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 7/7 | 1929 | chr8 | 85283278 | ||||||
| chr8:85283293 | G | A | 1 | a0001c0001t0019 | 1 | HG02273.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1944G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 7/7 | 1944 | chr8 | 85283293 | ||||||
| chr8:85283431 | T | A | 1 | a0001c0001t0024 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2082T>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 7/7 | 2082 | chr8 | 85283431 | ||||||
| chr8:85283435 | T | A | 1 | a0001c0001t0024 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2086T>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 7/7 | 2086 | chr8 | 85283435 | ||||||
| chr8:85283441 | ATTTTTTA others(31): Show |
A | 1 | a0001c0001t0024 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2093_*2130delTTTT others(34): Show |
CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 7/7 | 2093 | chr8 | 85283441 | ||||||
| chr8:85283442 | T | C | 16 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0007 others(13): Show |
158 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*2093T>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 7/7 | 2093 | chr8 | 85283442 | ||||||
| chr8:85283481 | A | AAAAAAAA others(50): Show |
1 | a0001c0001t0024 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2134_*2135insAAAA others(53): Show |
CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 7/7 | 2135 | INFO_REALIGN_3_PRIME | chr8 | 85283481 | |||||
| chr8:85283484 | T | A | 1 | a0001c0001t0024 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2135T>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 7/7 | 2135 | chr8 | 85283484 | ||||||
| chr8:85283485 | T | A | 1 | a0001c0001t0024 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2136T>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 7/7 | 2136 | chr8 | 85283485 | ||||||
| chr8:85283489 | T | A | 1 | a0001c0001t0024 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2140T>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 7/7 | 2140 | chr8 | 85283489 | ||||||
| chr8:85283491 | C | A | 1 | a0001c0001t0024 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2142C>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 7/7 | 2142 | chr8 | 85283491 | ||||||
| chr8:85283493 | C | A | 1 | a0001c0001t0024 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2144C>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 7/7 | 2144 | chr8 | 85283493 | ||||||
| chr8:85283494 | T | A | 1 | a0001c0001t0024 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2145T>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 7/7 | 2145 | chr8 | 85283494 | ||||||
| chr8:85283496 | T | A | 1 | a0001c0001t0024 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2147T>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 7/7 | 2147 | chr8 | 85283496 | ||||||
| chr8:85283500 | T | A | 1 | a0001c0001t0024 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2151T>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 7/7 | 2151 | chr8 | 85283500 | ||||||
| chr8:85283501 | T | A | 1 | a0001c0001t0024 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2152T>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 7/7 | 2152 | chr8 | 85283501 | ||||||
| chr8:85283504 | T | A | 1 | a0001c0001t0024 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2155T>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 7/7 | 2155 | chr8 | 85283504 | ||||||
| chr8:85283506 | T | A | 1 | a0001c0001t0024 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2157T>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 7/7 | 2157 | chr8 | 85283506 | ||||||
| chr8:85283509 | C | A | 1 | a0001c0001t0024 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2160C>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 7/7 | 2160 | chr8 | 85283509 | ||||||
| chr8:85283512 | G | A | 1 | a0001c0001t0024 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2163G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 7/7 | 2163 | chr8 | 85283512 | ||||||
| chr8:85283513 | T | A | 1 | a0001c0001t0024 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2164T>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 7/7 | 2164 | chr8 | 85283513 | ||||||
| chr8:85283518 | T | A | 1 | a0001c0001t0024 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2169T>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 7/7 | 2169 | chr8 | 85283518 | ||||||
| chr8:85283519 | ACATTGTC others(5): Show |
A | 1 | a0001c0001t0024 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2171_*2182delCATT others(8): Show |
CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 7/7 | 2171 | chr8 | 85283519 | ||||||
| chr8:85283536 | T | A | 1 | a0001c0001t0024 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2187T>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 7/7 | 2187 | chr8 | 85283536 | ||||||
| chr8:85283544 | T | G | 1 | a0001c0001t0024 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2195T>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 7/7 | 2195 | chr8 | 85283544 | ||||||
| chr8:85283545 | T | A | 1 | a0001c0001t0024 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2196T>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 7/7 | 2196 | chr8 | 85283545 | ||||||
| chr8:85283546 | T | A | 1 | a0001c0001t0024 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2197T>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 7/7 | 2197 | chr8 | 85283546 | ||||||
| chr8:85283547 | T | A | 1 | a0001c0001t0024 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2198T>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 7/7 | 2198 | chr8 | 85283547 | ||||||
| chr8:85283562 | T | C | 1 | a0001c0001t0025 | 1 | NA19055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2213T>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 7/7 | 2213 | chr8 | 85283562 | ||||||
| chr8:85283632 | T | G | 1 | a0001c0001t0011 | 3 | HG02647.hp1 HG02895.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2283T>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 7/7 | 2283 | chr8 | 85283632 | ||||||
| chr8:85283691 | A | C | 1 | a0001c0001t0009 | 4 | HG02145.hp2 HG02970.hp2 HG03195.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2342A>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 7/7 | 2342 | chr8 | 85283691 | ||||||
| chr8:85283713 | G | C | 1 | a0001c0001t0020 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2364G>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 7/7 | 2364 | chr8 | 85283713 | ||||||
| chr8:85284056 | G | A | 1 | a0001c0001t0014 | 2 | HG00280.hp2 HG01123.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2707G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 7/7 | 2707 | chr8 | 85284056 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:85245890 | G | C | 1 | a0001c0001t0001g0044 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.37+25G>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 1/6 | chr8 | 85245890 | |||||||
| chr8:85245895 | G | A | 1 | a0001c0001t0002g0045 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.37+30G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 1/6 | chr8 | 85245895 | |||||||
| chr8:85245988 | TTAAAC | T | 105 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(102): Show |
159 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.37+127_37+131delAC others(3): Show |
CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 85245988 | ||||||
| chr8:85246020 | C | T | 109 | a0001c0001t0001g0157 a0001c0001t0002g0001 a0001c0001t0002g0007 others(106): Show |
163 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.37+155C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 1/6 | chr8 | 85246020 | |||||||
| chr8:85246292 | A | G | 1 | a0001c0001t0021g0239 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.37+427A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 1/6 | chr8 | 85246292 | |||||||
| chr8:85246565 | A | G | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | HG01243.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.37+700A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 1/6 | chr8 | 85246565 | |||||||
| chr8:85246681 | CTGAT | C | 4 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(1): Show |
7 | HG02559.hp2 HG02572.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.37+819_37+822delAT others(2): Show |
CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 85246681 | ||||||
| chr8:85246715 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.37+850G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 1/6 | chr8 | 85246715 | |||||||
| chr8:85246894 | T | A | 1 | a0001c0001t0001g0047 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.37+1029T>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 1/6 | chr8 | 85246894 | |||||||
| chr8:85247249 | C | T | 10 | a0001c0001t0004g0009 a0001c0001t0004g0030 a0001c0001t0004g0143 others(7): Show |
14 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.37+1384C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 1/6 | chr8 | 85247249 | |||||||
| chr8:85247448 | C | T | 1 | a0001c0001t0002g0021 | 3 | HG00408.hp1 NA19010.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.37+1583C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 1/6 | chr8 | 85247448 | |||||||
| chr8:85247752 | G | C | 10 | a0001c0001t0005g0022 a0001c0001t0005g0048 a0001c0001t0005g0049 others(7): Show |
10 | HG01070.hp1 HG01261.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.37+1887G>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 1/6 | chr8 | 85247752 | |||||||
| chr8:85247889 | G | GT | 7 | a0001c0001t0001g0029 a0001c0001t0001g0141 a0001c0001t0001g0142 others(4): Show |
8 | HG00140.hp1 HG01243.hp1 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.37+2039dupT | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 85247889 | ||||||
| chr8:85247889 | G | T | 1 | a0001c0001t0004g0150 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.37+2024G>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 1/6 | chr8 | 85247889 | |||||||
| chr8:85247894 | T | G | 3 | a0001c0001t0011g0154 a0001c0001t0011g0155 a0001c0001t0023g0156 |
3 | HG02895.hp2 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.37+2029T>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 1/6 | chr8 | 85247894 | |||||||
| chr8:85247895 | T | G | 118 | a0001c0001t0001g0065 a0001c0001t0001g0157 a0001c0001t0002g0001 others(115): Show |
174 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.37+2030T>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 1/6 | chr8 | 85247895 | |||||||
| chr8:85247920 | T | TA | 151 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(148): Show |
214 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.37+2058dupA | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 85247920 | ||||||
| chr8:85247993 | C | T | 4 | a0001c0001t0002g0235 a0001c0001t0002g0236 a0001c0001t0002g0237 others(1): Show |
4 | NA18612.hp2 NA18979.hp2 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.37+2128C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 1/6 | chr8 | 85247993 | |||||||
| chr8:85248032 | A | C | 1 | a0001c0001t0001g0140 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.37+2167A>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 1/6 | chr8 | 85248032 | |||||||
| chr8:85248147 | A | G | 1 | a0001c0001t0002g0234 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.37+2282A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 1/6 | chr8 | 85248147 | |||||||
| chr8:85248262 | A | C | 105 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(102): Show |
159 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.37+2397A>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 1/6 | chr8 | 85248262 | |||||||
| chr8:85248286 | C | T | 5 | a0001c0001t0005g0050 a0001c0001t0005g0051 a0001c0001t0005g0052 others(2): Show |
5 | HG01261.hp2 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.37+2421C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 1/6 | chr8 | 85248286 | |||||||
| chr8:85248457 | C | CA | 15 | a0001c0001t0001g0070 a0001c0001t0002g0158 a0001c0001t0002g0159 others(12): Show |
15 | HG00438.hp2 HG00597.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.38-2266dupA | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 85248457 | ||||||
| chr8:85248489 | G | A | 3 | a0001c0001t0011g0154 a0001c0001t0011g0155 a0001c0001t0023g0156 |
3 | HG02895.hp2 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.38-2251G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 1/6 | chr8 | 85248489 | |||||||
| chr8:85248569 | G | T | 1 | a0001c0001t0002g0233 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.38-2171G>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 1/6 | chr8 | 85248569 | |||||||
| chr8:85248581 | G | C | 2 | a0001c0001t0002g0162 a0001c0001t0002g0163 |
2 | HG01891.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.38-2159G>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 1/6 | chr8 | 85248581 | |||||||
| chr8:85248599 | G | A | 3 | a0001c0001t0002g0034 a0001c0001t0002g0164 a0001c0001t0029g0034 |
3 | HG00735.hp1 HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.38-2141G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 1/6 | chr8 | 85248599 | |||||||
| chr8:85248622 | A | G | 106 | a0001c0001t0001g0157 a0001c0001t0002g0001 a0001c0001t0002g0007 others(103): Show |
160 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.38-2118A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 1/6 | chr8 | 85248622 | |||||||
| chr8:85248625 | A | G | 105 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(102): Show |
159 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.38-2115A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 1/6 | chr8 | 85248625 | |||||||
| chr8:85248656 | G | T | 1 | a0001c0001t0012g0232 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.38-2084G>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 1/6 | chr8 | 85248656 | |||||||
| chr8:85248671 | A | G | 10 | a0001c0001t0004g0009 a0001c0001t0004g0030 a0001c0001t0004g0143 others(7): Show |
14 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.38-2069A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 1/6 | chr8 | 85248671 | |||||||
| chr8:85249079 | A | G | 1 | a0001c0001t0001g0044 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.38-1661A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 1/6 | chr8 | 85249079 | |||||||
| chr8:85249212 | G | A | 3 | a0001c0001t0001g0025 a0001c0001t0001g0072 a0001c0001t0024g0071 |
4 | NA18941.hp2 NA18967.hp2 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.38-1528G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 1/6 | chr8 | 85249212 | |||||||
| chr8:85249213 | T | A | 1 | a0001c0001t0003g0056 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.38-1527T>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 1/6 | chr8 | 85249213 | |||||||
| chr8:85249228 | G | T | 1 | a0001c0001t0001g0139 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.38-1512G>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 1/6 | chr8 | 85249228 | |||||||
| chr8:85249308 | G | A | 106 | a0001c0001t0001g0157 a0001c0001t0002g0001 a0001c0001t0002g0007 others(103): Show |
160 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.38-1432G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 1/6 | chr8 | 85249308 | |||||||
| chr8:85249494 | C | CA | 115 | a0001c0001t0001g0157 a0001c0001t0002g0001 a0001c0001t0002g0007 others(112): Show |
171 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.38-1230dupA | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 85249494 | ||||||
| chr8:85249546 | T | C | 1 | a0001c0001t0002g0165 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.38-1194T>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 1/6 | chr8 | 85249546 | |||||||
| chr8:85249613 | G | A | 10 | a0001c0001t0005g0022 a0001c0001t0005g0048 a0001c0001t0005g0049 others(7): Show |
10 | HG01070.hp1 HG01261.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.38-1127G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 1/6 | chr8 | 85249613 | |||||||
| chr8:85249742 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.38-998T>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 1/6 | chr8 | 85249742 | |||||||
| chr8:85249761 | A | G | 8 | a0001c0001t0002g0020 a0001c0001t0002g0161 a0001c0001t0002g0227 others(5): Show |
11 | HG00099.hp1 HG00438.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.38-979A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 1/6 | chr8 | 85249761 | |||||||
| chr8:85250136 | G | A | 147 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(144): Show |
210 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.38-604G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 1/6 | chr8 | 85250136 | |||||||
| chr8:85250232 | G | T | 8 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0060 others(5): Show |
10 | HG00544.hp2 HG00597.hp1 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.38-508G>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 1/6 | chr8 | 85250232 | |||||||
| chr8:85250266 | G | A | 2 | a0001c0001t0002g0227 a0001c0001t0002g0228 |
2 | HG04115.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.38-474G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 1/6 | chr8 | 85250266 | |||||||
| chr8:85250485 | TAC | T | 17 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0040 others(14): Show |
24 | HG01109.hp2 HG01167.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.38-253_38-252delCA | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr8 | 85250485 | ||||||
| chr8:85250584 | A | G | 5 | a0001c0001t0005g0050 a0001c0001t0005g0051 a0001c0001t0005g0052 others(2): Show |
5 | HG01261.hp2 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.38-156A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 1/6 | chr8 | 85250584 | |||||||
| chr8:85250607 | C | T | 1 | a0001c0001t0002g0215 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.38-133C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 1/6 | chr8 | 85250607 | |||||||
| chr8:85250682 | A | G | 1 | a0001c0001t0001g0138 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.38-58A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 1/6 | chr8 | 85250682 | |||||||
| chr8:85251001 | CT | C | 46 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0044 others(43): Show |
54 | HG00140.hp2 HG00544.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.235+83delT | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr8 | 85251001 | ||||||
| chr8:85251001 | CTT | C | 100 | a0001c0001t0001g0031 a0001c0001t0001g0157 a0001c0001t0002g0001 others(97): Show |
154 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.235+82_235+83delTT | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr8 | 85251001 | ||||||
| chr8:85251001 | CTTT | C | 5 | a0001c0001t0002g0035 a0001c0001t0002g0166 a0001c0001t0002g0233 others(2): Show |
6 | HG01975.hp2 HG02965.hp1 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.235+81_235+83delTT others(1): Show |
CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr8 | 85251001 | ||||||
| chr8:85251041 | C | T | 1 | a0001c0001t0001g0137 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.235+104C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85251041 | |||||||
| chr8:85251047 | G | A | 1 | a0001c0001t0002g0166 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.235+110G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85251047 | |||||||
| chr8:85251058 | G | A | 3 | a0001c0001t0002g0020 a0002c0002t0010g0043 a0002c0002t0010g0231 |
6 | HG00099.hp1 HG01071.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.235+121G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85251058 | |||||||
| chr8:85251065 | G | A | 1 | a0001c0001t0004g0143 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.235+128G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85251065 | |||||||
| chr8:85251126 | C | T | 1 | a0001c0001t0004g0148 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.235+189C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85251126 | |||||||
| chr8:85251146 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.235+209C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85251146 | |||||||
| chr8:85251147 | G | A | 1 | a0001c0001t0003g0064 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.235+210G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85251147 | |||||||
| chr8:85251238 | G | A | 4 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(1): Show |
4 | HG01934.hp2 NA18983.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+301G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85251238 | |||||||
| chr8:85251244 | C | T | 2 | a0001c0001t0004g0030 a0001c0001t0004g0147 |
3 | HG01070.hp2 HG01071.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.235+307C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85251244 | |||||||
| chr8:85251258 | T | A | 106 | a0001c0001t0001g0157 a0001c0001t0002g0001 a0001c0001t0002g0007 others(103): Show |
160 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.235+321T>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85251258 | |||||||
| chr8:85251284 | G | A | 3 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 |
3 | NA18961.hp2 NA18963.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.235+347G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85251284 | |||||||
| chr8:85251373 | C | T | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | HG01243.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.235+436C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85251373 | |||||||
| chr8:85251392 | T | G | 3 | a0001c0001t0002g0040 a0001c0001t0002g0216 a0001c0001t0002g0217 |
4 | HG01167.hp2 HG01884.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.235+455T>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85251392 | |||||||
| chr8:85251398 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.235+461A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85251398 | |||||||
| chr8:85251587 | G | A | 4 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(1): Show |
7 | HG02559.hp2 HG02572.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.235+650G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85251587 | |||||||
| chr8:85251608 | G | C | 1 | a0001c0001t0001g0083 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.235+671G>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85251608 | |||||||
| chr8:85251623 | C | A | 1 | a0001c0001t0001g0084 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.235+686C>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85251623 | |||||||
| chr8:85251627 | TA | T | 151 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(148): Show |
214 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.235+692delA | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr8 | 85251627 | ||||||
| chr8:85251634 | C | A | 151 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(148): Show |
214 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.235+697C>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85251634 | |||||||
| chr8:85251637 | C | A | 3 | a0001c0001t0009g0036 a0001c0001t0009g0167 a0001c0001t0009g0230 |
4 | HG02145.hp2 HG02970.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.235+700C>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85251637 | |||||||
| chr8:85251765 | A | G | 1 | a0001c0001t0002g0212 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.235+828A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85251765 | |||||||
| chr8:85251809 | G | A | 1 | a0001c0001t0005g0048 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.235+872G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85251809 | |||||||
| chr8:85252047 | T | C | 147 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(144): Show |
210 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.235+1110T>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85252047 | |||||||
| chr8:85252058 | G | A | 10 | a0001c0001t0005g0022 a0001c0001t0005g0048 a0001c0001t0005g0049 others(7): Show |
10 | HG01070.hp1 HG01261.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.235+1121G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85252058 | |||||||
| chr8:85252294 | A | G | 4 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(1): Show |
7 | HG02559.hp2 HG02572.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.235+1357A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85252294 | |||||||
| chr8:85252433 | CT | C | 106 | a0001c0001t0001g0157 a0001c0001t0002g0001 a0001c0001t0002g0007 others(103): Show |
160 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.235+1502delT | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr8 | 85252433 | ||||||
| chr8:85252498 | A | G | 1 | a0001c0001t0001g0138 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.235+1561A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85252498 | |||||||
| chr8:85252936 | GT | G | 3 | a0001c0001t0002g0018 a0001c0001t0002g0218 a0001c0001t0002g0219 |
5 | HG01891.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.235+2008delT | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr8 | 85252936 | ||||||
| chr8:85253086 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.235+2149C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85253086 | |||||||
| chr8:85253170 | C | T | 2 | a0001c0001t0002g0210 a0001c0001t0020g0211 |
2 | NA18948.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.235+2233C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85253170 | |||||||
| chr8:85253191 | C | T | 2 | a0001c0001t0002g0225 a0001c0001t0002g0226 |
2 | HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.235+2254C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85253191 | |||||||
| chr8:85253252 | C | CTTAT | 9 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0073 others(6): Show |
15 | HG00621.hp1 NA18952.hp2 NA18968.hp1 others(12): Show |
intron_variant | MODIFIER | c.235+2338_235+2341d others(6): Show |
CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr8 | 85253252 | ||||||
| chr8:85253252 | CTTATTTA others(1): Show |
C | 5 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(2): Show |
8 | HG02559.hp2 HG02572.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.235+2334_235+2341d others(10): Show |
CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr8 | 85253252 | ||||||
| chr8:85253274 | TA | T | 14 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0003g0023 others(11): Show |
16 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.235+2338delA | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85253274 | |||||||
| chr8:85253290 | G | A | 2 | a0001c0001t0002g0162 a0001c0001t0002g0163 |
2 | HG01891.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.235+2353G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85253290 | |||||||
| chr8:85253424 | C | T | 1 | a0001c0001t0016g0209 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.235+2487C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85253424 | |||||||
| chr8:85253589 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.235+2652C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85253589 | |||||||
| chr8:85253712 | A | G | 1 | a0001c0001t0001g0133 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.235+2775A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85253712 | |||||||
| chr8:85253733 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.235+2796C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85253733 | |||||||
| chr8:85253871 | G | C | 1 | a0001c0001t0002g0161 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.235+2934G>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85253871 | |||||||
| chr8:85253987 | A | T | 1 | a0001c0001t0002g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.235+3050A>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85253987 | |||||||
| chr8:85254060 | C | A | 1 | a0001c0001t0002g0218 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.235+3123C>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85254060 | |||||||
| chr8:85254277 | C | CA | 108 | a0001c0001t0001g0070 a0001c0001t0001g0152 a0001c0001t0001g0153 others(105): Show |
162 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.235+3354dupA | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr8 | 85254277 | ||||||
| chr8:85254277 | C | CAA | 14 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0056 others(11): Show |
16 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.235+3353_235+3354d others(4): Show |
CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr8 | 85254277 | ||||||
| chr8:85254277 | CA | C | 14 | a0001c0001t0001g0044 a0001c0001t0001g0067 a0001c0001t0001g0068 others(11): Show |
18 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.235+3354delA | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr8 | 85254277 | ||||||
| chr8:85254292 | G | A | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | HG01243.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.235+3355G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85254292 | |||||||
| chr8:85254403 | A | G | 105 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(102): Show |
159 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.235+3466A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85254403 | |||||||
| chr8:85254483 | C | T | 1 | a0001c0001t0002g0166 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.235+3546C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85254483 | |||||||
| chr8:85254760 | A | G | 1 | a0001c0001t0002g0208 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.235+3823A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85254760 | |||||||
| chr8:85254772 | G | GT | 6 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(3): Show |
6 | HG00597.hp1 HG00609.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.235+3851dupT | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr8 | 85254772 | ||||||
| chr8:85254772 | G | GTTT | 62 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(59): Show |
105 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.235+3849_235+3851d others(5): Show |
CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr8 | 85254772 | ||||||
| chr8:85254772 | G | GTTTT | 33 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(30): Show |
43 | HG00099.hp1 HG01071.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.235+3848_235+3851d others(6): Show |
CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr8 | 85254772 | ||||||
| chr8:85254772 | G | GTTTTT | 7 | a0001c0001t0002g0160 a0001c0001t0002g0161 a0001c0001t0002g0166 others(4): Show |
8 | HG00438.hp2 HG02145.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.235+3847_235+3851d others(7): Show |
CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr8 | 85254772 | ||||||
| chr8:85254772 | GT | G | 6 | a0001c0001t0001g0044 a0001c0001t0001g0067 a0001c0001t0001g0068 others(3): Show |
6 | HG02055.hp1 HG03209.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.235+3851delT | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr8 | 85254772 | ||||||
| chr8:85254777 | TTTTTTTT others(11): Show |
T | 1 | a0001c0001t0003g0060 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.235+3851_235+3868d others(20): Show |
CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr8 | 85254777 | ||||||
| chr8:85254784 | T | G | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | HG01243.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.235+3847T>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85254784 | |||||||
| chr8:85254790 | G | T | 3 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0003g0061 |
3 | HG01243.hp1 HG03041.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.235+3853G>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85254790 | |||||||
| chr8:85254794 | T | G | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | HG01243.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.235+3857T>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85254794 | |||||||
| chr8:85254795 | G | T | 13 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0003g0023 others(10): Show |
15 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(12): Show |
intron_variant | MODIFIER | c.235+3858G>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85254795 | |||||||
| chr8:85254826 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.235+3889A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85254826 | |||||||
| chr8:85255242 | A | G | 1 | a0001c0001t0005g0053 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.236-4179A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85255242 | |||||||
| chr8:85255263 | A | AT | 7 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(4): Show |
10 | HG01928.hp2 HG02080.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.236-4141dupT | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr8 | 85255263 | ||||||
| chr8:85255263 | AT | A | 6 | a0001c0001t0001g0090 a0001c0001t0002g0173 a0001c0001t0002g0174 others(3): Show |
6 | HG02965.hp2 HG02976.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.236-4141delT | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr8 | 85255263 | ||||||
| chr8:85255326 | A | C | 2 | a0001c0001t0013g0223 a0001c0001t0013g0224 |
2 | HG02622.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.236-4095A>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85255326 | |||||||
| chr8:85255655 | G | A | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | HG01243.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.236-3766G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85255655 | |||||||
| chr8:85255744 | A | G | 1 | a0001c0001t0001g0079 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.236-3677A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85255744 | |||||||
| chr8:85255853 | C | T | 3 | a0001c0001t0002g0017 a0001c0001t0002g0202 a0001c0001t0002g0203 |
5 | HG01109.hp1 HG01361.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.236-3568C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85255853 | |||||||
| chr8:85256033 | C | CA | 6 | a0001c0001t0001g0091 a0001c0001t0001g0141 a0001c0001t0002g0175 others(3): Show |
6 | HG02074.hp2 HG04115.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.236-3372dupA | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr8 | 85256033 | ||||||
| chr8:85256033 | CA | C | 6 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(3): Show |
6 | HG02055.hp1 HG03471.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.236-3372delA | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr8 | 85256033 | ||||||
| chr8:85256124 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.236-3297G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85256124 | |||||||
| chr8:85256158 | T | G | 1 | a0001c0001t0001g0092 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.236-3263T>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85256158 | |||||||
| chr8:85256254 | A | T | 4 | a0001c0001t0001g0044 a0001c0001t0001g0067 a0001c0001t0001g0068 others(1): Show |
4 | HG02055.hp1 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.236-3167A>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85256254 | |||||||
| chr8:85256441 | C | T | 1 | a0001c0001t0002g0201 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.236-2980C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85256441 | |||||||
| chr8:85256449 | A | G | 1 | a0001c0001t0001g0126 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.236-2972A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85256449 | |||||||
| chr8:85256489 | T | G | 2 | a0002c0002t0010g0043 a0002c0002t0010g0231 |
3 | HG01256.hp2 HG01258.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.236-2932T>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85256489 | |||||||
| chr8:85256598 | T | C | 5 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 others(2): Show |
5 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.236-2823T>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85256598 | |||||||
| chr8:85256684 | C | T | 1 | a0001c0001t0001g0125 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.236-2737C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85256684 | |||||||
| chr8:85256801 | G | A | 1 | a0001c0001t0017g0177 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.236-2620G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85256801 | |||||||
| chr8:85256911 | C | T | 2 | a0001c0001t0002g0016 a0001c0001t0002g0176 |
4 | HG00738.hp2 HG01099.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.236-2510C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85256911 | |||||||
| chr8:85256956 | T | C | 10 | a0001c0001t0004g0009 a0001c0001t0004g0030 a0001c0001t0004g0143 others(7): Show |
14 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.236-2465T>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85256956 | |||||||
| chr8:85257705 | C | CA | 103 | a0001c0001t0001g0012 a0001c0001t0001g0098 a0001c0001t0001g0099 others(100): Show |
159 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.236-1704dupA | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr8 | 85257705 | ||||||
| chr8:85257705 | C | CAA | 6 | a0001c0001t0002g0178 a0001c0001t0002g0210 a0001c0001t0002g0213 others(3): Show |
6 | HG02074.hp1 HG02630.hp2 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.236-1705_236-1704d others(4): Show |
CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr8 | 85257705 | ||||||
| chr8:85257724 | C | T | 1 | a0001c0001t0002g0220 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.236-1697C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85257724 | |||||||
| chr8:85257742 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.236-1679C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85257742 | |||||||
| chr8:85257793 | AT | A | 7 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(4): Show |
7 | HG03098.hp2 HG03516.hp1 NA18971.hp2 others(4): Show |
intron_variant | MODIFIER | c.236-1615delT | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr8 | 85257793 | ||||||
| chr8:85257877 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.236-1544C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85257877 | |||||||
| chr8:85257908 | T | A | 1 | a0001c0001t0001g0100 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.236-1513T>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85257908 | |||||||
| chr8:85258103 | C | T | 1 | a0001c0001t0002g0207 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.236-1318C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85258103 | |||||||
| chr8:85258210 | A | G | 13 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(10): Show |
27 | HG00408.hp2 HG00423.hp2 HG02027.hp1 others(24): Show |
intron_variant | MODIFIER | c.236-1211A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85258210 | |||||||
| chr8:85258230 | A | G | 1 | a0001c0001t0002g0238 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.236-1191A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85258230 | |||||||
| chr8:85258304 | T | A | 1 | a0001c0001t0001g0076 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.236-1117T>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85258304 | |||||||
| chr8:85258355 | CT | C | 14 | a0001c0001t0001g0008 a0001c0001t0001g0076 a0001c0001t0001g0077 others(11): Show |
17 | HG01928.hp2 HG01934.hp2 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.236-1065delT | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85258355 | |||||||
| chr8:85258431 | T | C | 10 | a0001c0001t0004g0009 a0001c0001t0004g0030 a0001c0001t0004g0143 others(7): Show |
14 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.236-990T>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85258431 | |||||||
| chr8:85258511 | G | A | 10 | a0001c0001t0004g0009 a0001c0001t0004g0030 a0001c0001t0004g0143 others(7): Show |
14 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.236-910G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85258511 | |||||||
| chr8:85258758 | A | C | 2 | a0001c0001t0001g0029 a0001c0001t0001g0118 |
3 | HG00140.hp1 HG01358.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.236-663A>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85258758 | |||||||
| chr8:85258759 | C | CA | 35 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0044 others(32): Show |
42 | HG00544.hp1 HG01168.hp2 HG01175.hp2 others(39): Show |
intron_variant | MODIFIER | c.236-633dupA | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr8 | 85258759 | ||||||
| chr8:85258759 | C | CAA | 62 | a0001c0001t0001g0099 a0001c0001t0002g0001 a0001c0001t0002g0010 others(59): Show |
105 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.236-634_236-633dup others(2): Show |
CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr8 | 85258759 | ||||||
| chr8:85258759 | C | CAAA | 31 | a0001c0001t0002g0007 a0001c0001t0002g0161 a0001c0001t0002g0164 others(28): Show |
39 | HG00423.hp1 HG00438.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.236-635_236-633dup others(3): Show |
CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr8 | 85258759 | ||||||
| chr8:85258759 | C | CAAAA | 8 | a0001c0001t0002g0041 a0001c0001t0002g0160 a0001c0001t0002g0162 others(5): Show |
9 | HG01891.hp2 HG02486.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.236-636_236-633dup others(4): Show |
CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr8 | 85258759 | ||||||
| chr8:85258759 | CA | C | 10 | a0001c0001t0001g0031 a0001c0001t0001g0033 a0001c0001t0001g0116 others(7): Show |
12 | HG00099.hp2 HG01243.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.236-633delA | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr8 | 85258759 | ||||||
| chr8:85258759 | CAA | C | 8 | a0001c0001t0004g0009 a0001c0001t0004g0030 a0001c0001t0004g0143 others(5): Show |
12 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.236-634_236-633del others(2): Show |
CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr8 | 85258759 | ||||||
| chr8:85258759 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0003g0056 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.236-643_236-633del others(11): Show |
CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr8 | 85258759 | ||||||
| chr8:85259244 | A | G | 5 | a0001c0001t0001g0157 a0001c0001t0006g0011 a0001c0001t0006g0015 others(2): Show |
10 | HG03471.hp2 NA18939.hp2 NA18943.hp2 others(7): Show |
intron_variant | MODIFIER | c.236-177A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85259244 | |||||||
| chr8:85259284 | G | A | 1 | a0001c0001t0002g0180 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.236-137G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 2/6 | chr8 | 85259284 | |||||||
| chr8:85259557 | T | C | 105 | a0001c0001t0001g0157 a0001c0001t0002g0001 a0001c0001t0002g0007 others(102): Show |
159 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.354+18T>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 3/6 | chr8 | 85259557 | |||||||
| chr8:85260205 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.354+666T>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 3/6 | chr8 | 85260205 | |||||||
| chr8:85260388 | G | A | 105 | a0001c0001t0001g0157 a0001c0001t0002g0001 a0001c0001t0002g0007 others(102): Show |
159 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.354+849G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 3/6 | chr8 | 85260388 | |||||||
| chr8:85260557 | T | A | 147 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(144): Show |
210 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.354+1018T>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 3/6 | chr8 | 85260557 | |||||||
| chr8:85261022 | C | A | 15 | a0001c0001t0001g0008 a0001c0001t0001g0076 a0001c0001t0001g0077 others(12): Show |
18 | HG01928.hp2 HG01934.hp2 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.354+1483C>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 3/6 | chr8 | 85261022 | |||||||
| chr8:85261037 | T | C | 109 | a0001c0001t0001g0157 a0001c0001t0002g0001 a0001c0001t0002g0007 others(106): Show |
163 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.354+1498T>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 3/6 | chr8 | 85261037 | |||||||
| chr8:85261082 | G | T | 145 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(142): Show |
207 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.354+1543G>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 3/6 | chr8 | 85261082 | |||||||
| chr8:85261178 | T | C | 2 | a0001c0001t0001g0074 a0001c0001t0001g0107 |
2 | HG02735.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.354+1639T>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 3/6 | chr8 | 85261178 | |||||||
| chr8:85261437 | T | A | 1 | a0001c0001t0001g0076 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.354+1898T>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 3/6 | chr8 | 85261437 | |||||||
| chr8:85261718 | G | T | 2 | a0001c0001t0002g0160 a0001c0001t0002g0233 |
2 | HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.354+2179G>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 3/6 | chr8 | 85261718 | |||||||
| chr8:85261729 | G | GTA | 3 | a0001c0001t0002g0160 a0001c0001t0002g0233 a0001c0001t0004g0143 |
3 | HG06807.hp1 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.354+2204_354+2205d others(4): Show |
CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr8 | 85261729 | ||||||
| chr8:85261773 | A | G | 4 | a0001c0001t0001g0044 a0001c0001t0001g0067 a0001c0001t0001g0068 others(1): Show |
4 | HG02055.hp1 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.354+2234A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 3/6 | chr8 | 85261773 | |||||||
| chr8:85261890 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.354+2351G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 3/6 | chr8 | 85261890 | |||||||
| chr8:85262121 | A | ATGCCTGT others(126): Show |
5 | a0001c0001t0005g0022 a0001c0001t0005g0048 a0001c0001t0005g0049 others(2): Show |
5 | HG01070.hp1 HG02717.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.354+2598_354+2599i others(135): Show |
CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr8 | 85262121 | ||||||
| chr8:85262207 | T | G | 1 | a0001c0001t0001g0141 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.354+2668T>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 3/6 | chr8 | 85262207 | |||||||
| chr8:85262349 | C | A | 4 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(1): Show |
7 | HG02559.hp2 HG02572.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.354+2810C>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 3/6 | chr8 | 85262349 | |||||||
| chr8:85262479 | A | G | 2 | a0001c0001t0002g0162 a0001c0001t0002g0163 |
2 | HG01891.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.354+2940A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 3/6 | chr8 | 85262479 | |||||||
| chr8:85262519 | A | C | 1 | a0001c0001t0001g0069 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.354+2980A>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 3/6 | chr8 | 85262519 | |||||||
| chr8:85262583 | C | A | 4 | a0001c0001t0001g0044 a0001c0001t0001g0067 a0001c0001t0001g0068 others(1): Show |
4 | HG02055.hp1 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.354+3044C>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 3/6 | chr8 | 85262583 | |||||||
| chr8:85262643 | T | C | 1 | a0001c0001t0002g0206 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.354+3104T>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 3/6 | chr8 | 85262643 | |||||||
| chr8:85262702 | G | A | 10 | a0001c0001t0004g0009 a0001c0001t0004g0030 a0001c0001t0004g0143 others(7): Show |
14 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.354+3163G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 3/6 | chr8 | 85262702 | |||||||
| chr8:85262703 | G | T | 1 | a0001c0001t0023g0156 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.354+3164G>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 3/6 | chr8 | 85262703 | |||||||
| chr8:85262858 | TC | T | 4 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 others(1): Show |
4 | HG02145.hp1 HG02257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.354+3321delC | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr8 | 85262858 | ||||||
| chr8:85263118 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.355-3490G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 3/6 | chr8 | 85263118 | |||||||
| chr8:85263328 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.355-3280G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 3/6 | chr8 | 85263328 | |||||||
| chr8:85263414 | A | G | 1 | a0001c0001t0004g0146 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.355-3194A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 3/6 | chr8 | 85263414 | |||||||
| chr8:85263508 | G | A | 1 | a0001c0001t0001g0088 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.355-3100G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 3/6 | chr8 | 85263508 | |||||||
| chr8:85263851 | T | G | 10 | a0001c0001t0005g0022 a0001c0001t0005g0048 a0001c0001t0005g0049 others(7): Show |
10 | HG01070.hp1 HG01261.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.355-2757T>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 3/6 | chr8 | 85263851 | |||||||
| chr8:85264119 | C | T | 1 | a0001c0001t0002g0212 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.355-2489C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 3/6 | chr8 | 85264119 | |||||||
| chr8:85264134 | C | T | 1 | a0001c0001t0002g0199 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.355-2474C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 3/6 | chr8 | 85264134 | |||||||
| chr8:85264142 | C | T | 5 | a0001c0001t0005g0050 a0001c0001t0005g0051 a0001c0001t0005g0052 others(2): Show |
5 | HG01261.hp2 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.355-2466C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 3/6 | chr8 | 85264142 | |||||||
| chr8:85264697 | G | A | 3 | a0001c0001t0002g0038 a0001c0001t0002g0181 a0001c0001t0002g0213 |
4 | HG01496.hp2 HG01928.hp1 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.355-1911G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 3/6 | chr8 | 85264697 | |||||||
| chr8:85264784 | A | G | 1 | a0001c0001t0002g0215 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.355-1824A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 3/6 | chr8 | 85264784 | |||||||
| chr8:85265294 | G | A | 1 | a0001c0001t0005g0055 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.355-1314G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 3/6 | chr8 | 85265294 | |||||||
| chr8:85265425 | G | A | 1 | a0002c0002t0010g0043 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.355-1183G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 3/6 | chr8 | 85265425 | |||||||
| chr8:85265478 | C | T | 1 | a0001c0001t0002g0198 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.355-1130C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 3/6 | chr8 | 85265478 | |||||||
| chr8:85265659 | T | C | 4 | a0001c0001t0001g0070 a0001c0001t0001g0108 a0001c0001t0001g0109 others(1): Show |
4 | HG03490.hp2 HG03492.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.355-949T>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 3/6 | chr8 | 85265659 | |||||||
| chr8:85265702 | C | T | 1 | a0001c0001t0002g0236 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.355-906C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 3/6 | chr8 | 85265702 | |||||||
| chr8:85265870 | A | G | 3 | a0001c0001t0001g0028 a0001c0001t0001g0091 a0001c0001t0001g0132 |
4 | NA18948.hp2 NA18963.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.355-738A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 3/6 | chr8 | 85265870 | |||||||
| chr8:85266015 | C | A | 1 | a0001c0001t0004g0149 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.355-593C>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 3/6 | chr8 | 85266015 | |||||||
| chr8:85266050 | C | T | 1 | a0001c0001t0002g0186 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.355-558C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 3/6 | chr8 | 85266050 | |||||||
| chr8:85266189 | T | A | 2 | a0001c0001t0001g0067 a0001c0001t0001g0068 |
2 | HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.355-419T>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 3/6 | chr8 | 85266189 | |||||||
| chr8:85266207 | C | T | 5 | a0001c0001t0002g0045 a0001c0001t0002g0180 a0001c0001t0002g0185 others(2): Show |
5 | HG01358.hp1 HG01978.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.355-401C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 3/6 | chr8 | 85266207 | |||||||
| chr8:85266221 | C | T | 2 | a0001c0001t0002g0174 a0001c0001t0002g0196 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.355-387C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 3/6 | chr8 | 85266221 | |||||||
| chr8:85266408 | T | C | 1 | a0001c0001t0001g0072 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.355-200T>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 3/6 | chr8 | 85266408 | |||||||
| chr8:85266730 | A | G | 1 | a0001c0001t0002g0039 | 2 | HG01167.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.450+27A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 4/6 | chr8 | 85266730 | |||||||
| chr8:85266887 | T | C | 1 | a0001c0001t0001g0101 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.450+184T>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 4/6 | chr8 | 85266887 | |||||||
| chr8:85266898 | T | C | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | NA18964.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.450+195T>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 4/6 | chr8 | 85266898 | |||||||
| chr8:85267106 | T | A | 1 | a0001c0001t0002g0212 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.450+403T>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 4/6 | chr8 | 85267106 | |||||||
| chr8:85267131 | C | T | 3 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 |
3 | NA18961.hp2 NA18963.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.450+428C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 4/6 | chr8 | 85267131 | |||||||
| chr8:85267135 | C | T | 4 | a0001c0001t0011g0154 a0001c0001t0011g0155 a0001c0001t0011g0200 others(1): Show |
4 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.450+432C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 4/6 | chr8 | 85267135 | |||||||
| chr8:85267199 | G | A | 14 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0003g0023 others(11): Show |
16 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.450+496G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 4/6 | chr8 | 85267199 | |||||||
| chr8:85267277 | T | G | 4 | a0001c0001t0011g0154 a0001c0001t0011g0155 a0001c0001t0011g0200 others(1): Show |
4 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.450+574T>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 4/6 | chr8 | 85267277 | |||||||
| chr8:85267281 | C | T | 1 | a0001c0001t0002g0207 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.450+578C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 4/6 | chr8 | 85267281 | |||||||
| chr8:85267292 | A | G | 10 | a0001c0001t0002g0165 a0001c0001t0002g0184 a0001c0001t0002g0199 others(7): Show |
11 | HG01081.hp2 HG02630.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.450+589A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 4/6 | chr8 | 85267292 | |||||||
| chr8:85267395 | C | T | 1 | a0001c0001t0001g0027 | 2 | HG03017.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.451-507C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 4/6 | chr8 | 85267395 | |||||||
| chr8:85267523 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0073 |
3 | NA18968.hp1 NA18969.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.451-379G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 4/6 | chr8 | 85267523 | |||||||
| chr8:85267541 | A | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0133 |
5 | HG02027.hp2 HG02083.hp1 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.451-361A>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 4/6 | chr8 | 85267541 | |||||||
| chr8:85267667 | TGGGACTA others(8): Show |
T | 1 | a0001c0001t0025g0123 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.451-233_451-219del others(15): Show |
CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr8 | 85267667 | ||||||
| chr8:85268277 | A | C | 2 | a0001c0001t0002g0162 a0001c0001t0002g0163 |
2 | HG01891.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.514-195A>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 5/6 | chr8 | 85268277 | |||||||
| chr8:85268677 | CT | C | 123 | a0001c0001t0001g0157 a0001c0001t0002g0001 a0001c0001t0002g0007 others(120): Show |
181 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.669+67delT | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 85268677 | ||||||
| chr8:85268677 | CTT | C | 22 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(19): Show |
27 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(24): Show |
intron_variant | MODIFIER | c.669+66_669+67delTT | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 85268677 | ||||||
| chr8:85268715 | A | G | 108 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(105): Show |
162 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.669+88A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85268715 | |||||||
| chr8:85268720 | G | A | 12 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0056 others(9): Show |
14 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(11): Show |
intron_variant | MODIFIER | c.669+93G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85268720 | |||||||
| chr8:85268981 | C | T | 1 | a0001c0001t0004g0149 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.669+354C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85268981 | |||||||
| chr8:85269322 | A | C | 4 | a0001c0001t0001g0044 a0001c0001t0001g0067 a0001c0001t0001g0068 others(1): Show |
4 | HG02055.hp1 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.669+695A>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85269322 | |||||||
| chr8:85269481 | G | A | 2 | a0001c0001t0002g0182 a0001c0001t0002g0190 |
2 | HG00735.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.669+854G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85269481 | |||||||
| chr8:85269641 | T | C | 147 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(144): Show |
210 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.669+1014T>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85269641 | |||||||
| chr8:85269763 | G | A | 1 | a0001c0001t0001g0027 | 2 | HG03017.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.669+1136G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85269763 | |||||||
| chr8:85269875 | A | AT | 12 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0056 others(9): Show |
14 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(11): Show |
intron_variant | MODIFIER | c.669+1258dupT | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 85269875 | ||||||
| chr8:85269877 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.669+1250T>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85269877 | |||||||
| chr8:85270060 | A | G | 123 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0157 others(120): Show |
179 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.669+1433A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85270060 | |||||||
| chr8:85270157 | C | A | 4 | a0001c0001t0002g0040 a0001c0001t0002g0216 a0001c0001t0002g0217 others(1): Show |
5 | HG01167.hp2 HG01884.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.669+1530C>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85270157 | |||||||
| chr8:85270446 | A | G | 1 | a0001c0001t0002g0216 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.669+1819A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85270446 | |||||||
| chr8:85271150 | G | T | 1 | a0001c0001t0005g0053 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.669+2523G>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85271150 | |||||||
| chr8:85271244 | G | T | 13 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(10): Show |
27 | HG00408.hp2 HG00423.hp2 HG02027.hp1 others(24): Show |
intron_variant | MODIFIER | c.669+2617G>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85271244 | |||||||
| chr8:85271300 | A | T | 1 | a0001c0001t0005g0052 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.669+2673A>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85271300 | |||||||
| chr8:85271411 | C | A | 1 | a0001c0001t0001g0137 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.669+2784C>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85271411 | |||||||
| chr8:85271441 | T | C | 151 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(148): Show |
214 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.669+2814T>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85271441 | |||||||
| chr8:85271775 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.669+3148A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85271775 | |||||||
| chr8:85271987 | T | G | 1 | a0001c0001t0001g0157 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.669+3360T>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85271987 | |||||||
| chr8:85272310 | G | T | 10 | a0001c0001t0004g0009 a0001c0001t0004g0030 a0001c0001t0004g0143 others(7): Show |
14 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.669+3683G>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85272310 | |||||||
| chr8:85272412 | C | T | 1 | a0001c0001t0002g0215 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.669+3785C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85272412 | |||||||
| chr8:85272438 | T | C | 2 | a0001c0001t0002g0041 a0001c0001t0002g0222 |
3 | HG02486.hp2 HG02647.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.669+3811T>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85272438 | |||||||
| chr8:85272615 | A | T | 10 | a0001c0001t0005g0022 a0001c0001t0005g0048 a0001c0001t0005g0049 others(7): Show |
10 | HG01070.hp1 HG01261.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.669+3988A>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85272615 | |||||||
| chr8:85273002 | G | A | 1 | a0001c0001t0005g0055 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.669+4375G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85273002 | |||||||
| chr8:85273003 | A | T | 10 | a0001c0001t0005g0022 a0001c0001t0005g0048 a0001c0001t0005g0049 others(7): Show |
10 | HG01070.hp1 HG01261.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.669+4376A>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85273003 | |||||||
| chr8:85273261 | A | G | 1 | a0001c0001t0004g0150 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.669+4634A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85273261 | |||||||
| chr8:85273522 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.669+4895C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85273522 | |||||||
| chr8:85273544 | C | T | 2 | a0001c0001t0002g0174 a0001c0001t0002g0196 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.669+4917C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85273544 | |||||||
| chr8:85273617 | C | T | 1 | a0001c0001t0002g0161 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.669+4990C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85273617 | |||||||
| chr8:85273621 | C | A | 1 | a0001c0001t0002g0191 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.669+4994C>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85273621 | |||||||
| chr8:85273634 | G | C | 11 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0046 others(8): Show |
17 | HG00733.hp2 HG01175.hp2 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.669+5007G>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85273634 | |||||||
| chr8:85273807 | C | T | 1 | a0001c0001t0011g0200 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.669+5180C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85273807 | |||||||
| chr8:85273873 | G | A | 3 | a0001c0001t0001g0075 a0001c0001t0001g0113 a0001c0001t0001g0117 |
3 | HG00099.hp2 HG02258.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.669+5246G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85273873 | |||||||
| chr8:85273924 | G | A | 1 | a0001c0001t0013g0223 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.669+5297G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85273924 | |||||||
| chr8:85273984 | C | G | 1 | a0001c0001t0001g0044 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.669+5357C>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85273984 | |||||||
| chr8:85273995 | C | T | 104 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(101): Show |
158 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.669+5368C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85273995 | |||||||
| chr8:85274026 | G | A | 10 | a0001c0001t0004g0009 a0001c0001t0004g0030 a0001c0001t0004g0143 others(7): Show |
14 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.669+5399G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85274026 | |||||||
| chr8:85274274 | T | G | 1 | a0001c0001t0001g0157 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.669+5647T>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85274274 | |||||||
| chr8:85274330 | G | A | 10 | a0001c0001t0004g0009 a0001c0001t0004g0030 a0001c0001t0004g0143 others(7): Show |
14 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.669+5703G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85274330 | |||||||
| chr8:85274386 | A | G | 5 | a0001c0001t0001g0025 a0001c0001t0001g0072 a0001c0001t0001g0103 others(2): Show |
6 | HG00544.hp1 HG00609.hp2 NA18941.hp2 others(3): Show |
intron_variant | MODIFIER | c.669+5759A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85274386 | |||||||
| chr8:85274532 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.669+5905C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85274532 | |||||||
| chr8:85274570 | C | T | 2 | a0001c0001t0001g0104 a0001c0001t0001g0112 |
2 | HG00733.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.669+5943C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85274570 | |||||||
| chr8:85274592 | C | T | 2 | a0001c0001t0002g0162 a0001c0001t0002g0163 |
2 | HG01891.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.669+5965C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85274592 | |||||||
| chr8:85274667 | C | T | 1 | a0001c0001t0002g0203 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.669+6040C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85274667 | |||||||
| chr8:85274869 | A | T | 1 | a0001c0001t0001g0157 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.669+6242A>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85274869 | |||||||
| chr8:85274936 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.670-6294A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85274936 | |||||||
| chr8:85275090 | A | C | 1 | a0001c0001t0001g0092 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.670-6140A>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85275090 | |||||||
| chr8:85275196 | C | T | 2 | a0001c0001t0002g0215 a0001c0001t0016g0209 |
2 | HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.670-6034C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85275196 | |||||||
| chr8:85275197 | G | A | 56 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(53): Show |
98 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.670-6033G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85275197 | |||||||
| chr8:85275316 | C | T | 4 | a0001c0001t0001g0025 a0001c0001t0001g0072 a0001c0001t0001g0131 others(1): Show |
5 | HG00609.hp2 NA18941.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.670-5914C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85275316 | |||||||
| chr8:85275344 | G | C | 4 | a0001c0001t0001g0014 a0001c0001t0001g0027 a0001c0001t0001g0105 others(1): Show |
7 | HG00621.hp2 HG01168.hp2 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.670-5886G>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85275344 | |||||||
| chr8:85275465 | T | G | 1 | a0001c0001t0001g0157 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.670-5765T>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85275465 | |||||||
| chr8:85275482 | A | G | 4 | a0001c0001t0011g0154 a0001c0001t0011g0155 a0001c0001t0011g0200 others(1): Show |
4 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.670-5748A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85275482 | |||||||
| chr8:85275536 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.670-5694G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85275536 | |||||||
| chr8:85275730 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.670-5500A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85275730 | |||||||
| chr8:85275862 | G | T | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | HG01243.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.670-5368G>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85275862 | |||||||
| chr8:85275914 | C | T | 10 | a0001c0001t0005g0022 a0001c0001t0005g0048 a0001c0001t0005g0049 others(7): Show |
10 | HG01070.hp1 HG01261.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.670-5316C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85275914 | |||||||
| chr8:85275929 | A | G | 1 | a0001c0001t0001g0032 | 2 | HG02572.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.670-5301A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85275929 | |||||||
| chr8:85276261 | C | T | 2 | a0001c0001t0001g0026 a0001c0001t0001g0073 |
3 | NA18968.hp1 NA18969.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.670-4969C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85276261 | |||||||
| chr8:85276262 | G | A | 2 | a0001c0001t0002g0041 a0001c0001t0002g0222 |
3 | HG02486.hp2 HG02647.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.670-4968G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85276262 | |||||||
| chr8:85276262 | G | C | 145 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(142): Show |
207 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.670-4968G>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85276262 | |||||||
| chr8:85276307 | C | G | 4 | a0001c0001t0001g0025 a0001c0001t0001g0072 a0001c0001t0001g0131 others(1): Show |
5 | HG00609.hp2 NA18941.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.670-4923C>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85276307 | |||||||
| chr8:85276322 | T | C | 10 | a0001c0001t0005g0022 a0001c0001t0005g0048 a0001c0001t0005g0049 others(7): Show |
10 | HG01070.hp1 HG01261.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.670-4908T>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85276322 | |||||||
| chr8:85276330 | G | C | 1 | a0001c0001t0001g0157 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.670-4900G>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85276330 | |||||||
| chr8:85276409 | C | T | 4 | a0001c0001t0011g0154 a0001c0001t0011g0155 a0001c0001t0011g0200 others(1): Show |
4 | HG02647.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.670-4821C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85276409 | |||||||
| chr8:85276413 | C | T | 12 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0056 others(9): Show |
14 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(11): Show |
intron_variant | MODIFIER | c.670-4817C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85276413 | |||||||
| chr8:85276459 | C | T | 12 | a0001c0001t0002g0182 a0001c0001t0002g0190 a0001c0001t0005g0022 others(9): Show |
12 | HG00735.hp2 HG01070.hp1 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.670-4771C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85276459 | |||||||
| chr8:85276742 | A | G | 108 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(105): Show |
162 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.670-4488A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85276742 | |||||||
| chr8:85276768 | A | T | 1 | a0001c0001t0003g0059 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.670-4462A>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85276768 | |||||||
| chr8:85276775 | G | A | 14 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0003g0023 others(11): Show |
16 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.670-4455G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85276775 | |||||||
| chr8:85276793 | TC | T | 5 | a0001c0001t0005g0022 a0001c0001t0005g0048 a0001c0001t0005g0049 others(2): Show |
5 | HG01070.hp1 HG02717.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.670-4436delC | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85276793 | |||||||
| chr8:85276794 | C | G | 5 | a0001c0001t0002g0045 a0001c0001t0002g0180 a0001c0001t0002g0185 others(2): Show |
5 | HG01358.hp1 HG01978.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.670-4436C>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85276794 | |||||||
| chr8:85276795 | G | C | 4 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(1): Show |
7 | HG02559.hp2 HG02572.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.670-4435G>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85276795 | |||||||
| chr8:85276832 | G | A | 3 | a0001c0001t0002g0184 a0001c0001t0002g0199 a0001c0001t0002g0206 |
3 | HG02809.hp1 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.670-4398G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85276832 | |||||||
| chr8:85276870 | A | G | 1 | a0001c0001t0027g0114 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.670-4360A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85276870 | |||||||
| chr8:85276969 | A | C | 2 | a0001c0001t0002g0019 a0001c0001t0002g0042 |
5 | HG01109.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.670-4261A>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85276969 | |||||||
| chr8:85276973 | A | C | 1 | a0001c0001t0003g0059 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.670-4257A>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85276973 | |||||||
| chr8:85277035 | C | T | 1 | a0001c0001t0016g0209 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.670-4195C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85277035 | |||||||
| chr8:85277202 | A | C | 5 | a0001c0001t0007g0037 a0001c0001t0007g0171 a0001c0001t0007g0179 others(2): Show |
6 | HG01081.hp2 HG02630.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.670-4028A>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85277202 | |||||||
| chr8:85277259 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.670-3971T>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85277259 | |||||||
| chr8:85277261 | C | A | 2 | a0001c0001t0002g0041 a0001c0001t0002g0222 |
3 | HG02486.hp2 HG02647.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.670-3969C>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85277261 | |||||||
| chr8:85277310 | G | A | 56 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(53): Show |
98 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.670-3920G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85277310 | |||||||
| chr8:85277336 | C | T | 1 | a0001c0001t0002g0193 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.670-3894C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85277336 | |||||||
| chr8:85277361 | A | G | 1 | a0001c0001t0003g0057 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.670-3869A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85277361 | |||||||
| chr8:85277470 | T | C | 109 | a0001c0001t0001g0157 a0001c0001t0002g0001 a0001c0001t0002g0007 others(106): Show |
163 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.670-3760T>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85277470 | |||||||
| chr8:85277677 | T | C | 2 | a0001c0001t0001g0074 a0001c0001t0001g0107 |
2 | HG02735.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.670-3553T>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85277677 | |||||||
| chr8:85277745 | C | T | 1 | a0001c0001t0017g0177 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.670-3485C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85277745 | |||||||
| chr8:85277759 | G | C | 12 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0056 others(9): Show |
14 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(11): Show |
intron_variant | MODIFIER | c.670-3471G>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85277759 | |||||||
| chr8:85277864 | C | T | 108 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(105): Show |
162 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.670-3366C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85277864 | |||||||
| chr8:85277866 | C | T | 20 | a0001c0001t0004g0009 a0001c0001t0004g0030 a0001c0001t0004g0143 others(17): Show |
24 | HG00140.hp2 HG01070.hp1 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.670-3364C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85277866 | |||||||
| chr8:85277875 | C | T | 12 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0056 others(9): Show |
14 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(11): Show |
intron_variant | MODIFIER | c.670-3355C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85277875 | |||||||
| chr8:85277909 | G | A | 2 | a0001c0001t0002g0041 a0001c0001t0002g0222 |
3 | HG02486.hp2 HG02647.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.670-3321G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85277909 | |||||||
| chr8:85277940 | A | T | 104 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(101): Show |
158 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.670-3290A>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85277940 | |||||||
| chr8:85278099 | TA | T | 7 | a0001c0001t0001g0079 a0001c0001t0002g0212 a0001c0001t0011g0154 others(4): Show |
7 | HG02647.hp1 HG02895.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.670-3118delA | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 85278099 | ||||||
| chr8:85278105 | A | C | 2 | a0001c0001t0002g0160 a0001c0001t0002g0233 |
2 | HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.670-3125A>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85278105 | |||||||
| chr8:85278153 | C | T | 1 | a0001c0001t0002g0192 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.670-3077C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85278153 | |||||||
| chr8:85278265 | C | CA | 100 | a0001c0001t0001g0029 a0001c0001t0001g0033 a0001c0001t0001g0070 others(97): Show |
150 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.670-2942dupA | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 85278265 | ||||||
| chr8:85278265 | C | CAA | 13 | a0001c0001t0002g0010 a0001c0001t0002g0042 a0001c0001t0002g0158 others(10): Show |
17 | HG01074.hp2 HG01261.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.670-2943_670-2942d others(4): Show |
CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 85278265 | ||||||
| chr8:85278265 | CA | C | 12 | a0001c0001t0001g0031 a0001c0001t0001g0079 a0001c0001t0001g0087 others(9): Show |
13 | HG01070.hp1 HG01070.hp2 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.670-2942delA | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 85278265 | ||||||
| chr8:85278397 | G | T | 4 | a0001c0001t0001g0089 a0001c0001t0001g0119 a0001c0001t0001g0121 others(1): Show |
4 | NA18950.hp2 NA18968.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.670-2833G>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85278397 | |||||||
| chr8:85278434 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.670-2796C>T | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85278434 | |||||||
| chr8:85278544 | T | G | 2 | a0001c0001t0001g0108 a0001c0001t0001g0116 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.670-2686T>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85278544 | |||||||
| chr8:85278607 | T | C | 4 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(1): Show |
7 | HG02559.hp2 HG02572.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.670-2623T>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85278607 | |||||||
| chr8:85278647 | AAG | A | 78 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0010 others(75): Show |
124 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.670-2578_670-2577d others(4): Show |
CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | 85278647 | ||||||
| chr8:85278672 | T | C | 4 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(1): Show |
7 | HG02559.hp2 HG02572.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.670-2558T>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85278672 | |||||||
| chr8:85279358 | A | G | 1 | a0001c0001t0002g0229 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.670-1872A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85279358 | |||||||
| chr8:85279425 | A | G | 2 | a0001c0001t0002g0041 a0001c0001t0002g0222 |
3 | HG02486.hp2 HG02647.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.670-1805A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85279425 | |||||||
| chr8:85279472 | C | A | 2 | a0001c0001t0001g0106 a0001c0001t0001g0125 |
2 | NA19003.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.670-1758C>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85279472 | |||||||
| chr8:85279659 | C | G | 1 | a0001c0001t0002g0207 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.670-1571C>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85279659 | |||||||
| chr8:85279750 | C | G | 1 | a0001c0001t0002g0236 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.670-1480C>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85279750 | |||||||
| chr8:85279804 | G | A | 1 | a0001c0001t0002g0219 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.670-1426G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85279804 | |||||||
| chr8:85279821 | A | G | 4 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(1): Show |
7 | HG02559.hp2 HG02572.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.670-1409A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85279821 | |||||||
| chr8:85279889 | T | C | 4 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(1): Show |
7 | HG02559.hp2 HG02572.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.670-1341T>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85279889 | |||||||
| chr8:85280146 | G | A | 4 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(1): Show |
4 | HG01934.hp2 NA18983.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.670-1084G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85280146 | |||||||
| chr8:85280274 | G | A | 1 | a0001c0001t0002g0170 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.670-956G>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85280274 | |||||||
| chr8:85280311 | A | G | 1 | a0001c0001t0002g0042 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.670-919A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85280311 | |||||||
| chr8:85280528 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.670-702T>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85280528 | |||||||
| chr8:85280603 | T | G | 2 | a0001c0001t0002g0182 a0001c0001t0002g0190 |
2 | HG00735.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.670-627T>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85280603 | |||||||
| chr8:85280606 | T | C | 10 | a0001c0001t0005g0022 a0001c0001t0005g0048 a0001c0001t0005g0049 others(7): Show |
10 | HG01070.hp1 HG01261.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.670-624T>C | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85280606 | |||||||
| chr8:85280807 | T | G | 4 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(1): Show |
7 | HG02559.hp2 HG02572.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.670-423T>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85280807 | |||||||
| chr8:85280825 | A | G | 12 | a0001c0001t0003g0023 a0001c0001t0003g0024 a0001c0001t0003g0056 others(9): Show |
14 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(11): Show |
intron_variant | MODIFIER | c.670-405A>G | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85280825 | |||||||
| chr8:85281130 | T | A | 1 | a0001c0001t0003g0063 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.670-100T>A | CA13 | ENSG00000185015.8 | transcript | ENST00000321764.4 | protein_coding | 6/6 | chr8 | 85281130 |