Item | Value |
---|---|
geneid | 3099 |
ensemblid | ENSG00000159399.10 |
hgncid | 4923 |
symbol | HK2 |
name | hexokinase 2 |
refseq_nuc | NM_000189.5 |
refseq_prot | NP_000180.2 |
ensembl_nuc | ENST00000290573.7 |
ensembl_prot | ENSP00000290573.2 |
mane_status | MANE Select |
chr | chr2 |
start | 74834127 |
end | 74893359 |
strand | + |
ver | v1.2 |
region | chr2:74834127-74893359 |
region5000 | chr2:74829127-74898359 |
regionname0 | HK2_chr2_74834127_74893359 |
regionname5000 | HK2_chr2_74829127_74898359 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 917 | 241 | 33 | 47 | 113 | 15 | 32 | 87 | HK2_chr2_74829127_74898359 | HK2 | MIASH others(912): Show |
chr2 | 74829127 | 74898359 |
a0002 | 0/0 | 917 | 67 | 38 | 4 | 23 | 0 | 2 | 20 | HK2_chr2_74829127_74898359 | HK2 | MIASH others(912): Show |
chr2 | 74829127 | 74898359 |
a0003 | 0/1 | 917 | 61 | 4 | 13 | 33 | 3 | 7 | 26 | HK2_chr2_74829127_74898359 | HK2 | MIASH others(912): Show |
chr2 | 74829127 | 74898359 |
a0004 | 0/0 | 917 | 14 | 12 | 2 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | MIASH others(912): Show |
chr2 | 74829127 | 74898359 |
a0005 | 0/0 | 917 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | MIASH others(912): Show |
chr2 | 74829127 | 74898359 |
a0006 | 0/0 | 917 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | MIASH others(912): Show |
chr2 | 74829127 | 74898359 |
a0007 | 0/0 | 917 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | MIASH others(912): Show |
chr2 | 74829127 | 74898359 |
a0008 | 0/0 | 917 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | MIASH others(912): Show |
chr2 | 74829127 | 74898359 |
a0009 | 0/0 | 917 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | MIASH others(912): Show |
chr2 | 74829127 | 74898359 |
a0010 | 0/0 | 917 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | MIASH others(912): Show |
chr2 | 74829127 | 74898359 |
a0011 | 0/0 | 917 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | MIASH others(912): Show |
chr2 | 74829127 | 74898359 |
a0012 | 0/0 | 917 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | MIASH others(912): Show |
chr2 | 74829127 | 74898359 |
a0013 | 0/0 | 917 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | MIASH others(912): Show |
chr2 | 74829127 | 74898359 |
a0014 | 0/0 | 917 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | MIASH others(912): Show |
chr2 | 74829127 | 74898359 |
a0015 | 0/0 | 917 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | MIASH others(912): Show |
chr2 | 74829127 | 74898359 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2751 | 103 | 11 | 17 | 50 | 8 | 17 | HK2_chr2_74829127_74898359 | HK2 | ATGAT others(2746): Show |
chr2 | 74829127 | 74898359 | ||
a0001c0002 | 1/0 | 2751 | 89 | 5 | 23 | 49 | 5 | 6 | HK2_chr2_74829127_74898359 | HK2 | ATGAT others(2746): Show |
chr2 | 74829127 | 74898359 | ||
a0001c0005 | 0/0 | 2751 | 17 | 1 | 4 | 7 | 1 | 4 | HK2_chr2_74829127_74898359 | HK2 | ATGAT others(2746): Show |
chr2 | 74829127 | 74898359 | ||
a0001c0006 | 0/0 | 2751 | 14 | 3 | 1 | 5 | 1 | 4 | HK2_chr2_74829127_74898359 | HK2 | ATGAT others(2746): Show |
chr2 | 74829127 | 74898359 | ||
a0001c0009 | 0/0 | 2751 | 4 | 4 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ATGAT others(2746): Show |
chr2 | 74829127 | 74898359 | ||
a0001c0011 | 0/0 | 2751 | 3 | 3 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ATGAT others(2746): Show |
chr2 | 74829127 | 74898359 | ||
a0001c0012 | 0/0 | 2751 | 3 | 2 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | ATGAT others(2746): Show |
chr2 | 74829127 | 74898359 | ||
a0001c0014 | 0/0 | 2751 | 2 | 1 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ATGAT others(2746): Show |
chr2 | 74829127 | 74898359 | ||
a0001c0022 | 0/0 | 2751 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ATGAT others(2746): Show |
chr2 | 74829127 | 74898359 | ||
a0001c0024 | 0/0 | 2751 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ATGAT others(2746): Show |
chr2 | 74829127 | 74898359 | ||
a0001c0030 | 0/0 | 2751 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ATGAT others(2746): Show |
chr2 | 74829127 | 74898359 | ||
a0001c0034 | 0/0 | 2751 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ATGAT others(2746): Show |
chr2 | 74829127 | 74898359 | ||
a0001c0037 | 0/0 | 2751 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ATGAT others(2746): Show |
chr2 | 74829127 | 74898359 | ||
a0001c0039 | 0/0 | 2751 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ATGAT others(2746): Show |
chr2 | 74829127 | 74898359 | ||
a0002c0004 | 0/0 | 2751 | 46 | 24 | 1 | 21 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ATGAT others(2746): Show |
chr2 | 74829127 | 74898359 | ||
a0002c0007 | 0/0 | 2751 | 9 | 7 | 1 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ATGAT others(2746): Show |
chr2 | 74829127 | 74898359 | ||
a0002c0010 | 0/0 | 2751 | 4 | 3 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | ATGAT others(2746): Show |
chr2 | 74829127 | 74898359 | ||
a0002c0013 | 0/0 | 2751 | 2 | 2 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ATGAT others(2746): Show |
chr2 | 74829127 | 74898359 | ||
a0002c0021 | 0/0 | 2751 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ATGAT others(2746): Show |
chr2 | 74829127 | 74898359 | ||
a0002c0023 | 0/0 | 2751 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ATGAT others(2746): Show |
chr2 | 74829127 | 74898359 | ||
a0002c0025 | 0/0 | 2751 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ATGAT others(2746): Show |
chr2 | 74829127 | 74898359 | ||
a0002c0026 | 0/0 | 2751 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ATGAT others(2746): Show |
chr2 | 74829127 | 74898359 | ||
a0002c0035 | 0/0 | 2751 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ATGAT others(2746): Show |
chr2 | 74829127 | 74898359 | ||
a0002c0036 | 0/0 | 2751 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | ATGAT others(2746): Show |
chr2 | 74829127 | 74898359 | ||
a0003c0003 | 0/1 | 2751 | 53 | 3 | 11 | 28 | 3 | 7 | HK2_chr2_74829127_74898359 | HK2 | ATGAT others(2746): Show |
chr2 | 74829127 | 74898359 | ||
a0003c0015 | 0/0 | 2751 | 2 | 0 | 0 | 2 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ATGAT others(2746): Show |
chr2 | 74829127 | 74898359 | ||
a0003c0017 | 0/0 | 2751 | 2 | 0 | 0 | 2 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ATGAT others(2746): Show |
chr2 | 74829127 | 74898359 | ||
a0003c0040 | 0/0 | 2751 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ATGAT others(2746): Show |
chr2 | 74829127 | 74898359 | ||
a0003c0042 | 0/0 | 2751 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ATGAT others(2746): Show |
chr2 | 74829127 | 74898359 | ||
a0003c0044 | 0/0 | 2751 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ATGAT others(2746): Show |
chr2 | 74829127 | 74898359 | ||
a0003c0045 | 0/0 | 2751 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ATGAT others(2746): Show |
chr2 | 74829127 | 74898359 | ||
a0004c0008 | 0/0 | 2751 | 8 | 7 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ATGAT others(2746): Show |
chr2 | 74829127 | 74898359 | ||
a0004c0016 | 0/0 | 2751 | 2 | 2 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ATGAT others(2746): Show |
chr2 | 74829127 | 74898359 | ||
a0004c0018 | 0/0 | 2751 | 2 | 2 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ATGAT others(2746): Show |
chr2 | 74829127 | 74898359 | ||
a0004c0041 | 0/0 | 2751 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ATGAT others(2746): Show |
chr2 | 74829127 | 74898359 | ||
a0004c0043 | 0/0 | 2751 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ATGAT others(2746): Show |
chr2 | 74829127 | 74898359 | ||
a0005c0029 | 0/0 | 2751 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ATGAT others(2746): Show |
chr2 | 74829127 | 74898359 | ||
a0006c0027 | 0/0 | 2751 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ATGAT others(2746): Show |
chr2 | 74829127 | 74898359 | ||
a0007c0038 | 0/0 | 2751 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ATGAT others(2746): Show |
chr2 | 74829127 | 74898359 | ||
a0008c0033 | 0/0 | 2751 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ATGAT others(2746): Show |
chr2 | 74829127 | 74898359 | ||
a0009c0046 | 0/0 | 2751 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | ATGAT others(2746): Show |
chr2 | 74829127 | 74898359 | ||
a0010c0031 | 0/0 | 2751 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ATGAT others(2746): Show |
chr2 | 74829127 | 74898359 | ||
a0011c0020 | 0/0 | 2751 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ATGAT others(2746): Show |
chr2 | 74829127 | 74898359 | ||
a0012c0047 | 0/0 | 2751 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ATGAT others(2746): Show |
chr2 | 74829127 | 74898359 | ||
a0013c0028 | 0/0 | 2751 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ATGAT others(2746): Show |
chr2 | 74829127 | 74898359 | ||
a0014c0019 | 0/0 | 2751 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ATGAT others(2746): Show |
chr2 | 74829127 | 74898359 | ||
a0015c0032 | 0/0 | 2751 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ATGAT others(2746): Show |
chr2 | 74829127 | 74898359 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/0 | 5625 | 73 | 8 | 7 | 38 | 7 | 13 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5620): Show |
chr2 | 74829127 | 74898359 |
a0001c0001t0003 | 0/0 | 5623 | 2 | 0 | 1 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5618): Show |
chr2 | 74829127 | 74898359 |
a0001c0001t0005 | 0/0 | 5624 | 12 | 0 | 6 | 6 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5619): Show |
chr2 | 74829127 | 74898359 |
a0001c0001t0006 | 0/0 | 5624 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5619): Show |
chr2 | 74829127 | 74898359 |
a0001c0001t0007 | 0/0 | 5625 | 10 | 2 | 2 | 4 | 0 | 2 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5620): Show |
chr2 | 74829127 | 74898359 |
a0001c0001t0008 | 0/0 | 5623 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5618): Show |
chr2 | 74829127 | 74898359 |
a0001c0001t0014 | 0/0 | 5624 | 2 | 0 | 0 | 1 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5619): Show |
chr2 | 74829127 | 74898359 |
a0001c0001t0040 | 0/0 | 5625 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5620): Show |
chr2 | 74829127 | 74898359 |
a0001c0001t0041 | 0/0 | 5623 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5618): Show |
chr2 | 74829127 | 74898359 |
a0001c0002t0001 | 1/0 | 5626 | 73 | 3 | 20 | 43 | 4 | 2 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5621): Show |
chr2 | 74829127 | 74898359 |
a0001c0002t0005 | 0/0 | 5624 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5619): Show |
chr2 | 74829127 | 74898359 |
a0001c0002t0011 | 0/0 | 5626 | 7 | 2 | 2 | 0 | 1 | 2 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5621): Show |
chr2 | 74829127 | 74898359 |
a0001c0002t0017 | 0/0 | 5627 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5622): Show |
chr2 | 74829127 | 74898359 |
a0001c0002t0025 | 0/0 | 5625 | 2 | 0 | 0 | 2 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5620): Show |
chr2 | 74829127 | 74898359 |
a0001c0002t0027 | 0/0 | 5626 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5621): Show |
chr2 | 74829127 | 74898359 |
a0001c0002t0036 | 0/0 | 5627 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5622): Show |
chr2 | 74829127 | 74898359 |
a0001c0002t0046 | 0/0 | 5626 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5621): Show |
chr2 | 74829127 | 74898359 |
a0001c0002t0048 | 0/0 | 5623 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5618): Show |
chr2 | 74829127 | 74898359 |
a0001c0002t0049 | 0/0 | 5626 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5621): Show |
chr2 | 74829127 | 74898359 |
a0001c0005t0001 | 0/0 | 5626 | 4 | 0 | 0 | 1 | 1 | 2 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5621): Show |
chr2 | 74829127 | 74898359 |
a0001c0005t0003 | 0/0 | 5623 | 6 | 0 | 0 | 5 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5618): Show |
chr2 | 74829127 | 74898359 |
a0001c0005t0005 | 0/0 | 5624 | 2 | 0 | 2 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5619): Show |
chr2 | 74829127 | 74898359 |
a0001c0005t0007 | 0/0 | 5625 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5620): Show |
chr2 | 74829127 | 74898359 |
a0001c0005t0011 | 0/0 | 5626 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5621): Show |
chr2 | 74829127 | 74898359 |
a0001c0005t0017 | 0/0 | 5627 | 2 | 1 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5622): Show |
chr2 | 74829127 | 74898359 |
a0001c0005t0047 | 0/0 | 5628 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5623): Show |
chr2 | 74829127 | 74898359 |
a0001c0006t0001 | 0/0 | 5626 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5621): Show |
chr2 | 74829127 | 74898359 |
a0001c0006t0002 | 0/0 | 5625 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5620): Show |
chr2 | 74829127 | 74898359 |
a0001c0006t0003 | 0/0 | 5623 | 6 | 1 | 0 | 3 | 0 | 2 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5618): Show |
chr2 | 74829127 | 74898359 |
a0001c0006t0007 | 0/0 | 5625 | 2 | 0 | 0 | 0 | 1 | 1 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5620): Show |
chr2 | 74829127 | 74898359 |
a0001c0006t0008 | 0/0 | 5623 | 2 | 0 | 1 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5618): Show |
chr2 | 74829127 | 74898359 |
a0001c0006t0021 | 0/0 | 5625 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5620): Show |
chr2 | 74829127 | 74898359 |
a0001c0006t0031 | 0/0 | 5625 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5620): Show |
chr2 | 74829127 | 74898359 |
a0001c0009t0015 | 0/0 | 5623 | 3 | 3 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5618): Show |
chr2 | 74829127 | 74898359 |
a0001c0009t0034 | 0/0 | 5622 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5617): Show |
chr2 | 74829127 | 74898359 |
a0001c0011t0020 | 0/0 | 5626 | 2 | 2 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5621): Show |
chr2 | 74829127 | 74898359 |
a0001c0011t0037 | 0/0 | 5624 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5619): Show |
chr2 | 74829127 | 74898359 |
a0001c0012t0002 | 0/0 | 5625 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5620): Show |
chr2 | 74829127 | 74898359 |
a0001c0012t0021 | 0/0 | 5625 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5620): Show |
chr2 | 74829127 | 74898359 |
a0001c0012t0022 | 0/0 | 5625 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5620): Show |
chr2 | 74829127 | 74898359 |
a0001c0014t0001 | 0/0 | 5626 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5621): Show |
chr2 | 74829127 | 74898359 |
a0001c0014t0043 | 0/0 | 5624 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5619): Show |
chr2 | 74829127 | 74898359 |
a0001c0022t0001 | 0/0 | 5626 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5621): Show |
chr2 | 74829127 | 74898359 |
a0001c0024t0003 | 0/0 | 5623 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5618): Show |
chr2 | 74829127 | 74898359 |
a0001c0030t0007 | 0/0 | 5625 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5620): Show |
chr2 | 74829127 | 74898359 |
a0001c0034t0002 | 0/0 | 5625 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5620): Show |
chr2 | 74829127 | 74898359 |
a0001c0037t0022 | 0/0 | 5625 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5620): Show |
chr2 | 74829127 | 74898359 |
a0001c0039t0001 | 0/0 | 5626 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5621): Show |
chr2 | 74829127 | 74898359 |
a0002c0004t0001 | 0/0 | 5626 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5621): Show |
chr2 | 74829127 | 74898359 |
a0002c0004t0004 | 0/0 | 5624 | 17 | 0 | 0 | 17 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5619): Show |
chr2 | 74829127 | 74898359 |
a0002c0004t0006 | 0/0 | 5624 | 8 | 8 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5619): Show |
chr2 | 74829127 | 74898359 |
a0002c0004t0009 | 0/0 | 5624 | 5 | 5 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5619): Show |
chr2 | 74829127 | 74898359 |
a0002c0004t0010 | 0/0 | 5624 | 4 | 4 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5619): Show |
chr2 | 74829127 | 74898359 |
a0002c0004t0013 | 0/0 | 5624 | 3 | 0 | 0 | 3 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5619): Show |
chr2 | 74829127 | 74898359 |
a0002c0004t0018 | 0/0 | 5622 | 2 | 2 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5617): Show |
chr2 | 74829127 | 74898359 |
a0002c0004t0019 | 0/0 | 5623 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5618): Show |
chr2 | 74829127 | 74898359 |
a0002c0004t0023 | 0/0 | 5623 | 2 | 1 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5618): Show |
chr2 | 74829127 | 74898359 |
a0002c0004t0026 | 0/0 | 5624 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5619): Show |
chr2 | 74829127 | 74898359 |
a0002c0004t0038 | 0/0 | 5624 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5619): Show |
chr2 | 74829127 | 74898359 |
a0002c0004t0044 | 0/0 | 5622 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5617): Show |
chr2 | 74829127 | 74898359 |
a0002c0007t0006 | 0/0 | 5624 | 2 | 1 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5619): Show |
chr2 | 74829127 | 74898359 |
a0002c0007t0009 | 0/0 | 5624 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5619): Show |
chr2 | 74829127 | 74898359 |
a0002c0007t0010 | 0/0 | 5624 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5619): Show |
chr2 | 74829127 | 74898359 |
a0002c0007t0012 | 0/0 | 5623 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5618): Show |
chr2 | 74829127 | 74898359 |
a0002c0007t0016 | 0/0 | 5622 | 3 | 3 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5617): Show |
chr2 | 74829127 | 74898359 |
a0002c0007t0035 | 0/0 | 5624 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5619): Show |
chr2 | 74829127 | 74898359 |
a0002c0010t0004 | 0/0 | 5624 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5619): Show |
chr2 | 74829127 | 74898359 |
a0002c0010t0006 | 0/0 | 5624 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5619): Show |
chr2 | 74829127 | 74898359 |
a0002c0010t0009 | 0/0 | 5624 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5619): Show |
chr2 | 74829127 | 74898359 |
a0002c0010t0028 | 0/0 | 5623 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5618): Show |
chr2 | 74829127 | 74898359 |
a0002c0013t0009 | 0/0 | 5624 | 2 | 2 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5619): Show |
chr2 | 74829127 | 74898359 |
a0002c0021t0006 | 0/0 | 5624 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5619): Show |
chr2 | 74829127 | 74898359 |
a0002c0023t0006 | 0/0 | 5624 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5619): Show |
chr2 | 74829127 | 74898359 |
a0002c0025t0024 | 0/0 | 5624 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5619): Show |
chr2 | 74829127 | 74898359 |
a0002c0026t0013 | 0/0 | 5624 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5619): Show |
chr2 | 74829127 | 74898359 |
a0002c0035t0012 | 0/0 | 5623 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5618): Show |
chr2 | 74829127 | 74898359 |
a0002c0036t0004 | 0/0 | 5624 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5619): Show |
chr2 | 74829127 | 74898359 |
a0003c0003t0002 | 0/0 | 5625 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5620): Show |
chr2 | 74829127 | 74898359 |
a0003c0003t0003 | 0/0 | 5623 | 41 | 3 | 10 | 23 | 1 | 4 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5618): Show |
chr2 | 74829127 | 74898359 |
a0003c0003t0005 | 0/0 | 5624 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5619): Show |
chr2 | 74829127 | 74898359 |
a0003c0003t0008 | 0/0 | 5623 | 7 | 0 | 1 | 2 | 2 | 2 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5618): Show |
chr2 | 74829127 | 74898359 |
a0003c0003t0030 | 0/0 | 5622 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5617): Show |
chr2 | 74829127 | 74898359 |
a0003c0003t0042 | 0/0 | 5623 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5618): Show |
chr2 | 74829127 | 74898359 |
a0003c0003t0050 | 0/1 | 5623 | 1 | 0 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5618): Show |
chr2 | 74829127 | 74898359 |
a0003c0015t0001 | 0/0 | 5626 | 2 | 0 | 0 | 2 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5621): Show |
chr2 | 74829127 | 74898359 |
a0003c0017t0003 | 0/0 | 5623 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5618): Show |
chr2 | 74829127 | 74898359 |
a0003c0017t0014 | 0/0 | 5624 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5619): Show |
chr2 | 74829127 | 74898359 |
a0003c0040t0001 | 0/0 | 5626 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5621): Show |
chr2 | 74829127 | 74898359 |
a0003c0042t0033 | 0/0 | 5623 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5618): Show |
chr2 | 74829127 | 74898359 |
a0003c0044t0001 | 0/0 | 5626 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5621): Show |
chr2 | 74829127 | 74898359 |
a0003c0045t0008 | 0/0 | 5623 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5618): Show |
chr2 | 74829127 | 74898359 |
a0004c0008t0006 | 0/0 | 5624 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5619): Show |
chr2 | 74829127 | 74898359 |
a0004c0008t0009 | 0/0 | 5624 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5619): Show |
chr2 | 74829127 | 74898359 |
a0004c0008t0010 | 0/0 | 5624 | 5 | 4 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5619): Show |
chr2 | 74829127 | 74898359 |
a0004c0008t0019 | 0/0 | 5623 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5618): Show |
chr2 | 74829127 | 74898359 |
a0004c0016t0012 | 0/0 | 5623 | 2 | 2 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5618): Show |
chr2 | 74829127 | 74898359 |
a0004c0018t0024 | 0/0 | 5624 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5619): Show |
chr2 | 74829127 | 74898359 |
a0004c0018t0045 | 0/0 | 5623 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5618): Show |
chr2 | 74829127 | 74898359 |
a0004c0041t0029 | 0/0 | 5623 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5618): Show |
chr2 | 74829127 | 74898359 |
a0004c0043t0012 | 0/0 | 5623 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5618): Show |
chr2 | 74829127 | 74898359 |
a0005c0029t0001 | 0/0 | 5626 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5621): Show |
chr2 | 74829127 | 74898359 |
a0006c0027t0039 | 0/0 | 5623 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5618): Show |
chr2 | 74829127 | 74898359 |
a0007c0038t0012 | 0/0 | 5623 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5618): Show |
chr2 | 74829127 | 74898359 |
a0008c0033t0002 | 0/0 | 5625 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5620): Show |
chr2 | 74829127 | 74898359 |
a0009c0046t0001 | 0/0 | 5626 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5621): Show |
chr2 | 74829127 | 74898359 |
a0010c0031t0003 | 0/0 | 5623 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5618): Show |
chr2 | 74829127 | 74898359 |
a0011c0020t0032 | 0/0 | 5625 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5620): Show |
chr2 | 74829127 | 74898359 |
a0012c0047t0005 | 0/0 | 5624 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5619): Show |
chr2 | 74829127 | 74898359 |
a0013c0028t0001 | 0/0 | 5626 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5621): Show |
chr2 | 74829127 | 74898359 |
a0014c0019t0001 | 0/0 | 5626 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5621): Show |
chr2 | 74829127 | 74898359 |
a0015c0032t0006 | 0/0 | 5624 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | ACATT others(5619): Show |
chr2 | 74829127 | 74898359 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0371 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0002g0372 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0003g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0005g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0005g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0005g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0005g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0005g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0005g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0005g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0005g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0005g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0005g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0005g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0005g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0006g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0007g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0007g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0007g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0007g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0007g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0007g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0007g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0007g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0007g0386 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0008g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0014g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0014g0385 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0040g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0001t0041g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0027 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0379 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0380 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0001g0382 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0005g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0011g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0011g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0011g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0011g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0011g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0011g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0011g0376 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0017g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0025g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0025g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0027g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0036g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0046g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0048g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0002t0049g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0005t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0005t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0005t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0005t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0005t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0005t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0005t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0005t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0005t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0005t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0005t0005g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0005t0005g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0005t0007g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0005t0011g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0005t0017g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0005t0017g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0005t0047g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0006t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0006t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0006t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0006t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0006t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0006t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0006t0003g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0006t0003g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0006t0007g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0006t0007g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0006t0008g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0006t0008g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0006t0021g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0006t0031g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0009t0015g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0009t0015g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0009t0015g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0009t0034g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0011t0020g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0011t0020g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0011t0037g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0012t0002g0373 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0012t0021g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0012t0022g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0014t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0014t0043g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0022t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0024t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0030t0007g0387 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0034t0002g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0037t0022g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0001c0039t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0004g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0004g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0004g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0004g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0004g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0004g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0004g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0004g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0004g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0004g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0004g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0006g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0006g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0006g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0006g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0006g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0006g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0006g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0006g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0009g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0009g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0009g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0009g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0009g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0010g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0010g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0010g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0013g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0013g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0013g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0018g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0018g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0019g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0023g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0023g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0026g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0038g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0004t0044g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0007t0006g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0007t0006g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0007t0009g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0007t0010g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0007t0012g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0007t0016g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0007t0016g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0007t0016g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0007t0035g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0010t0004g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0010t0006g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0010t0009g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0010t0028g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0013t0009g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0013t0009g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0021t0006g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0023t0006g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0025t0024g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0026t0013g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0035t0012g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0002c0036t0004g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0003g0381 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0005g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0008g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0008g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0008g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0008g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0008g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0008g0383 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0008g0384 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0030g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0042g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0003t0050g0305 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0015t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0015t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0017t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0017t0014g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0040t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0042t0033g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0044t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0003c0045t0008g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0004c0008t0006g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0004c0008t0009g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0004c0008t0010g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0004c0008t0010g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0004c0008t0010g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0004c0008t0010g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0004c0008t0010g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0004c0008t0019g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0004c0016t0012g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0004c0016t0012g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0004c0018t0024g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0004c0018t0045g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0004c0041t0029g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0004c0043t0012g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0005c0029t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0006c0027t0039g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0007c0038t0012g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0008c0033t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0009c0046t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0010c0031t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0011c0020t0032g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0012c0047t0005g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0013c0028t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0014c0019t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
a0015c0032t0006g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0230 | EUR | GBR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00099 | hp2 | a0001 | c0001 | t0014 | g0385 | EUR | GBR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0132 | EUR | GBR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0208 | EUR | GBR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00280 | hp1 | a0001 | c0002 | t0011 | g0328 | EUR | FIN | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0045 | EUR | FIN | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00323 | hp1 | a0003 | c0003 | t0003 | g0279 | EUR | FIN | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00323 | hp2 | a0001 | c0006 | t0007 | g0330 | EUR | FIN | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00408 | hp1 | a0003 | c0003 | t0003 | g0117 | EAS | CHS | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | CHS | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00423 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | CHS | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | CHS | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00438 | hp1 | a0001 | c0002 | t0001 | g0210 | EAS | CHS | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00438 | hp2 | a0003 | c0003 | t0003 | g0063 | EAS | CHS | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00544 | hp1 | a0001 | c0002 | t0001 | g0025 | EAS | CHS | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | CHS | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | CHS | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00609 | hp2 | a0002 | c0004 | t0013 | g0098 | EAS | CHS | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00639 | hp1 | a0001 | c0039 | t0001 | g0056 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00639 | hp2 | a0003 | c0003 | t0003 | g0087 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0050 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00642 | hp2 | a0001 | c0001 | t0005 | g0271 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00673 | hp1 | a0001 | c0001 | t0007 | g0284 | EAS | CHS | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00673 | hp2 | a0001 | c0001 | t0007 | g0265 | EAS | CHS | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00735 | hp1 | a0004 | c0008 | t0010 | g0349 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00735 | hp2 | a0001 | c0001 | t0005 | g0274 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0344 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00738 | hp2 | a0004 | c0041 | t0029 | g0264 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00741 | hp1 | a0003 | c0003 | t0003 | g0206 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0129 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01069 | hp1 | a0001 | c0002 | t0001 | g0304 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01069 | hp2 | a0001 | c0005 | t0005 | g0043 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0280 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01070 | hp2 | a0003 | c0003 | t0003 | g0085 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0317 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01071 | hp2 | a0003 | c0003 | t0003 | g0086 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01081 | hp1 | a0001 | c0002 | t0001 | g0089 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0125 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01099 | hp1 | a0003 | c0044 | t0001 | g0077 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0306 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01106 | hp1 | a0001 | c0002 | t0011 | g0193 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01106 | hp2 | a0001 | c0002 | t0001 | g0219 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01109 | hp1 | a0002 | c0025 | t0024 | g0268 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01109 | hp2 | a0001 | c0002 | t0001 | g0051 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01168 | hp1 | a0001 | c0005 | t0017 | g0084 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01168 | hp2 | a0001 | c0001 | t0005 | g0159 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01169 | hp1 | a0001 | c0006 | t0008 | g0252 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01169 | hp2 | a0001 | c0005 | t0047 | g0015 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01175 | hp1 | a0005 | c0029 | t0001 | g0090 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01175 | hp2 | a0001 | c0001 | t0005 | g0281 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01192 | hp1 | a0001 | c0002 | t0001 | g0104 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0130 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01243 | hp1 | a0002 | c0007 | t0006 | g0106 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01243 | hp2 | a0002 | c0035 | t0012 | g0346 | AMR | PUR | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01255 | hp1 | a0003 | c0042 | t0033 | g0375 | AMR | CLM | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01255 | hp2 | a0003 | c0003 | t0003 | g0059 | AMR | CLM | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01256 | hp1 | a0001 | c0001 | t0007 | g0006 | AMR | CLM | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01256 | hp2 | a0003 | c0003 | t0008 | g0384 | AMR | CLM | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0378 | AMR | CLM | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01257 | hp2 | a0002 | c0004 | t0023 | g0244 | AMR | CLM | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01258 | hp1 | a0001 | c0002 | t0001 | g0379 | AMR | CLM | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01258 | hp2 | a0001 | c0001 | t0007 | g0006 | AMR | CLM | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01261 | hp1 | a0003 | c0003 | t0003 | g0166 | AMR | CLM | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01261 | hp2 | a0001 | c0014 | t0001 | g0078 | AMR | CLM | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01346 | hp1 | a0001 | c0002 | t0001 | g0049 | AMR | CLM | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01346 | hp2 | a0001 | c0001 | t0041 | g0147 | AMR | CLM | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0067 | AMR | CLM | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01358 | hp2 | a0003 | c0003 | t0003 | g0134 | AMR | CLM | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01361 | hp1 | a0003 | c0003 | t0003 | g0207 | AMR | CLM | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01361 | hp2 | a0001 | c0002 | t0001 | g0272 | AMR | CLM | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0052 | AMR | CLM | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01433 | hp2 | a0001 | c0002 | t0001 | g0285 | AMR | CLM | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01496 | hp1 | a0001 | c0002 | t0011 | g0298 | AMR | CLM | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0155 | AMR | CLM | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0060 | EUR | IBS | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01515 | hp2 | a0003 | c0003 | t0008 | g0310 | EUR | IBS | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01516 | hp1 | a0003 | c0003 | t0008 | g0237 | EUR | IBS | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01516 | hp2 | a0001 | c0002 | t0001 | g0216 | EUR | IBS | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01517 | hp1 | a0001 | c0002 | t0001 | g0217 | EUR | IBS | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0061 | EUR | IBS | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01884 | hp1 | a0004 | c0043 | t0012 | g0177 | AFR | ACB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01884 | hp2 | a0004 | c0008 | t0019 | g0190 | AFR | ACB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01891 | hp1 | a0006 | c0027 | t0039 | g0350 | AFR | ACB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01891 | hp2 | a0004 | c0008 | t0010 | g0353 | AFR | ACB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01952 | hp1 | a0001 | c0002 | t0001 | g0382 | AMR | PEL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01952 | hp2 | a0003 | c0003 | t0003 | g0381 | AMR | PEL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01978 | hp1 | a0001 | c0005 | t0005 | g0068 | AMR | PEL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01978 | hp2 | a0001 | c0002 | t0027 | g0066 | AMR | PEL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02004 | hp1 | a0001 | c0001 | t0005 | g0053 | AMR | PEL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02004 | hp2 | a0001 | c0002 | t0001 | g0032 | AMR | PEL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02015 | hp1 | a0003 | c0003 | t0008 | g0261 | EAS | KHV | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0367 | EAS | KHV | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02027 | hp1 | a0001 | c0002 | t0049 | g0293 | EAS | KHV | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0300 | EAS | KHV | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02040 | hp1 | a0002 | c0004 | t0004 | g0366 | EAS | KHV | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02040 | hp2 | a0003 | c0045 | t0008 | g0262 | EAS | KHV | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02055 | hp1 | a0001 | c0012 | t0022 | g0335 | AFR | ACB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02055 | hp2 | a0001 | c0009 | t0015 | g0360 | AFR | ACB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02056 | hp1 | a0003 | c0017 | t0003 | g0225 | EAS | KHV | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | KHV | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | KHV | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02083 | hp2 | a0003 | c0003 | t0003 | g0016 | EAS | KHV | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02129 | hp1 | a0001 | c0001 | t0007 | g0242 | EAS | KHV | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | KHV | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02132 | hp1 | a0001 | c0006 | t0003 | g0142 | EAS | KHV | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02132 | hp2 | a0001 | c0006 | t0001 | g0044 | EAS | KHV | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0133 | EAS | KHV | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02135 | hp2 | a0002 | c0007 | t0035 | g0007 | EAS | KHV | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02145 | hp1 | a0001 | c0006 | t0021 | g0109 | AFR | ACB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02145 | hp2 | a0003 | c0040 | t0001 | g0071 | AFR | ACB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02148 | hp1 | a0001 | c0002 | t0001 | g0282 | AMR | PEL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02148 | hp2 | a0001 | c0001 | t0005 | g0220 | AMR | PEL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0198 | EAS | CDX | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | CDX | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | CDX | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02165 | hp2 | a0001 | c0002 | t0001 | g0127 | EAS | CDX | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02257 | hp1 | a0002 | c0004 | t0018 | g0320 | AFR | ACB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0107 | AFR | ACB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02258 | hp1 | a0001 | c0002 | t0011 | g0307 | AFR | ACB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02258 | hp2 | a0002 | c0004 | t0001 | g0114 | AFR | ACB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02280 | hp1 | a0001 | c0011 | t0037 | g0245 | AFR | ACB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02280 | hp2 | a0002 | c0004 | t0018 | g0231 | AFR | ACB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02293 | hp1 | a0001 | c0002 | t0001 | g0042 | AMR | PEL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02293 | hp2 | a0001 | c0002 | t0001 | g0380 | AMR | PEL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0283 | AMR | PEL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02300 | hp2 | a0008 | c0033 | t0002 | g0157 | AMR | PEL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02451 | hp1 | a0002 | c0010 | t0028 | g0341 | AFR | ACB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02451 | hp2 | a0002 | c0004 | t0006 | g0361 | AFR | ACB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0018 | SAS | PJL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02602 | hp2 | a0001 | c0012 | t0002 | g0373 | SAS | PJL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02615 | hp1 | a0002 | c0004 | t0009 | g0340 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02615 | hp2 | a0004 | c0008 | t0010 | g0354 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02622 | hp1 | a0001 | c0037 | t0022 | g0364 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02622 | hp2 | a0002 | c0004 | t0006 | g0232 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02630 | hp1 | a0002 | c0004 | t0038 | g0352 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02630 | hp2 | a0002 | c0010 | t0006 | g0233 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02647 | hp1 | a0001 | c0002 | t0001 | g0214 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02647 | hp2 | a0002 | c0007 | t0016 | g0201 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0148 | SAS | PJL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02683 | hp2 | a0003 | c0003 | t0003 | g0154 | SAS | PJL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0371 | SAS | PJL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02698 | hp2 | a0003 | c0003 | t0042 | g0020 | SAS | PJL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0238 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02717 | hp2 | a0002 | c0004 | t0010 | g0247 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02723 | hp1 | a0002 | c0007 | t0016 | g0224 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02723 | hp2 | a0002 | c0013 | t0009 | g0322 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02738 | hp1 | a0001 | c0006 | t0003 | g0240 | SAS | PJL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02738 | hp2 | a0009 | c0046 | t0001 | g0165 | SAS | PJL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02809 | hp1 | a0001 | c0006 | t0031 | g0324 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0170 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02818 | hp1 | a0002 | c0004 | t0009 | g0321 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02818 | hp2 | a0002 | c0004 | t0006 | g0292 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02886 | hp1 | a0004 | c0008 | t0006 | g0105 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02886 | hp2 | a0002 | c0007 | t0010 | g0249 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02895 | hp1 | a0002 | c0023 | t0006 | g0374 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02895 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02896 | hp1 | a0002 | c0007 | t0006 | g0101 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02896 | hp2 | a0002 | c0004 | t0010 | g0004 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02897 | hp1 | a0001 | c0002 | t0001 | g0005 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02897 | hp2 | a0002 | c0004 | t0010 | g0004 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02922 | hp1 | a0002 | c0004 | t0010 | g0097 | AFR | ESN | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02922 | hp2 | a0002 | c0004 | t0009 | g0227 | AFR | ESN | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02965 | hp1 | a0002 | c0004 | t0044 | g0100 | AFR | ESN | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02965 | hp2 | a0001 | c0011 | t0020 | g0348 | AFR | ESN | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02976 | hp1 | a0001 | c0001 | t0007 | g0325 | AFR | ESN | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02976 | hp2 | a0001 | c0009 | t0015 | g0234 | AFR | ESN | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0176 | SAS | PJL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0173 | SAS | PJL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03041 | hp1 | a0002 | c0004 | t0006 | g0248 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03041 | hp2 | a0004 | c0018 | t0045 | g0246 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03098 | hp1 | a0004 | c0008 | t0010 | g0111 | AFR | MSL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03098 | hp2 | a0003 | c0003 | t0003 | g0291 | AFR | MSL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03130 | hp1 | a0002 | c0021 | t0006 | g0215 | AFR | ESN | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03130 | hp2 | a0002 | c0004 | t0006 | g0363 | AFR | ESN | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03139 | hp1 | a0002 | c0004 | t0023 | g0228 | AFR | ESN | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03139 | hp2 | a0002 | c0004 | t0006 | g0362 | AFR | ESN | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03209 | hp1 | a0004 | c0018 | t0024 | g0223 | AFR | MSL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03209 | hp2 | a0001 | c0001 | t0006 | g0357 | AFR | MSL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03225 | hp1 | a0004 | c0008 | t0009 | g0213 | AFR | MSL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03225 | hp2 | a0002 | c0004 | t0019 | g0342 | AFR | MSL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03239 | hp1 | a0001 | c0002 | t0011 | g0376 | SAS | PJL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03239 | hp2 | a0001 | c0005 | t0003 | g0095 | SAS | PJL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03453 | hp1 | a0010 | c0031 | t0003 | g0204 | AFR | MSL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0189 | AFR | MSL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03486 | hp1 | a0003 | c0003 | t0003 | g0202 | AFR | MSL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03486 | hp2 | a0003 | c0003 | t0003 | g0377 | AFR | MSL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03490 | hp1 | a0001 | c0006 | t0007 | g0309 | SAS | PJL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03490 | hp2 | a0001 | c0001 | t0007 | g0250 | SAS | PJL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03491 | hp1 | a0002 | c0010 | t0004 | g0058 | SAS | PJL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03491 | hp2 | a0003 | c0003 | t0008 | g0308 | SAS | PJL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03516 | hp1 | a0004 | c0008 | t0010 | g0351 | AFR | ESN | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03516 | hp2 | a0002 | c0007 | t0016 | g0123 | AFR | ESN | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03540 | hp1 | a0002 | c0004 | t0006 | g0092 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03540 | hp2 | a0002 | c0013 | t0009 | g0323 | AFR | GWD | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03579 | hp1 | a0011 | c0020 | t0032 | g0339 | AFR | MSL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0093 | AFR | MSL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0205 | SAS | PJL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03654 | hp2 | a0001 | c0006 | t0003 | g0162 | SAS | PJL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03669 | hp1 | a0001 | c0006 | t0008 | g0254 | SAS | PJL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03669 | hp2 | a0001 | c0002 | t0036 | g0010 | SAS | PJL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03688 | hp1 | a0001 | c0005 | t0001 | g0030 | SAS | STU | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03688 | hp2 | a0002 | c0036 | t0004 | g0012 | SAS | STU | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0124 | SAS | PJL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03704 | hp2 | a0003 | c0003 | t0008 | g0383 | SAS | PJL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03710 | hp1 | a0003 | c0003 | t0003 | g0158 | SAS | PJL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0179 | SAS | PJL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | BEB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0046 | SAS | BEB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03834 | hp1 | a0001 | c0001 | t0007 | g0386 | SAS | BEB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0156 | SAS | BEB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03942 | hp1 | a0001 | c0002 | t0011 | g0267 | SAS | BEB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03942 | hp2 | a0003 | c0003 | t0003 | g0218 | SAS | BEB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0023 | SAS | STU | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG04115 | hp2 | a0001 | c0001 | t0040 | g0164 | SAS | STU | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG04184 | hp1 | a0001 | c0001 | t0008 | g0314 | SAS | BEB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG04184 | hp2 | a0001 | c0005 | t0001 | g0088 | SAS | BEB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG04199 | hp1 | a0001 | c0002 | t0046 | g0163 | SAS | STU | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0038 | SAS | STU | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG04228 | hp1 | a0001 | c0005 | t0011 | g0297 | SAS | STU | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0149 | SAS | STU | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0222 | AFR | YRI | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18522 | hp2 | a0002 | c0010 | t0009 | g0338 | AFR | YRI | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18612 | hp1 | a0001 | c0001 | t0007 | g0186 | EAS | CHB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18612 | hp2 | a0001 | c0022 | t0001 | g0188 | EAS | CHB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18747 | hp1 | a0001 | c0002 | t0001 | g0076 | EAS | CHB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18747 | hp2 | a0003 | c0003 | t0003 | g0167 | EAS | CHB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18906 | hp1 | a0002 | c0004 | t0009 | g0326 | AFR | YRI | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0112 | AFR | YRI | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18939 | hp1 | a0001 | c0002 | t0005 | g0333 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18940 | hp1 | a0002 | c0004 | t0004 | g0138 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18940 | hp2 | a0003 | c0015 | t0001 | g0064 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18941 | hp1 | a0002 | c0004 | t0004 | g0174 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18941 | hp2 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18943 | hp1 | a0001 | c0002 | t0001 | g0180 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18943 | hp2 | a0003 | c0003 | t0003 | g0336 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18944 | hp1 | a0003 | c0003 | t0003 | g0139 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18944 | hp2 | a0001 | c0001 | t0005 | g0160 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18946 | hp1 | a0002 | c0026 | t0013 | g0258 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18946 | hp2 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18950 | hp1 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18950 | hp2 | a0002 | c0004 | t0004 | g0296 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18951 | hp1 | a0003 | c0003 | t0003 | g0070 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18951 | hp2 | a0012 | c0047 | t0005 | g0221 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18953 | hp2 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18954 | hp1 | a0002 | c0004 | t0013 | g0255 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18954 | hp2 | a0003 | c0003 | t0003 | g0332 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18957 | hp1 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18957 | hp2 | a0002 | c0004 | t0004 | g0318 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18959 | hp1 | a0003 | c0003 | t0030 | g0260 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18959 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18960 | hp2 | a0001 | c0005 | t0003 | g0081 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18961 | hp1 | a0002 | c0004 | t0004 | g0151 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18961 | hp2 | a0001 | c0002 | t0001 | g0278 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18962 | hp1 | a0001 | c0001 | t0014 | g0257 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18962 | hp2 | a0001 | c0002 | t0025 | g0028 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18964 | hp1 | a0003 | c0015 | t0001 | g0021 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18966 | hp1 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18966 | hp2 | a0003 | c0003 | t0003 | g0031 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18968 | hp1 | a0002 | c0004 | t0004 | g0013 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18968 | hp2 | a0001 | c0005 | t0003 | g0181 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18969 | hp1 | a0002 | c0004 | t0004 | g0128 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18969 | hp2 | a0001 | c0002 | t0001 | g0195 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18970 | hp1 | a0003 | c0003 | t0003 | g0311 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18970 | hp2 | a0001 | c0002 | t0001 | g0313 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18971 | hp1 | a0002 | c0004 | t0004 | g0211 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18975 | hp2 | a0003 | c0003 | t0003 | g0270 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18977 | hp1 | a0001 | c0006 | t0003 | g0026 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18977 | hp2 | a0003 | c0003 | t0003 | g0029 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18979 | hp1 | a0002 | c0004 | t0004 | g0368 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18979 | hp2 | a0003 | c0003 | t0003 | g0069 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18980 | hp1 | a0003 | c0003 | t0002 | g0294 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18980 | hp2 | a0003 | c0003 | t0008 | g0099 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18981 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18982 | hp1 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18982 | hp2 | a0001 | c0002 | t0001 | g0329 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18983 | hp2 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18985 | hp2 | a0003 | c0003 | t0003 | g0146 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18986 | hp1 | a0003 | c0003 | t0003 | g0169 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18986 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18987 | hp1 | a0002 | c0004 | t0004 | g0168 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18988 | hp1 | a0001 | c0001 | t0005 | g0116 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18988 | hp2 | a0003 | c0003 | t0003 | g0144 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18989 | hp2 | a0001 | c0002 | t0001 | g0161 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18990 | hp1 | a0001 | c0002 | t0001 | g0266 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18990 | hp2 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18994 | hp1 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18994 | hp2 | a0003 | c0003 | t0003 | g0288 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18998 | hp1 | a0003 | c0003 | t0003 | g0269 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18998 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18999 | hp1 | a0003 | c0017 | t0014 | g0251 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18999 | hp2 | a0002 | c0004 | t0004 | g0239 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19001 | hp1 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19002 | hp1 | a0001 | c0001 | t0005 | g0331 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19002 | hp2 | a0001 | c0034 | t0002 | g0369 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19004 | hp1 | a0002 | c0004 | t0004 | g0024 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19004 | hp2 | a0001 | c0002 | t0001 | g0289 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19006 | hp1 | a0001 | c0006 | t0003 | g0034 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19006 | hp2 | a0003 | c0003 | t0003 | g0287 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19007 | hp1 | a0001 | c0005 | t0003 | g0022 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19007 | hp2 | a0001 | c0002 | t0001 | g0275 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19009 | hp2 | a0001 | c0002 | t0001 | g0243 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19011 | hp1 | a0001 | c0005 | t0003 | g0315 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19011 | hp2 | a0003 | c0003 | t0003 | g0036 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19012 | hp1 | a0001 | c0005 | t0003 | g0312 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19012 | hp2 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19030 | hp1 | a0001 | c0014 | t0043 | g0345 | AFR | LWK | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19030 | hp2 | a0001 | c0009 | t0034 | g0184 | AFR | LWK | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19043 | hp1 | a0001 | c0006 | t0003 | g0359 | AFR | LWK | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19043 | hp2 | a0004 | c0016 | t0012 | g0347 | AFR | LWK | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19054 | hp1 | a0003 | c0003 | t0005 | g0122 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19054 | hp2 | a0001 | c0002 | t0017 | g0014 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19056 | hp1 | a0002 | c0004 | t0004 | g0276 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19057 | hp1 | a0001 | c0002 | t0001 | g0259 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19057 | hp2 | a0002 | c0004 | t0004 | g0017 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19058 | hp1 | a0001 | c0005 | t0001 | g0143 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19058 | hp2 | a0001 | c0002 | t0001 | g0236 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19060 | hp1 | a0001 | c0002 | t0048 | g0175 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19065 | hp1 | a0003 | c0003 | t0003 | g0062 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19065 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19066 | hp1 | a0002 | c0004 | t0004 | g0334 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19068 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0365 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19070 | hp1 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19070 | hp2 | a0001 | c0002 | t0025 | g0057 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19072 | hp1 | a0001 | c0002 | t0001 | g0303 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19072 | hp2 | a0001 | c0001 | t0002 | g0343 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19074 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19074 | hp2 | a0001 | c0001 | t0005 | g0035 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19077 | hp2 | a0001 | c0006 | t0002 | g0009 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19078 | hp2 | a0002 | c0004 | t0013 | g0185 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19079 | hp2 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19081 | hp1 | a0002 | c0004 | t0026 | g0370 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19081 | hp2 | a0001 | c0001 | t0003 | g0277 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19084 | hp1 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19085 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19085 | hp2 | a0003 | c0003 | t0003 | g0152 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19086 | hp1 | a0003 | c0003 | t0003 | g0286 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19086 | hp2 | a0001 | c0005 | t0007 | g0253 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19087 | hp2 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19091 | hp2 | a0002 | c0004 | t0004 | g0199 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19240 | hp1 | a0013 | c0028 | t0001 | g0172 | AFR | YRI | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA19240 | hp2 | a0002 | c0004 | t0009 | g0115 | AFR | YRI | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA20129 | hp1 | a0014 | c0019 | t0001 | g0113 | AFR | ASW | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA20129 | hp2 | a0004 | c0016 | t0012 | g0355 | AFR | ASW | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0263 | EUR | TSI | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0372 | EUR | TSI | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA20805 | hp1 | a0001 | c0005 | t0001 | g0094 | EUR | TSI | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA20805 | hp2 | a0001 | c0002 | t0001 | g0153 | EUR | TSI | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0011 | SAS | GIH | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA20905 | hp2 | a0003 | c0003 | t0003 | g0019 | SAS | GIH | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01123 | hp1 | a0003 | c0003 | t0003 | g0241 | AMR | CLM | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0150 | AMR | CLM | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02109 | hp1 | a0001 | c0001 | t0007 | g0319 | AFR | ACB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02109 | hp2 | a0007 | c0038 | t0012 | g0110 | AFR | ACB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02486 | hp1 | a0001 | c0011 | t0020 | g0096 | AFR | ACB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02486 | hp2 | a0001 | c0030 | t0007 | g0387 | AFR | ACB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02559 | hp1 | a0001 | c0005 | t0017 | g0047 | AFR | ACB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG02559 | hp2 | a0002 | c0004 | t0006 | g0108 | AFR | ACB | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03471 | hp1 | a0001 | c0024 | t0003 | g0183 | AFR | MSL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG03471 | hp2 | a0001 | c0002 | t0011 | g0337 | AFR | MSL | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0290 | AFR | USA | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
HG06807 | hp2 | a0001 | c0012 | t0021 | g0356 | AFR | USA | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18955 | hp1 | a0001 | c0001 | t0005 | g0141 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA20300 | hp1 | a0002 | c0007 | t0009 | g0327 | AFR | USA | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA20300 | hp2 | a0001 | c0009 | t0015 | g0358 | AFR | USA | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA21309 | hp1 | a0015 | c0032 | t0006 | g0102 | AFR | LWK | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
NA21309 | hp2 | a0002 | c0007 | t0012 | g0103 | AFR | LWK | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
homoSapiens | chm13v2 | a0003 | c0003 | t0050 | g0305 | REF | REF | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0027 | REF | REF | HK2_chr2_74829127_74898359 | HK2 | chr2 | 74829127 | 74898359 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:74834632 | C | G | 1 | a0012 | 1 | NA18951.hp2 | missense_variant | MODERATE | c.52C>G | p.Gln18Glu | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/18 | 506/5626 | 52/2754 | 18/917 | chr2 | 74834632 | |||
chr2:74854392 | A | G | 1 | a0009 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.163A>G | p.Thr55Ala | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/18 | 617/5626 | 163/2754 | 55/917 | chr2 | 74854392 | |||
chr2:74872350 | A | T | 2 | a0003 a0004 |
74 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(71): Show |
missense_variant | MODERATE | c.426A>T | p.Gln142His | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 4/18 | 880/5626 | 426/2754 | 142/917 | chr2 | 74872350 | |||
chr2:74874425 | G | A | 1 | a0005 | 1 | HG01175.hp1 | missense_variant | MODERATE | c.851G>A | p.Gly284Asp | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/18 | 1305/5626 | 851/2754 | 284/917 | chr2 | 74874425 | |||
chr2:74877252 | G | A | 1 | a0014 | 1 | NA20129.hp1 | missense_variant | MODERATE | c.962G>A | p.Gly321Glu | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/18 | 1416/5626 | 962/2754 | 321/917 | chr2 | 74877252 | |||
chr2:74877252 | G | C | 1 | a0010 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.962G>C | p.Gly321Ala | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/18 | 1416/5626 | 962/2754 | 321/917 | chr2 | 74877252 | |||
chr2:74878815 | G | T | 2 | a0006 a0013 |
2 | HG01891.hp1 NA19240.hp1 |
missense_variant | MODERATE | c.1159G>T | p.Ala387Ser | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 9/18 | 1613/5626 | 1159/2754 | 387/917 | chr2 | 74878815 | |||
chr2:74880329 | C | T | 1 | a0009 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.1330C>T | p.Arg444Cys | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 10/18 | 1784/5626 | 1330/2754 | 444/917 | chr2 | 74880329 | |||
chr2:74880392 | G | C | 2 | a0011 a0015 |
2 | HG03579.hp1 NA21309.hp1 |
missense_variant | MODERATE | c.1393G>C | p.Asp465His | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 10/18 | 1847/5626 | 1393/2754 | 465/917 | chr2 | 74880392 | |||
chr2:74880489 | G | A | 1 | a0008 | 1 | HG02300.hp2 | missense_variant | MODERATE | c.1490G>A | p.Arg497Gln | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 10/18 | 1944/5626 | 1490/2754 | 497/917 | chr2 | 74880489 | |||
chr2:74882147 | G | T | 1 | a0007 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.1747G>T | p.Ala583Ser | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/18 | 2201/5626 | 1747/2754 | 583/917 | chr2 | 74882147 | |||
chr2:74889400 | G | A | 6 | a0002 a0004 a0006 others(3): Show |
85 | HG00609.hp2 HG00735.hp1 HG00738.hp2 others(82): Show |
missense_variant | MODERATE | c.2531G>A | p.Arg844Lys | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 17/18 | 2985/5626 | 2531/2754 | 844/917 | chr2 | 74889400 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:74873855 | C | T | 1 | a0001c0039 | 1 | HG00639.hp1 | synonymous_variant | LOW | c.603C>T | p.Ile201Ile | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 6/18 | 1057/5626 | 603/2754 | 201/917 | chr2 | 74873855 | |||
chr2:74874327 | T | C | 26 | a0001c0009 a0001c0011 a0001c0012 others(23): Show |
140 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(137): Show |
synonymous_variant | LOW | c.753T>C | p.Asp251Asp | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/18 | 1207/5626 | 753/2754 | 251/917 | chr2 | 74874327 | |||
chr2:74877202 | G | A | 1 | a0001c0030 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.912G>A | p.Glu304Glu | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/18 | 1366/5626 | 912/2754 | 304/917 | chr2 | 74877202 | |||
chr2:74878760 | C | T | 1 | a0003c0045 | 1 | HG02040.hp2 | synonymous_variant | LOW | c.1104C>T | p.Cys368Cys | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 9/18 | 1558/5626 | 1104/2754 | 368/917 | chr2 | 74878760 | |||
chr2:74880289 | C | T | 1 | a0002c0026 | 1 | NA18946.hp1 | synonymous_variant | LOW | c.1290C>T | p.Thr430Thr | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 10/18 | 1744/5626 | 1290/2754 | 430/917 | chr2 | 74880289 | |||
chr2:74880544 | C | T | 1 | a0004c0018 | 2 | HG03041.hp2 HG03209.hp1 |
synonymous_variant | LOW | c.1545C>T | p.Tyr515Tyr | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 10/18 | 1999/5626 | 1545/2754 | 515/917 | chr2 | 74880544 | |||
chr2:74881739 | T | C | 1 | a0001c0034 | 1 | NA19002.hp2 | synonymous_variant | LOW | c.1599T>C | p.Leu533Leu | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 11/18 | 2053/5626 | 1599/2754 | 533/917 | chr2 | 74881739 | |||
chr2:74886350 | C | T | 1 | a0001c0037 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.1992C>T | p.Thr664Thr | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 14/18 | 2446/5626 | 1992/2754 | 664/917 | chr2 | 74886350 | |||
chr2:74886530 | C | T | 25 | a0001c0001 a0001c0009 a0001c0011 others(22): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
synonymous_variant | LOW | c.2076C>T | p.Asn692Asn | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 15/18 | 2530/5626 | 2076/2754 | 692/917 | chr2 | 74886530 | |||
chr2:74886662 | C | G | 25 | a0001c0001 a0001c0006 a0001c0012 others(22): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
synonymous_variant | LOW | c.2208C>G | p.Pro736Pro | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 15/18 | 2662/5626 | 2208/2754 | 736/917 | chr2 | 74886662 | |||
chr2:74887981 | A | G | 25 | a0001c0001 a0001c0005 a0001c0006 others(22): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
synonymous_variant | LOW | c.2298A>G | p.Leu766Leu | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 16/18 | 2752/5626 | 2298/2754 | 766/917 | chr2 | 74887981 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:74834191 | G | C | 1 | a0002c0004t0026 | 1 | NA19081.hp1 | 5_prime_UTR_variant | MODIFIER | c.-390G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/18 | 390 | chr2 | 74834191 | ||||||
chr2:74834212 | G | A | 1 | a0001c0002t0027 | 1 | HG01978.hp2 | 5_prime_UTR_variant | MODIFIER | c.-369G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/18 | 369 | chr2 | 74834212 | ||||||
chr2:74834348 | G | C | 27 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0014 others(24): Show |
59 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(56): Show |
5_prime_UTR_variant | MODIFIER | c.-233G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/18 | 233 | chr2 | 74834348 | ||||||
chr2:74834442 | T | C | 1 | a0002c0007t0035 | 1 | HG02135.hp2 | 5_prime_UTR_variant | MODIFIER | c.-139T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/18 | 139 | chr2 | 74834442 | ||||||
chr2:74891058 | C | A | 1 | a0001c0002t0036 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*117C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 117 | chr2 | 74891058 | ||||||
chr2:74891195 | A | G | 7 | a0002c0004t0004 a0002c0004t0013 a0002c0004t0026 others(4): Show |
25 | HG00609.hp2 HG02040.hp1 HG02135.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*254A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 254 | chr2 | 74891195 | ||||||
chr2:74891203 | T | G | 70 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(67): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
3_prime_UTR_variant | MODIFIER | c.*262T>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 262 | chr2 | 74891203 | ||||||
chr2:74891342 | A | C | 1 | a0001c0002t0049 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*401A>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 401 | chr2 | 74891342 | ||||||
chr2:74891480 | T | C | 1 | a0001c0002t0036 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*539T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 539 | chr2 | 74891480 | ||||||
chr2:74891493 | C | A | 25 | a0001c0001t0006 a0001c0011t0037 a0002c0004t0004 others(22): Show |
56 | HG00609.hp2 HG01243.hp1 HG01884.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*552C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 552 | chr2 | 74891493 | ||||||
chr2:74891558 | G | C | 1 | a0001c0014t0043 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*617G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 617 | chr2 | 74891558 | ||||||
chr2:74891610 | C | T | 64 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(61): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
3_prime_UTR_variant | MODIFIER | c.*669C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 669 | chr2 | 74891610 | ||||||
chr2:74891625 | C | T | 6 | a0001c0006t0021 a0001c0006t0031 a0001c0012t0021 others(3): Show |
6 | HG02055.hp1 HG02145.hp1 HG02622.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*684C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 684 | chr2 | 74891625 | ||||||
chr2:74891662 | G | A | 3 | a0001c0006t0021 a0001c0006t0031 a0001c0012t0021 |
3 | HG02145.hp1 HG02809.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*721G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 721 | chr2 | 74891662 | ||||||
chr2:74891729 | T | C | 66 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(63): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
3_prime_UTR_variant | MODIFIER | c.*788T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 788 | chr2 | 74891729 | ||||||
chr2:74891757 | G | GA | 85 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(82): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
3_prime_UTR_variant | MODIFIER | c.*817dupA | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 818 | INFO_REALIGN_3_PRIME | chr2 | 74891757 | |||||
chr2:74891786 | TAATG | T | 85 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(82): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
3_prime_UTR_variant | MODIFIER | c.*850_*853delAATG | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 850 | INFO_REALIGN_3_PRIME | chr2 | 74891786 | |||||
chr2:74891814 | T | C | 1 | a0001c0002t0046 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*873T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 873 | chr2 | 74891814 | ||||||
chr2:74891892 | G | C | 1 | a0002c0004t0038 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*951G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 951 | chr2 | 74891892 | ||||||
chr2:74891992 | C | T | 1 | a0004c0041t0029 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1051C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 1051 | chr2 | 74891992 | ||||||
chr2:74892046 | C | T | 3 | a0002c0025t0024 a0004c0018t0024 a0004c0018t0045 |
3 | HG01109.hp1 HG03041.hp2 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1105C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 1105 | chr2 | 74892046 | ||||||
chr2:74892264 | T | C | 1 | a0001c0001t0040 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1323T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 1323 | chr2 | 74892264 | ||||||
chr2:74892371 | A | G | 9 | a0001c0014t0043 a0002c0004t0018 a0002c0004t0044 others(6): Show |
13 | HG01243.hp2 HG01884.hp1 HG02109.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1430A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 1430 | chr2 | 74892371 | ||||||
chr2:74892394 | G | A | 1 | a0001c0009t0034 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1453G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 1453 | chr2 | 74892394 | ||||||
chr2:74892738 | C | T | 1 | a0004c0041t0029 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1797C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 1797 | chr2 | 74892738 | ||||||
chr2:74892742 | T | G | 1 | a0004c0041t0029 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1801T>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 1801 | chr2 | 74892742 | ||||||
chr2:74892862 | C | T | 1 | a0003c0003t0042 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1921C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 1921 | chr2 | 74892862 | ||||||
chr2:74892961 | G | A | 1 | a0001c0001t0041 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2020G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 2020 | chr2 | 74892961 | ||||||
chr2:74893032 | C | CT | 38 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0014 others(35): Show |
90 | HG00099.hp2 HG00609.hp2 HG00642.hp2 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*2107dupT | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 2108 | INFO_REALIGN_3_PRIME | chr2 | 74893032 | |||||
chr2:74893032 | C | CTT | 18 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0040 others(15): Show |
100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*2106_*2107dupTT | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 2108 | INFO_REALIGN_3_PRIME | chr2 | 74893032 | |||||
chr2:74893032 | CT | C | 6 | a0001c0002t0025 a0001c0009t0034 a0002c0004t0018 others(3): Show |
10 | HG02257.hp1 HG02280.hp2 HG02647.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2107delT | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 2107 | INFO_REALIGN_3_PRIME | chr2 | 74893032 | |||||
chr2:74893131 | T | C | 1 | a0001c0009t0034 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2190T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 2190 | chr2 | 74893131 | ||||||
chr2:74893249 | G | A | 1 | a0001c0009t0015 | 3 | HG02055.hp2 HG02976.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2308G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 2308 | chr2 | 74893249 | ||||||
chr2:74893254 | C | T | 2 | a0002c0004t0018 a0002c0007t0016 |
5 | HG02257.hp1 HG02280.hp2 HG02647.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2313C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 18/18 | 2313 | chr2 | 74893254 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:74834686 | G | A | 1 | a0002c0007t0035g0007 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.63+43G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74834686 | |||||||
chr2:74834746 | C | G | 295 | a0001c0001t0002g0107 a0001c0001t0002g0112 a0001c0001t0002g0124 others(292): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.63+103C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74834746 | |||||||
chr2:74834762 | AAAAGTTT others(73): Show |
A | 6 | a0001c0001t0007g0006 a0001c0001t0007g0386 a0001c0001t0014g0385 others(3): Show |
7 | HG00099.hp2 HG01256.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+121_63+200delAA others(78): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74834762 | ||||||
chr2:74834773 | C | T | 1 | a0006c0027t0039g0350 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.63+130C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74834773 | |||||||
chr2:74834783 | A | C | 3 | a0001c0002t0001g0178 a0001c0002t0001g0278 a0003c0003t0003g0287 |
3 | NA18961.hp2 NA19001.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.63+140A>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74834783 | |||||||
chr2:74834870 | C | T | 1 | a0001c0005t0003g0095 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.63+227C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74834870 | |||||||
chr2:74835102 | G | A | 2 | a0001c0011t0020g0096 a0002c0004t0010g0097 |
2 | HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.63+459G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74835102 | |||||||
chr2:74835169 | G | C | 2 | a0002c0004t0013g0098 a0003c0003t0008g0099 |
2 | HG00609.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.63+526G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74835169 | |||||||
chr2:74835335 | C | T | 5 | a0001c0002t0001g0378 a0001c0002t0001g0379 a0001c0002t0001g0380 others(2): Show |
5 | HG01257.hp1 HG01258.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+692C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74835335 | |||||||
chr2:74835377 | C | T | 1 | a0001c0005t0001g0094 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.63+734C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74835377 | |||||||
chr2:74835398 | C | T | 1 | a0003c0003t0003g0377 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.63+755C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74835398 | |||||||
chr2:74835459 | C | T | 2 | a0001c0002t0011g0376 a0003c0042t0033g0375 |
2 | HG01255.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.63+816C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74835459 | |||||||
chr2:74835472 | A | C | 1 | a0002c0023t0006g0374 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.63+829A>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74835472 | |||||||
chr2:74835603 | G | C | 8 | a0001c0001t0002g0107 a0001c0002t0001g0104 a0002c0004t0044g0100 others(5): Show |
8 | HG01192.hp1 HG01243.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.63+960G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74835603 | |||||||
chr2:74835629 | G | A | 3 | a0001c0006t0021g0109 a0002c0004t0006g0108 a0002c0004t0010g0004 |
4 | HG02145.hp1 HG02559.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+986G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74835629 | |||||||
chr2:74835652 | C | T | 2 | a0001c0001t0002g0372 a0001c0012t0002g0373 |
2 | HG02602.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.63+1009C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74835652 | |||||||
chr2:74835743 | G | A | 293 | a0001c0001t0002g0107 a0001c0001t0002g0112 a0001c0001t0002g0124 others(290): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.63+1100G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74835743 | |||||||
chr2:74836083 | A | G | 5 | a0001c0001t0002g0365 a0001c0001t0002g0367 a0001c0034t0002g0369 others(2): Show |
5 | HG02015.hp2 HG02040.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+1440A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74836083 | |||||||
chr2:74836475 | A | G | 25 | a0001c0001t0002g0371 a0001c0001t0006g0357 a0001c0006t0003g0359 others(22): Show |
26 | HG00735.hp1 HG01243.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.63+1832A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74836475 | |||||||
chr2:74836528 | C | A | 1 | a0001c0001t0002g0008 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.63+1885C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74836528 | |||||||
chr2:74836637 | T | C | 3 | a0001c0006t0021g0109 a0002c0004t0006g0108 a0002c0004t0010g0004 |
4 | HG02145.hp1 HG02559.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+1994T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74836637 | |||||||
chr2:74836704 | A | G | 3 | a0001c0006t0021g0109 a0002c0004t0006g0108 a0002c0004t0010g0004 |
4 | HG02145.hp1 HG02559.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+2061A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74836704 | |||||||
chr2:74836738 | A | G | 1 | a0001c0001t0002g0344 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.63+2095A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74836738 | |||||||
chr2:74836817 | T | A | 6 | a0001c0001t0002g0112 a0001c0014t0043g0345 a0002c0004t0001g0114 others(3): Show |
6 | HG02109.hp2 HG02258.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+2174T>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74836817 | |||||||
chr2:74836883 | C | T | 1 | a0001c0001t0002g0343 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.63+2240C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74836883 | |||||||
chr2:74836963 | A | G | 1 | a0002c0004t0001g0114 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.63+2320A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74836963 | |||||||
chr2:74837052 | C | T | 1 | a0002c0004t0019g0342 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.63+2409C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74837052 | |||||||
chr2:74837102 | T | A | 1 | a0002c0004t0009g0115 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.63+2459T>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74837102 | |||||||
chr2:74837106 | G | A | 1 | a0001c0001t0005g0116 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.63+2463G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74837106 | |||||||
chr2:74837235 | CG | C | 76 | a0001c0001t0002g0011 a0001c0001t0002g0124 a0001c0001t0002g0125 others(73): Show |
76 | HG00140.hp1 HG00408.hp1 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.63+2593delG | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74837235 | |||||||
chr2:74837246 | A | G | 1 | a0001c0002t0001g0173 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.63+2603A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74837246 | |||||||
chr2:74837265 | T | C | 77 | a0001c0001t0002g0011 a0001c0001t0002g0124 a0001c0001t0002g0125 others(74): Show |
77 | HG00140.hp1 HG00408.hp1 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.63+2622T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74837265 | |||||||
chr2:74837346 | G | A | 7 | a0001c0002t0001g0118 a0001c0002t0001g0119 a0001c0002t0001g0120 others(4): Show |
7 | HG00408.hp1 NA18946.hp2 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+2703G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74837346 | |||||||
chr2:74837583 | C | T | 4 | a0001c0002t0001g0378 a0001c0002t0001g0379 a0001c0002t0001g0380 others(1): Show |
4 | HG01257.hp1 HG01258.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+2940C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74837583 | |||||||
chr2:74837584 | G | T | 6 | a0001c0011t0020g0348 a0002c0023t0006g0374 a0004c0008t0010g0349 others(3): Show |
6 | HG00735.hp1 HG01891.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+2941G>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74837584 | |||||||
chr2:74837648 | C | G | 9 | a0001c0001t0002g0093 a0001c0006t0021g0109 a0001c0037t0022g0364 others(6): Show |
10 | HG02145.hp1 HG02451.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.63+3005C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74837648 | |||||||
chr2:74837672 | C | CT | 76 | a0001c0001t0002g0112 a0001c0001t0002g0290 a0001c0001t0002g0295 others(73): Show |
79 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.63+3051dupT | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74837672 | ||||||
chr2:74837672 | C | CTT | 10 | a0001c0001t0002g0107 a0001c0002t0011g0337 a0001c0012t0022g0335 others(7): Show |
10 | HG02055.hp1 HG02257.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.63+3050_63+3051dup others(2): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74837672 | ||||||
chr2:74837672 | CT | C | 81 | a0001c0001t0002g0011 a0001c0001t0002g0124 a0001c0001t0002g0125 others(78): Show |
82 | HG00140.hp1 HG00408.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.63+3051delT | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74837672 | ||||||
chr2:74837704 | T | C | 1 | a0002c0007t0016g0123 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.63+3061T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74837704 | |||||||
chr2:74837738 | C | T | 1 | a0001c0002t0001g0289 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.63+3095C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74837738 | |||||||
chr2:74837821 | G | A | 280 | a0001c0001t0002g0011 a0001c0001t0002g0093 a0001c0001t0002g0107 others(277): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.63+3178G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74837821 | |||||||
chr2:74837954 | G | A | 2 | a0001c0002t0001g0180 a0001c0005t0003g0181 |
2 | NA18943.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.63+3311G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74837954 | |||||||
chr2:74837964 | G | A | 1 | a0001c0001t0002g0290 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.63+3321G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74837964 | |||||||
chr2:74838204 | G | C | 1 | a0001c0001t0002g0124 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.63+3561G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74838204 | |||||||
chr2:74838265 | G | A | 2 | a0001c0012t0021g0356 a0004c0016t0012g0355 |
2 | HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.63+3622G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74838265 | |||||||
chr2:74838328 | G | A | 1 | a0002c0007t0035g0007 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.63+3685G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74838328 | |||||||
chr2:74838336 | A | C | 71 | a0001c0001t0002g0011 a0001c0001t0002g0124 a0001c0001t0002g0125 others(68): Show |
71 | HG00140.hp1 HG00408.hp1 HG00738.hp1 others(68): Show |
intron_variant | MODIFIER | c.63+3693A>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74838336 | |||||||
chr2:74838345 | C | T | 5 | a0001c0001t0002g0080 a0001c0002t0001g0079 a0001c0002t0001g0082 others(2): Show |
5 | NA18959.hp2 NA18960.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+3702C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74838345 | |||||||
chr2:74838346 | T | C | 139 | a0001c0001t0002g0107 a0001c0001t0002g0112 a0001c0001t0002g0176 others(136): Show |
140 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.63+3703T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74838346 | |||||||
chr2:74838402 | T | TCCAAAGC others(11): Show |
3 | a0001c0001t0002g0112 a0004c0008t0010g0111 a0007c0038t0012g0110 |
3 | HG02109.hp2 HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.63+3780_63+3797dup others(18): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74838402 | ||||||
chr2:74838518 | G | A | 2 | a0001c0012t0021g0356 a0004c0016t0012g0355 |
2 | HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.63+3875G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74838518 | |||||||
chr2:74838523 | G | A | 280 | a0001c0001t0002g0011 a0001c0001t0002g0093 a0001c0001t0002g0107 others(277): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.63+3880G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74838523 | |||||||
chr2:74838537 | A | AT | 44 | a0001c0001t0002g0093 a0001c0001t0002g0256 a0001c0001t0007g0242 others(41): Show |
45 | HG00609.hp2 HG00673.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.63+3913dupT | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74838537 | ||||||
chr2:74838537 | AT | A | 44 | a0001c0001t0002g0125 a0001c0001t0002g0126 a0001c0001t0002g0182 others(41): Show |
47 | HG00099.hp2 HG00639.hp2 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.63+3913delT | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74838537 | ||||||
chr2:74838601 | C | G | 81 | a0001c0001t0002g0176 a0001c0001t0002g0182 a0001c0001t0002g0189 others(78): Show |
82 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.63+3958C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74838601 | |||||||
chr2:74838625 | A | G | 280 | a0001c0001t0002g0011 a0001c0001t0002g0093 a0001c0001t0002g0107 others(277): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.63+3982A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74838625 | |||||||
chr2:74838631 | C | T | 2 | a0001c0001t0002g0107 a0003c0003t0003g0241 |
2 | HG01123.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.63+3988C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74838631 | |||||||
chr2:74838639 | C | T | 2 | a0001c0002t0001g0075 a0001c0002t0001g0076 |
2 | HG00423.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.63+3996C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74838639 | |||||||
chr2:74838653 | C | G | 2 | a0001c0012t0021g0356 a0004c0016t0012g0355 |
2 | HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.63+4010C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74838653 | |||||||
chr2:74838773 | C | T | 71 | a0001c0001t0002g0011 a0001c0001t0002g0124 a0001c0001t0002g0125 others(68): Show |
71 | HG00140.hp1 HG00408.hp1 HG00738.hp1 others(68): Show |
intron_variant | MODIFIER | c.63+4130C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74838773 | |||||||
chr2:74838853 | T | C | 6 | a0001c0011t0020g0348 a0002c0023t0006g0374 a0004c0008t0010g0349 others(3): Show |
6 | HG00735.hp1 HG01891.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+4210T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74838853 | |||||||
chr2:74839026 | A | T | 71 | a0001c0001t0002g0011 a0001c0001t0002g0124 a0001c0001t0002g0125 others(68): Show |
71 | HG00140.hp1 HG00408.hp1 HG00738.hp1 others(68): Show |
intron_variant | MODIFIER | c.63+4383A>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74839026 | |||||||
chr2:74839234 | A | G | 2 | a0001c0012t0021g0356 a0004c0016t0012g0355 |
2 | HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.63+4591A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74839234 | |||||||
chr2:74839241 | T | C | 4 | a0001c0001t0002g0112 a0002c0004t0001g0114 a0004c0008t0010g0111 others(1): Show |
4 | HG02109.hp2 HG02258.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+4598T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74839241 | |||||||
chr2:74839341 | C | T | 1 | a0001c0001t0002g0074 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.63+4698C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74839341 | |||||||
chr2:74839347 | G | A | 3 | a0001c0001t0005g0116 a0001c0002t0001g0127 a0002c0004t0004g0128 |
3 | HG02165.hp2 NA18969.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.63+4704G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74839347 | |||||||
chr2:74839473 | T | C | 2 | a0001c0012t0021g0356 a0004c0016t0012g0355 |
2 | HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.63+4830T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74839473 | |||||||
chr2:74839659 | A | AT | 27 | a0001c0001t0002g0072 a0001c0001t0002g0073 a0001c0001t0002g0107 others(24): Show |
27 | HG01192.hp1 HG01243.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.63+5031dupT | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74839659 | ||||||
chr2:74839659 | A | ATT | 13 | a0001c0006t0003g0359 a0001c0009t0034g0184 a0001c0011t0020g0348 others(10): Show |
13 | HG01257.hp2 HG01891.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.63+5030_63+5031dup others(2): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74839659 | ||||||
chr2:74839659 | A | ATTT | 23 | a0001c0001t0002g0256 a0001c0001t0007g0186 a0001c0001t0007g0250 others(20): Show |
23 | HG00609.hp2 HG00673.hp2 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.63+5029_63+5031dup others(3): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74839659 | ||||||
chr2:74839659 | AT | A | 9 | a0001c0001t0002g0093 a0001c0006t0021g0109 a0001c0037t0022g0364 others(6): Show |
10 | HG02145.hp1 HG02451.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.63+5031delT | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74839659 | ||||||
chr2:74839828 | T | TTGTA | 72 | a0001c0001t0002g0011 a0001c0001t0002g0124 a0001c0001t0002g0125 others(69): Show |
72 | HG00140.hp1 HG00408.hp1 HG00738.hp1 others(69): Show |
intron_variant | MODIFIER | c.63+5186_63+5187ins others(4): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74839828 | ||||||
chr2:74839883 | A | G | 1 | a0003c0003t0003g0288 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.63+5240A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74839883 | |||||||
chr2:74839951 | C | CT | 34 | a0001c0001t0002g0073 a0001c0001t0002g0074 a0001c0001t0002g0107 others(31): Show |
34 | HG00438.hp2 HG01192.hp1 HG01261.hp1 others(31): Show |
intron_variant | MODIFIER | c.63+5330dupT | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74839951 | ||||||
chr2:74839951 | CT | C | 62 | a0001c0001t0002g0018 a0001c0001t0002g0093 a0001c0001t0002g0182 others(59): Show |
66 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.63+5330delT | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74839951 | ||||||
chr2:74839951 | CTT | C | 18 | a0001c0001t0007g0319 a0001c0001t0007g0325 a0001c0002t0001g0187 others(15): Show |
18 | HG01243.hp1 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.63+5329_63+5330del others(2): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74839951 | ||||||
chr2:74840009 | A | G | 72 | a0001c0001t0002g0011 a0001c0001t0002g0124 a0001c0001t0002g0125 others(69): Show |
72 | HG00140.hp1 HG00408.hp1 HG00738.hp1 others(69): Show |
intron_variant | MODIFIER | c.63+5366A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840009 | |||||||
chr2:74840059 | C | T | 1 | a0013c0028t0001g0172 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.63+5416C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840059 | |||||||
chr2:74840116 | C | A | 1 | a0001c0009t0034g0184 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.63+5473C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840116 | |||||||
chr2:74840116 | C | T | 1 | a0001c0001t0007g0265 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.63+5473C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840116 | |||||||
chr2:74840238 | C | T | 1 | a0001c0002t0046g0163 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.63+5595C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840238 | |||||||
chr2:74840248 | C | T | 1 | a0001c0006t0003g0162 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.63+5605C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840248 | |||||||
chr2:74840258 | A | AT | 7 | a0001c0001t0002g0008 a0001c0001t0002g0200 a0001c0002t0001g0161 others(4): Show |
7 | HG01175.hp1 HG02055.hp2 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+5631dupT | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74840258 | ||||||
chr2:74840350 | G | A | 44 | a0001c0001t0002g0018 a0001c0001t0002g0290 a0001c0001t0002g0299 others(41): Show |
47 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.63+5707G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840350 | |||||||
chr2:74840372 | A | G | 2 | a0001c0012t0021g0356 a0004c0016t0012g0355 |
2 | HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.63+5729A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840372 | |||||||
chr2:74840458 | G | A | 1 | a0001c0001t0002g0008 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.63+5815G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840458 | |||||||
chr2:74840502 | G | A | 1 | a0001c0001t0002g0290 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.63+5859G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840502 | |||||||
chr2:74840505 | G | C | 1 | a0001c0002t0001g0129 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.63+5862G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840505 | |||||||
chr2:74840627 | A | G | 31 | a0001c0001t0002g0256 a0001c0001t0007g0186 a0001c0001t0007g0242 others(28): Show |
31 | HG00609.hp2 HG00673.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.63+5984A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840627 | |||||||
chr2:74840634 | A | G | 1 | a0001c0001t0005g0160 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.63+5991A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840634 | |||||||
chr2:74840649 | C | T | 72 | a0001c0001t0002g0176 a0001c0001t0002g0182 a0001c0001t0002g0191 others(69): Show |
73 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.63+6006C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840649 | |||||||
chr2:74840664 | A | G | 6 | a0001c0011t0020g0348 a0002c0023t0006g0374 a0004c0008t0010g0349 others(3): Show |
6 | HG00735.hp1 HG01891.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+6021A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840664 | |||||||
chr2:74840692 | C | A | 8 | a0001c0001t0002g0189 a0001c0009t0034g0184 a0001c0014t0043g0345 others(5): Show |
8 | HG01884.hp1 HG01884.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.63+6049C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840692 | |||||||
chr2:74840698 | T | C | 4 | a0001c0002t0001g0378 a0001c0002t0001g0379 a0001c0002t0001g0380 others(1): Show |
4 | HG01257.hp1 HG01258.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+6055T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840698 | |||||||
chr2:74840711 | C | CA | 11 | a0001c0001t0002g0072 a0001c0001t0002g0203 a0001c0001t0005g0271 others(8): Show |
11 | HG00642.hp2 HG01109.hp1 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.63+6086dupA | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74840711 | ||||||
chr2:74840711 | CA | C | 207 | a0001c0001t0002g0011 a0001c0001t0002g0060 a0001c0001t0002g0061 others(204): Show |
208 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(205): Show |
intron_variant | MODIFIER | c.63+6086delA | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74840711 | ||||||
chr2:74840711 | CAA | C | 59 | a0001c0001t0002g0018 a0001c0001t0002g0112 a0001c0001t0002g0170 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.63+6085_63+6086del others(2): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74840711 | ||||||
chr2:74840711 | CAAAAA | C | 5 | a0001c0001t0002g0093 a0001c0006t0021g0109 a0002c0004t0006g0092 others(2): Show |
6 | HG02145.hp1 HG02559.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+6082_63+6086del others(5): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74840711 | ||||||
chr2:74840714 | A | C | 1 | a0001c0002t0001g0089 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.63+6071A>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840714 | |||||||
chr2:74840754 | C | A | 16 | a0001c0001t0007g0319 a0001c0001t0007g0325 a0001c0002t0011g0337 others(13): Show |
16 | HG01243.hp1 HG02109.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.63+6111C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840754 | |||||||
chr2:74840803 | C | T | 1 | a0001c0024t0003g0183 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.63+6160C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840803 | |||||||
chr2:74840834 | G | T | 1 | a0002c0007t0016g0123 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.63+6191G>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840834 | |||||||
chr2:74840878 | C | CAAAAAAA others(3): Show |
6 | a0001c0001t0007g0325 a0001c0006t0031g0324 a0002c0004t0009g0340 others(3): Show |
6 | HG02451.hp1 HG02615.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+6252_63+6261dup others(10): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74840878 | ||||||
chr2:74840878 | C | CAAAAAAA others(4): Show |
6 | a0001c0002t0011g0337 a0002c0004t0009g0115 a0002c0004t0009g0321 others(3): Show |
6 | HG02257.hp1 HG02818.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+6251_63+6261dup others(11): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74840878 | ||||||
chr2:74840878 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0007g0319 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.63+6250_63+6261dup others(12): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74840878 | ||||||
chr2:74840878 | CA | C | 168 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0011 others(165): Show |
172 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.63+6261delA | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74840878 | ||||||
chr2:74840878 | CAA | C | 16 | a0001c0001t0002g0093 a0001c0001t0007g0250 a0001c0002t0017g0014 others(13): Show |
17 | HG00323.hp2 HG01169.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.63+6260_63+6261del others(2): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74840878 | ||||||
chr2:74840878 | CAAA | C | 18 | a0001c0001t0002g0256 a0001c0001t0007g0186 a0001c0001t0007g0242 others(15): Show |
18 | HG00609.hp2 HG00673.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.63+6259_63+6261del others(3): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74840878 | ||||||
chr2:74840878 | CAAAA | C | 6 | a0001c0011t0020g0348 a0002c0023t0006g0374 a0004c0008t0010g0349 others(3): Show |
6 | HG00735.hp1 HG01891.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+6258_63+6261del others(4): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74840878 | ||||||
chr2:74840878 | CAAAAAAA others(4): Show |
C | 4 | a0002c0004t0038g0352 a0003c0003t0003g0377 a0004c0008t0010g0353 others(1): Show |
4 | HG01891.hp2 HG02615.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+6251_63+6261del others(11): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74840878 | ||||||
chr2:74840878 | CAAAAAAA others(6): Show |
C | 5 | a0001c0001t0002g0132 a0001c0001t0005g0159 a0001c0002t0001g0129 others(2): Show |
5 | HG00140.hp1 HG00741.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+6249_63+6261del others(13): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74840878 | ||||||
chr2:74840904 | A | AAAAG | 18 | a0001c0001t0002g0209 a0001c0001t0002g0212 a0001c0001t0002g0365 others(15): Show |
18 | HG00438.hp1 HG01106.hp2 HG01516.hp2 others(15): Show |
intron_variant | MODIFIER | c.63+6261_63+6262ins others(4): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840904 | |||||||
chr2:74840904 | A | AAAG | 37 | a0001c0001t0002g0107 a0001c0001t0002g0176 a0001c0001t0002g0222 others(34): Show |
38 | HG00099.hp1 HG00544.hp2 HG01123.hp1 others(35): Show |
intron_variant | MODIFIER | c.63+6261_63+6262ins others(3): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840904 | |||||||
chr2:74840904 | A | AAG | 18 | a0001c0001t0002g0182 a0001c0001t0002g0189 a0001c0001t0002g0191 others(15): Show |
18 | HG01106.hp1 HG01516.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.63+6261_63+6262ins others(2): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840904 | |||||||
chr2:74840904 | A | AG | 14 | a0001c0001t0002g0112 a0001c0001t0002g0194 a0001c0001t0002g0196 others(11): Show |
14 | HG00408.hp2 HG01884.hp1 HG02602.hp2 others(11): Show |
intron_variant | MODIFIER | c.63+6262dupG | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74840904 | ||||||
chr2:74840904 | A | G | 6 | a0002c0004t0004g0199 a0002c0004t0010g0097 a0002c0004t0038g0352 others(3): Show |
6 | HG01891.hp2 HG02615.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+6261A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840904 | |||||||
chr2:74840955 | C | T | 6 | a0001c0011t0020g0348 a0002c0023t0006g0374 a0004c0008t0010g0349 others(3): Show |
6 | HG00735.hp1 HG01891.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+6312C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840955 | |||||||
chr2:74840986 | C | T | 70 | a0001c0001t0002g0112 a0001c0001t0002g0176 a0001c0001t0002g0191 others(67): Show |
71 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.63+6343C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74840986 | |||||||
chr2:74841039 | C | G | 4 | a0002c0004t0038g0352 a0003c0003t0003g0377 a0004c0008t0010g0353 others(1): Show |
4 | HG01891.hp2 HG02615.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+6396C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74841039 | |||||||
chr2:74841272 | G | A | 7 | a0001c0001t0002g0273 a0001c0001t0003g0277 a0001c0001t0005g0035 others(4): Show |
7 | HG00423.hp2 NA18961.hp2 NA19001.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+6629G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74841272 | |||||||
chr2:74841369 | C | G | 1 | a0001c0002t0001g0083 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.63+6726C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74841369 | |||||||
chr2:74841405 | C | G | 1 | a0001c0002t0001g0329 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.63+6762C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74841405 | |||||||
chr2:74841458 | G | C | 1 | a0003c0003t0008g0384 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.63+6815G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74841458 | |||||||
chr2:74841666 | C | T | 5 | a0001c0001t0002g0189 a0002c0007t0016g0201 a0003c0003t0003g0202 others(2): Show |
5 | HG01884.hp2 HG02647.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+7023C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74841666 | |||||||
chr2:74841715 | C | T | 167 | a0001c0001t0002g0018 a0001c0001t0002g0107 a0001c0001t0002g0112 others(164): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.63+7072C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74841715 | |||||||
chr2:74841717 | C | G | 2 | a0001c0024t0003g0183 a0002c0007t0016g0123 |
2 | HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.63+7074C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74841717 | |||||||
chr2:74841978 | C | T | 66 | a0001c0001t0002g0112 a0001c0001t0002g0176 a0001c0001t0002g0191 others(63): Show |
67 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.63+7335C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74841978 | |||||||
chr2:74842021 | A | T | 6 | a0001c0001t0002g0080 a0001c0002t0001g0079 a0001c0002t0001g0082 others(3): Show |
6 | NA18959.hp2 NA18960.hp2 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+7378A>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74842021 | |||||||
chr2:74842052 | A | C | 1 | a0001c0002t0001g0380 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.63+7409A>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74842052 | |||||||
chr2:74842115 | T | C | 1 | a0001c0002t0001g0129 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.63+7472T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74842115 | |||||||
chr2:74842232 | A | G | 1 | a0001c0014t0001g0078 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.63+7589A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74842232 | |||||||
chr2:74842237 | AT | A | 8 | a0001c0001t0002g0222 a0001c0024t0003g0183 a0002c0004t0006g0248 others(5): Show |
8 | HG02717.hp2 HG02723.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.63+7603delT | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74842237 | ||||||
chr2:74842298 | A | G | 15 | a0001c0009t0034g0184 a0001c0012t0021g0356 a0001c0014t0043g0345 others(12): Show |
15 | HG00639.hp1 HG01243.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.63+7655A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74842298 | |||||||
chr2:74842413 | C | T | 4 | a0001c0001t0002g0060 a0001c0001t0002g0061 a0001c0001t0002g0155 others(1): Show |
4 | HG01496.hp2 HG01515.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+7770C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74842413 | |||||||
chr2:74842473 | A | G | 1 | a0001c0002t0001g0055 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.63+7830A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74842473 | |||||||
chr2:74842728 | G | A | 1 | a0003c0003t0003g0158 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.63+8085G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74842728 | |||||||
chr2:74842782 | G | A | 1 | a0004c0016t0012g0347 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.63+8139G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74842782 | |||||||
chr2:74843089 | G | A | 64 | a0001c0001t0002g0170 a0001c0001t0002g0205 a0001c0001t0002g0208 others(61): Show |
67 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.63+8446G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74843089 | |||||||
chr2:74843115 | C | T | 5 | a0001c0001t0002g0189 a0002c0007t0016g0201 a0003c0003t0003g0202 others(2): Show |
5 | HG01884.hp2 HG02647.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+8472C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74843115 | |||||||
chr2:74843136 | C | A | 67 | a0001c0001t0002g0112 a0001c0001t0002g0176 a0001c0001t0002g0191 others(64): Show |
68 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.63+8493C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74843136 | |||||||
chr2:74843278 | C | A | 5 | a0001c0011t0020g0348 a0002c0023t0006g0374 a0004c0008t0010g0349 others(2): Show |
5 | HG00735.hp1 HG02895.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+8635C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74843278 | |||||||
chr2:74843281 | TC | T | 5 | a0001c0011t0020g0348 a0002c0023t0006g0374 a0004c0008t0010g0349 others(2): Show |
5 | HG00735.hp1 HG02895.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+8640delC | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74843281 | ||||||
chr2:74843440 | C | T | 89 | a0001c0001t0002g0112 a0001c0001t0002g0176 a0001c0001t0002g0189 others(86): Show |
90 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.63+8797C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74843440 | |||||||
chr2:74843547 | G | A | 7 | a0001c0001t0002g0182 a0001c0001t0002g0194 a0001c0002t0001g0180 others(4): Show |
7 | HG00408.hp2 NA18943.hp1 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+8904G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74843547 | |||||||
chr2:74843548 | C | T | 1 | a0001c0014t0043g0345 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.63+8905C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74843548 | |||||||
chr2:74843883 | T | C | 252 | a0001c0001t0002g0011 a0001c0001t0002g0023 a0001c0001t0002g0037 others(249): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.63+9240T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74843883 | |||||||
chr2:74844068 | GC | G | 6 | a0001c0001t0002g0107 a0001c0002t0001g0104 a0002c0004t0044g0100 others(3): Show |
6 | HG01192.hp1 HG02257.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+9428delC | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74844068 | ||||||
chr2:74844090 | C | T | 3 | a0001c0002t0001g0178 a0001c0002t0001g0278 a0003c0003t0003g0287 |
3 | NA18961.hp2 NA19001.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.63+9447C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74844090 | |||||||
chr2:74844224 | ATGT | A | 81 | a0001c0001t0002g0011 a0001c0001t0002g0023 a0001c0001t0002g0037 others(78): Show |
82 | HG00140.hp1 HG00408.hp1 HG00738.hp1 others(79): Show |
intron_variant | MODIFIER | c.63+9585_63+9587del others(3): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74844224 | ||||||
chr2:74844494 | T | C | 1 | a0009c0046t0001g0165 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.64-9799T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74844494 | |||||||
chr2:74844564 | T | C | 17 | a0001c0001t0002g0191 a0001c0001t0002g0192 a0001c0001t0002g0196 others(14): Show |
17 | HG00438.hp1 HG01106.hp1 HG01516.hp1 others(14): Show |
intron_variant | MODIFIER | c.64-9729T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74844564 | |||||||
chr2:74844590 | C | G | 1 | a0001c0001t0002g0205 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.64-9703C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74844590 | |||||||
chr2:74844634 | T | C | 63 | a0001c0001t0002g0176 a0001c0001t0002g0191 a0001c0001t0002g0192 others(60): Show |
64 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.64-9659T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74844634 | |||||||
chr2:74844674 | C | A | 1 | a0001c0002t0011g0298 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.64-9619C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74844674 | |||||||
chr2:74844738 | G | A | 5 | a0001c0001t0002g0093 a0001c0006t0021g0109 a0002c0004t0006g0092 others(2): Show |
6 | HG02145.hp1 HG02559.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-9555G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74844738 | |||||||
chr2:74844750 | G | T | 16 | a0001c0001t0007g0250 a0001c0002t0001g0263 a0001c0005t0011g0297 others(13): Show |
16 | HG00735.hp1 HG00738.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.64-9543G>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74844750 | |||||||
chr2:74844823 | C | G | 1 | a0001c0002t0001g0082 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.64-9470C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74844823 | |||||||
chr2:74844962 | G | T | 2 | a0003c0003t0003g0139 a0003c0003t0003g0169 |
2 | NA18944.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.64-9331G>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74844962 | |||||||
chr2:74845239 | A | G | 2 | a0001c0002t0046g0163 a0009c0046t0001g0165 |
2 | HG02738.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.64-9054A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74845239 | |||||||
chr2:74845335 | C | G | 1 | a0001c0001t0007g0250 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.64-8958C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74845335 | |||||||
chr2:74845567 | A | G | 5 | a0001c0005t0017g0084 a0001c0005t0047g0015 a0003c0003t0003g0085 others(2): Show |
5 | HG00639.hp2 HG01070.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-8726A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74845567 | |||||||
chr2:74845695 | C | A | 1 | a0001c0001t0002g0140 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.64-8598C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74845695 | |||||||
chr2:74845796 | T | C | 69 | a0001c0001t0002g0112 a0001c0001t0002g0176 a0001c0001t0002g0191 others(66): Show |
70 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.64-8497T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74845796 | |||||||
chr2:74845802 | G | A | 2 | a0001c0001t0002g0222 a0004c0018t0024g0223 |
2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.64-8491G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74845802 | |||||||
chr2:74845805 | G | C | 1 | a0002c0004t0006g0108 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.64-8488G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74845805 | |||||||
chr2:74845819 | C | A | 1 | a0004c0008t0010g0349 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.64-8474C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74845819 | |||||||
chr2:74845821 | G | T | 6 | a0001c0001t0002g0107 a0001c0002t0001g0104 a0002c0004t0044g0100 others(3): Show |
6 | HG01192.hp1 HG02257.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-8472G>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74845821 | |||||||
chr2:74845942 | T | G | 6 | a0001c0001t0002g0107 a0001c0002t0001g0104 a0002c0004t0044g0100 others(3): Show |
6 | HG01192.hp1 HG02257.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-8351T>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74845942 | |||||||
chr2:74846041 | C | T | 16 | a0001c0001t0007g0319 a0001c0001t0007g0325 a0001c0006t0031g0324 others(13): Show |
16 | HG01243.hp1 HG02109.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.64-8252C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74846041 | |||||||
chr2:74846124 | A | G | 2 | a0001c0024t0003g0183 a0002c0007t0016g0123 |
2 | HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.64-8169A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74846124 | |||||||
chr2:74846276 | T | C | 1 | a0001c0002t0017g0014 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.64-8017T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74846276 | |||||||
chr2:74846318 | C | CT | 255 | a0001c0001t0002g0011 a0001c0001t0002g0023 a0001c0001t0002g0037 others(252): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.64-7967dupT | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74846318 | ||||||
chr2:74846331 | C | T | 1 | a0003c0003t0003g0167 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.64-7962C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74846331 | |||||||
chr2:74846420 | C | G | 1 | a0004c0043t0012g0177 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.64-7873C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74846420 | |||||||
chr2:74846455 | G | A | 247 | a0001c0001t0002g0011 a0001c0001t0002g0023 a0001c0001t0002g0037 others(244): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.64-7838G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74846455 | |||||||
chr2:74846928 | G | T | 81 | a0001c0001t0002g0011 a0001c0001t0002g0023 a0001c0001t0002g0033 others(78): Show |
81 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.64-7365G>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74846928 | |||||||
chr2:74847078 | C | T | 2 | a0001c0011t0037g0245 a0004c0018t0045g0246 |
2 | HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.64-7215C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74847078 | |||||||
chr2:74847282 | T | C | 1 | a0003c0003t0003g0377 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.64-7011T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74847282 | |||||||
chr2:74847497 | G | T | 15 | a0001c0001t0007g0319 a0001c0001t0007g0325 a0001c0006t0031g0324 others(12): Show |
15 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.64-6796G>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74847497 | |||||||
chr2:74847511 | C | T | 1 | a0001c0014t0043g0345 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.64-6782C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74847511 | |||||||
chr2:74847548 | C | T | 9 | a0001c0001t0002g0222 a0001c0011t0020g0348 a0001c0037t0022g0364 others(6): Show |
9 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.64-6745C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74847548 | |||||||
chr2:74847626 | G | A | 9 | a0001c0001t0002g0222 a0001c0011t0020g0348 a0001c0037t0022g0364 others(6): Show |
9 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.64-6667G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74847626 | |||||||
chr2:74847662 | G | A | 17 | a0001c0001t0007g0319 a0001c0001t0007g0325 a0001c0006t0031g0324 others(14): Show |
17 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.64-6631G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74847662 | |||||||
chr2:74847704 | C | T | 5 | a0001c0001t0002g0093 a0001c0001t0002g0112 a0001c0006t0021g0109 others(2): Show |
5 | HG02145.hp1 HG02559.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-6589C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74847704 | |||||||
chr2:74847711 | TAAAC | T | 67 | a0001c0001t0002g0008 a0001c0001t0002g0018 a0001c0001t0002g0045 others(64): Show |
68 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.64-6577_64-6574del others(4): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74847711 | ||||||
chr2:74847766 | T | A | 2 | a0001c0012t0021g0356 a0004c0016t0012g0355 |
2 | HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.64-6527T>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74847766 | |||||||
chr2:74847799 | C | T | 1 | a0001c0001t0002g0343 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.64-6494C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74847799 | |||||||
chr2:74847805 | A | C | 59 | a0001c0001t0002g0107 a0001c0001t0002g0132 a0001c0001t0002g0140 others(56): Show |
62 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.64-6488A>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74847805 | |||||||
chr2:74847840 | T | C | 90 | a0001c0001t0002g0074 a0001c0001t0002g0080 a0001c0001t0002g0131 others(87): Show |
92 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.64-6453T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74847840 | |||||||
chr2:74847974 | C | G | 5 | a0001c0001t0006g0357 a0001c0011t0037g0245 a0002c0007t0010g0249 others(2): Show |
5 | HG01884.hp1 HG02280.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-6319C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74847974 | |||||||
chr2:74848055 | G | A | 15 | a0001c0001t0007g0319 a0001c0001t0007g0325 a0001c0006t0031g0324 others(12): Show |
15 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.64-6238G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74848055 | |||||||
chr2:74848128 | G | A | 142 | a0001c0001t0002g0074 a0001c0001t0002g0080 a0001c0001t0002g0093 others(139): Show |
147 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.64-6165G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74848128 | |||||||
chr2:74848275 | A | G | 303 | a0001c0001t0002g0008 a0001c0001t0002g0018 a0001c0001t0002g0038 others(300): Show |
309 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.64-6018A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74848275 | |||||||
chr2:74848304 | T | C | 1 | a0001c0002t0001g0133 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.64-5989T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74848304 | |||||||
chr2:74848405 | A | G | 85 | a0001c0001t0002g0074 a0001c0001t0002g0080 a0001c0001t0002g0093 others(82): Show |
87 | HG00099.hp1 HG00423.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.64-5888A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74848405 | |||||||
chr2:74848465 | C | T | 2 | a0002c0007t0012g0103 a0002c0025t0024g0268 |
2 | HG01109.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.64-5828C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74848465 | |||||||
chr2:74848469 | ATTAAT | A | 85 | a0001c0001t0002g0074 a0001c0001t0002g0080 a0001c0001t0002g0093 others(82): Show |
87 | HG00099.hp1 HG00423.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.64-5821_64-5817del others(5): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74848469 | ||||||
chr2:74848486 | TTA | T | 85 | a0001c0001t0002g0074 a0001c0001t0002g0080 a0001c0001t0002g0093 others(82): Show |
87 | HG00099.hp1 HG00423.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.64-5805_64-5804del others(2): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74848486 | ||||||
chr2:74849047 | A | G | 2 | a0001c0001t0002g0170 a0001c0011t0020g0096 |
2 | HG02486.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.64-5246A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74849047 | |||||||
chr2:74849054 | G | A | 1 | a0001c0002t0001g0042 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.64-5239G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74849054 | |||||||
chr2:74849252 | C | T | 1 | a0002c0004t0018g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.64-5041C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74849252 | |||||||
chr2:74849340 | A | G | 1 | a0001c0002t0001g0091 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.64-4953A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74849340 | |||||||
chr2:74849443 | C | T | 7 | a0001c0037t0022g0364 a0002c0004t0006g0092 a0002c0004t0038g0352 others(4): Show |
7 | HG01243.hp2 HG01891.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.64-4850C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74849443 | |||||||
chr2:74849662 | A | C | 221 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0018 others(218): Show |
223 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.64-4631A>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74849662 | |||||||
chr2:74849721 | G | C | 2 | a0001c0012t0022g0335 a0002c0004t0001g0114 |
2 | HG02055.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.64-4572G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74849721 | |||||||
chr2:74849754 | A | C | 84 | a0001c0001t0002g0008 a0001c0001t0002g0018 a0001c0001t0002g0033 others(81): Show |
85 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.64-4539A>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74849754 | |||||||
chr2:74849828 | C | T | 6 | a0001c0001t0002g0093 a0001c0001t0002g0112 a0001c0006t0021g0109 others(3): Show |
6 | HG01109.hp1 HG02145.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-4465C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74849828 | |||||||
chr2:74849869 | G | A | 1 | a0001c0001t0007g0250 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.64-4424G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74849869 | |||||||
chr2:74849927 | C | T | 2 | a0003c0003t0003g0202 a0003c0003t0003g0291 |
2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.64-4366C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74849927 | |||||||
chr2:74849943 | T | C | 2 | a0001c0012t0022g0335 a0002c0004t0001g0114 |
2 | HG02055.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.64-4350T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74849943 | |||||||
chr2:74849973 | A | C | 182 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0018 others(179): Show |
183 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.64-4320A>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74849973 | |||||||
chr2:74850067 | C | T | 84 | a0001c0001t0002g0008 a0001c0001t0002g0018 a0001c0001t0002g0033 others(81): Show |
85 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.64-4226C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74850067 | |||||||
chr2:74850105 | T | C | 36 | a0001c0001t0002g0107 a0001c0001t0002g0132 a0001c0001t0002g0290 others(33): Show |
37 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.64-4188T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74850105 | |||||||
chr2:74850185 | C | A | 4 | a0002c0004t0006g0092 a0002c0004t0023g0228 a0002c0004t0038g0352 others(1): Show |
4 | HG02630.hp1 HG03139.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-4108C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74850185 | |||||||
chr2:74850320 | T | G | 1 | a0014c0019t0001g0113 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.64-3973T>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74850320 | |||||||
chr2:74850413 | C | T | 5 | a0001c0001t0002g0130 a0001c0001t0002g0150 a0001c0001t0002g0344 others(2): Show |
5 | HG00099.hp2 HG00738.hp1 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-3880C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74850413 | |||||||
chr2:74850414 | G | A | 1 | a0006c0027t0039g0350 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.64-3879G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74850414 | |||||||
chr2:74850468 | T | C | 2 | a0003c0003t0003g0202 a0003c0003t0003g0291 |
2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.64-3825T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74850468 | |||||||
chr2:74850518 | C | T | 9 | a0001c0024t0003g0183 a0002c0004t0009g0326 a0002c0004t0019g0342 others(6): Show |
9 | HG01243.hp1 HG02896.hp1 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.64-3775C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74850518 | |||||||
chr2:74850550 | A | G | 84 | a0001c0001t0002g0008 a0001c0001t0002g0018 a0001c0001t0002g0033 others(81): Show |
85 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.64-3743A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74850550 | |||||||
chr2:74850628 | T | C | 2 | a0001c0002t0046g0163 a0003c0017t0014g0251 |
2 | HG04199.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.64-3665T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74850628 | |||||||
chr2:74850657 | C | G | 1 | a0001c0001t0002g0191 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.64-3636C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74850657 | |||||||
chr2:74850787 | G | A | 1 | a0001c0001t0002g0343 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.64-3506G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74850787 | |||||||
chr2:74850812 | C | T | 2 | a0003c0003t0003g0202 a0003c0003t0003g0291 |
2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.64-3481C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74850812 | |||||||
chr2:74850996 | A | ACTGTTTC others(10): Show |
84 | a0001c0001t0002g0008 a0001c0001t0002g0018 a0001c0001t0002g0033 others(81): Show |
85 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.64-3284_64-3268dup others(17): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74850996 | ||||||
chr2:74851074 | G | T | 88 | a0001c0001t0002g0003 a0001c0001t0002g0073 a0001c0001t0002g0093 others(85): Show |
88 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.64-3219G>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74851074 | |||||||
chr2:74851129 | C | T | 1 | a0002c0007t0016g0201 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.64-3164C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74851129 | |||||||
chr2:74851162 | C | T | 2 | a0001c0001t0002g0060 a0001c0001t0002g0061 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.64-3131C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74851162 | |||||||
chr2:74851253 | C | T | 3 | a0001c0002t0001g0025 a0001c0002t0001g0039 a0001c0002t0001g0040 |
3 | HG00544.hp1 NA18950.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.64-3040C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74851253 | |||||||
chr2:74851526 | C | T | 10 | a0001c0001t0002g0052 a0001c0002t0001g0032 a0001c0002t0001g0042 others(7): Show |
10 | HG00642.hp1 HG01109.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.64-2767C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74851526 | |||||||
chr2:74851546 | G | C | 2 | a0003c0003t0003g0202 a0003c0003t0003g0291 |
2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.64-2747G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74851546 | |||||||
chr2:74851627 | C | T | 1 | a0003c0003t0003g0019 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.64-2666C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74851627 | |||||||
chr2:74851632 | G | A | 1 | a0001c0006t0003g0142 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.64-2661G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74851632 | |||||||
chr2:74851644 | C | T | 1 | a0001c0002t0001g0156 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.64-2649C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74851644 | |||||||
chr2:74851666 | G | A | 4 | a0001c0001t0002g0205 a0001c0001t0002g0208 a0003c0003t0003g0206 others(1): Show |
4 | HG00140.hp2 HG00741.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-2627G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74851666 | |||||||
chr2:74851678 | C | T | 1 | a0001c0001t0007g0325 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.64-2615C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74851678 | |||||||
chr2:74851828 | A | G | 1 | a0001c0002t0001g0156 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.64-2465A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74851828 | |||||||
chr2:74851842 | A | C | 1 | a0002c0004t0006g0108 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.64-2451A>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74851842 | |||||||
chr2:74852031 | C | T | 4 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0002t0001g0137 others(1): Show |
4 | NA18941.hp2 NA18975.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-2262C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74852031 | |||||||
chr2:74852219 | A | T | 40 | a0001c0001t0002g0003 a0001c0001t0002g0073 a0001c0001t0002g0131 others(37): Show |
40 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.64-2074A>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74852219 | |||||||
chr2:74852292 | A | G | 183 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0018 others(180): Show |
184 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.64-2001A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74852292 | |||||||
chr2:74852334 | A | G | 12 | a0001c0001t0002g0170 a0001c0001t0006g0357 a0001c0009t0015g0358 others(9): Show |
12 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.64-1959A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74852334 | |||||||
chr2:74852521 | C | A | 5 | a0001c0002t0001g0118 a0001c0002t0001g0119 a0001c0002t0001g0120 others(2): Show |
5 | NA18946.hp2 NA18953.hp2 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-1772C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74852521 | |||||||
chr2:74852552 | A | G | 9 | a0001c0001t0002g0093 a0001c0001t0002g0112 a0001c0006t0021g0109 others(6): Show |
9 | HG01109.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.64-1741A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74852552 | |||||||
chr2:74852582 | G | T | 1 | a0001c0001t0005g0271 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.64-1711G>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74852582 | |||||||
chr2:74852689 | A | T | 7 | a0001c0001t0002g0023 a0001c0001t0002g0093 a0001c0001t0002g0112 others(4): Show |
7 | HG02145.hp1 HG02559.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-1604A>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74852689 | |||||||
chr2:74852698 | A | C | 83 | a0001c0001t0002g0008 a0001c0001t0002g0018 a0001c0001t0002g0033 others(80): Show |
84 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.64-1595A>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74852698 | |||||||
chr2:74852897 | T | C | 2 | a0003c0003t0003g0202 a0003c0003t0003g0291 |
2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.64-1396T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74852897 | |||||||
chr2:74852911 | C | T | 7 | a0001c0001t0002g0222 a0001c0011t0020g0348 a0002c0007t0016g0201 others(4): Show |
7 | HG00735.hp1 HG02647.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.64-1382C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74852911 | |||||||
chr2:74853149 | A | G | 2 | a0001c0001t0002g0131 a0001c0006t0002g0009 |
2 | NA18947.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.64-1144A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74853149 | |||||||
chr2:74853195 | A | G | 12 | a0001c0001t0007g0319 a0001c0001t0007g0325 a0001c0006t0031g0324 others(9): Show |
12 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.64-1098A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74853195 | |||||||
chr2:74853247 | T | C | 84 | a0001c0001t0002g0003 a0001c0001t0002g0073 a0001c0001t0002g0131 others(81): Show |
84 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.64-1046T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74853247 | |||||||
chr2:74853254 | C | A | 3 | a0001c0012t0022g0335 a0002c0004t0001g0114 a0002c0025t0024g0268 |
3 | HG01109.hp1 HG02055.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.64-1039C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74853254 | |||||||
chr2:74853280 | G | A | 41 | a0001c0001t0002g0003 a0001c0001t0002g0073 a0001c0001t0002g0131 others(38): Show |
41 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.64-1013G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74853280 | |||||||
chr2:74853323 | C | A | 84 | a0001c0001t0002g0003 a0001c0001t0002g0073 a0001c0001t0002g0131 others(81): Show |
84 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.64-970C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74853323 | |||||||
chr2:74853393 | T | C | 84 | a0001c0001t0002g0008 a0001c0001t0002g0018 a0001c0001t0002g0033 others(81): Show |
85 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.64-900T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74853393 | |||||||
chr2:74853518 | A | AAAC | 42 | a0001c0001t0002g0008 a0001c0001t0002g0018 a0001c0001t0002g0033 others(39): Show |
43 | HG00280.hp2 HG00609.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.64-730_64-728dupCA others(1): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74853518 | ||||||
chr2:74853518 | A | AAACAAC | 10 | a0001c0001t0002g0048 a0001c0001t0002g0052 a0001c0002t0001g0075 others(7): Show |
10 | HG00423.hp1 HG01123.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.64-733_64-728dupCA others(4): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74853518 | ||||||
chr2:74853518 | AAAC | A | 71 | a0001c0001t0002g0011 a0001c0001t0002g0023 a0001c0001t0002g0038 others(68): Show |
71 | HG00099.hp2 HG00438.hp2 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.64-730_64-728delCA others(1): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74853518 | ||||||
chr2:74853518 | AAACAAC | A | 18 | a0001c0001t0002g0205 a0001c0001t0002g0208 a0001c0002t0001g0041 others(15): Show |
18 | HG00140.hp2 HG00741.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.64-733_64-728delCA others(4): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74853518 | ||||||
chr2:74853518 | AAACAACA others(2): Show |
A | 119 | a0001c0001t0002g0003 a0001c0001t0002g0073 a0001c0001t0002g0107 others(116): Show |
121 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.64-736_64-728delCA others(7): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74853518 | ||||||
chr2:74853518 | AAACAACA others(5): Show |
A | 106 | a0001c0001t0002g0074 a0001c0001t0002g0080 a0001c0001t0002g0093 others(103): Show |
109 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.64-739_64-728delCA others(10): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74853518 | ||||||
chr2:74853688 | T | C | 84 | a0001c0001t0002g0008 a0001c0001t0002g0018 a0001c0001t0002g0033 others(81): Show |
85 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.64-605T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74853688 | |||||||
chr2:74853696 | C | CA | 44 | a0001c0001t0002g0003 a0001c0001t0002g0073 a0001c0001t0002g0131 others(41): Show |
44 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(41): Show |
intron_variant | MODIFIER | c.64-585dupA | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74853696 | ||||||
chr2:74853770 | CT | C | 84 | a0001c0001t0002g0008 a0001c0001t0002g0018 a0001c0001t0002g0033 others(81): Show |
85 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.64-520delT | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr2 | 74853770 | ||||||
chr2:74853785 | A | G | 16 | a0001c0001t0002g0192 a0001c0001t0002g0196 a0001c0001t0002g0197 others(13): Show |
16 | HG00099.hp1 HG00544.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.64-508A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74853785 | |||||||
chr2:74853828 | A | G | 1 | a0003c0003t0003g0381 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.64-465A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74853828 | |||||||
chr2:74853874 | C | T | 1 | a0001c0022t0001g0188 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.64-419C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74853874 | |||||||
chr2:74853946 | C | T | 1 | a0001c0001t0002g0073 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.64-347C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74853946 | |||||||
chr2:74853947 | T | G | 1 | a0001c0001t0002g0073 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.64-346T>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74853947 | |||||||
chr2:74854007 | C | T | 2 | a0002c0004t0004g0174 a0002c0004t0004g0199 |
2 | NA18941.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.64-286C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74854007 | |||||||
chr2:74854008 | G | A | 2 | a0001c0001t0002g0080 a0001c0006t0003g0034 |
2 | NA18987.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.64-285G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74854008 | |||||||
chr2:74854140 | G | A | 2 | a0003c0003t0003g0202 a0003c0003t0003g0291 |
2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.64-153G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 1/17 | chr2 | 74854140 | |||||||
chr2:74854458 | A | G | 1 | a0004c0008t0019g0190 | 1 | HG01884.hp2 | splice_region_variant&intron_variant | LOW | c.226+3A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74854458 | |||||||
chr2:74854556 | C | T | 1 | a0002c0004t0010g0004 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.226+101C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74854556 | |||||||
chr2:74854795 | C | T | 2 | a0001c0001t0002g0131 a0001c0006t0002g0009 |
2 | NA18947.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.226+340C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74854795 | |||||||
chr2:74854844 | C | T | 1 | a0002c0007t0035g0007 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.226+389C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74854844 | |||||||
chr2:74854864 | G | A | 1 | a0003c0003t0003g0117 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.226+409G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74854864 | |||||||
chr2:74854878 | C | T | 1 | a0001c0001t0002g0018 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.226+423C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74854878 | |||||||
chr2:74855008 | A | T | 1 | a0003c0003t0003g0167 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.226+553A>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74855008 | |||||||
chr2:74855089 | T | C | 173 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0018 others(170): Show |
174 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.226+634T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74855089 | |||||||
chr2:74855432 | T | A | 1 | a0001c0002t0001g0214 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.226+977T>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74855432 | |||||||
chr2:74855488 | G | A | 1 | a0001c0001t0002g0093 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.226+1033G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74855488 | |||||||
chr2:74855600 | G | A | 6 | a0001c0001t0002g0093 a0001c0001t0002g0112 a0001c0006t0021g0109 others(3): Show |
6 | HG02145.hp1 HG02559.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.226+1145G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74855600 | |||||||
chr2:74855623 | T | C | 2 | a0002c0004t0006g0232 a0002c0010t0006g0233 |
2 | HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.226+1168T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74855623 | |||||||
chr2:74855647 | T | C | 5 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0002t0001g0137 others(2): Show |
5 | NA18941.hp2 NA18975.hp1 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.226+1192T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74855647 | |||||||
chr2:74855707 | G | A | 1 | a0001c0001t0002g0372 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.226+1252G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74855707 | |||||||
chr2:74855717 | G | A | 6 | a0001c0001t0002g0093 a0001c0001t0002g0112 a0001c0006t0021g0109 others(3): Show |
6 | HG02145.hp1 HG02559.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.226+1262G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74855717 | |||||||
chr2:74855768 | G | A | 84 | a0001c0001t0002g0008 a0001c0001t0002g0018 a0001c0001t0002g0033 others(81): Show |
85 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.226+1313G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74855768 | |||||||
chr2:74855834 | G | A | 2 | a0003c0003t0003g0029 a0003c0003t0003g0332 |
2 | NA18954.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.226+1379G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74855834 | |||||||
chr2:74855845 | G | A | 1 | a0001c0001t0005g0274 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.226+1390G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74855845 | |||||||
chr2:74855846 | G | A | 15 | a0001c0001t0002g0192 a0001c0001t0002g0196 a0001c0001t0002g0197 others(12): Show |
15 | HG00544.hp1 HG01255.hp2 NA18747.hp2 others(12): Show |
intron_variant | MODIFIER | c.226+1391G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74855846 | |||||||
chr2:74855849 | G | A | 5 | a0001c0001t0002g0093 a0001c0001t0002g0112 a0001c0006t0021g0109 others(2): Show |
5 | HG02145.hp1 HG02559.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.226+1394G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74855849 | |||||||
chr2:74855863 | C | T | 2 | a0003c0003t0003g0202 a0003c0003t0003g0291 |
2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.226+1408C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74855863 | |||||||
chr2:74855931 | A | G | 84 | a0001c0001t0002g0008 a0001c0001t0002g0018 a0001c0001t0002g0033 others(81): Show |
85 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.226+1476A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74855931 | |||||||
chr2:74855987 | G | A | 8 | a0001c0024t0003g0183 a0002c0004t0009g0326 a0002c0004t0019g0342 others(5): Show |
8 | HG01243.hp1 HG02896.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.226+1532G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74855987 | |||||||
chr2:74856070 | C | T | 1 | a0001c0002t0001g0121 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.226+1615C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74856070 | |||||||
chr2:74856127 | T | G | 1 | a0001c0002t0001g0382 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.226+1672T>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74856127 | |||||||
chr2:74856131 | G | A | 2 | a0003c0003t0003g0202 a0003c0003t0003g0291 |
2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.226+1676G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74856131 | |||||||
chr2:74856174 | TG | T | 12 | a0001c0001t0002g0170 a0001c0001t0006g0357 a0001c0009t0015g0358 others(9): Show |
12 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.226+1722delG | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 74856174 | ||||||
chr2:74856185 | T | C | 1 | a0001c0006t0021g0109 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.226+1730T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74856185 | |||||||
chr2:74856458 | C | T | 4 | a0001c0001t0002g0130 a0001c0001t0002g0150 a0001c0001t0002g0344 others(1): Show |
4 | HG00099.hp2 HG00738.hp1 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.226+2003C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74856458 | |||||||
chr2:74856462 | C | T | 1 | a0004c0043t0012g0177 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.226+2007C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74856462 | |||||||
chr2:74856748 | C | A | 167 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0018 others(164): Show |
168 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.226+2293C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74856748 | |||||||
chr2:74856803 | G | C | 4 | a0001c0001t0002g0189 a0001c0012t0021g0356 a0004c0008t0019g0190 others(1): Show |
4 | HG01884.hp2 HG03453.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.226+2348G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74856803 | |||||||
chr2:74856864 | C | T | 1 | a0001c0001t0002g0170 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.226+2409C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74856864 | |||||||
chr2:74856911 | G | C | 1 | a0002c0035t0012g0346 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.226+2456G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74856911 | |||||||
chr2:74857177 | C | T | 84 | a0001c0001t0002g0008 a0001c0001t0002g0018 a0001c0001t0002g0033 others(81): Show |
85 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.226+2722C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74857177 | |||||||
chr2:74857216 | G | T | 84 | a0001c0001t0002g0008 a0001c0001t0002g0018 a0001c0001t0002g0033 others(81): Show |
85 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.226+2761G>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74857216 | |||||||
chr2:74857219 | T | A | 3 | a0001c0012t0022g0335 a0002c0004t0001g0114 a0002c0025t0024g0268 |
3 | HG01109.hp1 HG02055.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.226+2764T>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74857219 | |||||||
chr2:74857425 | C | A | 84 | a0001c0001t0002g0008 a0001c0001t0002g0018 a0001c0001t0002g0033 others(81): Show |
85 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.226+2970C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74857425 | |||||||
chr2:74857526 | A | G | 1 | a0004c0016t0012g0347 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.226+3071A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74857526 | |||||||
chr2:74857614 | C | A | 1 | a0001c0037t0022g0364 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.226+3159C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74857614 | |||||||
chr2:74857743 | A | C | 7 | a0001c0001t0002g0222 a0001c0011t0020g0348 a0002c0007t0016g0201 others(4): Show |
7 | HG00735.hp1 HG02647.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.226+3288A>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74857743 | |||||||
chr2:74857770 | A | T | 1 | a0001c0001t0002g0011 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.226+3315A>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74857770 | |||||||
chr2:74857778 | A | T | 1 | a0009c0046t0001g0165 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.226+3323A>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74857778 | |||||||
chr2:74858036 | C | T | 222 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0018 others(219): Show |
224 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.226+3581C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74858036 | |||||||
chr2:74858057 | T | C | 40 | a0001c0001t0002g0003 a0001c0001t0002g0073 a0001c0001t0002g0131 others(37): Show |
40 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.226+3602T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74858057 | |||||||
chr2:74858147 | A | T | 84 | a0001c0001t0002g0008 a0001c0001t0002g0018 a0001c0001t0002g0033 others(81): Show |
85 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.226+3692A>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74858147 | |||||||
chr2:74858153 | G | A | 2 | a0001c0002t0001g0329 a0001c0002t0017g0014 |
2 | NA18982.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.226+3698G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74858153 | |||||||
chr2:74858235 | CAGAACCT others(264): Show |
C | 1 | a0002c0004t0019g0342 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.226+3783_226+4053d others(2): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 74858235 | ||||||
chr2:74858332 | C | T | 1 | a0002c0004t0023g0244 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.226+3877C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74858332 | |||||||
chr2:74858440 | A | C | 179 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0018 others(176): Show |
180 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.226+3985A>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74858440 | |||||||
chr2:74858452 | A | G | 2 | a0001c0037t0022g0364 a0002c0035t0012g0346 |
2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.226+3997A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74858452 | |||||||
chr2:74858490 | C | T | 1 | a0001c0009t0034g0184 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.226+4035C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74858490 | |||||||
chr2:74858491 | G | A | 5 | a0001c0001t0002g0093 a0001c0001t0002g0112 a0001c0006t0021g0109 others(2): Show |
5 | HG02145.hp1 HG02559.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.226+4036G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74858491 | |||||||
chr2:74858886 | C | T | 1 | a0004c0018t0024g0223 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.226+4431C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74858886 | |||||||
chr2:74858889 | AG | A | 84 | a0001c0001t0002g0008 a0001c0001t0002g0018 a0001c0001t0002g0033 others(81): Show |
85 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.226+4438delG | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 74858889 | ||||||
chr2:74858929 | T | G | 1 | a0001c0006t0003g0240 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.226+4474T>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74858929 | |||||||
chr2:74858974 | A | G | 2 | a0001c0005t0017g0047 a0002c0010t0004g0058 |
2 | HG02559.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.226+4519A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74858974 | |||||||
chr2:74859035 | G | A | 37 | a0001c0001t0002g0003 a0001c0001t0002g0073 a0001c0001t0002g0131 others(34): Show |
37 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.226+4580G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74859035 | |||||||
chr2:74859054 | A | G | 79 | a0001c0001t0002g0074 a0001c0001t0002g0080 a0001c0001t0002g0140 others(76): Show |
83 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.226+4599A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74859054 | |||||||
chr2:74859081 | T | G | 2 | a0001c0012t0021g0356 a0004c0016t0012g0355 |
2 | HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.226+4626T>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74859081 | |||||||
chr2:74859399 | A | T | 1 | a0001c0002t0001g0303 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.226+4944A>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74859399 | |||||||
chr2:74859435 | C | A | 5 | a0001c0001t0002g0093 a0001c0001t0002g0112 a0001c0006t0021g0109 others(2): Show |
5 | HG02145.hp1 HG02559.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.226+4980C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74859435 | |||||||
chr2:74859458 | G | A | 6 | a0002c0004t0006g0092 a0002c0004t0023g0228 a0002c0004t0038g0352 others(3): Show |
6 | HG01891.hp2 HG02615.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.226+5003G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74859458 | |||||||
chr2:74859476 | G | A | 2 | a0003c0003t0003g0202 a0003c0003t0003g0291 |
2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.226+5021G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74859476 | |||||||
chr2:74859512 | C | T | 1 | a0003c0003t0003g0059 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.226+5057C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74859512 | |||||||
chr2:74859547 | G | A | 3 | a0001c0002t0001g0304 a0001c0002t0001g0317 a0003c0003t0008g0383 |
3 | HG01069.hp1 HG01071.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.226+5092G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74859547 | |||||||
chr2:74859585 | C | T | 1 | a0001c0002t0001g0283 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.226+5130C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74859585 | |||||||
chr2:74859621 | C | T | 40 | a0001c0001t0002g0003 a0001c0001t0002g0073 a0001c0001t0002g0131 others(37): Show |
40 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.226+5166C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74859621 | |||||||
chr2:74859622 | G | A | 87 | a0001c0001t0002g0008 a0001c0001t0002g0018 a0001c0001t0002g0033 others(84): Show |
88 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.226+5167G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74859622 | |||||||
chr2:74859665 | C | A | 1 | a0001c0002t0001g0303 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.226+5210C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74859665 | |||||||
chr2:74859666 | A | C | 1 | a0001c0002t0001g0303 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.226+5211A>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74859666 | |||||||
chr2:74859952 | C | A | 41 | a0001c0001t0002g0003 a0001c0001t0002g0073 a0001c0001t0002g0131 others(38): Show |
41 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.226+5497C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74859952 | |||||||
chr2:74859994 | T | C | 1 | a0003c0003t0003g0206 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.226+5539T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74859994 | |||||||
chr2:74860007 | T | A | 1 | a0001c0002t0001g0303 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.226+5552T>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74860007 | |||||||
chr2:74860133 | A | G | 2 | a0001c0002t0001g0329 a0001c0002t0017g0014 |
2 | NA18982.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.226+5678A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74860133 | |||||||
chr2:74860134 | A | T | 2 | a0001c0001t0002g0037 a0003c0003t0003g0036 |
2 | NA18953.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.226+5679A>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74860134 | |||||||
chr2:74860189 | C | T | 85 | a0001c0001t0002g0008 a0001c0001t0002g0018 a0001c0001t0002g0033 others(82): Show |
86 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.226+5734C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74860189 | |||||||
chr2:74860206 | G | A | 85 | a0001c0001t0002g0008 a0001c0001t0002g0018 a0001c0001t0002g0033 others(82): Show |
86 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.226+5751G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74860206 | |||||||
chr2:74860231 | T | A | 2 | a0001c0009t0015g0358 a0001c0009t0015g0360 |
2 | HG02055.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.226+5776T>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74860231 | |||||||
chr2:74860290 | A | G | 1 | a0002c0004t0018g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.226+5835A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74860290 | |||||||
chr2:74860332 | T | A | 1 | a0001c0002t0001g0210 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.226+5877T>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74860332 | |||||||
chr2:74860363 | C | T | 94 | a0001c0001t0002g0074 a0001c0001t0002g0080 a0001c0001t0002g0140 others(91): Show |
98 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.226+5908C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74860363 | |||||||
chr2:74860416 | C | T | 1 | a0002c0007t0016g0201 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.226+5961C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74860416 | |||||||
chr2:74860463 | A | G | 8 | a0001c0024t0003g0183 a0002c0004t0009g0326 a0002c0004t0019g0342 others(5): Show |
8 | HG01243.hp1 HG02896.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.226+6008A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74860463 | |||||||
chr2:74860534 | T | C | 2 | a0001c0001t0002g0299 a0001c0001t0002g0300 |
2 | HG02027.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.226+6079T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74860534 | |||||||
chr2:74860535 | C | A | 2 | a0003c0003t0003g0202 a0003c0003t0003g0291 |
2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.226+6080C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74860535 | |||||||
chr2:74860575 | G | A | 12 | a0001c0001t0002g0170 a0001c0001t0006g0357 a0001c0009t0015g0358 others(9): Show |
12 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.226+6120G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74860575 | |||||||
chr2:74860614 | G | C | 8 | a0001c0024t0003g0183 a0002c0004t0009g0326 a0002c0004t0019g0342 others(5): Show |
8 | HG01243.hp1 HG02896.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.226+6159G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74860614 | |||||||
chr2:74860652 | C | T | 1 | a0001c0002t0046g0163 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.226+6197C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74860652 | |||||||
chr2:74860726 | G | A | 1 | a0001c0002t0001g0049 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.226+6271G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74860726 | |||||||
chr2:74860747 | C | T | 8 | a0001c0024t0003g0183 a0002c0004t0009g0326 a0002c0004t0019g0342 others(5): Show |
8 | HG01243.hp1 HG02896.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.226+6292C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74860747 | |||||||
chr2:74860821 | C | T | 1 | a0003c0003t0003g0241 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.226+6366C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74860821 | |||||||
chr2:74860823 | C | A | 93 | a0001c0001t0002g0003 a0001c0001t0002g0073 a0001c0001t0002g0093 others(90): Show |
93 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.226+6368C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74860823 | |||||||
chr2:74860963 | C | T | 7 | a0001c0001t0002g0093 a0001c0001t0002g0112 a0001c0001t0002g0222 others(4): Show |
7 | HG02145.hp1 HG02559.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.226+6508C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74860963 | |||||||
chr2:74861029 | G | A | 1 | a0003c0003t0003g0144 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.226+6574G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74861029 | |||||||
chr2:74861054 | G | A | 85 | a0001c0001t0002g0008 a0001c0001t0002g0018 a0001c0001t0002g0033 others(82): Show |
86 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.227-6582G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74861054 | |||||||
chr2:74861083 | A | T | 2 | a0001c0037t0022g0364 a0002c0035t0012g0346 |
2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.227-6553A>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74861083 | |||||||
chr2:74861335 | G | A | 6 | a0001c0001t0002g0011 a0001c0001t0002g0124 a0001c0001t0002g0149 others(3): Show |
6 | HG00639.hp2 HG01070.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.227-6301G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74861335 | |||||||
chr2:74861638 | C | T | 1 | a0001c0001t0002g0273 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.227-5998C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74861638 | |||||||
chr2:74861679 | G | T | 1 | a0002c0004t0010g0004 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.227-5957G>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74861679 | |||||||
chr2:74861704 | G | A | 37 | a0001c0001t0002g0003 a0001c0001t0002g0073 a0001c0001t0002g0131 others(34): Show |
37 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.227-5932G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74861704 | |||||||
chr2:74861783 | A | T | 2 | a0001c0012t0022g0335 a0002c0025t0024g0268 |
2 | HG01109.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.227-5853A>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74861783 | |||||||
chr2:74861925 | G | A | 1 | a0011c0020t0032g0339 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.227-5711G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74861925 | |||||||
chr2:74862092 | C | A | 100 | a0001c0001t0002g0008 a0001c0001t0002g0018 a0001c0001t0002g0033 others(97): Show |
101 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.227-5544C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74862092 | |||||||
chr2:74862099 | G | A | 106 | a0001c0001t0002g0008 a0001c0001t0002g0018 a0001c0001t0002g0033 others(103): Show |
107 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(104): Show |
intron_variant | MODIFIER | c.227-5537G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74862099 | |||||||
chr2:74862327 | A | G | 52 | a0001c0001t0002g0107 a0001c0001t0002g0132 a0001c0001t0002g0205 others(49): Show |
53 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(50): Show |
intron_variant | MODIFIER | c.227-5309A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74862327 | |||||||
chr2:74862442 | A | G | 233 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0018 others(230): Show |
235 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.227-5194A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74862442 | |||||||
chr2:74862522 | A | G | 1 | a0001c0001t0002g0155 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.227-5114A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74862522 | |||||||
chr2:74862560 | CATGGAAG others(9): Show |
C | 1 | a0001c0012t0022g0335 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.227-5075_227-5060d others(18): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74862560 | |||||||
chr2:74862562 | T | C | 130 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0018 others(127): Show |
131 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.227-5074T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74862562 | |||||||
chr2:74862624 | G | A | 3 | a0001c0002t0001g0104 a0002c0004t0044g0100 a0004c0008t0006g0105 |
3 | HG01192.hp1 HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.227-5012G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74862624 | |||||||
chr2:74862674 | T | G | 181 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0018 others(178): Show |
182 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.227-4962T>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74862674 | |||||||
chr2:74862823 | G | A | 89 | a0001c0001t0002g0008 a0001c0001t0002g0018 a0001c0001t0002g0033 others(86): Show |
90 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.227-4813G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74862823 | |||||||
chr2:74863028 | G | A | 89 | a0001c0001t0002g0008 a0001c0001t0002g0018 a0001c0001t0002g0033 others(86): Show |
90 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.227-4608G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74863028 | |||||||
chr2:74863215 | GTGTTT | G | 3 | a0001c0001t0002g0212 a0001c0002t0049g0293 a0002c0004t0004g0211 |
3 | HG02027.hp1 HG02056.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.227-4419_227-4415d others(7): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 74863215 | ||||||
chr2:74863273 | T | C | 4 | a0001c0011t0020g0348 a0002c0007t0016g0201 a0004c0008t0010g0349 others(1): Show |
4 | HG00735.hp1 HG02647.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.227-4363T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74863273 | |||||||
chr2:74863454 | T | C | 1 | a0002c0007t0010g0249 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.227-4182T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74863454 | |||||||
chr2:74863572 | G | A | 89 | a0001c0001t0002g0008 a0001c0001t0002g0018 a0001c0001t0002g0033 others(86): Show |
90 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.227-4064G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74863572 | |||||||
chr2:74863632 | G | A | 1 | a0003c0003t0003g0286 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.227-4004G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74863632 | |||||||
chr2:74863638 | C | T | 83 | a0001c0001t0002g0008 a0001c0001t0002g0018 a0001c0001t0002g0033 others(80): Show |
84 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.227-3998C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74863638 | |||||||
chr2:74863639 | G | A | 37 | a0001c0001t0002g0003 a0001c0001t0002g0073 a0001c0001t0002g0131 others(34): Show |
37 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.227-3997G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74863639 | |||||||
chr2:74863653 | A | C | 1 | a0001c0014t0043g0345 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.227-3983A>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74863653 | |||||||
chr2:74863771 | T | A | 1 | a0001c0002t0001g0195 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.227-3865T>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74863771 | |||||||
chr2:74863789 | G | T | 2 | a0002c0004t0006g0292 a0002c0007t0016g0224 |
2 | HG02723.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.227-3847G>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74863789 | |||||||
chr2:74863827 | C | A | 1 | a0002c0004t0010g0004 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.227-3809C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74863827 | |||||||
chr2:74864074 | G | A | 83 | a0001c0001t0002g0008 a0001c0001t0002g0018 a0001c0001t0002g0033 others(80): Show |
84 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.227-3562G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74864074 | |||||||
chr2:74864145 | C | G | 83 | a0001c0001t0002g0008 a0001c0001t0002g0018 a0001c0001t0002g0033 others(80): Show |
84 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.227-3491C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74864145 | |||||||
chr2:74864238 | G | A | 14 | a0001c0001t0002g0170 a0001c0001t0006g0357 a0001c0009t0015g0358 others(11): Show |
14 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.227-3398G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74864238 | |||||||
chr2:74864514 | GT | G | 136 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0018 others(133): Show |
137 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.227-3112delT | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 74864514 | ||||||
chr2:74864567 | C | T | 96 | a0001c0001t0002g0074 a0001c0001t0002g0080 a0001c0001t0002g0140 others(93): Show |
100 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.227-3069C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74864567 | |||||||
chr2:74864568 | G | A | 1 | a0002c0021t0006g0215 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.227-3068G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74864568 | |||||||
chr2:74864612 | T | A | 1 | a0002c0007t0010g0249 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.227-3024T>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74864612 | |||||||
chr2:74864679 | G | A | 136 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0018 others(133): Show |
137 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.227-2957G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74864679 | |||||||
chr2:74864779 | A | T | 177 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0018 others(174): Show |
178 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.227-2857A>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74864779 | |||||||
chr2:74864823 | T | C | 12 | a0001c0001t0007g0319 a0001c0001t0007g0325 a0001c0006t0031g0324 others(9): Show |
12 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.227-2813T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74864823 | |||||||
chr2:74864850 | C | T | 1 | a0001c0002t0001g0127 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.227-2786C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74864850 | |||||||
chr2:74864865 | C | T | 1 | a0003c0003t0042g0020 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.227-2771C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74864865 | |||||||
chr2:74864959 | GCTGCTGA others(2314): Show |
G | 1 | a0002c0023t0006g0374 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.227-2675_227-355de others(1): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 74864959 | ||||||
chr2:74865004 | G | A | 4 | a0001c0001t0002g0212 a0001c0002t0001g0055 a0001c0002t0049g0293 others(1): Show |
4 | HG02027.hp1 HG02056.hp2 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.227-2632G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74865004 | |||||||
chr2:74865048 | G | A | 1 | a0004c0016t0012g0347 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.227-2588G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74865048 | |||||||
chr2:74865413 | C | T | 2 | a0001c0001t0002g0299 a0001c0001t0002g0300 |
2 | HG02027.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.227-2223C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74865413 | |||||||
chr2:74865434 | C | T | 8 | a0001c0024t0003g0183 a0002c0004t0009g0326 a0002c0004t0019g0342 others(5): Show |
8 | HG01243.hp1 HG02896.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.227-2202C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74865434 | |||||||
chr2:74865441 | C | T | 1 | a0002c0007t0016g0201 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.227-2195C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74865441 | |||||||
chr2:74865647 | A | G | 17 | a0001c0001t0002g0189 a0001c0001t0007g0319 a0001c0001t0007g0325 others(14): Show |
17 | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.227-1989A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74865647 | |||||||
chr2:74865706 | T | A | 1 | a0002c0035t0012g0346 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.227-1930T>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74865706 | |||||||
chr2:74865732 | C | T | 1 | a0001c0005t0001g0094 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.227-1904C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74865732 | |||||||
chr2:74865845 | C | T | 77 | a0001c0001t0002g0008 a0001c0001t0002g0018 a0001c0001t0002g0045 others(74): Show |
78 | HG00280.hp2 HG00423.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.227-1791C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74865845 | |||||||
chr2:74865869 | C | G | 83 | a0001c0001t0002g0008 a0001c0001t0002g0018 a0001c0001t0002g0045 others(80): Show |
84 | HG00280.hp2 HG00423.hp1 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.227-1767C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74865869 | |||||||
chr2:74865881 | T | C | 16 | a0001c0001t0002g0170 a0001c0001t0002g0222 a0001c0001t0006g0357 others(13): Show |
16 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.227-1755T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74865881 | |||||||
chr2:74866062 | G | A | 2 | a0001c0037t0022g0364 a0002c0035t0012g0346 |
2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.227-1574G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74866062 | |||||||
chr2:74866070 | C | T | 6 | a0001c0011t0020g0348 a0001c0037t0022g0364 a0002c0007t0016g0201 others(3): Show |
6 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.227-1566C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74866070 | |||||||
chr2:74866074 | G | A | 77 | a0001c0001t0002g0008 a0001c0001t0002g0018 a0001c0001t0002g0045 others(74): Show |
78 | HG00280.hp2 HG00423.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.227-1562G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74866074 | |||||||
chr2:74866120 | C | T | 6 | a0001c0011t0020g0348 a0001c0037t0022g0364 a0002c0007t0016g0201 others(3): Show |
6 | HG00735.hp1 HG01243.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.227-1516C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74866120 | |||||||
chr2:74866243 | T | G | 1 | a0001c0001t0002g0301 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.227-1393T>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74866243 | |||||||
chr2:74866283 | A | G | 10 | a0001c0001t0002g0074 a0001c0001t0002g0273 a0001c0001t0003g0277 others(7): Show |
10 | HG00423.hp2 HG02083.hp2 NA18955.hp1 others(7): Show |
intron_variant | MODIFIER | c.227-1353A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74866283 | |||||||
chr2:74866304 | G | C | 77 | a0001c0001t0002g0008 a0001c0001t0002g0018 a0001c0001t0002g0045 others(74): Show |
78 | HG00280.hp2 HG00423.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.227-1332G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74866304 | |||||||
chr2:74866341 | A | G | 83 | a0001c0001t0002g0008 a0001c0001t0002g0018 a0001c0001t0002g0045 others(80): Show |
84 | HG00280.hp2 HG00423.hp1 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.227-1295A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74866341 | |||||||
chr2:74866344 | C | G | 2 | a0003c0003t0003g0202 a0003c0003t0003g0291 |
2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.227-1292C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74866344 | |||||||
chr2:74866503 | G | C | 77 | a0001c0001t0002g0008 a0001c0001t0002g0018 a0001c0001t0002g0045 others(74): Show |
78 | HG00280.hp2 HG00423.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.227-1133G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74866503 | |||||||
chr2:74866504 | C | T | 1 | a0001c0001t0005g0141 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.227-1132C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74866504 | |||||||
chr2:74866509 | C | T | 1 | a0001c0030t0007g0387 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.227-1127C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74866509 | |||||||
chr2:74866649 | G | C | 1 | a0001c0001t0002g0046 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.227-987G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74866649 | |||||||
chr2:74866686 | T | C | 1 | a0001c0001t0002g0045 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.227-950T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74866686 | |||||||
chr2:74866854 | T | A | 79 | a0001c0001t0002g0008 a0001c0001t0002g0018 a0001c0001t0002g0045 others(76): Show |
80 | HG00280.hp2 HG00423.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.227-782T>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74866854 | |||||||
chr2:74866886 | G | A | 102 | a0001c0001t0002g0008 a0001c0001t0002g0018 a0001c0001t0002g0045 others(99): Show |
103 | HG00280.hp2 HG00423.hp1 HG00639.hp1 others(100): Show |
intron_variant | MODIFIER | c.227-750G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74866886 | |||||||
chr2:74866998 | C | T | 79 | a0001c0001t0002g0008 a0001c0001t0002g0018 a0001c0001t0002g0045 others(76): Show |
80 | HG00280.hp2 HG00423.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.227-638C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74866998 | |||||||
chr2:74867092 | G | A | 4 | a0001c0011t0020g0348 a0002c0007t0016g0201 a0004c0008t0010g0349 others(1): Show |
4 | HG00735.hp1 HG02647.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.227-544G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74867092 | |||||||
chr2:74867131 | C | T | 76 | a0001c0001t0002g0008 a0001c0001t0002g0018 a0001c0001t0002g0045 others(73): Show |
77 | HG00280.hp2 HG00423.hp1 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.227-505C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74867131 | |||||||
chr2:74867174 | G | A | 6 | a0001c0001t0002g0093 a0001c0001t0002g0112 a0001c0006t0021g0109 others(3): Show |
6 | HG02145.hp1 HG02559.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.227-462G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74867174 | |||||||
chr2:74867176 | C | G | 77 | a0001c0001t0002g0008 a0001c0001t0002g0018 a0001c0001t0002g0045 others(74): Show |
78 | HG00280.hp2 HG00423.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.227-460C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74867176 | |||||||
chr2:74867188 | T | C | 77 | a0001c0001t0002g0008 a0001c0001t0002g0018 a0001c0001t0002g0045 others(74): Show |
78 | HG00280.hp2 HG00423.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.227-448T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74867188 | |||||||
chr2:74867196 | A | G | 2 | a0001c0037t0022g0364 a0002c0035t0012g0346 |
2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.227-440A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74867196 | |||||||
chr2:74867219 | C | T | 1 | a0001c0001t0002g0125 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.227-417C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74867219 | |||||||
chr2:74867294 | G | A | 107 | a0001c0001t0002g0008 a0001c0001t0002g0018 a0001c0001t0002g0045 others(104): Show |
108 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.227-342G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74867294 | |||||||
chr2:74867310 | G | C | 3 | a0001c0002t0001g0378 a0001c0002t0001g0379 a0001c0002t0001g0380 |
3 | HG01257.hp1 HG01258.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.227-326G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74867310 | |||||||
chr2:74867399 | T | TAA | 13 | a0001c0001t0002g0170 a0001c0001t0006g0357 a0001c0009t0015g0358 others(10): Show |
13 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.227-228_227-227dup others(2): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr2 | 74867399 | ||||||
chr2:74867577 | C | T | 1 | a0001c0002t0001g0051 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.227-59C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74867577 | |||||||
chr2:74867619 | C | T | 1 | a0003c0003t0003g0154 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.227-17C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 2/17 | chr2 | 74867619 | |||||||
chr2:74867853 | C | G | 1 | a0002c0007t0016g0123 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.375+69C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74867853 | |||||||
chr2:74867976 | G | GTA | 41 | a0001c0001t0002g0107 a0001c0001t0002g0132 a0001c0001t0002g0205 others(38): Show |
42 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(39): Show |
intron_variant | MODIFIER | c.375+193_375+194dup others(2): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr2 | 74867976 | ||||||
chr2:74868044 | T | C | 1 | a0001c0001t0002g0155 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.375+260T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74868044 | |||||||
chr2:74868052 | C | T | 3 | a0001c0006t0007g0309 a0001c0006t0007g0330 a0003c0003t0008g0308 |
3 | HG00323.hp2 HG03490.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.375+268C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74868052 | |||||||
chr2:74868096 | C | T | 1 | a0001c0001t0002g0125 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.375+312C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74868096 | |||||||
chr2:74868164 | T | C | 1 | a0002c0004t0010g0004 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.375+380T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74868164 | |||||||
chr2:74868293 | C | T | 1 | a0001c0002t0001g0079 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.375+509C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74868293 | |||||||
chr2:74868682 | G | A | 39 | a0001c0001t0002g0131 a0001c0001t0002g0170 a0001c0001t0002g0182 others(36): Show |
39 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.375+898G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74868682 | |||||||
chr2:74868706 | C | T | 11 | a0001c0001t0002g0222 a0001c0009t0034g0184 a0001c0024t0003g0183 others(8): Show |
11 | HG01243.hp1 HG02896.hp1 HG03209.hp1 others(8): Show |
intron_variant | MODIFIER | c.375+922C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74868706 | |||||||
chr2:74868717 | A | G | 1 | a0001c0005t0001g0030 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.375+933A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74868717 | |||||||
chr2:74868765 | A | C | 15 | a0001c0001t0002g0222 a0001c0002t0001g0005 a0001c0002t0011g0337 others(12): Show |
16 | HG01243.hp1 HG02280.hp2 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.375+981A>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74868765 | |||||||
chr2:74868817 | C | A | 5 | a0001c0011t0020g0348 a0002c0007t0016g0201 a0004c0008t0010g0349 others(2): Show |
5 | HG00735.hp1 HG02647.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.375+1033C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74868817 | |||||||
chr2:74868888 | A | G | 10 | a0001c0001t0002g0170 a0001c0001t0006g0357 a0001c0009t0015g0358 others(7): Show |
10 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.375+1104A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74868888 | |||||||
chr2:74868901 | G | C | 45 | a0001c0001t0002g0131 a0001c0001t0002g0170 a0001c0001t0002g0182 others(42): Show |
46 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.375+1117G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74868901 | |||||||
chr2:74868935 | T | C | 10 | a0001c0001t0002g0170 a0001c0001t0006g0357 a0001c0009t0015g0358 others(7): Show |
10 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.375+1151T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74868935 | |||||||
chr2:74869027 | A | G | 1 | a0003c0003t0008g0310 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.375+1243A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74869027 | |||||||
chr2:74869120 | TA | T | 10 | a0001c0001t0002g0125 a0001c0001t0002g0170 a0001c0009t0015g0358 others(7): Show |
10 | HG01081.hp2 HG01884.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.375+1347delA | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr2 | 74869120 | ||||||
chr2:74869373 | T | C | 5 | a0001c0011t0037g0245 a0001c0037t0022g0364 a0002c0035t0012g0346 others(2): Show |
5 | HG01243.hp2 HG02280.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.375+1589T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74869373 | |||||||
chr2:74869595 | C | A | 2 | a0001c0022t0001g0188 a0003c0003t0005g0122 |
2 | NA18612.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.375+1811C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74869595 | |||||||
chr2:74869616 | C | T | 1 | a0001c0001t0005g0053 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.375+1832C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74869616 | |||||||
chr2:74869617 | G | A | 4 | a0001c0002t0001g0104 a0002c0004t0006g0248 a0002c0035t0012g0346 others(1): Show |
4 | HG01192.hp1 HG01243.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.375+1833G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74869617 | |||||||
chr2:74869626 | G | A | 4 | a0001c0002t0001g0104 a0002c0004t0006g0248 a0002c0035t0012g0346 others(1): Show |
4 | HG01192.hp1 HG01243.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.375+1842G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74869626 | |||||||
chr2:74869724 | G | A | 1 | a0001c0001t0002g0074 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.375+1940G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74869724 | |||||||
chr2:74869861 | T | C | 1 | a0002c0023t0006g0374 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.375+2077T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74869861 | |||||||
chr2:74869878 | A | G | 5 | a0001c0001t0002g0107 a0001c0001t0005g0141 a0002c0004t0019g0342 others(2): Show |
5 | HG02257.hp2 HG03209.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.375+2094A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74869878 | |||||||
chr2:74869881 | G | A | 2 | a0003c0003t0003g0029 a0003c0003t0003g0332 |
2 | NA18954.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.375+2097G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74869881 | |||||||
chr2:74869982 | G | GTCTTT | 3 | a0002c0004t0018g0231 a0002c0004t0018g0320 a0004c0043t0012g0177 |
3 | HG01884.hp1 HG02257.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.375+2200_375+2204d others(7): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr2 | 74869982 | ||||||
chr2:74869989 | T | C | 2 | a0001c0011t0037g0245 a0014c0019t0001g0113 |
2 | HG02280.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.375+2205T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74869989 | |||||||
chr2:74869991 | C | T | 2 | a0001c0011t0037g0245 a0014c0019t0001g0113 |
2 | HG02280.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.375+2207C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74869991 | |||||||
chr2:74870001 | C | CT | 8 | a0001c0001t0002g0008 a0001c0001t0002g0023 a0001c0001t0002g0149 others(5): Show |
8 | HG01243.hp1 HG02055.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.375+2235dupT | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr2 | 74870001 | ||||||
chr2:74870001 | CT | C | 176 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0045 others(173): Show |
178 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.375+2235delT | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr2 | 74870001 | ||||||
chr2:74870001 | CTT | C | 8 | a0001c0002t0001g0216 a0001c0002t0001g0217 a0004c0008t0006g0105 others(5): Show |
8 | HG00735.hp1 HG01516.hp2 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.375+2234_375+2235d others(4): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr2 | 74870001 | ||||||
chr2:74870063 | C | T | 1 | a0001c0002t0001g0137 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.376-2237C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74870063 | |||||||
chr2:74870078 | G | A | 2 | a0001c0002t0001g0039 a0001c0002t0048g0175 |
2 | NA18950.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.376-2222G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74870078 | |||||||
chr2:74870146 | C | A | 1 | a0002c0021t0006g0215 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.376-2154C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74870146 | |||||||
chr2:74870177 | T | G | 1 | a0003c0003t0003g0036 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.376-2123T>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74870177 | |||||||
chr2:74870270 | G | A | 2 | a0002c0004t0010g0097 a0002c0021t0006g0215 |
2 | HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.376-2030G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74870270 | |||||||
chr2:74870428 | C | T | 1 | a0001c0012t0022g0335 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.376-1872C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74870428 | |||||||
chr2:74870477 | T | TTGCTTTT others(156): Show |
2 | a0002c0013t0009g0322 a0002c0013t0009g0323 |
2 | HG02723.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.376-1807_376-1806i others(165): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr2 | 74870477 | ||||||
chr2:74870477 | T | TTGCTTTT others(156): Show |
13 | a0001c0006t0007g0309 a0001c0006t0007g0330 a0001c0006t0021g0109 others(10): Show |
13 | HG00323.hp2 HG01243.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.376-1807_376-1806i others(165): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr2 | 74870477 | ||||||
chr2:74870477 | T | TTGCTTTT others(157): Show |
1 | a0010c0031t0003g0204 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.376-1807_376-1806i others(166): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr2 | 74870477 | ||||||
chr2:74870554 | C | CT | 17 | a0001c0001t0002g0126 a0001c0001t0002g0191 a0001c0001t0002g0200 others(14): Show |
17 | HG00423.hp2 HG00741.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.376-1725dupT | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr2 | 74870554 | ||||||
chr2:74870554 | CT | C | 21 | a0001c0001t0002g0080 a0001c0001t0002g0212 a0001c0001t0002g0343 others(18): Show |
21 | HG00423.hp1 HG00735.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.376-1725delT | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr2 | 74870554 | ||||||
chr2:74870554 | CTTT | C | 72 | a0001c0006t0007g0309 a0001c0006t0007g0330 a0001c0006t0021g0109 others(69): Show |
73 | HG00323.hp2 HG00609.hp2 HG00738.hp2 others(70): Show |
intron_variant | MODIFIER | c.376-1727_376-1725d others(5): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr2 | 74870554 | ||||||
chr2:74870558 | T | C | 48 | a0001c0009t0034g0184 a0001c0011t0020g0096 a0001c0011t0020g0348 others(45): Show |
49 | HG00609.hp2 HG02040.hp1 HG02055.hp1 others(46): Show |
intron_variant | MODIFIER | c.376-1742T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74870558 | |||||||
chr2:74870559 | T | C | 2 | a0002c0004t0018g0231 a0002c0004t0018g0320 |
2 | HG02257.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.376-1741T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74870559 | |||||||
chr2:74870597 | A | G | 4 | a0001c0011t0020g0096 a0001c0011t0020g0348 a0002c0004t0006g0248 others(1): Show |
4 | HG02486.hp1 HG02818.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.376-1703A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74870597 | |||||||
chr2:74870686 | G | A | 1 | a0001c0005t0007g0253 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.376-1614G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74870686 | |||||||
chr2:74871010 | C | T | 1 | a0001c0001t0002g0033 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.376-1290C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74871010 | |||||||
chr2:74871056 | G | A | 278 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0011 others(275): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.376-1244G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74871056 | |||||||
chr2:74871239 | G | T | 1 | a0003c0003t0003g0016 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.376-1061G>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74871239 | |||||||
chr2:74871510 | G | A | 1 | a0001c0014t0043g0345 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.376-790G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74871510 | |||||||
chr2:74871573 | T | A | 1 | a0001c0001t0002g0295 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.376-727T>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74871573 | |||||||
chr2:74871766 | G | C | 1 | a0002c0004t0006g0292 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.376-534G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74871766 | |||||||
chr2:74871780 | G | A | 1 | a0004c0043t0012g0177 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.376-520G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74871780 | |||||||
chr2:74871803 | A | G | 2 | a0003c0003t0008g0237 a0003c0003t0008g0308 |
2 | HG01516.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.376-497A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74871803 | |||||||
chr2:74871827 | C | A | 6 | a0004c0008t0006g0105 a0004c0008t0010g0111 a0004c0008t0010g0349 others(3): Show |
6 | HG00735.hp1 HG01891.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.376-473C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74871827 | |||||||
chr2:74871827 | C | G | 2 | a0001c0001t0002g0008 a0001c0001t0002g0149 |
2 | HG03831.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.376-473C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74871827 | |||||||
chr2:74871959 | C | T | 1 | a0002c0036t0004g0012 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.376-341C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74871959 | |||||||
chr2:74872095 | G | A | 1 | a0002c0023t0006g0374 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.376-205G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74872095 | |||||||
chr2:74872110 | C | G | 47 | a0001c0011t0020g0096 a0001c0011t0020g0348 a0001c0011t0037g0245 others(44): Show |
48 | HG00609.hp2 HG02040.hp1 HG02055.hp1 others(45): Show |
intron_variant | MODIFIER | c.376-190C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74872110 | |||||||
chr2:74872197 | T | G | 1 | a0002c0023t0006g0374 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.376-103T>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74872197 | |||||||
chr2:74872254 | T | C | 75 | a0002c0004t0018g0320 a0003c0003t0002g0294 a0003c0003t0003g0016 others(72): Show |
75 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.376-46T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 3/17 | chr2 | 74872254 | |||||||
chr2:74872567 | G | A | 56 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0037 others(53): Show |
57 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.495+148G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 4/17 | chr2 | 74872567 | |||||||
chr2:74872571 | G | C | 1 | a0002c0004t0006g0092 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.495+152G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 4/17 | chr2 | 74872571 | |||||||
chr2:74872705 | A | G | 75 | a0001c0011t0037g0245 a0003c0003t0002g0294 a0003c0003t0003g0016 others(72): Show |
75 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.495+286A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 4/17 | chr2 | 74872705 | |||||||
chr2:74872745 | T | C | 75 | a0001c0011t0037g0245 a0003c0003t0002g0294 a0003c0003t0003g0016 others(72): Show |
75 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.495+326T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 4/17 | chr2 | 74872745 | |||||||
chr2:74872981 | A | G | 23 | a0001c0006t0007g0309 a0001c0006t0007g0330 a0001c0006t0021g0109 others(20): Show |
23 | HG00323.hp2 HG01243.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.496-295A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 4/17 | chr2 | 74872981 | |||||||
chr2:74872991 | C | G | 7 | a0002c0004t0018g0320 a0004c0008t0006g0105 a0004c0008t0010g0111 others(4): Show |
7 | HG00735.hp1 HG01891.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.496-285C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 4/17 | chr2 | 74872991 | |||||||
chr2:74873174 | C | T | 6 | a0004c0008t0006g0105 a0004c0008t0010g0111 a0004c0008t0010g0349 others(3): Show |
6 | HG00735.hp1 HG01891.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.496-102C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 4/17 | chr2 | 74873174 | |||||||
chr2:74873223 | G | T | 1 | a0004c0041t0029g0264 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.496-53G>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 4/17 | chr2 | 74873223 | |||||||
chr2:74873380 | G | A | 2 | a0001c0009t0034g0184 a0002c0025t0024g0268 |
2 | HG01109.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.591+9G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 5/17 | chr2 | 74873380 | |||||||
chr2:74873381 | G | A | 3 | a0001c0011t0020g0096 a0001c0011t0020g0348 a0002c0004t0009g0321 |
3 | HG02486.hp1 HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.591+10G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 5/17 | chr2 | 74873381 | |||||||
chr2:74873687 | A | C | 7 | a0004c0008t0006g0105 a0004c0008t0010g0111 a0004c0008t0010g0349 others(4): Show |
7 | HG00735.hp1 HG00738.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.592-157A>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 5/17 | chr2 | 74873687 | |||||||
chr2:74873724 | GA | G | 4 | a0002c0004t0010g0097 a0002c0004t0018g0231 a0002c0004t0018g0320 others(1): Show |
4 | HG02257.hp1 HG02280.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.592-119delA | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 5/17 | chr2 | 74873724 | |||||||
chr2:74873730 | G | A | 1 | a0004c0041t0029g0264 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.592-114G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 5/17 | chr2 | 74873730 | |||||||
chr2:74873746 | A | AAGAAGGA others(5): Show |
42 | a0001c0011t0020g0096 a0001c0011t0020g0348 a0001c0012t0021g0356 others(39): Show |
43 | HG00609.hp2 HG00738.hp2 HG02055.hp1 others(40): Show |
intron_variant | MODIFIER | c.592-96_592-95insAA others(10): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr2 | 74873746 | ||||||
chr2:74873746 | A | AAGAAGGA others(8): Show |
7 | a0002c0004t0009g0115 a0004c0008t0006g0105 a0004c0008t0010g0111 others(4): Show |
7 | HG00735.hp1 HG01891.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.592-96_592-95insAA others(13): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr2 | 74873746 | ||||||
chr2:74873746 | A | AAGG | 7 | a0001c0014t0043g0345 a0002c0004t0010g0097 a0002c0004t0023g0244 others(4): Show |
7 | HG01257.hp2 HG02451.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.592-77_592-75dupGA others(1): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr2 | 74873746 | ||||||
chr2:74873746 | A | AAGGAGG | 93 | a0001c0006t0007g0309 a0001c0006t0007g0330 a0001c0006t0021g0109 others(90): Show |
93 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.592-80_592-75dupGA others(4): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr2 | 74873746 | ||||||
chr2:74873746 | A | AAGGAGGA others(5): Show |
2 | a0002c0004t0004g0366 a0002c0004t0026g0370 |
2 | HG02040.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.592-86_592-75dupGA others(10): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr2 | 74873746 | ||||||
chr2:74873746 | A | AAGGAGGA others(8): Show |
1 | a0002c0010t0006g0233 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.592-89_592-75dupGA others(13): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr2 | 74873746 | ||||||
chr2:74873992 | G | A | 1 | a0001c0012t0021g0356 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.691+49G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 6/17 | chr2 | 74873992 | |||||||
chr2:74874069 | C | A | 1 | a0001c0006t0031g0324 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.691+126C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 6/17 | chr2 | 74874069 | |||||||
chr2:74874228 | G | A | 1 | a0001c0012t0021g0356 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.692-38G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 6/17 | chr2 | 74874228 | |||||||
chr2:74874237 | G | A | 36 | a0001c0012t0021g0356 a0001c0022t0001g0188 a0002c0004t0004g0013 others(33): Show |
36 | HG00609.hp2 HG02040.hp1 HG02451.hp2 others(33): Show |
intron_variant | MODIFIER | c.692-29G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 6/17 | chr2 | 74874237 | |||||||
chr2:74874517 | G | A | 1 | a0001c0005t0003g0181 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.875+68G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74874517 | |||||||
chr2:74874518 | C | A | 1 | a0001c0005t0003g0181 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.875+69C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74874518 | |||||||
chr2:74874523 | G | C | 1 | a0001c0002t0001g0076 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.875+74G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74874523 | |||||||
chr2:74874632 | G | A | 3 | a0001c0006t0007g0309 a0001c0006t0007g0330 a0010c0031t0003g0204 |
3 | HG00323.hp2 HG03453.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.875+183G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74874632 | |||||||
chr2:74874766 | G | A | 1 | a0001c0024t0003g0183 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.875+317G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74874766 | |||||||
chr2:74874793 | G | A | 1 | a0004c0041t0029g0264 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.875+344G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74874793 | |||||||
chr2:74875003 | A | G | 72 | a0001c0006t0007g0309 a0001c0006t0007g0330 a0001c0006t0021g0109 others(69): Show |
73 | HG00323.hp2 HG00609.hp2 HG01243.hp1 others(70): Show |
intron_variant | MODIFIER | c.875+554A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74875003 | |||||||
chr2:74875049 | A | G | 94 | a0001c0006t0007g0309 a0001c0006t0007g0330 a0001c0006t0021g0109 others(91): Show |
94 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.875+600A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74875049 | |||||||
chr2:74875112 | C | G | 27 | a0001c0006t0007g0309 a0001c0006t0007g0330 a0001c0006t0021g0109 others(24): Show |
27 | HG00323.hp2 HG00735.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.875+663C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74875112 | |||||||
chr2:74875206 | G | C | 4 | a0001c0009t0034g0184 a0002c0004t0001g0114 a0002c0004t0044g0100 others(1): Show |
4 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.875+757G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74875206 | |||||||
chr2:74875209 | C | A | 1 | a0001c0001t0002g0052 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.875+760C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74875209 | |||||||
chr2:74875226 | CTG | C | 5 | a0001c0002t0001g0083 a0001c0002t0001g0119 a0001c0002t0001g0120 others(2): Show |
5 | NA18953.hp2 NA18957.hp1 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.875+779_875+780del others(2): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 74875226 | ||||||
chr2:74875308 | C | T | 1 | a0001c0001t0002g0136 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.875+859C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74875308 | |||||||
chr2:74875327 | G | GT | 212 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0018 others(209): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.875+897dupT | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 74875327 | ||||||
chr2:74875327 | G | GTT | 31 | a0001c0001t0002g0008 a0001c0001t0002g0023 a0001c0001t0002g0046 others(28): Show |
31 | HG00735.hp1 HG01243.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.875+896_875+897dup others(2): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 74875327 | ||||||
chr2:74875327 | G | T | 1 | a0004c0043t0012g0177 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.875+878G>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74875327 | |||||||
chr2:74875327 | GT | G | 11 | a0001c0002t0001g0039 a0001c0009t0015g0234 a0001c0009t0015g0358 others(8): Show |
11 | HG01257.hp2 HG02055.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.875+897delT | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 74875327 | ||||||
chr2:74875365 | G | C | 6 | a0004c0008t0006g0105 a0004c0008t0010g0111 a0004c0008t0010g0349 others(3): Show |
6 | HG00735.hp1 HG01891.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.875+916G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74875365 | |||||||
chr2:74875379 | T | A | 1 | a0002c0004t0004g0296 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.875+930T>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74875379 | |||||||
chr2:74875397 | T | C | 153 | a0001c0006t0007g0309 a0001c0006t0007g0330 a0001c0006t0021g0109 others(150): Show |
154 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.875+948T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74875397 | |||||||
chr2:74875435 | TCTCCTAC others(5): Show |
T | 3 | a0003c0003t0003g0059 a0003c0003t0008g0384 a0003c0044t0001g0077 |
3 | HG01099.hp1 HG01255.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.875+989_875+1000de others(13): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | 74875435 | ||||||
chr2:74875473 | C | T | 1 | a0001c0024t0003g0183 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.875+1024C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74875473 | |||||||
chr2:74875567 | G | A | 1 | a0002c0021t0006g0215 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.875+1118G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74875567 | |||||||
chr2:74875571 | C | T | 32 | a0001c0006t0007g0309 a0001c0006t0007g0330 a0001c0006t0021g0109 others(29): Show |
32 | HG00323.hp2 HG01243.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.875+1122C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74875571 | |||||||
chr2:74875656 | G | T | 6 | a0004c0008t0006g0105 a0004c0008t0010g0111 a0004c0008t0010g0349 others(3): Show |
6 | HG00735.hp1 HG01891.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.875+1207G>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74875656 | |||||||
chr2:74875821 | C | T | 6 | a0001c0011t0020g0096 a0001c0011t0020g0348 a0002c0004t0006g0248 others(3): Show |
6 | HG02486.hp1 HG02723.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.876-1345C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74875821 | |||||||
chr2:74875837 | C | T | 3 | a0001c0002t0001g0005 a0001c0002t0001g0104 a0001c0002t0011g0337 |
4 | HG01192.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.876-1329C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74875837 | |||||||
chr2:74875949 | C | T | 1 | a0003c0003t0003g0031 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.876-1217C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74875949 | |||||||
chr2:74876090 | T | A | 1 | a0004c0041t0029g0264 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.876-1076T>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74876090 | |||||||
chr2:74876139 | G | A | 1 | a0014c0019t0001g0113 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.876-1027G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74876139 | |||||||
chr2:74876195 | C | T | 54 | a0003c0003t0003g0016 a0003c0003t0003g0029 a0003c0003t0003g0031 others(51): Show |
54 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.876-971C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74876195 | |||||||
chr2:74876248 | A | G | 1 | a0004c0041t0029g0264 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.876-918A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74876248 | |||||||
chr2:74876296 | C | T | 51 | a0001c0009t0015g0234 a0001c0009t0015g0358 a0001c0009t0015g0360 others(48): Show |
52 | HG00609.hp2 HG01257.hp2 HG02040.hp1 others(49): Show |
intron_variant | MODIFIER | c.876-870C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74876296 | |||||||
chr2:74876462 | C | A | 1 | a0001c0002t0049g0293 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.876-704C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74876462 | |||||||
chr2:74876515 | C | A | 1 | a0003c0015t0001g0064 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.876-651C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74876515 | |||||||
chr2:74876561 | G | A | 4 | a0001c0001t0002g0344 a0001c0006t0007g0309 a0001c0006t0007g0330 others(1): Show |
4 | HG00323.hp2 HG00738.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.876-605G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74876561 | |||||||
chr2:74876605 | C | G | 1 | a0001c0011t0020g0096 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.876-561C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74876605 | |||||||
chr2:74876671 | G | A | 1 | a0004c0008t0010g0353 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.876-495G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74876671 | |||||||
chr2:74876704 | C | T | 2 | a0002c0004t0001g0114 a0002c0004t0044g0100 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.876-462C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74876704 | |||||||
chr2:74876762 | A | G | 2 | a0003c0003t0003g0202 a0003c0003t0003g0291 |
2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.876-404A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74876762 | |||||||
chr2:74876807 | A | C | 1 | a0003c0003t0003g0377 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.876-359A>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74876807 | |||||||
chr2:74876825 | A | G | 6 | a0004c0008t0006g0105 a0004c0008t0010g0111 a0004c0008t0010g0349 others(3): Show |
6 | HG00735.hp1 HG01891.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.876-341A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74876825 | |||||||
chr2:74876868 | C | T | 45 | a0001c0001t0002g0003 a0001c0001t0002g0037 a0001c0001t0002g0048 others(42): Show |
45 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.876-298C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74876868 | |||||||
chr2:74876889 | C | A | 7 | a0001c0009t0034g0184 a0002c0004t0001g0114 a0002c0004t0044g0100 others(4): Show |
7 | HG01109.hp1 HG01891.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.876-277C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74876889 | |||||||
chr2:74876892 | G | T | 1 | a0001c0001t0002g0230 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.876-274G>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74876892 | |||||||
chr2:74876911 | T | C | 2 | a0001c0022t0001g0188 a0002c0004t0004g0318 |
2 | NA18612.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.876-255T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74876911 | |||||||
chr2:74876939 | T | A | 7 | a0001c0009t0034g0184 a0002c0004t0001g0114 a0002c0004t0044g0100 others(4): Show |
7 | HG01109.hp1 HG01891.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.876-227T>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74876939 | |||||||
chr2:74876992 | A | G | 78 | a0001c0009t0034g0184 a0001c0011t0020g0096 a0001c0011t0020g0348 others(75): Show |
78 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.876-174A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74876992 | |||||||
chr2:74877091 | A | G | 78 | a0001c0009t0034g0184 a0001c0011t0020g0096 a0001c0011t0020g0348 others(75): Show |
78 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.876-75A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74877091 | |||||||
chr2:74877115 | G | A | 3 | a0001c0001t0002g0189 a0001c0001t0002g0222 a0001c0006t0003g0359 |
3 | HG03453.hp2 NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.876-51G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 7/17 | chr2 | 74877115 | |||||||
chr2:74877342 | C | G | 1 | a0002c0004t0001g0114 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1031+21C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74877342 | |||||||
chr2:74877403 | C | T | 1 | a0010c0031t0003g0204 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1031+82C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74877403 | |||||||
chr2:74877443 | A | G | 74 | a0001c0009t0034g0184 a0001c0011t0037g0245 a0002c0004t0001g0114 others(71): Show |
74 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.1031+122A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74877443 | |||||||
chr2:74877448 | G | A | 67 | a0001c0011t0037g0245 a0002c0013t0009g0322 a0002c0013t0009g0323 others(64): Show |
67 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.1031+127G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74877448 | |||||||
chr2:74877500 | T | A | 1 | a0001c0012t0021g0356 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1031+179T>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74877500 | |||||||
chr2:74877501 | C | T | 3 | a0001c0001t0002g0008 a0001c0001t0002g0023 a0001c0001t0002g0149 |
3 | HG03831.hp1 HG04115.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1031+180C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74877501 | |||||||
chr2:74877543 | A | G | 1 | a0003c0003t0003g0279 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1031+222A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74877543 | |||||||
chr2:74877546 | G | A | 2 | a0001c0002t0001g0278 a0001c0005t0001g0143 |
2 | NA18961.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.1031+225G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74877546 | |||||||
chr2:74877620 | G | A | 5 | a0001c0009t0015g0234 a0001c0009t0015g0358 a0001c0009t0015g0360 others(2): Show |
5 | HG01257.hp2 HG02055.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1031+299G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74877620 | |||||||
chr2:74877719 | C | A | 1 | a0002c0004t0044g0100 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1031+398C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74877719 | |||||||
chr2:74877752 | C | T | 2 | a0002c0013t0009g0322 a0002c0013t0009g0323 |
2 | HG02723.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1031+431C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74877752 | |||||||
chr2:74877800 | C | T | 1 | a0003c0003t0003g0062 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1031+479C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74877800 | |||||||
chr2:74877818 | G | A | 66 | a0001c0011t0037g0245 a0002c0013t0009g0322 a0002c0013t0009g0323 others(63): Show |
66 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.1031+497G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74877818 | |||||||
chr2:74877836 | G | A | 1 | a0003c0003t0003g0146 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1031+515G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74877836 | |||||||
chr2:74877890 | C | G | 1 | a0003c0003t0008g0310 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1031+569C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74877890 | |||||||
chr2:74877920 | A | G | 4 | a0002c0004t0010g0097 a0002c0004t0018g0231 a0002c0004t0018g0320 others(1): Show |
4 | HG02257.hp1 HG02280.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1031+599A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74877920 | |||||||
chr2:74877963 | T | A | 1 | a0001c0001t0002g0023 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1031+642T>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74877963 | |||||||
chr2:74877985 | T | G | 2 | a0001c0002t0001g0075 a0001c0002t0001g0198 |
2 | HG00423.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.1031+664T>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74877985 | |||||||
chr2:74878124 | C | A | 1 | a0001c0037t0022g0364 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1032-564C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74878124 | |||||||
chr2:74878165 | A | T | 1 | a0001c0002t0001g0055 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1032-523A>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74878165 | |||||||
chr2:74878235 | G | A | 1 | a0013c0028t0001g0172 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1032-453G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74878235 | |||||||
chr2:74878302 | G | A | 2 | a0002c0013t0009g0322 a0002c0013t0009g0323 |
2 | HG02723.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1032-386G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74878302 | |||||||
chr2:74878334 | G | C | 1 | a0001c0001t0002g0046 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1032-354G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74878334 | |||||||
chr2:74878377 | A | T | 1 | a0001c0001t0006g0357 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1032-311A>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74878377 | |||||||
chr2:74878380 | A | G | 1 | a0001c0001t0005g0116 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1032-308A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74878380 | |||||||
chr2:74878381 | G | A | 1 | a0001c0001t0005g0116 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1032-307G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74878381 | |||||||
chr2:74878404 | C | T | 12 | a0001c0006t0021g0109 a0001c0006t0031g0324 a0001c0037t0022g0364 others(9): Show |
12 | HG01243.hp1 HG01243.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1032-284C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74878404 | |||||||
chr2:74878413 | C | CTG | 4 | a0001c0001t0002g0093 a0001c0001t0002g0112 a0001c0002t0011g0193 others(1): Show |
4 | HG01106.hp1 HG02738.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1032-250_1032-249d others(4): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr2 | 74878413 | ||||||
chr2:74878413 | CTG | C | 7 | a0001c0001t0002g0052 a0001c0001t0002g0170 a0001c0002t0001g0153 others(4): Show |
7 | HG01433.hp1 HG02257.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1032-250_1032-249d others(4): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr2 | 74878413 | ||||||
chr2:74878413 | CTGTG | C | 120 | a0001c0001t0002g0018 a0001c0001t0002g0023 a0001c0001t0002g0038 others(117): Show |
121 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.1032-252_1032-249d others(6): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr2 | 74878413 | ||||||
chr2:74878413 | CTGTGTG | C | 57 | a0003c0003t0003g0016 a0003c0003t0003g0029 a0003c0003t0003g0031 others(54): Show |
57 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.1032-254_1032-249d others(8): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr2 | 74878413 | ||||||
chr2:74878413 | CTGTGTGT others(1): Show |
C | 7 | a0003c0003t0003g0062 a0004c0008t0006g0105 a0004c0008t0010g0111 others(4): Show |
7 | HG00735.hp1 HG01891.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1032-256_1032-249d others(10): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr2 | 74878413 | ||||||
chr2:74878413 | CTGTGTGT others(9): Show |
C | 2 | a0001c0001t0002g0008 a0001c0001t0002g0149 |
2 | HG03831.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1032-264_1032-249d others(18): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr2 | 74878413 | ||||||
chr2:74878420 | TGTGTGTG others(31): Show |
T | 2 | a0002c0013t0009g0322 a0002c0013t0009g0323 |
2 | HG02723.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1032-256_1032-219d others(40): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr2 | 74878420 | ||||||
chr2:74878432 | T | TGTGTGTG others(21): Show |
2 | a0002c0004t0010g0097 a0002c0021t0006g0215 |
2 | HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1032-246_1032-245i others(30): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr2 | 74878432 | ||||||
chr2:74878438 | T | C | 3 | a0001c0014t0001g0078 a0001c0039t0001g0056 a0003c0003t0002g0294 |
3 | HG00639.hp1 HG01261.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.1032-250T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74878438 | |||||||
chr2:74878441 | G | A | 16 | a0001c0006t0007g0309 a0001c0006t0007g0330 a0001c0006t0021g0109 others(13): Show |
16 | HG00323.hp2 HG00738.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.1032-247G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74878441 | |||||||
chr2:74878453 | G | A | 2 | a0003c0003t0003g0241 a0003c0003t0008g0383 |
2 | HG01123.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1032-235G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74878453 | |||||||
chr2:74878457 | G | A | 2 | a0001c0001t0002g0301 a0001c0001t0007g0265 |
2 | HG00673.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.1032-231G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74878457 | |||||||
chr2:74878458 | C | T | 1 | a0002c0004t0004g0334 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1032-230C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74878458 | |||||||
chr2:74878459 | G | A | 1 | a0002c0004t0018g0231 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1032-229G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74878459 | |||||||
chr2:74878561 | A | G | 3 | a0002c0023t0006g0374 a0006c0027t0039g0350 a0013c0028t0001g0172 |
3 | HG01891.hp1 HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1032-127A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74878561 | |||||||
chr2:74878579 | C | T | 4 | a0001c0009t0034g0184 a0002c0004t0001g0114 a0002c0004t0044g0100 others(1): Show |
4 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1032-109C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74878579 | |||||||
chr2:74878583 | G | A | 3 | a0002c0023t0006g0374 a0006c0027t0039g0350 a0013c0028t0001g0172 |
3 | HG01891.hp1 HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1032-105G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74878583 | |||||||
chr2:74878671 | A | G | 382 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0011 others(379): Show |
388 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(385): Show |
intron_variant | MODIFIER | c.1032-17A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 8/17 | chr2 | 74878671 | |||||||
chr2:74879026 | G | T | 2 | a0002c0004t0010g0097 a0002c0021t0006g0215 |
2 | HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1265+105G>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 9/17 | chr2 | 74879026 | |||||||
chr2:74879193 | G | A | 3 | a0004c0008t0009g0213 a0004c0016t0012g0347 a0004c0016t0012g0355 |
3 | HG03225.hp1 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1265+272G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 9/17 | chr2 | 74879193 | |||||||
chr2:74879208 | C | T | 1 | a0001c0012t0021g0356 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1265+287C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 9/17 | chr2 | 74879208 | |||||||
chr2:74879314 | T | C | 150 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0011 others(147): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.1265+393T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 9/17 | chr2 | 74879314 | |||||||
chr2:74879542 | T | C | 2 | a0004c0018t0024g0223 a0004c0018t0045g0246 |
2 | HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1265+621T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 9/17 | chr2 | 74879542 | |||||||
chr2:74879543 | C | T | 1 | a0001c0001t0007g0325 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1265+622C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 9/17 | chr2 | 74879543 | |||||||
chr2:74879547 | T | C | 3 | a0001c0005t0003g0022 a0001c0005t0003g0081 a0001c0005t0003g0181 |
3 | NA18960.hp2 NA18968.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.1265+626T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 9/17 | chr2 | 74879547 | |||||||
chr2:74879785 | A | G | 3 | a0001c0006t0007g0309 a0001c0006t0007g0330 a0010c0031t0003g0204 |
3 | HG00323.hp2 HG03453.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.1266-480A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 9/17 | chr2 | 74879785 | |||||||
chr2:74879899 | C | G | 1 | a0001c0002t0048g0175 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1266-366C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 9/17 | chr2 | 74879899 | |||||||
chr2:74879921 | G | T | 194 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0011 others(191): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.1266-344G>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 9/17 | chr2 | 74879921 | |||||||
chr2:74879933 | A | T | 5 | a0001c0001t0002g0238 a0001c0002t0001g0005 a0001c0002t0001g0104 others(2): Show |
6 | HG01192.hp1 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1266-332A>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 9/17 | chr2 | 74879933 | |||||||
chr2:74879997 | T | G | 1 | a0002c0004t0023g0228 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1266-268T>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 9/17 | chr2 | 74879997 | |||||||
chr2:74880074 | G | A | 15 | a0001c0006t0007g0309 a0001c0006t0007g0330 a0001c0006t0021g0109 others(12): Show |
15 | HG00323.hp2 HG01243.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.1266-191G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 9/17 | chr2 | 74880074 | |||||||
chr2:74880119 | C | G | 24 | a0001c0006t0007g0309 a0001c0006t0007g0330 a0001c0006t0021g0109 others(21): Show |
24 | HG00323.hp2 HG00735.hp1 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.1266-146C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 9/17 | chr2 | 74880119 | |||||||
chr2:74880240 | T | G | 56 | a0003c0003t0002g0294 a0003c0003t0003g0016 a0003c0003t0003g0029 others(53): Show |
56 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.1266-25T>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 9/17 | chr2 | 74880240 | |||||||
chr2:74880247 | C | T | 6 | a0001c0002t0001g0216 a0001c0002t0001g0217 a0002c0007t0010g0249 others(3): Show |
6 | HG01516.hp2 HG01517.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1266-18C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 9/17 | chr2 | 74880247 | |||||||
chr2:74880677 | G | A | 3 | a0002c0007t0016g0123 a0002c0007t0016g0201 a0002c0007t0016g0224 |
3 | HG02647.hp2 HG02723.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1570+108G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 10/17 | chr2 | 74880677 | |||||||
chr2:74880747 | G | A | 1 | a0002c0004t0019g0342 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1570+178G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 10/17 | chr2 | 74880747 | |||||||
chr2:74880748 | T | C | 1 | a0004c0043t0012g0177 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1570+179T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 10/17 | chr2 | 74880748 | |||||||
chr2:74880889 | G | A | 1 | a0002c0025t0024g0268 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1570+320G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 10/17 | chr2 | 74880889 | |||||||
chr2:74881071 | T | TTTA | 271 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0011 others(268): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.1570+506_1570+508d others(5): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr2 | 74881071 | ||||||
chr2:74881085 | A | G | 1 | a0002c0023t0006g0374 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1570+516A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 10/17 | chr2 | 74881085 | |||||||
chr2:74881094 | C | T | 4 | a0001c0001t0002g0045 a0001c0001t0002g0124 a0001c0001t0002g0176 others(1): Show |
4 | HG00280.hp2 HG01168.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.1570+525C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 10/17 | chr2 | 74881094 | |||||||
chr2:74881182 | C | T | 6 | a0004c0008t0006g0105 a0004c0008t0010g0111 a0004c0008t0010g0349 others(3): Show |
6 | HG00735.hp1 HG01891.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1571-529C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 10/17 | chr2 | 74881182 | |||||||
chr2:74881312 | A | T | 2 | a0001c0006t0021g0109 a0001c0006t0031g0324 |
2 | HG02145.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1571-399A>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 10/17 | chr2 | 74881312 | |||||||
chr2:74881463 | C | T | 5 | a0004c0008t0010g0111 a0004c0008t0010g0349 a0004c0008t0010g0351 others(2): Show |
5 | HG00735.hp1 HG01891.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1571-248C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 10/17 | chr2 | 74881463 | |||||||
chr2:74881464 | G | A | 2 | a0002c0004t0010g0004 a0002c0004t0010g0247 |
3 | HG02717.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1571-247G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 10/17 | chr2 | 74881464 | |||||||
chr2:74881570 | T | A | 2 | a0001c0006t0007g0309 a0001c0006t0007g0330 |
2 | HG00323.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.1571-141T>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 10/17 | chr2 | 74881570 | |||||||
chr2:74881617 | A | G | 70 | a0001c0011t0020g0096 a0001c0011t0020g0348 a0001c0011t0037g0245 others(67): Show |
70 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.1571-94A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 10/17 | chr2 | 74881617 | |||||||
chr2:74881936 | C | G | 1 | a0002c0004t0004g0024 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1719+77C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 11/17 | chr2 | 74881936 | |||||||
chr2:74882051 | G | A | 1 | a0003c0003t0003g0167 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1720-69G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 11/17 | chr2 | 74882051 | |||||||
chr2:74882310 | G | T | 2 | a0004c0018t0024g0223 a0004c0018t0045g0246 |
2 | HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1839+71G>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74882310 | |||||||
chr2:74882461 | T | C | 2 | a0001c0009t0034g0184 a0002c0025t0024g0268 |
2 | HG01109.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1839+222T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74882461 | |||||||
chr2:74882473 | T | A | 1 | a0004c0043t0012g0177 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1839+234T>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74882473 | |||||||
chr2:74882604 | C | CATATATA others(41): Show |
1 | a0001c0006t0003g0162 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1839+365_1839+366i others(50): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74882604 | |||||||
chr2:74882605 | T | A | 1 | a0001c0006t0003g0162 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1839+366T>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74882605 | |||||||
chr2:74882605 | T | TTA | 10 | a0001c0002t0001g0049 a0001c0002t0027g0066 a0002c0013t0009g0322 others(7): Show |
10 | HG00735.hp1 HG01109.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.1839+381_1839+382d others(4): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | ||||||
chr2:74882605 | T | TTATA | 8 | a0002c0004t0044g0100 a0002c0007t0012g0103 a0004c0008t0006g0105 others(5): Show |
8 | HG01884.hp2 HG02109.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1839+379_1839+382d others(6): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | ||||||
chr2:74882605 | T | TTATATAT others(3): Show |
1 | a0002c0004t0004g0276 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1839+373_1839+382d others(12): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | ||||||
chr2:74882605 | T | TTATATAT others(5): Show |
7 | a0002c0004t0001g0114 a0002c0007t0006g0101 a0002c0007t0006g0106 others(4): Show |
7 | HG00738.hp2 HG01243.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1839+371_1839+382d others(14): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | ||||||
chr2:74882605 | T | TTATATAT others(7): Show |
6 | a0001c0006t0002g0009 a0002c0004t0004g0024 a0002c0007t0009g0327 others(3): Show |
6 | HG03041.hp2 HG03209.hp1 NA19004.hp1 others(3): Show |
intron_variant | MODIFIER | c.1839+369_1839+382d others(16): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | ||||||
chr2:74882605 | T | TTATATAT others(9): Show |
2 | a0001c0001t0002g0131 a0001c0001t0007g0265 |
2 | HG00673.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.1839+367_1839+382d others(18): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | ||||||
chr2:74882605 | T | TTATATAT others(11): Show |
3 | a0001c0006t0007g0330 a0006c0027t0039g0350 a0011c0020t0032g0339 |
3 | HG00323.hp2 HG01891.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1839+382_1839+383i others(20): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | ||||||
chr2:74882605 | T | TTATATAT others(13): Show |
3 | a0001c0001t0002g0238 a0001c0006t0007g0309 a0002c0023t0006g0374 |
3 | HG02717.hp1 HG02895.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.1839+382_1839+383i others(22): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | ||||||
chr2:74882605 | T | TTATATAT others(15): Show |
7 | a0001c0001t0002g0148 a0002c0004t0013g0098 a0003c0003t0003g0029 others(4): Show |
7 | HG00609.hp2 HG02300.hp2 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.1839+382_1839+383i others(24): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | ||||||
chr2:74882605 | T | TTATATAT others(17): Show |
20 | a0001c0001t0002g0037 a0001c0001t0002g0192 a0001c0001t0008g0314 others(17): Show |
20 | HG00323.hp1 HG00639.hp2 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.1839+382_1839+383i others(26): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | ||||||
chr2:74882605 | T | TTATATAT others(19): Show |
29 | a0001c0001t0002g0003 a0001c0001t0002g0054 a0001c0001t0002g0072 others(26): Show |
30 | HG00438.hp2 HG01099.hp1 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.1839+382_1839+383i others(28): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | ||||||
chr2:74882605 | T | TTATATAT others(21): Show |
19 | a0001c0001t0002g0011 a0001c0001t0002g0080 a0001c0001t0002g0212 others(16): Show |
19 | HG00544.hp2 HG01256.hp2 HG02015.hp2 others(16): Show |
intron_variant | MODIFIER | c.1839+382_1839+383i others(30): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | ||||||
chr2:74882605 | T | TTATATAT others(23): Show |
11 | a0001c0001t0002g0048 a0001c0001t0002g0182 a0001c0001t0002g0194 others(8): Show |
11 | HG00408.hp2 HG01123.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.1839+382_1839+383i others(32): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | ||||||
chr2:74882605 | T | TTATATAT others(25): Show |
17 | a0001c0001t0002g0074 a0001c0001t0002g0140 a0001c0001t0002g0230 others(14): Show |
17 | HG00099.hp1 HG00673.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.1839+382_1839+383i others(34): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | ||||||
chr2:74882605 | T | TTATATAT others(27): Show |
7 | a0001c0001t0002g0222 a0001c0001t0002g0372 a0001c0001t0005g0116 others(4): Show |
7 | HG01255.hp2 HG02280.hp1 HG03669.hp1 others(4): Show |
intron_variant | MODIFIER | c.1839+382_1839+383i others(36): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | ||||||
chr2:74882605 | T | TTATATAT others(29): Show |
12 | a0001c0001t0002g0209 a0001c0001t0002g0273 a0001c0002t0001g0303 others(9): Show |
12 | HG00423.hp2 HG02055.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1839+382_1839+383i others(38): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | ||||||
chr2:74882605 | T | TTATATAT others(31): Show |
13 | a0001c0001t0002g0290 a0001c0001t0007g0325 a0001c0005t0005g0043 others(10): Show |
13 | HG00741.hp1 HG01069.hp2 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.1839+382_1839+383i others(40): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | ||||||
chr2:74882605 | T | TTATATAT others(33): Show |
11 | a0001c0001t0002g0052 a0001c0001t0002g0060 a0001c0001t0002g0093 others(8): Show |
12 | HG00140.hp2 HG00408.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.1839+382_1839+383i others(42): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | ||||||
chr2:74882605 | T | TTATATAT others(35): Show |
28 | a0001c0001t0002g0033 a0001c0001t0002g0061 a0001c0001t0002g0107 others(25): Show |
28 | HG00609.hp1 HG00642.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.1839+382_1839+383i others(44): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | ||||||
chr2:74882605 | T | TTATATAT others(37): Show |
14 | a0001c0001t0002g0018 a0001c0001t0002g0045 a0001c0001t0002g0130 others(11): Show |
14 | HG00140.hp1 HG00280.hp2 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.1839+382_1839+383i others(46): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | ||||||
chr2:74882605 | T | TTATATAT others(39): Show |
13 | a0001c0001t0002g0008 a0001c0001t0002g0038 a0001c0001t0002g0112 others(10): Show |
13 | HG02027.hp2 HG02451.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.1839+382_1839+383i others(48): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | ||||||
chr2:74882605 | T | TTATATAT others(41): Show |
9 | a0001c0001t0002g0046 a0001c0001t0002g0150 a0001c0001t0002g0170 others(6): Show |
9 | HG01123.hp2 HG02717.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1839+382_1839+383i others(50): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | ||||||
chr2:74882605 | T | TTATATAT others(43): Show |
2 | a0001c0001t0002g0023 a0002c0004t0006g0248 |
2 | HG03041.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1839+382_1839+383i others(52): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | ||||||
chr2:74882605 | T | TTATATAT others(45): Show |
7 | a0001c0001t0002g0126 a0001c0001t0002g0155 a0001c0001t0002g0344 others(4): Show |
7 | HG00099.hp2 HG00738.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.1839+382_1839+383i others(54): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | ||||||
chr2:74882605 | T | TTATATAT others(47): Show |
1 | a0002c0004t0004g0239 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1839+382_1839+383i others(56): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | ||||||
chr2:74882605 | T | TTATATAT others(53): Show |
1 | a0001c0001t0002g0179 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1839+382_1839+383i others(62): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | ||||||
chr2:74882605 | T | TTTATATA others(28): Show |
1 | a0001c0001t0002g0125 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1839+367_1839+368i others(37): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr2 | 74882605 | ||||||
chr2:74882621 | A | ATATATAT others(49): Show |
1 | a0002c0004t0006g0363 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1839+382_1839+383i others(58): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74882621 | |||||||
chr2:74882629 | T | G | 1 | a0001c0006t0003g0034 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1839+390T>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74882629 | |||||||
chr2:74882683 | G | A | 47 | a0001c0011t0020g0096 a0001c0011t0020g0348 a0001c0011t0037g0245 others(44): Show |
48 | HG00609.hp2 HG02040.hp1 HG02055.hp1 others(45): Show |
intron_variant | MODIFIER | c.1839+444G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74882683 | |||||||
chr2:74882912 | C | G | 1 | a0001c0022t0001g0188 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1839+673C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74882912 | |||||||
chr2:74883055 | G | A | 1 | a0001c0002t0001g0065 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1839+816G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74883055 | |||||||
chr2:74883144 | T | A | 116 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0011 others(113): Show |
117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.1839+905T>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74883144 | |||||||
chr2:74883161 | T | C | 218 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0011 others(215): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1839+922T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74883161 | |||||||
chr2:74883225 | C | G | 1 | a0001c0001t0002g0011 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1839+986C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74883225 | |||||||
chr2:74883328 | C | T | 212 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0011 others(209): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.1839+1089C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74883328 | |||||||
chr2:74883377 | G | C | 1 | a0001c0002t0046g0163 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1839+1138G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74883377 | |||||||
chr2:74883501 | C | G | 6 | a0004c0008t0006g0105 a0004c0008t0010g0111 a0004c0008t0010g0349 others(3): Show |
6 | HG00735.hp1 HG01891.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1839+1262C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74883501 | |||||||
chr2:74883784 | G | A | 7 | a0001c0006t0003g0162 a0001c0006t0008g0254 a0003c0003t0003g0134 others(4): Show |
7 | HG00741.hp1 HG01261.hp1 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.1839+1545G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74883784 | |||||||
chr2:74883930 | A | G | 261 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0011 others(258): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.1840-1564A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74883930 | |||||||
chr2:74883975 | T | C | 260 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0011 others(257): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.1840-1519T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74883975 | |||||||
chr2:74884007 | T | C | 264 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0011 others(261): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.1840-1487T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74884007 | |||||||
chr2:74884041 | C | G | 260 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0011 others(257): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.1840-1453C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74884041 | |||||||
chr2:74884234 | G | A | 1 | a0001c0005t0003g0095 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1840-1260G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74884234 | |||||||
chr2:74884234 | G | C | 2 | a0001c0009t0034g0184 a0002c0025t0024g0268 |
2 | HG01109.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1840-1260G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74884234 | |||||||
chr2:74884308 | C | T | 219 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0018 others(216): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.1840-1186C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74884308 | |||||||
chr2:74884359 | A | G | 274 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0011 others(271): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.1840-1135A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74884359 | |||||||
chr2:74884547 | G | A | 1 | a0002c0007t0016g0201 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1840-947G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74884547 | |||||||
chr2:74884822 | C | T | 2 | a0001c0009t0034g0184 a0002c0025t0024g0268 |
2 | HG01109.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1840-672C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74884822 | |||||||
chr2:74884823 | G | A | 191 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0011 others(188): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.1840-671G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74884823 | |||||||
chr2:74884915 | C | T | 24 | a0002c0004t0001g0114 a0002c0004t0009g0321 a0002c0004t0010g0097 others(21): Show |
24 | HG00735.hp1 HG01243.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.1840-579C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74884915 | |||||||
chr2:74884953 | G | T | 5 | a0001c0009t0034g0184 a0002c0023t0006g0374 a0002c0025t0024g0268 others(2): Show |
5 | HG01109.hp1 HG01891.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1840-541G>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74884953 | |||||||
chr2:74885044 | T | C | 1 | a0001c0001t0002g0125 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1840-450T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74885044 | |||||||
chr2:74885144 | G | A | 1 | a0002c0023t0006g0374 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1840-350G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74885144 | |||||||
chr2:74885245 | C | T | 2 | a0002c0007t0012g0103 a0007c0038t0012g0110 |
2 | HG02109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1840-249C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74885245 | |||||||
chr2:74885377 | G | C | 3 | a0001c0002t0001g0187 a0001c0002t0001g0266 a0001c0002t0001g0289 |
3 | NA18982.hp1 NA18990.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.1840-117G>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74885377 | |||||||
chr2:74885383 | G | A | 24 | a0002c0004t0001g0114 a0002c0004t0009g0321 a0002c0004t0010g0097 others(21): Show |
24 | HG00735.hp1 HG01243.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.1840-111G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74885383 | |||||||
chr2:74885385 | G | A | 1 | a0013c0028t0001g0172 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1840-109G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 12/17 | chr2 | 74885385 | |||||||
chr2:74885714 | C | T | 24 | a0002c0004t0001g0114 a0002c0004t0009g0321 a0002c0004t0010g0097 others(21): Show |
24 | HG00735.hp1 HG01243.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.1935+125C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | chr2 | 74885714 | |||||||
chr2:74885737 | A | T | 1 | a0002c0004t0004g0168 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1935+148A>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | chr2 | 74885737 | |||||||
chr2:74885738 | C | G | 1 | a0002c0004t0004g0168 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1935+149C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | chr2 | 74885738 | |||||||
chr2:74885743 | T | G | 1 | a0002c0004t0004g0168 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1935+154T>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | chr2 | 74885743 | |||||||
chr2:74885845 | A | AAC | 38 | a0001c0001t0002g0011 a0001c0001t0002g0045 a0001c0001t0002g0048 others(35): Show |
40 | HG00280.hp2 HG00423.hp1 HG01168.hp2 others(37): Show |
intron_variant | MODIFIER | c.1935+296_1935+297d others(4): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 74885845 | ||||||
chr2:74885845 | A | AACAC | 35 | a0001c0001t0002g0074 a0001c0001t0002g0126 a0001c0001t0002g0176 others(32): Show |
35 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.1935+294_1935+297d others(6): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 74885845 | ||||||
chr2:74885845 | A | AACACAC | 7 | a0001c0001t0002g0140 a0001c0002t0001g0129 a0001c0002t0001g0153 others(4): Show |
7 | HG00741.hp2 HG01884.hp1 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.1935+292_1935+297d others(8): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 74885845 | ||||||
chr2:74885845 | A | AACACACA others(1): Show |
7 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0006t0008g0252 others(4): Show |
7 | HG01169.hp1 HG01891.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1935+290_1935+297d others(10): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 74885845 | ||||||
chr2:74885845 | A | AACACACA others(3): Show |
15 | a0001c0002t0011g0267 a0001c0011t0037g0245 a0002c0004t0006g0108 others(12): Show |
15 | HG00609.hp2 HG02280.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1935+288_1935+297d others(12): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 74885845 | ||||||
chr2:74885845 | A | AACACACA others(5): Show |
12 | a0001c0009t0034g0184 a0002c0004t0004g0017 a0002c0004t0004g0174 others(9): Show |
12 | HG01109.hp1 HG03130.hp1 HG03130.hp2 others(9): Show |
intron_variant | MODIFIER | c.1935+286_1935+297d others(14): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 74885845 | ||||||
chr2:74885845 | A | AACACACA others(7): Show |
8 | a0001c0009t0015g0234 a0001c0009t0015g0358 a0001c0009t0015g0360 others(5): Show |
8 | HG02055.hp2 HG02486.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1935+284_1935+297d others(16): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 74885845 | ||||||
chr2:74885845 | A | AACACACA others(9): Show |
7 | a0002c0004t0004g0013 a0002c0004t0004g0024 a0002c0004t0004g0138 others(4): Show |
7 | HG02040.hp1 NA18940.hp1 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.1935+282_1935+297d others(18): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 74885845 | ||||||
chr2:74885845 | A | AACACACA others(11): Show |
3 | a0002c0004t0004g0168 a0002c0004t0004g0276 a0002c0004t0010g0247 |
3 | HG02717.hp2 NA18987.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1935+280_1935+297d others(20): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 74885845 | ||||||
chr2:74885845 | A | AACACACA others(13): Show |
3 | a0002c0004t0023g0244 a0002c0004t0026g0370 a0002c0007t0035g0007 |
3 | HG01257.hp2 HG02135.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1935+278_1935+297d others(22): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 74885845 | ||||||
chr2:74885845 | A | AACACACA others(15): Show |
1 | a0002c0004t0004g0368 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1935+276_1935+297d others(24): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 74885845 | ||||||
chr2:74885845 | A | AACACACA others(17): Show |
1 | a0002c0004t0004g0128 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1935+274_1935+297d others(26): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 74885845 | ||||||
chr2:74885845 | A | AACACACA others(19): Show |
1 | a0001c0012t0021g0356 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1935+272_1935+297d others(28): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 74885845 | ||||||
chr2:74885845 | AAC | A | 17 | a0001c0001t0002g0033 a0001c0001t0002g0037 a0001c0001t0002g0072 others(14): Show |
17 | HG00609.hp1 HG00741.hp1 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.1935+296_1935+297d others(4): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 74885845 | ||||||
chr2:74885845 | AACAC | A | 6 | a0001c0001t0005g0035 a0001c0001t0005g0331 a0001c0001t0014g0257 others(3): Show |
6 | HG01346.hp1 HG01361.hp1 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.1935+294_1935+297d others(6): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 74885845 | ||||||
chr2:74885845 | AACACAC | A | 3 | a0001c0001t0007g0006 a0001c0001t0007g0250 a0004c0008t0010g0349 |
4 | HG00735.hp1 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1935+292_1935+297d others(8): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 74885845 | ||||||
chr2:74885845 | AACACACA others(3): Show |
A | 3 | a0001c0006t0003g0359 a0001c0024t0003g0183 a0002c0023t0006g0374 |
3 | HG02895.hp1 HG03471.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1935+288_1935+297d others(12): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 74885845 | ||||||
chr2:74885885 | C | A | 2 | a0004c0008t0010g0349 a0004c0018t0045g0246 |
2 | HG00735.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1935+296C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | chr2 | 74885885 | |||||||
chr2:74885885 | C | CACACAA | 13 | a0002c0004t0001g0114 a0002c0004t0009g0321 a0002c0004t0044g0100 others(10): Show |
13 | HG01243.hp1 HG02109.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1935+297_1935+298i others(8): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 74885885 | ||||||
chr2:74885885 | C | CACACACA others(3): Show |
2 | a0002c0004t0010g0097 a0004c0008t0019g0190 |
2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1935+297_1935+298i others(12): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 74885885 | ||||||
chr2:74885885 | C | CACACACA others(7): Show |
3 | a0004c0008t0010g0111 a0004c0008t0010g0351 a0004c0008t0010g0353 |
3 | HG01891.hp2 HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1935+297_1935+298i others(16): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 74885885 | ||||||
chr2:74885885 | C | CACACACA others(9): Show |
1 | a0004c0008t0010g0354 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1935+297_1935+298i others(18): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr2 | 74885885 | ||||||
chr2:74885923 | A | G | 216 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0011 others(213): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.1935+334A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | chr2 | 74885923 | |||||||
chr2:74885930 | T | C | 4 | a0001c0005t0017g0084 a0001c0005t0047g0015 a0001c0039t0001g0056 others(1): Show |
4 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1935+341T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | chr2 | 74885930 | |||||||
chr2:74885973 | T | C | 3 | a0002c0023t0006g0374 a0006c0027t0039g0350 a0013c0028t0001g0172 |
3 | HG01891.hp1 HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1936-321T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | chr2 | 74885973 | |||||||
chr2:74885987 | G | A | 2 | a0001c0009t0034g0184 a0004c0043t0012g0177 |
2 | HG01884.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1936-307G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | chr2 | 74885987 | |||||||
chr2:74886210 | T | C | 2 | a0003c0003t0003g0085 a0003c0003t0003g0086 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1936-84T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 13/17 | chr2 | 74886210 | |||||||
chr2:74886445 | G | A | 189 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0011 others(186): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.2036-45G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 14/17 | chr2 | 74886445 | |||||||
chr2:74886765 | C | T | 1 | a0002c0004t0006g0248 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2219+92C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 15/17 | chr2 | 74886765 | |||||||
chr2:74886772 | C | T | 1 | a0001c0009t0034g0184 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2219+99C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 15/17 | chr2 | 74886772 | |||||||
chr2:74886776 | A | G | 77 | a0001c0006t0001g0044 a0001c0006t0002g0009 a0001c0006t0003g0026 others(74): Show |
77 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.2219+103A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 15/17 | chr2 | 74886776 | |||||||
chr2:74886861 | C | T | 1 | a0014c0019t0001g0113 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2219+188C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 15/17 | chr2 | 74886861 | |||||||
chr2:74887030 | C | T | 1 | a0002c0023t0006g0374 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2219+357C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 15/17 | chr2 | 74887030 | |||||||
chr2:74887214 | C | T | 3 | a0001c0001t0002g0205 a0001c0001t0007g0386 a0001c0012t0002g0373 |
3 | HG02602.hp2 HG03654.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.2219+541C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 15/17 | chr2 | 74887214 | |||||||
chr2:74887229 | G | A | 2 | a0004c0018t0024g0223 a0004c0018t0045g0246 |
2 | HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2219+556G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 15/17 | chr2 | 74887229 | |||||||
chr2:74887245 | T | G | 50 | a0001c0011t0037g0245 a0001c0012t0021g0356 a0002c0004t0001g0114 others(47): Show |
51 | HG00609.hp2 HG01243.hp1 HG01884.hp2 others(48): Show |
intron_variant | MODIFIER | c.2219+572T>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 15/17 | chr2 | 74887245 | |||||||
chr2:74887413 | C | A | 1 | a0001c0005t0003g0095 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2220-490C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 15/17 | chr2 | 74887413 | |||||||
chr2:74887434 | ATGGGGGC | A | 83 | a0001c0001t0041g0147 a0001c0005t0003g0022 a0001c0005t0003g0081 others(80): Show |
83 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.2220-468_2220-462d others(9): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 15/17 | chr2 | 74887434 | |||||||
chr2:74887442 | C | A | 83 | a0001c0001t0041g0147 a0001c0005t0003g0022 a0001c0005t0003g0081 others(80): Show |
83 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.2220-461C>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 15/17 | chr2 | 74887442 | |||||||
chr2:74887523 | T | G | 86 | a0001c0001t0041g0147 a0001c0002t0001g0025 a0001c0002t0001g0133 others(83): Show |
86 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.2220-380T>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 15/17 | chr2 | 74887523 | |||||||
chr2:74887603 | C | T | 104 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0011 others(101): Show |
105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
intron_variant | MODIFIER | c.2220-300C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 15/17 | chr2 | 74887603 | |||||||
chr2:74887712 | A | G | 84 | a0001c0001t0041g0147 a0001c0005t0003g0022 a0001c0005t0003g0081 others(81): Show |
84 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.2220-191A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 15/17 | chr2 | 74887712 | |||||||
chr2:74888183 | T | G | 2 | a0006c0027t0039g0350 a0013c0028t0001g0172 |
2 | HG01891.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2375+125T>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 16/17 | chr2 | 74888183 | |||||||
chr2:74888252 | C | T | 195 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0011 others(192): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.2375+194C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 16/17 | chr2 | 74888252 | |||||||
chr2:74888256 | A | C | 69 | a0001c0011t0037g0245 a0002c0004t0001g0114 a0002c0004t0004g0013 others(66): Show |
70 | HG00609.hp2 HG00735.hp1 HG01243.hp1 others(67): Show |
intron_variant | MODIFIER | c.2375+198A>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 16/17 | chr2 | 74888256 | |||||||
chr2:74888343 | C | T | 1 | a0001c0012t0021g0356 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2375+285C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 16/17 | chr2 | 74888343 | |||||||
chr2:74888365 | A | G | 1 | a0001c0009t0034g0184 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2375+307A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 16/17 | chr2 | 74888365 | |||||||
chr2:74888560 | G | A | 57 | a0001c0011t0037g0245 a0002c0004t0001g0114 a0002c0004t0004g0013 others(54): Show |
57 | HG00609.hp2 HG00738.hp2 HG01243.hp1 others(54): Show |
intron_variant | MODIFIER | c.2375+502G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 16/17 | chr2 | 74888560 | |||||||
chr2:74888591 | T | C | 1 | a0002c0004t0004g0318 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2375+533T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 16/17 | chr2 | 74888591 | |||||||
chr2:74888599 | T | C | 196 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0011 others(193): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.2375+541T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 16/17 | chr2 | 74888599 | |||||||
chr2:74888638 | T | A | 1 | a0001c0002t0001g0002 | 2 | NA19074.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.2375+580T>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 16/17 | chr2 | 74888638 | |||||||
chr2:74888659 | T | C | 3 | a0001c0002t0001g0040 a0001c0002t0001g0041 a0001c0002t0025g0028 |
3 | NA18962.hp2 NA19068.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.2376-586T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 16/17 | chr2 | 74888659 | |||||||
chr2:74888873 | T | G | 1 | a0002c0023t0006g0374 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2376-372T>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 16/17 | chr2 | 74888873 | |||||||
chr2:74888887 | G | A | 39 | a0002c0004t0001g0114 a0002c0004t0004g0013 a0002c0004t0004g0017 others(36): Show |
39 | HG00609.hp2 HG02040.hp1 HG02135.hp2 others(36): Show |
intron_variant | MODIFIER | c.2376-358G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 16/17 | chr2 | 74888887 | |||||||
chr2:74889140 | T | C | 1 | a0001c0001t0002g0131 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2376-105T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 16/17 | chr2 | 74889140 | |||||||
chr2:74889500 | C | T | 280 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0011 others(277): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.2609+22C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 17/17 | chr2 | 74889500 | |||||||
chr2:74889613 | T | C | 2 | a0001c0002t0001g0025 a0001c0002t0001g0133 |
2 | HG00544.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.2609+135T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 17/17 | chr2 | 74889613 | |||||||
chr2:74889658 | C | G | 1 | a0013c0028t0001g0172 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2609+180C>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 17/17 | chr2 | 74889658 | |||||||
chr2:74889699 | A | G | 1 | a0001c0001t0007g0242 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2609+221A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 17/17 | chr2 | 74889699 | |||||||
chr2:74889848 | T | TGGCTGGC others(129): Show |
1 | a0001c0001t0002g0073 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2609+372_2609+507d others(138): Show |
HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr2 | 74889848 | ||||||
chr2:74890016 | T | C | 1 | a0001c0002t0001g0025 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2609+538T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 17/17 | chr2 | 74890016 | |||||||
chr2:74890065 | A | G | 11 | a0002c0004t0010g0004 a0002c0004t0010g0097 a0002c0004t0010g0247 others(8): Show |
12 | HG00735.hp1 HG01891.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.2609+587A>G | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 17/17 | chr2 | 74890065 | |||||||
chr2:74890377 | G | A | 1 | a0002c0004t0010g0004 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2610-420G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 17/17 | chr2 | 74890377 | |||||||
chr2:74890426 | C | T | 1 | a0001c0001t0002g0200 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2610-371C>T | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 17/17 | chr2 | 74890426 | |||||||
chr2:74890604 | G | A | 3 | a0001c0009t0015g0234 a0001c0009t0015g0358 a0001c0009t0015g0360 |
3 | HG02055.hp2 HG02976.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2610-193G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 17/17 | chr2 | 74890604 | |||||||
chr2:74890668 | T | C | 1 | a0002c0004t0023g0228 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2610-129T>C | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 17/17 | chr2 | 74890668 | |||||||
chr2:74890733 | G | A | 2 | a0001c0002t0001g0216 a0001c0002t0001g0217 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2610-64G>A | HK2 | ENSG00000159399.10 | transcript | ENST00000290573.7 | protein_coding | 17/17 | chr2 | 74890733 |