Item | Value |
---|---|
geneid | 3945 |
ensemblid | ENSG00000111716.14 |
hgncid | 6541 |
symbol | LDHB |
name | lactate dehydrogenase B |
refseq_nuc | NM_002300.8 |
refseq_prot | NP_002291.1 |
ensembl_nuc | ENST00000350669.5 |
ensembl_prot | ENSP00000229319.1 |
mane_status | MANE Select |
chr | chr12 |
start | 21635342 |
end | 21657842 |
strand | - |
ver | v1.2 |
region | chr12:21635342-21657842 |
region5000 | chr12:21630342-21662842 |
regionname0 | LDHB_chr12_21635342_21657842 |
regionname5000 | LDHB_chr12_21630342_21662842 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 334 | 325 | 92 | 68 | 110 | 14 | 39 | 78 | LDHB_chr12_21630342_21662842 | LDHB | MATLK others(329): Show |
chr12 | 21630342 | 21662842 |
a0002 | 0/0 | 334 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LDHB_chr12_21630342_21662842 | LDHB | MATLK others(329): Show |
chr12 | 21630342 | 21662842 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1002 | 303 | 71 | 68 | 110 | 14 | 39 | LDHB_chr12_21630342_21662842 | LDHB | ATGGC others(997): Show |
chr12 | 21630342 | 21662842 | ||
a0001c0002 | 1/0 | 1002 | 14 | 13 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | ATGGC others(997): Show |
chr12 | 21630342 | 21662842 | ||
a0001c0003 | 0/0 | 1002 | 7 | 7 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | ATGGC others(997): Show |
chr12 | 21630342 | 21662842 | ||
a0001c0004 | 0/0 | 1002 | 1 | 1 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | ATGGC others(997): Show |
chr12 | 21630342 | 21662842 | ||
a0002c0005 | 0/0 | 1002 | 1 | 0 | 0 | 0 | 0 | 1 | LDHB_chr12_21630342_21662842 | LDHB | ATGGC others(997): Show |
chr12 | 21630342 | 21662842 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 1303 | 299 | 68 | 67 | 110 | 14 | 39 | LDHB_chr12_21630342_21662842 | LDHB | CTTGC others(1298): Show |
chr12 | 21630342 | 21662842 |
a0001c0001t0002 | 0/0 | 1303 | 2 | 2 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | CTTGC others(1298): Show |
chr12 | 21630342 | 21662842 |
a0001c0001t0003 | 0/0 | 1303 | 1 | 0 | 1 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | CTTGC others(1298): Show |
chr12 | 21630342 | 21662842 |
a0001c0001t0004 | 0/0 | 1303 | 1 | 1 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | CTTGC others(1298): Show |
chr12 | 21630342 | 21662842 |
a0001c0002t0001 | 1/0 | 1303 | 14 | 13 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | CTTGC others(1298): Show |
chr12 | 21630342 | 21662842 |
a0001c0003t0002 | 0/0 | 1303 | 7 | 7 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | CTTGC others(1298): Show |
chr12 | 21630342 | 21662842 |
a0001c0004t0002 | 0/0 | 1303 | 1 | 1 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | CTTGC others(1298): Show |
chr12 | 21630342 | 21662842 |
a0002c0005t0001 | 0/0 | 1303 | 1 | 0 | 0 | 0 | 0 | 1 | LDHB_chr12_21630342_21662842 | LDHB | CTTGC others(1298): Show |
chr12 | 21630342 | 21662842 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 33 | 0 | 7 | 21 | 2 | 3 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0002 | 0/0 | 26 | 0 | 8 | 10 | 4 | 4 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0003 | 0/0 | 16 | 1 | 3 | 3 | 0 | 9 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0004 | 0/0 | 13 | 5 | 5 | 0 | 0 | 3 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0005 | 0/0 | 10 | 0 | 10 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0006 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0007 | 0/0 | 8 | 1 | 1 | 3 | 0 | 3 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0008 | 0/0 | 8 | 6 | 0 | 0 | 0 | 2 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0009 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0010 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0011 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0012 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0014 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0025 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0032 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0060 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0002g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0003g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0001t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0002t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0002t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0002t0001g0140 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0002t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0002t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0002t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0002t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0003t0002g0013 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0003t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0003t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0001c0004t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
a0002c0005t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0150 | EUR | GBR | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0050 | EUR | FIN | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0071 | EUR | FIN | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0106 | AMR | PUR | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0053 | EUR | IBS | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | IBS | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0052 | EUR | IBS | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0025 | EUR | IBS | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01884 | hp1 | a0001 | c0003 | t0002 | g0013 | AFR | ACB | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01891 | hp2 | a0001 | c0002 | t0001 | g0142 | AFR | ACB | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | CDX | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CDX | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02257 | hp1 | a0001 | c0003 | t0002 | g0013 | AFR | ACB | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02572 | hp1 | a0001 | c0004 | t0002 | g0042 | AFR | GWD | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02622 | hp2 | a0001 | c0002 | t0001 | g0019 | AFR | GWD | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02630 | hp2 | a0001 | c0003 | t0002 | g0040 | AFR | GWD | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02809 | hp1 | a0001 | c0002 | t0001 | g0143 | AFR | GWD | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02818 | hp2 | a0001 | c0002 | t0001 | g0036 | AFR | GWD | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02895 | hp2 | a0001 | c0003 | t0002 | g0041 | AFR | GWD | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02922 | hp1 | a0001 | c0003 | t0002 | g0013 | AFR | ESN | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02970 | hp1 | a0001 | c0003 | t0002 | g0013 | AFR | ESN | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02970 | hp2 | a0001 | c0002 | t0001 | g0144 | AFR | ESN | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | ESN | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG03098 | hp1 | a0001 | c0002 | t0001 | g0138 | AFR | MSL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | MSL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | ESN | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ESN | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG03195 | hp2 | a0001 | c0002 | t0001 | g0149 | AFR | ESN | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | MSL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG03486 | hp1 | a0001 | c0002 | t0001 | g0066 | AFR | MSL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG03491 | hp1 | a0002 | c0005 | t0001 | g0093 | SAS | PJL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | ESN | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | STU | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | BEB | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | BEB | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | STU | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | STU | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18522 | hp1 | a0001 | c0002 | t0001 | g0036 | AFR | YRI | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | YRI | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHB | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | CHB | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHB | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18906 | hp1 | a0001 | c0002 | t0001 | g0019 | AFR | YRI | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | LWK | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA19030 | hp2 | a0001 | c0002 | t0001 | g0139 | AFR | LWK | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | LWK | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA19043 | hp2 | a0001 | c0003 | t0002 | g0013 | AFR | LWK | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA19240 | hp1 | a0001 | c0002 | t0001 | g0019 | AFR | YRI | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | YRI | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ASW | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ASW | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0075 | EUR | TSI | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | GIH | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | USA | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | USA | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA20300 | hp1 | a0001 | c0001 | t0004 | g0122 | AFR | USA | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA20300 | hp2 | a0001 | c0002 | t0001 | g0141 | AFR | USA | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | LWK | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | LWK | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0060 | REF | REF | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0140 | REF | REF | LDHB_chr12_21630342_21662842 | LDHB | chr12 | 21630342 | 21662842 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:21642075 | G | A | 1 | a0002 | 1 | HG03491.hp1 | missense_variant | MODERATE | c.472C>T | p.Arg158Cys | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 5/8 | 570/1303 | 472/1005 | 158/334 | chr12 | 21642075 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:21635668 | T | C | 2 | a0001c0003 a0001c0004 |
8 | HG01884.hp1 HG02257.hp1 HG02572.hp1 others(5): Show |
synonymous_variant | LOW | c.879A>G | p.Pro293Pro | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 8/8 | 977/1303 | 879/1005 | 293/334 | chr12 | 21635668 | |||
chr12:21642112 | C | T | 1 | a0001c0004 | 1 | HG02572.hp1 | synonymous_variant | LOW | c.435G>A | p.Thr145Thr | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 5/8 | 533/1303 | 435/1005 | 145/334 | chr12 | 21642112 | |||
chr12:21644095 | A | G | 4 | a0001c0001 a0001c0003 a0001c0004 others(1): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
synonymous_variant | LOW | c.261T>C | p.Thr87Thr | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 4/8 | 359/1303 | 261/1005 | 87/334 | chr12 | 21644095 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:21635370 | C | A | 1 | a0001c0001t0004 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*172G>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 8/8 | 172 | chr12 | 21635370 | ||||||
chr12:21635420 | A | G | 1 | a0001c0001t0003 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*122T>C | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 8/8 | 122 | chr12 | 21635420 | ||||||
chr12:21657825 | C | G | 3 | a0001c0001t0002 a0001c0003t0002 a0001c0004t0002 |
10 | HG01884.hp1 HG02257.hp1 HG02572.hp1 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-81G>C | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 1/8 | 3154 | chr12 | 21657825 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:21635858 | G | C | 1 | a0001c0002t0001g0139 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.838-149C>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 7/7 | chr12 | 21635858 | |||||||
chr12:21636110 | C | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(135): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.838-401G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 7/7 | chr12 | 21636110 | |||||||
chr12:21636316 | C | G | 1 | a0001c0001t0001g0056 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.838-607G>C | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 7/7 | chr12 | 21636316 | |||||||
chr12:21636344 | T | TA | 8 | a0001c0001t0001g0029 a0001c0001t0001g0051 a0001c0001t0001g0062 others(5): Show |
9 | HG00597.hp2 HG01993.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.838-636dupT | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 7/7 | chr12 | 21636344 | |||||||
chr12:21636718 | CA | C | 2 | a0001c0001t0001g0038 a0001c0001t0001g0145 |
3 | HG01168.hp1 HG01169.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.837+352delT | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 7/7 | chr12 | 21636718 | |||||||
chr12:21636788 | A | C | 1 | a0001c0001t0001g0145 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.837+283T>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 7/7 | chr12 | 21636788 | |||||||
chr12:21636800 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.837+271G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 7/7 | chr12 | 21636800 | |||||||
chr12:21637034 | G | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(135): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.837+37C>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 7/7 | chr12 | 21637034 | |||||||
chr12:21637339 | T | C | 3 | a0001c0001t0001g0018 a0001c0001t0001g0039 a0001c0001t0001g0058 |
6 | HG01891.hp1 HG02109.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.714-145A>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 6/7 | chr12 | 21637339 | |||||||
chr12:21637402 | T | A | 4 | a0001c0003t0002g0013 a0001c0003t0002g0040 a0001c0003t0002g0041 others(1): Show |
8 | HG01884.hp1 HG02257.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.714-208A>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 6/7 | chr12 | 21637402 | |||||||
chr12:21637516 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.714-322A>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 6/7 | chr12 | 21637516 | |||||||
chr12:21637565 | G | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.714-371C>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 6/7 | chr12 | 21637565 | |||||||
chr12:21637598 | CAACT | C | 4 | a0001c0003t0002g0013 a0001c0003t0002g0040 a0001c0003t0002g0041 others(1): Show |
8 | HG01884.hp1 HG02257.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.714-408_714-405del others(4): Show |
LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 6/7 | chr12 | 21637598 | |||||||
chr12:21637685 | C | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.714-491G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 6/7 | chr12 | 21637685 | |||||||
chr12:21637704 | A | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.714-510T>C | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 6/7 | chr12 | 21637704 | |||||||
chr12:21637721 | T | C | 1 | a0001c0001t0001g0037 | 2 | HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.714-527A>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 6/7 | chr12 | 21637721 | |||||||
chr12:21637722 | T | C | 4 | a0001c0003t0002g0013 a0001c0003t0002g0040 a0001c0003t0002g0041 others(1): Show |
8 | HG01884.hp1 HG02257.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.714-528A>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 6/7 | chr12 | 21637722 | |||||||
chr12:21637770 | T | C | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(129): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.714-576A>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 6/7 | chr12 | 21637770 | |||||||
chr12:21637785 | A | G | 9 | a0001c0001t0001g0009 a0001c0001t0001g0033 a0001c0001t0001g0079 others(6): Show |
17 | HG00597.hp1 HG00621.hp2 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.713+568T>C | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 6/7 | chr12 | 21637785 | |||||||
chr12:21637817 | A | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.713+536T>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 6/7 | chr12 | 21637817 | |||||||
chr12:21637892 | C | A | 2 | a0001c0001t0001g0064 a0001c0001t0001g0065 |
2 | NA18974.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.713+461G>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 6/7 | chr12 | 21637892 | |||||||
chr12:21637901 | G | GA | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.713+451dupT | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 6/7 | chr12 | 21637901 | |||||||
chr12:21637959 | C | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(135): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.713+394G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 6/7 | chr12 | 21637959 | |||||||
chr12:21637993 | C | A | 1 | a0001c0001t0001g0113 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.713+360G>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 6/7 | chr12 | 21637993 | |||||||
chr12:21638128 | T | G | 1 | a0001c0001t0001g0092 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.713+225A>C | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 6/7 | chr12 | 21638128 | |||||||
chr12:21638338 | T | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.713+15A>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 6/7 | chr12 | 21638338 | |||||||
chr12:21638476 | TA | T | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(120): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
splice_region_variant&intron_variant | LOW | c.596-7delT | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 5/7 | chr12 | 21638476 | |||||||
chr12:21638478 | A | T | 1 | a0001c0001t0001g0050 | 1 | HG00280.hp1 | splice_region_variant&intron_variant | LOW | c.596-8T>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 5/7 | chr12 | 21638478 | |||||||
chr12:21638521 | A | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(135): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.596-51T>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 5/7 | chr12 | 21638521 | |||||||
chr12:21638631 | A | C | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(135): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.596-161T>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 5/7 | chr12 | 21638631 | |||||||
chr12:21638864 | C | T | 30 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0027 others(27): Show |
73 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.596-394G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 5/7 | chr12 | 21638864 | |||||||
chr12:21638941 | G | T | 1 | a0001c0001t0001g0038 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.596-471C>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 5/7 | chr12 | 21638941 | |||||||
chr12:21639013 | C | T | 1 | a0001c0003t0002g0040 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.596-543G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 5/7 | chr12 | 21639013 | |||||||
chr12:21639028 | T | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.596-558A>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 5/7 | chr12 | 21639028 | |||||||
chr12:21639121 | G | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(135): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.596-651C>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 5/7 | chr12 | 21639121 | |||||||
chr12:21639160 | C | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.596-690G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 5/7 | chr12 | 21639160 | |||||||
chr12:21639187 | G | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.596-717C>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 5/7 | chr12 | 21639187 | |||||||
chr12:21639335 | G | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.596-865C>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 5/7 | chr12 | 21639335 | |||||||
chr12:21639477 | C | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.596-1007G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 5/7 | chr12 | 21639477 | |||||||
chr12:21639555 | T | C | 2 | a0001c0001t0001g0052 a0001c0001t0001g0053 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.596-1085A>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 5/7 | chr12 | 21639555 | |||||||
chr12:21639833 | T | C | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(135): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.596-1363A>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 5/7 | chr12 | 21639833 | |||||||
chr12:21640035 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.596-1565C>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 5/7 | chr12 | 21640035 | |||||||
chr12:21640156 | T | TA | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(130): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.596-1687_596-1686i others(3): Show |
LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 5/7 | chr12 | 21640156 | |||||||
chr12:21640197 | A | G | 1 | a0001c0001t0001g0088 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.596-1727T>C | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 5/7 | chr12 | 21640197 | |||||||
chr12:21640208 | G | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.596-1738C>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 5/7 | chr12 | 21640208 | |||||||
chr12:21640284 | G | T | 4 | a0001c0003t0002g0013 a0001c0003t0002g0040 a0001c0003t0002g0041 others(1): Show |
8 | HG01884.hp1 HG02257.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.595+1668C>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 5/7 | chr12 | 21640284 | |||||||
chr12:21640341 | G | A | 4 | a0001c0001t0001g0010 a0001c0001t0001g0087 a0001c0001t0001g0114 others(1): Show |
10 | HG02258.hp1 HG02559.hp2 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.595+1611C>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 5/7 | chr12 | 21640341 | |||||||
chr12:21640348 | TAA | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.595+1602_595+1603d others(4): Show |
LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 5/7 | chr12 | 21640348 | |||||||
chr12:21640452 | TCATA | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0087 a0001c0001t0004g0122 |
9 | HG02258.hp1 HG02559.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.595+1496_595+1499d others(6): Show |
LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 5/7 | chr12 | 21640452 | |||||||
chr12:21640824 | T | C | 1 | a0001c0001t0001g0096 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.595+1128A>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 5/7 | chr12 | 21640824 | |||||||
chr12:21640837 | T | TA | 5 | a0001c0001t0001g0037 a0001c0001t0001g0131 a0001c0001t0001g0132 others(2): Show |
6 | HG01243.hp1 HG02451.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.595+1114dupT | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 5/7 | chr12 | 21640837 | |||||||
chr12:21640852 | G | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.595+1100C>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 5/7 | chr12 | 21640852 | |||||||
chr12:21640852 | G | C | 4 | a0001c0003t0002g0013 a0001c0003t0002g0040 a0001c0003t0002g0041 others(1): Show |
8 | HG01884.hp1 HG02257.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.595+1100C>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 5/7 | chr12 | 21640852 | |||||||
chr12:21640900 | T | C | 4 | a0001c0001t0001g0005 a0001c0001t0001g0067 a0001c0001t0001g0083 others(1): Show |
13 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.595+1052A>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 5/7 | chr12 | 21640900 | |||||||
chr12:21641040 | A | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.595+912T>C | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 5/7 | chr12 | 21641040 | |||||||
chr12:21641086 | T | C | 6 | a0001c0001t0001g0024 a0001c0001t0001g0046 a0001c0001t0001g0054 others(3): Show |
7 | HG02135.hp2 HG03017.hp2 HG03654.hp2 others(4): Show |
intron_variant | MODIFIER | c.595+866A>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 5/7 | chr12 | 21641086 | |||||||
chr12:21641116 | T | C | 4 | a0001c0003t0002g0013 a0001c0003t0002g0040 a0001c0003t0002g0041 others(1): Show |
8 | HG01884.hp1 HG02257.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.595+836A>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 5/7 | chr12 | 21641116 | |||||||
chr12:21641164 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.595+788T>C | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 5/7 | chr12 | 21641164 | |||||||
chr12:21641620 | C | T | 2 | a0001c0001t0001g0070 a0001c0001t0001g0075 |
2 | HG01074.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.595+332G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 5/7 | chr12 | 21641620 | |||||||
chr12:21641631 | T | G | 2 | a0001c0001t0001g0046 a0001c0001t0001g0054 |
2 | NA19009.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.595+321A>C | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 5/7 | chr12 | 21641631 | |||||||
chr12:21642359 | C | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.422-234G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 4/7 | chr12 | 21642359 | |||||||
chr12:21642577 | A | ATG | 4 | a0001c0003t0002g0013 a0001c0003t0002g0040 a0001c0003t0002g0041 others(1): Show |
8 | HG01884.hp1 HG02257.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.422-454_422-453dup others(2): Show |
LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 4/7 | chr12 | 21642577 | |||||||
chr12:21642695 | C | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(135): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.422-570G>C | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 4/7 | chr12 | 21642695 | |||||||
chr12:21642718 | T | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.422-593A>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 4/7 | chr12 | 21642718 | |||||||
chr12:21642755 | A | G | 1 | a0001c0001t0001g0038 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.422-630T>C | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 4/7 | chr12 | 21642755 | |||||||
chr12:21642800 | G | T | 1 | a0001c0001t0001g0148 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.422-675C>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 4/7 | chr12 | 21642800 | |||||||
chr12:21642838 | A | C | 1 | a0001c0001t0001g0111 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.422-713T>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 4/7 | chr12 | 21642838 | |||||||
chr12:21643066 | A | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.421+869T>C | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 4/7 | chr12 | 21643066 | |||||||
chr12:21643106 | A | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.421+829T>C | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 4/7 | chr12 | 21643106 | |||||||
chr12:21643107 | G | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.421+828C>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 4/7 | chr12 | 21643107 | |||||||
chr12:21643280 | A | T | 1 | a0001c0001t0001g0110 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.421+655T>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 4/7 | chr12 | 21643280 | |||||||
chr12:21643589 | A | G | 1 | a0001c0001t0001g0084 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.421+346T>C | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 4/7 | chr12 | 21643589 | |||||||
chr12:21643758 | C | G | 1 | a0001c0001t0001g0099 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.421+177G>C | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 4/7 | chr12 | 21643758 | |||||||
chr12:21643831 | T | C | 3 | a0001c0003t0002g0013 a0001c0003t0002g0040 a0001c0003t0002g0041 |
7 | HG01884.hp1 HG02257.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.421+104A>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 4/7 | chr12 | 21643831 | |||||||
chr12:21643880 | G | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(135): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.421+55C>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 4/7 | chr12 | 21643880 | |||||||
chr12:21643922 | T | C | 3 | a0001c0001t0001g0018 a0001c0001t0001g0039 a0001c0001t0001g0058 |
6 | HG01891.hp1 HG02109.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.421+13A>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 4/7 | chr12 | 21643922 | |||||||
chr12:21644219 | T | C | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(135): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.248-111A>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 3/7 | chr12 | 21644219 | |||||||
chr12:21644351 | G | A | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(132): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.248-243C>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 3/7 | chr12 | 21644351 | |||||||
chr12:21644424 | CA | C | 4 | a0001c0002t0001g0019 a0001c0002t0001g0138 a0001c0002t0001g0142 others(1): Show |
6 | HG01891.hp2 HG02622.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.248-317delT | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 3/7 | chr12 | 21644424 | |||||||
chr12:21644434 | A | AAAAC | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(124): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.248-327_248-326ins others(4): Show |
LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 3/7 | chr12 | 21644434 | |||||||
chr12:21644438 | A | ACAAAAAA others(6): Show |
1 | a0001c0001t0001g0038 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.248-331_248-330ins others(13): Show |
LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 3/7 | chr12 | 21644438 | |||||||
chr12:21644444 | AAC | A | 3 | a0001c0003t0002g0013 a0001c0003t0002g0040 a0001c0003t0002g0041 |
6 | HG01884.hp1 HG02630.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.248-338_248-337del others(2): Show |
LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 3/7 | chr12 | 21644444 | |||||||
chr12:21644446 | C | A | 1 | a0001c0001t0001g0038 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.248-338G>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 3/7 | chr12 | 21644446 | |||||||
chr12:21644446 | C | CAAAAAAA | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(128): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.248-339_248-338ins others(7): Show |
LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 3/7 | chr12 | 21644446 | |||||||
chr12:21644453 | A | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(134): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.248-345T>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 3/7 | chr12 | 21644453 | |||||||
chr12:21644464 | T | G | 1 | a0001c0004t0002g0042 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.248-356A>C | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 3/7 | chr12 | 21644464 | |||||||
chr12:21644660 | T | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.248-552A>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 3/7 | chr12 | 21644660 | |||||||
chr12:21644661 | G | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.248-553C>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 3/7 | chr12 | 21644661 | |||||||
chr12:21644797 | G | C | 1 | a0001c0004t0002g0042 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.248-689C>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 3/7 | chr12 | 21644797 | |||||||
chr12:21644893 | C | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.248-785G>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 3/7 | chr12 | 21644893 | |||||||
chr12:21645024 | T | C | 1 | a0001c0001t0001g0055 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.248-916A>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 3/7 | chr12 | 21645024 | |||||||
chr12:21645233 | C | G | 2 | a0001c0001t0001g0068 a0001c0001t0001g0086 |
2 | HG02148.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.248-1125G>C | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 3/7 | chr12 | 21645233 | |||||||
chr12:21645236 | T | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.248-1128A>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 3/7 | chr12 | 21645236 | |||||||
chr12:21645239 | A | AAGGCC | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.248-1136_248-1132d others(7): Show |
LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 3/7 | chr12 | 21645239 | |||||||
chr12:21645296 | G | A | 4 | a0001c0001t0001g0030 a0001c0001t0001g0038 a0001c0001t0001g0145 others(1): Show |
6 | HG01168.hp1 HG01169.hp1 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.248-1188C>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 3/7 | chr12 | 21645296 | |||||||
chr12:21645422 | G | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.248-1314C>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 3/7 | chr12 | 21645422 | |||||||
chr12:21645475 | G | C | 4 | a0001c0003t0002g0013 a0001c0003t0002g0040 a0001c0003t0002g0041 others(1): Show |
8 | HG01884.hp1 HG02257.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.248-1367C>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 3/7 | chr12 | 21645475 | |||||||
chr12:21645502 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.248-1394C>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 3/7 | chr12 | 21645502 | |||||||
chr12:21645577 | G | C | 1 | a0001c0001t0001g0097 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.247+1322C>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 3/7 | chr12 | 21645577 | |||||||
chr12:21645579 | C | T | 2 | a0001c0001t0001g0127 a0001c0001t0001g0130 |
2 | HG03017.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.247+1320G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 3/7 | chr12 | 21645579 | |||||||
chr12:21645810 | T | A | 1 | a0001c0001t0001g0098 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.247+1089A>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 3/7 | chr12 | 21645810 | |||||||
chr12:21645878 | C | T | 4 | a0001c0003t0002g0013 a0001c0003t0002g0040 a0001c0003t0002g0041 others(1): Show |
8 | HG01884.hp1 HG02257.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.247+1021G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 3/7 | chr12 | 21645878 | |||||||
chr12:21645888 | G | A | 1 | a0001c0001t0001g0022 | 2 | HG01255.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.247+1011C>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 3/7 | chr12 | 21645888 | |||||||
chr12:21646146 | A | G | 3 | a0001c0003t0002g0013 a0001c0003t0002g0040 a0001c0003t0002g0041 |
7 | HG01884.hp1 HG02257.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.247+753T>C | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 3/7 | chr12 | 21646146 | |||||||
chr12:21646189 | T | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.247+710A>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 3/7 | chr12 | 21646189 | |||||||
chr12:21646364 | G | C | 4 | a0001c0003t0002g0013 a0001c0003t0002g0040 a0001c0003t0002g0041 others(1): Show |
8 | HG01884.hp1 HG02257.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.247+535C>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 3/7 | chr12 | 21646364 | |||||||
chr12:21646568 | C | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.247+331G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 3/7 | chr12 | 21646568 | |||||||
chr12:21646615 | A | G | 4 | a0001c0003t0002g0013 a0001c0003t0002g0040 a0001c0003t0002g0041 others(1): Show |
8 | HG01884.hp1 HG02257.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.247+284T>C | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 3/7 | chr12 | 21646615 | |||||||
chr12:21646654 | G | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.247+245C>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 3/7 | chr12 | 21646654 | |||||||
chr12:21646682 | A | G | 1 | a0001c0001t0001g0085 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.247+217T>C | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 3/7 | chr12 | 21646682 | |||||||
chr12:21646732 | GC | G | 4 | a0001c0003t0002g0013 a0001c0003t0002g0040 a0001c0003t0002g0041 others(1): Show |
8 | HG01884.hp1 HG02257.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.247+166delG | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 3/7 | chr12 | 21646732 | |||||||
chr12:21646869 | T | G | 2 | a0001c0001t0001g0071 a0001c0001t0001g0105 |
2 | HG00280.hp2 HG00642.hp1 |
intron_variant | MODIFIER | c.247+30A>C | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 3/7 | chr12 | 21646869 | |||||||
chr12:21646878 | T | C | 1 | a0001c0004t0002g0042 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.247+21A>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 3/7 | chr12 | 21646878 | |||||||
chr12:21646895 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG02165.hp1 | splice_region_variant&intron_variant | LOW | c.247+4A>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 3/7 | chr12 | 21646895 | |||||||
chr12:21647065 | G | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.130-49C>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21647065 | |||||||
chr12:21647070 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.130-54G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21647070 | |||||||
chr12:21647172 | G | A | 4 | a0001c0003t0002g0013 a0001c0003t0002g0040 a0001c0003t0002g0041 others(1): Show |
8 | HG01884.hp1 HG02257.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.130-156C>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21647172 | |||||||
chr12:21647241 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.130-225G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21647241 | |||||||
chr12:21647653 | T | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.130-637A>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21647653 | |||||||
chr12:21647703 | C | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.130-687G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21647703 | |||||||
chr12:21647705 | G | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.130-689C>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21647705 | |||||||
chr12:21647711 | C | A | 1 | a0001c0004t0002g0042 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.130-695G>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21647711 | |||||||
chr12:21647713 | C | T | 1 | a0001c0001t0001g0015 | 4 | HG02257.hp2 HG02615.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-697G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21647713 | |||||||
chr12:21647716 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.130-700G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21647716 | |||||||
chr12:21647789 | C | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.130-773G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21647789 | |||||||
chr12:21647790 | GGGTTCA | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.130-780_130-775del others(6): Show |
LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21647790 | |||||||
chr12:21647797 | A | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.130-781T>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21647797 | |||||||
chr12:21647844 | G | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.130-828C>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21647844 | |||||||
chr12:21647856 | C | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0039 |
5 | HG02109.hp2 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.130-840G>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21647856 | |||||||
chr12:21648038 | GA | G | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(132): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.130-1023delT | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21648038 | |||||||
chr12:21648226 | A | C | 1 | a0001c0001t0001g0148 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.130-1210T>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21648226 | |||||||
chr12:21648394 | G | A | 1 | a0001c0002t0001g0142 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.130-1378C>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21648394 | |||||||
chr12:21648424 | C | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.130-1408G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21648424 | |||||||
chr12:21648445 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.130-1429G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21648445 | |||||||
chr12:21648462 | A | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.130-1446T>C | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21648462 | |||||||
chr12:21648535 | T | TG | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(132): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.130-1520dupC | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21648535 | |||||||
chr12:21648552 | G | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.130-1536C>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21648552 | |||||||
chr12:21648597 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.130-1581C>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21648597 | |||||||
chr12:21648645 | C | G | 5 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0067 others(2): Show |
15 | HG00140.hp2 HG00733.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.130-1629G>C | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21648645 | |||||||
chr12:21648717 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.130-1701G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21648717 | |||||||
chr12:21648850 | T | A | 6 | a0001c0001t0001g0037 a0001c0001t0001g0131 a0001c0001t0001g0132 others(3): Show |
7 | HG01243.hp1 HG02451.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.130-1834A>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21648850 | |||||||
chr12:21648863 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.130-1847C>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21648863 | |||||||
chr12:21648954 | A | C | 1 | a0001c0001t0001g0109 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.130-1938T>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21648954 | |||||||
chr12:21649026 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.130-2010T>C | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21649026 | |||||||
chr12:21649121 | G | A | 5 | a0001c0001t0001g0006 a0001c0001t0001g0099 a0001c0001t0001g0107 others(2): Show |
13 | HG00741.hp1 HG02055.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.130-2105C>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21649121 | |||||||
chr12:21649186 | G | A | 3 | a0001c0001t0001g0038 a0001c0001t0001g0145 a0001c0001t0001g0148 |
4 | HG01168.hp1 HG01169.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.130-2170C>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21649186 | |||||||
chr12:21649287 | C | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.130-2271G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21649287 | |||||||
chr12:21649294 | A | T | 1 | a0001c0001t0002g0020 | 2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.130-2278T>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21649294 | |||||||
chr12:21649387 | C | T | 6 | a0001c0002t0001g0019 a0001c0002t0001g0066 a0001c0002t0001g0138 others(3): Show |
8 | HG02622.hp2 HG02809.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.130-2371G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21649387 | |||||||
chr12:21649470 | T | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.130-2454A>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21649470 | |||||||
chr12:21649493 | C | G | 1 | a0001c0001t0001g0076 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.130-2477G>C | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21649493 | |||||||
chr12:21649500 | C | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.130-2484G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21649500 | |||||||
chr12:21649503 | G | C | 1 | a0001c0001t0001g0100 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.130-2487C>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21649503 | |||||||
chr12:21649632 | TA | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.130-2617delT | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21649632 | |||||||
chr12:21649674 | T | TA | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.130-2659dupT | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21649674 | |||||||
chr12:21649829 | T | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.130-2813A>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21649829 | |||||||
chr12:21649831 | C | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.130-2815G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21649831 | |||||||
chr12:21650096 | G | GA | 10 | a0001c0001t0001g0010 a0001c0001t0001g0039 a0001c0001t0001g0048 others(7): Show |
17 | HG01255.hp2 HG02015.hp1 HG02083.hp1 others(14): Show |
intron_variant | MODIFIER | c.130-3081dupT | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21650096 | |||||||
chr12:21650096 | G | GAAA | 58 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(55): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.130-3083_130-3081d others(5): Show |
LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21650096 | |||||||
chr12:21650103 | A | AAAAAT | 36 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(33): Show |
88 | HG00140.hp2 HG00642.hp1 HG00733.hp2 others(85): Show |
intron_variant | MODIFIER | c.130-3088_130-3087i others(7): Show |
LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21650103 | |||||||
chr12:21650103 | A | AAAAATAT | 20 | a0001c0001t0001g0014 a0001c0001t0001g0018 a0001c0001t0001g0021 others(17): Show |
29 | HG00642.hp2 HG01175.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.130-3088_130-3087i others(9): Show |
LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21650103 | |||||||
chr12:21650103 | A | AAT | 2 | a0001c0003t0002g0013 a0001c0003t0002g0040 |
6 | HG01884.hp1 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.130-3089_130-3088d others(4): Show |
LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21650103 | |||||||
chr12:21650104 | ATAC | A | 3 | a0001c0001t0001g0037 a0001c0001t0001g0118 a0001c0001t0001g0148 |
4 | HG01243.hp2 HG02647.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-3091_130-3089d others(5): Show |
LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21650104 | |||||||
chr12:21650104 | ATACACAC others(4): Show |
A | 1 | a0001c0001t0001g0076 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.130-3099_130-3089d others(13): Show |
LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21650104 | |||||||
chr12:21650105 | T | A | 11 | a0001c0001t0001g0010 a0001c0001t0001g0039 a0001c0001t0001g0048 others(8): Show |
18 | HG01255.hp2 HG02015.hp1 HG02083.hp1 others(15): Show |
intron_variant | MODIFIER | c.130-3089A>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21650105 | |||||||
chr12:21650105 | T | TAC | 6 | a0001c0002t0001g0019 a0001c0002t0001g0138 a0001c0002t0001g0139 others(3): Show |
6 | HG02809.hp1 HG02970.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.130-3091_130-3090d others(4): Show |
LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21650105 | |||||||
chr12:21650107 | C | A | 2 | a0001c0001t0001g0027 a0001c0001t0001g0048 |
3 | HG02015.hp2 HG02683.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.130-3091G>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21650107 | |||||||
chr12:21650107 | C | T | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(98): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.130-3091G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21650107 | |||||||
chr12:21650109 | C | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0118 |
3 | HG01243.hp2 HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.130-3093G>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21650109 | |||||||
chr12:21650109 | C | T | 58 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(55): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.130-3093G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21650109 | |||||||
chr12:21650111 | C | A | 1 | a0001c0001t0001g0022 | 2 | HG01255.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.130-3095G>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21650111 | |||||||
chr12:21650111 | C | T | 12 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0001t0001g0037 others(9): Show |
20 | HG01243.hp2 HG01255.hp2 HG02015.hp1 others(17): Show |
intron_variant | MODIFIER | c.130-3095G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21650111 | |||||||
chr12:21650113 | C | T | 5 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0037 others(2): Show |
8 | HG01243.hp2 HG01255.hp1 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.130-3097G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21650113 | |||||||
chr12:21650115 | C | T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0037 a0001c0001t0001g0148 |
5 | HG01255.hp1 HG01516.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.130-3099G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21650115 | |||||||
chr12:21650117 | C | A | 1 | a0001c0001t0001g0076 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.130-3101G>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21650117 | |||||||
chr12:21650117 | C | T | 2 | a0001c0001t0001g0022 a0001c0001t0001g0148 |
3 | HG01255.hp1 HG01516.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.130-3101G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21650117 | |||||||
chr12:21650119 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.130-3103G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21650119 | |||||||
chr12:21650121 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.130-3105G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21650121 | |||||||
chr12:21650123 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.130-3107G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21650123 | |||||||
chr12:21650145 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.130-3129G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21650145 | |||||||
chr12:21650147 | C | CAT | 5 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0056 others(2): Show |
13 | HG00642.hp2 HG01346.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.130-3132_130-3131i others(4): Show |
LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21650147 | |||||||
chr12:21650147 | C | T | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(115): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.130-3131G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21650147 | |||||||
chr12:21650149 | C | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(122): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.130-3133G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21650149 | |||||||
chr12:21650151 | C | CACACACA others(7): Show |
1 | a0001c0001t0001g0117 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.130-3136_130-3135i others(16): Show |
LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21650151 | |||||||
chr12:21650151 | C | CACATATA others(1): Show |
3 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0133 |
3 | HG01243.hp1 HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.130-3136_130-3135i others(10): Show |
LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21650151 | |||||||
chr12:21650151 | C | CATATAT | 3 | a0001c0001t0001g0038 a0001c0001t0001g0132 a0001c0001t0001g0145 |
4 | HG01168.hp1 HG01169.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.130-3136_130-3135i others(8): Show |
LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21650151 | |||||||
chr12:21650151 | C | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(123): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.130-3135G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21650151 | |||||||
chr12:21650152 | G | A | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(128): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.130-3136C>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21650152 | |||||||
chr12:21650152 | G | C | 7 | a0001c0001t0001g0037 a0001c0001t0001g0074 a0001c0001t0001g0131 others(4): Show |
8 | HG01243.hp1 HG02451.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.130-3136C>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21650152 | |||||||
chr12:21650154 | C | A | 3 | a0001c0001t0001g0034 a0001c0001t0001g0120 a0001c0001t0001g0146 |
4 | HG02615.hp1 HG02647.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.130-3138G>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21650154 | |||||||
chr12:21650190 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.130-3174G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21650190 | |||||||
chr12:21650343 | C | T | 6 | a0001c0001t0001g0037 a0001c0001t0001g0131 a0001c0001t0001g0132 others(3): Show |
7 | HG01243.hp1 HG02451.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.130-3327G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21650343 | |||||||
chr12:21650417 | T | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.130-3401A>C | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21650417 | |||||||
chr12:21650506 | G | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.130-3490C>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21650506 | |||||||
chr12:21650662 | G | C | 1 | a0001c0001t0001g0121 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.130-3646C>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21650662 | |||||||
chr12:21650751 | G | C | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(88): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.130-3735C>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21650751 | |||||||
chr12:21650770 | G | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.130-3754C>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21650770 | |||||||
chr12:21650836 | C | T | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(88): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.129+3707G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21650836 | |||||||
chr12:21650957 | A | G | 1 | a0001c0001t0001g0039 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.129+3586T>C | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21650957 | |||||||
chr12:21650985 | A | C | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(135): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.129+3558T>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21650985 | |||||||
chr12:21651074 | A | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.129+3469T>C | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21651074 | |||||||
chr12:21651251 | T | C | 4 | a0001c0003t0002g0013 a0001c0003t0002g0040 a0001c0003t0002g0041 others(1): Show |
8 | HG01884.hp1 HG02257.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.129+3292A>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21651251 | |||||||
chr12:21651464 | C | T | 4 | a0001c0002t0001g0019 a0001c0002t0001g0066 a0001c0002t0001g0138 others(1): Show |
6 | HG02622.hp2 HG02809.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.129+3079G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21651464 | |||||||
chr12:21651536 | G | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.129+3007C>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21651536 | |||||||
chr12:21651619 | AGC | A | 2 | a0001c0001t0001g0010 a0001c0001t0004g0122 |
8 | HG02258.hp1 HG02559.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.129+2922_129+2923d others(4): Show |
LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21651619 | |||||||
chr12:21651653 | T | C | 14 | a0001c0002t0001g0019 a0001c0002t0001g0036 a0001c0002t0001g0066 others(11): Show |
21 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.129+2890A>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21651653 | |||||||
chr12:21651675 | A | G | 1 | a0001c0001t0001g0048 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.129+2868T>C | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21651675 | |||||||
chr12:21651718 | T | C | 1 | a0001c0001t0001g0123 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.129+2825A>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21651718 | |||||||
chr12:21651822 | T | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.129+2721A>C | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21651822 | |||||||
chr12:21651944 | C | T | 2 | a0001c0001t0001g0038 a0001c0001t0001g0145 |
3 | HG01168.hp1 HG01169.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.129+2599G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21651944 | |||||||
chr12:21651987 | G | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(135): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.129+2556C>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21651987 | |||||||
chr12:21652105 | G | C | 1 | a0001c0001t0001g0124 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.129+2438C>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21652105 | |||||||
chr12:21652108 | T | TACA | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.129+2432_129+2434d others(5): Show |
LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21652108 | |||||||
chr12:21652359 | C | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.129+2184G>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21652359 | |||||||
chr12:21652374 | C | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.129+2169G>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21652374 | |||||||
chr12:21652402 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.129+2141G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21652402 | |||||||
chr12:21652584 | GTAGTTAC others(62): Show |
G | 1 | a0001c0001t0001g0047 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.129+1890_129+1958d others(71): Show |
LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21652584 | |||||||
chr12:21652598 | TATTGAAA others(131): Show |
T | 5 | a0001c0001t0001g0046 a0001c0001t0001g0054 a0001c0001t0001g0127 others(2): Show |
5 | HG02135.hp2 HG03017.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.129+1807_129+1944d others(2): Show |
LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21652598 | |||||||
chr12:21652603 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.129+1940T>C | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21652603 | |||||||
chr12:21652654 | T | CAGTTACC others(41): Show |
4 | a0001c0003t0002g0013 a0001c0003t0002g0040 a0001c0003t0002g0041 others(1): Show |
8 | HG01884.hp1 HG02257.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.129+1889_129+1890i others(50): Show |
LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21652654 | |||||||
chr12:21652720 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.129+1823A>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21652720 | |||||||
chr12:21652807 | T | C | 1 | a0001c0001t0001g0044 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.129+1736A>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21652807 | |||||||
chr12:21652913 | G | A | 5 | a0001c0001t0001g0037 a0001c0001t0001g0131 a0001c0001t0001g0132 others(2): Show |
6 | HG01243.hp1 HG02451.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.129+1630C>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21652913 | |||||||
chr12:21653039 | T | C | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(135): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.129+1504A>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21653039 | |||||||
chr12:21653042 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.129+1501T>C | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21653042 | |||||||
chr12:21653047 | T | C | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(130): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.129+1496A>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21653047 | |||||||
chr12:21653048 | A | C | 1 | a0001c0001t0001g0070 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.129+1495T>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21653048 | |||||||
chr12:21653245 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.129+1298C>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21653245 | |||||||
chr12:21653374 | C | T | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(142): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.129+1169G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21653374 | |||||||
chr12:21653504 | A | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(135): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.129+1039T>C | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21653504 | |||||||
chr12:21653570 | T | C | 1 | a0001c0002t0001g0142 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.129+973A>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21653570 | |||||||
chr12:21653666 | G | GTATGTAT others(1): Show |
138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(135): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.129+869_129+876dup others(8): Show |
LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21653666 | |||||||
chr12:21653888 | A | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.129+655T>C | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21653888 | |||||||
chr12:21653952 | T | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.129+591A>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21653952 | |||||||
chr12:21654190 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.129+353C>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21654190 | |||||||
chr12:21654362 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.129+181T>C | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21654362 | |||||||
chr12:21654498 | T | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.129+45A>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 2/7 | chr12 | 21654498 | |||||||
chr12:21654706 | G | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.-6-29C>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 1/7 | chr12 | 21654706 | |||||||
chr12:21654753 | C | G | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(88): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.-6-76G>C | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 1/7 | chr12 | 21654753 | |||||||
chr12:21654765 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-6-88G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 1/7 | chr12 | 21654765 | |||||||
chr12:21654827 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-6-150C>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 1/7 | chr12 | 21654827 | |||||||
chr12:21655011 | C | T | 4 | a0001c0003t0002g0013 a0001c0003t0002g0040 a0001c0003t0002g0041 others(1): Show |
8 | HG01884.hp1 HG02257.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-6-334G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 1/7 | chr12 | 21655011 | |||||||
chr12:21655335 | T | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.-6-658A>C | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 1/7 | chr12 | 21655335 | |||||||
chr12:21655497 | T | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.-6-820A>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 1/7 | chr12 | 21655497 | |||||||
chr12:21655498 | G | A | 1 | a0001c0001t0001g0045 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-6-821C>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 1/7 | chr12 | 21655498 | |||||||
chr12:21655730 | T | TA | 4 | a0001c0003t0002g0013 a0001c0003t0002g0040 a0001c0003t0002g0041 others(1): Show |
8 | HG01884.hp1 HG02257.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-6-1054dupT | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 1/7 | chr12 | 21655730 | |||||||
chr12:21655736 | A | C | 1 | a0001c0001t0001g0046 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-6-1059T>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 1/7 | chr12 | 21655736 | |||||||
chr12:21655737 | A | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.-6-1060T>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 1/7 | chr12 | 21655737 | |||||||
chr12:21655857 | G | A | 1 | a0001c0002t0001g0066 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-6-1180C>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 1/7 | chr12 | 21655857 | |||||||
chr12:21655868 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-6-1191G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 1/7 | chr12 | 21655868 | |||||||
chr12:21655957 | C | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.-6-1280G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 1/7 | chr12 | 21655957 | |||||||
chr12:21655982 | C | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.-6-1305G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 1/7 | chr12 | 21655982 | |||||||
chr12:21656118 | T | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(131): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.-6-1441A>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 1/7 | chr12 | 21656118 | |||||||
chr12:21656162 | C | T | 1 | a0001c0001t0001g0037 | 2 | HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-6-1485G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 1/7 | chr12 | 21656162 | |||||||
chr12:21656293 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-7+1458C>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 1/7 | chr12 | 21656293 | |||||||
chr12:21656402 | C | A | 1 | a0001c0001t0001g0035 | 2 | HG01175.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.-7+1349G>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 1/7 | chr12 | 21656402 | |||||||
chr12:21656452 | G | A | 1 | a0001c0002t0001g0143 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-7+1299C>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 1/7 | chr12 | 21656452 | |||||||
chr12:21656514 | G | A | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(130): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.-7+1237C>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 1/7 | chr12 | 21656514 | |||||||
chr12:21656532 | C | CCCTGTGT others(3): Show |
1 | a0001c0002t0001g0144 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-7+1218_-7+1219ins others(10): Show |
LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 1/7 | chr12 | 21656532 | |||||||
chr12:21656603 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-7+1148G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 1/7 | chr12 | 21656603 | |||||||
chr12:21656631 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-7+1120T>C | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 1/7 | chr12 | 21656631 | |||||||
chr12:21656707 | A | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(135): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.-7+1044T>C | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 1/7 | chr12 | 21656707 | |||||||
chr12:21656762 | C | CTGTAT | 8 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0043 others(5): Show |
14 | NA18612.hp2 NA18747.hp2 NA18959.hp2 others(11): Show |
intron_variant | MODIFIER | c.-7+988_-7+989insAT others(3): Show |
LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 1/7 | chr12 | 21656762 | |||||||
chr12:21656822 | T | C | 3 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0136 |
3 | NA18612.hp2 NA18977.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.-7+929A>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 1/7 | chr12 | 21656822 | |||||||
chr12:21656872 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-7+879C>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 1/7 | chr12 | 21656872 | |||||||
chr12:21656873 | C | T | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(130): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.-7+878G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 1/7 | chr12 | 21656873 | |||||||
chr12:21656937 | T | C | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(130): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.-7+814A>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 1/7 | chr12 | 21656937 | |||||||
chr12:21657015 | CA | C | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(130): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.-7+735delT | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 1/7 | chr12 | 21657015 | |||||||
chr12:21657048 | A | C | 1 | a0001c0002t0001g0138 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-7+703T>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 1/7 | chr12 | 21657048 | |||||||
chr12:21657194 | G | C | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(130): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.-7+557C>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 1/7 | chr12 | 21657194 | |||||||
chr12:21657346 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-7+405C>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 1/7 | chr12 | 21657346 | |||||||
chr12:21657561 | G | T | 3 | a0001c0001t0001g0026 a0001c0001t0001g0064 a0001c0001t0001g0065 |
4 | NA18952.hp2 NA18973.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7+190C>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 1/7 | chr12 | 21657561 | |||||||
chr12:21657573 | C | G | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(124): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.-7+178G>C | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 1/7 | chr12 | 21657573 | |||||||
chr12:21657596 | A | G | 5 | a0001c0001t0002g0020 a0001c0003t0002g0013 a0001c0003t0002g0040 others(2): Show |
10 | HG01884.hp1 HG02257.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-7+155T>C | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 1/7 | chr12 | 21657596 | |||||||
chr12:21657632 | G | A | 1 | a0001c0002t0001g0149 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-7+119C>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 1/7 | chr12 | 21657632 | |||||||
chr12:21657687 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-7+64A>G | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 1/7 | chr12 | 21657687 | |||||||
chr12:21657708 | C | A | 1 | a0001c0001t0001g0012 | 6 | NA18612.hp1 NA18944.hp2 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7+43G>T | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 1/7 | chr12 | 21657708 | |||||||
chr12:21657712 | C | T | 33 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0014 others(30): Show |
66 | HG00280.hp1 HG00642.hp2 HG01069.hp2 others(63): Show |
intron_variant | MODIFIER | c.-7+39G>A | LDHB | ENSG00000111716.14 | transcript | ENST00000350669.5 | protein_coding | 1/7 | chr12 | 21657712 |