Item | Value |
---|---|
geneid | 4803 |
ensemblid | ENSG00000134259.6 |
hgncid | 7808 |
symbol | NGF |
name | nerve growth factor |
refseq_nuc | NM_002506.3 |
refseq_prot | NP_002497.2 |
ensembl_nuc | ENST00000369512.3 |
ensembl_prot | ENSP00000358525.2 |
mane_status | MANE Select |
chr | chr1 |
start | 115285917 |
end | 115338249 |
strand | - |
ver | v1.2 |
region | chr1:115285917-115338249 |
region5000 | chr1:115280917-115343249 |
regionname0 | NGF_chr1_115285917_115338249 |
regionname5000 | NGF_chr1_115280917_115343249 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 241 | 323 | 84 | 57 | 141 | 5 | 34 | 115 | NGF_chr1_115280917_115343249 | NGF | MSMLF others(236): Show |
chr1 | 115280917 | 115343249 |
a0002 | 0/0 | 241 | 86 | 11 | 23 | 41 | 1 | 10 | 33 | NGF_chr1_115280917_115343249 | NGF | MSMLF others(236): Show |
chr1 | 115280917 | 115343249 |
a0003 | 0/0 | 241 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | NGF_chr1_115280917_115343249 | NGF | MSMLF others(236): Show |
chr1 | 115280917 | 115343249 |
a0004 | 0/0 | 241 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | NGF_chr1_115280917_115343249 | NGF | MSMLF others(236): Show |
chr1 | 115280917 | 115343249 |
a0005 | 0/0 | 241 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | MSMLF others(236): Show |
chr1 | 115280917 | 115343249 |
a0006 | 0/0 | 241 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | MSMLF others(236): Show |
chr1 | 115280917 | 115343249 |
a0007 | 0/0 | 241 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NGF_chr1_115280917_115343249 | NGF | MSMLF others(236): Show |
chr1 | 115280917 | 115343249 |
a0008 | 0/0 | 241 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | MSMLF others(236): Show |
chr1 | 115280917 | 115343249 |
a0009 | 0/0 | 241 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | MSMLF others(236): Show |
chr1 | 115280917 | 115343249 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 723 | 308 | 70 | 56 | 141 | 5 | 34 | NGF_chr1_115280917_115343249 | NGF | ATGTC others(718): Show |
chr1 | 115280917 | 115343249 | ||
a0001c0003 | 0/0 | 723 | 15 | 14 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | ATGTC others(718): Show |
chr1 | 115280917 | 115343249 | ||
a0002c0002 | 0/0 | 723 | 86 | 11 | 23 | 41 | 1 | 10 | NGF_chr1_115280917_115343249 | NGF | ATGTC others(718): Show |
chr1 | 115280917 | 115343249 | ||
a0003c0004 | 0/0 | 723 | 2 | 0 | 1 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | ATGTC others(718): Show |
chr1 | 115280917 | 115343249 | ||
a0004c0005 | 0/0 | 723 | 2 | 0 | 0 | 0 | 0 | 2 | NGF_chr1_115280917_115343249 | NGF | ATGTC others(718): Show |
chr1 | 115280917 | 115343249 | ||
a0005c0006 | 0/0 | 723 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | ATGTC others(718): Show |
chr1 | 115280917 | 115343249 | ||
a0006c0007 | 0/0 | 723 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | ATGTC others(718): Show |
chr1 | 115280917 | 115343249 | ||
a0007c0010 | 0/0 | 723 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | ATGTC others(718): Show |
chr1 | 115280917 | 115343249 | ||
a0008c0009 | 0/0 | 723 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | ATGTC others(718): Show |
chr1 | 115280917 | 115343249 | ||
a0009c0008 | 0/0 | 723 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | ATGTC others(718): Show |
chr1 | 115280917 | 115343249 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1061 | 307 | 70 | 56 | 141 | 5 | 33 | NGF_chr1_115280917_115343249 | NGF | GCTCC others(1056): Show |
chr1 | 115280917 | 115343249 |
a0001c0001t0002 | 0/0 | 1061 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | GCTCC others(1056): Show |
chr1 | 115280917 | 115343249 |
a0001c0003t0001 | 0/0 | 1061 | 15 | 14 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | GCTCC others(1056): Show |
chr1 | 115280917 | 115343249 |
a0002c0002t0001 | 0/0 | 1061 | 86 | 11 | 23 | 41 | 1 | 10 | NGF_chr1_115280917_115343249 | NGF | GCTCC others(1056): Show |
chr1 | 115280917 | 115343249 |
a0003c0004t0001 | 0/0 | 1061 | 2 | 0 | 1 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | GCTCC others(1056): Show |
chr1 | 115280917 | 115343249 |
a0004c0005t0001 | 0/0 | 1061 | 2 | 0 | 0 | 0 | 0 | 2 | NGF_chr1_115280917_115343249 | NGF | GCTCC others(1056): Show |
chr1 | 115280917 | 115343249 |
a0005c0006t0001 | 0/0 | 1061 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | GCTCC others(1056): Show |
chr1 | 115280917 | 115343249 |
a0006c0007t0001 | 0/0 | 1061 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | GCTCC others(1056): Show |
chr1 | 115280917 | 115343249 |
a0007c0010t0001 | 0/0 | 1061 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | GCTCC others(1056): Show |
chr1 | 115280917 | 115343249 |
a0008c0009t0001 | 0/0 | 1061 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | GCTCC others(1056): Show |
chr1 | 115280917 | 115343249 |
a0009c0008t0001 | 0/0 | 1061 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | GCTCC others(1056): Show |
chr1 | 115280917 | 115343249 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0135 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0287 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0368 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0377 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0380 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0384 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0387 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0389 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0390 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0391 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0001g0394 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0001t0002g0366 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0003t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0003t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0003t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0003t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0003t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0003t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0003t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0003t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0003t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0003t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0003t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0003t0001g0388 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0003t0001g0393 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0003t0001g0395 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0001c0003t0001g0396 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0004 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0369 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0379 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0383 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0392 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0002c0002t0001g0397 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0003c0004t0001g0381 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0003c0004t0001g0382 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0004c0005t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0004c0005t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0005c0006t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0006c0007t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0007c0010t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0008c0009t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
a0009c0008t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0368 | EUR | GBR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0353 | EUR | GBR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0136 | EUR | FIN | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0284 | EUR | FIN | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00408 | hp1 | a0002 | c0002 | t0001 | g0256 | EAS | CHS | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00438 | hp2 | a0002 | c0002 | t0001 | g0085 | EAS | CHS | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | CHS | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | CHS | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00621 | hp1 | a0002 | c0002 | t0001 | g0063 | EAS | CHS | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0358 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00639 | hp2 | a0002 | c0002 | t0001 | g0338 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00673 | hp2 | a0002 | c0002 | t0001 | g0089 | EAS | CHS | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0380 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00733 | hp2 | a0002 | c0002 | t0001 | g0342 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0315 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0336 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00738 | hp1 | a0002 | c0002 | t0001 | g0362 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00741 | hp1 | a0002 | c0002 | t0001 | g0375 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0318 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0330 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0317 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0352 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0326 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01099 | hp1 | a0002 | c0002 | t0001 | g0255 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01099 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01109 | hp2 | a0003 | c0004 | t0001 | g0382 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0325 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0343 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0324 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01175 | hp2 | a0002 | c0002 | t0001 | g0323 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01192 | hp1 | a0002 | c0002 | t0001 | g0244 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0376 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01243 | hp1 | a0002 | c0002 | t0001 | g0331 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01256 | hp2 | a0002 | c0002 | t0001 | g0234 | AMR | CLM | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | CLM | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0250 | AMR | CLM | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0329 | AMR | CLM | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01346 | hp1 | a0005 | c0006 | t0001 | g0265 | AMR | CLM | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0316 | AMR | CLM | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0367 | AMR | CLM | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0383 | AMR | CLM | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01361 | hp2 | a0002 | c0002 | t0001 | g0207 | AMR | CLM | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01433 | hp2 | a0001 | c0003 | t0001 | g0396 | AMR | CLM | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | ACB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0374 | AFR | ACB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0391 | AFR | ACB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0390 | AFR | ACB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PEL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | PEL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01943 | hp1 | a0002 | c0002 | t0001 | g0203 | AMR | PEL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0337 | AMR | PEL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01952 | hp1 | a0002 | c0002 | t0001 | g0360 | AMR | PEL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0363 | AMR | PEL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02004 | hp2 | a0002 | c0002 | t0001 | g0340 | AMR | PEL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | KHV | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02027 | hp2 | a0002 | c0002 | t0001 | g0168 | EAS | KHV | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02055 | hp2 | a0001 | c0003 | t0001 | g0395 | AFR | ACB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02056 | hp2 | a0002 | c0002 | t0001 | g0067 | EAS | KHV | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02071 | hp2 | a0002 | c0002 | t0001 | g0291 | EAS | KHV | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | KHV | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02145 | hp1 | a0001 | c0003 | t0001 | g0393 | AFR | ACB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02145 | hp2 | a0001 | c0003 | t0001 | g0195 | AFR | ACB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | CDX | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02155 | hp2 | a0002 | c0002 | t0001 | g0098 | EAS | CDX | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02257 | hp1 | a0001 | c0003 | t0001 | g0037 | AFR | ACB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | ACB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0394 | AFR | ACB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02273 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | ACB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02293 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02451 | hp1 | a0002 | c0002 | t0001 | g0034 | AFR | ACB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0302 | AFR | ACB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0366 | SAS | PJL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02615 | hp1 | a0002 | c0002 | t0001 | g0004 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02622 | hp1 | a0002 | c0002 | t0001 | g0397 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02647 | hp1 | a0001 | c0003 | t0001 | g0388 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02683 | hp1 | a0002 | c0002 | t0001 | g0359 | SAS | PJL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02683 | hp2 | a0002 | c0002 | t0001 | g0344 | SAS | PJL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02698 | hp1 | a0002 | c0002 | t0001 | g0369 | SAS | PJL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02698 | hp2 | a0002 | c0002 | t0001 | g0268 | SAS | PJL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02717 | hp1 | a0001 | c0003 | t0001 | g0038 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0385 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0377 | SAS | PJL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02738 | hp1 | a0002 | c0002 | t0001 | g0279 | SAS | PJL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0384 | SAS | PJL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02809 | hp1 | a0002 | c0002 | t0001 | g0186 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02818 | hp1 | a0002 | c0002 | t0001 | g0185 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02922 | hp1 | a0001 | c0003 | t0001 | g0310 | AFR | ESN | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | ESN | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | ESN | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0341 | SAS | PJL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03017 | hp2 | a0002 | c0002 | t0001 | g0155 | SAS | PJL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | MSL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | MSL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03130 | hp1 | a0001 | c0003 | t0001 | g0027 | AFR | ESN | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03130 | hp2 | a0002 | c0002 | t0001 | g0060 | AFR | ESN | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03139 | hp1 | a0001 | c0003 | t0001 | g0179 | AFR | ESN | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03195 | hp1 | a0001 | c0003 | t0001 | g0141 | AFR | ESN | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | ESN | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | MSL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0312 | AFR | MSL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0283 | SAS | PJL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03453 | hp1 | a0002 | c0002 | t0001 | g0392 | AFR | MSL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0389 | AFR | MSL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03486 | hp2 | a0002 | c0002 | t0001 | g0190 | AFR | MSL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03490 | hp1 | a0002 | c0002 | t0001 | g0321 | SAS | PJL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03490 | hp2 | a0004 | c0005 | t0001 | g0101 | SAS | PJL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03492 | hp1 | a0004 | c0005 | t0001 | g0102 | SAS | PJL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03516 | hp1 | a0006 | c0007 | t0001 | g0151 | AFR | ESN | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ESN | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | MSL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0319 | SAS | PJL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | STU | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0267 | SAS | STU | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0327 | SAS | PJL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0277 | SAS | PJL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03710 | hp1 | a0002 | c0002 | t0001 | g0259 | SAS | PJL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0334 | SAS | BEB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | BEB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | BEB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | BEB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03927 | hp1 | a0003 | c0004 | t0001 | g0381 | SAS | BEB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | BEB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | BEB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03942 | hp2 | a0002 | c0002 | t0001 | g0349 | SAS | BEB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | STU | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0335 | SAS | STU | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | BEB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | BEB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0346 | SAS | STU | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG04199 | hp2 | a0007 | c0010 | t0001 | g0288 | SAS | STU | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | STU | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0270 | SAS | STU | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | STU | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0293 | SAS | STU | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18522 | hp2 | a0001 | c0003 | t0001 | g0041 | AFR | YRI | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0371 | EAS | CHB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | CHB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0386 | AFR | YRI | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18906 | hp2 | a0001 | c0003 | t0001 | g0145 | AFR | YRI | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18940 | hp2 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0364 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18943 | hp2 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0378 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18946 | hp1 | a0002 | c0002 | t0001 | g0276 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0365 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18950 | hp1 | a0002 | c0002 | t0001 | g0129 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18953 | hp1 | a0002 | c0002 | t0001 | g0108 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18956 | hp2 | a0002 | c0002 | t0001 | g0264 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18962 | hp1 | a0002 | c0002 | t0001 | g0260 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0356 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18964 | hp1 | a0002 | c0002 | t0001 | g0049 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18965 | hp2 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18966 | hp2 | a0002 | c0002 | t0001 | g0061 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18967 | hp1 | a0002 | c0002 | t0001 | g0332 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18971 | hp1 | a0002 | c0002 | t0001 | g0139 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18972 | hp1 | a0002 | c0002 | t0001 | g0066 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18974 | hp1 | a0002 | c0002 | t0001 | g0046 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18978 | hp1 | a0002 | c0002 | t0001 | g0111 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18984 | hp1 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18987 | hp1 | a0008 | c0009 | t0001 | g0173 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18987 | hp2 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0354 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18991 | hp2 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0372 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0370 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18995 | hp2 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18998 | hp1 | a0002 | c0002 | t0001 | g0153 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19002 | hp2 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19007 | hp2 | a0002 | c0002 | t0001 | g0091 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19009 | hp2 | a0002 | c0002 | t0001 | g0254 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19012 | hp1 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0387 | AFR | LWK | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | LWK | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19056 | hp1 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19056 | hp2 | a0002 | c0002 | t0001 | g0313 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0357 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0083 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19072 | hp1 | a0002 | c0002 | t0001 | g0253 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19074 | hp2 | a0009 | c0008 | t0001 | g0243 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19076 | hp1 | a0002 | c0002 | t0001 | g0105 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19080 | hp2 | a0002 | c0002 | t0001 | g0093 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19081 | hp1 | a0002 | c0002 | t0001 | g0114 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19084 | hp2 | a0002 | c0002 | t0001 | g0086 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19086 | hp2 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0345 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ASW | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ASW | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA20805 | hp1 | a0002 | c0002 | t0001 | g0379 | EUR | TSI | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0183 | EUR | TSI | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | GIH | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA20905 | hp2 | a0002 | c0002 | t0001 | g0146 | SAS | GIH | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG01123 | hp2 | a0002 | c0002 | t0001 | g0361 | AMR | CLM | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0373 | AFR | ACB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | ACB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG02559 | hp2 | a0002 | c0002 | t0001 | g0320 | AFR | ACB | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG03471 | hp2 | a0001 | c0003 | t0001 | g0140 | AFR | MSL | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | USA | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
HG06807 | hp2 | a0002 | c0002 | t0001 | g0178 | AFR | USA | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA20300 | hp1 | a0001 | c0003 | t0001 | g0040 | AFR | USA | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | USA | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA21309 | hp1 | a0002 | c0002 | t0001 | g0035 | AFR | LWK | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | LWK | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0287 | REF | REF | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0135 | REF | REF | NGF_chr1_115280917_115343249 | NGF | chr1 | 115280917 | 115343249 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:115286474 | C | T | 1 | a0009 | 1 | NA19074.hp2 | missense_variant | MODERATE | c.322G>A | p.Gly108Ser | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 3/3 | 504/1061 | 322/726 | 108/241 | chr1 | 115286474 | |||
chr1:115286504 | C | T | 1 | a0004 | 2 | HG03490.hp2 HG03492.hp1 |
missense_variant | MODERATE | c.292G>A | p.Ala98Thr | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 3/3 | 474/1061 | 292/726 | 98/241 | chr1 | 115286504 | |||
chr1:115286557 | C | T | 1 | a0003 | 2 | HG01109.hp2 HG03927.hp1 |
missense_variant | MODERATE | c.239G>A | p.Arg80Gln | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 3/3 | 421/1061 | 239/726 | 80/241 | chr1 | 115286557 | |||
chr1:115286582 | C | T | 1 | a0006 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.214G>A | p.Val72Met | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 3/3 | 396/1061 | 214/726 | 72/241 | chr1 | 115286582 | |||
chr1:115286623 | G | A | 1 | a0007 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.173C>T | p.Ala58Val | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 3/3 | 355/1061 | 173/726 | 58/241 | chr1 | 115286623 | |||
chr1:115286641 | C | A | 1 | a0008 | 1 | NA18987.hp1 | missense_variant | MODERATE | c.155G>T | p.Arg52Leu | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 3/3 | 337/1061 | 155/726 | 52/241 | chr1 | 115286641 | |||
chr1:115286692 | G | A | 2 | a0002 a0007 |
87 | HG00408.hp1 HG00438.hp2 HG00621.hp1 others(84): Show |
missense_variant | MODERATE | c.104C>T | p.Ala35Val | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 3/3 | 286/1061 | 104/726 | 35/241 | chr1 | 115286692 | |||
chr1:115286753 | C | G | 1 | a0005 | 1 | HG01346.hp1 | missense_variant | MODERATE | c.43G>C | p.Gly15Arg | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 3/3 | 225/1061 | 43/726 | 15/241 | chr1 | 115286753 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:115286742 | C | T | 1 | a0001c0003 | 15 | HG01433.hp2 HG02055.hp2 HG02145.hp1 others(12): Show |
synonymous_variant | LOW | c.54G>A | p.Ala18Ala | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 3/3 | 236/1061 | 54/726 | 18/241 | chr1 | 115286742 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:115286057 | G | A | 1 | a0001c0001t0002 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 3/3 | 13 | chr1 | 115286057 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:115286925 | C | G | 2 | a0003c0004t0001g0381 a0003c0004t0001g0382 |
2 | HG01109.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-12-118G>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115286925 | |||||||
chr1:115286948 | G | T | 1 | a0002c0002t0001g0268 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-12-141C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115286948 | |||||||
chr1:115286962 | G | T | 1 | a0001c0003t0001g0179 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-12-155C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115286962 | |||||||
chr1:115286982 | C | T | 1 | a0001c0001t0001g0092 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-12-175G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115286982 | |||||||
chr1:115287181 | G | A | 3 | a0001c0001t0001g0059 a0001c0001t0001g0096 a0001c0001t0001g0301 |
3 | HG00423.hp1 NA19066.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.-12-374C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115287181 | |||||||
chr1:115287199 | T | C | 392 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(389): Show |
413 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(410): Show |
intron_variant | MODIFIER | c.-12-392A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115287199 | |||||||
chr1:115287273 | G | A | 4 | a0001c0001t0001g0133 a0001c0001t0001g0143 a0001c0001t0001g0302 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12-466C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115287273 | |||||||
chr1:115287294 | T | C | 2 | a0001c0001t0001g0081 a0001c0001t0001g0100 |
2 | NA18941.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.-12-487A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115287294 | |||||||
chr1:115287322 | C | A | 177 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(174): Show |
188 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.-12-515G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115287322 | |||||||
chr1:115287365 | C | T | 84 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0033 others(81): Show |
87 | HG00408.hp1 HG00438.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.-12-558G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115287365 | |||||||
chr1:115287539 | G | A | 1 | a0001c0001t0001g0245 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-12-732C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115287539 | |||||||
chr1:115287829 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0374 |
2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-12-1022G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115287829 | |||||||
chr1:115287840 | C | G | 30 | a0001c0001t0001g0031 a0001c0001t0001g0039 a0001c0001t0001g0097 others(27): Show |
30 | HG01433.hp2 HG02055.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.-12-1033G>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115287840 | |||||||
chr1:115287849 | T | C | 1 | a0001c0001t0001g0297 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-12-1042A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115287849 | |||||||
chr1:115287916 | C | T | 1 | a0001c0001t0001g0020 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-12-1109G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115287916 | |||||||
chr1:115287954 | C | T | 1 | a0001c0001t0001g0365 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-12-1147G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115287954 | |||||||
chr1:115288005 | A | C | 12 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0001g0030 others(9): Show |
13 | HG00423.hp1 HG00741.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.-12-1198T>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115288005 | |||||||
chr1:115288010 | T | C | 115 | a0001c0001t0001g0031 a0001c0001t0001g0042 a0001c0001t0001g0097 others(112): Show |
117 | HG00408.hp1 HG00438.hp2 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.-12-1203A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115288010 | |||||||
chr1:115288088 | C | G | 1 | a0001c0001t0001g0132 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-12-1281G>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115288088 | |||||||
chr1:115288232 | C | G | 12 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0001g0030 others(9): Show |
13 | HG00423.hp1 HG00741.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.-12-1425G>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115288232 | |||||||
chr1:115288270 | G | C | 1 | a0002c0002t0001g0276 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-12-1463C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115288270 | |||||||
chr1:115288290 | C | T | 15 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0018 others(12): Show |
19 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.-12-1483G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115288290 | |||||||
chr1:115288370 | G | A | 2 | a0001c0001t0001g0176 a0001c0001t0001g0180 |
2 | HG03098.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-12-1563C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115288370 | |||||||
chr1:115288581 | G | A | 2 | a0003c0004t0001g0381 a0003c0004t0001g0382 |
2 | HG01109.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-12-1774C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115288581 | |||||||
chr1:115288856 | A | G | 3 | a0001c0001t0001g0039 a0001c0001t0001g0172 a0001c0001t0001g0246 |
3 | HG02055.hp1 HG02559.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-12-2049T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115288856 | |||||||
chr1:115288940 | C | G | 1 | a0001c0001t0001g0039 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-12-2133G>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115288940 | |||||||
chr1:115289136 | C | T | 1 | a0001c0001t0001g0389 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-12-2329G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115289136 | |||||||
chr1:115289161 | G | A | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | HG00280.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-12-2354C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115289161 | |||||||
chr1:115289162 | C | T | 64 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0020 others(61): Show |
66 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.-12-2355G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115289162 | |||||||
chr1:115289210 | C | G | 2 | a0001c0001t0001g0208 a0001c0001t0001g0302 |
2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-12-2403G>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115289210 | |||||||
chr1:115289278 | A | C | 3 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0289 |
3 | HG00408.hp2 HG00621.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.-12-2471T>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115289278 | |||||||
chr1:115289372 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-12-2565G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115289372 | |||||||
chr1:115289374 | A | G | 1 | a0001c0001t0001g0365 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-12-2567T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115289374 | |||||||
chr1:115289382 | A | G | 2 | a0001c0001t0001g0208 a0001c0001t0001g0302 |
2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-12-2575T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115289382 | |||||||
chr1:115289515 | G | T | 392 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(389): Show |
413 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(410): Show |
intron_variant | MODIFIER | c.-12-2708C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115289515 | |||||||
chr1:115289991 | T | A | 1 | a0001c0001t0001g0252 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-12-3184A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115289991 | |||||||
chr1:115290261 | C | G | 64 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(61): Show |
69 | HG00423.hp1 HG00544.hp2 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.-13+3366G>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115290261 | |||||||
chr1:115290371 | A | T | 2 | a0001c0001t0001g0121 a0001c0001t0001g0343 |
2 | HG01168.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.-13+3256T>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115290371 | |||||||
chr1:115290385 | T | A | 1 | a0001c0001t0001g0295 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-13+3242A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115290385 | |||||||
chr1:115290386 | C | CT | 23 | a0001c0001t0001g0024 a0001c0001t0001g0042 a0001c0001t0001g0076 others(20): Show |
23 | HG00621.hp2 HG00673.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.-13+3240dupA | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115290386 | |||||||
chr1:115290386 | CT | C | 147 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(144): Show |
163 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(160): Show |
intron_variant | MODIFIER | c.-13+3240delA | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115290386 | |||||||
chr1:115290386 | CTT | C | 83 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0032 others(80): Show |
87 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.-13+3239_-13+3240d others(4): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115290386 | |||||||
chr1:115290386 | CTTT | C | 24 | a0001c0001t0001g0025 a0001c0001t0001g0036 a0001c0001t0001g0172 others(21): Show |
24 | HG01168.hp1 HG01433.hp2 HG01943.hp1 others(21): Show |
intron_variant | MODIFIER | c.-13+3238_-13+3240d others(5): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115290386 | |||||||
chr1:115290386 | CTTTTT | C | 7 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0298 others(4): Show |
7 | HG01081.hp1 HG01884.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.-13+3236_-13+3240d others(7): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115290386 | |||||||
chr1:115290386 | CTTTTTTT others(8): Show |
C | 6 | a0001c0001t0001g0022 a0001c0001t0001g0097 a0001c0001t0001g0217 others(3): Show |
6 | HG02451.hp1 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-13+3226_-13+3240d others(17): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115290386 | |||||||
chr1:115290405 | T | C | 2 | a0001c0003t0001g0388 a0001c0003t0001g0393 |
2 | HG02145.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-13+3222A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115290405 | |||||||
chr1:115290535 | A | G | 1 | a0001c0001t0001g0294 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-13+3092T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115290535 | |||||||
chr1:115290553 | G | A | 2 | a0001c0001t0001g0172 a0001c0001t0001g0246 |
2 | HG02559.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-13+3074C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115290553 | |||||||
chr1:115290676 | G | A | 9 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0077 others(6): Show |
9 | HG01884.hp2 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-13+2951C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115290676 | |||||||
chr1:115290796 | T | C | 2 | a0001c0003t0001g0388 a0001c0003t0001g0393 |
2 | HG02145.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-13+2831A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115290796 | |||||||
chr1:115290879 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0374 |
2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-13+2748G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115290879 | |||||||
chr1:115290960 | T | C | 297 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(294): Show |
317 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(314): Show |
intron_variant | MODIFIER | c.-13+2667A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115290960 | |||||||
chr1:115290967 | G | T | 2 | a0001c0001t0001g0132 a0001c0001t0001g0295 |
2 | HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-13+2660C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115290967 | |||||||
chr1:115291107 | G | T | 1 | a0001c0001t0001g0122 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-13+2520C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115291107 | |||||||
chr1:115291181 | T | A | 2 | a0001c0001t0001g0057 a0001c0001t0001g0198 |
2 | HG01993.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.-13+2446A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115291181 | |||||||
chr1:115291182 | A | T | 40 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0012 others(37): Show |
43 | HG00423.hp1 HG00735.hp2 HG01256.hp1 others(40): Show |
intron_variant | MODIFIER | c.-13+2445T>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115291182 | |||||||
chr1:115291227 | T | C | 149 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0015 others(146): Show |
155 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.-13+2400A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115291227 | |||||||
chr1:115291231 | G | GT | 25 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(22): Show |
29 | HG00544.hp1 HG00609.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.-13+2395dupA | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115291231 | |||||||
chr1:115291235 | A | T | 271 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(268): Show |
287 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.-13+2392T>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115291235 | |||||||
chr1:115291236 | A | T | 1 | a0002c0002t0001g0186 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-13+2391T>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115291236 | |||||||
chr1:115291246 | C | A | 1 | a0002c0002t0001g0063 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-13+2381G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115291246 | |||||||
chr1:115291570 | T | G | 11 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0032 others(8): Show |
11 | HG01081.hp1 HG01884.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-13+2057A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115291570 | |||||||
chr1:115291588 | G | T | 4 | a0001c0001t0001g0013 a0001c0001t0001g0209 a0001c0001t0001g0210 others(1): Show |
5 | HG00642.hp1 HG01069.hp1 HG01070.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13+2039C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115291588 | |||||||
chr1:115291721 | C | T | 2 | a0001c0003t0001g0388 a0001c0003t0001g0393 |
2 | HG02145.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-13+1906G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115291721 | |||||||
chr1:115291801 | A | G | 2 | a0001c0001t0001g0208 a0001c0001t0001g0302 |
2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-13+1826T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115291801 | |||||||
chr1:115291826 | G | C | 1 | a0001c0001t0001g0208 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-13+1801C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115291826 | |||||||
chr1:115291901 | C | G | 274 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(271): Show |
292 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(289): Show |
intron_variant | MODIFIER | c.-13+1726G>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115291901 | |||||||
chr1:115291930 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-13+1697A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115291930 | |||||||
chr1:115291949 | G | A | 2 | a0001c0001t0001g0029 a0002c0002t0001g0060 |
2 | HG02970.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-13+1678C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115291949 | |||||||
chr1:115292048 | G | T | 261 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(258): Show |
279 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.-13+1579C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115292048 | |||||||
chr1:115292099 | C | G | 8 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0296 others(5): Show |
8 | HG01081.hp1 HG01884.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.-13+1528G>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115292099 | |||||||
chr1:115292153 | T | A | 2 | a0004c0005t0001g0101 a0004c0005t0001g0102 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-13+1474A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115292153 | |||||||
chr1:115292181 | C | T | 23 | a0001c0001t0001g0062 a0001c0001t0001g0128 a0001c0001t0001g0134 others(20): Show |
23 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.-13+1446G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115292181 | |||||||
chr1:115292452 | T | C | 1 | a0001c0001t0001g0280 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-13+1175A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115292452 | |||||||
chr1:115292567 | G | A | 1 | a0001c0001t0001g0239 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-13+1060C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115292567 | |||||||
chr1:115292632 | G | A | 3 | a0002c0002t0001g0035 a0003c0004t0001g0381 a0003c0004t0001g0382 |
3 | HG01109.hp2 HG03927.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-13+995C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115292632 | |||||||
chr1:115292777 | A | G | 6 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 others(3): Show |
6 | HG00735.hp1 HG01069.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.-13+850T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115292777 | |||||||
chr1:115292859 | T | G | 1 | a0001c0001t0001g0184 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-13+768A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115292859 | |||||||
chr1:115292879 | T | G | 253 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(250): Show |
269 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.-13+748A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115292879 | |||||||
chr1:115292898 | C | A | 3 | a0001c0001t0001g0092 a0002c0002t0001g0086 a0002c0002t0001g0260 |
3 | NA18947.hp1 NA18962.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.-13+729G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115292898 | |||||||
chr1:115293090 | C | T | 2 | a0001c0001t0001g0132 a0001c0001t0001g0295 |
2 | HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-13+537G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115293090 | |||||||
chr1:115293093 | G | T | 9 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0077 others(6): Show |
9 | HG01884.hp2 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-13+534C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115293093 | |||||||
chr1:115293129 | G | T | 9 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0077 others(6): Show |
9 | HG01884.hp2 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-13+498C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115293129 | |||||||
chr1:115293135 | A | G | 2 | a0001c0001t0001g0121 a0001c0001t0001g0343 |
2 | HG01168.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.-13+492T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115293135 | |||||||
chr1:115293220 | T | C | 297 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(294): Show |
317 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(314): Show |
intron_variant | MODIFIER | c.-13+407A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115293220 | |||||||
chr1:115293290 | G | A | 3 | a0001c0001t0001g0172 a0001c0001t0001g0246 a0001c0001t0001g0303 |
3 | HG02257.hp2 HG02559.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-13+337C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115293290 | |||||||
chr1:115293308 | C | T | 3 | a0001c0001t0001g0031 a0001c0001t0001g0130 a0001c0001t0001g0394 |
3 | HG02258.hp1 HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-13+319G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115293308 | |||||||
chr1:115293341 | C | T | 30 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0018 others(27): Show |
35 | HG01099.hp2 HG01884.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.-13+286G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115293341 | |||||||
chr1:115293399 | C | T | 43 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0012 others(40): Show |
46 | HG00423.hp1 HG00735.hp2 HG01256.hp1 others(43): Show |
intron_variant | MODIFIER | c.-13+228G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115293399 | |||||||
chr1:115293442 | A | G | 2 | a0002c0002t0001g0034 a0002c0002t0001g0392 |
2 | HG02451.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-13+185T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115293442 | |||||||
chr1:115293482 | G | T | 22 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(19): Show |
26 | HG00544.hp1 HG00609.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.-13+145C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 2/2 | chr1 | 115293482 | |||||||
chr1:115293851 | G | C | 1 | a0001c0003t0001g0145 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-136-101C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115293851 | |||||||
chr1:115293893 | A | T | 1 | a0002c0002t0001g0279 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-136-143T>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115293893 | |||||||
chr1:115293916 | C | T | 3 | a0001c0001t0001g0031 a0001c0001t0001g0130 a0001c0001t0001g0394 |
3 | HG02258.hp1 HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-136-166G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115293916 | |||||||
chr1:115293917 | G | A | 23 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0057 others(20): Show |
25 | HG00280.hp2 HG00597.hp1 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.-136-167C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115293917 | |||||||
chr1:115293923 | T | G | 8 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0296 others(5): Show |
8 | HG01081.hp1 HG01884.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.-136-173A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115293923 | |||||||
chr1:115293967 | G | A | 3 | a0001c0001t0001g0006 a0001c0001t0001g0103 a0001c0001t0001g0116 |
4 | NA18944.hp2 NA18974.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.-136-217C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115293967 | |||||||
chr1:115294125 | C | A | 25 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(22): Show |
29 | HG00544.hp1 HG00609.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.-136-375G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115294125 | |||||||
chr1:115294174 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-136-424G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115294174 | |||||||
chr1:115294312 | A | G | 1 | a0001c0001t0001g0039 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-136-562T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115294312 | |||||||
chr1:115294355 | T | C | 1 | a0001c0001t0001g0073 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-136-605A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115294355 | |||||||
chr1:115294436 | A | T | 300 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(297): Show |
320 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(317): Show |
intron_variant | MODIFIER | c.-136-686T>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115294436 | |||||||
chr1:115294495 | T | A | 1 | a0001c0001t0001g0257 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-136-745A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115294495 | |||||||
chr1:115294661 | C | T | 3 | a0001c0001t0001g0031 a0001c0001t0001g0130 a0001c0001t0001g0394 |
3 | HG02258.hp1 HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-136-911G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115294661 | |||||||
chr1:115294827 | G | A | 1 | a0002c0002t0001g0360 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-136-1077C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115294827 | |||||||
chr1:115294934 | C | T | 1 | a0002c0002t0001g0046 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-136-1184G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115294934 | |||||||
chr1:115295052 | C | T | 8 | a0001c0001t0001g0010 a0001c0001t0001g0150 a0001c0001t0001g0175 others(5): Show |
9 | HG02615.hp2 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.-136-1302G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115295052 | |||||||
chr1:115295057 | A | C | 1 | a0001c0001t0001g0152 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-136-1307T>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115295057 | |||||||
chr1:115295088 | A | G | 270 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(267): Show |
288 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(285): Show |
intron_variant | MODIFIER | c.-136-1338T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115295088 | |||||||
chr1:115295242 | A | T | 1 | a0001c0001t0001g0275 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-136-1492T>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115295242 | |||||||
chr1:115295298 | C | T | 141 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0015 others(138): Show |
147 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.-136-1548G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115295298 | |||||||
chr1:115295340 | C | G | 1 | a0001c0001t0001g0394 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-136-1590G>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115295340 | |||||||
chr1:115295414 | C | T | 8 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0296 others(5): Show |
8 | HG01081.hp1 HG01884.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.-136-1664G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115295414 | |||||||
chr1:115295478 | G | A | 14 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0018 others(11): Show |
19 | HG01099.hp2 HG01891.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.-136-1728C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115295478 | |||||||
chr1:115295661 | G | T | 175 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(172): Show |
186 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(183): Show |
intron_variant | MODIFIER | c.-136-1911C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115295661 | |||||||
chr1:115295949 | T | A | 1 | a0001c0001t0001g0343 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-136-2199A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115295949 | |||||||
chr1:115296119 | TA | T | 22 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(19): Show |
26 | HG00544.hp1 HG00609.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.-136-2370delT | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115296119 | |||||||
chr1:115296303 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-136-2553G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115296303 | |||||||
chr1:115296331 | C | T | 10 | a0001c0001t0001g0132 a0001c0001t0001g0142 a0001c0001t0001g0295 others(7): Show |
10 | HG02145.hp1 HG02647.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.-136-2581G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115296331 | |||||||
chr1:115296434 | G | A | 1 | a0001c0001t0001g0028 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-136-2684C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115296434 | |||||||
chr1:115296514 | C | A | 1 | a0001c0001t0001g0206 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-136-2764G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115296514 | |||||||
chr1:115296523 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-136-2773T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115296523 | |||||||
chr1:115296575 | A | G | 49 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(46): Show |
53 | HG00544.hp1 HG00609.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.-136-2825T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115296575 | |||||||
chr1:115296646 | T | C | 9 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0077 others(6): Show |
9 | HG01884.hp2 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-136-2896A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115296646 | |||||||
chr1:115296696 | C | A | 1 | a0001c0001t0001g0120 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-136-2946G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115296696 | |||||||
chr1:115296703 | A | G | 49 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(46): Show |
53 | HG00544.hp1 HG00609.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.-136-2953T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115296703 | |||||||
chr1:115296837 | A | G | 1 | a0001c0001t0001g0364 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-136-3087T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115296837 | |||||||
chr1:115296858 | C | A | 6 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(3): Show |
6 | HG02717.hp2 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-136-3108G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115296858 | |||||||
chr1:115296890 | G | C | 2 | a0001c0001t0001g0208 a0001c0001t0001g0302 |
2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-136-3140C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115296890 | |||||||
chr1:115296905 | G | A | 3 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 |
3 | HG02717.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-136-3155C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115296905 | |||||||
chr1:115296974 | A | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(46): Show |
53 | HG00544.hp1 HG00609.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.-136-3224T>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115296974 | |||||||
chr1:115297027 | T | C | 1 | a0001c0001t0001g0023 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-136-3277A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115297027 | |||||||
chr1:115297031 | G | A | 10 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0208 others(7): Show |
10 | HG01081.hp1 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.-136-3281C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115297031 | |||||||
chr1:115297050 | T | C | 238 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(235): Show |
254 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.-136-3300A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115297050 | |||||||
chr1:115297059 | G | A | 47 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(44): Show |
51 | HG00544.hp1 HG00609.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.-136-3309C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115297059 | |||||||
chr1:115297065 | CATGCTTT others(1): Show |
C | 6 | a0002c0002t0001g0331 a0002c0002t0001g0358 a0002c0002t0001g0359 others(3): Show |
6 | HG00639.hp1 HG00738.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.-136-3323_-136-331 others(12): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115297065 | |||||||
chr1:115297112 | T | G | 300 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(297): Show |
320 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(317): Show |
intron_variant | MODIFIER | c.-136-3362A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115297112 | |||||||
chr1:115297147 | T | G | 1 | a0001c0001t0001g0304 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-136-3397A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115297147 | |||||||
chr1:115297151 | G | C | 21 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0018 others(18): Show |
26 | HG01099.hp2 HG01891.hp1 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.-136-3401C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115297151 | |||||||
chr1:115297157 | T | C | 89 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(86): Show |
96 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.-136-3407A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115297157 | |||||||
chr1:115297161 | A | G | 2 | a0002c0002t0001g0063 a0002c0002t0001g0064 |
2 | HG00621.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.-136-3411T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115297161 | |||||||
chr1:115297206 | C | A | 1 | a0001c0001t0001g0021 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-136-3456G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115297206 | |||||||
chr1:115297280 | G | T | 1 | a0002c0002t0001g0035 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-136-3530C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115297280 | |||||||
chr1:115297394 | T | C | 1 | a0001c0001t0001g0302 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-136-3644A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115297394 | |||||||
chr1:115297411 | C | T | 2 | a0002c0002t0001g0178 a0002c0002t0001g0190 |
2 | HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-136-3661G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115297411 | |||||||
chr1:115297749 | C | G | 2 | a0001c0001t0001g0363 a0001c0001t0001g0368 |
2 | HG00099.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.-136-3999G>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115297749 | |||||||
chr1:115297792 | T | G | 1 | a0001c0001t0001g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-136-4042A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115297792 | |||||||
chr1:115297817 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-136-4067C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115297817 | |||||||
chr1:115297828 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-136-4078G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115297828 | |||||||
chr1:115297896 | C | G | 49 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(46): Show |
53 | HG00544.hp1 HG00609.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.-136-4146G>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115297896 | |||||||
chr1:115298097 | T | A | 3 | a0001c0001t0001g0039 a0001c0003t0001g0145 a0001c0003t0001g0395 |
3 | HG02055.hp1 HG02055.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-136-4347A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115298097 | |||||||
chr1:115298134 | C | T | 6 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 others(3): Show |
6 | HG00735.hp1 HG01069.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.-136-4384G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115298134 | |||||||
chr1:115298218 | C | T | 3 | a0001c0001t0001g0031 a0001c0001t0001g0130 a0001c0001t0001g0394 |
3 | HG02258.hp1 HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-136-4468G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115298218 | |||||||
chr1:115298306 | AT | A | 7 | a0001c0001t0001g0022 a0001c0001t0001g0077 a0001c0001t0001g0078 others(4): Show |
7 | HG02717.hp2 HG02723.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136-4557delA | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115298306 | |||||||
chr1:115298466 | A | C | 1 | a0001c0001t0001g0230 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-136-4716T>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115298466 | |||||||
chr1:115298482 | A | G | 3 | a0001c0001t0001g0031 a0001c0001t0001g0130 a0001c0001t0001g0394 |
3 | HG02258.hp1 HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-136-4732T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115298482 | |||||||
chr1:115298489 | T | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0013 others(109): Show |
119 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.-136-4739A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115298489 | |||||||
chr1:115298771 | C | T | 67 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0032 others(64): Show |
70 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.-136-5021G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115298771 | |||||||
chr1:115298831 | G | T | 1 | a0001c0001t0001g0018 | 2 | HG02647.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-136-5081C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115298831 | |||||||
chr1:115298882 | G | A | 2 | a0001c0001t0001g0269 a0001c0001t0001g0384 |
2 | HG02602.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.-136-5132C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115298882 | |||||||
chr1:115298892 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-136-5142C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115298892 | |||||||
chr1:115298956 | T | G | 58 | a0001c0001t0001g0010 a0001c0001t0001g0029 a0001c0001t0001g0032 others(55): Show |
61 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.-136-5206A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115298956 | |||||||
chr1:115298981 | C | T | 8 | a0001c0001t0001g0042 a0001c0001t0001g0077 a0001c0001t0001g0078 others(5): Show |
8 | HG01884.hp2 HG02717.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.-136-5231G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115298981 | |||||||
chr1:115299112 | T | A | 1 | a0001c0001t0001g0275 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-136-5362A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115299112 | |||||||
chr1:115299399 | G | C | 122 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0013 others(119): Show |
129 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.-136-5649C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115299399 | |||||||
chr1:115299661 | T | C | 1 | a0001c0001t0001g0202 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-136-5911A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115299661 | |||||||
chr1:115299716 | A | G | 1 | a0001c0001t0001g0177 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-136-5966T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115299716 | |||||||
chr1:115299768 | C | G | 4 | a0001c0001t0001g0121 a0001c0001t0001g0343 a0001c0003t0001g0388 others(1): Show |
4 | HG01168.hp1 HG02145.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.-136-6018G>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115299768 | |||||||
chr1:115299881 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-136-6131C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115299881 | |||||||
chr1:115299937 | T | G | 2 | a0002c0002t0001g0360 a0002c0002t0001g0362 |
2 | HG00738.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.-136-6187A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115299937 | |||||||
chr1:115300037 | G | A | 36 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(33): Show |
40 | HG00544.hp1 HG00609.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.-136-6287C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115300037 | |||||||
chr1:115300145 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-136-6395A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115300145 | |||||||
chr1:115300189 | A | T | 122 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0013 others(119): Show |
129 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.-136-6439T>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115300189 | |||||||
chr1:115300277 | A | T | 3 | a0001c0001t0001g0031 a0001c0001t0001g0130 a0001c0001t0001g0394 |
3 | HG02258.hp1 HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-136-6527T>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115300277 | |||||||
chr1:115300286 | G | T | 122 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0013 others(119): Show |
129 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.-136-6536C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115300286 | |||||||
chr1:115300405 | G | A | 2 | a0001c0001t0001g0298 a0001c0001t0001g0301 |
2 | NA19066.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.-136-6655C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115300405 | |||||||
chr1:115300466 | T | C | 317 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(314): Show |
337 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(334): Show |
intron_variant | MODIFIER | c.-136-6716A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115300466 | |||||||
chr1:115300537 | G | A | 23 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0018 others(20): Show |
28 | HG01099.hp2 HG01891.hp1 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.-136-6787C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115300537 | |||||||
chr1:115300544 | G | A | 8 | a0001c0001t0001g0042 a0001c0001t0001g0077 a0001c0001t0001g0078 others(5): Show |
8 | HG01884.hp2 HG02717.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.-136-6794C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115300544 | |||||||
chr1:115300685 | A | C | 1 | a0001c0001t0001g0177 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-136-6935T>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115300685 | |||||||
chr1:115300962 | G | A | 2 | a0001c0003t0001g0388 a0001c0003t0001g0393 |
2 | HG02145.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-136-7212C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115300962 | |||||||
chr1:115300969 | T | C | 3 | a0002c0002t0001g0331 a0002c0002t0001g0358 a0002c0002t0001g0379 |
3 | HG00639.hp1 HG01243.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-136-7219A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115300969 | |||||||
chr1:115301137 | GAACAA | G | 6 | a0001c0001t0001g0092 a0002c0002t0001g0091 a0002c0002t0001g0093 others(3): Show |
6 | HG00408.hp1 NA18947.hp1 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.-136-7392_-136-738 others(9): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115301137 | |||||||
chr1:115301297 | C | A | 2 | a0001c0003t0001g0388 a0001c0003t0001g0393 |
2 | HG02145.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-136-7547G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115301297 | |||||||
chr1:115301306 | C | A | 122 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0013 others(119): Show |
129 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.-136-7556G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115301306 | |||||||
chr1:115301419 | A | C | 8 | a0001c0001t0001g0010 a0001c0001t0001g0150 a0001c0001t0001g0175 others(5): Show |
9 | HG02615.hp2 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.-136-7669T>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115301419 | |||||||
chr1:115301549 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-136-7799A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115301549 | |||||||
chr1:115301592 | C | T | 1 | a0001c0001t0001g0363 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-136-7842G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115301592 | |||||||
chr1:115301683 | T | C | 1 | a0001c0001t0001g0307 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-136-7933A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115301683 | |||||||
chr1:115302044 | G | A | 2 | a0002c0002t0001g0034 a0002c0002t0001g0392 |
2 | HG02451.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-136-8294C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115302044 | |||||||
chr1:115302076 | T | A | 2 | a0001c0001t0001g0042 a0001c0001t0001g0374 |
2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-136-8326A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115302076 | |||||||
chr1:115302101 | C | T | 17 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0018 others(14): Show |
22 | HG01099.hp2 HG01891.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.-136-8351G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115302101 | |||||||
chr1:115302425 | G | A | 78 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0028 others(75): Show |
80 | HG00597.hp2 HG00639.hp1 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.-136-8675C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115302425 | |||||||
chr1:115302438 | C | T | 14 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0018 others(11): Show |
19 | HG01099.hp2 HG01891.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.-136-8688G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115302438 | |||||||
chr1:115302568 | A | G | 6 | a0001c0001t0001g0084 a0001c0001t0001g0215 a0001c0001t0001g0218 others(3): Show |
6 | NA18940.hp1 NA18959.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.-136-8818T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115302568 | |||||||
chr1:115302736 | G | A | 121 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0013 others(118): Show |
128 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.-136-8986C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115302736 | |||||||
chr1:115302754 | G | C | 34 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(31): Show |
38 | HG00544.hp1 HG00609.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.-136-9004C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115302754 | |||||||
chr1:115302764 | T | C | 307 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(304): Show |
327 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(324): Show |
intron_variant | MODIFIER | c.-136-9014A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115302764 | |||||||
chr1:115302773 | C | A | 2 | a0003c0004t0001g0381 a0003c0004t0001g0382 |
2 | HG01109.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-136-9023G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115302773 | |||||||
chr1:115302815 | C | T | 2 | a0001c0001t0001g0121 a0001c0001t0001g0343 |
2 | HG01168.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.-136-9065G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115302815 | |||||||
chr1:115302884 | G | A | 22 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0018 others(19): Show |
27 | HG01099.hp2 HG01891.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.-136-9134C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115302884 | |||||||
chr1:115302907 | C | T | 121 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0013 others(118): Show |
128 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.-136-9157G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115302907 | |||||||
chr1:115303074 | T | TAAGAAAT others(331): Show |
1 | a0001c0003t0001g0388 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-136-9325_-136-932 others(342): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115303074 | |||||||
chr1:115303074 | T | TAAGAAAT others(332): Show |
1 | a0001c0003t0001g0393 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-136-9325_-136-932 others(343): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115303074 | |||||||
chr1:115303100 | A | C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0374 |
2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-136-9350T>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115303100 | |||||||
chr1:115303166 | C | T | 42 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(39): Show |
46 | HG00544.hp1 HG00609.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.-136-9416G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115303166 | |||||||
chr1:115303350 | G | C | 42 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(39): Show |
46 | HG00544.hp1 HG00609.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.-136-9600C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115303350 | |||||||
chr1:115303356 | C | T | 1 | a0002c0002t0001g0255 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-136-9606G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115303356 | |||||||
chr1:115303372 | A | C | 5 | a0001c0001t0001g0030 a0001c0001t0001g0296 a0001c0001t0001g0306 others(2): Show |
5 | HG01884.hp1 HG01891.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-136-9622T>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115303372 | |||||||
chr1:115303524 | C | T | 116 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0014 others(113): Show |
122 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.-136-9774G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115303524 | |||||||
chr1:115303555 | C | A | 2 | a0002c0002t0001g0360 a0002c0002t0001g0362 |
2 | HG00738.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.-136-9805G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115303555 | |||||||
chr1:115303560 | T | C | 304 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(301): Show |
324 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(321): Show |
intron_variant | MODIFIER | c.-136-9810A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115303560 | |||||||
chr1:115303600 | C | T | 122 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0013 others(119): Show |
129 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.-136-9850G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115303600 | |||||||
chr1:115303627 | A | G | 1 | a0001c0001t0001g0169 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-136-9877T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115303627 | |||||||
chr1:115303710 | CCAT | C | 4 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0204 others(1): Show |
4 | HG00408.hp2 HG00609.hp2 HG00621.hp2 others(1): Show |
intron_variant | MODIFIER | c.-136-9963_-136-996 others(7): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115303710 | |||||||
chr1:115303812 | T | A | 8 | a0001c0001t0001g0010 a0001c0001t0001g0150 a0001c0001t0001g0175 others(5): Show |
9 | HG02615.hp2 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.-136-10062A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115303812 | |||||||
chr1:115304019 | TTTTTC | T | 4 | a0001c0001t0001g0039 a0001c0001t0001g0208 a0001c0001t0001g0302 others(1): Show |
4 | HG02055.hp1 HG02280.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-136-10274_-136-10 others(11): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115304019 | |||||||
chr1:115304140 | C | T | 2 | a0001c0003t0001g0388 a0001c0003t0001g0393 |
2 | HG02145.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-136-10390G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115304140 | |||||||
chr1:115304177 | A | AT | 7 | a0001c0001t0001g0084 a0001c0001t0001g0215 a0001c0001t0001g0218 others(4): Show |
7 | HG01192.hp1 NA18940.hp1 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.-136-10428dupA | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115304177 | |||||||
chr1:115304210 | T | G | 10 | a0001c0001t0001g0036 a0001c0003t0001g0037 a0001c0003t0001g0038 others(7): Show |
10 | HG01433.hp2 HG02145.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-136-10460A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115304210 | |||||||
chr1:115304306 | G | A | 1 | a0001c0001t0001g0161 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-136-10556C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115304306 | |||||||
chr1:115304309 | C | T | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-136-10559G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115304309 | |||||||
chr1:115304329 | A | ATTTTTTT others(2): Show |
23 | a0001c0001t0001g0010 a0001c0001t0001g0022 a0001c0001t0001g0036 others(20): Show |
24 | HG01433.hp2 HG01884.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.-136-10588_-136-10 others(15): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115304329 | |||||||
chr1:115304329 | A | ATTTTTTT others(3): Show |
34 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(31): Show |
38 | HG00544.hp1 HG00609.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.-136-10589_-136-10 others(16): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115304329 | |||||||
chr1:115304329 | A | ATTTTTTT others(4): Show |
4 | a0001c0001t0001g0076 a0002c0002t0001g0035 a0002c0002t0001g0063 others(1): Show |
4 | HG00621.hp1 HG02027.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-136-10590_-136-10 others(17): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115304329 | |||||||
chr1:115304329 | A | ATTTTTTT others(7): Show |
8 | a0001c0001t0001g0121 a0001c0001t0001g0142 a0001c0001t0001g0177 others(5): Show |
8 | HG01168.hp1 HG02109.hp1 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.-136-10593_-136-10 others(20): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115304329 | |||||||
chr1:115304329 | A | ATTTTTTT others(8): Show |
4 | a0001c0001t0001g0267 a0001c0001t0001g0295 a0001c0001t0001g0296 others(1): Show |
4 | HG02071.hp2 HG02976.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.-136-10594_-136-10 others(21): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115304329 | |||||||
chr1:115304329 | A | ATTTTTTT others(9): Show |
119 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0012 others(116): Show |
126 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.-136-10595_-136-10 others(22): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115304329 | |||||||
chr1:115304329 | A | ATTTTTTT others(10): Show |
62 | a0001c0001t0001g0016 a0001c0001t0001g0028 a0001c0001t0001g0030 others(59): Show |
63 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.-136-10580_-136-10 others(23): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115304329 | |||||||
chr1:115304329 | A | ATTTTTTT others(11): Show |
14 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0029 others(11): Show |
16 | HG00738.hp2 HG01358.hp2 HG01975.hp1 others(13): Show |
intron_variant | MODIFIER | c.-136-10580_-136-10 others(24): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115304329 | |||||||
chr1:115304329 | A | ATTTTTTT others(12): Show |
4 | a0001c0001t0001g0044 a0001c0001t0001g0205 a0001c0001t0001g0261 others(1): Show |
4 | HG00544.hp2 HG01928.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.-136-10580_-136-10 others(25): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115304329 | |||||||
chr1:115304329 | A | ATTTTTTT others(14): Show |
1 | a0001c0001t0001g0158 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-136-10580_-136-10 others(27): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115304329 | |||||||
chr1:115304340 | T | TTTTTTTT others(9): Show |
1 | a0001c0003t0001g0395 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-136-10591_-136-10 others(22): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115304340 | |||||||
chr1:115304361 | A | G | 302 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(299): Show |
322 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(319): Show |
intron_variant | MODIFIER | c.-136-10611T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115304361 | |||||||
chr1:115304466 | G | A | 1 | a0001c0003t0001g0179 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-136-10716C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115304466 | |||||||
chr1:115304674 | T | G | 302 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(299): Show |
322 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(319): Show |
intron_variant | MODIFIER | c.-136-10924A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115304674 | |||||||
chr1:115304771 | C | T | 98 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(95): Show |
109 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.-136-11021G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115304771 | |||||||
chr1:115304813 | C | T | 1 | a0001c0001t0001g0372 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-136-11063G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115304813 | |||||||
chr1:115304830 | C | T | 2 | a0001c0001t0001g0300 a0001c0001t0001g0378 |
2 | NA18945.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.-136-11080G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115304830 | |||||||
chr1:115304925 | G | C | 236 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(233): Show |
251 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.-136-11175C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115304925 | |||||||
chr1:115305032 | T | C | 10 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0069 others(7): Show |
10 | NA18945.hp1 NA18950.hp2 NA18964.hp2 others(7): Show |
intron_variant | MODIFIER | c.-136-11282A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115305032 | |||||||
chr1:115305061 | A | G | 1 | a0001c0001t0001g0025 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-136-11311T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115305061 | |||||||
chr1:115305115 | A | G | 304 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(301): Show |
324 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(321): Show |
intron_variant | MODIFIER | c.-136-11365T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115305115 | |||||||
chr1:115305120 | T | A | 1 | a0001c0001t0001g0290 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-136-11370A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115305120 | |||||||
chr1:115305275 | T | A | 63 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0050 others(60): Show |
65 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.-136-11525A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115305275 | |||||||
chr1:115305307 | C | T | 3 | a0001c0001t0001g0324 a0001c0001t0001g0325 a0001c0001t0001g0326 |
3 | HG01081.hp2 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-136-11557G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115305307 | |||||||
chr1:115305375 | G | T | 1 | a0001c0001t0001g0347 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-136-11625C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115305375 | |||||||
chr1:115305460 | C | T | 8 | a0001c0001t0001g0010 a0001c0001t0001g0150 a0001c0001t0001g0175 others(5): Show |
9 | HG02615.hp2 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.-136-11710G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115305460 | |||||||
chr1:115305490 | C | T | 5 | a0001c0001t0001g0142 a0001c0001t0001g0305 a0001c0001t0001g0389 others(2): Show |
5 | HG03195.hp1 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.-136-11740G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115305490 | |||||||
chr1:115305767 | C | T | 77 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(74): Show |
83 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.-136-12017G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115305767 | |||||||
chr1:115305802 | T | C | 4 | a0002c0002t0001g0033 a0002c0002t0001g0061 a0002c0002t0001g0313 others(1): Show |
4 | NA18966.hp2 NA18967.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.-136-12052A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115305802 | |||||||
chr1:115305804 | C | T | 2 | a0001c0003t0001g0388 a0001c0003t0001g0393 |
2 | HG02145.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-136-12054G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115305804 | |||||||
chr1:115305829 | A | C | 77 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(74): Show |
83 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.-136-12079T>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115305829 | |||||||
chr1:115306089 | G | A | 2 | a0001c0001t0001g0121 a0001c0001t0001g0343 |
2 | HG01168.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.-136-12339C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115306089 | |||||||
chr1:115306399 | A | G | 2 | a0001c0001t0001g0187 a0001c0001t0001g0319 |
2 | HG02523.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-136-12649T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115306399 | |||||||
chr1:115306457 | T | A | 4 | a0001c0001t0001g0076 a0001c0001t0001g0232 a0001c0001t0001g0241 others(1): Show |
4 | HG01175.hp1 HG02280.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-136-12707A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115306457 | |||||||
chr1:115306882 | C | A | 1 | a0001c0001t0001g0236 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-136-13132G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115306882 | |||||||
chr1:115306887 | A | C | 8 | a0001c0001t0001g0010 a0001c0001t0001g0150 a0001c0001t0001g0175 others(5): Show |
9 | HG02615.hp2 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.-136-13137T>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115306887 | |||||||
chr1:115306947 | C | T | 28 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0043 others(25): Show |
30 | HG00544.hp2 HG00735.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.-136-13197G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115306947 | |||||||
chr1:115307154 | T | A | 8 | a0001c0001t0001g0010 a0001c0001t0001g0150 a0001c0001t0001g0175 others(5): Show |
9 | HG02615.hp2 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.-136-13404A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115307154 | |||||||
chr1:115307291 | G | C | 1 | a0001c0001t0001g0124 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-136-13541C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115307291 | |||||||
chr1:115307317 | G | A | 2 | a0001c0001t0001g0121 a0001c0001t0001g0343 |
2 | HG01168.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.-136-13567C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115307317 | |||||||
chr1:115307347 | C | T | 1 | a0001c0001t0001g0241 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-136-13597G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115307347 | |||||||
chr1:115307348 | G | A | 2 | a0001c0003t0001g0388 a0001c0003t0001g0393 |
2 | HG02145.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-136-13598C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115307348 | |||||||
chr1:115307385 | A | C | 2 | a0001c0003t0001g0388 a0001c0003t0001g0393 |
2 | HG02145.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-136-13635T>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115307385 | |||||||
chr1:115307506 | C | T | 4 | a0001c0001t0001g0039 a0001c0001t0001g0208 a0001c0001t0001g0302 others(1): Show |
4 | HG02055.hp1 HG02280.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-136-13756G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115307506 | |||||||
chr1:115307579 | A | G | 1 | a0001c0001t0001g0394 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-136-13829T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115307579 | |||||||
chr1:115307581 | G | A | 15 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0018 others(12): Show |
20 | HG01099.hp2 HG01891.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.-136-13831C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115307581 | |||||||
chr1:115307637 | A | G | 2 | a0001c0003t0001g0388 a0001c0003t0001g0393 |
2 | HG02145.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-136-13887T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115307637 | |||||||
chr1:115307747 | C | T | 1 | a0001c0001t0001g0053 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-136-13997G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115307747 | |||||||
chr1:115307995 | T | C | 1 | a0002c0002t0001g0291 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-136-14245A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115307995 | |||||||
chr1:115308378 | C | T | 32 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(29): Show |
36 | HG00544.hp1 HG00609.hp1 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.-136-14628G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115308378 | |||||||
chr1:115308643 | A | G | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG00544.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.-136-14893T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115308643 | |||||||
chr1:115308847 | G | A | 2 | a0001c0001t0001g0039 a0001c0003t0001g0145 |
2 | HG02055.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-136-15097C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115308847 | |||||||
chr1:115308870 | A | G | 137 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0028 others(134): Show |
141 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.-136-15120T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115308870 | |||||||
chr1:115308934 | T | TTTAGTTT others(2): Show |
8 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0296 others(5): Show |
8 | HG01081.hp1 HG01884.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.-136-15185_-136-15 others(15): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115308934 | |||||||
chr1:115308939 | A | G | 8 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0296 others(5): Show |
8 | HG01081.hp1 HG01884.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.-136-15189T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115308939 | |||||||
chr1:115308940 | A | ATTT | 8 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0296 others(5): Show |
8 | HG01081.hp1 HG01884.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.-136-15191_-136-15 others(9): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115308940 | |||||||
chr1:115309097 | G | C | 6 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(3): Show |
6 | HG02717.hp2 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-136-15347C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115309097 | |||||||
chr1:115309215 | C | T | 42 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(39): Show |
46 | HG00544.hp1 HG00609.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.-136-15465G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115309215 | |||||||
chr1:115309311 | G | C | 2 | a0001c0001t0001g0235 a0001c0001t0001g0251 |
2 | NA18973.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.-136-15561C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115309311 | |||||||
chr1:115309334 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-136-15584G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115309334 | |||||||
chr1:115309383 | C | T | 128 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0028 others(125): Show |
132 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.-136-15633G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115309383 | |||||||
chr1:115309411 | A | G | 82 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(79): Show |
88 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.-136-15661T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115309411 | |||||||
chr1:115309632 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-136-15882C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115309632 | |||||||
chr1:115309647 | C | T | 6 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(3): Show |
6 | HG02717.hp2 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-136-15897G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115309647 | |||||||
chr1:115309753 | C | T | 135 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0028 others(132): Show |
139 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.-136-16003G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115309753 | |||||||
chr1:115309766 | T | C | 82 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(79): Show |
88 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.-136-16016A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115309766 | |||||||
chr1:115309803 | G | A | 1 | a0001c0001t0001g0305 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-136-16053C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115309803 | |||||||
chr1:115309893 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-136-16143G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115309893 | |||||||
chr1:115310127 | T | A | 5 | a0001c0001t0001g0031 a0001c0001t0001g0130 a0001c0001t0001g0394 others(2): Show |
5 | HG02145.hp1 HG02258.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-136-16377A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115310127 | |||||||
chr1:115310170 | T | A | 1 | a0001c0001t0001g0021 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-136-16420A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115310170 | |||||||
chr1:115310199 | T | G | 20 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0018 others(17): Show |
25 | HG01099.hp2 HG01891.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.-136-16449A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115310199 | |||||||
chr1:115310363 | G | A | 135 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0028 others(132): Show |
139 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.-136-16613C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115310363 | |||||||
chr1:115310463 | T | C | 90 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(87): Show |
97 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.-136-16713A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115310463 | |||||||
chr1:115310833 | G | A | 42 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(39): Show |
46 | HG00544.hp1 HG00609.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.-136-17083C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115310833 | |||||||
chr1:115310898 | C | A | 1 | a0001c0001t0001g0006 | 2 | NA18982.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.-136-17148G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115310898 | |||||||
chr1:115311000 | G | A | 2 | a0001c0001t0001g0026 a0001c0003t0001g0027 |
2 | HG02630.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-136-17250C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115311000 | |||||||
chr1:115311130 | A | G | 1 | a0001c0001t0001g0307 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-136-17380T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115311130 | |||||||
chr1:115311135 | T | C | 4 | a0001c0001t0001g0039 a0001c0001t0001g0208 a0001c0001t0001g0302 others(1): Show |
4 | HG02055.hp1 HG02280.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-136-17385A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115311135 | |||||||
chr1:115311182 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-136-17432C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115311182 | |||||||
chr1:115311191 | T | C | 306 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(303): Show |
326 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(323): Show |
intron_variant | MODIFIER | c.-136-17441A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115311191 | |||||||
chr1:115311518 | G | C | 1 | a0001c0001t0001g0248 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-136-17768C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115311518 | |||||||
chr1:115311630 | G | A | 2 | a0001c0001t0001g0208 a0001c0001t0001g0302 |
2 | HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-136-17880C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115311630 | |||||||
chr1:115311707 | A | G | 138 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0028 others(135): Show |
142 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.-136-17957T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115311707 | |||||||
chr1:115311814 | A | G | 138 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0028 others(135): Show |
142 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.-136-18064T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115311814 | |||||||
chr1:115312075 | G | A | 1 | a0001c0001t0001g0345 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-136-18325C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115312075 | |||||||
chr1:115312172 | C | T | 3 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 |
3 | HG02717.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-136-18422G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115312172 | |||||||
chr1:115312247 | T | C | 1 | a0001c0001t0001g0025 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-136-18497A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115312247 | |||||||
chr1:115312344 | T | C | 2 | a0001c0003t0001g0388 a0001c0003t0001g0393 |
2 | HG02145.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-136-18594A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115312344 | |||||||
chr1:115312473 | T | C | 4 | a0001c0001t0001g0039 a0001c0001t0001g0208 a0001c0001t0001g0302 others(1): Show |
4 | HG02055.hp1 HG02280.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-136-18723A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115312473 | |||||||
chr1:115312487 | C | T | 2 | a0001c0001t0001g0174 a0001c0001t0001g0336 |
2 | HG00735.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-136-18737G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115312487 | |||||||
chr1:115312526 | G | A | 306 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(303): Show |
326 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(323): Show |
intron_variant | MODIFIER | c.-136-18776C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115312526 | |||||||
chr1:115312609 | G | C | 2 | a0001c0001t0001g0133 a0001c0001t0001g0143 |
2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-136-18859C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115312609 | |||||||
chr1:115312782 | C | T | 8 | a0002c0002t0001g0049 a0002c0002t0001g0063 a0002c0002t0001g0064 others(5): Show |
8 | HG00621.hp1 HG02027.hp2 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.-136-19032G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115312782 | |||||||
chr1:115312803 | G | A | 8 | a0001c0001t0001g0010 a0001c0001t0001g0150 a0001c0001t0001g0175 others(5): Show |
9 | HG02615.hp2 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.-136-19053C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115312803 | |||||||
chr1:115313169 | T | C | 2 | a0001c0001t0001g0156 a0001c0001t0001g0277 |
2 | HG01346.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-136-19419A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115313169 | |||||||
chr1:115313293 | G | T | 306 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(303): Show |
326 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(323): Show |
intron_variant | MODIFIER | c.-136-19543C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115313293 | |||||||
chr1:115313294 | T | G | 306 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(303): Show |
326 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(323): Show |
intron_variant | MODIFIER | c.-136-19544A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115313294 | |||||||
chr1:115313366 | T | C | 2 | a0001c0001t0001g0121 a0001c0001t0001g0343 |
2 | HG01168.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.-136-19616A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115313366 | |||||||
chr1:115313390 | G | T | 1 | a0005c0006t0001g0265 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-136-19640C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115313390 | |||||||
chr1:115313457 | C | T | 135 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0028 others(132): Show |
139 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.-136-19707G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115313457 | |||||||
chr1:115313485 | G | A | 7 | a0001c0001t0001g0132 a0001c0001t0001g0142 a0001c0001t0001g0295 others(4): Show |
7 | HG02886.hp2 HG03195.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136-19735C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115313485 | |||||||
chr1:115313539 | G | A | 5 | a0001c0001t0001g0183 a0001c0001t0001g0283 a0001c0001t0001g0324 others(2): Show |
5 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.-136-19789C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115313539 | |||||||
chr1:115313574 | C | A | 5 | a0001c0001t0001g0031 a0001c0001t0001g0130 a0001c0001t0001g0394 others(2): Show |
5 | HG02145.hp1 HG02258.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-136-19824G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115313574 | |||||||
chr1:115313613 | ATTGT | A | 8 | a0001c0001t0001g0010 a0001c0001t0001g0150 a0001c0001t0001g0175 others(5): Show |
9 | HG02615.hp2 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.-136-19867_-136-19 others(10): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115313613 | |||||||
chr1:115313626 | T | G | 1 | a0001c0001t0001g0305 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-136-19876A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115313626 | |||||||
chr1:115313723 | A | G | 138 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0028 others(135): Show |
142 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.-136-19973T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115313723 | |||||||
chr1:115313804 | G | C | 1 | a0002c0002t0001g0168 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-136-20054C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115313804 | |||||||
chr1:115314021 | G | A | 1 | a0002c0002t0001g0260 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-136-20271C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115314021 | |||||||
chr1:115314122 | G | A | 2 | a0001c0001t0001g0042 a0001c0001t0001g0374 |
2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-136-20372C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115314122 | |||||||
chr1:115314129 | A | T | 1 | a0001c0001t0001g0199 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-136-20379T>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115314129 | |||||||
chr1:115314158 | T | C | 8 | a0001c0001t0001g0010 a0001c0001t0001g0150 a0001c0001t0001g0175 others(5): Show |
9 | HG02615.hp2 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.-136-20408A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115314158 | |||||||
chr1:115314183 | C | T | 296 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(293): Show |
316 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(313): Show |
intron_variant | MODIFIER | c.-136-20433G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115314183 | |||||||
chr1:115314251 | A | G | 2 | a0002c0002t0001g0234 a0002c0002t0001g0250 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-136-20501T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115314251 | |||||||
chr1:115314266 | G | C | 1 | a0001c0001t0001g0326 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-136-20516C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115314266 | |||||||
chr1:115314281 | T | G | 1 | a0001c0001t0001g0198 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-136-20531A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115314281 | |||||||
chr1:115314500 | C | A | 1 | a0002c0002t0001g0035 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-136-20750G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115314500 | |||||||
chr1:115314630 | G | A | 127 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0028 others(124): Show |
131 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.-136-20880C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115314630 | |||||||
chr1:115314717 | G | A | 2 | a0001c0001t0001g0133 a0001c0001t0001g0143 |
2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-136-20967C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115314717 | |||||||
chr1:115314727 | T | G | 1 | a0001c0001t0001g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-136-20977A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115314727 | |||||||
chr1:115314810 | C | T | 4 | a0001c0001t0001g0032 a0001c0001t0001g0133 a0001c0001t0001g0143 others(1): Show |
4 | HG02486.hp2 HG03139.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-136-21060G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115314810 | |||||||
chr1:115314850 | A | G | 1 | a0001c0001t0001g0319 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-136-21100T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115314850 | |||||||
chr1:115314937 | G | A | 6 | a0001c0001t0001g0025 a0001c0001t0001g0172 a0001c0001t0001g0246 others(3): Show |
6 | HG02257.hp2 HG02258.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-136-21187C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115314937 | |||||||
chr1:115314987 | G | A | 1 | a0002c0002t0001g0146 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-136-21237C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115314987 | |||||||
chr1:115315027 | G | A | 2 | a0001c0001t0001g0133 a0001c0001t0001g0143 |
2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-136-21277C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115315027 | |||||||
chr1:115315295 | G | A | 67 | a0001c0001t0001g0007 a0001c0001t0001g0024 a0001c0001t0001g0056 others(64): Show |
68 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.-136-21545C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115315295 | |||||||
chr1:115315337 | T | C | 214 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(211): Show |
229 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(226): Show |
intron_variant | MODIFIER | c.-136-21587A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115315337 | |||||||
chr1:115315381 | A | G | 8 | a0001c0001t0001g0010 a0001c0001t0001g0150 a0001c0001t0001g0175 others(5): Show |
9 | HG02615.hp2 HG02895.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.-136-21631T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115315381 | |||||||
chr1:115315387 | C | T | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG00544.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.-136-21637G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115315387 | |||||||
chr1:115315412 | A | C | 13 | a0001c0001t0001g0015 a0001c0001t0001g0248 a0001c0001t0001g0339 others(10): Show |
14 | HG02523.hp1 NA18612.hp1 NA18940.hp2 others(11): Show |
intron_variant | MODIFIER | c.-136-21662T>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115315412 | |||||||
chr1:115315414 | T | C | 1 | a0001c0001t0001g0162 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-136-21664A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115315414 | |||||||
chr1:115315469 | G | A | 10 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(7): Show |
10 | HG02451.hp1 HG02622.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.-136-21719C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115315469 | |||||||
chr1:115315483 | G | A | 85 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(82): Show |
94 | HG00280.hp2 HG00423.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.-136-21733C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115315483 | |||||||
chr1:115315803 | G | A | 1 | a0002c0002t0001g0397 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-136-22053C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115315803 | |||||||
chr1:115315910 | G | A | 1 | a0002c0002t0001g0035 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-136-22160C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115315910 | |||||||
chr1:115315911 | C | G | 1 | a0001c0001t0001g0274 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-136-22161G>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115315911 | |||||||
chr1:115315917 | G | A | 27 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0057 others(24): Show |
28 | HG00280.hp2 HG00438.hp1 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.-136-22167C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115315917 | |||||||
chr1:115315983 | G | A | 4 | a0001c0001t0001g0029 a0001c0001t0001g0172 a0001c0001t0001g0376 others(1): Show |
4 | HG01192.hp2 HG02559.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.-137+22221C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115315983 | |||||||
chr1:115316002 | T | A | 1 | a0001c0001t0001g0160 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-137+22202A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115316002 | |||||||
chr1:115316006 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-137+22198C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115316006 | |||||||
chr1:115316117 | G | A | 4 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0003t0001g0140 others(1): Show |
4 | HG02486.hp2 HG03195.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-137+22087C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115316117 | |||||||
chr1:115316296 | G | A | 1 | a0001c0001t0001g0282 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-137+21908C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115316296 | |||||||
chr1:115316308 | G | C | 5 | a0001c0001t0001g0208 a0001c0001t0001g0246 a0001c0001t0001g0302 others(2): Show |
5 | HG01884.hp2 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-137+21896C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115316308 | |||||||
chr1:115316485 | A | G | 2 | a0001c0001t0001g0121 a0001c0001t0001g0172 |
2 | HG02300.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-137+21719T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115316485 | |||||||
chr1:115316494 | A | G | 2 | a0002c0002t0001g0331 a0002c0002t0001g0358 |
2 | HG00639.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.-137+21710T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115316494 | |||||||
chr1:115316562 | C | T | 9 | a0001c0001t0001g0036 a0001c0001t0001g0039 a0001c0001t0001g0042 others(6): Show |
9 | HG01433.hp2 HG02055.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-137+21642G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115316562 | |||||||
chr1:115316622 | T | C | 2 | a0001c0003t0001g0140 a0001c0003t0001g0141 |
2 | HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-137+21582A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115316622 | |||||||
chr1:115316806 | T | G | 6 | a0001c0001t0001g0208 a0001c0001t0001g0302 a0001c0001t0001g0374 others(3): Show |
6 | HG01884.hp2 HG02055.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-137+21398A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115316806 | |||||||
chr1:115316827 | T | A | 1 | a0001c0001t0001g0123 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-137+21377A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115316827 | |||||||
chr1:115316863 | G | C | 2 | a0001c0001t0001g0119 a0001c0001t0001g0206 |
2 | HG02976.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-137+21341C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115316863 | |||||||
chr1:115317012 | A | C | 2 | a0002c0002t0001g0190 a0002c0002t0001g0392 |
2 | HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-137+21192T>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115317012 | |||||||
chr1:115317012 | A | T | 2 | a0002c0002t0001g0058 a0002c0002t0001g0083 |
2 | NA18943.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.-137+21192T>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115317012 | |||||||
chr1:115317110 | TA | T | 13 | a0001c0001t0001g0122 a0001c0001t0001g0208 a0001c0001t0001g0302 others(10): Show |
13 | HG00621.hp1 HG01168.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.-137+21093delT | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115317110 | |||||||
chr1:115317187 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-137+21017G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115317187 | |||||||
chr1:115317352 | C | T | 10 | a0001c0001t0001g0036 a0001c0001t0001g0039 a0001c0001t0001g0042 others(7): Show |
10 | HG01433.hp2 HG02055.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-137+20852G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115317352 | |||||||
chr1:115317368 | T | A | 2 | a0001c0001t0001g0121 a0002c0002t0001g0323 |
2 | HG01175.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.-137+20836A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115317368 | |||||||
chr1:115317555 | A | G | 1 | a0001c0001t0001g0246 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-137+20649T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115317555 | |||||||
chr1:115317654 | G | A | 1 | a0002c0002t0001g0034 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-137+20550C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115317654 | |||||||
chr1:115317739 | C | T | 1 | a0001c0001t0001g0025 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-137+20465G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115317739 | |||||||
chr1:115317741 | T | G | 2 | a0001c0001t0001g0121 a0001c0001t0001g0172 |
2 | HG02300.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-137+20463A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115317741 | |||||||
chr1:115317930 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-137+20274G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115317930 | |||||||
chr1:115318078 | G | C | 2 | a0001c0001t0001g0121 a0001c0001t0001g0172 |
2 | HG02300.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-137+20126C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115318078 | |||||||
chr1:115318180 | C | A | 18 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0018 others(15): Show |
23 | HG01099.hp2 HG01884.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.-137+20024G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115318180 | |||||||
chr1:115318197 | C | T | 1 | a0001c0001t0001g0295 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-137+20007G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115318197 | |||||||
chr1:115318216 | G | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0295 |
2 | HG02258.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-137+19988C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115318216 | |||||||
chr1:115318221 | G | A | 2 | a0001c0001t0001g0121 a0001c0001t0001g0172 |
2 | HG02300.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-137+19983C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115318221 | |||||||
chr1:115318252 | T | A | 3 | a0001c0001t0001g0329 a0001c0001t0001g0376 a0001c0001t0001g0377 |
3 | HG01192.hp2 HG01261.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.-137+19952A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115318252 | |||||||
chr1:115318321 | T | C | 2 | a0001c0001t0001g0121 a0001c0001t0001g0172 |
2 | HG02300.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-137+19883A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115318321 | |||||||
chr1:115318342 | G | C | 1 | a0002c0002t0001g0066 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-137+19862C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115318342 | |||||||
chr1:115318400 | G | A | 1 | a0001c0001t0001g0306 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-137+19804C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115318400 | |||||||
chr1:115318638 | C | T | 1 | a0001c0003t0001g0395 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-137+19566G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115318638 | |||||||
chr1:115318644 | T | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(149): Show |
160 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.-137+19560A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115318644 | |||||||
chr1:115318863 | C | T | 1 | a0002c0002t0001g0359 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-137+19341G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115318863 | |||||||
chr1:115318878 | C | A | 5 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(2): Show |
5 | HG00544.hp1 NA18612.hp2 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.-137+19326G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115318878 | |||||||
chr1:115318906 | G | A | 2 | a0001c0001t0001g0121 a0001c0001t0001g0172 |
2 | HG02300.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-137+19298C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115318906 | |||||||
chr1:115318984 | G | A | 2 | a0002c0002t0001g0190 a0002c0002t0001g0392 |
2 | HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-137+19220C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115318984 | |||||||
chr1:115318998 | A | G | 8 | a0001c0001t0001g0122 a0002c0002t0001g0049 a0002c0002t0001g0063 others(5): Show |
8 | HG00621.hp1 HG02056.hp2 HG04115.hp1 others(5): Show |
intron_variant | MODIFIER | c.-137+19206T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115318998 | |||||||
chr1:115319258 | A | G | 1 | a0001c0001t0001g0039 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-137+18946T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115319258 | |||||||
chr1:115319402 | T | C | 1 | a0001c0001t0001g0216 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-137+18802A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115319402 | |||||||
chr1:115319536 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-137+18668G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115319536 | |||||||
chr1:115319613 | A | G | 1 | a0001c0001t0001g0295 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-137+18591T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115319613 | |||||||
chr1:115319633 | A | C | 309 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(306): Show |
327 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(324): Show |
intron_variant | MODIFIER | c.-137+18571T>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115319633 | |||||||
chr1:115319906 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-137+18298C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115319906 | |||||||
chr1:115319946 | C | T | 1 | a0001c0001t0001g0280 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-137+18258G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115319946 | |||||||
chr1:115319947 | G | A | 164 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0013 others(161): Show |
173 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.-137+18257C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115319947 | |||||||
chr1:115319996 | C | G | 309 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(306): Show |
327 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(324): Show |
intron_variant | MODIFIER | c.-137+18208G>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115319996 | |||||||
chr1:115320020 | T | G | 309 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(306): Show |
327 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(324): Show |
intron_variant | MODIFIER | c.-137+18184A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115320020 | |||||||
chr1:115320022 | C | T | 1 | a0001c0001t0001g0007 | 2 | HG01243.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.-137+18182G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115320022 | |||||||
chr1:115320049 | G | T | 18 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0018 others(15): Show |
23 | HG01099.hp2 HG01884.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.-137+18155C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115320049 | |||||||
chr1:115320192 | T | C | 3 | a0001c0001t0001g0149 a0001c0001t0001g0161 a0001c0001t0001g0162 |
3 | NA18956.hp1 NA18971.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.-137+18012A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115320192 | |||||||
chr1:115320199 | T | G | 75 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(72): Show |
81 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.-137+18005A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115320199 | |||||||
chr1:115320205 | C | T | 4 | a0001c0001t0001g0013 a0001c0001t0001g0209 a0001c0001t0001g0210 others(1): Show |
5 | HG00642.hp1 HG01069.hp1 HG01070.hp1 others(2): Show |
intron_variant | MODIFIER | c.-137+17999G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115320205 | |||||||
chr1:115320297 | T | A | 187 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(184): Show |
201 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.-137+17907A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115320297 | |||||||
chr1:115320383 | C | T | 1 | a0001c0001t0001g0239 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-137+17821G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115320383 | |||||||
chr1:115320441 | C | T | 1 | a0001c0001t0001g0295 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-137+17763G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115320441 | |||||||
chr1:115320446 | A | T | 1 | a0001c0001t0001g0286 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-137+17758T>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115320446 | |||||||
chr1:115320758 | T | C | 3 | a0001c0001t0001g0119 a0002c0002t0001g0190 a0002c0002t0001g0392 |
3 | HG03453.hp1 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-137+17446A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115320758 | |||||||
chr1:115320860 | C | T | 1 | a0001c0001t0001g0239 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-137+17344G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115320860 | |||||||
chr1:115320927 | C | G | 187 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(184): Show |
201 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.-137+17277G>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115320927 | |||||||
chr1:115321279 | T | C | 187 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(184): Show |
201 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.-137+16925A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321279 | |||||||
chr1:115321296 | A | T | 5 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(2): Show |
5 | HG00544.hp1 NA18612.hp2 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.-137+16908T>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321296 | |||||||
chr1:115321301 | G | A | 5 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(2): Show |
5 | HG00544.hp1 NA18612.hp2 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.-137+16903C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321301 | |||||||
chr1:115321305 | A | C | 10 | a0001c0001t0001g0010 a0001c0001t0001g0175 a0001c0001t0001g0176 others(7): Show |
11 | HG01891.hp1 HG02109.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.-137+16899T>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321305 | |||||||
chr1:115321445 | G | A | 1 | a0001c0003t0001g0395 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-137+16759C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321445 | |||||||
chr1:115321507 | G | T | 1 | a0001c0001t0001g0224 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-137+16697C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321507 | |||||||
chr1:115321508 | G | C | 1 | a0001c0001t0001g0224 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-137+16696C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321508 | |||||||
chr1:115321509 | A | C | 1 | a0001c0001t0001g0224 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-137+16695T>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321509 | |||||||
chr1:115321510 | C | A | 1 | a0001c0001t0001g0224 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-137+16694G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321510 | |||||||
chr1:115321512 | G | A | 1 | a0001c0001t0001g0224 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-137+16692C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321512 | |||||||
chr1:115321513 | C | G | 1 | a0001c0001t0001g0224 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-137+16691G>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321513 | |||||||
chr1:115321515 | G | T | 1 | a0001c0001t0001g0224 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-137+16689C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321515 | |||||||
chr1:115321517 | T | TTTTGCCA others(3): Show |
1 | a0001c0001t0001g0224 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-137+16686_-137+16 others(16): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321517 | |||||||
chr1:115321518 | C | A | 1 | a0001c0001t0001g0224 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-137+16686G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321518 | |||||||
chr1:115321551 | C | T | 1 | a0002c0002t0001g0034 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-137+16653G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321551 | |||||||
chr1:115321576 | A | ATG | 24 | a0001c0001t0001g0009 a0001c0001t0001g0044 a0001c0001t0001g0053 others(21): Show |
25 | HG00544.hp1 HG00544.hp2 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.-137+16626_-137+16 others(8): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321576 | |||||||
chr1:115321576 | A | ATGTG | 3 | a0001c0001t0001g0124 a0001c0001t0001g0166 a0001c0001t0001g0174 |
3 | HG03927.hp2 NA18968.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.-137+16624_-137+16 others(10): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321576 | |||||||
chr1:115321576 | ATG | A | 40 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0068 others(37): Show |
41 | HG00438.hp1 HG00639.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.-137+16626_-137+16 others(8): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321576 | |||||||
chr1:115321576 | ATGTG | A | 52 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(49): Show |
55 | HG00280.hp1 HG00609.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.-137+16624_-137+16 others(10): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321576 | |||||||
chr1:115321576 | ATGTGTG | A | 34 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0021 others(31): Show |
35 | HG00280.hp2 HG01123.hp1 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.-137+16622_-137+16 others(12): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321576 | |||||||
chr1:115321576 | ATGTGTGT others(1): Show |
A | 102 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0012 others(99): Show |
107 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.-137+16620_-137+16 others(14): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321576 | |||||||
chr1:115321576 | ATGTGTGT others(3): Show |
A | 27 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(24): Show |
31 | HG00609.hp1 HG00642.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.-137+16618_-137+16 others(16): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321576 | |||||||
chr1:115321576 | ATGTGTGT others(5): Show |
A | 11 | a0001c0001t0001g0090 a0001c0001t0001g0104 a0001c0001t0001g0122 others(8): Show |
11 | HG00621.hp1 HG00735.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.-137+16616_-137+16 others(18): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321576 | |||||||
chr1:115321576 | ATGTGTGT others(7): Show |
A | 3 | a0001c0001t0001g0316 a0001c0001t0001g0317 a0001c0001t0001g0318 |
3 | HG01069.hp2 HG01071.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.-137+16614_-137+16 others(20): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321576 | |||||||
chr1:115321576 | ATGTGTGT others(9): Show |
A | 1 | a0001c0001t0001g0295 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-137+16612_-137+16 others(22): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321576 | |||||||
chr1:115321576 | ATGTGTGT others(11): Show |
A | 14 | a0001c0001t0001g0031 a0001c0001t0001g0036 a0001c0001t0001g0039 others(11): Show |
14 | HG01433.hp2 HG02055.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-137+16610_-137+16 others(24): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321576 | |||||||
chr1:115321576 | ATGTGTGT others(13): Show |
A | 28 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0018 others(25): Show |
33 | HG00741.hp2 HG01099.hp2 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.-137+16608_-137+16 others(26): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321576 | |||||||
chr1:115321576 | ATGTGTGT others(17): Show |
A | 2 | a0001c0001t0001g0172 a0001c0001t0001g0305 |
2 | HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-137+16604_-137+16 others(30): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321576 | |||||||
chr1:115321576 | ATGTGTGT others(19): Show |
A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0121 |
2 | HG02300.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-137+16602_-137+16 others(32): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321576 | |||||||
chr1:115321768 | C | T | 6 | a0001c0001t0001g0130 a0001c0001t0001g0132 a0001c0001t0001g0196 others(3): Show |
6 | HG00741.hp2 HG02145.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-137+16436G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321768 | |||||||
chr1:115321928 | C | T | 168 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0013 others(165): Show |
177 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.-137+16276G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321928 | |||||||
chr1:115321966 | G | A | 1 | a0001c0003t0001g0195 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-137+16238C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321966 | |||||||
chr1:115321982 | G | A | 1 | a0002c0002t0001g0129 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-137+16222C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321982 | |||||||
chr1:115321983 | A | T | 1 | a0001c0001t0001g0025 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-137+16221T>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321983 | |||||||
chr1:115321986 | T | A | 1 | a0002c0002t0001g0186 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-137+16218A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115321986 | |||||||
chr1:115322002 | T | A | 18 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0018 others(15): Show |
23 | HG01099.hp2 HG01884.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.-137+16202A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115322002 | |||||||
chr1:115322035 | T | C | 2 | a0001c0001t0001g0269 a0001c0001t0001g0384 |
2 | HG02602.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.-137+16169A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115322035 | |||||||
chr1:115322068 | C | T | 3 | a0001c0001t0001g0119 a0002c0002t0001g0190 a0002c0002t0001g0392 |
3 | HG03453.hp1 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-137+16136G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115322068 | |||||||
chr1:115322098 | T | C | 1 | a0002c0002t0001g0313 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-137+16106A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115322098 | |||||||
chr1:115322329 | G | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0165 |
2 | NA18966.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.-137+15875C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115322329 | |||||||
chr1:115322486 | G | C | 3 | a0001c0001t0001g0121 a0001c0001t0001g0172 a0001c0003t0001g0395 |
3 | HG02055.hp2 HG02300.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-137+15718C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115322486 | |||||||
chr1:115322527 | C | A | 1 | a0001c0001t0001g0245 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-137+15677G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115322527 | |||||||
chr1:115322596 | A | C | 7 | a0001c0001t0001g0084 a0001c0001t0001g0215 a0001c0001t0001g0218 others(4): Show |
7 | NA18940.hp1 NA18957.hp1 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.-137+15608T>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115322596 | |||||||
chr1:115322610 | A | G | 1 | a0001c0001t0001g0385 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-137+15594T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115322610 | |||||||
chr1:115322698 | C | A | 1 | a0001c0001t0001g0389 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-137+15506G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115322698 | |||||||
chr1:115322771 | C | A | 9 | a0001c0001t0001g0036 a0001c0001t0001g0039 a0001c0001t0001g0042 others(6): Show |
9 | HG01433.hp2 HG02055.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-137+15433G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115322771 | |||||||
chr1:115322865 | A | G | 1 | a0001c0001t0001g0197 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-137+15339T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115322865 | |||||||
chr1:115322984 | C | T | 2 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-137+15220G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115322984 | |||||||
chr1:115322985 | A | C | 4 | a0001c0001t0001g0018 a0001c0001t0001g0032 a0001c0001t0001g0306 others(1): Show |
6 | HG01099.hp2 HG01884.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-137+15219T>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115322985 | |||||||
chr1:115323350 | A | G | 17 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(14): Show |
21 | HG00609.hp1 HG00642.hp1 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.-137+14854T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115323350 | |||||||
chr1:115323577 | A | G | 8 | a0001c0001t0001g0122 a0002c0002t0001g0049 a0002c0002t0001g0063 others(5): Show |
8 | HG00621.hp1 HG02056.hp2 HG04115.hp1 others(5): Show |
intron_variant | MODIFIER | c.-137+14627T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115323577 | |||||||
chr1:115323651 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-137+14553T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115323651 | |||||||
chr1:115323848 | A | G | 1 | a0001c0001t0001g0295 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-137+14356T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115323848 | |||||||
chr1:115323998 | C | T | 2 | a0004c0005t0001g0101 a0004c0005t0001g0102 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-137+14206G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115323998 | |||||||
chr1:115324286 | G | A | 8 | a0001c0001t0001g0133 a0001c0001t0001g0142 a0001c0001t0001g0143 others(5): Show |
8 | HG02486.hp2 HG02723.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-137+13918C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115324286 | |||||||
chr1:115324332 | G | T | 3 | a0001c0001t0001g0208 a0001c0001t0001g0302 a0001c0001t0001g0374 |
3 | HG01884.hp2 HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-137+13872C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115324332 | |||||||
chr1:115324345 | G | A | 3 | a0001c0001t0001g0208 a0001c0001t0001g0302 a0001c0001t0001g0374 |
3 | HG01884.hp2 HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-137+13859C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115324345 | |||||||
chr1:115324454 | C | T | 1 | a0002c0002t0001g0185 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-137+13750G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115324454 | |||||||
chr1:115324466 | T | A | 1 | a0001c0001t0001g0182 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-137+13738A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115324466 | |||||||
chr1:115324515 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-137+13689A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115324515 | |||||||
chr1:115324549 | C | A | 1 | a0002c0002t0001g0034 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-137+13655G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115324549 | |||||||
chr1:115324576 | G | T | 9 | a0001c0001t0001g0036 a0001c0001t0001g0039 a0001c0001t0001g0042 others(6): Show |
9 | HG01433.hp2 HG02055.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-137+13628C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115324576 | |||||||
chr1:115324595 | T | A | 84 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0012 others(81): Show |
88 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.-137+13609A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115324595 | |||||||
chr1:115324626 | A | G | 3 | a0001c0001t0001g0334 a0001c0001t0001g0335 a0001c0001t0001g0346 |
3 | HG03831.hp1 HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-137+13578T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115324626 | |||||||
chr1:115324650 | G | A | 296 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(293): Show |
314 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(311): Show |
intron_variant | MODIFIER | c.-137+13554C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115324650 | |||||||
chr1:115324701 | G | A | 1 | a0001c0001t0001g0286 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-137+13503C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115324701 | |||||||
chr1:115324713 | T | G | 11 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0175 others(8): Show |
12 | HG01891.hp1 HG02109.hp1 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.-137+13491A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115324713 | |||||||
chr1:115324950 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-137+13254G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115324950 | |||||||
chr1:115324996 | C | T | 84 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0011 others(81): Show |
87 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.-137+13208G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115324996 | |||||||
chr1:115325044 | G | A | 11 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0001c0001t0001g0069 others(8): Show |
11 | NA18945.hp1 NA18950.hp2 NA18964.hp2 others(8): Show |
intron_variant | MODIFIER | c.-137+13160C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115325044 | |||||||
chr1:115325121 | A | T | 81 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0012 others(78): Show |
85 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.-137+13083T>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115325121 | |||||||
chr1:115325185 | C | T | 4 | a0001c0001t0001g0167 a0001c0001t0001g0212 a0001c0001t0001g0213 others(1): Show |
4 | HG02155.hp1 NA18990.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.-137+13019G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115325185 | |||||||
chr1:115325223 | G | A | 1 | a0001c0003t0001g0395 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-137+12981C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115325223 | |||||||
chr1:115325264 | C | T | 9 | a0001c0001t0001g0036 a0001c0001t0001g0039 a0001c0001t0001g0042 others(6): Show |
9 | HG01433.hp2 HG02055.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-137+12940G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115325264 | |||||||
chr1:115325265 | G | A | 1 | a0001c0001t0001g0236 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-137+12939C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115325265 | |||||||
chr1:115325439 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-137+12765T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115325439 | |||||||
chr1:115325527 | A | T | 1 | a0001c0001t0001g0172 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-137+12677T>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115325527 | |||||||
chr1:115325761 | A | G | 50 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0018 others(47): Show |
55 | HG00621.hp1 HG00741.hp2 HG01099.hp2 others(52): Show |
intron_variant | MODIFIER | c.-137+12443T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115325761 | |||||||
chr1:115325805 | A | G | 40 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0018 others(37): Show |
45 | HG00621.hp1 HG00741.hp2 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.-137+12399T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115325805 | |||||||
chr1:115325930 | C | T | 9 | a0001c0001t0001g0100 a0001c0001t0001g0309 a0001c0001t0001g0322 others(6): Show |
9 | NA18954.hp1 NA18957.hp2 NA18962.hp2 others(6): Show |
intron_variant | MODIFIER | c.-137+12274G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115325930 | |||||||
chr1:115326157 | G | A | 1 | a0001c0001t0001g0295 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-137+12047C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115326157 | |||||||
chr1:115326178 | C | T | 2 | a0003c0004t0001g0381 a0003c0004t0001g0382 |
2 | HG01109.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-137+12026G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115326178 | |||||||
chr1:115326200 | T | C | 3 | a0001c0001t0001g0022 a0002c0002t0001g0034 a0002c0002t0001g0035 |
3 | HG02451.hp1 HG03471.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-137+12004A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115326200 | |||||||
chr1:115326261 | A | T | 83 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0012 others(80): Show |
87 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.-137+11943T>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115326261 | |||||||
chr1:115326339 | G | T | 1 | a0001c0001t0001g0122 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-137+11865C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115326339 | |||||||
chr1:115326468 | G | C | 207 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(204): Show |
219 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(216): Show |
intron_variant | MODIFIER | c.-137+11736C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115326468 | |||||||
chr1:115326471 | G | A | 81 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0012 others(78): Show |
85 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.-137+11733C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115326471 | |||||||
chr1:115326501 | G | T | 1 | a0001c0001t0001g0246 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-137+11703C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115326501 | |||||||
chr1:115326520 | T | A | 1 | a0001c0001t0001g0274 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-137+11684A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115326520 | |||||||
chr1:115326610 | T | G | 1 | a0001c0001t0001g0282 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-137+11594A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115326610 | |||||||
chr1:115326616 | A | G | 10 | a0001c0001t0001g0119 a0001c0001t0001g0133 a0001c0001t0001g0142 others(7): Show |
10 | HG02486.hp2 HG02723.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.-137+11588T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115326616 | |||||||
chr1:115326676 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-137+11528A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115326676 | |||||||
chr1:115326837 | G | T | 1 | a0001c0001t0001g0188 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-137+11367C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115326837 | |||||||
chr1:115326878 | G | A | 170 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0013 others(167): Show |
179 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.-137+11326C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115326878 | |||||||
chr1:115327074 | T | C | 1 | a0001c0001t0001g0312 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-137+11130A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115327074 | |||||||
chr1:115327209 | G | A | 6 | a0001c0001t0001g0130 a0001c0001t0001g0132 a0001c0001t0001g0196 others(3): Show |
6 | HG00741.hp2 HG02145.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-137+10995C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115327209 | |||||||
chr1:115327229 | T | C | 82 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0012 others(79): Show |
86 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.-137+10975A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115327229 | |||||||
chr1:115327306 | C | T | 7 | a0001c0001t0001g0120 a0001c0001t0001g0152 a0001c0001t0001g0189 others(4): Show |
7 | HG01106.hp1 HG01261.hp2 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.-137+10898G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115327306 | |||||||
chr1:115327346 | T | C | 1 | a0001c0001t0001g0390 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-137+10858A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115327346 | |||||||
chr1:115327505 | C | T | 8 | a0001c0001t0001g0122 a0002c0002t0001g0049 a0002c0002t0001g0063 others(5): Show |
8 | HG00621.hp1 HG02056.hp2 HG04115.hp1 others(5): Show |
intron_variant | MODIFIER | c.-137+10699G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115327505 | |||||||
chr1:115327576 | G | A | 3 | a0001c0001t0001g0208 a0001c0001t0001g0302 a0001c0001t0001g0374 |
3 | HG01884.hp2 HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-137+10628C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115327576 | |||||||
chr1:115327689 | A | G | 45 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0018 others(42): Show |
50 | HG00621.hp1 HG00741.hp2 HG01099.hp2 others(47): Show |
intron_variant | MODIFIER | c.-137+10515T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115327689 | |||||||
chr1:115327708 | T | C | 2 | a0004c0005t0001g0101 a0004c0005t0001g0102 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-137+10496A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115327708 | |||||||
chr1:115327854 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-137+10350G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115327854 | |||||||
chr1:115327911 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-137+10293G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115327911 | |||||||
chr1:115328165 | AG | A | 231 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(228): Show |
243 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(240): Show |
intron_variant | MODIFIER | c.-137+10038delC | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115328165 | |||||||
chr1:115328188 | TG | T | 133 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(130): Show |
142 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.-137+10015delC | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115328188 | |||||||
chr1:115328284 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-137+9920A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115328284 | |||||||
chr1:115328525 | C | T | 3 | a0001c0001t0001g0022 a0002c0002t0001g0034 a0002c0002t0001g0035 |
3 | HG02451.hp1 HG03471.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-137+9679G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115328525 | |||||||
chr1:115328550 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-137+9654C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115328550 | |||||||
chr1:115328568 | G | C | 1 | a0001c0001t0001g0096 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-137+9636C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115328568 | |||||||
chr1:115328733 | C | A | 184 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(181): Show |
191 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(188): Show |
intron_variant | MODIFIER | c.-137+9471G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115328733 | |||||||
chr1:115328795 | G | A | 1 | a0001c0001t0001g0166 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-137+9409C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115328795 | |||||||
chr1:115328853 | G | T | 5 | a0001c0001t0001g0014 a0001c0001t0001g0289 a0001c0001t0001g0290 others(2): Show |
6 | HG02056.hp1 HG02071.hp1 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.-137+9351C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115328853 | |||||||
chr1:115329014 | A | G | 78 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(75): Show |
83 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.-137+9190T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115329014 | |||||||
chr1:115329233 | A | G | 17 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(14): Show |
21 | HG00609.hp1 HG00642.hp1 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.-137+8971T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115329233 | |||||||
chr1:115329240 | A | AGTATGTA others(14): Show |
1 | a0001c0001t0001g0295 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-137+8943_-137+896 others(25): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115329240 | |||||||
chr1:115329245 | G | A | 1 | a0001c0001t0001g0262 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-137+8959C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115329245 | |||||||
chr1:115329269 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-137+8935G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115329269 | |||||||
chr1:115329287 | T | C | 6 | a0001c0001t0001g0130 a0001c0001t0001g0132 a0001c0001t0001g0196 others(3): Show |
6 | HG00741.hp2 HG02145.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-137+8917A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115329287 | |||||||
chr1:115329414 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-137+8790C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115329414 | |||||||
chr1:115329617 | C | T | 7 | a0002c0002t0001g0049 a0002c0002t0001g0063 a0002c0002t0001g0064 others(4): Show |
7 | HG00621.hp1 HG02056.hp2 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.-137+8587G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115329617 | |||||||
chr1:115329645 | T | G | 109 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(106): Show |
119 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.-137+8559A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115329645 | |||||||
chr1:115329694 | A | G | 1 | a0001c0001t0001g0374 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-137+8510T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115329694 | |||||||
chr1:115329744 | C | CT | 15 | a0001c0001t0001g0025 a0001c0001t0001g0119 a0001c0001t0001g0133 others(12): Show |
15 | HG02258.hp2 HG02486.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-137+8459dupA | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115329744 | |||||||
chr1:115329744 | CT | C | 188 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(185): Show |
196 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.-137+8459delA | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115329744 | |||||||
chr1:115329749 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-137+8455A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115329749 | |||||||
chr1:115329751 | T | C | 1 | a0001c0001t0001g0345 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-137+8453A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115329751 | |||||||
chr1:115329803 | G | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0389 a0001c0001t0001g0394 |
3 | HG02258.hp1 HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-137+8401C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115329803 | |||||||
chr1:115329907 | T | C | 217 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(214): Show |
229 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(226): Show |
intron_variant | MODIFIER | c.-137+8297A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115329907 | |||||||
chr1:115329933 | T | A | 1 | a0001c0001t0001g0172 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-137+8271A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115329933 | |||||||
chr1:115330013 | C | G | 1 | a0001c0001t0001g0121 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-137+8191G>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115330013 | |||||||
chr1:115330257 | T | G | 2 | a0001c0001t0001g0201 a0001c0001t0001g0245 |
2 | NA18939.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.-137+7947A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115330257 | |||||||
chr1:115330346 | G | A | 6 | a0001c0001t0001g0130 a0001c0001t0001g0132 a0001c0001t0001g0196 others(3): Show |
6 | HG00741.hp2 HG02145.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-137+7858C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115330346 | |||||||
chr1:115330426 | G | T | 254 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(251): Show |
268 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.-137+7778C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115330426 | |||||||
chr1:115330431 | C | G | 1 | a0001c0001t0001g0025 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-137+7773G>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115330431 | |||||||
chr1:115330695 | C | T | 1 | a0001c0003t0001g0395 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-137+7509G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115330695 | |||||||
chr1:115330703 | C | G | 1 | a0001c0001t0001g0172 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-137+7501G>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115330703 | |||||||
chr1:115330730 | TCACTC | T | 160 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(157): Show |
168 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.-137+7469_-137+747 others(9): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115330730 | |||||||
chr1:115330802 | A | G | 6 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0295 others(3): Show |
6 | HG02055.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-137+7402T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115330802 | |||||||
chr1:115330847 | G | A | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG00408.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.-137+7357C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115330847 | |||||||
chr1:115330984 | C | T | 1 | a0001c0001t0001g0020 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-137+7220G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115330984 | |||||||
chr1:115331110 | A | AG | 56 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0020 others(53): Show |
58 | HG00423.hp1 HG00438.hp2 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.-137+7093dupC | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115331110 | |||||||
chr1:115331133 | T | G | 3 | a0001c0001t0001g0208 a0001c0001t0001g0302 a0001c0001t0001g0374 |
3 | HG01884.hp2 HG02280.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-137+7071A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115331133 | |||||||
chr1:115331298 | T | G | 1 | a0001c0001t0001g0032 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-137+6906A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115331298 | |||||||
chr1:115331380 | C | T | 3 | a0001c0001t0001g0232 a0001c0001t0001g0241 a0001c0001t0001g0242 |
3 | HG01175.hp1 HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-137+6824G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115331380 | |||||||
chr1:115331453 | T | G | 1 | a0001c0001t0001g0249 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-137+6751A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115331453 | |||||||
chr1:115331829 | T | G | 2 | a0001c0001t0001g0311 a0001c0003t0001g0310 |
2 | HG02622.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-137+6375A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115331829 | |||||||
chr1:115331891 | A | C | 23 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(20): Show |
24 | HG00741.hp2 HG01891.hp1 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.-137+6313T>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115331891 | |||||||
chr1:115331978 | A | G | 2 | a0002c0002t0001g0234 a0002c0002t0001g0250 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-137+6226T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115331978 | |||||||
chr1:115332082 | T | A | 1 | a0001c0001t0001g0270 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-137+6122A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115332082 | |||||||
chr1:115332133 | C | T | 2 | a0002c0002t0001g0033 a0002c0002t0001g0332 |
2 | NA18967.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.-137+6071G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115332133 | |||||||
chr1:115332310 | A | G | 383 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(380): Show |
403 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(400): Show |
intron_variant | MODIFIER | c.-137+5894T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115332310 | |||||||
chr1:115332339 | T | A | 3 | a0001c0001t0001g0380 a0003c0004t0001g0381 a0003c0004t0001g0382 |
3 | HG00733.hp1 HG01109.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-137+5865A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115332339 | |||||||
chr1:115332516 | TA | T | 206 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(203): Show |
214 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.-137+5687delT | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115332516 | |||||||
chr1:115332573 | A | C | 109 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(106): Show |
114 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.-137+5631T>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115332573 | |||||||
chr1:115332588 | G | A | 1 | a0001c0001t0001g0346 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-137+5616C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115332588 | |||||||
chr1:115332939 | C | T | 2 | a0001c0001t0001g0246 a0001c0003t0001g0395 |
2 | HG02055.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-137+5265G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115332939 | |||||||
chr1:115333024 | C | T | 206 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(203): Show |
214 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.-137+5180G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333024 | |||||||
chr1:115333049 | T | C | 2 | a0001c0001t0001g0113 a0001c0001t0001g0115 |
2 | NA19068.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.-137+5155A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333049 | |||||||
chr1:115333279 | A | G | 2 | a0001c0001t0001g0246 a0001c0003t0001g0395 |
2 | HG02055.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-137+4925T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333279 | |||||||
chr1:115333499 | T | TA | 77 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(74): Show |
81 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.-137+4704dupT | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333499 | |||||||
chr1:115333499 | T | TAA | 15 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0025 others(12): Show |
16 | HG02055.hp2 HG02258.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.-137+4703_-137+470 others(6): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333499 | |||||||
chr1:115333499 | T | TAAA | 104 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(101): Show |
107 | HG00408.hp2 HG00609.hp2 HG00621.hp2 others(104): Show |
intron_variant | MODIFIER | c.-137+4702_-137+470 others(7): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333499 | |||||||
chr1:115333499 | T | TAAAA | 21 | a0001c0001t0001g0039 a0001c0001t0001g0044 a0001c0001t0001g0143 others(18): Show |
21 | HG00544.hp2 HG01261.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.-137+4701_-137+470 others(8): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333499 | |||||||
chr1:115333647 | C | G | 88 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(85): Show |
91 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.-137+4557G>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333647 | |||||||
chr1:115333655 | C | CTCTT | 5 | a0001c0001t0001g0322 a0001c0001t0001g0376 a0002c0002t0001g0320 others(2): Show |
5 | HG01175.hp2 HG01192.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.-137+4545_-137+454 others(8): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333655 | |||||||
chr1:115333655 | CTCTT | C | 19 | a0001c0001t0001g0068 a0001c0001t0001g0136 a0001c0001t0001g0187 others(16): Show |
19 | HG00280.hp1 HG00639.hp2 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.-137+4545_-137+454 others(8): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333655 | |||||||
chr1:115333655 | CTCTTTCT others(1): Show |
C | 24 | a0001c0001t0001g0069 a0001c0001t0001g0106 a0001c0001t0001g0137 others(21): Show |
24 | HG00099.hp2 HG00639.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.-137+4541_-137+454 others(12): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333655 | |||||||
chr1:115333655 | CTCTTTCT others(5): Show |
C | 14 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0050 others(11): Show |
16 | HG01358.hp2 HG01433.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.-137+4537_-137+454 others(16): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333655 | |||||||
chr1:115333655 | CTCTTTCT others(9): Show |
C | 6 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0368 others(3): Show |
6 | HG00099.hp1 HG02698.hp1 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.-137+4533_-137+454 others(20): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333655 | |||||||
chr1:115333655 | CTCTTTCT others(13): Show |
C | 1 | a0001c0001t0001g0174 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-137+4529_-137+454 others(24): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333655 | |||||||
chr1:115333662 | T | C | 1 | a0002c0002t0001g0112 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-137+4542A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333662 | |||||||
chr1:115333677 | CTTTCTTT others(6): Show |
C | 1 | a0001c0001t0001g0372 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-137+4514_-137+452 others(17): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333677 | |||||||
chr1:115333677 | CTTTCTTT others(30): Show |
C | 2 | a0001c0001t0001g0142 a0001c0001t0001g0143 |
2 | HG02486.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-137+4490_-137+452 others(41): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333677 | |||||||
chr1:115333678 | TTTCTTTC others(8): Show |
T | 11 | a0001c0001t0001g0010 a0001c0001t0001g0175 a0001c0001t0001g0176 others(8): Show |
12 | HG01891.hp1 HG02109.hp1 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.-137+4511_-137+452 others(19): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333678 | |||||||
chr1:115333681 | CTTTCTTT others(26): Show |
C | 2 | a0001c0003t0001g0140 a0001c0003t0001g0141 |
2 | HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-137+4490_-137+452 others(37): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333681 | |||||||
chr1:115333682 | TTTCTTTC others(4): Show |
T | 64 | a0001c0001t0001g0011 a0001c0001t0001g0024 a0001c0001t0001g0043 others(61): Show |
65 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.-137+4511_-137+452 others(15): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333682 | |||||||
chr1:115333682 | TTTCTTTC others(8): Show |
T | 1 | a0001c0001t0001g0009 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-137+4507_-137+452 others(19): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333682 | |||||||
chr1:115333686 | TTTCTTTC | T | 10 | a0001c0001t0001g0124 a0001c0001t0001g0130 a0001c0001t0001g0147 others(7): Show |
10 | HG00741.hp2 HG02145.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-137+4511_-137+451 others(11): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333686 | |||||||
chr1:115333689 | CTTTCTTT others(18): Show |
C | 1 | a0001c0001t0001g0315 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-137+4490_-137+451 others(29): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333689 | |||||||
chr1:115333693 | CTTTCTTT others(14): Show |
C | 14 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0110 others(11): Show |
14 | HG00609.hp1 HG02129.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.-137+4490_-137+451 others(25): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333693 | |||||||
chr1:115333693 | CTTTCTTT others(15): Show |
C | 1 | a0002c0002t0001g0397 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-137+4489_-137+451 others(26): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333693 | |||||||
chr1:115333697 | CTTTCTTT others(10): Show |
C | 40 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(37): Show |
42 | HG00408.hp1 HG00544.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.-137+4490_-137+450 others(21): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333697 | |||||||
chr1:115333701 | CTTTCTTT others(6): Show |
C | 48 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0022 others(45): Show |
49 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(46): Show |
intron_variant | MODIFIER | c.-137+4490_-137+450 others(17): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333701 | |||||||
chr1:115333702 | TTTCTTTC others(18): Show |
T | 1 | a0001c0001t0001g0057 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-137+4477_-137+450 others(29): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333702 | |||||||
chr1:115333702 | TTTCTTTC others(25): Show |
T | 1 | a0001c0001t0001g0097 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-137+4470_-137+450 others(36): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333702 | |||||||
chr1:115333705 | CTTTCTTT others(2): Show |
C | 31 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0039 others(28): Show |
31 | HG00280.hp2 HG00423.hp2 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.-137+4490_-137+449 others(13): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333705 | |||||||
chr1:115333706 | TTTCTTTC others(14): Show |
T | 1 | a0001c0001t0001g0281 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-137+4477_-137+449 others(25): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333706 | |||||||
chr1:115333706 | TTTCTTTC others(21): Show |
T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0226 |
2 | HG01978.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.-137+4470_-137+449 others(32): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333706 | |||||||
chr1:115333709 | CTTTCT | C | 21 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0042 others(18): Show |
21 | HG00741.hp1 HG01070.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.-137+4490_-137+449 others(9): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333709 | |||||||
chr1:115333710 | TTTCTTTT others(17): Show |
T | 15 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0076 others(12): Show |
16 | HG00438.hp1 HG01496.hp1 HG02717.hp2 others(13): Show |
intron_variant | MODIFIER | c.-137+4470_-137+449 others(28): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333710 | |||||||
chr1:115333713 | CT | C | 20 | a0001c0001t0001g0021 a0001c0001t0001g0052 a0001c0001t0001g0094 others(17): Show |
20 | HG01123.hp1 HG02056.hp2 HG02071.hp1 others(17): Show |
intron_variant | MODIFIER | c.-137+4490delA | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333713 | |||||||
chr1:115333714 | TTTTCTTT others(6): Show |
T | 20 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0082 others(17): Show |
22 | HG00438.hp2 HG00597.hp1 HG00673.hp2 others(19): Show |
intron_variant | MODIFIER | c.-137+4477_-137+448 others(17): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333714 | |||||||
chr1:115333714 | TTTTCTTT others(13): Show |
T | 21 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0059 others(18): Show |
22 | HG00423.hp1 HG01243.hp2 HG01928.hp1 others(19): Show |
intron_variant | MODIFIER | c.-137+4470_-137+448 others(24): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333714 | |||||||
chr1:115333715 | TTTCTTTC others(4): Show |
T | 1 | a0002c0002t0001g0264 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-137+4478_-137+448 others(15): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333715 | |||||||
chr1:115333723 | TTTCCTTC others(4): Show |
T | 8 | a0001c0001t0001g0021 a0001c0001t0001g0094 a0001c0001t0001g0123 others(5): Show |
8 | HG02080.hp1 HG02080.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.-137+4470_-137+448 others(15): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333723 | |||||||
chr1:115333727 | C | T | 2 | a0001c0001t0001g0052 a0001c0001t0001g0218 |
2 | NA18949.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.-137+4477G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333727 | |||||||
chr1:115333731 | TTTC | T | 22 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0052 others(19): Show |
24 | HG00438.hp2 HG00597.hp1 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.-137+4470_-137+447 others(7): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333731 | |||||||
chr1:115333734 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-137+4470G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333734 | |||||||
chr1:115333738 | C | T | 3 | a0001c0001t0001g0081 a0002c0002t0001g0051 a0002c0002t0001g0080 |
3 | NA18941.hp2 NA18984.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-137+4466G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333738 | |||||||
chr1:115333741 | T | C | 1 | a0001c0001t0001g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-137+4463A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333741 | |||||||
chr1:115333747 | T | A | 1 | a0001c0001t0001g0246 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-137+4457A>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333747 | |||||||
chr1:115333748 | T | C | 1 | a0001c0001t0001g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-137+4456A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333748 | |||||||
chr1:115333760 | C | CCT | 229 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(226): Show |
245 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(242): Show |
intron_variant | MODIFIER | c.-137+4442_-137+444 others(6): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333760 | |||||||
chr1:115333760 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-137+4444G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333760 | |||||||
chr1:115333794 | C | CTTTCTTT others(13): Show |
1 | a0001c0001t0001g0294 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-137+4409_-137+441 others(24): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333794 | |||||||
chr1:115333794 | CTTTCTTT others(9): Show |
C | 10 | a0001c0001t0001g0010 a0001c0001t0001g0175 a0001c0001t0001g0176 others(7): Show |
11 | HG02109.hp1 HG02895.hp2 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.-137+4394_-137+440 others(20): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333794 | |||||||
chr1:115333804 | T | C | 1 | a0002c0002t0001g0375 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-137+4400A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333804 | |||||||
chr1:115333804 | T | TTCTC | 226 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(223): Show |
242 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(239): Show |
intron_variant | MODIFIER | c.-137+4396_-137+439 others(8): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333804 | |||||||
chr1:115333810 | T | C | 3 | a0001c0001t0001g0217 a0001c0001t0001g0296 a0001c0001t0001g0297 |
3 | HG02723.hp2 HG02809.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-137+4394A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333810 | |||||||
chr1:115333812 | T | C | 3 | a0001c0001t0001g0217 a0001c0001t0001g0296 a0001c0001t0001g0297 |
3 | HG02723.hp2 HG02809.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-137+4392A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333812 | |||||||
chr1:115333814 | C | T | 3 | a0001c0001t0001g0217 a0001c0001t0001g0296 a0001c0001t0001g0297 |
3 | HG02723.hp2 HG02809.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-137+4390G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333814 | |||||||
chr1:115333882 | G | A | 109 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(106): Show |
120 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.-137+4322C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333882 | |||||||
chr1:115333915 | G | A | 2 | a0001c0001t0001g0116 a0002c0002t0001g0105 |
2 | NA18944.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.-137+4289C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333915 | |||||||
chr1:115333962 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-137+4242G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333962 | |||||||
chr1:115333997 | G | T | 312 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(309): Show |
331 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(328): Show |
intron_variant | MODIFIER | c.-137+4207C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115333997 | |||||||
chr1:115334350 | G | A | 2 | a0002c0002t0001g0111 a0002c0002t0001g0112 |
2 | NA18940.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.-137+3854C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115334350 | |||||||
chr1:115334381 | A | G | 4 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(1): Show |
4 | HG02717.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-137+3823T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115334381 | |||||||
chr1:115334410 | A | G | 4 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(1): Show |
4 | HG02717.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-137+3794T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115334410 | |||||||
chr1:115334455 | A | G | 108 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(105): Show |
115 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.-137+3749T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115334455 | |||||||
chr1:115334541 | G | T | 4 | a0002c0002t0001g0045 a0002c0002t0001g0046 a0002c0002t0001g0047 others(1): Show |
4 | NA18965.hp2 NA18974.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.-137+3663C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115334541 | |||||||
chr1:115334580 | C | T | 1 | a0002c0002t0001g0034 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-137+3624G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115334580 | |||||||
chr1:115334597 | A | C | 1 | a0001c0001t0001g0121 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-137+3607T>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115334597 | |||||||
chr1:115334808 | C | A | 1 | a0001c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-137+3396G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115334808 | |||||||
chr1:115334901 | C | T | 212 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(209): Show |
225 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(222): Show |
intron_variant | MODIFIER | c.-137+3303G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115334901 | |||||||
chr1:115334906 | C | T | 3 | a0001c0001t0001g0022 a0002c0002t0001g0034 a0002c0002t0001g0035 |
3 | HG02451.hp1 HG03471.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-137+3298G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115334906 | |||||||
chr1:115334907 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-137+3297C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115334907 | |||||||
chr1:115335003 | G | A | 90 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(87): Show |
93 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.-137+3201C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115335003 | |||||||
chr1:115335009 | A | G | 1 | a0002c0002t0001g0061 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-137+3195T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115335009 | |||||||
chr1:115335232 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-137+2972G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115335232 | |||||||
chr1:115335592 | G | A | 2 | a0003c0004t0001g0381 a0003c0004t0001g0382 |
2 | HG01109.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-137+2612C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115335592 | |||||||
chr1:115335621 | T | G | 321 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(318): Show |
340 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(337): Show |
intron_variant | MODIFIER | c.-137+2583A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115335621 | |||||||
chr1:115335649 | CT | C | 321 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(318): Show |
340 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(337): Show |
intron_variant | MODIFIER | c.-137+2554delA | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115335649 | |||||||
chr1:115335685 | T | C | 1 | a0001c0001t0001g0280 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-137+2519A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115335685 | |||||||
chr1:115335916 | C | T | 12 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0023 others(9): Show |
15 | HG01884.hp1 HG01884.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-137+2288G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115335916 | |||||||
chr1:115335954 | G | A | 1 | a0001c0001t0001g0117 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-137+2250C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115335954 | |||||||
chr1:115336183 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-137+2021G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115336183 | |||||||
chr1:115336184 | G | A | 4 | a0001c0001t0001g0380 a0002c0002t0001g0379 a0003c0004t0001g0381 others(1): Show |
4 | HG00733.hp1 HG01109.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-137+2020C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115336184 | |||||||
chr1:115336372 | C | T | 1 | a0001c0001t0001g0134 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.-137+1832G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115336372 | |||||||
chr1:115336444 | A | T | 42 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0022 others(39): Show |
44 | HG00733.hp1 HG01081.hp1 HG01099.hp2 others(41): Show |
intron_variant | MODIFIER | c.-137+1760T>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115336444 | |||||||
chr1:115336506 | G | T | 3 | a0001c0001t0001g0131 a0001c0001t0001g0293 a0007c0010t0001g0288 |
3 | HG03688.hp1 HG04199.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-137+1698C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115336506 | |||||||
chr1:115336605 | G | C | 1 | a0001c0001t0001g0281 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-137+1599C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115336605 | |||||||
chr1:115336780 | G | C | 1 | a0001c0001t0001g0106 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-137+1424C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115336780 | |||||||
chr1:115336810 | G | A | 1 | a0002c0002t0001g0207 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-137+1394C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115336810 | |||||||
chr1:115336815 | T | C | 1 | a0002c0002t0001g0060 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-137+1389A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115336815 | |||||||
chr1:115337176 | C | T | 1 | a0002c0002t0001g0313 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-137+1028G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337176 | |||||||
chr1:115337200 | G | C | 84 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0018 others(81): Show |
88 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(85): Show |
intron_variant | MODIFIER | c.-137+1004C>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337200 | |||||||
chr1:115337250 | TTTTTTGT others(4): Show |
T | 7 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0303 others(4): Show |
10 | HG01884.hp2 HG02257.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.-137+943_-137+953d others(13): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337250 | |||||||
chr1:115337256 | GTTTTGT | G | 4 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0001g0133 others(1): Show |
4 | HG01081.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-137+942_-137+947d others(8): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337256 | |||||||
chr1:115337257 | TTTTGTTT others(3): Show |
T | 3 | a0001c0001t0001g0023 a0001c0001t0001g0312 a0001c0001t0001g0373 |
3 | HG02109.hp2 HG02970.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-137+937_-137+946d others(12): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337257 | |||||||
chr1:115337267 | G | GT | 25 | a0001c0001t0001g0015 a0001c0001t0001g0183 a0001c0001t0001g0309 others(22): Show |
26 | HG00099.hp2 HG00733.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.-137+936dupA | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | |||||||
chr1:115337267 | G | GTT | 8 | a0001c0001t0001g0016 a0001c0001t0001g0317 a0001c0001t0001g0354 others(5): Show |
9 | HG01071.hp2 HG01243.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.-137+935_-137+936d others(4): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | |||||||
chr1:115337267 | G | GTTTGTTT others(10): Show |
1 | a0001c0001t0001g0143 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-137+936_-137+937i others(19): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | |||||||
chr1:115337267 | G | GTTTGTTT others(13): Show |
1 | a0001c0003t0001g0141 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-137+936_-137+937i others(22): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | |||||||
chr1:115337267 | G | GTTTGTTT others(14): Show |
1 | a0001c0003t0001g0140 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-137+936_-137+937i others(23): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | |||||||
chr1:115337267 | G | GTTTGTTT others(16): Show |
1 | a0001c0001t0001g0142 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-137+936_-137+937i others(25): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | |||||||
chr1:115337267 | G | GTTTGTTT others(5): Show |
1 | a0001c0001t0001g0159 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-137+936_-137+937i others(14): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | |||||||
chr1:115337267 | G | GTTTGTTT others(6): Show |
4 | a0001c0001t0001g0150 a0001c0001t0001g0160 a0001c0001t0001g0164 others(1): Show |
4 | HG03209.hp1 HG03516.hp1 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-137+936_-137+937i others(15): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | |||||||
chr1:115337267 | G | GTTTGTTT others(7): Show |
2 | a0001c0001t0001g0152 a0001c0001t0001g0171 |
2 | HG03831.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.-137+936_-137+937i others(16): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | |||||||
chr1:115337267 | G | GTTTGTTT others(8): Show |
2 | a0001c0001t0001g0024 a0001c0001t0001g0165 |
2 | NA18966.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.-137+936_-137+937i others(17): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | |||||||
chr1:115337267 | G | GTTTGTTT others(9): Show |
5 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(2): Show |
5 | HG01346.hp2 NA18959.hp2 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.-137+936_-137+937i others(18): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | |||||||
chr1:115337267 | G | GTTTGTTT others(10): Show |
3 | a0001c0001t0001g0148 a0001c0001t0001g0172 a0002c0002t0001g0155 |
3 | HG02559.hp1 HG03017.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.-137+936_-137+937i others(19): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | |||||||
chr1:115337267 | G | GTTTGTTT others(11): Show |
4 | a0001c0001t0001g0009 a0001c0001t0001g0147 a0001c0001t0001g0154 others(1): Show |
4 | HG02083.hp1 HG03491.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.-137+936_-137+937i others(20): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | |||||||
chr1:115337267 | G | GTTTGTTT others(12): Show |
4 | a0001c0001t0001g0009 a0001c0001t0001g0166 a0001c0001t0001g0177 others(1): Show |
4 | HG02027.hp2 HG02109.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.-137+936_-137+937i others(21): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | |||||||
chr1:115337267 | G | GTTTGTTT others(13): Show |
1 | a0001c0001t0001g0180 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-137+936_-137+937i others(22): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | |||||||
chr1:115337267 | G | GTTTGTTT others(14): Show |
3 | a0001c0001t0001g0134 a0001c0001t0001g0163 a0001c0001t0001g0182 |
3 | NA18961.hp2 NA19072.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-137+936_-137+937i others(23): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | |||||||
chr1:115337267 | G | GTTTGTTT others(15): Show |
4 | a0001c0001t0001g0176 a0001c0003t0001g0179 a0002c0002t0001g0146 others(1): Show |
4 | HG03139.hp1 HG03579.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-137+936_-137+937i others(24): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | |||||||
chr1:115337267 | G | GTTTGTTT others(17): Show |
1 | a0001c0001t0001g0010 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-137+936_-137+937i others(26): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | |||||||
chr1:115337267 | G | GTTTGTTT others(18): Show |
3 | a0001c0001t0001g0010 a0001c0001t0001g0149 a0001c0001t0001g0162 |
3 | HG02895.hp2 NA18956.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.-137+936_-137+937i others(27): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | |||||||
chr1:115337267 | G | GTTTGTTT others(19): Show |
1 | a0001c0001t0001g0127 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-137+936_-137+937i others(28): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | |||||||
chr1:115337267 | G | GTTTGTTT others(22): Show |
1 | a0001c0001t0001g0174 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-137+936_-137+937i others(31): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | |||||||
chr1:115337267 | G | GTTTTTTT others(4): Show |
1 | a0001c0001t0001g0187 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-137+926_-137+936d others(13): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | |||||||
chr1:115337267 | G | GTTTTTTT others(9): Show |
1 | a0001c0001t0001g0175 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-137+921_-137+936d others(18): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | |||||||
chr1:115337267 | G | GTTTTTTT others(10): Show |
1 | a0001c0001t0001g0144 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-137+920_-137+936d others(19): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | |||||||
chr1:115337267 | G | GTTTTTTT others(11): Show |
1 | a0001c0001t0001g0181 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-137+919_-137+936d others(20): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | |||||||
chr1:115337267 | G | GTTTTTTT others(13): Show |
1 | a0002c0002t0001g0153 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-137+917_-137+936d others(22): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | |||||||
chr1:115337267 | G | GTTTTTTT others(18): Show |
1 | a0001c0001t0001g0170 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-137+912_-137+936d others(27): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | |||||||
chr1:115337267 | G | GTTTTTTT others(19): Show |
1 | a0001c0001t0001g0161 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-137+911_-137+936d others(28): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | |||||||
chr1:115337267 | G | T | 4 | a0001c0001t0001g0122 a0001c0001t0001g0133 a0001c0001t0001g0386 others(1): Show |
4 | HG02683.hp2 HG03139.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.-137+937C>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | |||||||
chr1:115337267 | GTT | G | 6 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0042 others(3): Show |
6 | HG00741.hp1 HG02145.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-137+935_-137+936d others(4): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | |||||||
chr1:115337267 | GTTT | G | 29 | a0001c0001t0001g0018 a0001c0001t0001g0032 a0001c0001t0001g0050 others(26): Show |
31 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(28): Show |
intron_variant | MODIFIER | c.-137+934_-137+936d others(5): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | |||||||
chr1:115337267 | GTTTT | G | 81 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(78): Show |
86 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.-137+933_-137+936d others(6): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | |||||||
chr1:115337267 | GTTTTT | G | 10 | a0001c0001t0001g0107 a0001c0001t0001g0208 a0001c0001t0001g0209 others(7): Show |
10 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.-137+932_-137+936d others(7): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | |||||||
chr1:115337267 | GTTTTTTT others(3): Show |
G | 1 | a0001c0001t0002g0366 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-137+927_-137+936d others(12): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | |||||||
chr1:115337267 | GTTTTTTT others(4): Show |
G | 3 | a0001c0001t0001g0113 a0001c0001t0001g0232 a0001c0001t0001g0233 |
3 | HG01175.hp1 NA19070.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.-137+926_-137+936d others(13): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | |||||||
chr1:115337267 | GTTTTTTT others(5): Show |
G | 23 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0115 others(20): Show |
26 | HG00609.hp1 HG01192.hp1 HG01256.hp2 others(23): Show |
intron_variant | MODIFIER | c.-137+925_-137+936d others(14): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | |||||||
chr1:115337267 | GTTTTTTT others(6): Show |
G | 57 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0109 others(54): Show |
61 | HG00408.hp1 HG00597.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.-137+924_-137+936d others(15): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | |||||||
chr1:115337267 | GTTTTTTT others(7): Show |
G | 6 | a0001c0001t0001g0138 a0001c0001t0001g0283 a0001c0001t0001g0284 others(3): Show |
6 | HG00280.hp2 HG01258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-137+923_-137+936d others(16): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337267 | |||||||
chr1:115337269 | T | TTG | 6 | a0001c0001t0001g0389 a0001c0001t0001g0390 a0001c0001t0001g0391 others(3): Show |
6 | HG01891.hp1 HG01891.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-137+934_-137+935i others(4): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337269 | |||||||
chr1:115337270 | T | G | 1 | a0001c0001t0001g0373 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-137+934A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337270 | |||||||
chr1:115337270 | T | TG | 4 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0003t0001g0393 others(1): Show |
4 | HG01981.hp2 HG02145.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-137+933_-137+934i others(3): Show |
NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337270 | |||||||
chr1:115337271 | T | G | 12 | a0001c0001t0001g0036 a0001c0001t0001g0039 a0001c0001t0001g0191 others(9): Show |
12 | HG01884.hp2 HG01978.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.-137+933A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337271 | |||||||
chr1:115337272 | T | G | 3 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0003t0001g0396 |
3 | HG01109.hp1 HG01261.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.-137+932A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337272 | |||||||
chr1:115337273 | T | G | 7 | a0001c0001t0001g0020 a0001c0001t0001g0042 a0001c0001t0001g0376 others(4): Show |
7 | HG00741.hp1 HG01192.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-137+931A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337273 | |||||||
chr1:115337274 | T | G | 25 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0053 others(22): Show |
25 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.-137+930A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337274 | |||||||
chr1:115337275 | T | G | 81 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(78): Show |
86 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.-137+929A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337275 | |||||||
chr1:115337276 | T | G | 10 | a0001c0001t0001g0107 a0001c0001t0001g0208 a0001c0001t0001g0209 others(7): Show |
10 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.-137+928A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337276 | |||||||
chr1:115337277 | T | G | 3 | a0001c0001t0001g0020 a0001c0001t0001g0213 a0002c0002t0001g0045 |
3 | HG02965.hp1 NA18965.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.-137+927A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337277 | |||||||
chr1:115337278 | T | G | 19 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0053 others(16): Show |
19 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(16): Show |
intron_variant | MODIFIER | c.-137+926A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337278 | |||||||
chr1:115337279 | T | G | 66 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(63): Show |
70 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.-137+925A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337279 | |||||||
chr1:115337280 | T | G | 5 | a0001c0001t0001g0107 a0001c0001t0001g0230 a0001c0001t0001g0231 others(2): Show |
5 | HG01256.hp1 NA18945.hp1 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.-137+924A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337280 | |||||||
chr1:115337281 | T | G | 1 | a0001c0001t0001g0020 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-137+923A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337281 | |||||||
chr1:115337282 | T | G | 3 | a0001c0001t0001g0113 a0001c0001t0001g0232 a0001c0001t0001g0233 |
3 | HG01175.hp1 NA19070.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.-137+922A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337282 | |||||||
chr1:115337283 | T | G | 30 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0014 others(27): Show |
34 | HG00609.hp1 HG00733.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.-137+921A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337283 | |||||||
chr1:115337284 | T | G | 57 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0109 others(54): Show |
61 | HG00408.hp1 HG00597.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.-137+920A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337284 | |||||||
chr1:115337285 | T | G | 6 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0285 others(3): Show |
6 | HG00280.hp2 HG01258.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-137+919A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337285 | |||||||
chr1:115337286 | T | G | 1 | a0001c0001t0001g0113 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-137+918A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337286 | |||||||
chr1:115337287 | T | G | 11 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0115 others(8): Show |
14 | HG00609.hp1 HG02056.hp1 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.-137+917A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337287 | |||||||
chr1:115337288 | T | G | 14 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 others(11): Show |
14 | HG01975.hp2 HG02451.hp2 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.-137+916A>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337288 | |||||||
chr1:115337511 | G | A | 89 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(86): Show |
94 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.-137+693C>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337511 | |||||||
chr1:115337575 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-137+629G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337575 | |||||||
chr1:115337710 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-137+494G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337710 | |||||||
chr1:115337754 | C | T | 1 | a0001c0001t0001g0021 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-137+450G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337754 | |||||||
chr1:115337776 | C | A | 1 | a0001c0001t0001g0123 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-137+428G>T | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337776 | |||||||
chr1:115337972 | A | G | 6 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 others(3): Show |
6 | HG00673.hp1 HG02083.hp2 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.-137+232T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115337972 | |||||||
chr1:115338054 | A | C | 110 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(107): Show |
116 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.-137+150T>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115338054 | |||||||
chr1:115338113 | A | G | 1 | a0001c0001t0001g0020 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-137+91T>C | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115338113 | |||||||
chr1:115338118 | T | C | 13 | a0001c0001t0001g0018 a0001c0001t0001g0386 a0001c0001t0001g0387 others(10): Show |
14 | HG01433.hp2 HG01891.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.-137+86A>G | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115338118 | |||||||
chr1:115338191 | C | T | 1 | a0001c0001t0001g0019 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-137+13G>A | NGF | ENSG00000134259.6 | transcript | ENST00000369512.3 | protein_coding | 1/2 | chr1 | 115338191 |