Item | Value |
---|---|
geneid | 5049 |
ensemblid | ENSG00000168092.14 |
hgncid | 8575 |
symbol | PAFAH1B2 |
name | platelet activating factor acetylhydrolase 1b catalytic subunit 2 |
refseq_nuc | NM_002572.4 |
refseq_prot | NP_002563.1 |
ensembl_nuc | ENST00000527958.6 |
ensembl_prot | ENSP00000435289.1 |
mane_status | MANE Select |
chr | chr11 |
start | 117144287 |
end | 117171045 |
strand | + |
ver | v1.2 |
region | chr11:117144287-117171045 |
region5000 | chr11:117139287-117176045 |
regionname0 | PAFAH1B2_chr11_117144287_117171045 |
regionname5000 | PAFAH1B2_chr11_117139287_117176045 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 687 | 432 | 90 | 78 | 200 | 16 | 46 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | ATGAG others(682): Show |
chr11 | 117139287 | 117176045 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 4175 | 88 | 3 | 9 | 65 | 1 | 9 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4170): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0002 | 0/0 | 4186 | 46 | 7 | 14 | 17 | 7 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4181): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0003 | 0/1 | 4185 | 37 | 4 | 10 | 17 | 1 | 4 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4180): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0004 | 0/0 | 4176 | 22 | 0 | 4 | 16 | 0 | 2 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4171): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0005 | 0/0 | 4181 | 17 | 0 | 0 | 17 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4176): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0006 | 0/0 | 4188 | 13 | 3 | 3 | 2 | 1 | 4 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4183): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0007 | 0/0 | 4172 | 13 | 0 | 3 | 2 | 3 | 5 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4167): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0008 | 0/0 | 4168 | 10 | 0 | 0 | 10 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4163): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0009 | 0/0 | 4187 | 10 | 0 | 0 | 7 | 2 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4182): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0010 | 0/0 | 4176 | 9 | 1 | 1 | 6 | 0 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4171): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0011 | 0/0 | 4175 | 9 | 9 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4170): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0012 | 0/0 | 4186 | 8 | 0 | 4 | 4 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4181): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0013 | 0/0 | 4186 | 8 | 1 | 0 | 7 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4181): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0014 | 0/0 | 4189 | 8 | 1 | 4 | 2 | 0 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4184): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0015 | 0/0 | 4175 | 8 | 7 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4170): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0016 | 0/0 | 4173 | 6 | 0 | 0 | 3 | 0 | 3 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4168): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0017 | 0/0 | 4185 | 6 | 0 | 0 | 6 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4180): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0018 | 0/0 | 4175 | 6 | 6 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4170): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0019 | 0/0 | 4187 | 5 | 2 | 1 | 2 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4182): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0020 | 0/0 | 4176 | 4 | 4 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4171): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0021 | 0/0 | 4177 | 4 | 1 | 1 | 1 | 0 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4172): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0022 | 0/0 | 4190 | 4 | 3 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4185): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0023 | 0/0 | 4179 | 3 | 3 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4174): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0024 | 0/0 | 4201 | 3 | 2 | 0 | 0 | 0 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4196): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0025 | 0/0 | 4181 | 3 | 2 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4176): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0026 | 0/0 | 4190 | 3 | 1 | 2 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4185): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0027 | 0/0 | 4175 | 3 | 0 | 0 | 3 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4170): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0028 | 0/0 | 4161 | 3 | 2 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4156): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0029 | 0/0 | 4166 | 3 | 2 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4161): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0030 | 0/0 | 4175 | 3 | 1 | 2 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4170): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0031 | 0/0 | 4174 | 3 | 3 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4169): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0032 | 0/0 | 4175 | 2 | 2 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4170): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0033 | 0/0 | 4187 | 2 | 2 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4182): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0034 | 0/0 | 4198 | 2 | 0 | 2 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4193): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0035 | 0/0 | 4202 | 2 | 0 | 0 | 0 | 0 | 2 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4197): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0036 | 0/0 | 4175 | 2 | 0 | 0 | 1 | 0 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4170): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0037 | 0/0 | 4187 | 2 | 0 | 1 | 0 | 0 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4182): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0038 | 0/0 | 4190 | 2 | 0 | 0 | 0 | 0 | 2 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4185): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0039 | 0/0 | 4176 | 2 | 1 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4171): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0040 | 0/0 | 4191 | 2 | 1 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4186): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0041 | 0/0 | 4195 | 2 | 1 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4190): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0042 | 0/0 | 4186 | 2 | 0 | 2 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4181): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0043 | 0/0 | 4181 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4176): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0044 | 0/0 | 4175 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4170): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0045 | 0/0 | 4176 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4171): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0046 | 0/0 | 4185 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4180): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0047 | 0/0 | 4191 | 1 | 0 | 0 | 0 | 1 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4186): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0048 | 0/0 | 4214 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4209): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0049 | 0/0 | 4165 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4160): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0050 | 0/0 | 4187 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4182): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0051 | 0/0 | 4188 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4183): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0052 | 0/0 | 4187 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4182): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0053 | 0/0 | 4189 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4184): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0054 | 0/0 | 4190 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4185): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0055 | 0/0 | 4167 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4162): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0056 | 0/0 | 4177 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4172): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0057 | 0/0 | 4176 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4171): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0058 | 0/0 | 4175 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4170): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0059 | 0/0 | 4189 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4184): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0060 | 0/0 | 4185 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4180): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0061 | 0/0 | 4185 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4180): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0062 | 0/0 | 4186 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4181): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0063 | 0/0 | 4186 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4181): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0064 | 0/0 | 4186 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4181): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0065 | 0/0 | 4188 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4183): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0066 | 0/0 | 4190 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4185): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0067 | 0/0 | 4185 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4180): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0068 | 0/0 | 4192 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4187): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0069 | 0/0 | 4193 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4188): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0070 | 0/0 | 4166 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4161): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0071 | 0/0 | 4189 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4184): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0072 | 0/0 | 4190 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4185): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0073 | 0/0 | 4176 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4171): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0074 | 0/0 | 4175 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4170): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0075 | 0/0 | 4176 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4171): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0076 | 0/0 | 4175 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4170): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0077 | 0/0 | 4176 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4171): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0078 | 0/0 | 4175 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4170): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0079 | 0/0 | 4175 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4170): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0080 | 0/0 | 4175 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4170): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0081 | 0/0 | 4176 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4171): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0082 | 0/0 | 4176 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4171): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0083 | 0/0 | 4176 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4171): Show |
chr11 | 117139287 | 117176045 |
a0001c0001t0084 | 0/0 | 4175 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | GGAGG others(4170): Show |
chr11 | 117139287 | 117176045 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 1/0 | 17 | 2 | 2 | 8 | 1 | 3 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0005 | 0/0 | 8 | 0 | 1 | 7 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0002g0002 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0002g0003 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0002g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0002g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0003g0002 | 0/0 | 8 | 2 | 2 | 4 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0003g0003 | 0/0 | 6 | 1 | 0 | 4 | 1 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0003g0224 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0003g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0003g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0003g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0003g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0003g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0003g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0004g0001 | 0/0 | 5 | 0 | 3 | 1 | 0 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0004g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0004g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0004g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0004g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0004g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0004g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0004g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0004g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0004g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0004g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0004g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0005g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0005g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0005g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0005g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0005g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0005g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0005g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0005g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0005g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0006g0006 | 0/0 | 3 | 2 | 0 | 0 | 0 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0006g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0006g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0006g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0006g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0006g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0006g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0006g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0006g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0006g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0006g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0007g0008 | 0/0 | 5 | 0 | 1 | 0 | 2 | 2 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0007g0014 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0007g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0007g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0007g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0007g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0008g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0008g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0008g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0008g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0009g0006 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0009g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0009g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0009g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0009g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0009g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0009g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0009g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0010g0001 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0010g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0010g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0010g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0010g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0010g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0010g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0011g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0011g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0011g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0011g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0011g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0012g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0012g0003 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0012g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0012g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0012g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0012g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0012g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0013g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0013g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0013g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0013g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0013g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0013g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0014g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0014g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0014g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0014g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0014g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0014g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0014g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0014g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0015g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0015g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0015g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0015g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0015g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0015g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0015g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0016g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0016g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0016g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0016g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0016g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0016g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0017g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0017g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0017g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0017g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0018g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0018g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0018g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0018g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0018g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0018g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0019g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0019g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0019g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0019g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0019g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0020g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0020g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0021g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0021g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0021g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0021g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0022g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0022g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0022g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0022g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0023g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0024g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0024g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0024g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0025g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0025g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0025g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0026g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0026g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0026g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0027g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0027g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0027g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0028g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0028g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0028g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0029g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0029g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0029g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0030g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0030g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0031g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0031g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0031g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0032g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0032g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0033g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0033g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0034g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0034g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0035g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0035g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0036g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0036g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0037g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0037g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0038g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0038g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0039g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0039g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0040g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0040g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0041g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0041g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0042g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0043g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0044g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0045g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0046g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0047g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0048g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0049g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0050g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0051g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0052g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0053g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0054g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0055g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0056g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0057g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0058g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0059g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0060g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0061g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0062g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0063g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0064g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0065g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0066g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0067g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0068g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0069g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0070g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0071g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0072g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0073g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0074g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0075g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0076g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0077g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0078g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0079g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0080g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0081g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0082g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0083g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
a0001c0001t0084g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0003 | EUR | GBR | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG00099 | hp2 | a0001 | c0001 | t0009 | g0006 | EUR | GBR | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG00280 | hp1 | a0001 | c0001 | t0009 | g0074 | EUR | FIN | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG00280 | hp2 | a0001 | c0001 | t0007 | g0008 | EUR | FIN | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0236 | EUR | FIN | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG00323 | hp2 | a0001 | c0001 | t0047 | g0093 | EUR | FIN | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG00408 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG00423 | hp2 | a0001 | c0001 | t0012 | g0255 | EAS | CHS | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG00438 | hp1 | a0001 | c0001 | t0064 | g0266 | EAS | CHS | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG00438 | hp2 | a0001 | c0001 | t0017 | g0002 | EAS | CHS | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG00544 | hp1 | a0001 | c0001 | t0010 | g0011 | EAS | CHS | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG00558 | hp1 | a0001 | c0001 | t0061 | g0002 | EAS | CHS | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG00597 | hp1 | a0001 | c0001 | t0016 | g0210 | EAS | CHS | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG00597 | hp2 | a0001 | c0001 | t0004 | g0185 | EAS | CHS | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG00609 | hp2 | a0001 | c0001 | t0005 | g0018 | EAS | CHS | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG00639 | hp1 | a0001 | c0001 | t0006 | g0071 | AMR | PUR | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0279 | AMR | PUR | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0263 | AMR | PUR | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG00642 | hp2 | a0001 | c0001 | t0057 | g0010 | AMR | PUR | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG00673 | hp1 | a0001 | c0001 | t0010 | g0012 | EAS | CHS | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG00733 | hp2 | a0001 | c0001 | t0012 | g0002 | AMR | PUR | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG00735 | hp1 | a0001 | c0001 | t0076 | g0019 | AMR | PUR | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG00735 | hp2 | a0001 | c0001 | t0014 | g0073 | AMR | PUR | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG00738 | hp1 | a0001 | c0001 | t0022 | g0066 | AMR | PUR | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0243 | AMR | PUR | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG00741 | hp1 | a0001 | c0001 | t0037 | g0275 | AMR | PUR | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01069 | hp1 | a0001 | c0001 | t0042 | g0003 | AMR | PUR | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01069 | hp2 | a0001 | c0001 | t0030 | g0019 | AMR | PUR | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01071 | hp1 | a0001 | c0001 | t0042 | g0003 | AMR | PUR | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0281 | AMR | PUR | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01074 | hp1 | a0001 | c0001 | t0028 | g0124 | AMR | PUR | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01074 | hp2 | a0001 | c0001 | t0034 | g0092 | AMR | PUR | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0250 | AMR | PUR | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01081 | hp2 | a0001 | c0001 | t0006 | g0024 | AMR | PUR | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0249 | AMR | PUR | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01099 | hp2 | a0001 | c0001 | t0019 | g0288 | AMR | PUR | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01106 | hp1 | a0001 | c0001 | t0012 | g0003 | AMR | PUR | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01106 | hp2 | a0001 | c0001 | t0039 | g0108 | AMR | PUR | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01109 | hp1 | a0001 | c0001 | t0029 | g0214 | AMR | PUR | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01109 | hp2 | a0001 | c0001 | t0060 | g0219 | AMR | PUR | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0262 | AMR | PUR | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0252 | AMR | PUR | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01175 | hp2 | a0001 | c0001 | t0025 | g0078 | AMR | PUR | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01243 | hp1 | a0001 | c0001 | t0015 | g0031 | AMR | PUR | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01243 | hp2 | a0001 | c0001 | t0034 | g0094 | AMR | PUR | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0280 | AMR | CLM | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | CLM | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01256 | hp1 | a0001 | c0001 | t0014 | g0048 | AMR | CLM | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0278 | AMR | CLM | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01257 | hp1 | a0001 | c0001 | t0007 | g0207 | AMR | CLM | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0261 | AMR | CLM | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01258 | hp1 | a0001 | c0001 | t0026 | g0049 | AMR | CLM | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01258 | hp2 | a0001 | c0001 | t0007 | g0014 | AMR | CLM | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01261 | hp1 | a0001 | c0001 | t0078 | g0205 | AMR | CLM | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01261 | hp2 | a0001 | c0001 | t0046 | g0009 | AMR | CLM | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01346 | hp1 | a0001 | c0001 | t0007 | g0008 | AMR | CLM | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | CLM | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0247 | AMR | CLM | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01496 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | CLM | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01496 | hp2 | a0001 | c0001 | t0004 | g0201 | AMR | CLM | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0041 | EUR | IBS | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0271 | EUR | IBS | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01516 | hp2 | a0001 | c0001 | t0007 | g0008 | EUR | IBS | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01517 | hp1 | a0001 | c0001 | t0007 | g0014 | EUR | IBS | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0273 | EUR | IBS | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01891 | hp1 | a0001 | c0001 | t0045 | g0100 | AFR | ACB | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01891 | hp2 | a0001 | c0001 | t0082 | g0132 | AFR | ACB | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01928 | hp2 | a0001 | c0001 | t0010 | g0005 | AMR | PEL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0254 | AMR | PEL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01934 | hp2 | a0001 | c0001 | t0003 | g0245 | AMR | PEL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01943 | hp2 | a0001 | c0001 | t0003 | g0040 | AMR | PEL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01975 | hp1 | a0001 | c0001 | t0014 | g0065 | AMR | PEL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01975 | hp2 | a0001 | c0001 | t0066 | g0277 | AMR | PEL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01978 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | PEL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01978 | hp2 | a0001 | c0001 | t0052 | g0091 | AMR | PEL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01981 | hp1 | a0001 | c0001 | t0012 | g0040 | AMR | PEL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01981 | hp2 | a0001 | c0001 | t0040 | g0025 | AMR | PEL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02004 | hp1 | a0001 | c0001 | t0026 | g0077 | AMR | PEL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02015 | hp1 | a0001 | c0001 | t0068 | g0052 | EAS | KHV | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | KHV | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02027 | hp2 | a0001 | c0001 | t0004 | g0164 | EAS | KHV | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02040 | hp1 | a0001 | c0001 | t0008 | g0103 | EAS | KHV | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02055 | hp1 | a0001 | c0001 | t0010 | g0001 | AFR | ACB | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02055 | hp2 | a0001 | c0001 | t0011 | g0032 | AFR | ACB | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02056 | hp2 | a0001 | c0001 | t0003 | g0223 | EAS | KHV | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02071 | hp1 | a0001 | c0001 | t0012 | g0287 | EAS | KHV | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | KHV | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | KHV | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02080 | hp1 | a0001 | c0001 | t0010 | g0169 | EAS | KHV | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02080 | hp2 | a0001 | c0001 | t0008 | g0004 | EAS | KHV | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02129 | hp2 | a0001 | c0001 | t0008 | g0004 | EAS | KHV | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02132 | hp1 | a0001 | c0001 | t0004 | g0152 | EAS | KHV | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02132 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | KHV | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02135 | hp1 | a0001 | c0001 | t0017 | g0003 | EAS | KHV | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | KHV | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02145 | hp1 | a0001 | c0001 | t0011 | g0134 | AFR | ACB | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02145 | hp2 | a0001 | c0001 | t0032 | g0121 | AFR | ACB | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02148 | hp1 | a0001 | c0001 | t0030 | g0019 | AMR | PEL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02148 | hp2 | a0001 | c0001 | t0012 | g0246 | AMR | PEL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02155 | hp1 | a0001 | c0001 | t0004 | g0165 | EAS | CDX | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02155 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | CDX | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | CDX | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | CDX | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02257 | hp1 | a0001 | c0001 | t0049 | g0111 | AFR | ACB | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02257 | hp2 | a0001 | c0001 | t0032 | g0123 | AFR | ACB | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02258 | hp1 | a0001 | c0001 | t0011 | g0133 | AFR | ACB | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02258 | hp2 | a0001 | c0001 | t0069 | g0082 | AFR | ACB | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02273 | hp2 | a0001 | c0001 | t0006 | g0025 | AMR | PEL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02280 | hp1 | a0001 | c0001 | t0006 | g0006 | AFR | ACB | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02280 | hp2 | a0001 | c0001 | t0020 | g0016 | AFR | ACB | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02293 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | PEL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02293 | hp2 | a0001 | c0001 | t0014 | g0051 | AMR | PEL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02300 | hp1 | a0001 | c0001 | t0021 | g0001 | AMR | PEL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02300 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02451 | hp1 | a0001 | c0001 | t0083 | g0193 | AFR | ACB | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02451 | hp2 | a0001 | c0001 | t0020 | g0096 | AFR | ACB | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02523 | hp1 | a0001 | c0001 | t0008 | g0004 | EAS | KHV | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02602 | hp2 | a0001 | c0001 | t0036 | g0004 | SAS | PJL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02622 | hp1 | a0001 | c0001 | t0025 | g0030 | AFR | GWD | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02622 | hp2 | a0001 | c0001 | t0024 | g0101 | AFR | GWD | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0268 | AFR | GWD | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0043 | AFR | GWD | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02647 | hp1 | a0001 | c0001 | t0033 | g0076 | AFR | GWD | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02647 | hp2 | a0001 | c0001 | t0023 | g0020 | AFR | GWD | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02698 | hp1 | a0001 | c0001 | t0075 | g0257 | SAS | PJL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02717 | hp1 | a0001 | c0001 | t0039 | g0110 | AFR | GWD | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02717 | hp2 | a0001 | c0001 | t0018 | g0046 | AFR | GWD | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02723 | hp2 | a0001 | c0001 | t0011 | g0010 | AFR | GWD | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02735 | hp1 | a0001 | c0001 | t0014 | g0081 | SAS | PJL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02735 | hp2 | a0001 | c0001 | t0003 | g0232 | SAS | PJL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02738 | hp1 | a0001 | c0001 | t0050 | g0039 | SAS | PJL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02738 | hp2 | a0001 | c0001 | t0003 | g0039 | SAS | PJL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02809 | hp1 | a0001 | c0001 | t0055 | g0217 | AFR | GWD | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02809 | hp2 | a0001 | c0001 | t0003 | g0228 | AFR | GWD | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0285 | AFR | GWD | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02818 | hp2 | a0001 | c0001 | t0018 | g0116 | AFR | GWD | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02886 | hp1 | a0001 | c0001 | t0015 | g0031 | AFR | GWD | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02886 | hp2 | a0001 | c0001 | t0033 | g0064 | AFR | GWD | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02896 | hp1 | a0001 | c0001 | t0015 | g0114 | AFR | GWD | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02896 | hp2 | a0001 | c0001 | t0040 | g0059 | AFR | GWD | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0269 | AFR | GWD | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02897 | hp2 | a0001 | c0001 | t0015 | g0113 | AFR | GWD | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02922 | hp1 | a0001 | c0001 | t0072 | g0203 | AFR | ESN | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02922 | hp2 | a0001 | c0001 | t0019 | g0235 | AFR | ESN | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02965 | hp1 | a0001 | c0001 | t0019 | g0043 | AFR | ESN | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02965 | hp2 | a0001 | c0001 | t0011 | g0029 | AFR | ESN | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02970 | hp2 | a0001 | c0001 | t0006 | g0006 | AFR | ESN | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02976 | hp1 | a0001 | c0001 | t0074 | g0127 | AFR | ESN | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02976 | hp2 | a0001 | c0001 | t0020 | g0016 | AFR | ESN | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03017 | hp1 | a0001 | c0001 | t0007 | g0037 | SAS | PJL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03017 | hp2 | a0001 | c0001 | t0035 | g0099 | SAS | PJL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03041 | hp1 | a0001 | c0001 | t0029 | g0204 | AFR | GWD | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03041 | hp2 | a0001 | c0001 | t0030 | g0109 | AFR | GWD | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03098 | hp1 | a0001 | c0001 | t0025 | g0117 | AFR | MSL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03098 | hp2 | a0001 | c0001 | t0015 | g0128 | AFR | MSL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03130 | hp1 | a0001 | c0001 | t0018 | g0119 | AFR | ESN | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03130 | hp2 | a0001 | c0001 | t0028 | g0125 | AFR | ESN | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03139 | hp1 | a0001 | c0001 | t0015 | g0130 | AFR | ESN | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03139 | hp2 | a0001 | c0001 | t0013 | g0045 | AFR | ESN | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03195 | hp1 | a0001 | c0001 | t0022 | g0057 | AFR | ESN | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03195 | hp2 | a0001 | c0001 | t0020 | g0016 | AFR | ESN | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03209 | hp1 | a0001 | c0001 | t0022 | g0056 | AFR | MSL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03209 | hp2 | a0001 | c0001 | t0031 | g0137 | AFR | MSL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0267 | AFR | MSL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03225 | hp2 | a0001 | c0001 | t0014 | g0024 | AFR | MSL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03239 | hp1 | a0001 | c0001 | t0010 | g0172 | SAS | PJL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03239 | hp2 | a0001 | c0001 | t0007 | g0008 | SAS | PJL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0284 | AFR | MSL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03453 | hp2 | a0001 | c0001 | t0084 | g0001 | AFR | MSL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03486 | hp1 | a0001 | c0001 | t0011 | g0029 | AFR | MSL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03486 | hp2 | a0001 | c0001 | t0018 | g0118 | AFR | MSL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03490 | hp2 | a0001 | c0001 | t0080 | g0150 | SAS | PJL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03491 | hp1 | a0001 | c0001 | t0024 | g0102 | SAS | PJL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03491 | hp2 | a0001 | c0001 | t0006 | g0072 | SAS | PJL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03492 | hp2 | a0001 | c0001 | t0006 | g0075 | SAS | PJL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03516 | hp1 | a0001 | c0001 | t0018 | g0047 | AFR | ESN | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03516 | hp2 | a0001 | c0001 | t0023 | g0020 | AFR | ESN | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03540 | hp2 | a0001 | c0001 | t0011 | g0010 | AFR | GWD | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03579 | hp1 | a0001 | c0001 | t0028 | g0126 | AFR | MSL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03579 | hp2 | a0001 | c0001 | t0024 | g0097 | AFR | MSL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03654 | hp2 | a0001 | c0001 | t0009 | g0044 | SAS | PJL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03669 | hp1 | a0001 | c0001 | t0021 | g0200 | SAS | PJL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03669 | hp2 | a0001 | c0001 | t0006 | g0006 | SAS | PJL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0227 | SAS | STU | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03688 | hp2 | a0001 | c0001 | t0004 | g0174 | SAS | STU | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03704 | hp1 | a0001 | c0001 | t0048 | g0004 | SAS | PJL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0233 | SAS | PJL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03710 | hp2 | a0001 | c0001 | t0007 | g0014 | SAS | PJL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | BEB | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03831 | hp2 | a0001 | c0001 | t0056 | g0206 | SAS | BEB | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | BEB | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0234 | SAS | BEB | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03927 | hp1 | a0001 | c0001 | t0037 | g0282 | SAS | BEB | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03927 | hp2 | a0001 | c0001 | t0016 | g0208 | SAS | BEB | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03942 | hp1 | a0001 | c0001 | t0006 | g0069 | SAS | BEB | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03942 | hp2 | a0001 | c0001 | t0016 | g0037 | SAS | BEB | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG04115 | hp1 | a0001 | c0001 | t0065 | g0256 | SAS | STU | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG04115 | hp2 | a0001 | c0001 | t0038 | g0006 | SAS | STU | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG04184 | hp1 | a0001 | c0001 | t0038 | g0079 | SAS | BEB | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG04184 | hp2 | a0001 | c0001 | t0016 | g0218 | SAS | BEB | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG04204 | hp1 | a0001 | c0001 | t0007 | g0014 | SAS | STU | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG04204 | hp2 | a0001 | c0001 | t0035 | g0004 | SAS | STU | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG04228 | hp1 | a0001 | c0001 | t0004 | g0001 | SAS | STU | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG04228 | hp2 | a0001 | c0001 | t0073 | g0283 | SAS | STU | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18522 | hp1 | a0001 | c0001 | t0029 | g0216 | AFR | YRI | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18522 | hp2 | a0001 | c0001 | t0015 | g0131 | AFR | YRI | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18612 | hp1 | a0001 | c0001 | t0067 | g0086 | EAS | CHB | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18612 | hp2 | a0001 | c0001 | t0004 | g0011 | EAS | CHB | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0222 | EAS | CHB | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18906 | hp1 | a0001 | c0001 | t0011 | g0010 | AFR | YRI | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18906 | hp2 | a0001 | c0001 | t0015 | g0129 | AFR | YRI | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18939 | hp1 | a0001 | c0001 | t0013 | g0054 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18941 | hp2 | a0001 | c0001 | t0013 | g0053 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18942 | hp2 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18943 | hp1 | a0001 | c0001 | t0006 | g0085 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18943 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18944 | hp1 | a0001 | c0001 | t0006 | g0026 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18945 | hp1 | a0001 | c0001 | t0019 | g0264 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18945 | hp2 | a0001 | c0001 | t0063 | g0244 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18946 | hp1 | a0001 | c0001 | t0010 | g0197 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18946 | hp2 | a0001 | c0001 | t0017 | g0258 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18947 | hp1 | a0001 | c0001 | t0008 | g0004 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18948 | hp1 | a0001 | c0001 | t0021 | g0190 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18948 | hp2 | a0001 | c0001 | t0008 | g0004 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18950 | hp2 | a0001 | c0001 | t0062 | g0259 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18951 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18951 | hp2 | a0001 | c0001 | t0003 | g0270 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18953 | hp1 | a0001 | c0001 | t0081 | g0033 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18953 | hp2 | a0001 | c0001 | t0013 | g0007 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18956 | hp2 | a0001 | c0001 | t0007 | g0212 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18957 | hp1 | a0001 | c0001 | t0005 | g0018 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18957 | hp2 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18959 | hp1 | a0001 | c0001 | t0004 | g0177 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18962 | hp1 | a0001 | c0001 | t0053 | g0083 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18963 | hp1 | a0001 | c0001 | t0004 | g0021 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18963 | hp2 | a0001 | c0001 | t0009 | g0090 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18965 | hp1 | a0001 | c0001 | t0005 | g0017 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18965 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18966 | hp1 | a0001 | c0001 | t0009 | g0007 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18968 | hp1 | a0001 | c0001 | t0027 | g0050 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18968 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18969 | hp2 | a0001 | c0001 | t0007 | g0211 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18970 | hp2 | a0001 | c0001 | t0009 | g0006 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18971 | hp1 | a0001 | c0001 | t0077 | g0253 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18971 | hp2 | a0001 | c0001 | t0010 | g0001 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18973 | hp1 | a0001 | c0001 | t0005 | g0028 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18973 | hp2 | a0001 | c0001 | t0003 | g0260 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18975 | hp1 | a0001 | c0001 | t0005 | g0009 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18977 | hp2 | a0001 | c0001 | t0012 | g0003 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18978 | hp1 | a0001 | c0001 | t0036 | g0106 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18978 | hp2 | a0001 | c0001 | t0014 | g0060 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18979 | hp1 | a0001 | c0001 | t0051 | g0015 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18981 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18983 | hp1 | a0001 | c0001 | t0017 | g0002 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18983 | hp2 | a0001 | c0001 | t0005 | g0027 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18984 | hp2 | a0001 | c0001 | t0005 | g0107 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18986 | hp2 | a0001 | c0001 | t0008 | g0104 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18987 | hp1 | a0001 | c0001 | t0017 | g0251 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18989 | hp1 | a0001 | c0001 | t0005 | g0105 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18990 | hp1 | a0001 | c0001 | t0005 | g0017 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18990 | hp2 | a0001 | c0001 | t0017 | g0002 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18994 | hp1 | a0001 | c0001 | t0004 | g0188 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18994 | hp2 | a0001 | c0001 | t0005 | g0028 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18995 | hp1 | a0001 | c0001 | t0004 | g0184 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18995 | hp2 | a0001 | c0001 | t0004 | g0189 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18997 | hp1 | a0001 | c0001 | t0005 | g0009 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18999 | hp2 | a0001 | c0001 | t0005 | g0009 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19000 | hp1 | a0001 | c0001 | t0019 | g0226 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19005 | hp1 | a0001 | c0001 | t0013 | g0007 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19007 | hp1 | a0001 | c0001 | t0009 | g0026 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19007 | hp2 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19009 | hp2 | a0001 | c0001 | t0014 | g0087 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19012 | hp1 | a0001 | c0001 | t0009 | g0007 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19012 | hp2 | a0001 | c0001 | t0013 | g0062 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19030 | hp1 | a0001 | c0001 | t0018 | g0030 | AFR | LWK | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19030 | hp2 | a0001 | c0001 | t0021 | g0135 | AFR | LWK | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19043 | hp1 | a0001 | c0001 | t0031 | g0001 | AFR | LWK | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19043 | hp2 | a0001 | c0001 | t0044 | g0122 | AFR | LWK | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19054 | hp2 | a0001 | c0001 | t0005 | g0018 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19056 | hp1 | a0001 | c0001 | t0005 | g0017 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19060 | hp1 | a0001 | c0001 | t0009 | g0088 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19060 | hp2 | a0001 | c0001 | t0012 | g0238 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19062 | hp1 | a0001 | c0001 | t0016 | g0209 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19063 | hp2 | a0001 | c0001 | t0008 | g0004 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19064 | hp1 | a0001 | c0001 | t0004 | g0180 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19064 | hp2 | a0001 | c0001 | t0005 | g0095 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19066 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19068 | hp2 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19072 | hp1 | a0001 | c0001 | t0005 | g0027 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19072 | hp2 | a0001 | c0001 | t0079 | g0153 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19074 | hp2 | a0001 | c0001 | t0013 | g0007 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19075 | hp1 | a0001 | c0001 | t0027 | g0058 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19075 | hp2 | a0001 | c0001 | t0004 | g0145 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19080 | hp1 | a0001 | c0001 | t0008 | g0004 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19081 | hp1 | a0001 | c0001 | t0009 | g0089 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19081 | hp2 | a0001 | c0001 | t0059 | g0229 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19082 | hp1 | a0001 | c0001 | t0004 | g0179 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19084 | hp1 | a0001 | c0001 | t0013 | g0084 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19084 | hp2 | a0001 | c0001 | t0004 | g0034 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19087 | hp1 | a0001 | c0001 | t0008 | g0098 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19087 | hp2 | a0001 | c0001 | t0027 | g0006 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19088 | hp2 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19090 | hp1 | a0001 | c0001 | t0010 | g0001 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19240 | hp1 | a0001 | c0001 | t0022 | g0055 | AFR | YRI | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA19240 | hp2 | a0001 | c0001 | t0011 | g0032 | AFR | YRI | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | ASW | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA20129 | hp2 | a0001 | c0001 | t0070 | g0215 | AFR | ASW | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA20752 | hp2 | a0001 | c0001 | t0006 | g0070 | EUR | TSI | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0041 | EUR | TSI | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0038 | EUR | TSI | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA20905 | hp1 | a0001 | c0001 | t0007 | g0008 | SAS | GIH | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | GIH | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG01123 | hp2 | a0001 | c0001 | t0041 | g0063 | AMR | CLM | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02109 | hp1 | a0001 | c0001 | t0006 | g0061 | AFR | ACB | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02109 | hp2 | a0001 | c0001 | t0054 | g0080 | AFR | ACB | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02486 | hp1 | a0001 | c0001 | t0058 | g0138 | AFR | ACB | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02486 | hp2 | a0001 | c0001 | t0071 | g0202 | AFR | ACB | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02559 | hp1 | a0001 | c0001 | t0043 | g0120 | AFR | ACB | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG02559 | hp2 | a0001 | c0001 | t0026 | g0067 | AFR | ACB | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03471 | hp1 | a0001 | c0001 | t0041 | g0068 | AFR | MSL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0286 | AFR | MSL | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18955 | hp1 | a0001 | c0001 | t0016 | g0213 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA18955 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA20300 | hp1 | a0001 | c0001 | t0031 | g0140 | AFR | USA | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | USA | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | LWK | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
NA21309 | hp2 | a0001 | c0001 | t0023 | g0020 | AFR | LWK | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0224 | REF | REF | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | PAFAH1B2_chr11_117139287_117176045 | PAFAH1B2 | chr11 | 117139287 | 117176045 |
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 |
---|
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:117144294 | C | T | 1 | a0001c0001t0084 | 1 | HG03453.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-132C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/6 | chr11 | 117144294 | |||||||
chr11:117144353 | C | T | 1 | a0001c0001t0042 | 2 | HG01069.hp1 HG01071.hp1 |
5_prime_UTR_variant | MODIFIER | c.-73C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/6 | 8095 | chr11 | 117144353 | ||||||
chr11:117167731 | C | A | 4 | a0001c0001t0023 a0001c0001t0032 a0001c0001t0043 others(1): Show |
7 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*32C>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 32 | chr11 | 117167731 | ||||||
chr11:117167814 | T | C | 1 | a0001c0001t0033 | 2 | HG02647.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*115T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 115 | chr11 | 117167814 | ||||||
chr11:117168025 | T | A | 11 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0020 others(8): Show |
44 | HG00323.hp2 HG00609.hp2 HG01074.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*326T>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 326 | chr11 | 117168025 | ||||||
chr11:117168252 | T | C | 3 | a0001c0001t0023 a0001c0001t0032 a0001c0001t0043 |
6 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*553T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 553 | chr11 | 117168252 | ||||||
chr11:117168419 | TTTCCCCT others(3): Show |
T | 1 | a0001c0001t0049 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*727_*736delTTCATT others(4): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 727 | INFO_REALIGN_3_PRIME | chr11 | 117168419 | |||||
chr11:117168438 | G | A | 11 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0020 others(8): Show |
44 | HG00323.hp2 HG00609.hp2 HG01074.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*739G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 739 | chr11 | 117168438 | ||||||
chr11:117168441 | A | AC | 8 | a0001c0001t0010 a0001c0001t0016 a0001c0001t0021 others(5): Show |
25 | HG00544.hp1 HG00597.hp1 HG00642.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*746dupC | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 747 | INFO_REALIGN_3_PRIME | chr11 | 117168441 | |||||
chr11:117168445 | C | CCGTTTGT others(3): Show |
1 | a0001c0001t0012 | 8 | HG00423.hp2 HG00733.hp2 HG01106.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*746_*747insCGTTTG others(4): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 747 | chr11 | 117168445 | ||||||
chr11:117168445 | C | CCGTTTGT others(4): Show |
2 | a0001c0001t0037 a0001c0001t0050 |
3 | HG00741.hp1 HG02738.hp1 HG03927.hp1 |
3_prime_UTR_variant | MODIFIER | c.*746_*747insCGTTTG others(5): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 747 | chr11 | 117168445 | ||||||
chr11:117168445 | C | CCGTTTGT others(5): Show |
1 | a0001c0001t0051 | 1 | NA18979.hp1 | 3_prime_UTR_variant | MODIFIER | c.*746_*747insCGTTTG others(6): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 747 | chr11 | 117168445 | ||||||
chr11:117168445 | C | CCGTTTGT others(5): Show |
1 | a0001c0001t0052 | 1 | HG01978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*746_*747insCGTTTG others(6): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 747 | chr11 | 117168445 | ||||||
chr11:117168445 | C | CCGTTTGT others(7): Show |
1 | a0001c0001t0053 | 1 | NA18962.hp1 | 3_prime_UTR_variant | MODIFIER | c.*746_*747insCGTTTG others(8): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 747 | chr11 | 117168445 | ||||||
chr11:117168445 | C | CCGTTTGT others(8): Show |
2 | a0001c0001t0038 a0001c0001t0054 |
3 | HG02109.hp2 HG04115.hp2 HG04184.hp1 |
3_prime_UTR_variant | MODIFIER | c.*746_*747insCGTTTG others(9): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 747 | chr11 | 117168445 | ||||||
chr11:117168445 | C | CGTTT | 1 | a0001c0001t0023 | 3 | HG02647.hp2 HG03516.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*747_*750dupGTTT | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 751 | INFO_REALIGN_3_PRIME | chr11 | 117168445 | |||||
chr11:117168446 | G | GT | 5 | a0001c0001t0004 a0001c0001t0021 a0001c0001t0081 others(2): Show |
29 | HG00597.hp2 HG01496.hp1 HG01496.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*772dupT | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 773 | INFO_REALIGN_3_PRIME | chr11 | 117168446 | |||||
chr11:117168446 | G | GTTTCGTT others(6): Show |
1 | a0001c0001t0059 | 1 | NA19081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*750_*751insCGTTGT others(7): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 751 | INFO_REALIGN_3_PRIME | chr11 | 117168446 | |||||
chr11:117168446 | G | GTTTGTT | 3 | a0001c0001t0005 a0001c0001t0025 a0001c0001t0043 |
21 | HG00609.hp2 HG01175.hp2 HG02559.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*750_*751insGTTTTT | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 751 | INFO_REALIGN_3_PRIME | chr11 | 117168446 | |||||
chr11:117168446 | G | GTTTGTTG others(2): Show |
4 | a0001c0001t0003 a0001c0001t0017 a0001c0001t0060 others(1): Show |
44 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*750_*751insGTTGTT others(3): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 751 | INFO_REALIGN_3_PRIME | chr11 | 117168446 | |||||
chr11:117168446 | G | GTTTGTTG others(3): Show |
5 | a0001c0001t0002 a0001c0001t0042 a0001c0001t0062 others(2): Show |
51 | HG00323.hp1 HG00438.hp1 HG00639.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*750_*751insGTTGTT others(4): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 751 | INFO_REALIGN_3_PRIME | chr11 | 117168446 | |||||
chr11:117168446 | G | GTTTGTTG others(4): Show |
1 | a0001c0001t0019 | 5 | HG01099.hp2 HG02922.hp2 HG02965.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*750_*751insGTTGTT others(5): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 751 | INFO_REALIGN_3_PRIME | chr11 | 117168446 | |||||
chr11:117168446 | G | GTTTGTTG others(5): Show |
1 | a0001c0001t0065 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*750_*751insGTTGTT others(6): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 751 | INFO_REALIGN_3_PRIME | chr11 | 117168446 | |||||
chr11:117168446 | G | GTTTGTTG others(7): Show |
1 | a0001c0001t0066 | 1 | HG01975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*750_*751insGTTGTT others(8): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 751 | INFO_REALIGN_3_PRIME | chr11 | 117168446 | |||||
chr11:117168446 | G | GTTTGTTT others(3): Show |
2 | a0001c0001t0046 a0001c0001t0067 |
2 | HG01261.hp2 NA18612.hp1 |
3_prime_UTR_variant | MODIFIER | c.*750_*751insGTTTTT others(4): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 751 | INFO_REALIGN_3_PRIME | chr11 | 117168446 | |||||
chr11:117168446 | G | GTTTGTTT others(4): Show |
1 | a0001c0001t0013 | 8 | HG03139.hp2 NA18939.hp1 NA18941.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*750_*751insGTTTTT others(5): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 751 | INFO_REALIGN_3_PRIME | chr11 | 117168446 | |||||
chr11:117168446 | G | GTTTGTTT others(5): Show |
2 | a0001c0001t0009 a0001c0001t0033 |
12 | HG00099.hp2 HG00280.hp1 HG02647.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*750_*751insGTTTTT others(6): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 751 | INFO_REALIGN_3_PRIME | chr11 | 117168446 | |||||
chr11:117168446 | G | GTTTGTTT others(6): Show |
1 | a0001c0001t0006 | 13 | HG00639.hp1 HG01081.hp2 HG02109.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*750_*751insGTTTTT others(7): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 751 | INFO_REALIGN_3_PRIME | chr11 | 117168446 | |||||
chr11:117168446 | G | GTTTGTTT others(7): Show |
1 | a0001c0001t0014 | 8 | HG00735.hp2 HG01256.hp1 HG01975.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*750_*751insGTTTTT others(8): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 751 | INFO_REALIGN_3_PRIME | chr11 | 117168446 | |||||
chr11:117168446 | G | GTTTGTTT others(8): Show |
2 | a0001c0001t0022 a0001c0001t0026 |
7 | HG00738.hp1 HG01258.hp1 HG02004.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*750_*751insGTTTTT others(9): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 751 | INFO_REALIGN_3_PRIME | chr11 | 117168446 | |||||
chr11:117168446 | G | GTTTGTTT others(9): Show |
2 | a0001c0001t0040 a0001c0001t0047 |
3 | HG00323.hp2 HG01981.hp2 HG02896.hp2 |
3_prime_UTR_variant | MODIFIER | c.*750_*751insGTTTTT others(10): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 751 | INFO_REALIGN_3_PRIME | chr11 | 117168446 | |||||
chr11:117168446 | G | GTTTGTTT others(10): Show |
1 | a0001c0001t0068 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*750_*751insGTTTTT others(11): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 751 | INFO_REALIGN_3_PRIME | chr11 | 117168446 | |||||
chr11:117168446 | G | GTTTGTTT others(11): Show |
1 | a0001c0001t0069 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*750_*751insGTTTTT others(12): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 751 | INFO_REALIGN_3_PRIME | chr11 | 117168446 | |||||
chr11:117168446 | G | GTTTGTTT others(13): Show |
1 | a0001c0001t0041 | 2 | HG01123.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*750_*751insGTTTTT others(14): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 751 | INFO_REALIGN_3_PRIME | chr11 | 117168446 | |||||
chr11:117168446 | G | GTTTGTTT others(16): Show |
1 | a0001c0001t0034 | 2 | HG01074.hp2 HG01243.hp2 |
3_prime_UTR_variant | MODIFIER | c.*750_*751insGTTTTT others(17): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 751 | INFO_REALIGN_3_PRIME | chr11 | 117168446 | |||||
chr11:117168446 | G | GTTTGTTT others(19): Show |
1 | a0001c0001t0024 | 3 | HG02622.hp2 HG03491.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*750_*751insGTTTTT others(20): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 751 | INFO_REALIGN_3_PRIME | chr11 | 117168446 | |||||
chr11:117168446 | G | GTTTGTTT others(20): Show |
1 | a0001c0001t0035 | 2 | HG03017.hp2 HG04204.hp2 |
3_prime_UTR_variant | MODIFIER | c.*750_*751insGTTTTT others(21): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 751 | INFO_REALIGN_3_PRIME | chr11 | 117168446 | |||||
chr11:117168446 | G | GTTTGTTT others(32): Show |
1 | a0001c0001t0048 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*750_*751insGTTTTT others(33): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 751 | INFO_REALIGN_3_PRIME | chr11 | 117168446 | |||||
chr11:117168446 | G | T | 8 | a0001c0001t0012 a0001c0001t0037 a0001c0001t0038 others(5): Show |
17 | HG00423.hp2 HG00733.hp2 HG00741.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*747G>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 747 | chr11 | 117168446 | ||||||
chr11:117168446 | GTTTT | G | 2 | a0001c0001t0007 a0001c0001t0016 |
19 | HG00280.hp2 HG00597.hp1 HG01257.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*769_*772delTTTT | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 769 | INFO_REALIGN_3_PRIME | chr11 | 117168446 | |||||
chr11:117168446 | GTTTTTTT | G | 1 | a0001c0001t0008 | 10 | HG02040.hp1 HG02080.hp2 HG02129.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*766_*772delTTTTTT others(1): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 766 | INFO_REALIGN_3_PRIME | chr11 | 117168446 | |||||
chr11:117168446 | GTTTTTTT others(2): Show |
G | 4 | a0001c0001t0028 a0001c0001t0029 a0001c0001t0055 others(1): Show |
8 | HG01074.hp1 HG01109.hp1 HG02809.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*764_*772delTTTTTT others(3): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 764 | INFO_REALIGN_3_PRIME | chr11 | 117168446 | |||||
chr11:117168449 | T | TG | 2 | a0001c0001t0020 a0001c0001t0045 |
5 | HG01891.hp1 HG02280.hp2 HG02451.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*750_*751insG | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 751 | chr11 | 117168449 | ||||||
chr11:117168451 | T | G | 1 | a0001c0001t0033 | 2 | HG02647.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*752T>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 752 | chr11 | 117168451 | ||||||
chr11:117168452 | T | G | 1 | a0001c0001t0027 | 3 | NA18968.hp1 NA19075.hp1 NA19087.hp2 |
3_prime_UTR_variant | MODIFIER | c.*753T>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 753 | chr11 | 117168452 | ||||||
chr11:117168455 | T | G | 1 | a0001c0001t0049 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*756T>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 756 | chr11 | 117168455 | ||||||
chr11:117168456 | T | TTTTTTTT others(7): Show |
1 | a0001c0001t0071 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*770_*771insGTTTTT others(8): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 771 | INFO_REALIGN_3_PRIME | chr11 | 117168456 | |||||
chr11:117168456 | T | TTTTTTTT others(8): Show |
1 | a0001c0001t0072 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*771_*772insGTTTTT others(9): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 772 | INFO_REALIGN_3_PRIME | chr11 | 117168456 | |||||
chr11:117168457 | T | G | 1 | a0001c0001t0008 | 10 | HG02040.hp1 HG02080.hp2 HG02129.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*758T>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 758 | chr11 | 117168457 | ||||||
chr11:117168492 | G | A | 4 | a0001c0001t0007 a0001c0001t0016 a0001c0001t0056 others(1): Show |
21 | HG00280.hp2 HG00597.hp1 HG01257.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*793G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 793 | chr11 | 117168492 | ||||||
chr11:117168521 | C | G | 1 | a0001c0001t0083 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*822C>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 822 | chr11 | 117168521 | ||||||
chr11:117168582 | T | C | 1 | a0001c0001t0050 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*883T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 883 | chr11 | 117168582 | ||||||
chr11:117168609 | T | G | 71 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(68): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
3_prime_UTR_variant | MODIFIER | c.*910T>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 910 | chr11 | 117168609 | ||||||
chr11:117168636 | G | A | 1 | a0001c0001t0015 | 8 | HG01243.hp1 HG02886.hp1 HG02896.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*937G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 937 | chr11 | 117168636 | ||||||
chr11:117168652 | T | TC | 4 | a0001c0001t0007 a0001c0001t0016 a0001c0001t0056 others(1): Show |
21 | HG00280.hp2 HG00597.hp1 HG01257.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*956dupC | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 957 | INFO_REALIGN_3_PRIME | chr11 | 117168652 | |||||
chr11:117168680 | T | G | 1 | a0001c0001t0060 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*981T>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 981 | chr11 | 117168680 | ||||||
chr11:117168708 | T | C | 1 | a0001c0001t0045 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1009T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 1009 | chr11 | 117168708 | ||||||
chr11:117168712 | C | G | 1 | a0001c0001t0045 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1013C>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 1013 | chr11 | 117168712 | ||||||
chr11:117168713 | A | T | 1 | a0001c0001t0045 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1014A>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 1014 | chr11 | 117168713 | ||||||
chr11:117168716 | C | T | 1 | a0001c0001t0045 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1017C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 1017 | chr11 | 117168716 | ||||||
chr11:117168719 | T | G | 1 | a0001c0001t0045 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1020T>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 1020 | chr11 | 117168719 | ||||||
chr11:117168721 | G | A | 1 | a0001c0001t0045 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1022G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 1022 | chr11 | 117168721 | ||||||
chr11:117168722 | C | A | 1 | a0001c0001t0045 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1023C>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 1023 | chr11 | 117168722 | ||||||
chr11:117168724 | C | T | 1 | a0001c0001t0045 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1025C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 1025 | chr11 | 117168724 | ||||||
chr11:117168731 | T | A | 1 | a0001c0001t0045 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1032T>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 1032 | chr11 | 117168731 | ||||||
chr11:117168732 | T | A | 1 | a0001c0001t0045 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1033T>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 1033 | chr11 | 117168732 | ||||||
chr11:117168733 | A | C | 1 | a0001c0001t0045 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1034A>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 1034 | chr11 | 117168733 | ||||||
chr11:117168734 | T | G | 1 | a0001c0001t0045 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1035T>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 1035 | chr11 | 117168734 | ||||||
chr11:117168735 | T | A | 1 | a0001c0001t0045 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1036T>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 1036 | chr11 | 117168735 | ||||||
chr11:117168736 | T | A | 1 | a0001c0001t0045 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1037T>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 1037 | chr11 | 117168736 | ||||||
chr11:117168737 | C | G | 1 | a0001c0001t0045 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1038C>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 1038 | chr11 | 117168737 | ||||||
chr11:117168741 | T | G | 1 | a0001c0001t0045 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1042T>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 1042 | chr11 | 117168741 | ||||||
chr11:117168742 | T | A | 1 | a0001c0001t0045 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1043T>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 1043 | chr11 | 117168742 | ||||||
chr11:117168743 | T | A | 1 | a0001c0001t0045 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1044T>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 1044 | chr11 | 117168743 | ||||||
chr11:117168745 | A | C | 10 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0020 others(7): Show |
43 | HG00323.hp2 HG00609.hp2 HG01074.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*1046A>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 1046 | chr11 | 117168745 | ||||||
chr11:117168746 | T | A | 1 | a0001c0001t0045 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1047T>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 1047 | chr11 | 117168746 | ||||||
chr11:117168749 | T | C | 1 | a0001c0001t0045 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1050T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 1050 | chr11 | 117168749 | ||||||
chr11:117168752 | C | T | 1 | a0001c0001t0045 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1053C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 1053 | chr11 | 117168752 | ||||||
chr11:117168757 | G | A | 1 | a0001c0001t0045 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1058G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 1058 | chr11 | 117168757 | ||||||
chr11:117168758 | G | A | 1 | a0001c0001t0045 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1059G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 1059 | chr11 | 117168758 | ||||||
chr11:117168762 | A | T | 1 | a0001c0001t0045 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1063A>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 1063 | chr11 | 117168762 | ||||||
chr11:117168763 | T | A | 1 | a0001c0001t0045 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1064T>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 1064 | chr11 | 117168763 | ||||||
chr11:117168779 | T | C | 2 | a0001c0001t0015 a0001c0001t0074 |
9 | HG01243.hp1 HG02886.hp1 HG02896.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1080T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 1080 | chr11 | 117168779 | ||||||
chr11:117168792 | TTTTTG | T | 1 | a0001c0001t0028 | 3 | HG01074.hp1 HG03130.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1107_*1111delTGTT others(1): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 1107 | INFO_REALIGN_3_PRIME | chr11 | 117168792 | |||||
chr11:117168839 | G | A | 3 | a0001c0001t0017 a0001c0001t0062 a0001c0001t0075 |
8 | HG00438.hp2 HG02135.hp1 HG02698.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1140G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 1140 | chr11 | 117168839 | ||||||
chr11:117168845 | C | T | 4 | a0001c0001t0022 a0001c0001t0041 a0001c0001t0054 others(1): Show |
8 | HG00738.hp1 HG01123.hp2 HG02109.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1146C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 1146 | chr11 | 117168845 | ||||||
chr11:117169081 | G | A | 54 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(51): Show |
241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
3_prime_UTR_variant | MODIFIER | c.*1382G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 1382 | chr11 | 117169081 | ||||||
chr11:117169298 | TA | T | 2 | a0001c0001t0031 a0001c0001t0058 |
4 | HG02486.hp1 HG03209.hp2 NA19043.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1607delA | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 1607 | INFO_REALIGN_3_PRIME | chr11 | 117169298 | |||||
chr11:117169375 | A | G | 3 | a0001c0001t0011 a0001c0001t0057 a0001c0001t0082 |
11 | HG00642.hp2 HG01891.hp2 HG02055.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1676A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 1676 | chr11 | 117169375 | ||||||
chr11:117169402 | C | G | 3 | a0001c0001t0023 a0001c0001t0032 a0001c0001t0043 |
6 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1703C>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 1703 | chr11 | 117169402 | ||||||
chr11:117169474 | G | T | 1 | a0001c0001t0074 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1775G>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 1775 | chr11 | 117169474 | ||||||
chr11:117169482 | G | GT | 19 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0012 others(16): Show |
117 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*1784dupT | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 1785 | INFO_REALIGN_3_PRIME | chr11 | 117169482 | |||||
chr11:117169520 | G | A | 1 | a0001c0001t0063 | 1 | NA18945.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1821G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 1821 | chr11 | 117169520 | ||||||
chr11:117169575 | C | A | 1 | a0001c0001t0079 | 1 | NA19072.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1876C>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 1876 | chr11 | 117169575 | ||||||
chr11:117169789 | G | C | 11 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0020 others(8): Show |
44 | HG00323.hp2 HG00609.hp2 HG01074.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*2090G>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 2090 | chr11 | 117169789 | ||||||
chr11:117169824 | G | A | 1 | a0001c0001t0080 | 1 | HG03490.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2125G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 2125 | chr11 | 117169824 | ||||||
chr11:117170023 | A | G | 3 | a0001c0001t0030 a0001c0001t0039 a0001c0001t0076 |
6 | HG00735.hp1 HG01069.hp2 HG01106.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2324A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 2324 | chr11 | 117170023 | ||||||
chr11:117170250 | T | A | 1 | a0001c0001t0070 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2551T>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 2551 | chr11 | 117170250 | ||||||
chr11:117170256 | T | C | 1 | a0001c0001t0061 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2557T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 2557 | chr11 | 117170256 | ||||||
chr11:117170424 | T | C | 1 | a0001c0001t0084 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2725T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 2725 | chr11 | 117170424 | ||||||
chr11:117170475 | C | T | 1 | a0001c0001t0071 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2776C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 2776 | chr11 | 117170475 | ||||||
chr11:117170506 | C | T | 1 | a0001c0001t0083 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2807C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 2807 | chr11 | 117170506 | ||||||
chr11:117170626 | T | TA | 7 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(4): Show |
23 | HG00673.hp1 HG01069.hp1 HG01071.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2948dupA | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 2949 | INFO_REALIGN_3_PRIME | chr11 | 117170626 | |||||
chr11:117170626 | TA | T | 45 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(42): Show |
139 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(136): Show |
3_prime_UTR_variant | MODIFIER | c.*2948delA | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 2948 | INFO_REALIGN_3_PRIME | chr11 | 117170626 | |||||
chr11:117170626 | TAA | T | 7 | a0001c0001t0008 a0001c0001t0014 a0001c0001t0029 others(4): Show |
10 | HG01109.hp1 HG01256.hp1 HG02148.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2947_*2948delAA | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 2947 | INFO_REALIGN_3_PRIME | chr11 | 117170626 | |||||
chr11:117170626 | TAAA | T | 3 | a0001c0001t0018 a0001c0001t0025 a0001c0001t0044 |
7 | HG02622.hp1 HG02818.hp2 HG03098.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2946_*2948delAAA | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 2946 | INFO_REALIGN_3_PRIME | chr11 | 117170626 | |||||
chr11:117170626 | TAAAA | T | 3 | a0001c0001t0023 a0001c0001t0032 a0001c0001t0043 |
6 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2945_*2948delAAAA | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 2945 | INFO_REALIGN_3_PRIME | chr11 | 117170626 | |||||
chr11:117170786 | T | C | 1 | a0001c0001t0070 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3087T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 3087 | chr11 | 117170786 | ||||||
chr11:117170888 | C | T | 1 | a0001c0001t0064 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3189C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 3189 | chr11 | 117170888 | ||||||
chr11:117170965 | G | A | 1 | a0001c0001t0081 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3266G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 6/6 | 3266 | chr11 | 117170965 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:117144473 | G | C | 60 | a0001c0001t0006g0006 a0001c0001t0006g0024 a0001c0001t0006g0025 others(57): Show |
66 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.-8+55G>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117144473 | |||||||
chr11:117144479 | C | T | 93 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0015 others(90): Show |
118 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.-8+61C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117144479 | |||||||
chr11:117144501 | C | T | 19 | a0001c0001t0007g0008 a0001c0001t0007g0014 a0001c0001t0007g0037 others(16): Show |
26 | HG00280.hp2 HG00597.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.-8+83C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117144501 | |||||||
chr11:117144502 | G | C | 19 | a0001c0001t0007g0008 a0001c0001t0007g0014 a0001c0001t0007g0037 others(16): Show |
26 | HG00280.hp2 HG00597.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.-8+84G>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117144502 | |||||||
chr11:117144522 | C | A | 28 | a0001c0001t0005g0004 a0001c0001t0005g0009 a0001c0001t0005g0017 others(25): Show |
44 | HG00323.hp2 HG00609.hp2 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.-8+104C>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117144522 | |||||||
chr11:117144559 | G | T | 13 | a0001c0001t0006g0026 a0001c0001t0006g0085 a0001c0001t0009g0007 others(10): Show |
16 | HG01978.hp2 NA18612.hp1 NA18943.hp1 others(13): Show |
intron_variant | MODIFIER | c.-8+141G>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117144559 | |||||||
chr11:117144561 | G | A | 1 | a0001c0001t0009g0044 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-8+143G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117144561 | |||||||
chr11:117144574 | G | A | 5 | a0001c0001t0030g0019 a0001c0001t0030g0109 a0001c0001t0039g0108 others(2): Show |
6 | HG00735.hp1 HG01069.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8+156G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117144574 | |||||||
chr11:117144585 | C | T | 2 | a0001c0001t0071g0202 a0001c0001t0072g0203 |
2 | HG02486.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-8+167C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117144585 | |||||||
chr11:117144646 | C | G | 2 | a0001c0001t0001g0036 a0001c0001t0004g0201 |
3 | HG01496.hp2 HG01928.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.-8+228C>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117144646 | |||||||
chr11:117144742 | C | CGCCCG | 6 | a0001c0001t0019g0288 a0001c0001t0030g0019 a0001c0001t0030g0109 others(3): Show |
7 | HG00735.hp1 HG01069.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8+328_-8+329insGG others(3): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 117144742 | ||||||
chr11:117144747 | C | CGCCCT | 4 | a0001c0001t0001g0115 a0001c0001t0015g0113 a0001c0001t0015g0114 others(1): Show |
4 | HG00558.hp2 HG01109.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+348_-8+352dupCT others(3): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 117144747 | ||||||
chr11:117144747 | C | CGCCCTGC others(3): Show |
2 | a0001c0001t0001g0112 a0001c0001t0029g0204 |
2 | HG03041.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.-8+343_-8+352dupCT others(8): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 117144747 | ||||||
chr11:117144747 | C | T | 6 | a0001c0001t0019g0288 a0001c0001t0030g0019 a0001c0001t0030g0109 others(3): Show |
7 | HG00735.hp1 HG01069.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8+329C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117144747 | |||||||
chr11:117144752 | T | C | 1 | a0001c0001t0049g0111 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-8+334T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117144752 | |||||||
chr11:117144770 | C | G | 1 | a0001c0001t0021g0200 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-8+352C>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117144770 | |||||||
chr11:117144800 | C | G | 30 | a0001c0001t0005g0004 a0001c0001t0005g0009 a0001c0001t0005g0017 others(27): Show |
46 | HG00323.hp2 HG00609.hp2 HG01074.hp2 others(43): Show |
intron_variant | MODIFIER | c.-8+382C>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117144800 | |||||||
chr11:117144816 | G | A | 1 | a0001c0001t0078g0205 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-8+398G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117144816 | |||||||
chr11:117144827 | C | T | 1 | a0001c0001t0001g0199 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-8+409C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117144827 | |||||||
chr11:117144894 | C | G | 5 | a0001c0001t0002g0043 a0001c0001t0002g0284 a0001c0001t0002g0285 others(2): Show |
5 | HG02630.hp2 HG02818.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8+476C>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117144894 | |||||||
chr11:117144896 | C | G | 5 | a0001c0001t0029g0204 a0001c0001t0029g0214 a0001c0001t0029g0216 others(2): Show |
5 | HG01109.hp1 HG02809.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8+478C>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117144896 | |||||||
chr11:117144987 | T | G | 1 | a0001c0001t0002g0220 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-8+569T>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117144987 | |||||||
chr11:117145076 | C | T | 1 | a0001c0001t0016g0213 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-8+658C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117145076 | |||||||
chr11:117145362 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-8+944C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117145362 | |||||||
chr11:117145374 | G | A | 3 | a0001c0001t0002g0221 a0001c0001t0003g0222 a0001c0001t0003g0223 |
3 | HG02056.hp2 HG02074.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.-8+956G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117145374 | |||||||
chr11:117145447 | C | CG | 237 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0015 others(234): Show |
299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.-8+1034dupG | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 117145447 | ||||||
chr11:117145539 | G | C | 1 | a0001c0001t0021g0135 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-8+1121G>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117145539 | |||||||
chr11:117145664 | G | A | 1 | a0001c0001t0011g0029 | 2 | HG02965.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-8+1246G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117145664 | |||||||
chr11:117145734 | C | T | 28 | a0001c0001t0005g0004 a0001c0001t0005g0009 a0001c0001t0005g0017 others(25): Show |
44 | HG00323.hp2 HG00609.hp2 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.-8+1316C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117145734 | |||||||
chr11:117145870 | T | C | 1 | a0001c0001t0013g0045 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-8+1452T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117145870 | |||||||
chr11:117145989 | C | A | 11 | a0001c0001t0018g0030 a0001c0001t0018g0116 a0001c0001t0018g0118 others(8): Show |
13 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8+1571C>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117145989 | |||||||
chr11:117146108 | T | G | 163 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0015 others(160): Show |
196 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.-8+1690T>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117146108 | |||||||
chr11:117146112 | T | G | 3 | a0001c0001t0002g0015 a0001c0001t0002g0023 a0001c0001t0002g0248 |
3 | HG02074.hp2 HG02165.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.-8+1694T>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117146112 | |||||||
chr11:117146113 | T | C | 3 | a0001c0001t0002g0267 a0001c0001t0002g0268 a0001c0001t0002g0269 |
3 | HG02630.hp1 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-8+1695T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117146113 | |||||||
chr11:117146114 | C | CT | 6 | a0001c0001t0001g0178 a0001c0001t0004g0188 a0001c0001t0010g0001 others(3): Show |
6 | HG01261.hp1 HG02055.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8+1715dupT | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 117146114 | ||||||
chr11:117146114 | CT | C | 14 | a0001c0001t0001g0154 a0001c0001t0002g0015 a0001c0001t0002g0023 others(11): Show |
14 | HG00735.hp1 HG01069.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.-8+1715delT | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 117146114 | ||||||
chr11:117146114 | CTT | C | 191 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0015 others(188): Show |
236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.-8+1714_-8+1715del others(2): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 117146114 | ||||||
chr11:117146117 | T | TC | 4 | a0001c0001t0001g0139 a0001c0001t0031g0137 a0001c0001t0031g0140 others(1): Show |
4 | HG02486.hp1 HG03209.hp2 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+1699_-8+1700ins others(1): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117146117 | |||||||
chr11:117146118 | T | C | 1 | a0001c0001t0001g0136 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-8+1700T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117146118 | |||||||
chr11:117146126 | T | G | 2 | a0001c0001t0002g0038 a0001c0001t0003g0038 |
2 | NA18957.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-8+1708T>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117146126 | |||||||
chr11:117146128 | T | G | 66 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0038 others(63): Show |
86 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.-8+1710T>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117146128 | |||||||
chr11:117146130 | T | G | 92 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0015 others(89): Show |
117 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.-8+1712T>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117146130 | |||||||
chr11:117146132 | T | G | 112 | a0001c0001t0001g0141 a0001c0001t0002g0002 a0001c0001t0002g0003 others(109): Show |
144 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.-8+1714T>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117146132 | |||||||
chr11:117146281 | C | T | 152 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0015 others(149): Show |
183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.-8+1863C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117146281 | |||||||
chr11:117146385 | A | G | 1 | a0001c0001t0032g0123 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-8+1967A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117146385 | |||||||
chr11:117146392 | T | G | 1 | a0001c0001t0071g0202 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-8+1974T>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117146392 | |||||||
chr11:117146401 | T | C | 1 | a0001c0001t0019g0264 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-8+1983T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117146401 | |||||||
chr11:117146406 | C | T | 1 | a0001c0001t0069g0082 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-8+1988C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117146406 | |||||||
chr11:117146412 | A | T | 2 | a0001c0001t0071g0202 a0001c0001t0072g0203 |
2 | HG02486.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-8+1994A>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117146412 | |||||||
chr11:117146609 | A | G | 3 | a0001c0001t0028g0124 a0001c0001t0028g0125 a0001c0001t0028g0126 |
3 | HG01074.hp1 HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-8+2191A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117146609 | |||||||
chr11:117146708 | A | G | 1 | a0001c0001t0002g0263 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-8+2290A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117146708 | |||||||
chr11:117146739 | T | G | 28 | a0001c0001t0005g0004 a0001c0001t0005g0009 a0001c0001t0005g0017 others(25): Show |
44 | HG00323.hp2 HG00609.hp2 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.-8+2321T>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117146739 | |||||||
chr11:117146814 | A | G | 28 | a0001c0001t0005g0004 a0001c0001t0005g0009 a0001c0001t0005g0017 others(25): Show |
44 | HG00323.hp2 HG00609.hp2 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.-8+2396A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117146814 | |||||||
chr11:117146827 | C | A | 2 | a0001c0001t0071g0202 a0001c0001t0072g0203 |
2 | HG02486.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-8+2409C>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117146827 | |||||||
chr11:117146837 | TG | T | 11 | a0001c0001t0018g0030 a0001c0001t0018g0116 a0001c0001t0018g0118 others(8): Show |
13 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8+2421delG | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 117146837 | ||||||
chr11:117146838 | G | GA | 3 | a0001c0001t0028g0124 a0001c0001t0028g0125 a0001c0001t0028g0126 |
3 | HG01074.hp1 HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-8+2420_-8+2421ins others(1): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117146838 | |||||||
chr11:117146838 | GGA | G | 151 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0015 others(148): Show |
182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.-8+2421_-8+2422del others(2): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117146838 | |||||||
chr11:117146839 | G | A | 3 | a0001c0001t0028g0124 a0001c0001t0028g0125 a0001c0001t0028g0126 |
3 | HG01074.hp1 HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-8+2421G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117146839 | |||||||
chr11:117146839 | GA | G | 15 | a0001c0001t0001g0035 a0001c0001t0001g0136 a0001c0001t0001g0194 others(12): Show |
17 | HG00735.hp1 HG01069.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.-8+2437delA | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 117146839 | ||||||
chr11:117146839 | GAAA | G | 28 | a0001c0001t0005g0004 a0001c0001t0005g0009 a0001c0001t0005g0017 others(25): Show |
44 | HG00323.hp2 HG00609.hp2 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.-8+2435_-8+2437del others(3): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 117146839 | ||||||
chr11:117146989 | C | T | 5 | a0001c0001t0007g0211 a0001c0001t0007g0212 a0001c0001t0016g0209 others(2): Show |
5 | HG00597.hp1 NA18955.hp1 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8+2571C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117146989 | |||||||
chr11:117146990 | C | T | 5 | a0001c0001t0030g0019 a0001c0001t0030g0109 a0001c0001t0039g0108 others(2): Show |
6 | HG00735.hp1 HG01069.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8+2572C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117146990 | |||||||
chr11:117146994 | C | T | 6 | a0001c0001t0001g0192 a0001c0001t0023g0020 a0001c0001t0032g0121 others(3): Show |
8 | HG02083.hp1 HG02145.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-8+2576C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117146994 | |||||||
chr11:117146998 | G | A | 28 | a0001c0001t0005g0004 a0001c0001t0005g0009 a0001c0001t0005g0017 others(25): Show |
44 | HG00323.hp2 HG00609.hp2 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.-8+2580G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117146998 | |||||||
chr11:117147043 | C | T | 8 | a0001c0001t0011g0010 a0001c0001t0011g0029 a0001c0001t0011g0032 others(5): Show |
12 | HG00642.hp2 HG01891.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.-8+2625C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117147043 | |||||||
chr11:117147046 | A | C | 28 | a0001c0001t0005g0004 a0001c0001t0005g0009 a0001c0001t0005g0017 others(25): Show |
44 | HG00323.hp2 HG00609.hp2 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.-8+2628A>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117147046 | |||||||
chr11:117147123 | G | C | 3 | a0001c0001t0034g0092 a0001c0001t0034g0094 a0001c0001t0047g0093 |
3 | HG00323.hp2 HG01074.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.-8+2705G>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117147123 | |||||||
chr11:117147224 | C | T | 1 | a0001c0001t0014g0081 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-8+2806C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117147224 | |||||||
chr11:117147260 | C | T | 5 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0280 others(2): Show |
5 | HG01071.hp2 HG01168.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8+2842C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117147260 | |||||||
chr11:117147315 | G | T | 5 | a0001c0001t0030g0019 a0001c0001t0030g0109 a0001c0001t0039g0108 others(2): Show |
6 | HG00735.hp1 HG01069.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8+2897G>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117147315 | |||||||
chr11:117147436 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-8+3018A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117147436 | |||||||
chr11:117147715 | G | C | 1 | a0001c0001t0029g0214 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-8+3297G>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117147715 | |||||||
chr11:117147728 | CAAAG | C | 4 | a0001c0001t0023g0020 a0001c0001t0032g0121 a0001c0001t0032g0123 others(1): Show |
6 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8+3314_-8+3317del others(4): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 117147728 | ||||||
chr11:117147756 | T | G | 1 | a0001c0001t0001g0142 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-8+3338T>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117147756 | |||||||
chr11:117148038 | CTTTTTTC others(4): Show |
C | 1 | a0001c0001t0049g0111 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-8+3638_-8+3648del others(11): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 117148038 | ||||||
chr11:117148048 | T | G | 1 | a0001c0001t0009g0006 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-8+3630T>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117148048 | |||||||
chr11:117148056 | C | CT | 7 | a0001c0001t0004g0188 a0001c0001t0004g0189 a0001c0001t0021g0190 others(4): Show |
9 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8+3652dupT | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 117148056 | ||||||
chr11:117148056 | CTT | C | 28 | a0001c0001t0005g0004 a0001c0001t0005g0009 a0001c0001t0005g0017 others(25): Show |
44 | HG00323.hp2 HG00609.hp2 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.-8+3651_-8+3652del others(2): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 117148056 | ||||||
chr11:117148112 | T | C | 2 | a0001c0001t0014g0048 a0001c0001t0026g0049 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-8+3694T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117148112 | |||||||
chr11:117148204 | A | G | 4 | a0001c0001t0001g0005 a0001c0001t0001g0186 a0001c0001t0001g0187 others(1): Show |
11 | HG00544.hp2 HG00609.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.-8+3786A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117148204 | |||||||
chr11:117148294 | C | T | 167 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0015 others(164): Show |
200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.-8+3876C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117148294 | |||||||
chr11:117148304 | C | T | 6 | a0001c0001t0002g0261 a0001c0001t0002g0262 a0001c0001t0002g0279 others(3): Show |
6 | HG00639.hp2 HG01071.hp2 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8+3886C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117148304 | |||||||
chr11:117148519 | A | G | 1 | a0001c0001t0054g0080 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-7-3922A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117148519 | |||||||
chr11:117148684 | A | G | 1 | a0001c0001t0003g0260 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-7-3757A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117148684 | |||||||
chr11:117148700 | A | G | 2 | a0001c0001t0071g0202 a0001c0001t0072g0203 |
2 | HG02486.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-7-3741A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117148700 | |||||||
chr11:117148710 | C | A | 1 | a0001c0001t0005g0095 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-7-3731C>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117148710 | |||||||
chr11:117148753 | C | G | 1 | a0001c0001t0038g0079 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-7-3688C>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117148753 | |||||||
chr11:117148774 | C | T | 7 | a0001c0001t0015g0031 a0001c0001t0015g0113 a0001c0001t0015g0114 others(4): Show |
8 | HG01243.hp1 HG02886.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-7-3667C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117148774 | |||||||
chr11:117148792 | C | T | 3 | a0001c0001t0017g0258 a0001c0001t0062g0259 a0001c0001t0075g0257 |
3 | HG02698.hp1 NA18946.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.-7-3649C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117148792 | |||||||
chr11:117148809 | T | C | 4 | a0001c0001t0002g0225 a0001c0001t0002g0265 a0001c0001t0019g0226 others(1): Show |
4 | HG00438.hp1 HG02027.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7-3632T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117148809 | |||||||
chr11:117148814 | G | A | 3 | a0001c0001t0030g0019 a0001c0001t0039g0108 a0001c0001t0076g0019 |
4 | HG00735.hp1 HG01069.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7-3627G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117148814 | |||||||
chr11:117148875 | A | T | 1 | a0001c0001t0038g0079 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-7-3566A>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117148875 | |||||||
chr11:117148967 | G | A | 3 | a0001c0001t0002g0227 a0001c0001t0071g0202 a0001c0001t0072g0203 |
3 | HG02486.hp2 HG02922.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.-7-3474G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117148967 | |||||||
chr11:117148978 | C | T | 1 | a0001c0001t0005g0107 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-7-3463C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117148978 | |||||||
chr11:117149033 | A | ATTT | 28 | a0001c0001t0005g0004 a0001c0001t0005g0009 a0001c0001t0005g0017 others(25): Show |
44 | HG00323.hp2 HG00609.hp2 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.-7-3388_-7-3386dup others(3): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 117149033 | ||||||
chr11:117149033 | AT | A | 26 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0146 others(23): Show |
33 | HG00280.hp2 HG00597.hp1 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.-7-3386delT | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 117149033 | ||||||
chr11:117149033 | ATT | A | 70 | a0001c0001t0002g0220 a0001c0001t0006g0006 a0001c0001t0006g0024 others(67): Show |
77 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.-7-3387_-7-3386del others(2): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 117149033 | ||||||
chr11:117149033 | ATTT | A | 112 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0015 others(109): Show |
140 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.-7-3388_-7-3386del others(3): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 117149033 | ||||||
chr11:117149114 | C | T | 2 | a0001c0001t0071g0202 a0001c0001t0072g0203 |
2 | HG02486.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-7-3327C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117149114 | |||||||
chr11:117149151 | A | G | 28 | a0001c0001t0005g0004 a0001c0001t0005g0009 a0001c0001t0005g0017 others(25): Show |
44 | HG00323.hp2 HG00609.hp2 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.-7-3290A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117149151 | |||||||
chr11:117149256 | AT | A | 238 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0015 others(235): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.-7-3178delT | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 117149256 | ||||||
chr11:117149370 | G | C | 1 | a0001c0001t0002g0280 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-7-3071G>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117149370 | |||||||
chr11:117149371 | C | T | 1 | a0001c0001t0004g0185 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-7-3070C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117149371 | |||||||
chr11:117149426 | A | G | 14 | a0001c0001t0007g0008 a0001c0001t0007g0014 a0001c0001t0007g0037 others(11): Show |
21 | HG00280.hp2 HG00597.hp1 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.-7-3015A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117149426 | |||||||
chr11:117149429 | C | CTTTTTTT others(5): Show |
2 | a0001c0001t0009g0007 a0001c0001t0013g0007 |
5 | NA18953.hp2 NA18966.hp1 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.-7-3012_-7-3011ins others(12): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117149429 | |||||||
chr11:117149429 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0078g0205 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-7-3012_-7-3011ins others(14): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117149429 | |||||||
chr11:117149430 | G | GGTTTTTT others(9): Show |
1 | a0001c0001t0016g0209 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-7-3011_-7-3010ins others(16): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117149430 | |||||||
chr11:117149430 | G | GGTTTTTT others(10): Show |
1 | a0001c0001t0016g0210 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-7-3011_-7-3010ins others(17): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117149430 | |||||||
chr11:117149430 | G | GT | 12 | a0001c0001t0001g0139 a0001c0001t0001g0148 a0001c0001t0001g0178 others(9): Show |
12 | HG02145.hp1 HG03831.hp1 NA18946.hp1 others(9): Show |
intron_variant | MODIFIER | c.-7-2997dupT | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 117149430 | ||||||
chr11:117149430 | G | GTTTTTTT others(4): Show |
10 | a0001c0001t0002g0261 a0001c0001t0002g0280 a0001c0001t0002g0281 others(7): Show |
10 | HG01071.hp2 HG01074.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.-7-3007_-7-2997dup others(11): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 117149430 | ||||||
chr11:117149430 | G | GTTTTTTT others(5): Show |
48 | a0001c0001t0002g0002 a0001c0001t0002g0023 a0001c0001t0002g0038 others(45): Show |
60 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.-7-3008_-7-2997dup others(12): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 117149430 | ||||||
chr11:117149430 | G | GTTTTTTT others(6): Show |
64 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0042 others(61): Show |
79 | HG00099.hp1 HG00438.hp1 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.-7-3009_-7-2997dup others(13): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 117149430 | ||||||
chr11:117149430 | G | GTTTTTTT others(7): Show |
36 | a0001c0001t0002g0227 a0001c0001t0002g0286 a0001c0001t0003g0040 others(33): Show |
41 | HG00099.hp2 HG00639.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.-7-3010_-7-2997dup others(14): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 117149430 | ||||||
chr11:117149430 | G | GTTTTTTT others(8): Show |
29 | a0001c0001t0005g0004 a0001c0001t0005g0017 a0001c0001t0005g0027 others(26): Show |
38 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.-7-2997_-7-2996ins others(15): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 117149430 | ||||||
chr11:117149430 | G | GTTTTTTT others(9): Show |
21 | a0001c0001t0005g0009 a0001c0001t0005g0018 a0001c0001t0005g0028 others(18): Show |
30 | HG00280.hp2 HG00609.hp2 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.-7-2997_-7-2996ins others(16): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 117149430 | ||||||
chr11:117149430 | G | GTTTTTTT others(10): Show |
10 | a0001c0001t0007g0014 a0001c0001t0007g0037 a0001c0001t0007g0212 others(7): Show |
13 | HG01258.hp2 HG01517.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.-7-2997_-7-2996ins others(17): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 117149430 | ||||||
chr11:117149430 | G | GTTTTTTT others(11): Show |
2 | a0001c0001t0018g0119 a0001c0001t0036g0106 |
2 | HG03130.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.-7-2997_-7-2996ins others(18): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 117149430 | ||||||
chr11:117149430 | G | GTTTTTTT others(12): Show |
1 | a0001c0001t0072g0203 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-7-2997_-7-2996ins others(19): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 117149430 | ||||||
chr11:117149430 | G | T | 3 | a0001c0001t0009g0007 a0001c0001t0013g0007 a0001c0001t0078g0205 |
6 | HG01261.hp1 NA18953.hp2 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7-3011G>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117149430 | |||||||
chr11:117149467 | C | T | 11 | a0001c0001t0018g0030 a0001c0001t0018g0116 a0001c0001t0018g0118 others(8): Show |
13 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.-7-2974C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117149467 | |||||||
chr11:117149479 | T | C | 1 | a0001c0001t0082g0132 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-7-2962T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117149479 | |||||||
chr11:117149528 | G | A | 1 | a0001c0001t0083g0193 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-7-2913G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117149528 | |||||||
chr11:117149575 | C | T | 2 | a0001c0001t0033g0064 a0001c0001t0033g0076 |
2 | HG02647.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-7-2866C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117149575 | |||||||
chr11:117149584 | G | A | 6 | a0001c0001t0018g0030 a0001c0001t0018g0116 a0001c0001t0018g0118 others(3): Show |
6 | HG02622.hp1 HG02818.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7-2857G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117149584 | |||||||
chr11:117149608 | A | G | 1 | a0001c0001t0032g0123 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-7-2833A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117149608 | |||||||
chr11:117149695 | G | A | 1 | a0001c0001t0013g0054 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-7-2746G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117149695 | |||||||
chr11:117149754 | A | G | 197 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0015 others(194): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.-7-2687A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117149754 | |||||||
chr11:117150189 | T | G | 3 | a0001c0001t0001g0149 a0001c0001t0021g0200 a0001c0001t0080g0150 |
3 | HG02129.hp1 HG03490.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-7-2252T>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117150189 | |||||||
chr11:117150376 | C | T | 1 | a0001c0001t0002g0236 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-7-2065C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117150376 | |||||||
chr11:117150381 | C | G | 1 | a0001c0001t0006g0071 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-7-2060C>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117150381 | |||||||
chr11:117150418 | A | T | 197 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0015 others(194): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.-7-2023A>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117150418 | |||||||
chr11:117150449 | C | T | 1 | a0001c0001t0006g0070 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-7-1992C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117150449 | |||||||
chr11:117150459 | G | GT | 15 | a0001c0001t0002g0274 a0001c0001t0003g0039 a0001c0001t0011g0010 others(12): Show |
21 | HG00642.hp2 HG01891.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.-7-1970dupT | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 117150459 | ||||||
chr11:117150605 | G | T | 1 | a0001c0001t0078g0205 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-7-1836G>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117150605 | |||||||
chr11:117150634 | A | G | 6 | a0001c0001t0018g0030 a0001c0001t0018g0116 a0001c0001t0018g0118 others(3): Show |
6 | HG02622.hp1 HG02818.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7-1807A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117150634 | |||||||
chr11:117150641 | G | A | 1 | a0001c0001t0065g0256 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-7-1800G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117150641 | |||||||
chr11:117150657 | G | A | 1 | a0001c0001t0002g0279 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-7-1784G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117150657 | |||||||
chr11:117150710 | G | C | 60 | a0001c0001t0006g0006 a0001c0001t0006g0024 a0001c0001t0006g0025 others(57): Show |
66 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.-7-1731G>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117150710 | |||||||
chr11:117150750 | A | G | 1 | a0001c0001t0002g0279 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-7-1691A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117150750 | |||||||
chr11:117150763 | C | T | 1 | a0001c0001t0036g0106 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-7-1678C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117150763 | |||||||
chr11:117150783 | C | T | 1 | a0001c0001t0013g0054 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-7-1658C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117150783 | |||||||
chr11:117150880 | T | C | 1 | a0001c0001t0001g0178 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-7-1561T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117150880 | |||||||
chr11:117150954 | C | T | 1 | a0001c0001t0011g0032 | 2 | HG02055.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-7-1487C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117150954 | |||||||
chr11:117150964 | G | A | 4 | a0001c0001t0023g0020 a0001c0001t0032g0121 a0001c0001t0032g0123 others(1): Show |
6 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7-1477G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117150964 | |||||||
chr11:117150989 | G | GA | 8 | a0001c0001t0003g0237 a0001c0001t0003g0250 a0001c0001t0004g0188 others(5): Show |
8 | HG01081.hp1 HG01975.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.-7-1436dupA | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 117150989 | ||||||
chr11:117150989 | GAA | G | 33 | a0001c0001t0005g0004 a0001c0001t0005g0009 a0001c0001t0005g0017 others(30): Show |
51 | HG00323.hp2 HG00609.hp2 HG01074.hp2 others(48): Show |
intron_variant | MODIFIER | c.-7-1437_-7-1436del others(2): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 117150989 | ||||||
chr11:117151043 | T | A | 195 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0015 others(192): Show |
244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.-7-1398T>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117151043 | |||||||
chr11:117151145 | T | A | 3 | a0001c0001t0028g0124 a0001c0001t0028g0125 a0001c0001t0028g0126 |
3 | HG01074.hp1 HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-7-1296T>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117151145 | |||||||
chr11:117151161 | G | C | 195 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0015 others(192): Show |
244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.-7-1280G>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117151161 | |||||||
chr11:117151185 | T | C | 1 | a0001c0001t0049g0111 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-7-1256T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117151185 | |||||||
chr11:117151207 | C | T | 152 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0015 others(149): Show |
183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.-7-1234C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117151207 | |||||||
chr11:117151232 | T | C | 6 | a0001c0001t0018g0030 a0001c0001t0018g0116 a0001c0001t0018g0118 others(3): Show |
6 | HG02622.hp1 HG02818.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7-1209T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117151232 | |||||||
chr11:117151233 | C | CT | 217 | a0001c0001t0001g0148 a0001c0001t0002g0002 a0001c0001t0002g0003 others(214): Show |
273 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.-7-1194dupT | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 117151233 | ||||||
chr11:117151233 | C | CTT | 10 | a0001c0001t0002g0262 a0001c0001t0007g0037 a0001c0001t0016g0037 others(7): Show |
12 | HG01168.hp2 HG02145.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-7-1195_-7-1194dup others(2): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 117151233 | ||||||
chr11:117151390 | C | T | 1 | a0001c0001t0006g0069 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-7-1051C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117151390 | |||||||
chr11:117151560 | A | G | 195 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0015 others(192): Show |
244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.-7-881A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117151560 | |||||||
chr11:117151612 | A | G | 5 | a0001c0001t0001g0034 a0001c0001t0004g0034 a0001c0001t0004g0177 others(2): Show |
5 | NA18939.hp2 NA18948.hp1 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.-7-829A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117151612 | |||||||
chr11:117151636 | A | C | 92 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0015 others(89): Show |
117 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.-7-805A>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117151636 | |||||||
chr11:117151637 | C | T | 5 | a0001c0001t0005g0017 a0001c0001t0005g0028 a0001c0001t0005g0105 others(2): Show |
8 | NA18965.hp1 NA18973.hp1 NA18978.hp1 others(5): Show |
intron_variant | MODIFIER | c.-7-804C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117151637 | |||||||
chr11:117151760 | G | A | 1 | a0001c0001t0009g0044 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-7-681G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117151760 | |||||||
chr11:117151769 | C | T | 2 | a0001c0001t0039g0108 a0001c0001t0044g0122 |
2 | HG01106.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-7-672C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117151769 | |||||||
chr11:117151867 | C | T | 2 | a0001c0001t0033g0064 a0001c0001t0033g0076 |
2 | HG02647.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-7-574C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117151867 | |||||||
chr11:117152131 | A | G | 1 | a0001c0001t0054g0080 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-7-310A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117152131 | |||||||
chr11:117152233 | C | A | 2 | a0001c0001t0012g0238 a0001c0001t0059g0229 |
2 | NA19060.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.-7-208C>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117152233 | |||||||
chr11:117152267 | A | G | 1 | a0001c0001t0066g0277 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-7-174A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117152267 | |||||||
chr11:117152290 | G | C | 1 | a0001c0001t0001g0151 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-7-151G>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117152290 | |||||||
chr11:117152394 | A | G | 1 | a0001c0001t0038g0079 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-7-47A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 1/5 | chr11 | 117152394 | |||||||
chr11:117152587 | T | A | 5 | a0001c0001t0023g0020 a0001c0001t0032g0121 a0001c0001t0032g0123 others(2): Show |
7 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.81+59T>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117152587 | |||||||
chr11:117152592 | T | C | 5 | a0001c0001t0023g0020 a0001c0001t0032g0121 a0001c0001t0032g0123 others(2): Show |
7 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.81+64T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117152592 | |||||||
chr11:117152634 | T | C | 1 | a0001c0001t0070g0215 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.81+106T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117152634 | |||||||
chr11:117152696 | G | A | 1 | a0001c0001t0065g0256 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.81+168G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117152696 | |||||||
chr11:117152771 | A | C | 200 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0015 others(197): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.81+243A>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117152771 | |||||||
chr11:117152828 | T | C | 1 | a0001c0001t0004g0152 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.81+300T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117152828 | |||||||
chr11:117152898 | C | G | 2 | a0001c0001t0002g0041 a0001c0001t0002g0273 |
3 | HG01515.hp2 HG01517.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.81+370C>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117152898 | |||||||
chr11:117152981 | GC | G | 4 | a0001c0001t0015g0031 a0001c0001t0015g0128 a0001c0001t0015g0129 others(1): Show |
5 | HG01243.hp1 HG02886.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+454delC | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117152981 | |||||||
chr11:117152990 | C | T | 28 | a0001c0001t0005g0004 a0001c0001t0005g0009 a0001c0001t0005g0017 others(25): Show |
44 | HG00323.hp2 HG00609.hp2 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.81+462C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117152990 | |||||||
chr11:117152998 | G | A | 1 | a0001c0001t0002g0239 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.81+470G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117152998 | |||||||
chr11:117153050 | G | A | 8 | a0001c0001t0015g0031 a0001c0001t0015g0128 a0001c0001t0015g0129 others(5): Show |
9 | HG01243.hp1 HG02451.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.81+522G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117153050 | |||||||
chr11:117153178 | T | C | 1 | a0001c0001t0014g0051 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.81+650T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117153178 | |||||||
chr11:117153224 | A | G | 5 | a0001c0001t0029g0204 a0001c0001t0029g0214 a0001c0001t0029g0216 others(2): Show |
5 | HG01109.hp1 HG02809.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.81+696A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117153224 | |||||||
chr11:117153371 | GTT | G | 6 | a0001c0001t0002g0225 a0001c0001t0002g0230 a0001c0001t0002g0240 others(3): Show |
6 | HG00438.hp1 HG02027.hp1 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+852_81+853delTT | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 117153371 | ||||||
chr11:117153372 | T | C | 1 | a0001c0001t0083g0193 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.81+844T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117153372 | |||||||
chr11:117153379 | T | G | 9 | a0001c0001t0011g0133 a0001c0001t0021g0135 a0001c0001t0029g0204 others(6): Show |
9 | HG01109.hp1 HG02258.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.81+851T>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117153379 | |||||||
chr11:117153379 | T | TG | 148 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0015 others(145): Show |
179 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.81+851_81+852insG | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117153379 | |||||||
chr11:117153406 | T | C | 1 | a0001c0001t0001g0195 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.81+878T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117153406 | |||||||
chr11:117153540 | G | A | 14 | a0001c0001t0007g0008 a0001c0001t0007g0014 a0001c0001t0007g0037 others(11): Show |
21 | HG00280.hp2 HG00597.hp1 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.81+1012G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117153540 | |||||||
chr11:117153548 | G | A | 153 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0015 others(150): Show |
184 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.81+1020G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117153548 | |||||||
chr11:117153586 | C | T | 238 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0015 others(235): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.81+1058C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117153586 | |||||||
chr11:117153719 | A | G | 3 | a0001c0001t0030g0019 a0001c0001t0039g0108 a0001c0001t0076g0019 |
4 | HG00735.hp1 HG01069.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.81+1191A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117153719 | |||||||
chr11:117153755 | A | G | 1 | a0001c0001t0011g0133 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.81+1227A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117153755 | |||||||
chr11:117153765 | T | C | 231 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0015 others(228): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.81+1237T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117153765 | |||||||
chr11:117153802 | A | G | 4 | a0001c0001t0003g0040 a0001c0001t0003g0249 a0001c0001t0003g0254 others(1): Show |
4 | HG01099.hp1 HG01934.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.81+1274A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117153802 | |||||||
chr11:117153821 | A | G | 5 | a0001c0001t0030g0019 a0001c0001t0030g0109 a0001c0001t0039g0108 others(2): Show |
6 | HG00735.hp1 HG01069.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.81+1293A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117153821 | |||||||
chr11:117153928 | C | CT | 12 | a0001c0001t0015g0031 a0001c0001t0015g0114 a0001c0001t0015g0128 others(9): Show |
13 | HG01243.hp1 HG02622.hp1 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.81+1413dupT | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 117153928 | ||||||
chr11:117153928 | CT | C | 13 | a0001c0001t0001g0021 a0001c0001t0001g0142 a0001c0001t0001g0143 others(10): Show |
14 | HG01168.hp2 HG02486.hp2 HG02922.hp1 others(11): Show |
intron_variant | MODIFIER | c.81+1413delT | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 117153928 | ||||||
chr11:117153968 | T | A | 5 | a0001c0001t0023g0020 a0001c0001t0032g0121 a0001c0001t0032g0123 others(2): Show |
7 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.81+1440T>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117153968 | |||||||
chr11:117153986 | G | A | 3 | a0001c0001t0002g0267 a0001c0001t0002g0268 a0001c0001t0002g0269 |
3 | HG02630.hp1 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.81+1458G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117153986 | |||||||
chr11:117154119 | G | GA | 195 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0015 others(192): Show |
244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.81+1599dupA | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 117154119 | ||||||
chr11:117154123 | A | G | 9 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0035 others(6): Show |
14 | HG00408.hp1 NA18956.hp1 NA18962.hp2 others(11): Show |
intron_variant | MODIFIER | c.81+1595A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117154123 | |||||||
chr11:117154170 | C | T | 1 | a0001c0001t0001g0176 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.81+1642C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117154170 | |||||||
chr11:117154310 | G | C | 1 | a0001c0001t0025g0078 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.81+1782G>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117154310 | |||||||
chr11:117154476 | G | GGCACCAT others(8): Show |
8 | a0001c0001t0015g0031 a0001c0001t0015g0113 a0001c0001t0015g0114 others(5): Show |
9 | HG01243.hp1 HG02451.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.81+1974_81+1988dup others(15): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 117154476 | ||||||
chr11:117154481 | C | CATTACAG others(12): Show |
1 | a0001c0001t0074g0127 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.81+1954_81+1972dup others(19): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 117154481 | ||||||
chr11:117154521 | G | C | 2 | a0001c0001t0022g0055 a0001c0001t0054g0080 |
2 | HG02109.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.81+1993G>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117154521 | |||||||
chr11:117154565 | T | C | 1 | a0001c0001t0043g0120 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.81+2037T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117154565 | |||||||
chr11:117154603 | A | AT | 28 | a0001c0001t0005g0004 a0001c0001t0005g0009 a0001c0001t0005g0017 others(25): Show |
44 | HG00323.hp2 HG00609.hp2 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.81+2083dupT | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 117154603 | ||||||
chr11:117154641 | A | G | 60 | a0001c0001t0006g0006 a0001c0001t0006g0024 a0001c0001t0006g0025 others(57): Show |
66 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.81+2113A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117154641 | |||||||
chr11:117154776 | A | G | 1 | a0001c0001t0049g0111 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.81+2248A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117154776 | |||||||
chr11:117155058 | C | T | 6 | a0001c0001t0018g0030 a0001c0001t0018g0116 a0001c0001t0018g0118 others(3): Show |
6 | HG02622.hp1 HG02818.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+2530C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117155058 | |||||||
chr11:117155075 | C | G | 1 | a0001c0001t0002g0280 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.81+2547C>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117155075 | |||||||
chr11:117155108 | A | G | 8 | a0001c0001t0015g0031 a0001c0001t0015g0113 a0001c0001t0015g0114 others(5): Show |
9 | HG01243.hp1 HG02886.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.81+2580A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117155108 | |||||||
chr11:117155113 | C | T | 1 | a0001c0001t0078g0205 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.81+2585C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117155113 | |||||||
chr11:117155144 | G | A | 4 | a0001c0001t0001g0021 a0001c0001t0001g0143 a0001c0001t0004g0021 others(1): Show |
5 | NA18959.hp2 NA18963.hp1 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+2616G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117155144 | |||||||
chr11:117155145 | A | T | 1 | a0001c0001t0013g0062 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.81+2617A>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117155145 | |||||||
chr11:117155168 | C | T | 1 | a0001c0001t0065g0256 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.81+2640C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117155168 | |||||||
chr11:117155216 | A | G | 28 | a0001c0001t0005g0004 a0001c0001t0005g0009 a0001c0001t0005g0017 others(25): Show |
44 | HG00323.hp2 HG00609.hp2 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.81+2688A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117155216 | |||||||
chr11:117155228 | TAC | T | 11 | a0001c0001t0018g0030 a0001c0001t0018g0116 a0001c0001t0018g0118 others(8): Show |
13 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.81+2702_81+2703del others(2): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 117155228 | ||||||
chr11:117155251 | C | G | 1 | a0001c0001t0002g0248 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.81+2723C>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117155251 | |||||||
chr11:117155339 | A | G | 3 | a0001c0001t0030g0019 a0001c0001t0039g0108 a0001c0001t0076g0019 |
4 | HG00735.hp1 HG01069.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.81+2811A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117155339 | |||||||
chr11:117155368 | C | T | 1 | a0001c0001t0078g0205 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.81+2840C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117155368 | |||||||
chr11:117155405 | A | G | 1 | a0001c0001t0003g0247 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.81+2877A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117155405 | |||||||
chr11:117155421 | T | C | 8 | a0001c0001t0022g0055 a0001c0001t0022g0056 a0001c0001t0022g0057 others(5): Show |
8 | HG00738.hp1 HG01123.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.81+2893T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117155421 | |||||||
chr11:117155438 | T | C | 16 | a0001c0001t0015g0031 a0001c0001t0015g0113 a0001c0001t0015g0114 others(13): Show |
18 | HG00735.hp1 HG01069.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.81+2910T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117155438 | |||||||
chr11:117155473 | C | T | 7 | a0001c0001t0011g0010 a0001c0001t0011g0029 a0001c0001t0011g0032 others(4): Show |
11 | HG00642.hp2 HG01891.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.81+2945C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117155473 | |||||||
chr11:117155606 | C | T | 2 | a0001c0001t0018g0046 a0001c0001t0018g0047 |
2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.81+3078C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117155606 | |||||||
chr11:117155633 | C | T | 3 | a0001c0001t0028g0124 a0001c0001t0028g0125 a0001c0001t0028g0126 |
3 | HG01074.hp1 HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.81+3105C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117155633 | |||||||
chr11:117155658 | A | C | 238 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0015 others(235): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.81+3130A>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117155658 | |||||||
chr11:117155771 | G | C | 2 | a0001c0001t0002g0225 a0001c0001t0002g0265 |
2 | HG02027.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.81+3243G>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117155771 | |||||||
chr11:117155804 | T | A | 1 | a0001c0001t0002g0230 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.81+3276T>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117155804 | |||||||
chr11:117155860 | C | A | 1 | a0001c0001t0078g0205 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.81+3332C>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117155860 | |||||||
chr11:117155868 | T | G | 2 | a0001c0001t0002g0221 a0001c0001t0003g0223 |
2 | HG02056.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.81+3340T>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117155868 | |||||||
chr11:117155963 | A | G | 7 | a0001c0001t0015g0031 a0001c0001t0015g0113 a0001c0001t0015g0114 others(4): Show |
8 | HG01243.hp1 HG02886.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.81+3435A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117155963 | |||||||
chr11:117155979 | C | T | 1 | a0001c0001t0044g0122 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.81+3451C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117155979 | |||||||
chr11:117156143 | A | G | 1 | a0001c0001t0002g0272 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.81+3615A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117156143 | |||||||
chr11:117156157 | A | G | 1 | a0001c0001t0022g0057 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.81+3629A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117156157 | |||||||
chr11:117156169 | G | A | 194 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0015 others(191): Show |
243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.81+3641G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117156169 | |||||||
chr11:117156203 | G | A | 1 | a0001c0001t0083g0193 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.81+3675G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117156203 | |||||||
chr11:117156209 | A | T | 6 | a0001c0001t0018g0030 a0001c0001t0018g0116 a0001c0001t0018g0118 others(3): Show |
6 | HG02622.hp1 HG02818.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+3681A>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117156209 | |||||||
chr11:117156217 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.81+3689T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117156217 | |||||||
chr11:117156298 | A | C | 1 | a0001c0001t0004g0189 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.82-3636A>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117156298 | |||||||
chr11:117156298 | A | T | 3 | a0001c0001t0031g0137 a0001c0001t0031g0140 a0001c0001t0058g0138 |
3 | HG02486.hp1 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.82-3636A>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117156298 | |||||||
chr11:117156467 | G | A | 2 | a0001c0001t0001g0144 a0001c0001t0001g0154 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.82-3467G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117156467 | |||||||
chr11:117156485 | C | T | 3 | a0001c0001t0028g0124 a0001c0001t0028g0125 a0001c0001t0028g0126 |
3 | HG01074.hp1 HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.82-3449C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117156485 | |||||||
chr11:117156500 | A | G | 4 | a0001c0001t0029g0204 a0001c0001t0029g0216 a0001c0001t0055g0217 others(1): Show |
4 | HG02809.hp1 HG03041.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-3434A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117156500 | |||||||
chr11:117156765 | G | A | 192 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0015 others(189): Show |
241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.82-3169G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117156765 | |||||||
chr11:117156769 | T | A | 6 | a0001c0001t0018g0030 a0001c0001t0018g0116 a0001c0001t0018g0118 others(3): Show |
6 | HG02622.hp1 HG02818.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.82-3165T>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117156769 | |||||||
chr11:117156951 | G | A | 5 | a0001c0001t0029g0204 a0001c0001t0029g0214 a0001c0001t0029g0216 others(2): Show |
5 | HG01109.hp1 HG02809.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.82-2983G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117156951 | |||||||
chr11:117157032 | C | CA | 18 | a0001c0001t0002g0227 a0001c0001t0007g0008 a0001c0001t0007g0014 others(15): Show |
26 | HG00280.hp2 HG00597.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.82-2896dupA | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 117157032 | ||||||
chr11:117157038 | AG | A | 44 | a0001c0001t0002g0269 a0001c0001t0002g0278 a0001c0001t0002g0279 others(41): Show |
60 | HG00323.hp2 HG00609.hp2 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.82-2895delG | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117157038 | |||||||
chr11:117157039 | G | A | 190 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0015 others(187): Show |
234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.82-2895G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117157039 | |||||||
chr11:117157051 | G | A | 4 | a0001c0001t0029g0204 a0001c0001t0029g0216 a0001c0001t0055g0217 others(1): Show |
4 | HG02809.hp1 HG03041.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-2883G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117157051 | |||||||
chr11:117157159 | T | C | 1 | a0001c0001t0049g0111 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.82-2775T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117157159 | |||||||
chr11:117157226 | T | C | 7 | a0001c0001t0030g0019 a0001c0001t0030g0109 a0001c0001t0039g0108 others(4): Show |
8 | HG00735.hp1 HG01069.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.82-2708T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117157226 | |||||||
chr11:117157232 | A | G | 1 | a0001c0001t0080g0150 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.82-2702A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117157232 | |||||||
chr11:117157287 | A | AAT | 36 | a0001c0001t0001g0187 a0001c0001t0002g0015 a0001c0001t0002g0023 others(33): Show |
40 | HG00438.hp1 HG01099.hp2 HG01255.hp2 others(37): Show |
intron_variant | MODIFIER | c.82-2631_82-2630dup others(2): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 117157287 | ||||||
chr11:117157304 | AGTTT | A | 5 | a0001c0001t0029g0204 a0001c0001t0029g0214 a0001c0001t0029g0216 others(2): Show |
5 | HG01109.hp1 HG02809.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.82-2617_82-2614del others(4): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 117157304 | ||||||
chr11:117157402 | A | G | 3 | a0001c0001t0028g0124 a0001c0001t0028g0125 a0001c0001t0028g0126 |
3 | HG01074.hp1 HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.82-2532A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117157402 | |||||||
chr11:117157404 | A | G | 1 | a0001c0001t0044g0122 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.82-2530A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117157404 | |||||||
chr11:117157428 | T | C | 1 | a0001c0001t0078g0205 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.82-2506T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117157428 | |||||||
chr11:117157548 | G | A | 7 | a0001c0001t0015g0031 a0001c0001t0015g0113 a0001c0001t0015g0114 others(4): Show |
8 | HG01243.hp1 HG02886.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.82-2386G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117157548 | |||||||
chr11:117157577 | A | T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0182 a0001c0001t0010g0012 |
5 | HG00673.hp1 NA18961.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.82-2357A>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117157577 | |||||||
chr11:117157764 | A | G | 3 | a0001c0001t0028g0124 a0001c0001t0028g0125 a0001c0001t0028g0126 |
3 | HG01074.hp1 HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.82-2170A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117157764 | |||||||
chr11:117157832 | G | A | 1 | a0001c0001t0016g0218 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.82-2102G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117157832 | |||||||
chr11:117157872 | T | G | 1 | a0001c0001t0028g0124 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.82-2062T>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117157872 | |||||||
chr11:117157876 | G | A | 1 | a0001c0001t0063g0244 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.82-2058G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117157876 | |||||||
chr11:117158011 | G | A | 28 | a0001c0001t0005g0004 a0001c0001t0005g0009 a0001c0001t0005g0017 others(25): Show |
44 | HG00323.hp2 HG00609.hp2 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.82-1923G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117158011 | |||||||
chr11:117158095 | G | A | 1 | a0001c0001t0078g0205 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.82-1839G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117158095 | |||||||
chr11:117158101 | A | G | 4 | a0001c0001t0001g0146 a0001c0001t0001g0175 a0001c0001t0001g0196 others(1): Show |
4 | NA18942.hp1 NA18986.hp1 NA19072.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-1833A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117158101 | |||||||
chr11:117158173 | T | C | 5 | a0001c0001t0022g0056 a0001c0001t0022g0057 a0001c0001t0022g0066 others(2): Show |
5 | HG00738.hp1 HG01123.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.82-1761T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117158173 | |||||||
chr11:117158206 | CTTTCTTT others(4): Show |
C | 1 | a0001c0001t0020g0096 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.82-1726_82-1716del others(11): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 117158206 | ||||||
chr11:117158459 | G | A | 8 | a0001c0001t0015g0031 a0001c0001t0015g0113 a0001c0001t0015g0114 others(5): Show |
9 | HG01243.hp1 HG02886.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.82-1475G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117158459 | |||||||
chr11:117158489 | T | C | 5 | a0001c0001t0029g0204 a0001c0001t0029g0214 a0001c0001t0029g0216 others(2): Show |
5 | HG01109.hp1 HG02809.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.82-1445T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117158489 | |||||||
chr11:117158602 | G | T | 5 | a0001c0001t0029g0204 a0001c0001t0029g0214 a0001c0001t0029g0216 others(2): Show |
5 | HG01109.hp1 HG02809.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.82-1332G>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117158602 | |||||||
chr11:117158640 | C | CT | 7 | a0001c0001t0001g0171 a0001c0001t0001g0173 a0001c0001t0001g0181 others(4): Show |
7 | HG03239.hp1 HG03688.hp2 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.82-1273dupT | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 117158640 | ||||||
chr11:117158640 | CT | C | 198 | a0001c0001t0001g0155 a0001c0001t0001g0187 a0001c0001t0001g0194 others(195): Show |
250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.82-1273delT | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 117158640 | ||||||
chr11:117158640 | CTT | C | 31 | a0001c0001t0007g0008 a0001c0001t0007g0014 a0001c0001t0007g0037 others(28): Show |
40 | HG00280.hp2 HG00597.hp1 HG01258.hp2 others(37): Show |
intron_variant | MODIFIER | c.82-1274_82-1273del others(2): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 117158640 | ||||||
chr11:117158680 | T | C | 1 | a0001c0001t0001g0139 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.82-1254T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117158680 | |||||||
chr11:117158726 | C | T | 6 | a0001c0001t0018g0030 a0001c0001t0018g0116 a0001c0001t0018g0118 others(3): Show |
6 | HG02622.hp1 HG02818.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.82-1208C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117158726 | |||||||
chr11:117158833 | C | T | 1 | a0001c0001t0004g0174 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.82-1101C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117158833 | |||||||
chr11:117158834 | G | A | 3 | a0001c0001t0028g0124 a0001c0001t0028g0125 a0001c0001t0028g0126 |
3 | HG01074.hp1 HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.82-1100G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117158834 | |||||||
chr11:117159069 | A | T | 28 | a0001c0001t0005g0004 a0001c0001t0005g0009 a0001c0001t0005g0017 others(25): Show |
44 | HG00323.hp2 HG00609.hp2 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.82-865A>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117159069 | |||||||
chr11:117159137 | A | G | 1 | a0001c0001t0001g0170 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.82-797A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117159137 | |||||||
chr11:117159265 | C | T | 1 | a0001c0001t0010g0169 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.82-669C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117159265 | |||||||
chr11:117159435 | T | TA | 4 | a0001c0001t0028g0124 a0001c0001t0028g0125 a0001c0001t0028g0126 others(1): Show |
4 | HG01074.hp1 HG02257.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-492dupA | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 117159435 | ||||||
chr11:117159471 | A | C | 14 | a0001c0001t0007g0008 a0001c0001t0007g0014 a0001c0001t0007g0037 others(11): Show |
21 | HG00280.hp2 HG00597.hp1 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.82-463A>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117159471 | |||||||
chr11:117159536 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.82-398C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117159536 | |||||||
chr11:117159678 | T | G | 2 | a0001c0001t0002g0241 a0001c0001t0002g0248 |
2 | NA18941.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.82-256T>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117159678 | |||||||
chr11:117159709 | T | C | 1 | a0001c0001t0038g0079 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.82-225T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117159709 | |||||||
chr11:117159736 | GA | G | 12 | a0001c0001t0001g0167 a0001c0001t0002g0269 a0001c0001t0003g0234 others(9): Show |
16 | HG00323.hp2 HG00642.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.82-183delA | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 117159736 | ||||||
chr11:117159743 | A | G | 1 | a0001c0001t0008g0103 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.82-191A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117159743 | |||||||
chr11:117159792 | T | C | 2 | a0001c0001t0015g0128 a0001c0001t0015g0130 |
2 | HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.82-142T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117159792 | |||||||
chr11:117159865 | T | A | 195 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0015 others(192): Show |
244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.82-69T>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117159865 | |||||||
chr11:117159908 | AT | A | 169 | a0001c0001t0001g0167 a0001c0001t0002g0002 a0001c0001t0002g0003 others(166): Show |
202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.82-15delT | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 117159908 | ||||||
chr11:117159917 | T | C | 28 | a0001c0001t0005g0004 a0001c0001t0005g0009 a0001c0001t0005g0017 others(25): Show |
44 | HG00323.hp2 HG00609.hp2 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.82-17T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 2/5 | chr11 | 117159917 | |||||||
chr11:117160430 | A | G | 1 | a0001c0001t0022g0066 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.171+407A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 3/5 | chr11 | 117160430 | |||||||
chr11:117160521 | G | A | 2 | a0001c0001t0074g0127 a0001c0001t0083g0193 |
2 | HG02451.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.171+498G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 3/5 | chr11 | 117160521 | |||||||
chr11:117160537 | A | G | 1 | a0001c0001t0078g0205 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.171+514A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 3/5 | chr11 | 117160537 | |||||||
chr11:117160647 | G | A | 27 | a0001c0001t0005g0004 a0001c0001t0005g0009 a0001c0001t0005g0017 others(24): Show |
43 | HG00323.hp2 HG00609.hp2 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.172-498G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 3/5 | chr11 | 117160647 | |||||||
chr11:117160648 | G | A | 2 | a0001c0001t0002g0221 a0001c0001t0003g0223 |
2 | HG02056.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.172-497G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 3/5 | chr11 | 117160648 | |||||||
chr11:117160649 | G | T | 1 | a0001c0001t0036g0106 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.172-496G>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 3/5 | chr11 | 117160649 | |||||||
chr11:117160701 | C | T | 1 | a0001c0001t0071g0202 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.172-444C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 3/5 | chr11 | 117160701 | |||||||
chr11:117160755 | C | G | 4 | a0001c0001t0023g0020 a0001c0001t0032g0121 a0001c0001t0032g0123 others(1): Show |
6 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.172-390C>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 3/5 | chr11 | 117160755 | |||||||
chr11:117160773 | A | G | 1 | a0001c0001t0025g0117 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.172-372A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 3/5 | chr11 | 117160773 | |||||||
chr11:117160779 | C | CT | 21 | a0001c0001t0001g0166 a0001c0001t0007g0008 a0001c0001t0007g0014 others(18): Show |
28 | HG00280.hp2 HG00597.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.172-350dupT | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr11 | 117160779 | ||||||
chr11:117160779 | CT | C | 10 | a0001c0001t0002g0267 a0001c0001t0002g0279 a0001c0001t0004g0184 others(7): Show |
11 | HG00639.hp2 HG00735.hp1 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.172-350delT | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr11 | 117160779 | ||||||
chr11:117161052 | A | G | 1 | a0001c0001t0011g0032 | 2 | HG02055.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.172-93A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 3/5 | chr11 | 117161052 | |||||||
chr11:117161080 | T | C | 1 | a0001c0001t0011g0134 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.172-65T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 3/5 | chr11 | 117161080 | |||||||
chr11:117161086 | C | T | 1 | a0001c0001t0004g0201 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.172-59C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 3/5 | chr11 | 117161086 | |||||||
chr11:117161278 | T | C | 1 | a0001c0001t0014g0087 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.288+17T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 4/5 | chr11 | 117161278 | |||||||
chr11:117161381 | C | A | 1 | a0001c0001t0001g0112 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.288+120C>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 4/5 | chr11 | 117161381 | |||||||
chr11:117161409 | G | T | 147 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0015 others(144): Show |
175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.288+148G>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 4/5 | chr11 | 117161409 | |||||||
chr11:117161512 | G | GT | 196 | a0001c0001t0001g0022 a0001c0001t0001g0139 a0001c0001t0002g0002 others(193): Show |
247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.288+265dupT | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 117161512 | ||||||
chr11:117161512 | G | GTT | 11 | a0001c0001t0003g0039 a0001c0001t0015g0031 a0001c0001t0015g0113 others(8): Show |
12 | HG01243.hp1 HG02738.hp1 HG02738.hp2 others(9): Show |
intron_variant | MODIFIER | c.288+264_288+265dup others(2): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 117161512 | ||||||
chr11:117161665 | G | T | 1 | a0001c0001t0049g0111 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.288+404G>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 4/5 | chr11 | 117161665 | |||||||
chr11:117161925 | T | C | 20 | a0001c0001t0007g0008 a0001c0001t0007g0014 a0001c0001t0007g0037 others(17): Show |
27 | HG00280.hp2 HG00597.hp1 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.288+664T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 4/5 | chr11 | 117161925 | |||||||
chr11:117162218 | C | T | 14 | a0001c0001t0007g0008 a0001c0001t0007g0014 a0001c0001t0007g0037 others(11): Show |
21 | HG00280.hp2 HG00597.hp1 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.288+957C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 4/5 | chr11 | 117162218 | |||||||
chr11:117162243 | A | G | 43 | a0001c0001t0005g0004 a0001c0001t0005g0009 a0001c0001t0005g0017 others(40): Show |
61 | HG00323.hp2 HG00609.hp2 HG01074.hp2 others(58): Show |
intron_variant | MODIFIER | c.288+982A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 4/5 | chr11 | 117162243 | |||||||
chr11:117162284 | C | A | 1 | a0001c0001t0049g0111 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.288+1023C>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 4/5 | chr11 | 117162284 | |||||||
chr11:117162347 | C | G | 1 | a0001c0001t0002g0227 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.288+1086C>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 4/5 | chr11 | 117162347 | |||||||
chr11:117162447 | A | AT | 212 | a0001c0001t0001g0163 a0001c0001t0001g0183 a0001c0001t0002g0002 others(209): Show |
265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.288+1200dupT | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 117162447 | ||||||
chr11:117162586 | G | A | 1 | a0001c0001t0002g0272 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.289-1184G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 4/5 | chr11 | 117162586 | |||||||
chr11:117162605 | T | TA | 9 | a0001c0001t0001g0156 a0001c0001t0004g0164 a0001c0001t0019g0226 others(6): Show |
10 | HG00735.hp1 HG01069.hp2 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.289-1148dupA | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 117162605 | ||||||
chr11:117162690 | G | A | 5 | a0001c0001t0006g0025 a0001c0001t0014g0051 a0001c0001t0014g0065 others(2): Show |
5 | HG01975.hp1 HG01981.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.289-1080G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 4/5 | chr11 | 117162690 | |||||||
chr11:117162733 | G | A | 8 | a0001c0001t0015g0031 a0001c0001t0015g0113 a0001c0001t0015g0114 others(5): Show |
9 | HG01243.hp1 HG02886.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.289-1037G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 4/5 | chr11 | 117162733 | |||||||
chr11:117162922 | G | A | 2 | a0001c0001t0011g0032 a0001c0001t0011g0133 |
3 | HG02055.hp2 HG02258.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.289-848G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 4/5 | chr11 | 117162922 | |||||||
chr11:117163043 | TTGAGAAA others(9): Show |
T | 1 | a0001c0001t0059g0229 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.289-724_289-709del others(16): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 117163043 | ||||||
chr11:117163070 | T | C | 1 | a0001c0001t0003g0242 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.289-700T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 4/5 | chr11 | 117163070 | |||||||
chr11:117163075 | T | C | 1 | a0001c0001t0029g0204 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.289-695T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 4/5 | chr11 | 117163075 | |||||||
chr11:117163092 | C | T | 19 | a0001c0001t0002g0015 a0001c0001t0002g0023 a0001c0001t0002g0225 others(16): Show |
22 | HG00438.hp1 HG01099.hp2 HG01975.hp2 others(19): Show |
intron_variant | MODIFIER | c.289-678C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 4/5 | chr11 | 117163092 | |||||||
chr11:117163187 | C | CTGGCTGA others(6): Show |
197 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0015 others(194): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.289-578_289-577ins others(13): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 117163187 | ||||||
chr11:117163288 | T | G | 1 | a0001c0001t0001g0157 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.289-482T>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 4/5 | chr11 | 117163288 | |||||||
chr11:117163393 | C | T | 1 | a0001c0001t0065g0256 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.289-377C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 4/5 | chr11 | 117163393 | |||||||
chr11:117163394 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.289-376G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 4/5 | chr11 | 117163394 | |||||||
chr11:117163604 | C | T | 14 | a0001c0001t0007g0008 a0001c0001t0007g0014 a0001c0001t0007g0037 others(11): Show |
21 | HG00280.hp2 HG00597.hp1 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.289-166C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 4/5 | chr11 | 117163604 | |||||||
chr11:117163642 | C | T | 5 | a0001c0001t0023g0020 a0001c0001t0032g0121 a0001c0001t0032g0123 others(2): Show |
7 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.289-128C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 4/5 | chr11 | 117163642 | |||||||
chr11:117163651 | T | C | 5 | a0001c0001t0029g0204 a0001c0001t0029g0214 a0001c0001t0029g0216 others(2): Show |
5 | HG01109.hp1 HG02809.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.289-119T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 4/5 | chr11 | 117163651 | |||||||
chr11:117163672 | C | CA | 6 | a0001c0001t0028g0124 a0001c0001t0028g0125 a0001c0001t0028g0126 others(3): Show |
6 | HG01074.hp1 HG03130.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.289-80dupA | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 117163672 | ||||||
chr11:117163672 | CAAAAAA | C | 152 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0015 others(149): Show |
183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.289-85_289-80delAA others(4): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 117163672 | ||||||
chr11:117163709 | G | A | 1 | a0001c0001t0083g0193 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.289-61G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 4/5 | chr11 | 117163709 | |||||||
chr11:117163903 | G | T | 238 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0015 others(235): Show |
300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.411+11G>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117163903 | |||||||
chr11:117163967 | T | C | 5 | a0001c0001t0029g0204 a0001c0001t0029g0214 a0001c0001t0029g0216 others(2): Show |
5 | HG01109.hp1 HG02809.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.411+75T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117163967 | |||||||
chr11:117164013 | T | C | 146 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0015 others(143): Show |
176 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.411+121T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117164013 | |||||||
chr11:117164033 | G | C | 1 | a0001c0001t0040g0059 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.411+141G>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117164033 | |||||||
chr11:117164136 | T | G | 1 | a0001c0001t0026g0067 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.411+244T>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117164136 | |||||||
chr11:117164145 | C | T | 3 | a0001c0001t0018g0030 a0001c0001t0025g0030 a0001c0001t0025g0117 |
3 | HG02622.hp1 HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.411+253C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117164145 | |||||||
chr11:117164189 | C | T | 6 | a0001c0001t0018g0030 a0001c0001t0018g0116 a0001c0001t0018g0118 others(3): Show |
6 | HG02622.hp1 HG02818.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.411+297C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117164189 | |||||||
chr11:117164223 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.411+331C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117164223 | |||||||
chr11:117164227 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.411+335G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117164227 | |||||||
chr11:117164264 | G | A | 6 | a0001c0001t0002g0042 a0001c0001t0002g0043 a0001c0001t0002g0284 others(3): Show |
7 | HG01255.hp2 HG01346.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.411+372G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117164264 | |||||||
chr11:117164268 | G | A | 8 | a0001c0001t0011g0010 a0001c0001t0011g0029 a0001c0001t0011g0032 others(5): Show |
12 | HG00642.hp2 HG01891.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.411+376G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117164268 | |||||||
chr11:117164279 | C | A | 1 | a0001c0001t0001g0160 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.411+387C>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117164279 | |||||||
chr11:117164300 | G | A | 28 | a0001c0001t0005g0004 a0001c0001t0005g0009 a0001c0001t0005g0017 others(25): Show |
44 | HG00323.hp2 HG00609.hp2 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.411+408G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117164300 | |||||||
chr11:117164360 | T | G | 3 | a0001c0001t0020g0016 a0001c0001t0020g0096 a0001c0001t0045g0100 |
5 | HG01891.hp1 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.411+468T>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117164360 | |||||||
chr11:117164406 | C | CAA | 193 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0015 others(190): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.411+524_411+525dup others(2): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr11 | 117164406 | ||||||
chr11:117164479 | T | C | 1 | a0001c0001t0001g0139 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.411+587T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117164479 | |||||||
chr11:117164494 | G | A | 2 | a0001c0001t0003g0254 a0001c0001t0054g0080 |
2 | HG01934.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.411+602G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117164494 | |||||||
chr11:117164494 | G | T | 1 | a0001c0001t0002g0272 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.411+602G>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117164494 | |||||||
chr11:117164512 | T | C | 5 | a0001c0001t0030g0019 a0001c0001t0030g0109 a0001c0001t0039g0108 others(2): Show |
6 | HG00735.hp1 HG01069.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.411+620T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117164512 | |||||||
chr11:117164517 | T | C | 5 | a0001c0001t0006g0025 a0001c0001t0014g0051 a0001c0001t0014g0065 others(2): Show |
5 | HG01975.hp1 HG01981.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.411+625T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117164517 | |||||||
chr11:117164526 | A | G | 1 | a0001c0001t0019g0235 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.411+634A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117164526 | |||||||
chr11:117164596 | C | A | 1 | a0001c0001t0008g0103 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.411+704C>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117164596 | |||||||
chr11:117164603 | A | G | 23 | a0001c0001t0005g0004 a0001c0001t0005g0009 a0001c0001t0005g0017 others(20): Show |
37 | HG00323.hp2 HG00609.hp2 HG01074.hp2 others(34): Show |
intron_variant | MODIFIER | c.411+711A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117164603 | |||||||
chr11:117164757 | C | T | 2 | a0001c0001t0005g0018 a0001c0001t0005g0027 |
5 | HG00609.hp2 NA18957.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.411+865C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117164757 | |||||||
chr11:117164764 | G | A | 7 | a0001c0001t0015g0031 a0001c0001t0015g0113 a0001c0001t0015g0114 others(4): Show |
8 | HG01243.hp1 HG02886.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.411+872G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117164764 | |||||||
chr11:117164786 | A | G | 92 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0015 others(89): Show |
117 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.411+894A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117164786 | |||||||
chr11:117164807 | G | A | 1 | a0001c0001t0021g0200 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.411+915G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117164807 | |||||||
chr11:117164807 | G | C | 1 | a0001c0001t0002g0042 | 2 | HG01255.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.411+915G>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117164807 | |||||||
chr11:117164808 | G | A | 1 | a0001c0001t0049g0111 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.411+916G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117164808 | |||||||
chr11:117164863 | G | A | 14 | a0001c0001t0006g0026 a0001c0001t0006g0085 a0001c0001t0009g0007 others(11): Show |
17 | HG01978.hp2 NA18612.hp1 NA18943.hp1 others(14): Show |
intron_variant | MODIFIER | c.411+971G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117164863 | |||||||
chr11:117164906 | C | T | 14 | a0001c0001t0007g0008 a0001c0001t0007g0014 a0001c0001t0007g0037 others(11): Show |
21 | HG00280.hp2 HG00597.hp1 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.411+1014C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117164906 | |||||||
chr11:117164935 | C | A | 1 | a0001c0001t0003g0243 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.411+1043C>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117164935 | |||||||
chr11:117164958 | C | CT | 150 | a0001c0001t0001g0148 a0001c0001t0002g0002 a0001c0001t0002g0003 others(147): Show |
181 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.411+1081dupT | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr11 | 117164958 | ||||||
chr11:117164965 | T | C | 1 | a0001c0001t0083g0193 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.411+1073T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117164965 | |||||||
chr11:117165078 | C | T | 1 | a0001c0001t0003g0233 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.411+1186C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117165078 | |||||||
chr11:117165100 | C | T | 41 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0022 others(38): Show |
48 | HG00408.hp1 HG00544.hp1 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.411+1208C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117165100 | |||||||
chr11:117165169 | G | A | 1 | a0001c0001t0006g0085 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.411+1277G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117165169 | |||||||
chr11:117165188 | G | C | 3 | a0001c0001t0028g0124 a0001c0001t0028g0125 a0001c0001t0028g0126 |
3 | HG01074.hp1 HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.411+1296G>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117165188 | |||||||
chr11:117165219 | T | G | 3 | a0001c0001t0028g0124 a0001c0001t0028g0125 a0001c0001t0028g0126 |
3 | HG01074.hp1 HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.411+1327T>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117165219 | |||||||
chr11:117165243 | C | A | 1 | a0001c0001t0078g0205 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.411+1351C>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117165243 | |||||||
chr11:117165248 | G | A | 1 | a0001c0001t0078g0205 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.411+1356G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117165248 | |||||||
chr11:117165349 | CA | C | 217 | a0001c0001t0001g0143 a0001c0001t0001g0146 a0001c0001t0002g0002 others(214): Show |
275 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.411+1473delA | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr11 | 117165349 | ||||||
chr11:117165444 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.411+1552T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117165444 | |||||||
chr11:117165641 | A | G | 1 | a0001c0001t0064g0266 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.411+1749A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117165641 | |||||||
chr11:117165690 | G | A | 1 | a0001c0001t0029g0216 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.412-1731G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117165690 | |||||||
chr11:117165834 | AT | A | 34 | a0001c0001t0001g0033 a0001c0001t0001g0155 a0001c0001t0002g0248 others(31): Show |
50 | HG00323.hp2 HG00609.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.412-1569delT | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr11 | 117165834 | ||||||
chr11:117165872 | C | G | 2 | a0001c0001t0024g0102 a0001c0001t0035g0099 |
2 | HG03017.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.412-1549C>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117165872 | |||||||
chr11:117165997 | C | T | 1 | a0001c0001t0006g0061 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.412-1424C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117165997 | |||||||
chr11:117166089 | C | T | 194 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0015 others(191): Show |
243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.412-1332C>T | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117166089 | |||||||
chr11:117166095 | A | G | 3 | a0001c0001t0028g0124 a0001c0001t0028g0125 a0001c0001t0028g0126 |
3 | HG01074.hp1 HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.412-1326A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117166095 | |||||||
chr11:117166240 | T | A | 7 | a0001c0001t0015g0031 a0001c0001t0015g0113 a0001c0001t0015g0114 others(4): Show |
8 | HG01243.hp1 HG02886.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.412-1181T>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117166240 | |||||||
chr11:117166349 | T | C | 92 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0015 others(89): Show |
117 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.412-1072T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117166349 | |||||||
chr11:117166364 | A | G | 3 | a0001c0001t0028g0124 a0001c0001t0028g0125 a0001c0001t0028g0126 |
3 | HG01074.hp1 HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.412-1057A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117166364 | |||||||
chr11:117166521 | T | C | 1 | a0001c0001t0013g0045 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.412-900T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117166521 | |||||||
chr11:117166549 | T | C | 1 | a0001c0001t0078g0205 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.412-872T>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117166549 | |||||||
chr11:117166569 | G | A | 1 | a0001c0001t0078g0205 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.412-852G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117166569 | |||||||
chr11:117166590 | G | A | 3 | a0001c0001t0020g0016 a0001c0001t0020g0096 a0001c0001t0045g0100 |
5 | HG01891.hp1 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.412-831G>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117166590 | |||||||
chr11:117166645 | A | G | 231 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0015 others(228): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.412-776A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117166645 | |||||||
chr11:117166657 | A | C | 1 | a0001c0001t0001g0173 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.412-764A>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117166657 | |||||||
chr11:117166859 | A | G | 1 | a0001c0001t0001g0170 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.412-562A>G | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117166859 | |||||||
chr11:117167103 | A | C | 3 | a0001c0001t0028g0124 a0001c0001t0028g0125 a0001c0001t0028g0126 |
3 | HG01074.hp1 HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.412-318A>C | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117167103 | |||||||
chr11:117167153 | AAGAGATC others(27): Show |
A | 1 | a0001c0001t0083g0193 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.412-263_412-230del others(34): Show |
PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr11 | 117167153 | ||||||
chr11:117167350 | C | A | 1 | a0001c0001t0072g0203 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.412-71C>A | PAFAH1B2 | ENSG00000168092.14 | transcript | ENST00000527958.6 | protein_coding | 5/5 | chr11 | 117167350 |