Item | Value |
---|---|
geneid | 55035 |
ensemblid | ENSG00000198000.12 |
hgncid | 23387 |
symbol | NOL8 |
name | nucleolar protein 8 |
refseq_nuc | NM_017948.6 |
refseq_prot | NP_060418.4 |
ensembl_nuc | ENST00000442668.7 |
ensembl_prot | ENSP00000401177.2 |
mane_status | MANE Select |
chr | chr9 |
start | 92297358 |
end | 92325350 |
strand | - |
ver | v1.2 |
region | chr9:92297358-92325350 |
region5000 | chr9:92292358-92330350 |
regionname0 | NOL8_chr9_92297358_92325350 |
regionname5000 | NOL8_chr9_92292358_92330350 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1167 | 346 | 71 | 67 | 158 | 13 | 35 | 134 | NOL8_chr9_92292358_92330350 | NOL8 | MKVNR others(1162): Show |
chr9 | 92292358 | 92330350 |
a0002 | 0/0 | 1167 | 22 | 1 | 3 | 13 | 1 | 4 | 11 | NOL8_chr9_92292358_92330350 | NOL8 | MKVNR others(1162): Show |
chr9 | 92292358 | 92330350 |
a0003 | 0/0 | 1167 | 12 | 10 | 2 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | MKVNR others(1162): Show |
chr9 | 92292358 | 92330350 |
a0004 | 0/0 | 1167 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | MKVNR others(1162): Show |
chr9 | 92292358 | 92330350 |
a0005 | 0/0 | 1167 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | NOL8_chr9_92292358_92330350 | NOL8 | MKVNR others(1162): Show |
chr9 | 92292358 | 92330350 |
a0006 | 0/0 | 1167 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | MKVNR others(1162): Show |
chr9 | 92292358 | 92330350 |
a0007 | 0/0 | 1167 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | MKVNR others(1162): Show |
chr9 | 92292358 | 92330350 |
a0008 | 0/0 | 1167 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | MKVNR others(1162): Show |
chr9 | 92292358 | 92330350 |
a0009 | 0/0 | 1167 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | MKVNR others(1162): Show |
chr9 | 92292358 | 92330350 |
a0010 | 0/0 | 1167 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | MKVNR others(1162): Show |
chr9 | 92292358 | 92330350 |
a0011 | 0/0 | 1167 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | MKVNR others(1162): Show |
chr9 | 92292358 | 92330350 |
a0012 | 0/0 | 1167 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | MKVNR others(1162): Show |
chr9 | 92292358 | 92330350 |
a0013 | 0/0 | 1167 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | MKVNR others(1162): Show |
chr9 | 92292358 | 92330350 |
a0014 | 0/0 | 1167 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | MKVNR others(1162): Show |
chr9 | 92292358 | 92330350 |
a0015 | 0/0 | 1167 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | MKVNR others(1162): Show |
chr9 | 92292358 | 92330350 |
a0016 | 0/0 | 1167 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | MKVNR others(1162): Show |
chr9 | 92292358 | 92330350 |
a0017 | 0/0 | 1167 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NOL8_chr9_92292358_92330350 | NOL8 | MKVNR others(1162): Show |
chr9 | 92292358 | 92330350 |
a0018 | 0/0 | 1167 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NOL8_chr9_92292358_92330350 | NOL8 | MKVNR others(1162): Show |
chr9 | 92292358 | 92330350 |
a0019 | 0/0 | 1167 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NOL8_chr9_92292358_92330350 | NOL8 | MKVNR others(1162): Show |
chr9 | 92292358 | 92330350 |
a0020 | 0/0 | 1167 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | MKVNR others(1162): Show |
chr9 | 92292358 | 92330350 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 3501 | 220 | 12 | 52 | 122 | 8 | 24 | NOL8_chr9_92292358_92330350 | NOL8 | ATGAA others(3496): Show |
chr9 | 92292358 | 92330350 | ||
a0001c0002 | 0/0 | 3501 | 124 | 58 | 15 | 35 | 5 | 11 | NOL8_chr9_92292358_92330350 | NOL8 | ATGAA others(3496): Show |
chr9 | 92292358 | 92330350 | ||
a0001c0013 | 0/0 | 3501 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | ATGAA others(3496): Show |
chr9 | 92292358 | 92330350 | ||
a0001c0014 | 0/0 | 3501 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | ATGAA others(3496): Show |
chr9 | 92292358 | 92330350 | ||
a0002c0003 | 0/0 | 3501 | 22 | 1 | 3 | 13 | 1 | 4 | NOL8_chr9_92292358_92330350 | NOL8 | ATGAA others(3496): Show |
chr9 | 92292358 | 92330350 | ||
a0003c0004 | 0/0 | 3501 | 12 | 10 | 2 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | ATGAA others(3496): Show |
chr9 | 92292358 | 92330350 | ||
a0004c0005 | 0/0 | 3501 | 5 | 5 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | ATGAA others(3496): Show |
chr9 | 92292358 | 92330350 | ||
a0005c0006 | 0/0 | 3501 | 3 | 0 | 0 | 3 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | ATGAA others(3496): Show |
chr9 | 92292358 | 92330350 | ||
a0006c0007 | 0/0 | 3501 | 2 | 0 | 1 | 0 | 0 | 1 | NOL8_chr9_92292358_92330350 | NOL8 | ATGAA others(3496): Show |
chr9 | 92292358 | 92330350 | ||
a0007c0008 | 0/0 | 3501 | 2 | 0 | 0 | 0 | 2 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | ATGAA others(3496): Show |
chr9 | 92292358 | 92330350 | ||
a0008c0009 | 0/0 | 3501 | 2 | 0 | 0 | 0 | 2 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | ATGAA others(3496): Show |
chr9 | 92292358 | 92330350 | ||
a0009c0018 | 0/0 | 3501 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | ATGAA others(3496): Show |
chr9 | 92292358 | 92330350 | ||
a0009c0020 | 0/0 | 3501 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | ATGAA others(3496): Show |
chr9 | 92292358 | 92330350 | ||
a0010c0010 | 0/0 | 3501 | 2 | 2 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | ATGAA others(3496): Show |
chr9 | 92292358 | 92330350 | ||
a0011c0016 | 0/0 | 3501 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | ATGAA others(3496): Show |
chr9 | 92292358 | 92330350 | ||
a0012c0023 | 0/0 | 3501 | 1 | 0 | 1 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | ATGAA others(3496): Show |
chr9 | 92292358 | 92330350 | ||
a0013c0021 | 0/0 | 3501 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | ATGAA others(3496): Show |
chr9 | 92292358 | 92330350 | ||
a0014c0022 | 0/0 | 3501 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | ATGAA others(3496): Show |
chr9 | 92292358 | 92330350 | ||
a0015c0012 | 0/0 | 3501 | 1 | 0 | 0 | 0 | 0 | 1 | NOL8_chr9_92292358_92330350 | NOL8 | ATGAA others(3496): Show |
chr9 | 92292358 | 92330350 | ||
a0016c0011 | 0/0 | 3501 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | ATGAA others(3496): Show |
chr9 | 92292358 | 92330350 | ||
a0017c0024 | 0/0 | 3501 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | ATGAA others(3496): Show |
chr9 | 92292358 | 92330350 | ||
a0018c0017 | 0/0 | 3501 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | ATGAA others(3496): Show |
chr9 | 92292358 | 92330350 | ||
a0019c0019 | 0/0 | 3501 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | ATGAA others(3496): Show |
chr9 | 92292358 | 92330350 | ||
a0020c0015 | 0/0 | 3501 | 1 | 0 | 0 | 0 | 0 | 1 | NOL8_chr9_92292358_92330350 | NOL8 | ATGAA others(3496): Show |
chr9 | 92292358 | 92330350 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/0 | 4075 | 122 | 11 | 29 | 62 | 4 | 16 | NOL8_chr9_92292358_92330350 | NOL8 | AGAAG others(4070): Show |
chr9 | 92292358 | 92330350 |
a0001c0001t0003 | 1/1 | 4075 | 98 | 1 | 23 | 60 | 4 | 8 | NOL8_chr9_92292358_92330350 | NOL8 | AGAAG others(4070): Show |
chr9 | 92292358 | 92330350 |
a0001c0002t0001 | 0/0 | 4075 | 119 | 54 | 14 | 35 | 5 | 11 | NOL8_chr9_92292358_92330350 | NOL8 | AGAAG others(4070): Show |
chr9 | 92292358 | 92330350 |
a0001c0002t0002 | 0/0 | 4075 | 2 | 2 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | AGAAG others(4070): Show |
chr9 | 92292358 | 92330350 |
a0001c0002t0005 | 0/0 | 4075 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | AGAAG others(4070): Show |
chr9 | 92292358 | 92330350 |
a0001c0002t0006 | 0/0 | 4075 | 1 | 0 | 1 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | AGAAG others(4070): Show |
chr9 | 92292358 | 92330350 |
a0001c0002t0007 | 0/0 | 4075 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | AGAAG others(4070): Show |
chr9 | 92292358 | 92330350 |
a0001c0013t0001 | 0/0 | 4075 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | AGAAG others(4070): Show |
chr9 | 92292358 | 92330350 |
a0001c0014t0003 | 0/0 | 4075 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | AGAAG others(4070): Show |
chr9 | 92292358 | 92330350 |
a0002c0003t0004 | 0/0 | 4075 | 22 | 1 | 3 | 13 | 1 | 4 | NOL8_chr9_92292358_92330350 | NOL8 | AGAAG others(4070): Show |
chr9 | 92292358 | 92330350 |
a0003c0004t0001 | 0/0 | 4075 | 12 | 10 | 2 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | AGAAG others(4070): Show |
chr9 | 92292358 | 92330350 |
a0004c0005t0001 | 0/0 | 4075 | 5 | 5 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | AGAAG others(4070): Show |
chr9 | 92292358 | 92330350 |
a0005c0006t0003 | 0/0 | 4075 | 3 | 0 | 0 | 3 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | AGAAG others(4070): Show |
chr9 | 92292358 | 92330350 |
a0006c0007t0001 | 0/0 | 4075 | 2 | 0 | 1 | 0 | 0 | 1 | NOL8_chr9_92292358_92330350 | NOL8 | AGAAG others(4070): Show |
chr9 | 92292358 | 92330350 |
a0007c0008t0002 | 0/0 | 4075 | 2 | 0 | 0 | 0 | 2 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | AGAAG others(4070): Show |
chr9 | 92292358 | 92330350 |
a0008c0009t0001 | 0/0 | 4075 | 2 | 0 | 0 | 0 | 2 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | AGAAG others(4070): Show |
chr9 | 92292358 | 92330350 |
a0009c0018t0001 | 0/0 | 4075 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | AGAAG others(4070): Show |
chr9 | 92292358 | 92330350 |
a0009c0020t0001 | 0/0 | 4075 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | AGAAG others(4070): Show |
chr9 | 92292358 | 92330350 |
a0010c0010t0001 | 0/0 | 4075 | 2 | 2 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | AGAAG others(4070): Show |
chr9 | 92292358 | 92330350 |
a0011c0016t0002 | 0/0 | 4075 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | AGAAG others(4070): Show |
chr9 | 92292358 | 92330350 |
a0012c0023t0004 | 0/0 | 4075 | 1 | 0 | 1 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | AGAAG others(4070): Show |
chr9 | 92292358 | 92330350 |
a0013c0021t0005 | 0/0 | 4075 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | AGAAG others(4070): Show |
chr9 | 92292358 | 92330350 |
a0014c0022t0001 | 0/0 | 4075 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | AGAAG others(4070): Show |
chr9 | 92292358 | 92330350 |
a0015c0012t0003 | 0/0 | 4075 | 1 | 0 | 0 | 0 | 0 | 1 | NOL8_chr9_92292358_92330350 | NOL8 | AGAAG others(4070): Show |
chr9 | 92292358 | 92330350 |
a0016c0011t0002 | 0/0 | 4075 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | AGAAG others(4070): Show |
chr9 | 92292358 | 92330350 |
a0017c0024t0001 | 0/0 | 4075 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | AGAAG others(4070): Show |
chr9 | 92292358 | 92330350 |
a0018c0017t0001 | 0/0 | 4075 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | AGAAG others(4070): Show |
chr9 | 92292358 | 92330350 |
a0019c0019t0001 | 0/0 | 4075 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | AGAAG others(4070): Show |
chr9 | 92292358 | 92330350 |
a0020c0015t0003 | 0/0 | 4075 | 1 | 0 | 0 | 0 | 0 | 1 | NOL8_chr9_92292358_92330350 | NOL8 | AGAAG others(4070): Show |
chr9 | 92292358 | 92330350 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0001 | 0/0 | 32 | 2 | 12 | 18 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0004 | 0/0 | 18 | 0 | 8 | 5 | 2 | 3 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0006 | 0/0 | 8 | 0 | 1 | 3 | 0 | 4 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0017 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0019 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0020 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0045 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0046 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0003g0002 | 1/1 | 24 | 1 | 9 | 7 | 0 | 5 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0003g0005 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0003g0007 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0003g0018 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0003g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0003g0032 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0003g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0003g0034 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0003g0036 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0003g0037 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0003g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0003g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0003g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0003g0058 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0003g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0001t0003g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0003 | 0/0 | 19 | 0 | 0 | 19 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0008 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0009 | 0/0 | 6 | 3 | 0 | 1 | 1 | 1 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0010 | 0/0 | 5 | 2 | 1 | 0 | 2 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0014 | 0/0 | 4 | 3 | 0 | 0 | 0 | 1 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0022 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0023 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0026 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0028 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0053 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0054 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0002g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0005g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0006g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0002t0007g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0013t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0001c0014t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0002c0003t0004g0015 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0002c0003t0004g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0002c0003t0004g0030 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0002c0003t0004g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0002c0003t0004g0056 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0002c0003t0004g0057 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0002c0003t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0002c0003t0004g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0002c0003t0004g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0002c0003t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0002c0003t0004g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0002c0003t0004g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0003c0004t0001g0011 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0003c0004t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0003c0004t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0003c0004t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0003c0004t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0003c0004t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0004c0005t0001g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0004c0005t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0005c0006t0003g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0005c0006t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0006c0007t0001g0050 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0007c0008t0002g0044 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0008c0009t0001g0052 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0009c0018t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0009c0020t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0010c0010t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0010c0010t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0011c0016t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0012c0023t0004g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0013c0021t0005g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0014c0022t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0015c0012t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0016c0011t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0017c0024t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0018c0017t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0019c0019t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
a0020c0015t0003g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0001 | g0009 | EUR | GBR | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0037 | EUR | GBR | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG00140 | hp1 | a0001 | c0001 | t0003 | g0036 | EUR | GBR | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG00140 | hp2 | a0001 | c0002 | t0001 | g0028 | EUR | GBR | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0032 | EUR | FIN | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG00280 | hp2 | a0002 | c0003 | t0004 | g0198 | EUR | FIN | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0098 | EUR | FIN | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG00323 | hp2 | a0001 | c0002 | t0001 | g0010 | EUR | FIN | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | CHS | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG00408 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | CHS | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | CHS | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG00423 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | CHS | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG00438 | hp1 | a0005 | c0006 | t0003 | g0106 | EAS | CHS | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | CHS | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | CHS | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG00558 | hp2 | a0011 | c0016 | t0002 | g0083 | EAS | CHS | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG00597 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | CHS | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | CHS | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0036 | AMR | PUR | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0054 | AMR | PUR | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG00642 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG00642 | hp2 | a0012 | c0023 | t0004 | g0196 | AMR | PUR | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG00673 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | CHS | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG00673 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | CHS | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0135 | AMR | PUR | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG00735 | hp2 | a0001 | c0002 | t0001 | g0023 | AMR | PUR | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0117 | AMR | PUR | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0034 | AMR | PUR | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0133 | AMR | PUR | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01074 | hp1 | a0006 | c0007 | t0001 | g0050 | AMR | PUR | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01081 | hp1 | a0001 | c0002 | t0001 | g0203 | AMR | PUR | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01081 | hp2 | a0003 | c0004 | t0001 | g0146 | AMR | PUR | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01099 | hp1 | a0001 | c0002 | t0001 | g0023 | AMR | PUR | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0090 | AMR | PUR | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01106 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0103 | AMR | PUR | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | PUR | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01109 | hp2 | a0001 | c0002 | t0001 | g0159 | AMR | PUR | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01167 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01168 | hp1 | a0001 | c0002 | t0001 | g0023 | AMR | PUR | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01168 | hp2 | a0002 | c0003 | t0004 | g0015 | AMR | PUR | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01169 | hp2 | a0002 | c0003 | t0004 | g0015 | AMR | PUR | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01243 | hp2 | a0001 | c0002 | t0006 | g0188 | AMR | PUR | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01255 | hp1 | a0003 | c0004 | t0001 | g0011 | AMR | CLM | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0194 | AMR | CLM | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0033 | AMR | CLM | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01257 | hp2 | a0001 | c0002 | t0001 | g0010 | AMR | CLM | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01258 | hp2 | a0001 | c0001 | t0003 | g0033 | AMR | CLM | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0091 | AMR | CLM | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01346 | hp1 | a0001 | c0001 | t0003 | g0137 | AMR | CLM | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01346 | hp2 | a0002 | c0003 | t0004 | g0015 | AMR | CLM | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01358 | hp2 | a0001 | c0002 | t0001 | g0049 | AMR | CLM | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0136 | AMR | CLM | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0153 | AMR | CLM | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0180 | AMR | CLM | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01515 | hp1 | a0001 | c0002 | t0001 | g0191 | EUR | IBS | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01515 | hp2 | a0007 | c0008 | t0002 | g0044 | EUR | IBS | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01516 | hp1 | a0008 | c0009 | t0001 | g0052 | EUR | IBS | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01516 | hp2 | a0001 | c0002 | t0001 | g0010 | EUR | IBS | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01517 | hp1 | a0008 | c0009 | t0001 | g0052 | EUR | IBS | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01517 | hp2 | a0007 | c0008 | t0002 | g0044 | EUR | IBS | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01884 | hp1 | a0013 | c0021 | t0005 | g0208 | AFR | ACB | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01884 | hp2 | a0001 | c0002 | t0001 | g0014 | AFR | ACB | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01928 | hp1 | a0001 | c0001 | t0003 | g0139 | AMR | PEL | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0087 | AMR | PEL | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01943 | hp1 | a0001 | c0002 | t0001 | g0028 | AMR | PEL | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | PEL | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0032 | AMR | PEL | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0062 | AMR | PEL | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01975 | hp2 | a0001 | c0002 | t0001 | g0028 | AMR | PEL | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01978 | hp1 | a0001 | c0001 | t0003 | g0138 | AMR | PEL | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | KHV | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02015 | hp2 | a0002 | c0003 | t0004 | g0195 | EAS | KHV | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | KHV | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0105 | EAS | KHV | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | ACB | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02055 | hp2 | a0001 | c0002 | t0002 | g0047 | AFR | ACB | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0089 | EAS | KHV | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | KHV | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | KHV | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | KHV | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | KHV | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | KHV | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02145 | hp1 | a0004 | c0005 | t0001 | g0164 | AFR | ACB | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02145 | hp2 | a0001 | c0002 | t0007 | g0207 | AFR | ACB | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02165 | hp1 | a0002 | c0003 | t0004 | g0030 | EAS | CDX | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | CDX | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02257 | hp1 | a0003 | c0004 | t0001 | g0031 | AFR | ACB | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02257 | hp2 | a0001 | c0002 | t0002 | g0047 | AFR | ACB | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02258 | hp1 | a0001 | c0002 | t0001 | g0170 | AFR | ACB | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02258 | hp2 | a0001 | c0002 | t0001 | g0161 | AFR | ACB | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0080 | AMR | PEL | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0097 | AMR | PEL | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02300 | hp2 | a0001 | c0002 | t0001 | g0049 | AMR | PEL | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02451 | hp1 | a0001 | c0002 | t0001 | g0008 | AFR | ACB | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02451 | hp2 | a0001 | c0002 | t0001 | g0026 | AFR | ACB | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02572 | hp1 | a0001 | c0002 | t0001 | g0152 | AFR | GWD | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02572 | hp2 | a0001 | c0002 | t0001 | g0025 | AFR | GWD | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0205 | SAS | PJL | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02615 | hp1 | a0001 | c0002 | t0001 | g0160 | AFR | GWD | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0113 | AFR | GWD | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02622 | hp1 | a0001 | c0002 | t0001 | g0059 | AFR | GWD | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02622 | hp2 | a0001 | c0002 | t0001 | g0171 | AFR | GWD | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02630 | hp1 | a0001 | c0002 | t0001 | g0027 | AFR | GWD | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02630 | hp2 | a0003 | c0004 | t0001 | g0065 | AFR | GWD | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02647 | hp1 | a0001 | c0002 | t0001 | g0025 | AFR | GWD | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02647 | hp2 | a0001 | c0002 | t0001 | g0192 | AFR | GWD | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02698 | hp1 | a0001 | c0002 | t0001 | g0189 | SAS | PJL | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02717 | hp1 | a0004 | c0005 | t0001 | g0012 | AFR | GWD | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02717 | hp2 | a0001 | c0002 | t0001 | g0182 | AFR | GWD | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02723 | hp2 | a0001 | c0002 | t0001 | g0027 | AFR | GWD | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02735 | hp2 | a0001 | c0002 | t0001 | g0053 | SAS | PJL | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02738 | hp2 | a0001 | c0001 | t0003 | g0018 | SAS | PJL | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02809 | hp1 | a0009 | c0020 | t0001 | g0163 | AFR | GWD | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02809 | hp2 | a0001 | c0002 | t0001 | g0066 | AFR | GWD | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02818 | hp1 | a0014 | c0022 | t0001 | g0167 | AFR | GWD | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02818 | hp2 | a0003 | c0004 | t0001 | g0031 | AFR | GWD | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02886 | hp1 | a0001 | c0002 | t0001 | g0061 | AFR | GWD | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0112 | AFR | GWD | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02895 | hp1 | a0001 | c0002 | t0001 | g0183 | AFR | GWD | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02895 | hp2 | a0001 | c0002 | t0001 | g0169 | AFR | GWD | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02896 | hp1 | a0004 | c0005 | t0001 | g0012 | AFR | GWD | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02896 | hp2 | a0001 | c0002 | t0001 | g0024 | AFR | GWD | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02897 | hp1 | a0001 | c0002 | t0001 | g0157 | AFR | GWD | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02897 | hp2 | a0004 | c0005 | t0001 | g0012 | AFR | GWD | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02922 | hp1 | a0001 | c0002 | t0001 | g0010 | AFR | ESN | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02922 | hp2 | a0001 | c0002 | t0001 | g0014 | AFR | ESN | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02965 | hp1 | a0001 | c0002 | t0001 | g0149 | AFR | ESN | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02965 | hp2 | a0001 | c0002 | t0001 | g0168 | AFR | ESN | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02970 | hp1 | a0003 | c0004 | t0001 | g0011 | AFR | ESN | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02970 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | ESN | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02976 | hp1 | a0001 | c0002 | t0001 | g0024 | AFR | ESN | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02976 | hp2 | a0010 | c0010 | t0001 | g0145 | AFR | ESN | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG03017 | hp1 | a0015 | c0012 | t0003 | g0107 | SAS | PJL | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG03041 | hp1 | a0001 | c0002 | t0001 | g0008 | AFR | GWD | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG03041 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | GWD | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG03098 | hp1 | a0001 | c0002 | t0001 | g0172 | AFR | MSL | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG03098 | hp2 | a0001 | c0013 | t0001 | g0156 | AFR | MSL | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG03130 | hp1 | a0001 | c0002 | t0001 | g0024 | AFR | ESN | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG03130 | hp2 | a0009 | c0018 | t0001 | g0141 | AFR | ESN | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG03139 | hp1 | a0001 | c0002 | t0001 | g0008 | AFR | ESN | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG03139 | hp2 | a0001 | c0002 | t0001 | g0142 | AFR | ESN | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG03195 | hp1 | a0003 | c0004 | t0001 | g0016 | AFR | ESN | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG03195 | hp2 | a0003 | c0004 | t0001 | g0011 | AFR | ESN | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG03209 | hp1 | a0001 | c0002 | t0001 | g0060 | AFR | MSL | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | MSL | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG03225 | hp1 | a0001 | c0002 | t0001 | g0008 | AFR | MSL | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG03225 | hp2 | a0016 | c0011 | t0002 | g0111 | AFR | MSL | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0081 | SAS | PJL | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG03453 | hp1 | a0001 | c0002 | t0001 | g0009 | AFR | MSL | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | MSL | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG03490 | hp1 | a0001 | c0001 | t0003 | g0068 | SAS | PJL | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG03490 | hp2 | a0001 | c0002 | t0001 | g0022 | SAS | PJL | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0022 | SAS | PJL | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG03516 | hp1 | a0001 | c0002 | t0001 | g0166 | AFR | ESN | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG03516 | hp2 | a0001 | c0002 | t0001 | g0014 | AFR | ESN | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG03540 | hp1 | a0001 | c0002 | t0001 | g0202 | AFR | GWD | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG03540 | hp2 | a0001 | c0002 | t0001 | g0185 | AFR | GWD | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG03579 | hp1 | a0001 | c0002 | t0001 | g0026 | AFR | MSL | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG03579 | hp2 | a0001 | c0002 | t0001 | g0025 | AFR | MSL | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG03688 | hp1 | a0001 | c0002 | t0001 | g0190 | SAS | STU | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0129 | SAS | STU | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0094 | SAS | PJL | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG03704 | hp2 | a0006 | c0007 | t0001 | g0050 | SAS | PJL | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG03710 | hp2 | a0002 | c0003 | t0004 | g0015 | SAS | PJL | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG03831 | hp1 | a0002 | c0003 | t0004 | g0056 | SAS | BEB | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | BEB | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0045 | SAS | BEB | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0009 | SAS | BEB | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG03927 | hp1 | a0001 | c0002 | t0001 | g0054 | SAS | BEB | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0099 | SAS | BEB | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | BEB | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG03942 | hp2 | a0002 | c0003 | t0004 | g0200 | SAS | BEB | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG04115 | hp1 | a0002 | c0003 | t0004 | g0201 | SAS | STU | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG04115 | hp2 | a0001 | c0002 | t0001 | g0022 | SAS | STU | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0053 | SAS | BEB | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | BEB | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG04199 | hp1 | a0001 | c0002 | t0001 | g0014 | SAS | STU | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG04199 | hp2 | a0001 | c0002 | t0001 | g0181 | SAS | STU | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | STU | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0118 | SAS | STU | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG04228 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | STU | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0067 | SAS | STU | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18522 | hp1 | a0001 | c0002 | t0001 | g0027 | AFR | YRI | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0043 | AFR | YRI | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0043 | AFR | YRI | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18906 | hp2 | a0003 | c0004 | t0001 | g0016 | AFR | YRI | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18939 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18939 | hp2 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18940 | hp2 | a0001 | c0002 | t0001 | g0177 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18942 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18943 | hp2 | a0001 | c0002 | t0001 | g0165 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18944 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18944 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18946 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18947 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18950 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18950 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18951 | hp1 | a0002 | c0003 | t0004 | g0199 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18951 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18952 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18956 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18956 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18957 | hp1 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18957 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18959 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18961 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18961 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18962 | hp1 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18962 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18963 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18963 | hp2 | a0002 | c0003 | t0004 | g0029 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18964 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18964 | hp2 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18965 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18966 | hp1 | a0017 | c0024 | t0001 | g0204 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18968 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18968 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18969 | hp2 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18972 | hp2 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18973 | hp2 | a0002 | c0003 | t0004 | g0057 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18975 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18977 | hp2 | a0001 | c0002 | t0001 | g0155 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18979 | hp2 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18980 | hp1 | a0002 | c0003 | t0004 | g0030 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0123 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18981 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18984 | hp1 | a0002 | c0003 | t0004 | g0029 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18984 | hp2 | a0001 | c0001 | t0003 | g0132 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18985 | hp2 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18986 | hp1 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18986 | hp2 | a0001 | c0014 | t0003 | g0078 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18990 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18992 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18992 | hp2 | a0005 | c0006 | t0003 | g0040 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18993 | hp1 | a0002 | c0003 | t0004 | g0029 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18993 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18994 | hp2 | a0001 | c0002 | t0001 | g0174 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18995 | hp2 | a0002 | c0003 | t0004 | g0030 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18997 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18997 | hp2 | a0001 | c0002 | t0001 | g0176 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19000 | hp1 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19000 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19001 | hp1 | a0005 | c0006 | t0003 | g0040 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19001 | hp2 | a0002 | c0003 | t0004 | g0197 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19003 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19005 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19007 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19007 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19009 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19011 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19012 | hp2 | a0018 | c0017 | t0001 | g0154 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19030 | hp1 | a0001 | c0002 | t0001 | g0151 | AFR | LWK | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19030 | hp2 | a0003 | c0004 | t0001 | g0064 | AFR | LWK | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19043 | hp1 | a0001 | c0002 | t0005 | g0209 | AFR | LWK | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19043 | hp2 | a0001 | c0002 | t0001 | g0186 | AFR | LWK | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19054 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19054 | hp2 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19055 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19055 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19056 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19056 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19058 | hp1 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19058 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19062 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19062 | hp2 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19063 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19064 | hp1 | a0019 | c0019 | t0001 | g0175 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19066 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19068 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19070 | hp2 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19075 | hp1 | a0002 | c0003 | t0004 | g0055 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19075 | hp2 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19076 | hp1 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19076 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19078 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19078 | hp2 | a0002 | c0003 | t0004 | g0057 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19079 | hp2 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19083 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19084 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19087 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19087 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19089 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19089 | hp2 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19091 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19091 | hp2 | a0002 | c0003 | t0004 | g0055 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19240 | hp1 | a0003 | c0004 | t0001 | g0011 | AFR | YRI | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA19240 | hp2 | a0010 | c0010 | t0001 | g0144 | AFR | YRI | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA20129 | hp1 | a0001 | c0002 | t0001 | g0009 | AFR | ASW | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | ASW | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0114 | EUR | TSI | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0004 | EUR | TSI | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0084 | EUR | TSI | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0004 | EUR | TSI | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA20905 | hp1 | a0020 | c0015 | t0003 | g0082 | SAS | GIH | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0019 | SAS | GIH | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02109 | hp1 | a0001 | c0002 | t0001 | g0193 | AFR | ACB | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02109 | hp2 | a0001 | c0002 | t0001 | g0158 | AFR | ACB | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02486 | hp1 | a0003 | c0004 | t0001 | g0016 | AFR | ACB | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02486 | hp2 | a0002 | c0003 | t0004 | g0056 | AFR | ACB | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0130 | AFR | ACB | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0148 | AFR | ACB | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG03471 | hp1 | a0001 | c0002 | t0001 | g0150 | AFR | MSL | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG03471 | hp2 | a0001 | c0002 | t0001 | g0187 | AFR | MSL | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG06807 | hp1 | a0001 | c0002 | t0001 | g0010 | AFR | USA | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
HG06807 | hp2 | a0004 | c0005 | t0001 | g0012 | AFR | USA | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18955 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA20300 | hp1 | a0001 | c0002 | t0001 | g0008 | AFR | USA | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | USA | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA21309 | hp1 | a0001 | c0002 | t0001 | g0162 | AFR | LWK | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
NA21309 | hp2 | a0001 | c0002 | t0001 | g0184 | AFR | LWK | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0002 | REF | REF | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0002 | REF | REF | NOL8_chr9_92292358_92330350 | NOL8 | chr9 | 92292358 | 92330350 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:92299996 | C | T | 1 | a0004 | 5 | HG02145.hp1 HG02717.hp1 HG02896.hp1 others(2): Show |
missense_variant | MODERATE | c.3196G>A | p.Val1066Met | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 14/17 | 3289/4075 | 3196/3504 | 1066/1167 | chr9 | 92299996 | |||
chr9:92301599 | C | T | 1 | a0019 | 1 | NA19064.hp1 | missense_variant | MODERATE | c.3127G>A | p.Gly1043Arg | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 13/17 | 3220/4075 | 3127/3504 | 1043/1167 | chr9 | 92301599 | |||
chr9:92301665 | C | T | 2 | a0002 a0012 |
23 | HG00280.hp2 HG00642.hp2 HG01168.hp2 others(20): Show |
missense_variant | MODERATE | c.3061G>A | p.Gly1021Ser | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 13/17 | 3154/4075 | 3061/3504 | 1021/1167 | chr9 | 92301665 | |||
chr9:92301762 | T | G | 1 | a0010 | 2 | HG02976.hp2 NA19240.hp2 |
missense_variant | MODERATE | c.2964A>C | p.Glu988Asp | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 13/17 | 3057/4075 | 2964/3504 | 988/1167 | chr9 | 92301762 | |||
chr9:92310218 | C | T | 1 | a0009 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.2639G>A | p.Arg880His | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 10/17 | 2732/4075 | 2639/3504 | 880/1167 | chr9 | 92310218 | |||
chr9:92310219 | G | A | 1 | a0009 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.2638C>T | p.Arg880Cys | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 10/17 | 2731/4075 | 2638/3504 | 880/1167 | chr9 | 92310219 | |||
chr9:92310625 | G | C | 4 | a0002 a0003 a0010 others(1): Show |
37 | HG00280.hp2 HG00642.hp2 HG01081.hp2 others(34): Show |
missense_variant | MODERATE | c.2523C>G | p.Asp841Glu | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 9/17 | 2616/4075 | 2523/3504 | 841/1167 | chr9 | 92310625 | |||
chr9:92314383 | C | G | 4 | a0002 a0003 a0010 others(1): Show |
37 | HG00280.hp2 HG00642.hp2 HG01081.hp2 others(34): Show |
missense_variant | MODERATE | c.2242G>C | p.Val748Leu | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 7/17 | 2335/4075 | 2242/3504 | 748/1167 | chr9 | 92314383 | |||
chr9:92314718 | G | A | 2 | a0013 a0014 |
2 | HG01884.hp1 HG02818.hp1 |
missense_variant | MODERATE | c.1907C>T | p.Ala636Val | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 7/17 | 2000/4075 | 1907/3504 | 636/1167 | chr9 | 92314718 | |||
chr9:92314844 | G | A | 1 | a0005 | 3 | HG00438.hp1 NA18992.hp2 NA19001.hp1 |
missense_variant | MODERATE | c.1781C>T | p.Ala594Val | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 7/17 | 1874/4075 | 1781/3504 | 594/1167 | chr9 | 92314844 | |||
chr9:92314858 | C | G | 1 | a0018 | 1 | NA19012.hp2 | missense_variant | MODERATE | c.1767G>C | p.Leu589Phe | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 7/17 | 1860/4075 | 1767/3504 | 589/1167 | chr9 | 92314858 | |||
chr9:92314938 | C | T | 1 | a0011 | 1 | HG00558.hp2 | missense_variant | MODERATE | c.1687G>A | p.Glu563Lys | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 7/17 | 1780/4075 | 1687/3504 | 563/1167 | chr9 | 92314938 | |||
chr9:92315188 | T | A | 1 | a0002 | 22 | HG00280.hp2 HG01168.hp2 HG01169.hp2 others(19): Show |
missense_variant | MODERATE | c.1437A>T | p.Lys479Asn | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 7/17 | 1530/4075 | 1437/3504 | 479/1167 | chr9 | 92315188 | |||
chr9:92315216 | C | T | 2 | a0003 a0010 |
14 | HG01081.hp2 HG01255.hp1 HG02257.hp1 others(11): Show |
missense_variant | MODERATE | c.1409G>A | p.Gly470Glu | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 7/17 | 1502/4075 | 1409/3504 | 470/1167 | chr9 | 92315216 | |||
chr9:92315406 | T | C | 1 | a0014 | 1 | HG02818.hp1 | missense_variant | MODERATE | c.1219A>G | p.Thr407Ala | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 7/17 | 1312/4075 | 1219/3504 | 407/1167 | chr9 | 92315406 | |||
chr9:92315409 | A | G | 1 | a0020 | 1 | NA20905.hp1 | missense_variant | MODERATE | c.1216T>C | p.Ser406Pro | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 7/17 | 1309/4075 | 1216/3504 | 406/1167 | chr9 | 92315409 | |||
chr9:92315687 | G | A | 1 | a0007 | 2 | HG01515.hp2 HG01517.hp2 |
missense_variant | MODERATE | c.938C>T | p.Ala313Val | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 7/17 | 1031/4075 | 938/3504 | 313/1167 | chr9 | 92315687 | |||
chr9:92315784 | G | T | 1 | a0015 | 1 | HG03017.hp1 | missense_variant | MODERATE | c.841C>A | p.Leu281Ile | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 7/17 | 934/4075 | 841/3504 | 281/1167 | chr9 | 92315784 | |||
chr9:92315810 | A | G | 1 | a0016 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.815T>C | p.Val272Ala | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 7/17 | 908/4075 | 815/3504 | 272/1167 | chr9 | 92315810 | |||
chr9:92316131 | T | C | 1 | a0008 | 2 | HG01516.hp1 HG01517.hp1 |
missense_variant | MODERATE | c.494A>G | p.Lys165Arg | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 7/17 | 587/4075 | 494/3504 | 165/1167 | chr9 | 92316131 | |||
chr9:92318622 | C | T | 1 | a0006 | 2 | HG01074.hp1 HG03704.hp2 |
missense_variant | MODERATE | c.482G>A | p.Arg161His | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 6/17 | 575/4075 | 482/3504 | 161/1167 | chr9 | 92318622 | |||
chr9:92324092 | G | C | 1 | a0017 | 1 | NA18966.hp1 | missense_variant | MODERATE | c.70C>G | p.Leu24Val | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 2/17 | 163/4075 | 70/3504 | 24/1167 | chr9 | 92324092 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:92305764 | C | T | 16 | a0001c0002 a0001c0013 a0002c0003 others(13): Show |
178 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(175): Show |
synonymous_variant | LOW | c.2892G>A | p.Lys964Lys | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 12/17 | 2985/4075 | 2892/3504 | 964/1167 | chr9 | 92305764 | |||
chr9:92315467 | C | T | 1 | a0001c0014 | 1 | NA18986.hp2 | synonymous_variant | LOW | c.1158G>A | p.Ala386Ala | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 7/17 | 1251/4075 | 1158/3504 | 386/1167 | chr9 | 92315467 | |||
chr9:92315545 | G | A | 2 | a0002c0003 a0012c0023 |
23 | HG00280.hp2 HG00642.hp2 HG01168.hp2 others(20): Show |
synonymous_variant | LOW | c.1080C>T | p.Val360Val | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 7/17 | 1173/4075 | 1080/3504 | 360/1167 | chr9 | 92315545 | |||
chr9:92315686 | C | T | 1 | a0001c0013 | 1 | HG03098.hp2 | synonymous_variant | LOW | c.939G>A | p.Ala313Ala | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 7/17 | 1032/4075 | 939/3504 | 313/1167 | chr9 | 92315686 | |||
chr9:92319287 | T | C | 2 | a0003c0004 a0010c0010 |
14 | HG01081.hp2 HG01255.hp1 HG02257.hp1 others(11): Show |
synonymous_variant | LOW | c.351A>G | p.Leu117Leu | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 5/17 | 444/4075 | 351/3504 | 117/1167 | chr9 | 92319287 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:92297508 | T | A | 19 | a0001c0002t0001 a0001c0002t0005 a0001c0002t0006 others(16): Show |
176 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(173): Show |
3_prime_UTR_variant | MODIFIER | c.*328A>T | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 17/17 | 328 | chr9 | 92297508 | ||||||
chr9:92297522 | A | G | 24 | a0001c0001t0002 a0001c0002t0001 a0001c0002t0002 others(21): Show |
304 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(301): Show |
3_prime_UTR_variant | MODIFIER | c.*314T>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 17/17 | 314 | chr9 | 92297522 | ||||||
chr9:92297551 | G | C | 2 | a0002c0003t0004 a0012c0023t0004 |
23 | HG00280.hp2 HG00642.hp2 HG01168.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*285C>G | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 17/17 | 285 | chr9 | 92297551 | ||||||
chr9:92297629 | T | C | 1 | a0001c0002t0006 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*207A>G | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 17/17 | 207 | chr9 | 92297629 | ||||||
chr9:92325340 | C | A | 1 | a0001c0002t0007 | 1 | HG02145.hp2 | 5_prime_UTR_variant | MODIFIER | c.-83G>T | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 1/17 | 1179 | chr9 | 92325340 | ||||||
chr9:92325341 | C | A | 2 | a0001c0002t0005 a0013c0021t0005 |
2 | HG01884.hp1 NA19043.hp1 |
5_prime_UTR_variant | MODIFIER | c.-84G>T | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 1/17 | 1180 | chr9 | 92325341 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:92297892 | A | G | 1 | a0001c0001t0003g0093 | 1 | NA19000.hp1 | splice_region_variant&intron_variant | LOW | c.3454-6T>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 16/16 | chr9 | 92297892 | |||||||
chr9:92298101 | A | G | 1 | a0001c0001t0002g0081 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3453+156T>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 16/16 | chr9 | 92298101 | |||||||
chr9:92298141 | T | C | 1 | a0009c0018t0001g0141 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3453+116A>G | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 16/16 | chr9 | 92298141 | |||||||
chr9:92298208 | T | C | 1 | a0001c0001t0002g0130 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3453+49A>G | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 16/16 | chr9 | 92298208 | |||||||
chr9:92298211 | G | T | 1 | a0002c0003t0004g0201 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3453+46C>A | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 16/16 | chr9 | 92298211 | |||||||
chr9:92298212 | T | TAAC | 22 | a0001c0002t0002g0047 a0002c0003t0004g0015 a0002c0003t0004g0029 others(19): Show |
39 | HG00280.hp2 HG00642.hp2 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.3453+42_3453+44dup others(3): Show |
NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 16/16 | chr9 | 92298212 | |||||||
chr9:92298348 | A | G | 12 | a0002c0003t0004g0015 a0002c0003t0004g0029 a0002c0003t0004g0030 others(9): Show |
22 | HG00280.hp2 HG01168.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.3374-12T>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 15/16 | chr9 | 92298348 | |||||||
chr9:92298463 | A | G | 2 | a0001c0001t0002g0095 a0001c0001t0002g0124 |
2 | HG00423.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.3374-127T>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 15/16 | chr9 | 92298463 | |||||||
chr9:92298772 | A | G | 1 | a0001c0001t0002g0114 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.3373+112T>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 15/16 | chr9 | 92298772 | |||||||
chr9:92298804 | C | G | 1 | a0001c0001t0002g0087 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.3373+80G>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 15/16 | chr9 | 92298804 | |||||||
chr9:92298831 | G | C | 3 | a0003c0004t0001g0016 a0003c0004t0001g0064 a0003c0004t0001g0065 |
5 | HG02486.hp1 HG02630.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.3373+53C>G | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 15/16 | chr9 | 92298831 | |||||||
chr9:92298851 | A | T | 4 | a0001c0002t0001g0022 a0001c0002t0001g0049 a0001c0002t0005g0209 others(1): Show |
7 | HG01358.hp2 HG01884.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.3373+33T>A | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 15/16 | chr9 | 92298851 | |||||||
chr9:92299133 | T | C | 1 | a0001c0002t0002g0047 | 2 | HG02055.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.3303-179A>G | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 14/16 | chr9 | 92299133 | |||||||
chr9:92299161 | T | A | 1 | a0001c0002t0002g0047 | 2 | HG02055.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.3303-207A>T | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 14/16 | chr9 | 92299161 | |||||||
chr9:92299175 | T | C | 1 | a0001c0002t0001g0059 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3303-221A>G | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 14/16 | chr9 | 92299175 | |||||||
chr9:92299218 | C | G | 1 | a0001c0001t0002g0100 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.3303-264G>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 14/16 | chr9 | 92299218 | |||||||
chr9:92299520 | G | A | 13 | a0002c0003t0004g0015 a0002c0003t0004g0029 a0002c0003t0004g0030 others(10): Show |
23 | HG00280.hp2 HG00642.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.3302+370C>T | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 14/16 | chr9 | 92299520 | |||||||
chr9:92299579 | C | T | 1 | a0001c0001t0002g0096 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3302+311G>A | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 14/16 | chr9 | 92299579 | |||||||
chr9:92299759 | A | T | 3 | a0001c0002t0001g0185 a0001c0002t0002g0047 a0013c0021t0005g0208 |
4 | HG01884.hp1 HG02055.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.3302+131T>A | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 14/16 | chr9 | 92299759 | |||||||
chr9:92299774 | A | G | 1 | a0001c0002t0001g0151 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3302+116T>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 14/16 | chr9 | 92299774 | |||||||
chr9:92300090 | A | T | 1 | a0001c0001t0002g0095 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.3176-74T>A | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 13/16 | chr9 | 92300090 | |||||||
chr9:92300103 | C | T | 1 | a0002c0003t0004g0199 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.3176-87G>A | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 13/16 | chr9 | 92300103 | |||||||
chr9:92300110 | A | T | 4 | a0001c0001t0003g0070 a0001c0001t0003g0071 a0001c0001t0003g0072 others(1): Show |
4 | NA18939.hp2 NA18986.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.3176-94T>A | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 13/16 | chr9 | 92300110 | |||||||
chr9:92300263 | A | C | 14 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0038 others(11): Show |
20 | HG00323.hp1 HG00408.hp1 HG02080.hp1 others(17): Show |
intron_variant | MODIFIER | c.3176-247T>G | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 13/16 | chr9 | 92300263 | |||||||
chr9:92300308 | A | T | 1 | a0002c0003t0004g0195 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.3176-292T>A | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 13/16 | chr9 | 92300308 | |||||||
chr9:92300369 | G | T | 22 | a0001c0002t0002g0047 a0002c0003t0004g0015 a0002c0003t0004g0029 others(19): Show |
39 | HG00280.hp2 HG00642.hp2 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.3176-353C>A | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 13/16 | chr9 | 92300369 | |||||||
chr9:92300576 | A | C | 3 | a0001c0002t0001g0013 a0001c0002t0001g0176 a0001c0002t0001g0179 |
6 | HG00673.hp2 NA18950.hp2 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.3176-560T>G | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 13/16 | chr9 | 92300576 | |||||||
chr9:92300663 | A | G | 3 | a0001c0002t0001g0022 a0001c0002t0001g0049 a0001c0002t0005g0209 |
6 | HG01358.hp2 HG02300.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.3176-647T>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 13/16 | chr9 | 92300663 | |||||||
chr9:92300814 | CA | C | 38 | a0001c0001t0003g0132 a0001c0002t0001g0008 a0001c0002t0001g0009 others(35): Show |
66 | HG00099.hp1 HG00323.hp2 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.3175+736delT | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 13/16 | chr9 | 92300814 | |||||||
chr9:92300855 | T | C | 12 | a0002c0003t0004g0015 a0002c0003t0004g0029 a0002c0003t0004g0030 others(9): Show |
22 | HG00280.hp2 HG01168.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.3175+696A>G | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 13/16 | chr9 | 92300855 | |||||||
chr9:92301130 | T | C | 1 | a0001c0002t0002g0047 | 2 | HG02055.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.3175+421A>G | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 13/16 | chr9 | 92301130 | |||||||
chr9:92301143 | A | G | 13 | a0002c0003t0004g0015 a0002c0003t0004g0029 a0002c0003t0004g0030 others(10): Show |
23 | HG00280.hp2 HG00642.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.3175+408T>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 13/16 | chr9 | 92301143 | |||||||
chr9:92301183 | C | G | 1 | a0001c0001t0002g0148 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3175+368G>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 13/16 | chr9 | 92301183 | |||||||
chr9:92301467 | T | C | 13 | a0002c0003t0004g0015 a0002c0003t0004g0029 a0002c0003t0004g0030 others(10): Show |
23 | HG00280.hp2 HG00642.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.3175+84A>G | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 13/16 | chr9 | 92301467 | |||||||
chr9:92301486 | T | C | 1 | a0001c0002t0001g0142 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3175+65A>G | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 13/16 | chr9 | 92301486 | |||||||
chr9:92301957 | A | G | 1 | a0001c0001t0002g0121 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2904-135T>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 12/16 | chr9 | 92301957 | |||||||
chr9:92301992 | A | T | 1 | a0001c0001t0002g0101 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2904-170T>A | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 12/16 | chr9 | 92301992 | |||||||
chr9:92302280 | G | C | 100 | a0001c0002t0001g0003 a0001c0002t0001g0008 a0001c0002t0001g0009 others(97): Show |
178 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.2904-458C>G | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 12/16 | chr9 | 92302280 | |||||||
chr9:92302285 | T | C | 2 | a0001c0001t0002g0043 a0016c0011t0002g0111 |
3 | HG03225.hp2 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2904-463A>G | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 12/16 | chr9 | 92302285 | |||||||
chr9:92302322 | G | A | 22 | a0001c0002t0002g0047 a0002c0003t0004g0015 a0002c0003t0004g0029 others(19): Show |
39 | HG00280.hp2 HG00642.hp2 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.2904-500C>T | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 12/16 | chr9 | 92302322 | |||||||
chr9:92302480 | G | A | 72 | a0001c0002t0001g0003 a0001c0002t0001g0008 a0001c0002t0001g0009 others(69): Show |
133 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.2904-658C>T | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 12/16 | chr9 | 92302480 | |||||||
chr9:92302506 | G | A | 1 | a0001c0002t0001g0162 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2904-684C>T | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 12/16 | chr9 | 92302506 | |||||||
chr9:92302543 | C | T | 1 | a0002c0003t0004g0199 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2904-721G>A | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 12/16 | chr9 | 92302543 | |||||||
chr9:92302561 | C | G | 100 | a0001c0002t0001g0003 a0001c0002t0001g0008 a0001c0002t0001g0009 others(97): Show |
178 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.2904-739G>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 12/16 | chr9 | 92302561 | |||||||
chr9:92303089 | A | C | 1 | a0001c0002t0006g0188 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2904-1267T>G | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 12/16 | chr9 | 92303089 | |||||||
chr9:92303238 | T | A | 13 | a0002c0003t0004g0015 a0002c0003t0004g0029 a0002c0003t0004g0030 others(10): Show |
23 | HG00280.hp2 HG00642.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.2904-1416A>T | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 12/16 | chr9 | 92303238 | |||||||
chr9:92303284 | T | C | 8 | a0003c0004t0001g0011 a0003c0004t0001g0016 a0003c0004t0001g0031 others(5): Show |
14 | HG01081.hp2 HG01255.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2904-1462A>G | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 12/16 | chr9 | 92303284 | |||||||
chr9:92303386 | C | A | 1 | a0001c0001t0003g0084 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2904-1564G>T | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 12/16 | chr9 | 92303386 | |||||||
chr9:92303456 | G | A | 4 | a0001c0001t0002g0043 a0001c0001t0002g0112 a0001c0001t0002g0113 others(1): Show |
5 | HG02615.hp2 HG02886.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.2904-1634C>T | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 12/16 | chr9 | 92303456 | |||||||
chr9:92303470 | A | G | 1 | a0014c0022t0001g0167 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2904-1648T>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 12/16 | chr9 | 92303470 | |||||||
chr9:92303527 | A | G | 2 | a0010c0010t0001g0144 a0010c0010t0001g0145 |
2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2904-1705T>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 12/16 | chr9 | 92303527 | |||||||
chr9:92303652 | A | T | 1 | a0001c0001t0003g0092 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.2904-1830T>A | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 12/16 | chr9 | 92303652 | |||||||
chr9:92303740 | G | A | 5 | a0001c0002t0001g0182 a0001c0002t0001g0183 a0001c0002t0001g0184 others(2): Show |
5 | HG01081.hp1 HG02717.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2904-1918C>T | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 12/16 | chr9 | 92303740 | |||||||
chr9:92303805 | A | G | 1 | a0001c0002t0001g0160 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2903+1948T>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 12/16 | chr9 | 92303805 | |||||||
chr9:92304017 | A | G | 1 | a0001c0001t0002g0099 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2903+1736T>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 12/16 | chr9 | 92304017 | |||||||
chr9:92304244 | A | G | 11 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0051 others(8): Show |
33 | HG00597.hp1 HG00673.hp2 NA18940.hp2 others(30): Show |
intron_variant | MODIFIER | c.2903+1509T>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 12/16 | chr9 | 92304244 | |||||||
chr9:92304564 | A | T | 5 | a0001c0001t0003g0007 a0001c0001t0003g0039 a0001c0001t0003g0079 others(2): Show |
13 | NA18942.hp1 NA18952.hp1 NA18956.hp1 others(10): Show |
intron_variant | MODIFIER | c.2903+1189T>A | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 12/16 | chr9 | 92304564 | |||||||
chr9:92304592 | A | G | 1 | a0001c0002t0001g0159 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2903+1161T>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 12/16 | chr9 | 92304592 | |||||||
chr9:92304860 | C | G | 8 | a0003c0004t0001g0011 a0003c0004t0001g0016 a0003c0004t0001g0031 others(5): Show |
14 | HG01081.hp2 HG01255.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2903+893G>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 12/16 | chr9 | 92304860 | |||||||
chr9:92304910 | C | T | 13 | a0002c0003t0004g0015 a0002c0003t0004g0029 a0002c0003t0004g0030 others(10): Show |
23 | HG00280.hp2 HG00642.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.2903+843G>A | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 12/16 | chr9 | 92304910 | |||||||
chr9:92304975 | T | C | 23 | a0001c0002t0002g0047 a0002c0003t0004g0015 a0002c0003t0004g0029 others(20): Show |
40 | HG00280.hp2 HG00642.hp2 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.2903+778A>G | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 12/16 | chr9 | 92304975 | |||||||
chr9:92304994 | A | T | 4 | a0001c0002t0001g0022 a0001c0002t0001g0049 a0001c0002t0005g0209 others(1): Show |
7 | HG01358.hp2 HG01884.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.2903+759T>A | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 12/16 | chr9 | 92304994 | |||||||
chr9:92305022 | C | T | 12 | a0002c0003t0004g0015 a0002c0003t0004g0029 a0002c0003t0004g0030 others(9): Show |
22 | HG00280.hp2 HG01168.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.2903+731G>A | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 12/16 | chr9 | 92305022 | |||||||
chr9:92305480 | C | T | 1 | a0001c0001t0003g0091 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2903+273G>A | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 12/16 | chr9 | 92305480 | |||||||
chr9:92305525 | G | T | 1 | a0001c0002t0001g0185 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2903+228C>A | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 12/16 | chr9 | 92305525 | |||||||
chr9:92305657 | C | T | 1 | a0002c0003t0004g0015 | 4 | HG01168.hp2 HG01169.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.2903+96G>A | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 12/16 | chr9 | 92305657 | |||||||
chr9:92305903 | A | T | 1 | a0001c0002t0001g0158 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2826-73T>A | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 11/16 | chr9 | 92305903 | |||||||
chr9:92306079 | C | T | 1 | a0001c0001t0003g0090 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2826-249G>A | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 11/16 | chr9 | 92306079 | |||||||
chr9:92306113 | C | A | 1 | a0001c0002t0001g0142 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2826-283G>T | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 11/16 | chr9 | 92306113 | |||||||
chr9:92306237 | G | A | 13 | a0002c0003t0004g0015 a0002c0003t0004g0029 a0002c0003t0004g0030 others(10): Show |
23 | HG00280.hp2 HG00642.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.2826-407C>T | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 11/16 | chr9 | 92306237 | |||||||
chr9:92306316 | A | G | 1 | a0002c0003t0004g0201 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2826-486T>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 11/16 | chr9 | 92306316 | |||||||
chr9:92306375 | C | T | 1 | a0001c0002t0001g0181 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2825+511G>A | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 11/16 | chr9 | 92306375 | |||||||
chr9:92306423 | T | C | 13 | a0002c0003t0004g0015 a0002c0003t0004g0029 a0002c0003t0004g0030 others(10): Show |
23 | HG00280.hp2 HG00642.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.2825+463A>G | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 11/16 | chr9 | 92306423 | |||||||
chr9:92306429 | A | C | 1 | a0001c0001t0003g0089 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2825+457T>G | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 11/16 | chr9 | 92306429 | |||||||
chr9:92306601 | C | G | 1 | a0001c0001t0002g0147 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2825+285G>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 11/16 | chr9 | 92306601 | |||||||
chr9:92307082 | A | T | 1 | a0002c0003t0004g0197 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2687-58T>A | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 10/16 | chr9 | 92307082 | |||||||
chr9:92307211 | G | A | 1 | a0001c0002t0001g0142 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2687-187C>T | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 10/16 | chr9 | 92307211 | |||||||
chr9:92307309 | G | A | 1 | a0001c0002t0001g0054 | 2 | HG00639.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.2687-285C>T | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 10/16 | chr9 | 92307309 | |||||||
chr9:92307325 | C | T | 3 | a0001c0002t0001g0022 a0001c0002t0001g0049 a0001c0002t0005g0209 |
6 | HG01358.hp2 HG02300.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.2687-301G>A | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 10/16 | chr9 | 92307325 | |||||||
chr9:92307381 | CAT | C | 13 | a0002c0003t0004g0015 a0002c0003t0004g0029 a0002c0003t0004g0030 others(10): Show |
23 | HG00280.hp2 HG00642.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.2687-359_2687-358d others(4): Show |
NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 10/16 | chr9 | 92307381 | |||||||
chr9:92307478 | T | G | 2 | a0001c0001t0002g0115 a0001c0001t0002g0143 |
2 | HG02083.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.2687-454A>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 10/16 | chr9 | 92307478 | |||||||
chr9:92307813 | A | G | 119 | a0001c0001t0002g0004 a0001c0001t0002g0043 a0001c0001t0002g0073 others(116): Show |
216 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.2687-789T>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 10/16 | chr9 | 92307813 | |||||||
chr9:92308272 | T | C | 1 | a0009c0018t0001g0141 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2687-1248A>G | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 10/16 | chr9 | 92308272 | |||||||
chr9:92308364 | AAAAAAT | A | 5 | a0001c0002t0001g0185 a0001c0002t0001g0186 a0001c0002t0001g0192 others(2): Show |
5 | HG02109.hp1 HG02145.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2687-1346_2687-134 others(10): Show |
NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 10/16 | chr9 | 92308364 | |||||||
chr9:92308442 | A | C | 8 | a0003c0004t0001g0011 a0003c0004t0001g0016 a0003c0004t0001g0031 others(5): Show |
14 | HG01081.hp2 HG01255.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2687-1418T>G | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 10/16 | chr9 | 92308442 | |||||||
chr9:92308505 | G | A | 2 | a0001c0002t0001g0010 a0001c0002t0001g0162 |
6 | HG00323.hp2 HG01257.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.2687-1481C>T | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 10/16 | chr9 | 92308505 | |||||||
chr9:92308785 | T | C | 1 | a0001c0002t0001g0024 | 3 | HG02896.hp2 HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2686+1386A>G | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 10/16 | chr9 | 92308785 | |||||||
chr9:92308880 | G | A | 1 | a0001c0001t0003g0094 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2686+1291C>T | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 10/16 | chr9 | 92308880 | |||||||
chr9:92309812 | G | C | 21 | a0002c0003t0004g0015 a0002c0003t0004g0029 a0002c0003t0004g0030 others(18): Show |
37 | HG00280.hp2 HG00642.hp2 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.2686+359C>G | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 10/16 | chr9 | 92309812 | |||||||
chr9:92310033 | G | A | 1 | a0001c0001t0002g0101 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2686+138C>T | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 10/16 | chr9 | 92310033 | |||||||
chr9:92310490 | T | A | 1 | a0001c0002t0001g0152 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2595+63A>T | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 9/16 | chr9 | 92310490 | |||||||
chr9:92310695 | T | G | 1 | a0001c0001t0003g0139 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2473-20A>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 8/16 | chr9 | 92310695 | |||||||
chr9:92310774 | G | A | 1 | a0001c0001t0003g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2473-99C>T | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 8/16 | chr9 | 92310774 | |||||||
chr9:92310775 | A | G | 1 | a0001c0001t0003g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2473-100T>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 8/16 | chr9 | 92310775 | |||||||
chr9:92310870 | T | C | 22 | a0001c0002t0002g0047 a0002c0003t0004g0015 a0002c0003t0004g0029 others(19): Show |
39 | HG00280.hp2 HG00642.hp2 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.2473-195A>G | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 8/16 | chr9 | 92310870 | |||||||
chr9:92311020 | G | T | 1 | a0001c0001t0003g0109 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.2472+126C>A | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 8/16 | chr9 | 92311020 | |||||||
chr9:92311045 | T | C | 2 | a0010c0010t0001g0144 a0010c0010t0001g0145 |
2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2472+101A>G | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 8/16 | chr9 | 92311045 | |||||||
chr9:92311093 | T | A | 2 | a0001c0001t0002g0048 a0001c0001t0002g0147 |
3 | NA18952.hp2 NA18973.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.2472+53A>T | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 8/16 | chr9 | 92311093 | |||||||
chr9:92311393 | CT | C | 22 | a0001c0002t0002g0047 a0002c0003t0004g0015 a0002c0003t0004g0029 others(19): Show |
39 | HG00280.hp2 HG00642.hp2 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.2359-135delA | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 7/16 | chr9 | 92311393 | |||||||
chr9:92311401 | C | A | 6 | a0001c0001t0002g0006 a0001c0001t0002g0045 a0001c0001t0002g0067 others(3): Show |
14 | HG00738.hp1 HG01361.hp2 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.2359-142G>T | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 7/16 | chr9 | 92311401 | |||||||
chr9:92311676 | C | A | 1 | a0001c0001t0002g0148 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2359-417G>T | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 7/16 | chr9 | 92311676 | |||||||
chr9:92311765 | A | G | 1 | a0001c0001t0003g0088 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2359-506T>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 7/16 | chr9 | 92311765 | |||||||
chr9:92311893 | T | C | 6 | a0003c0004t0001g0011 a0003c0004t0001g0016 a0003c0004t0001g0031 others(3): Show |
12 | HG01081.hp2 HG01255.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.2359-634A>G | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 7/16 | chr9 | 92311893 | |||||||
chr9:92311901 | T | C | 1 | a0001c0002t0001g0166 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2359-642A>G | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 7/16 | chr9 | 92311901 | |||||||
chr9:92312264 | A | G | 8 | a0003c0004t0001g0011 a0003c0004t0001g0016 a0003c0004t0001g0031 others(5): Show |
14 | HG01081.hp2 HG01255.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2359-1005T>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 7/16 | chr9 | 92312264 | |||||||
chr9:92312309 | C | G | 1 | a0009c0018t0001g0141 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2359-1050G>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 7/16 | chr9 | 92312309 | |||||||
chr9:92312415 | C | T | 32 | a0001c0001t0002g0001 a0001c0001t0002g0017 a0001c0001t0002g0019 others(29): Show |
73 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.2359-1156G>A | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 7/16 | chr9 | 92312415 | |||||||
chr9:92312446 | T | TA | 24 | a0001c0001t0002g0073 a0001c0001t0002g0095 a0001c0001t0002g0096 others(21): Show |
29 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.2359-1188dupT | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 7/16 | chr9 | 92312446 | |||||||
chr9:92312446 | TA | T | 57 | a0001c0001t0002g0098 a0001c0001t0002g0112 a0001c0001t0002g0128 others(54): Show |
100 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.2359-1188delT | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 7/16 | chr9 | 92312446 | |||||||
chr9:92312446 | TAA | T | 35 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0010 others(32): Show |
63 | HG00099.hp1 HG00323.hp2 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.2359-1189_2359-118 others(6): Show |
NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 7/16 | chr9 | 92312446 | |||||||
chr9:92312446 | TAAA | T | 7 | a0003c0004t0001g0011 a0003c0004t0001g0016 a0003c0004t0001g0031 others(4): Show |
13 | HG01081.hp2 HG01255.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.2359-1190_2359-118 others(7): Show |
NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 7/16 | chr9 | 92312446 | |||||||
chr9:92312446 | TAAAAAAA others(6): Show |
T | 1 | a0001c0001t0002g0086 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2359-1200_2359-118 others(17): Show |
NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 7/16 | chr9 | 92312446 | |||||||
chr9:92312570 | T | G | 1 | a0001c0001t0002g0148 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2359-1311A>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 7/16 | chr9 | 92312570 | |||||||
chr9:92312642 | C | A | 1 | a0010c0010t0001g0145 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2359-1383G>T | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 7/16 | chr9 | 92312642 | |||||||
chr9:92312706 | A | G | 13 | a0002c0003t0004g0015 a0002c0003t0004g0029 a0002c0003t0004g0030 others(10): Show |
23 | HG00280.hp2 HG00642.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.2359-1447T>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 7/16 | chr9 | 92312706 | |||||||
chr9:92312815 | A | G | 4 | a0001c0002t0001g0051 a0001c0002t0001g0173 a0001c0002t0001g0174 others(1): Show |
5 | NA18940.hp2 NA18951.hp2 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.2358+1452T>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 7/16 | chr9 | 92312815 | |||||||
chr9:92312827 | C | CA | 21 | a0001c0001t0002g0019 a0001c0001t0002g0063 a0001c0001t0002g0067 others(18): Show |
23 | HG00323.hp1 HG00408.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.2358+1439dupT | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 7/16 | chr9 | 92312827 | |||||||
chr9:92312827 | C | CAA | 9 | a0001c0001t0002g0020 a0001c0001t0002g0048 a0001c0001t0002g0104 others(6): Show |
13 | HG01358.hp2 HG01884.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.2358+1438_2358+143 others(6): Show |
NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 7/16 | chr9 | 92312827 | |||||||
chr9:92312827 | CA | C | 30 | a0001c0001t0002g0004 a0001c0001t0002g0043 a0001c0001t0002g0073 others(27): Show |
52 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.2358+1439delT | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 7/16 | chr9 | 92312827 | |||||||
chr9:92312843 | A | AAAG | 9 | a0002c0003t0004g0015 a0002c0003t0004g0030 a0002c0003t0004g0055 others(6): Show |
17 | HG00280.hp2 HG01168.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.2358+1423_2358+142 others(7): Show |
NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 7/16 | chr9 | 92312843 | |||||||
chr9:92312843 | A | AAG | 12 | a0001c0002t0002g0047 a0002c0003t0004g0029 a0002c0003t0004g0199 others(9): Show |
21 | HG00642.hp2 HG01081.hp2 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.2358+1423_2358+142 others(6): Show |
NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 7/16 | chr9 | 92312843 | |||||||
chr9:92312844 | A | G | 1 | a0001c0001t0003g0084 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2358+1423T>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 7/16 | chr9 | 92312844 | |||||||
chr9:92312845 | A | G | 1 | a0001c0001t0002g0035 | 2 | HG03209.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2358+1422T>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 7/16 | chr9 | 92312845 | |||||||
chr9:92312884 | T | G | 8 | a0003c0004t0001g0011 a0003c0004t0001g0016 a0003c0004t0001g0031 others(5): Show |
14 | HG01081.hp2 HG01255.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2358+1383A>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 7/16 | chr9 | 92312884 | |||||||
chr9:92312910 | A | G | 13 | a0002c0003t0004g0015 a0002c0003t0004g0029 a0002c0003t0004g0030 others(10): Show |
23 | HG00280.hp2 HG00642.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.2358+1357T>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 7/16 | chr9 | 92312910 | |||||||
chr9:92312932 | C | G | 1 | a0002c0003t0004g0198 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2358+1335G>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 7/16 | chr9 | 92312932 | |||||||
chr9:92312981 | G | A | 1 | a0001c0001t0002g0119 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2358+1286C>T | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 7/16 | chr9 | 92312981 | |||||||
chr9:92312999 | T | TTG | 22 | a0001c0002t0002g0047 a0002c0003t0004g0015 a0002c0003t0004g0029 others(19): Show |
39 | HG00280.hp2 HG00642.hp2 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.2358+1266_2358+126 others(6): Show |
NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 7/16 | chr9 | 92312999 | |||||||
chr9:92313279 | C | T | 12 | a0001c0002t0001g0008 a0001c0002t0001g0025 a0001c0002t0001g0027 others(9): Show |
21 | HG01109.hp2 HG02109.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.2358+988G>A | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 7/16 | chr9 | 92313279 | |||||||
chr9:92313421 | T | G | 1 | a0001c0001t0003g0105 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2358+846A>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 7/16 | chr9 | 92313421 | |||||||
chr9:92313502 | A | G | 2 | a0001c0001t0003g0021 a0001c0001t0003g0108 |
4 | NA18950.hp1 NA19062.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.2358+765T>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 7/16 | chr9 | 92313502 | |||||||
chr9:92313544 | C | G | 13 | a0002c0003t0004g0015 a0002c0003t0004g0029 a0002c0003t0004g0030 others(10): Show |
23 | HG00280.hp2 HG00642.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.2358+723G>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 7/16 | chr9 | 92313544 | |||||||
chr9:92313838 | A | C | 8 | a0003c0004t0001g0011 a0003c0004t0001g0016 a0003c0004t0001g0031 others(5): Show |
14 | HG01081.hp2 HG01255.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2358+429T>G | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 7/16 | chr9 | 92313838 | |||||||
chr9:92314167 | C | G | 1 | a0001c0001t0003g0068 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2358+100G>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 7/16 | chr9 | 92314167 | |||||||
chr9:92316143 | C | T | 1 | a0009c0018t0001g0141 | 1 | HG03130.hp2 | splice_region_variant&intron_variant | LOW | c.487-5G>A | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 6/16 | chr9 | 92316143 | |||||||
chr9:92316340 | T | C | 7 | a0001c0001t0003g0005 a0001c0001t0003g0021 a0001c0001t0003g0041 others(4): Show |
19 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.487-202A>G | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 6/16 | chr9 | 92316340 | |||||||
chr9:92316421 | G | A | 2 | a0001c0001t0002g0110 a0001c0001t0003g0042 |
3 | NA18983.hp1 NA19066.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.487-283C>T | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 6/16 | chr9 | 92316421 | |||||||
chr9:92316441 | T | C | 15 | a0001c0001t0002g0004 a0001c0001t0002g0073 a0001c0001t0002g0080 others(12): Show |
33 | HG00741.hp1 HG01074.hp2 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.487-303A>G | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 6/16 | chr9 | 92316441 | |||||||
chr9:92316489 | A | G | 1 | a0001c0002t0001g0024 | 3 | HG02896.hp2 HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.487-351T>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 6/16 | chr9 | 92316489 | |||||||
chr9:92316536 | C | G | 8 | a0003c0004t0001g0011 a0003c0004t0001g0016 a0003c0004t0001g0031 others(5): Show |
14 | HG01081.hp2 HG01255.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.487-398G>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 6/16 | chr9 | 92316536 | |||||||
chr9:92316570 | C | A | 76 | a0001c0002t0001g0003 a0001c0002t0001g0008 a0001c0002t0001g0009 others(73): Show |
137 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.487-432G>T | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 6/16 | chr9 | 92316570 | |||||||
chr9:92316753 | C | A | 1 | a0003c0004t0001g0146 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.487-615G>T | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 6/16 | chr9 | 92316753 | |||||||
chr9:92317019 | C | T | 6 | a0001c0001t0002g0006 a0001c0001t0002g0045 a0001c0001t0002g0067 others(3): Show |
14 | HG00738.hp1 HG01361.hp2 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.487-881G>A | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 6/16 | chr9 | 92317019 | |||||||
chr9:92317259 | C | T | 5 | a0001c0002t0001g0028 a0001c0002t0001g0180 a0001c0002t0001g0181 others(2): Show |
8 | HG00140.hp2 HG01496.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.487-1121G>A | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 6/16 | chr9 | 92317259 | |||||||
chr9:92317460 | G | A | 20 | a0001c0001t0002g0004 a0001c0001t0002g0043 a0001c0001t0002g0073 others(17): Show |
39 | HG00741.hp1 HG01074.hp2 HG01123.hp2 others(36): Show |
intron_variant | MODIFIER | c.486+1158C>T | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 6/16 | chr9 | 92317460 | |||||||
chr9:92317512 | G | A | 14 | a0001c0002t0001g0189 a0002c0003t0004g0015 a0002c0003t0004g0029 others(11): Show |
24 | HG00280.hp2 HG00642.hp2 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.486+1106C>T | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 6/16 | chr9 | 92317512 | |||||||
chr9:92317744 | C | T | 13 | a0002c0003t0004g0015 a0002c0003t0004g0029 a0002c0003t0004g0030 others(10): Show |
23 | HG00280.hp2 HG00642.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.486+874G>A | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 6/16 | chr9 | 92317744 | |||||||
chr9:92317759 | G | A | 1 | a0001c0002t0001g0177 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.486+859C>T | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 6/16 | chr9 | 92317759 | |||||||
chr9:92317898 | G | C | 1 | a0001c0001t0003g0120 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.486+720C>G | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 6/16 | chr9 | 92317898 | |||||||
chr9:92317919 | C | T | 8 | a0003c0004t0001g0011 a0003c0004t0001g0016 a0003c0004t0001g0031 others(5): Show |
14 | HG01081.hp2 HG01255.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.486+699G>A | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 6/16 | chr9 | 92317919 | |||||||
chr9:92318033 | C | CA | 25 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0121 others(22): Show |
31 | HG01071.hp1 HG01361.hp2 HG02083.hp2 others(28): Show |
intron_variant | MODIFIER | c.486+584dupT | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 6/16 | chr9 | 92318033 | |||||||
chr9:92318033 | C | CAA | 6 | a0001c0001t0002g0134 a0001c0001t0003g0132 a0001c0001t0003g0133 others(3): Show |
7 | HG01071.hp2 HG01884.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.486+583_486+584dup others(2): Show |
NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 6/16 | chr9 | 92318033 | |||||||
chr9:92318033 | C | CAAA | 11 | a0001c0002t0001g0152 a0002c0003t0004g0015 a0002c0003t0004g0029 others(8): Show |
20 | HG00280.hp2 HG01168.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.486+582_486+584dup others(3): Show |
NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 6/16 | chr9 | 92318033 | |||||||
chr9:92318033 | C | CAAAAA | 6 | a0003c0004t0001g0011 a0003c0004t0001g0016 a0003c0004t0001g0065 others(3): Show |
11 | HG01081.hp2 HG01255.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.486+580_486+584dup others(5): Show |
NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 6/16 | chr9 | 92318033 | |||||||
chr9:92318033 | CA | C | 10 | a0001c0001t0002g0017 a0001c0001t0002g0080 a0001c0001t0003g0034 others(7): Show |
13 | HG00438.hp2 HG01070.hp1 HG01943.hp2 others(10): Show |
intron_variant | MODIFIER | c.486+584delT | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 6/16 | chr9 | 92318033 | |||||||
chr9:92318033 | CAAAAAAA | C | 27 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0028 others(24): Show |
52 | HG00140.hp2 HG00597.hp1 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.486+578_486+584del others(7): Show |
NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 6/16 | chr9 | 92318033 | |||||||
chr9:92318033 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0002g0067 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.486+575_486+584del others(10): Show |
NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 6/16 | chr9 | 92318033 | |||||||
chr9:92318121 | G | C | 1 | a0002c0003t0004g0201 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.486+497C>G | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 6/16 | chr9 | 92318121 | |||||||
chr9:92318372 | C | T | 1 | a0001c0002t0001g0142 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.486+246G>A | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 6/16 | chr9 | 92318372 | |||||||
chr9:92318470 | G | A | 1 | a0001c0002t0001g0179 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.486+148C>T | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 6/16 | chr9 | 92318470 | |||||||
chr9:92318576 | C | T | 1 | a0001c0002t0001g0059 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.486+42G>A | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 6/16 | chr9 | 92318576 | |||||||
chr9:92318597 | T | C | 22 | a0001c0002t0002g0047 a0002c0003t0004g0015 a0002c0003t0004g0029 others(19): Show |
39 | HG00280.hp2 HG00642.hp2 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.486+21A>G | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 6/16 | chr9 | 92318597 | |||||||
chr9:92318761 | T | C | 1 | a0001c0001t0003g0135 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.418-75A>G | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 5/16 | chr9 | 92318761 | |||||||
chr9:92318797 | G | T | 2 | a0001c0002t0001g0023 a0001c0002t0001g0153 |
4 | HG00735.hp2 HG01099.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.418-111C>A | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 5/16 | chr9 | 92318797 | |||||||
chr9:92318910 | G | C | 32 | a0001c0002t0001g0008 a0001c0002t0001g0009 a0001c0002t0001g0010 others(29): Show |
63 | HG00099.hp1 HG00323.hp2 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.418-224C>G | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 5/16 | chr9 | 92318910 | |||||||
chr9:92318944 | G | A | 1 | a0001c0002t0001g0191 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.418-258C>T | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 5/16 | chr9 | 92318944 | |||||||
chr9:92319405 | G | A | 1 | a0001c0001t0002g0136 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.282-49C>T | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 4/16 | chr9 | 92319405 | |||||||
chr9:92319519 | C | T | 2 | a0010c0010t0001g0144 a0010c0010t0001g0145 |
2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.282-163G>A | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 4/16 | chr9 | 92319519 | |||||||
chr9:92319994 | C | T | 1 | a0001c0001t0003g0033 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.282-638G>A | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 4/16 | chr9 | 92319994 | |||||||
chr9:92320176 | C | T | 1 | a0001c0001t0003g0077 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.282-820G>A | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 4/16 | chr9 | 92320176 | |||||||
chr9:92320446 | A | T | 1 | a0002c0003t0004g0195 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.282-1090T>A | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 4/16 | chr9 | 92320446 | |||||||
chr9:92320522 | A | G | 74 | a0001c0002t0001g0003 a0001c0002t0001g0008 a0001c0002t0001g0009 others(71): Show |
135 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.281+1146T>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 4/16 | chr9 | 92320522 | |||||||
chr9:92320595 | C | CT | 24 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0051 others(21): Show |
56 | HG00280.hp2 HG00597.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.281+1072dupA | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 4/16 | chr9 | 92320595 | |||||||
chr9:92320595 | CT | C | 9 | a0001c0002t0001g0027 a0001c0002t0001g0168 a0001c0002t0001g0169 others(6): Show |
13 | HG01884.hp1 HG02258.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.281+1072delA | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 4/16 | chr9 | 92320595 | |||||||
chr9:92320607 | T | C | 1 | a0001c0001t0002g0076 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.281+1061A>G | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 4/16 | chr9 | 92320607 | |||||||
chr9:92320609 | C | T | 1 | a0001c0001t0002g0076 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.281+1059G>A | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 4/16 | chr9 | 92320609 | |||||||
chr9:92320627 | C | G | 2 | a0001c0002t0001g0173 a0001c0002t0001g0174 |
2 | NA18994.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.281+1041G>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 4/16 | chr9 | 92320627 | |||||||
chr9:92320630 | G | C | 2 | a0001c0002t0001g0192 a0001c0002t0001g0193 |
2 | HG02109.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.281+1038C>G | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 4/16 | chr9 | 92320630 | |||||||
chr9:92320718 | T | C | 1 | a0001c0002t0001g0172 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.281+950A>G | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 4/16 | chr9 | 92320718 | |||||||
chr9:92320853 | C | T | 1 | a0009c0018t0001g0141 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.281+815G>A | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 4/16 | chr9 | 92320853 | |||||||
chr9:92320859 | G | A | 1 | a0001c0001t0002g0206 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.281+809C>T | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 4/16 | chr9 | 92320859 | |||||||
chr9:92320898 | T | C | 3 | a0001c0001t0003g0137 a0001c0001t0003g0138 a0001c0001t0003g0139 |
3 | HG01346.hp1 HG01928.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.281+770A>G | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 4/16 | chr9 | 92320898 | |||||||
chr9:92320903 | G | A | 1 | a0001c0001t0002g0140 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.281+765C>T | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 4/16 | chr9 | 92320903 | |||||||
chr9:92320959 | C | T | 8 | a0003c0004t0001g0011 a0003c0004t0001g0016 a0003c0004t0001g0031 others(5): Show |
14 | HG01081.hp2 HG01255.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.281+709G>A | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 4/16 | chr9 | 92320959 | |||||||
chr9:92321134 | A | G | 1 | a0001c0002t0002g0047 | 2 | HG02055.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.281+534T>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 4/16 | chr9 | 92321134 | |||||||
chr9:92321225 | C | T | 1 | a0001c0001t0002g0075 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.281+443G>A | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 4/16 | chr9 | 92321225 | |||||||
chr9:92321234 | T | C | 22 | a0001c0002t0002g0047 a0002c0003t0004g0015 a0002c0003t0004g0029 others(19): Show |
39 | HG00280.hp2 HG00642.hp2 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.281+434A>G | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 4/16 | chr9 | 92321234 | |||||||
chr9:92321365 | C | T | 1 | a0001c0001t0002g0074 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.281+303G>A | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 4/16 | chr9 | 92321365 | |||||||
chr9:92321541 | A | G | 1 | a0001c0001t0002g0073 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.281+127T>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 4/16 | chr9 | 92321541 | |||||||
chr9:92321543 | C | G | 3 | a0001c0001t0003g0070 a0001c0001t0003g0071 a0001c0001t0003g0072 |
3 | NA18986.hp1 NA19084.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.281+125G>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 4/16 | chr9 | 92321543 | |||||||
chr9:92321551 | A | AT | 13 | a0002c0003t0004g0015 a0002c0003t0004g0029 a0002c0003t0004g0030 others(10): Show |
23 | HG00280.hp2 HG00642.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.281+116dupA | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 4/16 | chr9 | 92321551 | |||||||
chr9:92321552 | T | TA | 87 | a0001c0002t0001g0003 a0001c0002t0001g0008 a0001c0002t0001g0009 others(84): Show |
155 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.281+115dupT | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 4/16 | chr9 | 92321552 | |||||||
chr9:92321583 | T | C | 1 | a0006c0007t0001g0050 | 2 | HG01074.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.281+85A>G | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 4/16 | chr9 | 92321583 | |||||||
chr9:92321772 | T | C | 1 | a0001c0001t0002g0143 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.203-26A>G | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 3/16 | chr9 | 92321772 | |||||||
chr9:92321784 | T | C | 21 | a0002c0003t0004g0015 a0002c0003t0004g0029 a0002c0003t0004g0030 others(18): Show |
37 | HG00280.hp2 HG00642.hp2 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.203-38A>G | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 3/16 | chr9 | 92321784 | |||||||
chr9:92321965 | G | C | 1 | a0001c0002t0002g0047 | 2 | HG02055.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.203-219C>G | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 3/16 | chr9 | 92321965 | |||||||
chr9:92321983 | G | A | 2 | a0001c0001t0002g0048 a0001c0001t0002g0147 |
3 | NA18952.hp2 NA18973.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.203-237C>T | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 3/16 | chr9 | 92321983 | |||||||
chr9:92322215 | G | A | 34 | a0001c0002t0001g0003 a0001c0002t0001g0013 a0001c0002t0001g0014 others(31): Show |
64 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.203-469C>T | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 3/16 | chr9 | 92322215 | |||||||
chr9:92322757 | G | A | 1 | a0001c0002t0001g0203 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.202+684C>T | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 3/16 | chr9 | 92322757 | |||||||
chr9:92322789 | T | C | 1 | a0001c0001t0002g0148 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.202+652A>G | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 3/16 | chr9 | 92322789 | |||||||
chr9:92322813 | T | G | 3 | a0001c0002t0001g0022 a0001c0002t0001g0049 a0001c0002t0005g0209 |
6 | HG01358.hp2 HG02300.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.202+628A>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 3/16 | chr9 | 92322813 | |||||||
chr9:92322872 | C | G | 13 | a0002c0003t0004g0015 a0002c0003t0004g0029 a0002c0003t0004g0030 others(10): Show |
23 | HG00280.hp2 HG00642.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.202+569G>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 3/16 | chr9 | 92322872 | |||||||
chr9:92323083 | G | A | 72 | a0001c0002t0001g0003 a0001c0002t0001g0008 a0001c0002t0001g0009 others(69): Show |
130 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.202+358C>T | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 3/16 | chr9 | 92323083 | |||||||
chr9:92323137 | T | C | 1 | a0001c0001t0003g0194 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.202+304A>G | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 3/16 | chr9 | 92323137 | |||||||
chr9:92323413 | C | T | 1 | a0001c0001t0003g0069 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.202+28G>A | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 3/16 | chr9 | 92323413 | |||||||
chr9:92323508 | A | AAAAC | 2 | a0001c0001t0003g0032 a0001c0001t0003g0068 |
3 | HG00280.hp1 HG01952.hp1 HG03490.hp1 |
splice_region_variant&intron_variant | LOW | c.140-9_140-6dupGTTT | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 2/16 | chr9 | 92323508 | |||||||
chr9:92323520 | C | G | 1 | a0001c0001t0002g0067 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.140-17G>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 2/16 | chr9 | 92323520 | |||||||
chr9:92323566 | T | C | 1 | a0002c0003t0004g0057 | 2 | NA18973.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.140-63A>G | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 2/16 | chr9 | 92323566 | |||||||
chr9:92323587 | TA | T | 6 | a0001c0002t0001g0066 a0003c0004t0001g0011 a0003c0004t0001g0016 others(3): Show |
12 | HG01255.hp1 HG02257.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.140-85delT | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 2/16 | chr9 | 92323587 | |||||||
chr9:92323680 | C | CA | 13 | a0002c0003t0004g0015 a0002c0003t0004g0029 a0002c0003t0004g0030 others(10): Show |
23 | HG00280.hp2 HG00642.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.140-178dupT | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 2/16 | chr9 | 92323680 | |||||||
chr9:92323950 | G | A | 2 | a0001c0002t0001g0202 a0001c0002t0001g0203 |
2 | HG01081.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.139+73C>T | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 2/16 | chr9 | 92323950 | |||||||
chr9:92324407 | C | T | 1 | a0001c0001t0002g0063 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-48-198G>A | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 1/16 | chr9 | 92324407 | |||||||
chr9:92324480 | C | T | 4 | a0001c0002t0001g0059 a0001c0002t0001g0060 a0001c0002t0001g0061 others(1): Show |
4 | HG01952.hp2 HG02622.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48-271G>A | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 1/16 | chr9 | 92324480 | |||||||
chr9:92324511 | G | A | 1 | a0001c0001t0003g0058 | 2 | NA18944.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.-48-302C>T | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 1/16 | chr9 | 92324511 | |||||||
chr9:92324580 | G | A | 1 | a0001c0001t0002g0205 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-48-371C>T | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 1/16 | chr9 | 92324580 | |||||||
chr9:92324606 | T | G | 1 | a0001c0001t0002g0206 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-48-397A>C | NOL8 | ENSG00000198000.12 | transcript | ENST00000442668.7 | protein_coding | 1/16 | chr9 | 92324606 |