Item | Value |
---|---|
geneid | 2934 |
ensemblid | ENSG00000148180.22 |
hgncid | 4620 |
symbol | GSN |
name | gelsolin |
refseq_nuc | NM_198252.3 |
refseq_prot | NP_937895.1 |
ensembl_nuc | ENST00000432226.7 |
ensembl_prot | ENSP00000404226.2 |
mane_status | MANE Select |
chr | chr9 |
start | 121268162 |
end | 121332842 |
strand | + |
ver | v1.2 |
region | chr9:121268162-121332842 |
region5000 | chr9:121263162-121337842 |
regionname0 | GSN_chr9_121268162_121332842 |
regionname5000 | GSN_chr9_121263162_121337842 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 731 | 242 | 58 | 52 | 98 | 13 | 20 | 71 | GSN_chr9_121263162_121337842 | GSN | MVVEH others(726): Show |
chr9 | 121263162 | 121337842 |
a0002 | 0/0 | 731 | 47 | 2 | 12 | 28 | 0 | 5 | 22 | GSN_chr9_121263162_121337842 | GSN | MVVEH others(726): Show |
chr9 | 121263162 | 121337842 |
a0003 | 0/0 | 731 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | MVVEH others(726): Show |
chr9 | 121263162 | 121337842 |
a0004 | 0/0 | 731 | 6 | 3 | 1 | 0 | 0 | 2 | 0 | GSN_chr9_121263162_121337842 | GSN | MVVEH others(726): Show |
chr9 | 121263162 | 121337842 |
a0005 | 0/0 | 731 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | MVVEH others(726): Show |
chr9 | 121263162 | 121337842 |
a0006 | 0/0 | 731 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | MVVEH others(726): Show |
chr9 | 121263162 | 121337842 |
a0007 | 0/1 | 731 | 2 | 0 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | MVVEH others(726): Show |
chr9 | 121263162 | 121337842 |
a0008 | 0/0 | 731 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | MVVEH others(726): Show |
chr9 | 121263162 | 121337842 |
a0009 | 0/0 | 731 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | MVVEH others(726): Show |
chr9 | 121263162 | 121337842 |
a0010 | 0/0 | 731 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | MVVEH others(726): Show |
chr9 | 121263162 | 121337842 |
a0011 | 0/0 | 731 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | MVVEH others(726): Show |
chr9 | 121263162 | 121337842 |
a0012 | 0/0 | 731 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GSN_chr9_121263162_121337842 | GSN | MVVEH others(726): Show |
chr9 | 121263162 | 121337842 |
a0013 | 0/0 | 731 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | MVVEH others(726): Show |
chr9 | 121263162 | 121337842 |
a0014 | 0/0 | 731 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | MVVEH others(726): Show |
chr9 | 121263162 | 121337842 |
a0015 | 0/0 | 731 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | MVVEH others(726): Show |
chr9 | 121263162 | 121337842 |
a0016 | 0/0 | 731 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | MVVEH others(726): Show |
chr9 | 121263162 | 121337842 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2193 | 203 | 50 | 46 | 75 | 13 | 18 | GSN_chr9_121263162_121337842 | GSN | ATGGT others(2188): Show |
chr9 | 121263162 | 121337842 | ||
a0001c0003 | 0/0 | 2193 | 28 | 6 | 2 | 19 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | ATGGT others(2188): Show |
chr9 | 121263162 | 121337842 | ||
a0001c0004 | 0/0 | 2193 | 8 | 0 | 3 | 4 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | ATGGT others(2188): Show |
chr9 | 121263162 | 121337842 | ||
a0001c0010 | 0/0 | 2193 | 2 | 1 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | ATGGT others(2188): Show |
chr9 | 121263162 | 121337842 | ||
a0001c0023 | 0/0 | 2193 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | ATGGT others(2188): Show |
chr9 | 121263162 | 121337842 | ||
a0002c0002 | 0/0 | 2193 | 40 | 2 | 11 | 23 | 0 | 4 | GSN_chr9_121263162_121337842 | GSN | ATGGT others(2188): Show |
chr9 | 121263162 | 121337842 | ||
a0002c0007 | 0/0 | 2193 | 5 | 0 | 0 | 4 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | ATGGT others(2188): Show |
chr9 | 121263162 | 121337842 | ||
a0002c0014 | 0/0 | 2193 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | ATGGT others(2188): Show |
chr9 | 121263162 | 121337842 | ||
a0002c0015 | 0/0 | 2193 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | ATGGT others(2188): Show |
chr9 | 121263162 | 121337842 | ||
a0003c0005 | 0/0 | 2193 | 8 | 8 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | ATGGT others(2188): Show |
chr9 | 121263162 | 121337842 | ||
a0004c0006 | 0/0 | 2193 | 6 | 3 | 1 | 0 | 0 | 2 | GSN_chr9_121263162_121337842 | GSN | ATGGT others(2188): Show |
chr9 | 121263162 | 121337842 | ||
a0005c0008 | 0/0 | 2193 | 3 | 2 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | ATGGT others(2188): Show |
chr9 | 121263162 | 121337842 | ||
a0006c0009 | 0/0 | 2193 | 3 | 3 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | ATGGT others(2188): Show |
chr9 | 121263162 | 121337842 | ||
a0007c0018 | 0/1 | 2193 | 1 | 0 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | ATGGT others(2188): Show |
chr9 | 121263162 | 121337842 | ||
a0007c0022 | 0/0 | 2193 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | ATGGT others(2188): Show |
chr9 | 121263162 | 121337842 | ||
a0008c0012 | 0/0 | 2193 | 2 | 2 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | ATGGT others(2188): Show |
chr9 | 121263162 | 121337842 | ||
a0009c0011 | 0/0 | 2193 | 2 | 2 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | ATGGT others(2188): Show |
chr9 | 121263162 | 121337842 | ||
a0010c0021 | 0/0 | 2193 | 1 | 0 | 0 | 0 | 1 | 0 | GSN_chr9_121263162_121337842 | GSN | ATGGT others(2188): Show |
chr9 | 121263162 | 121337842 | ||
a0011c0019 | 0/0 | 2193 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | ATGGT others(2188): Show |
chr9 | 121263162 | 121337842 | ||
a0012c0017 | 0/0 | 2193 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | ATGGT others(2188): Show |
chr9 | 121263162 | 121337842 | ||
a0013c0013 | 0/0 | 2193 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | ATGGT others(2188): Show |
chr9 | 121263162 | 121337842 | ||
a0014c0020 | 0/0 | 2193 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | ATGGT others(2188): Show |
chr9 | 121263162 | 121337842 | ||
a0015c0024 | 0/0 | 2193 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | ATGGT others(2188): Show |
chr9 | 121263162 | 121337842 | ||
a0016c0016 | 0/0 | 2193 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | ATGGT others(2188): Show |
chr9 | 121263162 | 121337842 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 2595 | 192 | 44 | 42 | 74 | 13 | 18 | GSN_chr9_121263162_121337842 | GSN | GGAAC others(2590): Show |
chr9 | 121263162 | 121337842 |
a0001c0001t0003 | 0/0 | 2597 | 10 | 6 | 4 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | GGAAC others(2592): Show |
chr9 | 121263162 | 121337842 |
a0001c0001t0006 | 0/0 | 2595 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | GGAAC others(2590): Show |
chr9 | 121263162 | 121337842 |
a0001c0003t0001 | 0/0 | 2595 | 28 | 6 | 2 | 19 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | GGAAC others(2590): Show |
chr9 | 121263162 | 121337842 |
a0001c0004t0002 | 0/0 | 2597 | 8 | 0 | 3 | 4 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | GGAAC others(2592): Show |
chr9 | 121263162 | 121337842 |
a0001c0010t0001 | 0/0 | 2595 | 2 | 1 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | GGAAC others(2590): Show |
chr9 | 121263162 | 121337842 |
a0001c0023t0003 | 0/0 | 2597 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | GGAAC others(2592): Show |
chr9 | 121263162 | 121337842 |
a0002c0002t0002 | 0/0 | 2597 | 37 | 0 | 10 | 23 | 0 | 4 | GSN_chr9_121263162_121337842 | GSN | GGAAC others(2592): Show |
chr9 | 121263162 | 121337842 |
a0002c0002t0004 | 0/0 | 2599 | 2 | 2 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | GGAAC others(2594): Show |
chr9 | 121263162 | 121337842 |
a0002c0002t0007 | 0/0 | 2597 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | GGAAC others(2592): Show |
chr9 | 121263162 | 121337842 |
a0002c0007t0001 | 0/0 | 2595 | 5 | 0 | 0 | 4 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | GGAAC others(2590): Show |
chr9 | 121263162 | 121337842 |
a0002c0014t0002 | 0/0 | 2597 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | GGAAC others(2592): Show |
chr9 | 121263162 | 121337842 |
a0002c0015t0001 | 0/0 | 2595 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | GGAAC others(2590): Show |
chr9 | 121263162 | 121337842 |
a0003c0005t0001 | 0/0 | 2595 | 8 | 8 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | GGAAC others(2590): Show |
chr9 | 121263162 | 121337842 |
a0004c0006t0004 | 0/0 | 2599 | 5 | 2 | 1 | 0 | 0 | 2 | GSN_chr9_121263162_121337842 | GSN | GGAAC others(2594): Show |
chr9 | 121263162 | 121337842 |
a0004c0006t0005 | 0/0 | 2595 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | GGAAC others(2590): Show |
chr9 | 121263162 | 121337842 |
a0005c0008t0001 | 0/0 | 2595 | 3 | 2 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | GGAAC others(2590): Show |
chr9 | 121263162 | 121337842 |
a0006c0009t0004 | 0/0 | 2599 | 3 | 3 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | GGAAC others(2594): Show |
chr9 | 121263162 | 121337842 |
a0007c0018t0001 | 0/1 | 2595 | 1 | 0 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | GGAAC others(2590): Show |
chr9 | 121263162 | 121337842 |
a0007c0022t0001 | 0/0 | 2595 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | GGAAC others(2590): Show |
chr9 | 121263162 | 121337842 |
a0008c0012t0001 | 0/0 | 2595 | 2 | 2 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | GGAAC others(2590): Show |
chr9 | 121263162 | 121337842 |
a0009c0011t0001 | 0/0 | 2595 | 2 | 2 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | GGAAC others(2590): Show |
chr9 | 121263162 | 121337842 |
a0010c0021t0001 | 0/0 | 2595 | 1 | 0 | 0 | 0 | 1 | 0 | GSN_chr9_121263162_121337842 | GSN | GGAAC others(2590): Show |
chr9 | 121263162 | 121337842 |
a0011c0019t0001 | 0/0 | 2595 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | GGAAC others(2590): Show |
chr9 | 121263162 | 121337842 |
a0012c0017t0001 | 0/0 | 2595 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | GGAAC others(2590): Show |
chr9 | 121263162 | 121337842 |
a0013c0013t0001 | 0/0 | 2595 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | GGAAC others(2590): Show |
chr9 | 121263162 | 121337842 |
a0014c0020t0001 | 0/0 | 2595 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | GGAAC others(2590): Show |
chr9 | 121263162 | 121337842 |
a0015c0024t0001 | 0/0 | 2595 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | GGAAC others(2590): Show |
chr9 | 121263162 | 121337842 |
a0016c0016t0001 | 0/0 | 2595 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | GGAAC others(2590): Show |
chr9 | 121263162 | 121337842 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0006 | 0/0 | 4 | 2 | 1 | 0 | 1 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0030 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0034 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0003g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0001t0006g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0003t0001g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0003t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0003t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0003t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0003t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0003t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0003t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0003t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0003t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0003t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0003t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0003t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0003t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0003t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0003t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0003t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0003t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0003t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0003t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0004t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0004t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0004t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0004t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0004t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0004t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0004t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0004t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0010t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0010t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0001c0023t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0002 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0007 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0002t0007g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0007t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0007t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0007t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0007t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0007t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0014t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0002c0015t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0003c0005t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0003c0005t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0003c0005t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0003c0005t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0003c0005t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0003c0005t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0003c0005t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0004c0006t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0004c0006t0004g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0004c0006t0004g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0004c0006t0004g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0004c0006t0004g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0004c0006t0005g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0005c0008t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0005c0008t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0005c0008t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0006c0009t0004g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0006c0009t0004g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0007c0018t0001g0254 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0007c0022t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0008c0012t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0008c0012t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0009c0011t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0010c0021t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0011c0019t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0012c0017t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0013c0013t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0014c0020t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0015c0024t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
a0016c0016t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0034 | EUR | GBR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | GBR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | GBR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0163 | EUR | GBR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0153 | EUR | FIN | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | FIN | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00323 | hp1 | a0010 | c0021 | t0001 | g0107 | EUR | FIN | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0118 | EUR | FIN | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00408 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | CHS | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00438 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | CHS | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00438 | hp2 | a0002 | c0002 | t0002 | g0013 | EAS | CHS | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00558 | hp1 | a0001 | c0001 | t0006 | g0031 | EAS | CHS | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00558 | hp2 | a0001 | c0003 | t0001 | g0009 | EAS | CHS | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00597 | hp1 | a0002 | c0002 | t0002 | g0060 | EAS | CHS | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00621 | hp1 | a0001 | c0004 | t0002 | g0155 | EAS | CHS | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | CHS | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00639 | hp1 | a0002 | c0015 | t0001 | g0047 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00735 | hp1 | a0001 | c0003 | t0001 | g0129 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01071 | hp2 | a0004 | c0006 | t0004 | g0222 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01074 | hp2 | a0001 | c0003 | t0001 | g0150 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01081 | hp1 | a0002 | c0002 | t0007 | g0076 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01106 | hp1 | a0002 | c0002 | t0002 | g0059 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01109 | hp1 | a0001 | c0010 | t0001 | g0114 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01168 | hp2 | a0002 | c0002 | t0002 | g0063 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01243 | hp1 | a0005 | c0008 | t0001 | g0095 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0148 | AMR | CLM | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | CLM | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01346 | hp2 | a0002 | c0002 | t0002 | g0011 | AMR | CLM | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | CLM | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01433 | hp2 | a0002 | c0002 | t0002 | g0067 | AMR | CLM | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0084 | EUR | IBS | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0165 | EUR | IBS | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0083 | EUR | IBS | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0213 | EUR | IBS | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01884 | hp1 | a0004 | c0006 | t0005 | g0236 | AFR | ACB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01884 | hp2 | a0004 | c0006 | t0004 | g0184 | AFR | ACB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01891 | hp2 | a0001 | c0023 | t0003 | g0044 | AFR | ACB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01928 | hp1 | a0002 | c0002 | t0002 | g0058 | AMR | PEL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01928 | hp2 | a0001 | c0004 | t0002 | g0139 | AMR | PEL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0027 | AMR | PEL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01952 | hp1 | a0002 | c0002 | t0002 | g0066 | AMR | PEL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01981 | hp2 | a0002 | c0002 | t0002 | g0010 | AMR | PEL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01993 | hp1 | a0001 | c0004 | t0002 | g0045 | AMR | PEL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02015 | hp1 | a0001 | c0003 | t0001 | g0009 | EAS | KHV | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02015 | hp2 | a0007 | c0022 | t0001 | g0181 | EAS | KHV | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02027 | hp2 | a0002 | c0007 | t0001 | g0061 | EAS | KHV | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02071 | hp2 | a0002 | c0002 | t0002 | g0075 | EAS | KHV | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02083 | hp2 | a0002 | c0002 | t0002 | g0013 | EAS | KHV | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02129 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | KHV | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02132 | hp2 | a0001 | c0003 | t0001 | g0009 | EAS | KHV | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0116 | AFR | ACB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02155 | hp1 | a0001 | c0003 | t0001 | g0195 | EAS | CDX | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | CDX | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02273 | hp1 | a0002 | c0002 | t0002 | g0007 | AMR | PEL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02273 | hp2 | a0001 | c0001 | t0003 | g0162 | AMR | PEL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | ACB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02280 | hp2 | a0003 | c0005 | t0001 | g0039 | AFR | ACB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0151 | AMR | PEL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02293 | hp2 | a0002 | c0002 | t0002 | g0010 | AMR | PEL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02300 | hp2 | a0001 | c0004 | t0002 | g0046 | AMR | PEL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02451 | hp1 | a0003 | c0005 | t0001 | g0242 | AFR | ACB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02451 | hp2 | a0008 | c0012 | t0001 | g0097 | AFR | ACB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02572 | hp1 | a0002 | c0002 | t0004 | g0055 | AFR | GWD | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02647 | hp1 | a0001 | c0001 | t0003 | g0017 | AFR | GWD | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02647 | hp2 | a0006 | c0009 | t0004 | g0038 | AFR | GWD | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02717 | hp2 | a0009 | c0011 | t0001 | g0041 | AFR | GWD | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02738 | hp1 | a0004 | c0006 | t0004 | g0223 | SAS | PJL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02809 | hp1 | a0008 | c0012 | t0001 | g0101 | AFR | GWD | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02818 | hp1 | a0001 | c0001 | t0003 | g0017 | AFR | GWD | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02818 | hp2 | a0002 | c0002 | t0004 | g0054 | AFR | GWD | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02886 | hp1 | a0003 | c0005 | t0001 | g0243 | AFR | GWD | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02895 | hp1 | a0003 | c0005 | t0001 | g0241 | AFR | GWD | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02896 | hp1 | a0006 | c0009 | t0004 | g0038 | AFR | GWD | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02922 | hp1 | a0005 | c0008 | t0001 | g0094 | AFR | ESN | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02922 | hp2 | a0001 | c0003 | t0001 | g0225 | AFR | ESN | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02965 | hp1 | a0001 | c0003 | t0001 | g0226 | AFR | ESN | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | ESN | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03017 | hp2 | a0012 | c0017 | t0001 | g0090 | SAS | PJL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03041 | hp1 | a0005 | c0008 | t0001 | g0096 | AFR | GWD | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03098 | hp1 | a0009 | c0011 | t0001 | g0041 | AFR | MSL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ESN | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03139 | hp2 | a0001 | c0003 | t0001 | g0201 | AFR | ESN | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03195 | hp1 | a0003 | c0005 | t0001 | g0246 | AFR | ESN | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03195 | hp2 | a0001 | c0003 | t0001 | g0261 | AFR | ESN | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | MSL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | MSL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03225 | hp2 | a0013 | c0013 | t0001 | g0260 | AFR | MSL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0108 | AFR | MSL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | MSL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03486 | hp2 | a0014 | c0020 | t0001 | g0257 | AFR | MSL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03490 | hp1 | a0002 | c0002 | t0002 | g0062 | SAS | PJL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03516 | hp1 | a0001 | c0003 | t0001 | g0212 | AFR | ESN | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0115 | AFR | ESN | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03579 | hp1 | a0004 | c0006 | t0004 | g0256 | AFR | MSL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03579 | hp2 | a0006 | c0009 | t0004 | g0239 | AFR | MSL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03654 | hp1 | a0002 | c0002 | t0002 | g0050 | SAS | PJL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03669 | hp2 | a0001 | c0003 | t0001 | g0237 | SAS | PJL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03688 | hp1 | a0002 | c0002 | t0002 | g0057 | SAS | STU | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | STU | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03710 | hp2 | a0002 | c0007 | t0001 | g0049 | SAS | PJL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | BEB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03831 | hp2 | a0001 | c0004 | t0002 | g0245 | SAS | BEB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | BEB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03834 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | BEB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | BEB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | BEB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | STU | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG04199 | hp1 | a0004 | c0006 | t0004 | g0238 | SAS | STU | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18522 | hp1 | a0001 | c0010 | t0001 | g0113 | AFR | YRI | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | YRI | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18612 | hp1 | a0002 | c0002 | t0002 | g0069 | EAS | CHB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18612 | hp2 | a0001 | c0003 | t0001 | g0131 | EAS | CHB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | CHB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18906 | hp1 | a0001 | c0003 | t0001 | g0211 | AFR | YRI | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18906 | hp2 | a0015 | c0024 | t0001 | g0100 | AFR | YRI | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18939 | hp2 | a0002 | c0014 | t0002 | g0048 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18941 | hp1 | a0002 | c0002 | t0002 | g0070 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18942 | hp1 | a0001 | c0003 | t0001 | g0133 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18943 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18944 | hp1 | a0002 | c0007 | t0001 | g0056 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18945 | hp2 | a0002 | c0002 | t0002 | g0053 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18948 | hp1 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18949 | hp2 | a0001 | c0004 | t0002 | g0122 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18952 | hp1 | a0001 | c0003 | t0001 | g0203 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18952 | hp2 | a0001 | c0004 | t0002 | g0174 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18954 | hp2 | a0002 | c0007 | t0001 | g0072 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18957 | hp2 | a0001 | c0004 | t0002 | g0171 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18964 | hp2 | a0002 | c0002 | t0002 | g0052 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18969 | hp2 | a0002 | c0002 | t0002 | g0071 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18971 | hp2 | a0001 | c0003 | t0001 | g0099 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18975 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18979 | hp1 | a0002 | c0002 | t0002 | g0074 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18981 | hp1 | a0001 | c0003 | t0001 | g0216 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18985 | hp2 | a0002 | c0002 | t0002 | g0253 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18986 | hp1 | a0001 | c0003 | t0001 | g0218 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18986 | hp2 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18988 | hp2 | a0001 | c0003 | t0001 | g0016 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18990 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18997 | hp2 | a0002 | c0002 | t0002 | g0073 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18999 | hp1 | a0002 | c0007 | t0001 | g0065 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19003 | hp1 | a0002 | c0002 | t0002 | g0077 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19004 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19004 | hp2 | a0001 | c0003 | t0001 | g0219 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19010 | hp1 | a0002 | c0002 | t0002 | g0051 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19011 | hp1 | a0001 | c0003 | t0001 | g0169 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19012 | hp2 | a0001 | c0003 | t0001 | g0016 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19043 | hp1 | a0003 | c0005 | t0001 | g0244 | AFR | LWK | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19058 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19066 | hp1 | a0016 | c0016 | t0001 | g0259 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19070 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19083 | hp1 | a0002 | c0002 | t0002 | g0064 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA19084 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ASW | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA20129 | hp2 | a0003 | c0005 | t0001 | g0039 | AFR | ASW | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | TSI | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0120 | EUR | TSI | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG01123 | hp2 | a0002 | c0002 | t0002 | g0011 | AMR | CLM | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0231 | AFR | ACB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG02559 | hp2 | a0011 | c0019 | t0001 | g0230 | AFR | ACB | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG03471 | hp2 | a0003 | c0005 | t0001 | g0240 | AFR | MSL | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | USA | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | USA | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18955 | hp1 | a0002 | c0002 | t0002 | g0068 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | LWK | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | LWK | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
homoSapiens | chm13v2 | a0007 | c0018 | t0001 | g0254 | REF | REF | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0030 | REF | REF | GSN_chr9_121263162_121337842 | GSN | chr9 | 121263162 | 121337842 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:121302000 | A | G | 2 | a0003 a0006 |
11 | HG02280.hp2 HG02451.hp1 HG02647.hp2 others(8): Show |
missense_variant | MODERATE | c.29A>G | p.Lys10Arg | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 3/18 | 189/2595 | 29/2196 | 10/731 | chr9 | 121302000 | |||
chr9:121302046 | C | G | 2 | a0008 a0015 |
3 | HG02451.hp2 HG02809.hp1 NA18906.hp2 |
missense_variant | MODERATE | c.75C>G | p.Phe25Leu | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 3/18 | 235/2595 | 75/2196 | 25/731 | chr9 | 121302046 | |||
chr9:121302098 | G | T | 1 | a0009 | 2 | HG02717.hp2 HG03098.hp1 |
missense_variant | MODERATE | c.127G>T | p.Ala43Ser | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 3/18 | 287/2595 | 127/2196 | 43/731 | chr9 | 121302098 | |||
chr9:121302104 | G | A | 1 | a0013 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.133G>A | p.Val45Ile | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 3/18 | 293/2595 | 133/2196 | 45/731 | chr9 | 121302104 | |||
chr9:121302946 | G | A | 2 | a0002 a0016 |
48 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(45): Show |
missense_variant | MODERATE | c.232G>A | p.Ala78Thr | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/18 | 392/2595 | 232/2196 | 78/731 | chr9 | 121302946 | |||
chr9:121312363 | A | G | 1 | a0005 | 3 | HG01243.hp1 HG02922.hp1 HG03041.hp1 |
missense_variant | MODERATE | c.538A>G | p.Asn180Asp | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 6/18 | 698/2595 | 538/2196 | 180/731 | chr9 | 121312363 | |||
chr9:121312456 | G | C | 1 | a0012 | 1 | HG03017.hp2 | missense_variant | MODERATE | c.631G>C | p.Glu211Gln | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 6/18 | 791/2595 | 631/2196 | 211/731 | chr9 | 121312456 | |||
chr9:121314000 | C | T | 1 | a0016 | 1 | NA19066.hp1 | missense_variant | MODERATE | c.730C>T | p.Arg244Cys | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 7/18 | 890/2595 | 730/2196 | 244/731 | chr9 | 121314000 | |||
chr9:121326630 | C | G | 1 | a0004 | 6 | HG01071.hp2 HG01884.hp1 HG01884.hp2 others(3): Show |
missense_variant | MODERATE | c.1535C>G | p.Thr512Ser | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 13/18 | 1695/2595 | 1535/2196 | 512/731 | chr9 | 121326630 | |||
chr9:121327357 | A | G | 1 | a0010 | 1 | HG00323.hp1 | missense_variant | MODERATE | c.1637A>G | p.Lys546Arg | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 14/18 | 1797/2595 | 1637/2196 | 546/731 | chr9 | 121327357 | |||
chr9:121327414 | C | T | 4 | a0003 a0004 a0014 others(1): Show |
16 | HG01071.hp2 HG01884.hp1 HG01884.hp2 others(13): Show |
missense_variant | MODERATE | c.1694C>T | p.Thr565Met | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 14/18 | 1854/2595 | 1694/2196 | 565/731 | chr9 | 121327414 | |||
chr9:121328978 | G | T | 1 | a0011 | 1 | HG02559.hp2 | missense_variant | MODERATE | c.1850G>T | p.Arg617Leu | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 15/18 | 2010/2595 | 1850/2196 | 617/731 | chr9 | 121328978 | |||
chr9:121329281 | C | T | 1 | a0007 | 1 | HG02015.hp2 | missense_variant | MODERATE | c.1931C>T | p.Thr644Met | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 16/18 | 2091/2595 | 1931/2196 | 644/731 | chr9 | 121329281 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:121302157 | C | T | 1 | a0009c0011 | 2 | HG02717.hp2 HG03098.hp1 |
synonymous_variant | LOW | c.186C>T | p.His62His | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 3/18 | 346/2595 | 186/2196 | 62/731 | chr9 | 121302157 | |||
chr9:121302957 | C | T | 1 | a0001c0023 | 1 | HG01891.hp2 | synonymous_variant | LOW | c.243C>T | p.Thr81Thr | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/18 | 403/2595 | 243/2196 | 81/731 | chr9 | 121302957 | |||
chr9:121321315 | A | G | 1 | a0001c0010 | 2 | HG01109.hp1 NA18522.hp1 |
synonymous_variant | LOW | c.1239A>G | p.Thr413Thr | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/18 | 1399/2595 | 1239/2196 | 413/731 | chr9 | 121321315 | |||
chr9:121321336 | C | T | 2 | a0001c0003 a0002c0015 |
29 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(26): Show |
synonymous_variant | LOW | c.1260C>T | p.Gly420Gly | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/18 | 1420/2595 | 1260/2196 | 420/731 | chr9 | 121321336 | |||
chr9:121326538 | C | T | 1 | a0002c0014 | 1 | NA18939.hp2 | synonymous_variant | LOW | c.1443C>T | p.Pro481Pro | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 13/18 | 1603/2595 | 1443/2196 | 481/731 | chr9 | 121326538 | |||
chr9:121326580 | C | T | 1 | a0007c0022 | 1 | HG02015.hp2 | synonymous_variant | LOW | c.1485C>T | p.Ile495Ile | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 13/18 | 1645/2595 | 1485/2196 | 495/731 | chr9 | 121326580 | |||
chr9:121332522 | T | C | 8 | a0001c0004 a0002c0002 a0002c0014 others(5): Show |
64 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(61): Show |
synonymous_variant | LOW | c.2115T>C | p.Phe705Phe | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 18/18 | 2275/2595 | 2115/2196 | 705/731 | chr9 | 121332522 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:121268202 | C | G | 1 | a0002c0002t0007 | 1 | HG01081.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-120C>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/18 | chr9 | 121268202 | |||||||
chr9:121281478 | C | T | 1 | a0001c0001t0006 | 1 | HG00558.hp1 | 5_prime_UTR_variant | MODIFIER | c.-94C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/18 | 20494 | chr9 | 121281478 | ||||||
chr9:121281480 | T | C | 1 | a0004c0006t0005 | 1 | HG01884.hp1 | 5_prime_UTR_variant | MODIFIER | c.-92T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/18 | 20492 | chr9 | 121281480 | ||||||
chr9:121332699 | A | AGT | 2 | a0001c0001t0003 a0001c0023t0003 |
11 | HG01255.hp1 HG01891.hp2 HG01934.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*115_*116dupGT | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 18/18 | 117 | INFO_REALIGN_3_PRIME | chr9 | 121332699 | |||||
chr9:121332699 | A | AGTGT | 3 | a0002c0002t0004 a0004c0006t0004 a0006c0009t0004 |
10 | HG01071.hp2 HG01884.hp2 HG02572.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*113_*116dupGTGT | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 18/18 | 117 | INFO_REALIGN_3_PRIME | chr9 | 121332699 | |||||
chr9:121332719 | T | TG | 4 | a0001c0004t0002 a0002c0002t0002 a0002c0002t0007 others(1): Show |
47 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*116_*117insG | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 18/18 | 117 | chr9 | 121332719 | ||||||
chr9:121332723 | T | TG | 4 | a0001c0004t0002 a0002c0002t0002 a0002c0002t0007 others(1): Show |
47 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*120_*121insG | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 18/18 | 121 | chr9 | 121332723 | ||||||
chr9:121332725 | C | T | 4 | a0001c0004t0002 a0002c0002t0002 a0002c0002t0007 others(1): Show |
47 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*122C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 18/18 | 122 | chr9 | 121332725 | ||||||
chr9:121332727 | T | C | 4 | a0001c0004t0002 a0002c0002t0002 a0002c0002t0007 others(1): Show |
47 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*124T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 18/18 | 124 | chr9 | 121332727 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:121268281 | T | C | 1 | a0001c0001t0001g0043 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-103+62T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121268281 | |||||||
chr9:121268283 | C | T | 2 | a0001c0001t0001g0263 a0001c0001t0001g0264 |
2 | NA18953.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.-103+64C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121268283 | |||||||
chr9:121268305 | A | G | 3 | a0001c0001t0001g0042 a0001c0001t0001g0262 a0001c0003t0001g0261 |
4 | HG02976.hp2 HG03130.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-103+86A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121268305 | |||||||
chr9:121268803 | G | T | 1 | a0013c0013t0001g0260 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-103+584G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121268803 | |||||||
chr9:121269474 | G | A | 1 | a0001c0023t0003g0044 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-103+1255G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121269474 | |||||||
chr9:121269615 | C | T | 1 | a0016c0016t0001g0259 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-103+1396C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121269615 | |||||||
chr9:121269769 | T | C | 2 | a0001c0004t0002g0045 a0001c0004t0002g0046 |
2 | HG01993.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.-103+1550T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121269769 | |||||||
chr9:121269809 | A | C | 1 | a0009c0011t0001g0041 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-103+1590A>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121269809 | |||||||
chr9:121269824 | A | T | 4 | a0001c0001t0001g0258 a0004c0006t0004g0256 a0013c0013t0001g0260 others(1): Show |
4 | HG03209.hp2 HG03225.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-103+1605A>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121269824 | |||||||
chr9:121269857 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-103+1638C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121269857 | |||||||
chr9:121270102 | G | A | 1 | a0002c0015t0001g0047 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-103+1883G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121270102 | |||||||
chr9:121270710 | G | T | 1 | a0002c0002t0002g0253 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-103+2491G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121270710 | |||||||
chr9:121270766 | C | A | 98 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0018 others(95): Show |
115 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.-103+2547C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121270766 | |||||||
chr9:121270902 | GTGTGTAT others(3): Show |
G | 1 | a0001c0001t0001g0123 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-103+2686_-103+269 others(14): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 121270902 | ||||||
chr9:121272098 | C | T | 3 | a0001c0001t0001g0040 a0001c0001t0001g0251 a0001c0001t0001g0252 |
4 | HG02129.hp1 NA18943.hp1 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.-103+3879C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121272098 | |||||||
chr9:121272111 | G | C | 1 | a0002c0014t0002g0048 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-103+3892G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121272111 | |||||||
chr9:121272117 | G | C | 1 | a0004c0006t0004g0256 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-103+3898G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121272117 | |||||||
chr9:121272234 | C | T | 4 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0249 others(1): Show |
4 | NA18939.hp1 NA18960.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.-103+4015C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121272234 | |||||||
chr9:121272431 | ATAATGTC others(4): Show |
A | 1 | a0001c0001t0001g0258 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-103+4214_-103+422 others(15): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 121272431 | ||||||
chr9:121272531 | G | A | 80 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(77): Show |
97 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.-103+4312G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121272531 | |||||||
chr9:121272581 | G | A | 1 | a0001c0023t0003g0044 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-103+4362G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121272581 | |||||||
chr9:121272700 | C | T | 1 | a0003c0005t0001g0246 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-103+4481C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121272700 | |||||||
chr9:121272702 | A | G | 1 | a0001c0004t0002g0245 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-103+4483A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121272702 | |||||||
chr9:121272783 | C | T | 10 | a0001c0023t0003g0044 a0003c0005t0001g0039 a0003c0005t0001g0240 others(7): Show |
12 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-103+4564C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121272783 | |||||||
chr9:121272866 | T | A | 1 | a0007c0022t0001g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-103+4647T>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121272866 | |||||||
chr9:121272950 | A | G | 10 | a0001c0023t0003g0044 a0003c0005t0001g0039 a0003c0005t0001g0240 others(7): Show |
12 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-103+4731A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121272950 | |||||||
chr9:121273021 | G | C | 1 | a0001c0001t0001g0182 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-103+4802G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121273021 | |||||||
chr9:121273038 | A | T | 1 | a0001c0001t0001g0250 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-103+4819A>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121273038 | |||||||
chr9:121273102 | T | C | 141 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(138): Show |
173 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.-103+4883T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121273102 | |||||||
chr9:121273129 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-103+4910G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121273129 | |||||||
chr9:121273267 | A | G | 95 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(92): Show |
117 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.-103+5048A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121273267 | |||||||
chr9:121273449 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-103+5230C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121273449 | |||||||
chr9:121273818 | A | G | 95 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(92): Show |
117 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.-103+5599A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121273818 | |||||||
chr9:121273863 | G | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0179 |
4 | NA18977.hp1 NA18985.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.-103+5644G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121273863 | |||||||
chr9:121273925 | G | A | 39 | a0002c0002t0002g0002 a0002c0002t0002g0007 a0002c0002t0002g0010 others(36): Show |
48 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.-103+5706G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121273925 | |||||||
chr9:121273967 | A | T | 39 | a0002c0002t0002g0002 a0002c0002t0002g0007 a0002c0002t0002g0010 others(36): Show |
48 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.-103+5748A>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121273967 | |||||||
chr9:121274253 | CT | C | 5 | a0001c0001t0001g0005 a0001c0001t0001g0182 a0001c0001t0001g0185 others(2): Show |
8 | HG01261.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-103+6043delT | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 121274253 | ||||||
chr9:121274342 | C | T | 1 | a0001c0001t0001g0020 | 2 | HG02809.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-103+6123C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121274342 | |||||||
chr9:121274509 | T | TA | 15 | a0001c0001t0001g0005 a0001c0001t0001g0182 a0001c0001t0001g0185 others(12): Show |
20 | HG01261.hp1 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.-103+6300dupA | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 121274509 | ||||||
chr9:121274519 | A | T | 1 | a0004c0006t0004g0238 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-103+6300A>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121274519 | |||||||
chr9:121274543 | G | A | 1 | a0002c0007t0001g0049 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-103+6324G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121274543 | |||||||
chr9:121274745 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-103+6526G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121274745 | |||||||
chr9:121274992 | C | G | 1 | a0014c0020t0001g0257 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-102-6478C>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121274992 | |||||||
chr9:121275008 | C | T | 1 | a0001c0001t0001g0178 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-102-6462C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121275008 | |||||||
chr9:121275022 | C | T | 1 | a0001c0003t0001g0237 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-102-6448C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121275022 | |||||||
chr9:121275073 | G | C | 1 | a0002c0002t0002g0050 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-102-6397G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121275073 | |||||||
chr9:121275189 | A | G | 2 | a0001c0001t0001g0042 a0001c0001t0001g0262 |
3 | HG02976.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-102-6281A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121275189 | |||||||
chr9:121275329 | C | T | 81 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(78): Show |
98 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.-102-6141C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121275329 | |||||||
chr9:121275493 | G | A | 15 | a0001c0001t0001g0005 a0001c0001t0001g0182 a0001c0001t0001g0185 others(12): Show |
20 | HG01261.hp1 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.-102-5977G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121275493 | |||||||
chr9:121275613 | C | T | 1 | a0004c0006t0005g0236 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-102-5857C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121275613 | |||||||
chr9:121275739 | A | T | 1 | a0001c0001t0001g0187 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-102-5731A>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121275739 | |||||||
chr9:121275941 | A | G | 1 | a0001c0001t0001g0235 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-102-5529A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121275941 | |||||||
chr9:121275954 | A | T | 3 | a0001c0001t0001g0037 a0001c0001t0001g0233 a0001c0001t0001g0234 |
4 | HG01070.hp1 HG01071.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.-102-5516A>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121275954 | |||||||
chr9:121275977 | A | G | 7 | a0001c0001t0001g0121 a0001c0001t0001g0183 a0001c0001t0001g0258 others(4): Show |
7 | HG01884.hp2 HG02109.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-102-5493A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121275977 | |||||||
chr9:121276172 | G | A | 5 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 others(2): Show |
5 | HG01070.hp2 HG01358.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.-102-5298G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121276172 | |||||||
chr9:121276189 | C | A | 81 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(78): Show |
98 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.-102-5281C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121276189 | |||||||
chr9:121276216 | C | G | 1 | a0001c0001t0001g0232 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-102-5254C>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121276216 | |||||||
chr9:121276313 | C | T | 7 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0175 others(4): Show |
7 | HG00621.hp2 HG02071.hp1 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.-102-5157C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121276313 | |||||||
chr9:121276366 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-102-5104T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121276366 | |||||||
chr9:121276534 | C | G | 201 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(198): Show |
241 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.-102-4936C>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121276534 | |||||||
chr9:121276848 | G | A | 81 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(78): Show |
98 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.-102-4622G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121276848 | |||||||
chr9:121277025 | T | C | 3 | a0001c0001t0001g0183 a0001c0001t0001g0258 a0004c0006t0004g0256 |
3 | HG02109.hp2 HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-102-4445T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121277025 | |||||||
chr9:121277448 | A | T | 1 | a0003c0005t0001g0246 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-102-4022A>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121277448 | |||||||
chr9:121277456 | A | T | 96 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(93): Show |
118 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.-102-4014A>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121277456 | |||||||
chr9:121277593 | C | T | 81 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(78): Show |
98 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.-102-3877C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121277593 | |||||||
chr9:121277618 | C | T | 1 | a0009c0011t0001g0041 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-102-3852C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121277618 | |||||||
chr9:121277653 | T | TAAAATAC others(308): Show |
1 | a0002c0015t0001g0047 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-102-3801_-102-380 others(319): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 121277653 | ||||||
chr9:121277653 | T | TAAAATAC others(310): Show |
1 | a0002c0002t0007g0076 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-102-3801_-102-380 others(321): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 121277653 | ||||||
chr9:121277653 | T | TAAAATAC others(312): Show |
2 | a0002c0002t0002g0013 a0002c0002t0002g0075 |
3 | HG00438.hp2 HG02071.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.-102-3801_-102-380 others(323): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 121277653 | ||||||
chr9:121277653 | T | TAAAATAC others(313): Show |
2 | a0002c0002t0002g0074 a0002c0002t0002g0253 |
2 | NA18979.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.-102-3801_-102-380 others(324): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 121277653 | ||||||
chr9:121277653 | T | TAAAATAC others(314): Show |
1 | a0002c0002t0002g0073 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-102-3801_-102-380 others(325): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 121277653 | ||||||
chr9:121277653 | T | TAAAATAC others(327): Show |
7 | a0002c0002t0002g0007 a0002c0002t0002g0012 a0002c0002t0002g0068 others(4): Show |
10 | HG02273.hp1 NA18612.hp1 NA18941.hp1 others(7): Show |
intron_variant | MODIFIER | c.-102-3801_-102-380 others(338): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 121277653 | ||||||
chr9:121277653 | T | TAAAATAC others(328): Show |
10 | a0002c0002t0002g0002 a0002c0002t0002g0011 a0002c0002t0002g0062 others(7): Show |
14 | HG01123.hp2 HG01168.hp2 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.-102-3801_-102-380 others(339): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 121277653 | ||||||
chr9:121277653 | T | TAAAATAC others(329): Show |
5 | a0002c0002t0002g0010 a0002c0002t0002g0058 a0002c0002t0002g0059 others(2): Show |
6 | HG00597.hp1 HG01106.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.-102-3801_-102-380 others(340): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 121277653 | ||||||
chr9:121277653 | T | TAAAATAC others(330): Show |
4 | a0002c0002t0002g0050 a0002c0002t0002g0057 a0002c0002t0004g0055 others(1): Show |
4 | HG02572.hp1 HG03654.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.-102-3801_-102-380 others(341): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 121277653 | ||||||
chr9:121277653 | T | TAAAATAC others(331): Show |
1 | a0002c0002t0004g0054 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-102-3801_-102-380 others(342): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 121277653 | ||||||
chr9:121277653 | T | TAAAATAC others(332): Show |
1 | a0002c0002t0002g0053 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-102-3801_-102-380 others(343): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 121277653 | ||||||
chr9:121277653 | T | TAAAATAC others(334): Show |
1 | a0002c0007t0001g0049 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-102-3801_-102-380 others(345): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 121277653 | ||||||
chr9:121277653 | T | TAAAATAC others(337): Show |
2 | a0002c0002t0002g0051 a0002c0002t0002g0052 |
2 | NA18964.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.-102-3801_-102-380 others(348): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 121277653 | ||||||
chr9:121277653 | T | TAAAATAC others(326): Show |
1 | a0002c0002t0002g0077 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-102-3801_-102-380 others(337): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 121277653 | ||||||
chr9:121277866 | C | T | 52 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0018 others(49): Show |
59 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.-102-3604C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121277866 | |||||||
chr9:121277918 | TAACA | T | 52 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0018 others(49): Show |
59 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.-102-3542_-102-353 others(8): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 121277918 | ||||||
chr9:121278030 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-102-3440G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121278030 | |||||||
chr9:121278051 | CT | C | 6 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(3): Show |
6 | HG00735.hp1 HG01070.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.-102-3405delT | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 121278051 | ||||||
chr9:121278307 | A | G | 2 | a0001c0001t0001g0170 a0001c0003t0001g0169 |
2 | NA18967.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.-102-3163A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121278307 | |||||||
chr9:121278343 | C | T | 1 | a0001c0003t0001g0261 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-102-3127C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121278343 | |||||||
chr9:121278400 | C | T | 52 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0018 others(49): Show |
59 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.-102-3070C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121278400 | |||||||
chr9:121278450 | A | C | 202 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(199): Show |
242 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.-102-3020A>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121278450 | |||||||
chr9:121278511 | C | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0119 a0001c0001t0001g0120 |
4 | HG00280.hp2 HG01099.hp2 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.-102-2959C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121278511 | |||||||
chr9:121278594 | T | C | 1 | a0004c0006t0005g0236 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-102-2876T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121278594 | |||||||
chr9:121278678 | AC | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0182 a0001c0001t0001g0185 others(2): Show |
8 | HG01261.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-102-2789delC | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr9 | 121278678 | ||||||
chr9:121278719 | G | C | 81 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(78): Show |
98 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.-102-2751G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121278719 | |||||||
chr9:121278907 | C | A | 1 | a0001c0001t0001g0263 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-102-2563C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121278907 | |||||||
chr9:121278948 | G | A | 1 | a0002c0002t0002g0068 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-102-2522G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121278948 | |||||||
chr9:121278968 | C | T | 15 | a0001c0001t0001g0005 a0001c0001t0001g0182 a0001c0001t0001g0185 others(12): Show |
20 | HG01261.hp1 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.-102-2502C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121278968 | |||||||
chr9:121279061 | C | T | 1 | a0002c0015t0001g0047 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-102-2409C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121279061 | |||||||
chr9:121279072 | G | T | 1 | a0002c0007t0001g0049 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-102-2398G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121279072 | |||||||
chr9:121279393 | T | A | 141 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(138): Show |
173 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.-102-2077T>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121279393 | |||||||
chr9:121279539 | C | T | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.-102-1931C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121279539 | |||||||
chr9:121279623 | G | A | 1 | a0001c0001t0001g0020 | 2 | HG02809.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-102-1847G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121279623 | |||||||
chr9:121279766 | G | A | 1 | a0009c0011t0001g0041 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-102-1704G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121279766 | |||||||
chr9:121279774 | C | T | 2 | a0001c0001t0003g0231 a0011c0019t0001g0230 |
2 | HG02486.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-102-1696C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121279774 | |||||||
chr9:121279810 | G | A | 2 | a0013c0013t0001g0260 a0014c0020t0001g0257 |
2 | HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-102-1660G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121279810 | |||||||
chr9:121279915 | G | A | 193 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(190): Show |
232 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.-102-1555G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121279915 | |||||||
chr9:121279946 | T | C | 12 | a0001c0001t0001g0014 a0001c0001t0001g0080 a0001c0001t0001g0083 others(9): Show |
13 | HG00099.hp2 HG00738.hp2 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.-102-1524T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121279946 | |||||||
chr9:121280322 | G | A | 1 | a0004c0006t0004g0184 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-102-1148G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121280322 | |||||||
chr9:121280457 | C | T | 14 | a0001c0001t0001g0005 a0001c0001t0001g0182 a0001c0001t0001g0185 others(11): Show |
19 | HG01261.hp1 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.-102-1013C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121280457 | |||||||
chr9:121280522 | T | C | 6 | a0001c0001t0001g0183 a0001c0001t0001g0258 a0004c0006t0004g0184 others(3): Show |
6 | HG01884.hp2 HG02109.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.-102-948T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121280522 | |||||||
chr9:121280540 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-102-930C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121280540 | |||||||
chr9:121280666 | C | T | 261 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(258): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.-102-804C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121280666 | |||||||
chr9:121280912 | TA | T | 14 | a0001c0001t0001g0005 a0001c0001t0001g0182 a0001c0001t0001g0185 others(11): Show |
19 | HG01261.hp1 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.-102-557delA | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121280912 | |||||||
chr9:121281150 | C | T | 1 | a0001c0001t0001g0036 | 2 | HG03239.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-102-320C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121281150 | |||||||
chr9:121281173 | G | T | 1 | a0001c0001t0001g0117 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-102-297G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121281173 | |||||||
chr9:121281189 | G | A | 52 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0018 others(49): Show |
59 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.-102-281G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121281189 | |||||||
chr9:121281282 | G | T | 2 | a0001c0001t0003g0115 a0001c0001t0003g0116 |
2 | HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-102-188G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 1/17 | chr9 | 121281282 | |||||||
chr9:121281582 | CA | C | 36 | a0002c0002t0002g0002 a0002c0002t0002g0007 a0002c0002t0002g0010 others(33): Show |
45 | HG00438.hp2 HG00597.hp1 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.-10+21delA | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121281582 | |||||||
chr9:121281589 | C | T | 96 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(93): Show |
118 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.-10+27C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121281589 | |||||||
chr9:121282054 | C | T | 1 | a0001c0001t0001g0228 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-10+492C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121282054 | |||||||
chr9:121282131 | G | T | 2 | a0001c0001t0001g0168 a0001c0001t0001g0227 |
2 | HG02486.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.-10+569G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121282131 | |||||||
chr9:121282209 | T | A | 1 | a0001c0001t0001g0194 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-10+647T>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121282209 | |||||||
chr9:121282340 | G | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0182 a0001c0001t0001g0185 others(2): Show |
8 | HG01261.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-10+778G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121282340 | |||||||
chr9:121282373 | T | G | 3 | a0001c0001t0001g0042 a0001c0001t0001g0262 a0006c0009t0004g0038 |
5 | HG02647.hp2 HG02896.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10+811T>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121282373 | |||||||
chr9:121282441 | G | A | 1 | a0001c0001t0001g0247 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-10+879G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121282441 | |||||||
chr9:121282708 | C | T | 1 | a0001c0001t0001g0120 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-10+1146C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121282708 | |||||||
chr9:121282717 | C | T | 81 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(78): Show |
98 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.-10+1155C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121282717 | |||||||
chr9:121282760 | A | G | 1 | a0002c0002t0002g0068 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-10+1198A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121282760 | |||||||
chr9:121282868 | C | A | 2 | a0001c0001t0001g0042 a0001c0001t0001g0262 |
3 | HG02976.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-10+1306C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121282868 | |||||||
chr9:121282873 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-10+1311A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121282873 | |||||||
chr9:121282906 | C | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0119 a0001c0001t0001g0120 |
4 | HG00280.hp2 HG01099.hp2 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+1344C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121282906 | |||||||
chr9:121282915 | A | G | 1 | a0013c0013t0001g0260 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-10+1353A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121282915 | |||||||
chr9:121282919 | C | T | 1 | a0001c0003t0001g0261 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-10+1357C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121282919 | |||||||
chr9:121283138 | TTCTCTTT others(71): Show |
T | 1 | a0002c0002t0002g0060 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-10+1611_-10+1688d others(80): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr9 | 121283138 | ||||||
chr9:121283180 | TAGTTAGG others(14): Show |
T | 5 | a0001c0001t0001g0183 a0001c0001t0001g0258 a0004c0006t0004g0256 others(2): Show |
5 | HG02109.hp2 HG03209.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10+1630_-10+1650d others(23): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr9 | 121283180 | ||||||
chr9:121283250 | G | A | 1 | a0001c0003t0001g0195 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-10+1688G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121283250 | |||||||
chr9:121283301 | CT | C | 84 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(81): Show |
101 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.-10+1754delT | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr9 | 121283301 | ||||||
chr9:121283393 | G | A | 2 | a0001c0001t0001g0091 a0001c0001t0001g0092 |
2 | HG01074.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.-10+1831G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121283393 | |||||||
chr9:121283458 | C | T | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
4 | HG01123.hp1 HG01358.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+1896C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121283458 | |||||||
chr9:121283498 | A | G | 1 | a0001c0003t0001g0226 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-10+1936A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121283498 | |||||||
chr9:121283644 | C | A | 1 | a0004c0006t0004g0184 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-10+2082C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121283644 | |||||||
chr9:121283671 | G | GTTCA | 33 | a0001c0001t0001g0042 a0001c0001t0001g0262 a0001c0001t0003g0231 others(30): Show |
42 | HG00438.hp2 HG00597.hp1 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.-10+2143_-10+2146d others(6): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr9 | 121283671 | ||||||
chr9:121283671 | G | GTTCATTC others(1): Show |
14 | a0001c0001t0001g0183 a0001c0001t0001g0258 a0002c0002t0002g0011 others(11): Show |
15 | HG01106.hp1 HG01123.hp2 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.-10+2139_-10+2146d others(10): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr9 | 121283671 | ||||||
chr9:121283671 | G | GTTCATTC others(5): Show |
1 | a0002c0002t0007g0076 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-10+2135_-10+2146d others(14): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr9 | 121283671 | ||||||
chr9:121283671 | GTTCA | G | 104 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(101): Show |
125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
intron_variant | MODIFIER | c.-10+2143_-10+2146d others(6): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr9 | 121283671 | ||||||
chr9:121283671 | GTTCATTC others(1): Show |
G | 2 | a0001c0001t0001g0093 a0009c0011t0001g0041 |
3 | HG02717.hp2 HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-10+2139_-10+2146d others(10): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr9 | 121283671 | ||||||
chr9:121283671 | GTTCATTC others(9): Show |
G | 81 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(78): Show |
98 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.-10+2131_-10+2146d others(18): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr9 | 121283671 | ||||||
chr9:121283680 | T | C | 14 | a0001c0001t0001g0005 a0001c0001t0001g0182 a0001c0001t0001g0185 others(11): Show |
19 | HG01261.hp1 HG02055.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.-10+2118T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121283680 | |||||||
chr9:121283684 | T | C | 1 | a0001c0023t0003g0044 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-10+2122T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121283684 | |||||||
chr9:121283696 | T | C | 81 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(78): Show |
98 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.-10+2134T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121283696 | |||||||
chr9:121283800 | G | A | 1 | a0002c0002t0004g0055 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-10+2238G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121283800 | |||||||
chr9:121284033 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-10+2471G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121284033 | |||||||
chr9:121284355 | G | T | 3 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 |
3 | HG00140.hp2 HG01261.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.-10+2793G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121284355 | |||||||
chr9:121284413 | G | T | 53 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0018 others(50): Show |
60 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.-10+2851G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121284413 | |||||||
chr9:121284444 | C | T | 81 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(78): Show |
98 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.-10+2882C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121284444 | |||||||
chr9:121284499 | A | G | 15 | a0001c0001t0001g0005 a0001c0001t0001g0182 a0001c0001t0001g0185 others(12): Show |
20 | HG01261.hp1 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.-10+2937A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121284499 | |||||||
chr9:121284552 | CT | C | 261 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(258): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.-10+2992delT | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr9 | 121284552 | ||||||
chr9:121284787 | G | A | 5 | a0001c0001t0001g0183 a0001c0001t0001g0258 a0004c0006t0004g0256 others(2): Show |
5 | HG02109.hp2 HG03209.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10+3225G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121284787 | |||||||
chr9:121284818 | A | G | 1 | a0001c0001t0003g0162 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-10+3256A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121284818 | |||||||
chr9:121284898 | C | T | 1 | a0001c0001t0001g0247 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-10+3336C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121284898 | |||||||
chr9:121284957 | G | A | 3 | a0005c0008t0001g0094 a0005c0008t0001g0095 a0005c0008t0001g0096 |
3 | HG01243.hp1 HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-10+3395G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121284957 | |||||||
chr9:121284959 | T | C | 53 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0018 others(50): Show |
60 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.-10+3397T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121284959 | |||||||
chr9:121284968 | A | C | 195 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(192): Show |
234 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.-10+3406A>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121284968 | |||||||
chr9:121284980 | A | G | 14 | a0001c0001t0001g0005 a0001c0001t0001g0182 a0001c0001t0001g0185 others(11): Show |
19 | HG01261.hp1 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.-10+3418A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121284980 | |||||||
chr9:121285219 | C | T | 1 | a0013c0013t0001g0260 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-10+3657C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121285219 | |||||||
chr9:121285496 | A | G | 39 | a0002c0002t0002g0002 a0002c0002t0002g0007 a0002c0002t0002g0010 others(36): Show |
48 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.-10+3934A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121285496 | |||||||
chr9:121285555 | T | C | 3 | a0001c0001t0001g0019 a0001c0001t0001g0119 a0001c0001t0001g0120 |
4 | HG00280.hp2 HG01099.hp2 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+3993T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121285555 | |||||||
chr9:121285558 | T | C | 2 | a0001c0001t0001g0091 a0001c0001t0001g0092 |
2 | HG01074.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.-10+3996T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121285558 | |||||||
chr9:121285706 | A | G | 1 | a0003c0005t0001g0244 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-10+4144A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121285706 | |||||||
chr9:121285797 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-10+4235T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121285797 | |||||||
chr9:121285900 | C | A | 1 | a0002c0007t0001g0049 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-10+4338C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121285900 | |||||||
chr9:121286020 | G | A | 50 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0018 others(47): Show |
57 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.-10+4458G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121286020 | |||||||
chr9:121286030 | C | T | 1 | a0001c0001t0001g0161 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-10+4468C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121286030 | |||||||
chr9:121286183 | T | C | 45 | a0001c0001t0001g0183 a0001c0001t0001g0258 a0002c0002t0002g0002 others(42): Show |
54 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.-10+4621T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121286183 | |||||||
chr9:121286343 | A | G | 5 | a0001c0001t0001g0018 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
6 | HG01109.hp2 HG02109.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+4781A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121286343 | |||||||
chr9:121286351 | C | G | 1 | a0001c0001t0001g0112 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-10+4789C>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121286351 | |||||||
chr9:121286361 | G | T | 1 | a0001c0001t0001g0160 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-10+4799G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121286361 | |||||||
chr9:121286378 | G | A | 1 | a0001c0001t0001g0178 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-10+4816G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121286378 | |||||||
chr9:121286449 | C | T | 96 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(93): Show |
118 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.-10+4887C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121286449 | |||||||
chr9:121286526 | C | T | 2 | a0001c0001t0001g0221 a0001c0001t0001g0227 |
2 | HG01175.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.-10+4964C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121286526 | |||||||
chr9:121287005 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-10+5443C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121287005 | |||||||
chr9:121287065 | G | C | 5 | a0001c0001t0001g0005 a0001c0001t0001g0182 a0001c0001t0001g0185 others(2): Show |
8 | HG01261.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-10+5503G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121287065 | |||||||
chr9:121287226 | G | A | 1 | a0008c0012t0001g0097 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-10+5664G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121287226 | |||||||
chr9:121287358 | G | T | 1 | a0003c0005t0001g0244 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-10+5796G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121287358 | |||||||
chr9:121287383 | G | A | 1 | a0001c0003t0001g0131 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-10+5821G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121287383 | |||||||
chr9:121287435 | G | A | 52 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0018 others(49): Show |
59 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.-10+5873G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121287435 | |||||||
chr9:121287439 | C | T | 39 | a0002c0002t0002g0002 a0002c0002t0002g0007 a0002c0002t0002g0010 others(36): Show |
48 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.-10+5877C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121287439 | |||||||
chr9:121287459 | T | C | 3 | a0001c0001t0001g0020 a0001c0001t0001g0098 a0001c0001t0001g0121 |
4 | HG02809.hp2 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+5897T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121287459 | |||||||
chr9:121287630 | G | A | 1 | a0013c0013t0001g0260 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-10+6068G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121287630 | |||||||
chr9:121287678 | T | C | 81 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(78): Show |
98 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.-10+6116T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121287678 | |||||||
chr9:121287682 | C | CT | 188 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(185): Show |
226 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.-10+6129dupT | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr9 | 121287682 | ||||||
chr9:121287692 | C | T | 3 | a0001c0001t0001g0080 a0001c0001t0001g0161 a0001c0001t0001g0177 |
3 | NA18959.hp1 NA18969.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.-10+6130C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121287692 | |||||||
chr9:121287693 | T | C | 2 | a0001c0001t0001g0080 a0001c0001t0001g0161 |
2 | NA18959.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.-10+6131T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121287693 | |||||||
chr9:121287702 | T | A | 15 | a0001c0001t0001g0005 a0001c0001t0001g0182 a0001c0001t0001g0185 others(12): Show |
20 | HG01261.hp1 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.-10+6140T>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121287702 | |||||||
chr9:121287703 | A | T | 1 | a0002c0002t0002g0067 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-10+6141A>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121287703 | |||||||
chr9:121287901 | C | T | 1 | a0009c0011t0001g0041 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-10+6339C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121287901 | |||||||
chr9:121287981 | C | T | 45 | a0001c0001t0001g0183 a0001c0001t0001g0258 a0002c0002t0002g0002 others(42): Show |
54 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.-10+6419C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121287981 | |||||||
chr9:121288051 | C | T | 1 | a0002c0007t0001g0049 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-10+6489C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121288051 | |||||||
chr9:121288389 | C | T | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
4 | HG01123.hp1 HG01358.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+6827C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121288389 | |||||||
chr9:121288461 | G | C | 1 | a0007c0022t0001g0181 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-10+6899G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121288461 | |||||||
chr9:121288530 | A | G | 3 | a0001c0001t0001g0018 a0001c0001t0001g0110 a0001c0001t0001g0111 |
4 | HG01109.hp2 HG02109.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+6968A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121288530 | |||||||
chr9:121288560 | G | A | 11 | a0001c0001t0001g0006 a0001c0001t0001g0037 a0001c0001t0001g0123 others(8): Show |
15 | HG00140.hp1 HG00741.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.-10+6998G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121288560 | |||||||
chr9:121288813 | A | ATAG | 4 | a0001c0001t0003g0017 a0001c0001t0003g0108 a0001c0001t0003g0115 others(1): Show |
5 | HG02145.hp2 HG02647.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10+7254_-10+7256d others(5): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr9 | 121288813 | ||||||
chr9:121288820 | A | G | 1 | a0009c0011t0001g0041 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-10+7258A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121288820 | |||||||
chr9:121289004 | A | G | 15 | a0001c0001t0001g0005 a0001c0001t0001g0182 a0001c0001t0001g0185 others(12): Show |
20 | HG01261.hp1 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.-10+7442A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121289004 | |||||||
chr9:121289122 | A | G | 196 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(193): Show |
235 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.-10+7560A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121289122 | |||||||
chr9:121289161 | T | G | 1 | a0001c0001t0001g0132 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-10+7599T>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121289161 | |||||||
chr9:121289240 | G | A | 1 | a0001c0003t0001g0099 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-10+7678G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121289240 | |||||||
chr9:121289313 | G | A | 1 | a0004c0006t0005g0236 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-10+7751G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121289313 | |||||||
chr9:121289334 | G | A | 1 | a0004c0006t0004g0222 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-10+7772G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121289334 | |||||||
chr9:121289545 | G | T | 1 | a0009c0011t0001g0041 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-10+7983G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121289545 | |||||||
chr9:121289557 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-10+7995C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121289557 | |||||||
chr9:121289622 | C | T | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | HG01934.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.-10+8060C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121289622 | |||||||
chr9:121289623 | C | T | 1 | a0001c0001t0001g0258 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-10+8061C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121289623 | |||||||
chr9:121289653 | G | A | 39 | a0002c0002t0002g0002 a0002c0002t0002g0007 a0002c0002t0002g0010 others(36): Show |
48 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.-10+8091G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121289653 | |||||||
chr9:121289794 | G | T | 40 | a0002c0002t0002g0002 a0002c0002t0002g0007 a0002c0002t0002g0010 others(37): Show |
50 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.-10+8232G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121289794 | |||||||
chr9:121289984 | A | G | 2 | a0002c0002t0002g0057 a0002c0002t0002g0062 |
2 | HG03490.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.-10+8422A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121289984 | |||||||
chr9:121289999 | A | G | 141 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(138): Show |
173 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.-10+8437A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121289999 | |||||||
chr9:121290120 | G | C | 3 | a0001c0001t0001g0042 a0001c0001t0001g0262 a0001c0003t0001g0261 |
4 | HG02976.hp2 HG03130.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+8558G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121290120 | |||||||
chr9:121290262 | C | T | 2 | a0001c0001t0001g0081 a0001c0001t0001g0082 |
2 | HG01891.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-10+8700C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121290262 | |||||||
chr9:121290266 | A | G | 1 | a0009c0011t0001g0041 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-10+8704A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121290266 | |||||||
chr9:121290367 | T | A | 3 | a0001c0001t0001g0042 a0001c0001t0001g0262 a0001c0003t0001g0261 |
4 | HG02976.hp2 HG03130.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+8805T>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121290367 | |||||||
chr9:121290518 | T | C | 1 | a0004c0006t0004g0184 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-10+8956T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121290518 | |||||||
chr9:121290572 | T | C | 1 | a0001c0001t0001g0132 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-10+9010T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121290572 | |||||||
chr9:121290610 | G | C | 4 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0200 others(1): Show |
4 | HG02257.hp2 HG02258.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+9048G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121290610 | |||||||
chr9:121290622 | G | T | 3 | a0001c0001t0001g0040 a0001c0001t0001g0251 a0001c0001t0001g0252 |
4 | HG02129.hp1 NA18943.hp1 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10+9060G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121290622 | |||||||
chr9:121290706 | G | A | 15 | a0001c0001t0001g0005 a0001c0001t0001g0182 a0001c0001t0001g0185 others(12): Show |
20 | HG01261.hp1 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.-10+9144G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121290706 | |||||||
chr9:121290783 | T | G | 1 | a0001c0001t0001g0188 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-10+9221T>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121290783 | |||||||
chr9:121290875 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0262 |
3 | HG02976.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-10+9313C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121290875 | |||||||
chr9:121291367 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-10+9805C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121291367 | |||||||
chr9:121291401 | T | C | 3 | a0005c0008t0001g0094 a0005c0008t0001g0095 a0005c0008t0001g0096 |
3 | HG01243.hp1 HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-10+9839T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121291401 | |||||||
chr9:121291416 | CT | C | 14 | a0001c0001t0001g0042 a0001c0001t0001g0156 a0001c0001t0001g0262 others(11): Show |
15 | HG01109.hp1 HG01884.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-10+9874delT | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr9 | 121291416 | ||||||
chr9:121291416 | CTT | C | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(174): Show |
213 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.-10+9873_-10+9874d others(4): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr9 | 121291416 | ||||||
chr9:121291416 | CTTT | C | 11 | a0001c0001t0001g0005 a0001c0001t0001g0126 a0001c0001t0001g0182 others(8): Show |
14 | HG01261.hp1 HG02055.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.-10+9872_-10+9874d others(5): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr9 | 121291416 | ||||||
chr9:121291482 | G | A | 1 | a0002c0002t0002g0051 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-10+9920G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121291482 | |||||||
chr9:121291482 | G | T | 1 | a0004c0006t0004g0256 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-10+9920G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121291482 | |||||||
chr9:121291494 | C | T | 3 | a0001c0001t0001g0183 a0001c0001t0001g0258 a0004c0006t0004g0256 |
3 | HG02109.hp2 HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-10+9932C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121291494 | |||||||
chr9:121291580 | G | A | 96 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(93): Show |
118 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.-10+10018G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121291580 | |||||||
chr9:121291608 | T | C | 201 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(198): Show |
241 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.-10+10046T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121291608 | |||||||
chr9:121292564 | G | A | 2 | a0001c0001t0001g0083 a0001c0001t0001g0084 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-9-9399G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121292564 | |||||||
chr9:121292809 | T | C | 5 | a0001c0001t0001g0042 a0001c0001t0001g0262 a0001c0001t0003g0231 others(2): Show |
6 | HG02486.hp2 HG02559.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-9154T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121292809 | |||||||
chr9:121292958 | C | T | 38 | a0002c0002t0002g0002 a0002c0002t0002g0007 a0002c0002t0002g0010 others(35): Show |
47 | HG00438.hp2 HG00597.hp1 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.-9-9005C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121292958 | |||||||
chr9:121293026 | A | G | 1 | a0010c0021t0001g0107 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-9-8937A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121293026 | |||||||
chr9:121293039 | G | A | 1 | a0001c0001t0001g0134 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-9-8924G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121293039 | |||||||
chr9:121293040 | A | G | 1 | a0001c0001t0001g0134 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-9-8923A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121293040 | |||||||
chr9:121293113 | G | A | 4 | a0001c0001t0001g0117 a0008c0012t0001g0097 a0008c0012t0001g0101 others(1): Show |
4 | HG02451.hp2 HG02809.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9-8850G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121293113 | |||||||
chr9:121293133 | C | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0262 a0001c0003t0001g0261 |
4 | HG02976.hp2 HG03130.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9-8830C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121293133 | |||||||
chr9:121293146 | G | T | 1 | a0001c0001t0001g0134 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-9-8817G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121293146 | |||||||
chr9:121293292 | G | A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0135 |
3 | HG01106.hp2 HG01192.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.-9-8671G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121293292 | |||||||
chr9:121293409 | AT | A | 201 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(198): Show |
241 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.-9-8541delT | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr9 | 121293409 | ||||||
chr9:121293577 | C | A | 1 | a0001c0001t0001g0136 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-9-8386C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121293577 | |||||||
chr9:121293608 | A | T | 81 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(78): Show |
98 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.-9-8355A>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121293608 | |||||||
chr9:121293654 | C | T | 16 | a0001c0001t0001g0014 a0001c0001t0001g0078 a0001c0001t0001g0080 others(13): Show |
17 | HG00099.hp2 HG00323.hp2 HG01516.hp1 others(14): Show |
intron_variant | MODIFIER | c.-9-8309C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121293654 | |||||||
chr9:121293697 | CA | C | 45 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0217 others(42): Show |
54 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.-9-8248delA | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr9 | 121293697 | ||||||
chr9:121293697 | CAA | C | 93 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(90): Show |
115 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.-9-8249_-9-8248del others(2): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr9 | 121293697 | ||||||
chr9:121293743 | T | C | 81 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(78): Show |
98 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.-9-8220T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121293743 | |||||||
chr9:121293765 | G | A | 1 | a0004c0006t0004g0223 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-9-8198G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121293765 | |||||||
chr9:121293769 | T | G | 1 | a0001c0003t0001g0261 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-9-8194T>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121293769 | |||||||
chr9:121293958 | A | G | 3 | a0001c0001t0001g0042 a0001c0001t0001g0262 a0001c0003t0001g0261 |
4 | HG02976.hp2 HG03130.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9-8005A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121293958 | |||||||
chr9:121293968 | AG | A | 81 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(78): Show |
98 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.-9-7994delG | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121293968 | |||||||
chr9:121294150 | G | A | 81 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(78): Show |
98 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.-9-7813G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121294150 | |||||||
chr9:121294236 | C | T | 10 | a0001c0023t0003g0044 a0003c0005t0001g0039 a0003c0005t0001g0240 others(7): Show |
12 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-9-7727C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121294236 | |||||||
chr9:121294254 | T | C | 6 | a0001c0001t0001g0020 a0001c0001t0001g0098 a0001c0001t0001g0121 others(3): Show |
7 | HG01243.hp1 HG02809.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9-7709T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121294254 | |||||||
chr9:121294348 | C | G | 201 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(198): Show |
241 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.-9-7615C>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121294348 | |||||||
chr9:121294352 | C | T | 1 | a0001c0004t0002g0155 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-9-7611C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121294352 | |||||||
chr9:121294451 | T | C | 1 | a0009c0011t0001g0041 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-9-7512T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121294451 | |||||||
chr9:121294903 | AG | A | 3 | a0008c0012t0001g0097 a0008c0012t0001g0101 a0015c0024t0001g0100 |
3 | HG02451.hp2 HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-9-7059delG | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121294903 | |||||||
chr9:121295254 | G | A | 1 | a0001c0004t0002g0171 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-9-6709G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121295254 | |||||||
chr9:121295301 | G | A | 1 | a0002c0015t0001g0047 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-9-6662G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121295301 | |||||||
chr9:121295404 | C | T | 81 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(78): Show |
98 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.-9-6559C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121295404 | |||||||
chr9:121295559 | G | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0127 |
2 | HG01358.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-9-6404G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121295559 | |||||||
chr9:121295561 | G | C | 1 | a0001c0001t0001g0159 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-9-6402G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121295561 | |||||||
chr9:121295709 | C | T | 1 | a0001c0003t0001g0216 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-9-6254C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121295709 | |||||||
chr9:121295807 | G | A | 12 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0130 others(9): Show |
14 | HG00621.hp2 HG02071.hp1 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.-9-6156G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121295807 | |||||||
chr9:121295935 | T | C | 95 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(92): Show |
117 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.-9-6028T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121295935 | |||||||
chr9:121295989 | C | A | 1 | a0002c0015t0001g0047 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-9-5974C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121295989 | |||||||
chr9:121296081 | C | T | 81 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(78): Show |
98 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.-9-5882C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121296081 | |||||||
chr9:121296098 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-9-5865C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121296098 | |||||||
chr9:121296521 | T | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(93): Show |
118 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.-9-5442T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121296521 | |||||||
chr9:121296665 | C | T | 81 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(78): Show |
98 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.-9-5298C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121296665 | |||||||
chr9:121296769 | G | C | 201 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(198): Show |
241 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.-9-5194G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121296769 | |||||||
chr9:121296807 | G | C | 1 | a0001c0001t0001g0102 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-9-5156G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121296807 | |||||||
chr9:121296899 | T | C | 95 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(92): Show |
117 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.-9-5064T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121296899 | |||||||
chr9:121297372 | C | A | 1 | a0001c0001t0001g0188 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-9-4591C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121297372 | |||||||
chr9:121297651 | T | G | 1 | a0014c0020t0001g0257 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-9-4312T>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121297651 | |||||||
chr9:121297697 | G | T | 2 | a0001c0001t0001g0091 a0001c0001t0001g0092 |
2 | HG01074.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.-9-4266G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121297697 | |||||||
chr9:121297774 | G | A | 36 | a0002c0002t0002g0002 a0002c0002t0002g0007 a0002c0002t0002g0010 others(33): Show |
45 | HG00438.hp2 HG00597.hp1 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.-9-4189G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121297774 | |||||||
chr9:121297901 | A | C | 10 | a0001c0023t0003g0044 a0003c0005t0001g0039 a0003c0005t0001g0240 others(7): Show |
12 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-9-4062A>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121297901 | |||||||
chr9:121297952 | T | C | 6 | a0001c0001t0001g0183 a0001c0001t0001g0258 a0004c0006t0004g0184 others(3): Show |
6 | HG01884.hp2 HG02109.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-4011T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121297952 | |||||||
chr9:121298026 | C | T | 78 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(75): Show |
95 | HG00280.hp1 HG00408.hp1 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.-9-3937C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121298026 | |||||||
chr9:121298144 | G | A | 87 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(84): Show |
107 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.-9-3819G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121298144 | |||||||
chr9:121298305 | C | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0182 a0001c0001t0001g0185 others(2): Show |
8 | HG01261.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-9-3658C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121298305 | |||||||
chr9:121298472 | C | T | 1 | a0001c0023t0003g0044 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-9-3491C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121298472 | |||||||
chr9:121298601 | T | C | 201 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(198): Show |
241 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.-9-3362T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121298601 | |||||||
chr9:121298681 | G | T | 1 | a0016c0016t0001g0259 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-9-3282G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121298681 | |||||||
chr9:121298711 | C | G | 81 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(78): Show |
98 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.-9-3252C>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121298711 | |||||||
chr9:121298986 | A | G | 40 | a0002c0002t0002g0002 a0002c0002t0002g0007 a0002c0002t0002g0010 others(37): Show |
50 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.-9-2977A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121298986 | |||||||
chr9:121299012 | G | C | 1 | a0001c0003t0001g0131 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-9-2951G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121299012 | |||||||
chr9:121299119 | T | C | 1 | a0001c0003t0001g0009 | 3 | HG00558.hp2 HG02015.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.-9-2844T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121299119 | |||||||
chr9:121299522 | TAGGTGCG others(3): Show |
T | 1 | a0004c0006t0004g0223 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-9-2437_-9-2428del others(10): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr9 | 121299522 | ||||||
chr9:121299557 | C | T | 45 | a0001c0001t0001g0183 a0001c0001t0001g0258 a0002c0002t0002g0002 others(42): Show |
55 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.-9-2406C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121299557 | |||||||
chr9:121299582 | C | T | 1 | a0001c0001t0001g0215 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-9-2381C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121299582 | |||||||
chr9:121299590 | C | A | 2 | a0001c0001t0001g0042 a0001c0001t0001g0262 |
3 | HG02976.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-9-2373C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121299590 | |||||||
chr9:121299614 | A | C | 2 | a0001c0001t0001g0153 a0001c0001t0001g0167 |
2 | HG00280.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.-9-2349A>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121299614 | |||||||
chr9:121299622 | C | A | 2 | a0001c0010t0001g0113 a0001c0010t0001g0114 |
2 | HG01109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-9-2341C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121299622 | |||||||
chr9:121299624 | C | T | 87 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(84): Show |
107 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.-9-2339C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121299624 | |||||||
chr9:121299666 | G | A | 1 | a0004c0006t0005g0236 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-9-2297G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121299666 | |||||||
chr9:121299685 | G | A | 52 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0018 others(49): Show |
59 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.-9-2278G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121299685 | |||||||
chr9:121299752 | G | A | 1 | a0001c0003t0001g0218 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-9-2211G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121299752 | |||||||
chr9:121299849 | C | G | 1 | a0001c0001t0001g0136 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-9-2114C>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121299849 | |||||||
chr9:121300482 | C | T | 1 | a0001c0010t0001g0114 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-9-1481C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121300482 | |||||||
chr9:121300737 | C | T | 45 | a0001c0001t0001g0183 a0001c0001t0001g0258 a0002c0002t0002g0002 others(42): Show |
55 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.-9-1226C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121300737 | |||||||
chr9:121300960 | G | A | 2 | a0001c0001t0001g0042 a0001c0001t0001g0262 |
3 | HG02976.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-9-1003G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121300960 | |||||||
chr9:121300979 | C | A | 1 | a0009c0011t0001g0041 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-9-984C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121300979 | |||||||
chr9:121301032 | C | A | 1 | a0001c0001t0001g0121 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-9-931C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121301032 | |||||||
chr9:121301036 | C | T | 2 | a0001c0003t0001g0016 a0001c0003t0001g0099 |
3 | NA18971.hp2 NA18988.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.-9-927C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121301036 | |||||||
chr9:121301046 | C | T | 1 | a0001c0001t0001g0023 | 2 | HG02083.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.-9-917C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121301046 | |||||||
chr9:121301074 | G | A | 87 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(84): Show |
107 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.-9-889G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121301074 | |||||||
chr9:121301346 | G | C | 5 | a0001c0001t0001g0183 a0001c0001t0001g0258 a0004c0006t0004g0256 others(2): Show |
5 | HG02109.hp2 HG03209.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-9-617G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121301346 | |||||||
chr9:121301352 | C | T | 7 | a0001c0001t0001g0020 a0001c0001t0001g0098 a0001c0001t0001g0121 others(4): Show |
8 | HG01106.hp1 HG01243.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-9-611C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121301352 | |||||||
chr9:121301429 | C | T | 6 | a0001c0001t0001g0005 a0001c0001t0001g0182 a0001c0001t0001g0185 others(3): Show |
9 | HG01261.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-9-534C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121301429 | |||||||
chr9:121301493 | T | G | 194 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(191): Show |
233 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.-9-470T>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121301493 | |||||||
chr9:121301550 | C | T | 6 | a0001c0001t0001g0005 a0001c0001t0001g0182 a0001c0001t0001g0185 others(3): Show |
9 | HG01261.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-9-413C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121301550 | |||||||
chr9:121301574 | C | T | 1 | a0004c0006t0005g0236 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-9-389C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121301574 | |||||||
chr9:121301625 | C | CA | 15 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0037 others(12): Show |
18 | HG00621.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.-9-319dupA | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr9 | 121301625 | ||||||
chr9:121301625 | CA | C | 19 | a0001c0001t0001g0042 a0001c0001t0001g0084 a0001c0001t0001g0106 others(16): Show |
21 | HG00323.hp1 HG01109.hp1 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.-9-319delA | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr9 | 121301625 | ||||||
chr9:121301625 | CAAAAAAA | C | 9 | a0003c0005t0001g0039 a0003c0005t0001g0240 a0003c0005t0001g0241 others(6): Show |
11 | HG02280.hp2 HG02451.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.-9-325_-9-319delAA others(5): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr9 | 121301625 | ||||||
chr9:121301639 | A | G | 38 | a0002c0002t0002g0002 a0002c0002t0002g0007 a0002c0002t0002g0010 others(35): Show |
47 | HG00438.hp2 HG00597.hp1 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.-9-324A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121301639 | |||||||
chr9:121301640 | A | G | 1 | a0001c0001t0001g0214 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-9-323A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121301640 | |||||||
chr9:121301778 | C | G | 9 | a0003c0005t0001g0039 a0003c0005t0001g0240 a0003c0005t0001g0241 others(6): Show |
11 | HG02280.hp2 HG02451.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.-9-185C>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121301778 | |||||||
chr9:121301877 | G | C | 1 | a0009c0011t0001g0041 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-9-86G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121301877 | |||||||
chr9:121301932 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-9-31C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 2/17 | chr9 | 121301932 | |||||||
chr9:121302322 | C | A | 1 | a0002c0015t0001g0047 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.196+155C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 3/17 | chr9 | 121302322 | |||||||
chr9:121302356 | C | T | 4 | a0001c0003t0001g0201 a0001c0003t0001g0211 a0001c0003t0001g0212 others(1): Show |
4 | HG02965.hp1 HG03139.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.196+189C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 3/17 | chr9 | 121302356 | |||||||
chr9:121302501 | C | A | 3 | a0001c0001t0001g0005 a0001c0001t0001g0185 a0001c0001t0001g0187 |
6 | HG02055.hp1 HG02559.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.196+334C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 3/17 | chr9 | 121302501 | |||||||
chr9:121302520 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.196+353C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 3/17 | chr9 | 121302520 | |||||||
chr9:121302570 | TG | T | 3 | a0004c0006t0004g0222 a0004c0006t0004g0223 a0004c0006t0004g0238 |
3 | HG01071.hp2 HG02738.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.197-340delG | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 3/17 | chr9 | 121302570 | |||||||
chr9:121302572 | C | A | 3 | a0004c0006t0004g0222 a0004c0006t0004g0223 a0004c0006t0004g0238 |
3 | HG01071.hp2 HG02738.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.197-339C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 3/17 | chr9 | 121302572 | |||||||
chr9:121302585 | G | A | 6 | a0001c0001t0001g0005 a0001c0001t0001g0182 a0001c0001t0001g0185 others(3): Show |
9 | HG01261.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.197-326G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 3/17 | chr9 | 121302585 | |||||||
chr9:121302650 | G | T | 81 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(78): Show |
98 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.197-261G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 3/17 | chr9 | 121302650 | |||||||
chr9:121302670 | G | C | 2 | a0001c0010t0001g0113 a0001c0010t0001g0114 |
2 | HG01109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.197-241G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 3/17 | chr9 | 121302670 | |||||||
chr9:121302685 | G | C | 1 | a0001c0001t0001g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.197-226G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 3/17 | chr9 | 121302685 | |||||||
chr9:121302746 | G | T | 3 | a0001c0001t0001g0005 a0001c0001t0001g0185 a0001c0001t0001g0187 |
6 | HG02055.hp1 HG02559.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.197-165G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 3/17 | chr9 | 121302746 | |||||||
chr9:121302906 | C | T | 1 | a0001c0003t0001g0212 | 1 | HG03516.hp1 | splice_region_variant&intron_variant | LOW | c.197-5C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 3/17 | chr9 | 121302906 | |||||||
chr9:121303138 | A | G | 2 | a0001c0010t0001g0113 a0001c0010t0001g0114 |
2 | HG01109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.351+73A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121303138 | |||||||
chr9:121303238 | G | A | 5 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0247 others(2): Show |
5 | HG01074.hp1 HG02148.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.351+173G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121303238 | |||||||
chr9:121303411 | G | A | 1 | a0001c0003t0001g0195 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.351+346G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121303411 | |||||||
chr9:121303443 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.351+378C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121303443 | |||||||
chr9:121303456 | C | T | 1 | a0001c0001t0003g0151 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.351+391C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121303456 | |||||||
chr9:121303764 | C | A | 1 | a0001c0001t0001g0178 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.351+699C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121303764 | |||||||
chr9:121304038 | A | G | 1 | a0001c0001t0001g0210 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.351+973A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121304038 | |||||||
chr9:121304222 | CAGAT | C | 4 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0200 others(1): Show |
4 | HG02257.hp2 HG02258.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.351+1160_351+1163d others(6): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr9 | 121304222 | ||||||
chr9:121304228 | G | A | 2 | a0001c0003t0001g0016 a0001c0003t0001g0099 |
3 | NA18971.hp2 NA18988.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.351+1163G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121304228 | |||||||
chr9:121304375 | T | C | 2 | a0001c0001t0001g0138 a0001c0004t0002g0155 |
2 | HG00621.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.351+1310T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121304375 | |||||||
chr9:121304572 | G | A | 7 | a0001c0001t0001g0005 a0001c0001t0001g0182 a0001c0001t0001g0185 others(4): Show |
10 | HG01109.hp1 HG01261.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.351+1507G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121304572 | |||||||
chr9:121304722 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.351+1657G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121304722 | |||||||
chr9:121304936 | C | T | 1 | a0001c0003t0001g0261 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.351+1871C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121304936 | |||||||
chr9:121305053 | A | G | 2 | a0001c0001t0001g0221 a0001c0001t0001g0227 |
2 | HG01175.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.351+1988A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121305053 | |||||||
chr9:121305167 | A | G | 1 | a0004c0006t0004g0184 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.351+2102A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121305167 | |||||||
chr9:121305234 | A | G | 5 | a0003c0005t0001g0240 a0003c0005t0001g0241 a0003c0005t0001g0242 others(2): Show |
5 | HG02451.hp1 HG02886.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.351+2169A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121305234 | |||||||
chr9:121305483 | A | G | 1 | a0001c0001t0001g0089 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.351+2418A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121305483 | |||||||
chr9:121305498 | G | A | 1 | a0001c0003t0001g0129 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.351+2433G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121305498 | |||||||
chr9:121305511 | G | A | 78 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(75): Show |
96 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.351+2446G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121305511 | |||||||
chr9:121305570 | A | G | 1 | a0002c0015t0001g0047 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.351+2505A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121305570 | |||||||
chr9:121305849 | C | T | 1 | a0001c0003t0001g0261 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.351+2784C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121305849 | |||||||
chr9:121306122 | A | G | 1 | a0002c0015t0001g0047 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.351+3057A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121306122 | |||||||
chr9:121306136 | C | T | 6 | a0002c0002t0002g0013 a0002c0002t0002g0053 a0002c0002t0002g0071 others(3): Show |
7 | HG00438.hp2 HG02071.hp2 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.351+3071C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121306136 | |||||||
chr9:121306506 | T | TATATATC | 78 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(75): Show |
96 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.351+3446_351+3447i others(9): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr9 | 121306506 | ||||||
chr9:121306554 | C | T | 14 | a0001c0001t0001g0005 a0001c0001t0001g0182 a0001c0001t0001g0183 others(11): Show |
17 | HG01109.hp1 HG01261.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.351+3489C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121306554 | |||||||
chr9:121306844 | A | T | 1 | a0001c0003t0001g0129 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.351+3779A>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121306844 | |||||||
chr9:121306879 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.352-3805C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121306879 | |||||||
chr9:121307183 | A | T | 1 | a0001c0001t0001g0137 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.352-3501A>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121307183 | |||||||
chr9:121307243 | A | G | 87 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(84): Show |
107 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.352-3441A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121307243 | |||||||
chr9:121307310 | T | A | 4 | a0001c0001t0001g0031 a0001c0001t0001g0214 a0001c0001t0001g0215 others(1): Show |
4 | HG00558.hp1 NA18942.hp2 NA18949.hp1 others(1): Show |
intron_variant | MODIFIER | c.352-3374T>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121307310 | |||||||
chr9:121307360 | T | A | 1 | a0004c0006t0004g0222 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.352-3324T>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121307360 | |||||||
chr9:121307391 | T | C | 1 | a0004c0006t0004g0256 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.352-3293T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121307391 | |||||||
chr9:121307537 | A | G | 63 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(60): Show |
78 | HG00140.hp1 HG00438.hp2 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.352-3147A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121307537 | |||||||
chr9:121307545 | C | T | 47 | a0002c0002t0002g0002 a0002c0002t0002g0007 a0002c0002t0002g0010 others(44): Show |
58 | HG00438.hp2 HG00597.hp1 HG01081.hp1 others(55): Show |
intron_variant | MODIFIER | c.352-3139C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121307545 | |||||||
chr9:121307758 | G | C | 1 | a0001c0003t0001g0261 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.352-2926G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121307758 | |||||||
chr9:121307780 | C | T | 39 | a0002c0002t0002g0002 a0002c0002t0002g0007 a0002c0002t0002g0010 others(36): Show |
48 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.352-2904C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121307780 | |||||||
chr9:121307787 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.352-2897G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121307787 | |||||||
chr9:121307787 | G | T | 1 | a0001c0003t0001g0261 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.352-2897G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121307787 | |||||||
chr9:121307872 | G | A | 1 | a0011c0019t0001g0230 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.352-2812G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121307872 | |||||||
chr9:121307881 | G | A | 1 | a0001c0003t0001g0226 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.352-2803G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121307881 | |||||||
chr9:121307954 | G | A | 1 | a0010c0021t0001g0107 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.352-2730G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121307954 | |||||||
chr9:121308246 | C | T | 1 | a0001c0001t0001g0250 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.352-2438C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121308246 | |||||||
chr9:121308459 | C | G | 1 | a0004c0006t0005g0236 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.352-2225C>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121308459 | |||||||
chr9:121308636 | C | T | 1 | a0009c0011t0001g0041 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.352-2048C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121308636 | |||||||
chr9:121308792 | G | C | 1 | a0009c0011t0001g0041 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.352-1892G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121308792 | |||||||
chr9:121308801 | A | G | 1 | a0001c0023t0003g0044 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.352-1883A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121308801 | |||||||
chr9:121309054 | G | A | 1 | a0001c0023t0003g0044 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.352-1630G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121309054 | |||||||
chr9:121309066 | C | T | 19 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(16): Show |
24 | HG00140.hp1 HG00741.hp2 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.352-1618C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121309066 | |||||||
chr9:121309113 | G | C | 3 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 |
3 | HG00140.hp2 HG01261.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.352-1571G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121309113 | |||||||
chr9:121309180 | A | G | 1 | a0001c0001t0001g0207 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.352-1504A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121309180 | |||||||
chr9:121309237 | G | C | 1 | a0001c0001t0001g0163 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.352-1447G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121309237 | |||||||
chr9:121309307 | A | T | 1 | a0001c0001t0001g0112 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.352-1377A>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121309307 | |||||||
chr9:121309332 | C | T | 1 | a0001c0003t0001g0261 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.352-1352C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121309332 | |||||||
chr9:121309466 | G | A | 40 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0002c0002t0002g0002 others(37): Show |
51 | HG00438.hp2 HG00597.hp1 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.352-1218G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121309466 | |||||||
chr9:121309843 | T | TTACTTAG others(10): Show |
1 | a0001c0003t0001g0150 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.352-841_352-840ins others(17): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121309843 | |||||||
chr9:121309849 | C | T | 70 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(67): Show |
86 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.352-835C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121309849 | |||||||
chr9:121309915 | T | C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0262 |
3 | HG02976.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.352-769T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121309915 | |||||||
chr9:121309983 | C | T | 1 | a0001c0001t0001g0252 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.352-701C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121309983 | |||||||
chr9:121309984 | G | A | 1 | a0014c0020t0001g0257 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.352-700G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121309984 | |||||||
chr9:121310015 | A | G | 4 | a0001c0001t0003g0017 a0001c0001t0003g0108 a0001c0001t0003g0115 others(1): Show |
5 | HG02145.hp2 HG02647.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.352-669A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121310015 | |||||||
chr9:121310134 | A | G | 1 | a0001c0003t0001g0226 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.352-550A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121310134 | |||||||
chr9:121310319 | C | T | 90 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(87): Show |
103 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.352-365C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121310319 | |||||||
chr9:121310374 | G | T | 94 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(91): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.352-310G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121310374 | |||||||
chr9:121310623 | T | C | 1 | a0001c0001t0001g0130 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.352-61T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 4/17 | chr9 | 121310623 | |||||||
chr9:121310864 | T | C | 2 | a0009c0011t0001g0041 a0014c0020t0001g0257 |
3 | HG02717.hp2 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.513+19T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 5/17 | chr9 | 121310864 | |||||||
chr9:121310898 | T | C | 244 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(241): Show |
297 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.513+53T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 5/17 | chr9 | 121310898 | |||||||
chr9:121310968 | G | C | 2 | a0001c0001t0001g0032 a0001c0001t0001g0210 |
3 | NA18993.hp2 NA19012.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.513+123G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 5/17 | chr9 | 121310968 | |||||||
chr9:121311025 | G | A | 2 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
2 | HG00621.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.513+180G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 5/17 | chr9 | 121311025 | |||||||
chr9:121311138 | C | A | 1 | a0001c0001t0001g0250 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.513+293C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 5/17 | chr9 | 121311138 | |||||||
chr9:121311275 | G | A | 241 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(238): Show |
293 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.513+430G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 5/17 | chr9 | 121311275 | |||||||
chr9:121311324 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.513+479C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 5/17 | chr9 | 121311324 | |||||||
chr9:121311330 | G | C | 1 | a0001c0004t0002g0045 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.513+485G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 5/17 | chr9 | 121311330 | |||||||
chr9:121311567 | T | C | 241 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(238): Show |
293 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.513+722T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 5/17 | chr9 | 121311567 | |||||||
chr9:121311981 | G | C | 1 | a0001c0001t0001g0185 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.514-358G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 5/17 | chr9 | 121311981 | |||||||
chr9:121312131 | C | G | 1 | a0002c0002t0002g0066 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.514-208C>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 5/17 | chr9 | 121312131 | |||||||
chr9:121312142 | G | A | 241 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(238): Show |
293 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.514-197G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 5/17 | chr9 | 121312142 | |||||||
chr9:121312513 | T | G | 2 | a0001c0001t0001g0091 a0001c0001t0001g0092 |
2 | HG01074.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.663+25T>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 6/17 | chr9 | 121312513 | |||||||
chr9:121312594 | C | T | 5 | a0001c0001t0001g0147 a0001c0001t0001g0220 a0001c0010t0001g0113 others(2): Show |
5 | HG00609.hp2 HG01109.hp1 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.663+106C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 6/17 | chr9 | 121312594 | |||||||
chr9:121312684 | G | T | 1 | a0001c0023t0003g0044 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.663+196G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 6/17 | chr9 | 121312684 | |||||||
chr9:121312687 | G | C | 132 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(129): Show |
154 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.663+199G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 6/17 | chr9 | 121312687 | |||||||
chr9:121312753 | G | A | 3 | a0001c0001t0001g0117 a0001c0004t0002g0045 a0001c0004t0002g0046 |
3 | HG01993.hp1 HG02300.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.663+265G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 6/17 | chr9 | 121312753 | |||||||
chr9:121312788 | A | G | 1 | a0001c0001t0001g0205 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.663+300A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 6/17 | chr9 | 121312788 | |||||||
chr9:121312865 | C | T | 1 | a0001c0001t0001g0020 | 2 | HG02809.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.663+377C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 6/17 | chr9 | 121312865 | |||||||
chr9:121312976 | G | A | 132 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(129): Show |
154 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.663+488G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 6/17 | chr9 | 121312976 | |||||||
chr9:121312981 | G | A | 81 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(78): Show |
92 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.663+493G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 6/17 | chr9 | 121312981 | |||||||
chr9:121313007 | C | A | 241 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(238): Show |
293 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.663+519C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 6/17 | chr9 | 121313007 | |||||||
chr9:121313132 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.663+644C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 6/17 | chr9 | 121313132 | |||||||
chr9:121313266 | G | A | 132 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(129): Show |
154 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.664-668G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 6/17 | chr9 | 121313266 | |||||||
chr9:121313514 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.664-420T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 6/17 | chr9 | 121313514 | |||||||
chr9:121313594 | G | C | 2 | a0001c0010t0001g0113 a0001c0010t0001g0114 |
2 | HG01109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.664-340G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 6/17 | chr9 | 121313594 | |||||||
chr9:121313625 | G | T | 1 | a0001c0001t0001g0137 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.664-309G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 6/17 | chr9 | 121313625 | |||||||
chr9:121313671 | C | T | 1 | a0002c0002t0007g0076 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.664-263C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 6/17 | chr9 | 121313671 | |||||||
chr9:121313698 | C | T | 7 | a0003c0005t0001g0039 a0003c0005t0001g0240 a0003c0005t0001g0241 others(4): Show |
8 | HG02280.hp2 HG02451.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.664-236C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 6/17 | chr9 | 121313698 | |||||||
chr9:121313738 | G | A | 132 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(129): Show |
154 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.664-196G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 6/17 | chr9 | 121313738 | |||||||
chr9:121313888 | C | A | 1 | a0011c0019t0001g0230 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.664-46C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 6/17 | chr9 | 121313888 | |||||||
chr9:121313930 | A | G | 1 | a0011c0019t0001g0230 | 1 | HG02559.hp2 | splice_region_variant&intron_variant | LOW | c.664-4A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 6/17 | chr9 | 121313930 | |||||||
chr9:121314054 | A | C | 1 | a0001c0001t0001g0197 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.753+31A>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 7/17 | chr9 | 121314054 | |||||||
chr9:121314125 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.753+102C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 7/17 | chr9 | 121314125 | |||||||
chr9:121314316 | A | T | 1 | a0001c0001t0001g0104 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.753+293A>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 7/17 | chr9 | 121314316 | |||||||
chr9:121314326 | G | T | 1 | a0001c0001t0001g0093 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.753+303G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 7/17 | chr9 | 121314326 | |||||||
chr9:121314367 | T | C | 1 | a0001c0003t0001g0099 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.753+344T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 7/17 | chr9 | 121314367 | |||||||
chr9:121314389 | G | A | 1 | a0001c0023t0003g0044 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.753+366G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 7/17 | chr9 | 121314389 | |||||||
chr9:121314538 | C | T | 243 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(240): Show |
295 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.753+515C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 7/17 | chr9 | 121314538 | |||||||
chr9:121315009 | C | T | 109 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(106): Show |
139 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.753+986C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 7/17 | chr9 | 121315009 | |||||||
chr9:121315142 | T | C | 2 | a0004c0006t0004g0184 a0004c0006t0004g0256 |
2 | HG01884.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.753+1119T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 7/17 | chr9 | 121315142 | |||||||
chr9:121315446 | C | T | 1 | a0001c0001t0001g0020 | 2 | HG02809.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.753+1423C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 7/17 | chr9 | 121315446 | |||||||
chr9:121315447 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.753+1424G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 7/17 | chr9 | 121315447 | |||||||
chr9:121315505 | T | C | 1 | a0002c0002t0007g0076 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.753+1482T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 7/17 | chr9 | 121315505 | |||||||
chr9:121315518 | C | T | 173 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(170): Show |
209 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.753+1495C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 7/17 | chr9 | 121315518 | |||||||
chr9:121315562 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.754-1524G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 7/17 | chr9 | 121315562 | |||||||
chr9:121315725 | C | T | 44 | a0001c0004t0002g0045 a0001c0004t0002g0046 a0001c0004t0002g0122 others(41): Show |
54 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.754-1361C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 7/17 | chr9 | 121315725 | |||||||
chr9:121315767 | T | A | 70 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(67): Show |
86 | HG00140.hp1 HG00438.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.754-1319T>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 7/17 | chr9 | 121315767 | |||||||
chr9:121316094 | T | G | 9 | a0003c0005t0001g0039 a0003c0005t0001g0240 a0003c0005t0001g0241 others(6): Show |
10 | HG02280.hp2 HG02451.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.754-992T>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 7/17 | chr9 | 121316094 | |||||||
chr9:121316295 | G | A | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | HG01934.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.754-791G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 7/17 | chr9 | 121316295 | |||||||
chr9:121316531 | C | T | 44 | a0001c0004t0002g0045 a0001c0004t0002g0046 a0001c0004t0002g0122 others(41): Show |
54 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.754-555C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 7/17 | chr9 | 121316531 | |||||||
chr9:121316660 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.754-426G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 7/17 | chr9 | 121316660 | |||||||
chr9:121316682 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.754-404G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 7/17 | chr9 | 121316682 | |||||||
chr9:121316700 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.754-386G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 7/17 | chr9 | 121316700 | |||||||
chr9:121316832 | C | G | 187 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(184): Show |
227 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.754-254C>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 7/17 | chr9 | 121316832 | |||||||
chr9:121316959 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0262 |
3 | HG02976.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.754-127C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 7/17 | chr9 | 121316959 | |||||||
chr9:121317237 | G | T | 1 | a0001c0001t0001g0227 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.886+19G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 8/17 | chr9 | 121317237 | |||||||
chr9:121317253 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.886+35G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 8/17 | chr9 | 121317253 | |||||||
chr9:121317523 | T | C | 56 | a0001c0001t0001g0042 a0001c0001t0001g0262 a0001c0001t0003g0151 others(53): Show |
68 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.886+305T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 8/17 | chr9 | 121317523 | |||||||
chr9:121317569 | C | T | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG02109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.886+351C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 8/17 | chr9 | 121317569 | |||||||
chr9:121317766 | C | G | 1 | a0009c0011t0001g0041 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.886+548C>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 8/17 | chr9 | 121317766 | |||||||
chr9:121317995 | G | A | 9 | a0003c0005t0001g0039 a0003c0005t0001g0240 a0003c0005t0001g0241 others(6): Show |
10 | HG02280.hp2 HG02451.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.887-411G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 8/17 | chr9 | 121317995 | |||||||
chr9:121318075 | C | CCTTATAG others(21): Show |
1 | a0001c0001t0001g0233 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.887-327_887-300dup others(28): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr9 | 121318075 | ||||||
chr9:121318075 | C | T | 1 | a0001c0003t0001g0129 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.887-331C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 8/17 | chr9 | 121318075 | |||||||
chr9:121318096 | G | C | 1 | a0001c0001t0001g0130 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.887-310G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 8/17 | chr9 | 121318096 | |||||||
chr9:121318279 | G | C | 2 | a0001c0010t0001g0113 a0001c0010t0001g0114 |
2 | HG01109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.887-127G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 8/17 | chr9 | 121318279 | |||||||
chr9:121318365 | C | T | 3 | a0001c0001t0001g0005 a0001c0001t0001g0185 a0001c0001t0001g0187 |
6 | HG02055.hp1 HG02559.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.887-41C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 8/17 | chr9 | 121318365 | |||||||
chr9:121318537 | G | C | 19 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0001t0001g0085 others(16): Show |
21 | HG00280.hp2 HG00323.hp1 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.975+43G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 9/17 | chr9 | 121318537 | |||||||
chr9:121318547 | G | T | 1 | a0001c0001t0001g0232 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.975+53G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 9/17 | chr9 | 121318547 | |||||||
chr9:121318558 | G | A | 2 | a0004c0006t0004g0184 a0004c0006t0004g0256 |
2 | HG01884.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.975+64G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 9/17 | chr9 | 121318558 | |||||||
chr9:121318916 | C | T | 1 | a0012c0017t0001g0090 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1191+36C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 10/17 | chr9 | 121318916 | |||||||
chr9:121318985 | T | C | 12 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0032 others(9): Show |
16 | HG02523.hp2 NA18944.hp1 NA18953.hp1 others(13): Show |
intron_variant | MODIFIER | c.1191+105T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 10/17 | chr9 | 121318985 | |||||||
chr9:121319487 | C | CT | 12 | a0001c0001t0001g0146 a0001c0010t0001g0113 a0001c0010t0001g0114 others(9): Show |
13 | HG01109.hp1 HG02280.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1191+622dupT | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr9 | 121319487 | ||||||
chr9:121319548 | C | G | 1 | a0001c0003t0001g0129 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1191+668C>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 10/17 | chr9 | 121319548 | |||||||
chr9:121319551 | G | C | 39 | a0001c0004t0002g0045 a0001c0004t0002g0046 a0001c0004t0002g0122 others(36): Show |
48 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.1191+671G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 10/17 | chr9 | 121319551 | |||||||
chr9:121319791 | A | G | 1 | a0001c0001t0001g0232 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1191+911A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 10/17 | chr9 | 121319791 | |||||||
chr9:121320074 | G | C | 3 | a0004c0006t0004g0222 a0004c0006t0004g0223 a0004c0006t0004g0238 |
3 | HG01071.hp2 HG02738.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1191+1194G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 10/17 | chr9 | 121320074 | |||||||
chr9:121320106 | T | C | 1 | a0001c0010t0001g0114 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1192-1162T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 10/17 | chr9 | 121320106 | |||||||
chr9:121320205 | C | T | 1 | a0011c0019t0001g0230 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1192-1063C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 10/17 | chr9 | 121320205 | |||||||
chr9:121320537 | C | T | 1 | a0001c0023t0003g0044 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1192-731C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 10/17 | chr9 | 121320537 | |||||||
chr9:121320652 | CA | C | 6 | a0001c0001t0001g0080 a0001c0001t0001g0192 a0001c0001t0001g0233 others(3): Show |
6 | HG01070.hp1 HG02896.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1192-602delA | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr9 | 121320652 | ||||||
chr9:121320652 | CAAAAAAA others(3): Show |
C | 1 | a0001c0004t0002g0155 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1192-611_1192-602d others(12): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr9 | 121320652 | ||||||
chr9:121320687 | G | A | 6 | a0001c0001t0001g0018 a0001c0001t0001g0103 a0001c0001t0001g0109 others(3): Show |
7 | HG01109.hp2 HG02109.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1192-581G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 10/17 | chr9 | 121320687 | |||||||
chr9:121320806 | T | A | 1 | a0001c0001t0001g0233 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1192-462T>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 10/17 | chr9 | 121320806 | |||||||
chr9:121320897 | G | A | 23 | a0001c0003t0001g0001 a0001c0003t0001g0009 a0001c0003t0001g0016 others(20): Show |
30 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.1192-371G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 10/17 | chr9 | 121320897 | |||||||
chr9:121321142 | G | A | 27 | a0001c0001t0001g0033 a0001c0003t0001g0001 a0001c0003t0001g0009 others(24): Show |
35 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.1192-126G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 10/17 | chr9 | 121321142 | |||||||
chr9:121321193 | C | T | 17 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(14): Show |
22 | HG00140.hp1 HG00741.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.1192-75C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 10/17 | chr9 | 121321193 | |||||||
chr9:121321207 | C | T | 1 | a0001c0001t0001g0204 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1192-61C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 10/17 | chr9 | 121321207 | |||||||
chr9:121321484 | G | A | 1 | a0009c0011t0001g0041 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1325+83G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121321484 | |||||||
chr9:121321542 | C | A | 1 | a0002c0002t0002g0063 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1325+141C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121321542 | |||||||
chr9:121321565 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1325+164A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121321565 | |||||||
chr9:121321594 | T | A | 1 | a0001c0001t0001g0233 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1325+193T>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121321594 | |||||||
chr9:121321636 | A | C | 1 | a0001c0001t0001g0138 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1325+235A>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121321636 | |||||||
chr9:121321670 | A | G | 23 | a0001c0003t0001g0001 a0001c0003t0001g0009 a0001c0003t0001g0016 others(20): Show |
30 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.1325+269A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121321670 | |||||||
chr9:121321731 | G | GTTTA | 3 | a0001c0001t0001g0153 a0001c0001t0001g0163 a0001c0001t0001g0167 |
3 | HG00140.hp2 HG00280.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.1325+354_1325+357d others(6): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr9 | 121321731 | ||||||
chr9:121321731 | GTTTA | G | 119 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0014 others(116): Show |
143 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.1325+354_1325+357d others(6): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr9 | 121321731 | ||||||
chr9:121321757 | T | A | 1 | a0001c0001t0001g0233 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1325+356T>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121321757 | |||||||
chr9:121321762 | G | A | 42 | a0001c0004t0002g0045 a0001c0004t0002g0046 a0001c0004t0002g0122 others(39): Show |
52 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.1325+361G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121321762 | |||||||
chr9:121321812 | G | A | 145 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(142): Show |
172 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.1325+411G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121321812 | |||||||
chr9:121321825 | T | A | 1 | a0001c0001t0001g0233 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1325+424T>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121321825 | |||||||
chr9:121321842 | A | G | 1 | a0001c0003t0001g0237 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1325+441A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121321842 | |||||||
chr9:121321861 | CCT | C | 3 | a0004c0006t0004g0222 a0004c0006t0004g0223 a0004c0006t0004g0238 |
3 | HG01071.hp2 HG02738.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1325+465_1325+466d others(4): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr9 | 121321861 | ||||||
chr9:121321916 | T | C | 1 | a0001c0001t0001g0249 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1325+515T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121321916 | |||||||
chr9:121322133 | C | A | 1 | a0001c0001t0001g0233 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1325+732C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121322133 | |||||||
chr9:121322192 | C | G | 3 | a0004c0006t0004g0222 a0004c0006t0004g0223 a0004c0006t0004g0238 |
3 | HG01071.hp2 HG02738.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1325+791C>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121322192 | |||||||
chr9:121322205 | TTCCAGTA others(44): Show |
T | 1 | a0001c0001t0001g0085 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1325+805_1325+855d others(53): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121322205 | |||||||
chr9:121322306 | C | A | 2 | a0001c0001t0001g0033 a0001c0023t0003g0044 |
3 | HG00639.hp2 HG00735.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.1325+905C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121322306 | |||||||
chr9:121322330 | T | G | 1 | a0001c0001t0001g0202 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1325+929T>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121322330 | |||||||
chr9:121322335 | A | G | 1 | a0001c0003t0001g0212 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1325+934A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121322335 | |||||||
chr9:121322667 | C | A | 1 | a0001c0001t0001g0164 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1325+1266C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121322667 | |||||||
chr9:121322702 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1325+1301G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121322702 | |||||||
chr9:121322733 | G | C | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | HG01934.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1325+1332G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121322733 | |||||||
chr9:121322783 | T | C | 2 | a0001c0001t0001g0021 a0001c0001t0001g0135 |
3 | HG01106.hp2 HG01192.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1325+1382T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121322783 | |||||||
chr9:121322807 | CT | C | 3 | a0001c0001t0001g0098 a0001c0001t0001g0121 a0001c0001t0001g0233 |
3 | HG01070.hp1 HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1325+1411delT | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr9 | 121322807 | ||||||
chr9:121322833 | A | AT | 185 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(182): Show |
225 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.1325+1447dupT | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr9 | 121322833 | ||||||
chr9:121322871 | G | C | 42 | a0001c0004t0002g0045 a0001c0004t0002g0046 a0001c0004t0002g0122 others(39): Show |
52 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.1325+1470G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121322871 | |||||||
chr9:121322912 | C | G | 11 | a0001c0001t0001g0006 a0001c0001t0001g0037 a0001c0001t0001g0123 others(8): Show |
15 | HG00140.hp1 HG00741.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.1325+1511C>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121322912 | |||||||
chr9:121322993 | A | G | 246 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(243): Show |
299 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.1326-1561A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121322993 | |||||||
chr9:121323036 | T | C | 1 | a0001c0001t0001g0079 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1326-1518T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121323036 | |||||||
chr9:121323055 | G | A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0135 |
3 | HG01106.hp2 HG01192.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1326-1499G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121323055 | |||||||
chr9:121323122 | C | T | 1 | a0011c0019t0001g0230 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1326-1432C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121323122 | |||||||
chr9:121323205 | C | T | 15 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(12): Show |
20 | HG00140.hp1 HG00741.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.1326-1349C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121323205 | |||||||
chr9:121323229 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1326-1325A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121323229 | |||||||
chr9:121323284 | A | C | 3 | a0004c0006t0004g0222 a0004c0006t0004g0223 a0004c0006t0004g0238 |
3 | HG01071.hp2 HG02738.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1326-1270A>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121323284 | |||||||
chr9:121323371 | G | GTTTTT | 113 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(110): Show |
132 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.1326-1169_1326-116 others(9): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr9 | 121323371 | ||||||
chr9:121323371 | G | GTTTTTT | 30 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0018 others(27): Show |
38 | HG00597.hp2 HG01106.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.1326-1170_1326-116 others(10): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr9 | 121323371 | ||||||
chr9:121323400 | T | A | 1 | a0001c0001t0001g0233 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1326-1154T>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121323400 | |||||||
chr9:121323440 | G | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0182 a0001c0001t0001g0185 others(2): Show |
8 | HG01261.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1326-1114G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121323440 | |||||||
chr9:121323450 | A | G | 1 | a0004c0006t0005g0236 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1326-1104A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121323450 | |||||||
chr9:121323562 | GT | G | 145 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(142): Show |
172 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.1326-989delT | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr9 | 121323562 | ||||||
chr9:121323768 | C | T | 13 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0104 others(10): Show |
14 | HG01074.hp1 HG02145.hp2 HG02148.hp1 others(11): Show |
intron_variant | MODIFIER | c.1326-786C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121323768 | |||||||
chr9:121323874 | A | T | 9 | a0003c0005t0001g0039 a0003c0005t0001g0240 a0003c0005t0001g0241 others(6): Show |
10 | HG02280.hp2 HG02451.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1326-680A>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121323874 | |||||||
chr9:121324015 | A | G | 3 | a0001c0001t0001g0132 a0001c0001t0001g0145 a0001c0001t0001g0175 |
3 | HG02155.hp2 NA18971.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.1326-539A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121324015 | |||||||
chr9:121324056 | A | T | 3 | a0001c0001t0001g0117 a0008c0012t0001g0097 a0008c0012t0001g0101 |
3 | HG02451.hp2 HG02809.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1326-498A>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121324056 | |||||||
chr9:121324298 | A | C | 9 | a0003c0005t0001g0039 a0003c0005t0001g0240 a0003c0005t0001g0241 others(6): Show |
10 | HG02280.hp2 HG02451.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1326-256A>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121324298 | |||||||
chr9:121324415 | G | C | 1 | a0001c0003t0001g0203 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1326-139G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | chr9 | 121324415 | |||||||
chr9:121324438 | CTCTA | C | 3 | a0004c0006t0004g0222 a0004c0006t0004g0223 a0004c0006t0004g0238 |
3 | HG01071.hp2 HG02738.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1326-112_1326-109d others(6): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr9 | 121324438 | ||||||
chr9:121324739 | ATCTG | A | 2 | a0001c0001t0001g0042 a0001c0001t0001g0262 |
3 | HG02976.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1416+106_1416+109d others(6): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr9 | 121324739 | ||||||
chr9:121324751 | G | GTCCA | 37 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0021 others(34): Show |
46 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.1416+149_1416+152d others(6): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr9 | 121324751 | ||||||
chr9:121324751 | G | GTCCATCC others(1): Show |
6 | a0001c0001t0001g0043 a0001c0001t0001g0152 a0001c0001t0001g0175 others(3): Show |
6 | HG01243.hp1 HG01256.hp1 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.1416+145_1416+152d others(10): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr9 | 121324751 | ||||||
chr9:121324751 | G | GTCCATCC others(9): Show |
1 | a0001c0001t0001g0166 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1416+137_1416+152d others(18): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr9 | 121324751 | ||||||
chr9:121324751 | GTCCA | G | 4 | a0001c0001t0001g0082 a0004c0006t0004g0222 a0004c0006t0004g0223 others(1): Show |
4 | HG01071.hp2 HG02738.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1416+149_1416+152d others(6): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr9 | 121324751 | ||||||
chr9:121324751 | GTCCATCC others(1): Show |
G | 4 | a0001c0001t0001g0144 a0001c0001t0001g0149 a0001c0001t0001g0157 others(1): Show |
4 | HG01934.hp2 HG02738.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.1416+145_1416+152d others(10): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr9 | 121324751 | ||||||
chr9:121324755 | A | G | 2 | a0001c0001t0001g0042 a0001c0001t0001g0262 |
3 | HG02976.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1416+111A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | chr9 | 121324755 | |||||||
chr9:121324776 | T | C | 42 | a0001c0004t0002g0045 a0001c0004t0002g0046 a0001c0004t0002g0122 others(39): Show |
52 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.1416+132T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | chr9 | 121324776 | |||||||
chr9:121324835 | C | T | 38 | a0001c0004t0002g0045 a0001c0004t0002g0046 a0001c0004t0002g0122 others(35): Show |
47 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.1416+191C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | chr9 | 121324835 | |||||||
chr9:121325087 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1416+443T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | chr9 | 121325087 | |||||||
chr9:121325349 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1416+705A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | chr9 | 121325349 | |||||||
chr9:121325388 | C | T | 187 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(184): Show |
227 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.1416+744C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | chr9 | 121325388 | |||||||
chr9:121325637 | C | T | 238 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(235): Show |
289 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.1417-875C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | chr9 | 121325637 | |||||||
chr9:121325656 | C | A | 2 | a0001c0001t0001g0042 a0001c0001t0001g0262 |
3 | HG02976.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1417-856C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | chr9 | 121325656 | |||||||
chr9:121325715 | A | G | 1 | a0001c0001t0001g0178 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1417-797A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | chr9 | 121325715 | |||||||
chr9:121325842 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1417-670C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | chr9 | 121325842 | |||||||
chr9:121325890 | C | G | 1 | a0001c0001t0001g0178 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1417-622C>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | chr9 | 121325890 | |||||||
chr9:121325899 | G | A | 1 | a0002c0007t0001g0056 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1417-613G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | chr9 | 121325899 | |||||||
chr9:121325929 | T | C | 238 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(235): Show |
289 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.1417-583T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | chr9 | 121325929 | |||||||
chr9:121325948 | G | A | 1 | a0002c0002t0002g0059 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1417-564G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | chr9 | 121325948 | |||||||
chr9:121325961 | C | T | 3 | a0002c0002t0002g0064 a0002c0002t0002g0069 a0002c0002t0002g0077 |
3 | NA18612.hp1 NA19003.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1417-551C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | chr9 | 121325961 | |||||||
chr9:121325962 | A | G | 42 | a0001c0004t0002g0045 a0001c0004t0002g0046 a0001c0004t0002g0122 others(39): Show |
52 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.1417-550A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | chr9 | 121325962 | |||||||
chr9:121326081 | C | T | 25 | a0001c0001t0001g0033 a0001c0003t0001g0001 a0001c0003t0001g0009 others(22): Show |
33 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.1417-431C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | chr9 | 121326081 | |||||||
chr9:121326160 | G | C | 1 | a0001c0001t0001g0128 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1417-352G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | chr9 | 121326160 | |||||||
chr9:121326177 | A | C | 42 | a0001c0004t0002g0045 a0001c0004t0002g0046 a0001c0004t0002g0122 others(39): Show |
52 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.1417-335A>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | chr9 | 121326177 | |||||||
chr9:121326256 | C | G | 1 | a0002c0014t0002g0048 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1417-256C>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | chr9 | 121326256 | |||||||
chr9:121326453 | A | G | 49 | a0001c0004t0002g0045 a0001c0004t0002g0046 a0001c0004t0002g0122 others(46): Show |
60 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.1417-59A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | chr9 | 121326453 | |||||||
chr9:121326462 | C | A | 2 | a0004c0006t0004g0223 a0004c0006t0004g0238 |
2 | HG02738.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1417-50C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | chr9 | 121326462 | |||||||
chr9:121326490 | T | C | 247 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(244): Show |
300 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.1417-22T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | chr9 | 121326490 | |||||||
chr9:121326491 | G | A | 1 | a0013c0013t0001g0260 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1417-21G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 12/17 | chr9 | 121326491 | |||||||
chr9:121326728 | A | G | 9 | a0003c0005t0001g0039 a0003c0005t0001g0240 a0003c0005t0001g0241 others(6): Show |
10 | HG02280.hp2 HG02451.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1587+46A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 13/17 | chr9 | 121326728 | |||||||
chr9:121326760 | C | T | 1 | a0001c0004t0002g0171 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1587+78C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 13/17 | chr9 | 121326760 | |||||||
chr9:121326774 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1587+92G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 13/17 | chr9 | 121326774 | |||||||
chr9:121326894 | A | G | 1 | a0001c0001t0001g0197 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1587+212A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 13/17 | chr9 | 121326894 | |||||||
chr9:121326895 | C | T | 238 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(235): Show |
289 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.1587+213C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 13/17 | chr9 | 121326895 | |||||||
chr9:121327186 | T | C | 2 | a0001c0010t0001g0113 a0001c0010t0001g0114 |
2 | HG01109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1588-122T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 13/17 | chr9 | 121327186 | |||||||
chr9:121327230 | GC | G | 38 | a0001c0004t0002g0045 a0001c0004t0002g0046 a0001c0004t0002g0122 others(35): Show |
47 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.1588-77delC | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 13/17 | chr9 | 121327230 | |||||||
chr9:121327231 | C | T | 4 | a0002c0002t0004g0054 a0002c0002t0004g0055 a0006c0009t0004g0038 others(1): Show |
5 | HG02572.hp1 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1588-77C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 13/17 | chr9 | 121327231 | |||||||
chr9:121327232 | G | T | 38 | a0001c0004t0002g0045 a0001c0004t0002g0046 a0001c0004t0002g0122 others(35): Show |
47 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.1588-76G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 13/17 | chr9 | 121327232 | |||||||
chr9:121327566 | A | C | 4 | a0002c0002t0004g0054 a0002c0002t0004g0055 a0006c0009t0004g0038 others(1): Show |
5 | HG02572.hp1 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1762+84A>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 14/17 | chr9 | 121327566 | |||||||
chr9:121327716 | G | GTAATCCC others(128): Show |
9 | a0003c0005t0001g0039 a0003c0005t0001g0240 a0003c0005t0001g0241 others(6): Show |
10 | HG02280.hp2 HG02451.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1762+245_1762+379d others(137): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 121327716 | ||||||
chr9:121327740 | A | C | 17 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(14): Show |
22 | HG00140.hp1 HG00741.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.1762+258A>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 14/17 | chr9 | 121327740 | |||||||
chr9:121327828 | C | T | 6 | a0004c0006t0004g0184 a0004c0006t0004g0222 a0004c0006t0004g0223 others(3): Show |
6 | HG01071.hp2 HG01884.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.1762+346C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 14/17 | chr9 | 121327828 | |||||||
chr9:121327833 | A | G | 1 | a0002c0002t0002g0050 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1762+351A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 14/17 | chr9 | 121327833 | |||||||
chr9:121327845 | G | A | 75 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(72): Show |
93 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.1762+363G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 14/17 | chr9 | 121327845 | |||||||
chr9:121327846 | C | T | 6 | a0004c0006t0004g0184 a0004c0006t0004g0222 a0004c0006t0004g0223 others(3): Show |
6 | HG01071.hp2 HG01884.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.1762+364C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 14/17 | chr9 | 121327846 | |||||||
chr9:121327904 | T | G | 249 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(246): Show |
302 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.1762+422T>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 14/17 | chr9 | 121327904 | |||||||
chr9:121327955 | C | T | 42 | a0001c0004t0002g0045 a0001c0004t0002g0046 a0001c0004t0002g0122 others(39): Show |
52 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.1762+473C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 14/17 | chr9 | 121327955 | |||||||
chr9:121327980 | G | GAAGA | 3 | a0001c0001t0001g0042 a0001c0001t0001g0170 a0001c0001t0001g0262 |
4 | HG02976.hp2 HG03130.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1762+514_1762+517d others(6): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 121327980 | ||||||
chr9:121328060 | G | GC | 17 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(14): Show |
22 | HG00140.hp1 HG00741.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.1762+580dupC | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 121328060 | ||||||
chr9:121328083 | C | G | 9 | a0003c0005t0001g0039 a0003c0005t0001g0240 a0003c0005t0001g0241 others(6): Show |
10 | HG02280.hp2 HG02451.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1762+601C>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 14/17 | chr9 | 121328083 | |||||||
chr9:121328180 | C | T | 9 | a0003c0005t0001g0039 a0003c0005t0001g0240 a0003c0005t0001g0241 others(6): Show |
10 | HG02280.hp2 HG02451.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1762+698C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 14/17 | chr9 | 121328180 | |||||||
chr9:121328202 | G | A | 2 | a0001c0001t0001g0081 a0001c0001t0001g0082 |
2 | HG01891.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1763-689G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 14/17 | chr9 | 121328202 | |||||||
chr9:121328237 | C | A | 1 | a0004c0006t0005g0236 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1763-654C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 14/17 | chr9 | 121328237 | |||||||
chr9:121328344 | T | TTGTGTTT others(44): Show |
1 | a0001c0001t0001g0085 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1763-546_1763-545i others(53): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr9 | 121328344 | ||||||
chr9:121328346 | T | G | 1 | a0001c0001t0001g0085 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1763-545T>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 14/17 | chr9 | 121328346 | |||||||
chr9:121328367 | G | A | 42 | a0001c0004t0002g0045 a0001c0004t0002g0046 a0001c0004t0002g0122 others(39): Show |
52 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.1763-524G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 14/17 | chr9 | 121328367 | |||||||
chr9:121328500 | A | G | 1 | a0001c0001t0001g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1763-391A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 14/17 | chr9 | 121328500 | |||||||
chr9:121328506 | G | A | 240 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(237): Show |
292 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.1763-385G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 14/17 | chr9 | 121328506 | |||||||
chr9:121328521 | G | T | 9 | a0003c0005t0001g0039 a0003c0005t0001g0240 a0003c0005t0001g0241 others(6): Show |
10 | HG02280.hp2 HG02451.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1763-370G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 14/17 | chr9 | 121328521 | |||||||
chr9:121328715 | C | T | 4 | a0001c0001t0001g0130 a0001c0001t0001g0137 a0001c0001t0001g0166 others(1): Show |
4 | NA18747.hp2 NA18975.hp1 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.1763-176C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 14/17 | chr9 | 121328715 | |||||||
chr9:121328777 | G | A | 1 | a0002c0015t0001g0047 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1763-114G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 14/17 | chr9 | 121328777 | |||||||
chr9:121328857 | G | A | 238 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(235): Show |
289 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.1763-34G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 14/17 | chr9 | 121328857 | |||||||
chr9:121329061 | G | T | 1 | a0009c0011t0001g0041 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1887+46G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 15/17 | chr9 | 121329061 | |||||||
chr9:121329201 | G | GAAGACAT others(4): Show |
1 | a0002c0002t0002g0253 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1888-36_1888-26dup others(11): Show |
GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr9 | 121329201 | ||||||
chr9:121329459 | C | T | 1 | a0009c0011t0001g0041 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1965+144C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 16/17 | chr9 | 121329459 | |||||||
chr9:121329507 | G | A | 21 | a0001c0003t0001g0001 a0001c0003t0001g0009 a0001c0003t0001g0016 others(18): Show |
28 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(25): Show |
intron_variant | MODIFIER | c.1965+192G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 16/17 | chr9 | 121329507 | |||||||
chr9:121329507 | G | C | 2 | a0004c0006t0004g0184 a0004c0006t0004g0256 |
2 | HG01884.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1965+192G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 16/17 | chr9 | 121329507 | |||||||
chr9:121329705 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1965+390G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 16/17 | chr9 | 121329705 | |||||||
chr9:121329706 | G | A | 4 | a0002c0002t0004g0054 a0002c0002t0004g0055 a0006c0009t0004g0038 others(1): Show |
5 | HG02572.hp1 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1965+391G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 16/17 | chr9 | 121329706 | |||||||
chr9:121329728 | C | A | 2 | a0001c0001t0001g0042 a0001c0001t0001g0262 |
3 | HG02976.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1965+413C>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 16/17 | chr9 | 121329728 | |||||||
chr9:121329771 | T | G | 1 | a0009c0011t0001g0041 | 2 | HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1965+456T>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 16/17 | chr9 | 121329771 | |||||||
chr9:121329983 | C | T | 52 | a0001c0004t0002g0045 a0001c0004t0002g0046 a0001c0004t0002g0122 others(49): Show |
64 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.1965+668C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 16/17 | chr9 | 121329983 | |||||||
chr9:121330077 | C | T | 64 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0018 others(61): Show |
70 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.1965+762C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 16/17 | chr9 | 121330077 | |||||||
chr9:121330107 | A | T | 1 | a0001c0001t0001g0209 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1965+792A>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 16/17 | chr9 | 121330107 | |||||||
chr9:121330139 | G | C | 1 | a0001c0001t0001g0089 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1965+824G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 16/17 | chr9 | 121330139 | |||||||
chr9:121330467 | T | C | 52 | a0001c0004t0002g0045 a0001c0004t0002g0046 a0001c0004t0002g0122 others(49): Show |
64 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.1966-921T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 16/17 | chr9 | 121330467 | |||||||
chr9:121330560 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1966-828G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 16/17 | chr9 | 121330560 | |||||||
chr9:121330593 | T | C | 54 | a0001c0001t0001g0042 a0001c0001t0001g0262 a0001c0004t0002g0045 others(51): Show |
67 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.1966-795T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 16/17 | chr9 | 121330593 | |||||||
chr9:121331121 | G | C | 1 | a0001c0001t0003g0148 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1966-267G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 16/17 | chr9 | 121331121 | |||||||
chr9:121331213 | T | A | 1 | a0001c0001t0001g0252 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1966-175T>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 16/17 | chr9 | 121331213 | |||||||
chr9:121331484 | T | C | 52 | a0001c0004t0002g0045 a0001c0004t0002g0046 a0001c0004t0002g0122 others(49): Show |
64 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.2026+36T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 17/17 | chr9 | 121331484 | |||||||
chr9:121331535 | G | A | 1 | a0001c0001t0001g0258 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2026+87G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 17/17 | chr9 | 121331535 | |||||||
chr9:121331662 | A | G | 247 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(244): Show |
300 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.2026+214A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 17/17 | chr9 | 121331662 | |||||||
chr9:121331663 | A | G | 1 | a0001c0001t0001g0252 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2026+215A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 17/17 | chr9 | 121331663 | |||||||
chr9:121331719 | G | C | 5 | a0004c0006t0004g0184 a0004c0006t0004g0222 a0004c0006t0004g0223 others(2): Show |
5 | HG01071.hp2 HG01884.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.2026+271G>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 17/17 | chr9 | 121331719 | |||||||
chr9:121331736 | A | G | 248 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(245): Show |
301 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.2026+288A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 17/17 | chr9 | 121331736 | |||||||
chr9:121331747 | G | T | 1 | a0001c0001t0001g0143 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2026+299G>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 17/17 | chr9 | 121331747 | |||||||
chr9:121331870 | A | G | 1 | a0001c0001t0001g0206 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2026+422A>G | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 17/17 | chr9 | 121331870 | |||||||
chr9:121331881 | T | C | 52 | a0001c0004t0002g0045 a0001c0004t0002g0046 a0001c0004t0002g0122 others(49): Show |
64 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.2026+433T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 17/17 | chr9 | 121331881 | |||||||
chr9:121331973 | T | C | 9 | a0003c0005t0001g0039 a0003c0005t0001g0240 a0003c0005t0001g0241 others(6): Show |
10 | HG02280.hp2 HG02451.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.2027-461T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 17/17 | chr9 | 121331973 | |||||||
chr9:121332012 | C | T | 2 | a0001c0001t0001g0153 a0001c0001t0001g0163 |
2 | HG00140.hp2 HG00280.hp1 |
intron_variant | MODIFIER | c.2027-422C>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 17/17 | chr9 | 121332012 | |||||||
chr9:121332157 | T | C | 50 | a0001c0004t0002g0045 a0001c0004t0002g0046 a0001c0004t0002g0122 others(47): Show |
62 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.2027-277T>C | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 17/17 | chr9 | 121332157 | |||||||
chr9:121332312 | A | T | 42 | a0001c0001t0001g0006 a0001c0001t0001g0033 a0001c0001t0001g0036 others(39): Show |
55 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.2027-122A>T | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 17/17 | chr9 | 121332312 | |||||||
chr9:121332402 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2027-32G>A | GSN | ENSG00000148180.22 | transcript | ENST00000432226.7 | protein_coding | 17/17 | chr9 | 121332402 |