Item | Value |
---|---|
geneid | 2022 |
ensemblid | ENSG00000106991.14 |
hgncid | 3349 |
symbol | ENG |
name | endoglin |
refseq_nuc | NM_001114753.3 |
refseq_prot | NP_001108225.1 |
ensembl_nuc | ENST00000373203.9 |
ensembl_prot | ENSP00000362299.4 |
mane_status | MANE Select |
chr | chr9 |
start | 127815016 |
end | 127854658 |
strand | - |
ver | v1.2 |
region | chr9:127815016-127854658 |
region5000 | chr9:127810016-127859658 |
regionname0 | ENG_chr9_127815016_127854658 |
regionname5000 | ENG_chr9_127810016_127859658 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 658 | 303 | 75 | 52 | 121 | 11 | 42 | 85 | ENG_chr9_127810016_127859658 | ENG | MDRGT others(653): Show |
chr9 | 127810016 | 127859658 |
a0002 | 0/0 | 658 | 16 | 0 | 0 | 16 | 0 | 0 | 10 | ENG_chr9_127810016_127859658 | ENG | MDRGT others(653): Show |
chr9 | 127810016 | 127859658 |
a0003 | 0/0 | 658 | 13 | 10 | 3 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | MDRGM others(653): Show |
chr9 | 127810016 | 127859658 |
a0004 | 0/0 | 658 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | MDRGT others(653): Show |
chr9 | 127810016 | 127859658 |
a0005 | 0/0 | 658 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | MDRGT others(653): Show |
chr9 | 127810016 | 127859658 |
a0006 | 0/0 | 658 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | MDRGT others(653): Show |
chr9 | 127810016 | 127859658 |
a0007 | 0/0 | 658 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | MDRGT others(653): Show |
chr9 | 127810016 | 127859658 |
a0008 | 0/0 | 658 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | MDRGT others(653): Show |
chr9 | 127810016 | 127859658 |
a0009 | 0/0 | 658 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ENG_chr9_127810016_127859658 | ENG | MDRGT others(653): Show |
chr9 | 127810016 | 127859658 |
a0010 | 0/0 | 658 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | MDRGT others(653): Show |
chr9 | 127810016 | 127859658 |
a0011 | 0/0 | 658 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ENG_chr9_127810016_127859658 | ENG | MDRGT others(653): Show |
chr9 | 127810016 | 127859658 |
a0012 | 0/0 | 658 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | MDRGT others(653): Show |
chr9 | 127810016 | 127859658 |
a0013 | 0/0 | 658 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | MDRGT others(653): Show |
chr9 | 127810016 | 127859658 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1974 | 230 | 44 | 36 | 107 | 9 | 32 | ENG_chr9_127810016_127859658 | ENG | ATGGA others(1969): Show |
chr9 | 127810016 | 127859658 | ||
a0001c0002 | 0/0 | 1974 | 35 | 21 | 7 | 5 | 1 | 1 | ENG_chr9_127810016_127859658 | ENG | ATGGA others(1969): Show |
chr9 | 127810016 | 127859658 | ||
a0001c0003 | 0/0 | 1974 | 18 | 2 | 3 | 4 | 1 | 8 | ENG_chr9_127810016_127859658 | ENG | ATGGA others(1969): Show |
chr9 | 127810016 | 127859658 | ||
a0001c0006 | 0/0 | 1974 | 5 | 3 | 1 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | ATGGA others(1969): Show |
chr9 | 127810016 | 127859658 | ||
a0001c0007 | 0/0 | 1974 | 4 | 0 | 2 | 2 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATGGA others(1969): Show |
chr9 | 127810016 | 127859658 | ||
a0001c0008 | 0/0 | 1974 | 2 | 1 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATGGA others(1969): Show |
chr9 | 127810016 | 127859658 | ||
a0001c0010 | 0/0 | 1974 | 2 | 0 | 0 | 2 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATGGA others(1969): Show |
chr9 | 127810016 | 127859658 | ||
a0001c0013 | 0/0 | 1974 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATGGA others(1969): Show |
chr9 | 127810016 | 127859658 | ||
a0001c0014 | 0/0 | 1974 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATGGA others(1969): Show |
chr9 | 127810016 | 127859658 | ||
a0001c0016 | 0/0 | 1974 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATGGA others(1969): Show |
chr9 | 127810016 | 127859658 | ||
a0001c0021 | 0/0 | 1974 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATGGA others(1969): Show |
chr9 | 127810016 | 127859658 | ||
a0001c0022 | 0/0 | 1974 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATGGA others(1969): Show |
chr9 | 127810016 | 127859658 | ||
a0001c0024 | 0/0 | 1974 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATGGA others(1969): Show |
chr9 | 127810016 | 127859658 | ||
a0001c0025 | 0/0 | 1974 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATGGA others(1969): Show |
chr9 | 127810016 | 127859658 | ||
a0002c0004 | 0/0 | 1974 | 15 | 0 | 0 | 15 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATGGA others(1969): Show |
chr9 | 127810016 | 127859658 | ||
a0002c0012 | 0/0 | 1974 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATGGA others(1969): Show |
chr9 | 127810016 | 127859658 | ||
a0003c0005 | 0/0 | 1974 | 11 | 8 | 3 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATGGA others(1969): Show |
chr9 | 127810016 | 127859658 | ||
a0003c0029 | 0/0 | 1974 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATGGA others(1969): Show |
chr9 | 127810016 | 127859658 | ||
a0003c0030 | 0/0 | 1974 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATGGA others(1969): Show |
chr9 | 127810016 | 127859658 | ||
a0004c0009 | 0/0 | 1974 | 2 | 2 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATGGA others(1969): Show |
chr9 | 127810016 | 127859658 | ||
a0004c0015 | 0/0 | 1974 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATGGA others(1969): Show |
chr9 | 127810016 | 127859658 | ||
a0005c0011 | 0/0 | 1974 | 1 | 0 | 0 | 0 | 1 | 0 | ENG_chr9_127810016_127859658 | ENG | ATGGA others(1969): Show |
chr9 | 127810016 | 127859658 | ||
a0006c0028 | 0/0 | 1974 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATGGA others(1969): Show |
chr9 | 127810016 | 127859658 | ||
a0007c0023 | 0/0 | 1974 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATGGA others(1969): Show |
chr9 | 127810016 | 127859658 | ||
a0008c0019 | 0/0 | 1974 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATGGA others(1969): Show |
chr9 | 127810016 | 127859658 | ||
a0009c0026 | 0/0 | 1974 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | ATGGA others(1969): Show |
chr9 | 127810016 | 127859658 | ||
a0010c0018 | 0/0 | 1974 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATGGA others(1969): Show |
chr9 | 127810016 | 127859658 | ||
a0011c0027 | 0/0 | 1974 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | ATGGA others(1969): Show |
chr9 | 127810016 | 127859658 | ||
a0012c0020 | 0/0 | 1974 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATGGA others(1969): Show |
chr9 | 127810016 | 127859658 | ||
a0013c0017 | 0/0 | 1974 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATGGA others(1969): Show |
chr9 | 127810016 | 127859658 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2946 | 218 | 41 | 36 | 99 | 9 | 31 | ENG_chr9_127810016_127859658 | ENG | ATACC others(2941): Show |
chr9 | 127810016 | 127859658 |
a0001c0001t0003 | 0/0 | 2946 | 4 | 0 | 0 | 4 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATACC others(2941): Show |
chr9 | 127810016 | 127859658 |
a0001c0001t0004 | 0/0 | 2946 | 4 | 0 | 0 | 4 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATACC others(2941): Show |
chr9 | 127810016 | 127859658 |
a0001c0001t0008 | 0/0 | 2946 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATACC others(2941): Show |
chr9 | 127810016 | 127859658 |
a0001c0001t0009 | 0/0 | 2946 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | ATACC others(2941): Show |
chr9 | 127810016 | 127859658 |
a0001c0001t0011 | 0/0 | 2946 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATACC others(2941): Show |
chr9 | 127810016 | 127859658 |
a0001c0001t0012 | 0/0 | 2946 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATACC others(2941): Show |
chr9 | 127810016 | 127859658 |
a0001c0002t0001 | 0/0 | 2946 | 34 | 20 | 7 | 5 | 1 | 1 | ENG_chr9_127810016_127859658 | ENG | ATACC others(2941): Show |
chr9 | 127810016 | 127859658 |
a0001c0002t0006 | 0/0 | 2946 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATACC others(2941): Show |
chr9 | 127810016 | 127859658 |
a0001c0003t0001 | 0/0 | 2946 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATACC others(2941): Show |
chr9 | 127810016 | 127859658 |
a0001c0003t0002 | 0/0 | 2942 | 17 | 2 | 3 | 3 | 1 | 8 | ENG_chr9_127810016_127859658 | ENG | ATACC others(2937): Show |
chr9 | 127810016 | 127859658 |
a0001c0006t0001 | 0/0 | 2946 | 4 | 3 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATACC others(2941): Show |
chr9 | 127810016 | 127859658 |
a0001c0006t0010 | 0/0 | 2946 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | ATACC others(2941): Show |
chr9 | 127810016 | 127859658 |
a0001c0007t0001 | 0/0 | 2946 | 4 | 0 | 2 | 2 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATACC others(2941): Show |
chr9 | 127810016 | 127859658 |
a0001c0008t0001 | 0/0 | 2946 | 2 | 1 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATACC others(2941): Show |
chr9 | 127810016 | 127859658 |
a0001c0010t0001 | 0/0 | 2946 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATACC others(2941): Show |
chr9 | 127810016 | 127859658 |
a0001c0010t0007 | 0/0 | 2946 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATACC others(2941): Show |
chr9 | 127810016 | 127859658 |
a0001c0013t0001 | 0/0 | 2946 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATACC others(2941): Show |
chr9 | 127810016 | 127859658 |
a0001c0014t0001 | 0/0 | 2946 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATACC others(2941): Show |
chr9 | 127810016 | 127859658 |
a0001c0016t0001 | 0/0 | 2946 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATACC others(2941): Show |
chr9 | 127810016 | 127859658 |
a0001c0021t0001 | 0/0 | 2946 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATACC others(2941): Show |
chr9 | 127810016 | 127859658 |
a0001c0022t0001 | 0/0 | 2946 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATACC others(2941): Show |
chr9 | 127810016 | 127859658 |
a0001c0024t0001 | 0/0 | 2946 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATACC others(2941): Show |
chr9 | 127810016 | 127859658 |
a0001c0025t0001 | 0/0 | 2946 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATACC others(2941): Show |
chr9 | 127810016 | 127859658 |
a0002c0004t0001 | 0/0 | 2946 | 15 | 0 | 0 | 15 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATACC others(2941): Show |
chr9 | 127810016 | 127859658 |
a0002c0012t0001 | 0/0 | 2946 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATACC others(2941): Show |
chr9 | 127810016 | 127859658 |
a0003c0005t0001 | 0/0 | 2946 | 11 | 8 | 3 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATACC others(2941): Show |
chr9 | 127810016 | 127859658 |
a0003c0029t0001 | 0/0 | 2946 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATACC others(2941): Show |
chr9 | 127810016 | 127859658 |
a0003c0030t0001 | 0/0 | 2946 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATACC others(2941): Show |
chr9 | 127810016 | 127859658 |
a0004c0009t0001 | 0/0 | 2946 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATACC others(2941): Show |
chr9 | 127810016 | 127859658 |
a0004c0009t0005 | 0/0 | 2946 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATACC others(2941): Show |
chr9 | 127810016 | 127859658 |
a0004c0015t0005 | 0/0 | 2946 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATACC others(2941): Show |
chr9 | 127810016 | 127859658 |
a0005c0011t0001 | 0/0 | 2946 | 1 | 0 | 0 | 0 | 1 | 0 | ENG_chr9_127810016_127859658 | ENG | ATACC others(2941): Show |
chr9 | 127810016 | 127859658 |
a0006c0028t0001 | 0/0 | 2946 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATACC others(2941): Show |
chr9 | 127810016 | 127859658 |
a0007c0023t0001 | 0/0 | 2946 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATACC others(2941): Show |
chr9 | 127810016 | 127859658 |
a0008c0019t0001 | 0/0 | 2946 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATACC others(2941): Show |
chr9 | 127810016 | 127859658 |
a0009c0026t0001 | 0/0 | 2946 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | ATACC others(2941): Show |
chr9 | 127810016 | 127859658 |
a0010c0018t0001 | 0/0 | 2946 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATACC others(2941): Show |
chr9 | 127810016 | 127859658 |
a0011c0027t0001 | 0/0 | 2946 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | ATACC others(2941): Show |
chr9 | 127810016 | 127859658 |
a0012c0020t0001 | 0/0 | 2946 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATACC others(2941): Show |
chr9 | 127810016 | 127859658 |
a0013c0017t0001 | 0/0 | 2946 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | ATACC others(2941): Show |
chr9 | 127810016 | 127859658 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0063 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0286 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0003g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0003g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0003g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0003g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0004g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0008g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0009g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0011g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0001t0012g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0002t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0002t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0002t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0002t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0002t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0002t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0002t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0002t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0002t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0002t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0002t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0002t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0002t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0002t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0002t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0002t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0002t0006g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0003t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0003t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0003t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0003t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0003t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0003t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0003t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0003t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0003t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0003t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0003t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0003t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0003t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0003t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0003t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0003t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0003t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0003t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0006t0001g0004 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0006t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0006t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0006t0010g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0007t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0007t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0007t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0007t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0008t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0008t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0010t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0010t0007g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0013t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0014t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0016t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0021t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0022t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0024t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0001c0025t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0002c0004t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0002c0004t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0002c0004t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0002c0004t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0002c0004t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0002c0004t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0002c0004t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0002c0004t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0002c0004t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0002c0004t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0002c0004t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0002c0004t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0002c0004t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0002c0004t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0002c0004t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0002c0012t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0003c0005t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0003c0005t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0003c0005t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0003c0005t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0003c0005t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0003c0005t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0003c0005t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0003c0005t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0003c0005t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0003c0005t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0003c0005t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0003c0029t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0003c0030t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0004c0009t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0004c0009t0005g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0004c0015t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0005c0011t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0006c0028t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0007c0023t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0008c0019t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0009c0026t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0010c0018t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0011c0027t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0012c0020t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
a0013c0017t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0207 | EUR | GBR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG00323 | hp1 | a0001 | c0003 | t0002 | g0259 | EUR | FIN | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG00323 | hp2 | a0005 | c0011 | t0001 | g0023 | EUR | FIN | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG00438 | hp1 | a0002 | c0004 | t0001 | g0092 | EAS | CHS | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG00544 | hp1 | a0002 | c0004 | t0001 | g0190 | EAS | CHS | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | CHS | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | CHS | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG00639 | hp2 | a0003 | c0005 | t0001 | g0333 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG00642 | hp1 | a0001 | c0025 | t0001 | g0257 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG00673 | hp1 | a0001 | c0007 | t0001 | g0164 | EAS | CHS | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | CHS | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG01069 | hp1 | a0003 | c0005 | t0001 | g0331 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG01070 | hp1 | a0001 | c0003 | t0002 | g0121 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG01070 | hp2 | a0001 | c0002 | t0001 | g0027 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0028 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG01074 | hp1 | a0001 | c0013 | t0001 | g0040 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG01081 | hp1 | a0001 | c0002 | t0001 | g0039 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG01081 | hp2 | a0001 | c0007 | t0001 | g0214 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG01099 | hp1 | a0001 | c0008 | t0001 | g0017 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG01106 | hp1 | a0001 | c0003 | t0002 | g0087 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG01109 | hp1 | a0003 | c0005 | t0001 | g0327 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG01109 | hp2 | a0001 | c0002 | t0001 | g0042 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG01167 | hp1 | a0001 | c0006 | t0001 | g0004 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG01192 | hp1 | a0001 | c0002 | t0001 | g0021 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG01192 | hp2 | a0001 | c0002 | t0001 | g0038 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG01255 | hp1 | a0006 | c0028 | t0001 | g0148 | AMR | CLM | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG01346 | hp1 | a0001 | c0002 | t0001 | g0295 | AMR | CLM | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG01346 | hp2 | a0007 | c0023 | t0001 | g0150 | AMR | CLM | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG01433 | hp2 | a0008 | c0019 | t0001 | g0156 | AMR | CLM | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0118 | EUR | IBS | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0221 | EUR | IBS | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0220 | EUR | IBS | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG01517 | hp2 | a0001 | c0002 | t0001 | g0031 | EUR | IBS | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | ACB | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG01891 | hp1 | a0001 | c0002 | t0001 | g0034 | AFR | ACB | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG01891 | hp2 | a0001 | c0002 | t0001 | g0041 | AFR | ACB | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0304 | AMR | PEL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PEL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | KHV | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | KHV | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02040 | hp1 | a0002 | c0004 | t0001 | g0234 | EAS | KHV | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | ACB | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | KHV | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | KHV | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | KHV | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | KHV | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02135 | hp1 | a0002 | c0004 | t0001 | g0083 | EAS | KHV | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02135 | hp2 | a0001 | c0007 | t0001 | g0208 | EAS | KHV | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02155 | hp1 | a0002 | c0004 | t0001 | g0284 | EAS | CDX | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | CDX | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02165 | hp1 | a0002 | c0004 | t0001 | g0089 | EAS | CDX | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | CDX | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | ACB | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02300 | hp1 | a0001 | c0007 | t0001 | g0213 | AMR | PEL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02451 | hp1 | a0003 | c0005 | t0001 | g0335 | AFR | ACB | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02451 | hp2 | a0003 | c0005 | t0001 | g0330 | AFR | ACB | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | KHV | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02615 | hp2 | a0003 | c0005 | t0001 | g0324 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0318 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0316 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02630 | hp2 | a0001 | c0003 | t0002 | g0014 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02647 | hp1 | a0004 | c0015 | t0005 | g0032 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0274 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02683 | hp2 | a0009 | c0026 | t0001 | g0262 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02698 | hp1 | a0001 | c0003 | t0002 | g0258 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02717 | hp2 | a0001 | c0002 | t0001 | g0024 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02723 | hp1 | a0001 | c0006 | t0001 | g0058 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02723 | hp2 | a0001 | c0002 | t0001 | g0037 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02735 | hp2 | a0001 | c0003 | t0002 | g0122 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02738 | hp2 | a0001 | c0006 | t0010 | g0336 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02809 | hp1 | a0010 | c0018 | t0001 | g0265 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02809 | hp2 | a0001 | c0002 | t0001 | g0019 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02818 | hp1 | a0004 | c0009 | t0001 | g0053 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02818 | hp2 | a0001 | c0014 | t0001 | g0030 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02886 | hp2 | a0001 | c0001 | t0008 | g0138 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02895 | hp1 | a0003 | c0005 | t0001 | g0329 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02896 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02897 | hp1 | a0003 | c0005 | t0001 | g0328 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02897 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02922 | hp1 | a0001 | c0001 | t0011 | g0337 | AFR | ESN | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02922 | hp2 | a0003 | c0029 | t0001 | g0334 | AFR | ESN | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | ESN | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02970 | hp2 | a0001 | c0002 | t0001 | g0022 | AFR | ESN | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02976 | hp1 | a0001 | c0002 | t0001 | g0035 | AFR | ESN | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ESN | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG03017 | hp1 | a0011 | c0027 | t0001 | g0186 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG03041 | hp1 | a0001 | c0002 | t0001 | g0051 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | MSL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG03098 | hp2 | a0004 | c0009 | t0005 | g0054 | AFR | MSL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG03130 | hp1 | a0001 | c0024 | t0001 | g0140 | AFR | ESN | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG03130 | hp2 | a0001 | c0002 | t0001 | g0036 | AFR | ESN | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0321 | AFR | ESN | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG03139 | hp2 | a0001 | c0002 | t0001 | g0043 | AFR | ESN | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG03195 | hp1 | a0012 | c0020 | t0001 | g0060 | AFR | ESN | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG03195 | hp2 | a0001 | c0002 | t0001 | g0033 | AFR | ESN | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG03209 | hp1 | a0003 | c0005 | t0001 | g0325 | AFR | MSL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | MSL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | MSL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | MSL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0320 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG03453 | hp1 | a0003 | c0005 | t0001 | g0326 | AFR | MSL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG03453 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | MSL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | MSL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG03486 | hp2 | a0001 | c0002 | t0001 | g0018 | AFR | MSL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0281 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG03490 | hp2 | a0001 | c0003 | t0002 | g0127 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0280 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG03516 | hp1 | a0003 | c0005 | t0001 | g0323 | AFR | ESN | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG03516 | hp2 | a0001 | c0006 | t0001 | g0057 | AFR | ESN | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG03540 | hp1 | a0001 | c0008 | t0001 | g0029 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG03579 | hp1 | a0001 | c0002 | t0006 | g0056 | AFR | MSL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | MSL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG03654 | hp2 | a0001 | c0002 | t0001 | g0020 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | STU | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG03688 | hp2 | a0001 | c0003 | t0002 | g0126 | SAS | STU | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0282 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | BEB | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG03831 | hp2 | a0001 | c0003 | t0002 | g0133 | SAS | BEB | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG03834 | hp1 | a0001 | c0003 | t0002 | g0135 | SAS | BEB | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | BEB | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG03942 | hp1 | a0001 | c0001 | t0009 | g0201 | SAS | BEB | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | BEB | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG04184 | hp1 | a0001 | c0003 | t0002 | g0153 | SAS | BEB | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0315 | SAS | BEB | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0266 | SAS | STU | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | STU | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG04228 | hp1 | a0001 | c0003 | t0002 | g0130 | SAS | STU | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | STU | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0297 | AFR | YRI | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | YRI | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18612 | hp1 | a0001 | c0010 | t0001 | g0194 | EAS | CHB | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | CHB | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | CHB | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | CHB | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18906 | hp1 | a0001 | c0006 | t0001 | g0004 | AFR | YRI | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18906 | hp2 | a0001 | c0002 | t0001 | g0025 | AFR | YRI | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18943 | hp1 | a0001 | c0001 | t0004 | g0081 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18944 | hp1 | a0001 | c0003 | t0002 | g0132 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18947 | hp1 | a0002 | c0004 | t0001 | g0074 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18950 | hp1 | a0001 | c0001 | t0004 | g0185 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18950 | hp2 | a0002 | c0004 | t0001 | g0076 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18957 | hp2 | a0002 | c0004 | t0001 | g0205 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18959 | hp1 | a0001 | c0021 | t0001 | g0073 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18963 | hp2 | a0001 | c0002 | t0001 | g0311 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18964 | hp2 | a0002 | c0004 | t0001 | g0066 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18966 | hp2 | a0001 | c0003 | t0002 | g0117 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18971 | hp2 | a0002 | c0004 | t0001 | g0167 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18977 | hp1 | a0002 | c0004 | t0001 | g0075 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18979 | hp2 | a0013 | c0017 | t0001 | g0120 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18981 | hp1 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18984 | hp1 | a0001 | c0001 | t0004 | g0096 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18988 | hp2 | a0002 | c0004 | t0001 | g0204 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18990 | hp2 | a0001 | c0001 | t0004 | g0078 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18993 | hp1 | a0001 | c0003 | t0001 | g0012 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18995 | hp2 | a0002 | c0004 | t0001 | g0197 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA19002 | hp1 | a0001 | c0002 | t0001 | g0314 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0312 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA19012 | hp2 | a0001 | c0003 | t0002 | g0065 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA19030 | hp1 | a0001 | c0001 | t0012 | g0338 | AFR | LWK | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA19030 | hp2 | a0003 | c0030 | t0001 | g0332 | AFR | LWK | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA19043 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | LWK | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA19043 | hp2 | a0001 | c0022 | t0001 | g0049 | AFR | LWK | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA19064 | hp2 | a0002 | c0004 | t0001 | g0235 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA19066 | hp1 | a0001 | c0002 | t0001 | g0313 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA19070 | hp2 | a0002 | c0012 | t0001 | g0308 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA19081 | hp1 | a0001 | c0010 | t0007 | g0193 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | YRI | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | YRI | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0300 | AFR | ASW | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | ASW | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0223 | EUR | TSI | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0215 | EUR | TSI | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0303 | EUR | TSI | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0267 | EUR | TSI | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0290 | SAS | GIH | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | GIH | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG01123 | hp1 | a0001 | c0003 | t0002 | g0088 | AMR | CLM | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | ACB | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG03471 | hp1 | a0001 | c0002 | t0001 | g0055 | AFR | MSL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG03471 | hp2 | a0001 | c0002 | t0001 | g0026 | AFR | MSL | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | USA | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
HG06807 | hp2 | a0001 | c0003 | t0002 | g0301 | AFR | USA | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA20300 | hp1 | a0001 | c0016 | t0001 | g0059 | AFR | USA | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | USA | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | LWK | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
NA21309 | hp2 | a0001 | c0002 | t0001 | g0016 | AFR | LWK | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0286 | REF | REF | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0063 | REF | REF | ENG_chr9_127810016_127859658 | ENG | chr9 | 127810016 | 127859658 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:127818169 | G | A | 1 | a0012 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.1637C>T | p.Thr546Ile | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 12/15 | 1940/2946 | 1637/1977 | 546/658 | chr9 | 127818169 | |||
chr9:127818173 | C | T | 1 | a0008 | 1 | HG01433.hp2 | missense_variant | MODERATE | c.1633G>A | p.Gly545Ser | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 12/15 | 1936/2946 | 1633/1977 | 545/658 | chr9 | 127818173 | |||
chr9:127818296 | C | T | 1 | a0004 | 3 | HG02647.hp1 HG02818.hp1 HG03098.hp2 |
missense_variant | MODERATE | c.1510G>A | p.Val504Met | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 12/15 | 1813/2946 | 1510/1977 | 504/658 | chr9 | 127818296 | |||
chr9:127824338 | G | C | 1 | a0007 | 1 | HG01346.hp2 | missense_variant | MODERATE | c.1100C>G | p.Ala367Gly | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/15 | 1403/2946 | 1100/1977 | 367/658 | chr9 | 127824338 | |||
chr9:127824342 | C | G | 1 | a0002 | 16 | HG00438.hp1 HG00544.hp1 HG02040.hp1 others(13): Show |
missense_variant | MODERATE | c.1096G>C | p.Asp366His | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/15 | 1399/2946 | 1096/1977 | 366/658 | chr9 | 127824342 | |||
chr9:127824811 | G | T | 1 | a0005 | 1 | HG00323.hp2 | missense_variant | MODERATE | c.980C>A | p.Ala327Asp | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 7/15 | 1283/2946 | 980/1977 | 327/658 | chr9 | 127824811 | |||
chr9:127825744 | C | T | 1 | a0010 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.640G>A | p.Gly214Ser | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 5/15 | 943/2946 | 640/1977 | 214/658 | chr9 | 127825744 | |||
chr9:127825788 | C | T | 1 | a0013 | 1 | NA18979.hp2 | missense_variant | MODERATE | c.596G>A | p.Arg199His | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 5/15 | 899/2946 | 596/1977 | 199/658 | chr9 | 127825788 | |||
chr9:127825810 | G | C | 1 | a0009 | 1 | HG02683.hp2 | missense_variant | MODERATE | c.574C>G | p.Arg192Gly | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 5/15 | 877/2946 | 574/1977 | 192/658 | chr9 | 127825810 | |||
chr9:127826641 | G | A | 1 | a0011 | 1 | HG03017.hp1 | missense_variant | MODERATE | c.392C>T | p.Pro131Leu | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 4/15 | 695/2946 | 392/1977 | 131/658 | chr9 | 127826641 | |||
chr9:127843143 | G | C | 1 | a0006 | 1 | HG01255.hp1 | missense_variant | MODERATE | c.170C>G | p.Ala57Gly | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/15 | 473/2946 | 170/1977 | 57/658 | chr9 | 127843143 | |||
chr9:127854342 | G | A | 1 | a0003 | 13 | HG00639.hp2 HG01069.hp1 HG01109.hp1 others(10): Show |
missense_variant | MODERATE | c.14C>T | p.Thr5Met | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/15 | 317/2946 | 14/1977 | 5/658 | chr9 | 127854342 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:127815727 | G | A | 1 | a0001c0007 | 4 | HG00673.hp1 HG01081.hp2 HG02135.hp2 others(1): Show |
synonymous_variant | LOW | c.1932C>T | p.Ile644Ile | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 15/15 | 2235/2946 | 1932/1977 | 644/658 | chr9 | 127815727 | |||
chr9:127816001 | A | G | 2 | a0001c0006 a0001c0014 |
6 | HG01167.hp1 HG02723.hp1 HG02738.hp2 others(3): Show |
synonymous_variant | LOW | c.1794T>C | p.Gly598Gly | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 14/15 | 2097/2946 | 1794/1977 | 598/658 | chr9 | 127816001 | |||
chr9:127818174 | G | A | 1 | a0001c0021 | 1 | NA18959.hp1 | synonymous_variant | LOW | c.1632C>T | p.Thr544Thr | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 12/15 | 1935/2946 | 1632/1977 | 544/658 | chr9 | 127818174 | |||
chr9:127818354 | G | A | 2 | a0004c0009 a0004c0015 |
3 | HG02647.hp1 HG02818.hp1 HG03098.hp2 |
synonymous_variant | LOW | c.1452C>T | p.Ser484Ser | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 12/15 | 1755/2946 | 1452/1977 | 484/658 | chr9 | 127818354 | |||
chr9:127818360 | G | A | 1 | a0003c0029 | 1 | HG02922.hp2 | synonymous_variant | LOW | c.1446C>T | p.Ser482Ser | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 12/15 | 1749/2946 | 1446/1977 | 482/658 | chr9 | 127818360 | |||
chr9:127818737 | C | T | 1 | a0001c0013 | 1 | HG01074.hp1 | synonymous_variant | LOW | c.1407G>A | p.Pro469Pro | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 11/15 | 1710/2946 | 1407/1977 | 469/658 | chr9 | 127818737 | |||
chr9:127818770 | T | C | 1 | a0001c0025 | 1 | HG00642.hp1 | synonymous_variant | LOW | c.1374A>G | p.Pro458Pro | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 11/15 | 1677/2946 | 1374/1977 | 458/658 | chr9 | 127818770 | |||
chr9:127819939 | G | A | 1 | a0001c0022 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.1233C>T | p.Ser411Ser | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 9/15 | 1536/2946 | 1233/1977 | 411/658 | chr9 | 127819939 | |||
chr9:127824378 | G | A | 4 | a0001c0008 a0001c0024 a0001c0025 others(1): Show |
5 | HG00642.hp1 HG01099.hp1 HG03130.hp1 others(2): Show |
synonymous_variant | LOW | c.1060C>T | p.Leu354Leu | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/15 | 1363/2946 | 1060/1977 | 354/658 | chr9 | 127824378 | |||
chr9:127824409 | G | A | 1 | a0001c0003 | 18 | HG00323.hp1 HG01070.hp1 HG01106.hp1 others(15): Show |
synonymous_variant | LOW | c.1029C>T | p.Thr343Thr | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/15 | 1332/2946 | 1029/1977 | 343/658 | chr9 | 127824409 | |||
chr9:127829813 | C | T | 1 | a0001c0016 | 1 | NA20300.hp1 | synonymous_variant | LOW | c.234G>A | p.Leu78Leu | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/15 | 537/2946 | 234/1977 | 78/658 | chr9 | 127829813 | |||
chr9:127829822 | C | T | 1 | a0001c0016 | 1 | NA20300.hp1 | synonymous_variant | LOW | c.225G>A | p.Pro75Pro | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/15 | 528/2946 | 225/1977 | 75/658 | chr9 | 127829822 | |||
chr9:127843106 | C | T | 7 | a0001c0002 a0001c0008 a0001c0013 others(4): Show |
42 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(39): Show |
synonymous_variant | LOW | c.207G>A | p.Leu69Leu | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/15 | 510/2946 | 207/1977 | 69/658 | chr9 | 127843106 | |||
chr9:127843154 | G | A | 1 | a0001c0010 | 2 | NA18612.hp1 NA19081.hp1 |
synonymous_variant | LOW | c.159C>T | p.Cys53Cys | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/15 | 462/2946 | 159/1977 | 53/658 | chr9 | 127843154 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:127815124 | T | C | 1 | a0001c0010t0007 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*558A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 15/15 | 558 | chr9 | 127815124 | ||||||
chr9:127815190 | C | T | 1 | a0001c0001t0004 | 4 | NA18943.hp1 NA18950.hp1 NA18984.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*492G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 15/15 | 492 | chr9 | 127815190 | ||||||
chr9:127815213 | CAGTT | C | 1 | a0001c0003t0002 | 17 | HG00323.hp1 HG01070.hp1 HG01106.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*465_*468delAACT | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 15/15 | 465 | chr9 | 127815213 | ||||||
chr9:127815533 | C | G | 2 | a0004c0009t0005 a0004c0015t0005 |
2 | HG02647.hp1 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*149G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 15/15 | 149 | chr9 | 127815533 | ||||||
chr9:127815564 | G | A | 1 | a0001c0001t0008 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*118C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 15/15 | 118 | chr9 | 127815564 | ||||||
chr9:127815573 | G | A | 1 | a0001c0001t0009 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*109C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 15/15 | 109 | chr9 | 127815573 | ||||||
chr9:127815619 | C | T | 1 | a0001c0002t0006 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*63G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 15/15 | 63 | chr9 | 127815619 | ||||||
chr9:127854409 | G | T | 1 | a0001c0001t0003 | 4 | HG00609.hp1 HG02027.hp2 HG02129.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-54C>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/15 | 54 | chr9 | 127854409 | ||||||
chr9:127854425 | G | A | 1 | a0001c0006t0010 | 1 | HG02738.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-70C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/15 | chr9 | 127854425 | |||||||
chr9:127854475 | C | A | 1 | a0001c0001t0011 | 1 | HG02922.hp1 | 5_prime_UTR_variant | MODIFIER | c.-120G>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/15 | 120 | chr9 | 127854475 | ||||||
chr9:127854476 | G | A | 1 | a0001c0001t0012 | 1 | NA19030.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-121C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/15 | chr9 | 127854476 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:127815829 | G | A | 1 | a0012c0020t0001g0060 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1853-23C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 14/14 | chr9 | 127815829 | |||||||
chr9:127816068 | C | T | 1 | a0001c0001t0001g0011 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1742-15G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 13/14 | chr9 | 127816068 | |||||||
chr9:127816125 | A | G | 183 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(180): Show |
188 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.1742-72T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 13/14 | chr9 | 127816125 | |||||||
chr9:127816188 | C | T | 2 | a0001c0003t0002g0014 a0001c0003t0002g0301 |
2 | HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1742-135G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 13/14 | chr9 | 127816188 | |||||||
chr9:127816214 | G | T | 1 | a0001c0003t0002g0117 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1742-161C>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 13/14 | chr9 | 127816214 | |||||||
chr9:127816346 | G | A | 19 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0137 others(16): Show |
20 | HG02280.hp1 HG02280.hp2 HG02615.hp1 others(17): Show |
intron_variant | MODIFIER | c.1742-293C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 13/14 | chr9 | 127816346 | |||||||
chr9:127816461 | G | A | 1 | a0001c0025t0001g0257 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1742-408C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 13/14 | chr9 | 127816461 | |||||||
chr9:127816539 | A | G | 4 | a0001c0008t0001g0017 a0001c0008t0001g0029 a0001c0024t0001g0140 others(1): Show |
4 | HG01099.hp1 HG03130.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1742-486T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 13/14 | chr9 | 127816539 | |||||||
chr9:127816543 | G | A | 7 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0229 others(4): Show |
7 | HG01891.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1742-490C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 13/14 | chr9 | 127816543 | |||||||
chr9:127816639 | T | C | 1 | a0012c0020t0001g0060 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1741+510A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 13/14 | chr9 | 127816639 | |||||||
chr9:127816756 | G | C | 1 | a0001c0025t0001g0257 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1741+393C>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 13/14 | chr9 | 127816756 | |||||||
chr9:127816770 | C | T | 1 | a0001c0010t0001g0194 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1741+379G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 13/14 | chr9 | 127816770 | |||||||
chr9:127816921 | C | G | 5 | a0001c0008t0001g0017 a0001c0008t0001g0029 a0001c0016t0001g0059 others(2): Show |
5 | HG01099.hp1 HG03130.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1741+228G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 13/14 | chr9 | 127816921 | |||||||
chr9:127816928 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1741+221G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 13/14 | chr9 | 127816928 | |||||||
chr9:127817320 | C | T | 118 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(115): Show |
121 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.1687-117G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 12/14 | chr9 | 127817320 | |||||||
chr9:127817360 | C | G | 5 | a0001c0002t0001g0003 a0001c0002t0001g0041 a0001c0002t0001g0042 others(2): Show |
6 | HG01109.hp2 HG01891.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1687-157G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 12/14 | chr9 | 127817360 | |||||||
chr9:127817425 | C | G | 2 | a0001c0002t0001g0312 a0001c0002t0001g0314 |
2 | NA19002.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1687-222G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 12/14 | chr9 | 127817425 | |||||||
chr9:127817531 | C | G | 191 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(188): Show |
196 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.1687-328G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 12/14 | chr9 | 127817531 | |||||||
chr9:127817625 | A | G | 25 | a0001c0001t0001g0050 a0001c0001t0001g0299 a0001c0002t0001g0051 others(22): Show |
25 | HG00438.hp1 HG00544.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.1687-422T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 12/14 | chr9 | 127817625 | |||||||
chr9:127817760 | T | C | 1 | a0001c0001t0001g0242 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1686+360A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 12/14 | chr9 | 127817760 | |||||||
chr9:127817781 | A | G | 1 | a0001c0022t0001g0049 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1686+339T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 12/14 | chr9 | 127817781 | |||||||
chr9:127817803 | T | C | 1 | a0001c0001t0001g0129 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1686+317A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 12/14 | chr9 | 127817803 | |||||||
chr9:127817808 | G | A | 1 | a0001c0025t0001g0257 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1686+312C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 12/14 | chr9 | 127817808 | |||||||
chr9:127817814 | T | C | 192 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(189): Show |
197 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.1686+306A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 12/14 | chr9 | 127817814 | |||||||
chr9:127817996 | C | A | 4 | a0001c0008t0001g0017 a0001c0008t0001g0029 a0001c0024t0001g0140 others(1): Show |
4 | HG01099.hp1 HG03130.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1686+124G>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 12/14 | chr9 | 127817996 | |||||||
chr9:127817997 | C | A | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG00673.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1686+123G>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 12/14 | chr9 | 127817997 | |||||||
chr9:127818660 | C | T | 1 | a0001c0001t0001g0290 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1428+56G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 11/14 | chr9 | 127818660 | |||||||
chr9:127818690 | C | T | 1 | a0001c0016t0001g0059 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1428+26G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 11/14 | chr9 | 127818690 | |||||||
chr9:127818870 | G | A | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG00673.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1312-38C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 10/14 | chr9 | 127818870 | |||||||
chr9:127818940 | C | CT | 45 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0052 others(42): Show |
46 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.1312-109dupA | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 10/14 | chr9 | 127818940 | |||||||
chr9:127818942 | T | C | 1 | a0012c0020t0001g0060 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1312-110A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 10/14 | chr9 | 127818942 | |||||||
chr9:127818968 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1312-136G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 10/14 | chr9 | 127818968 | |||||||
chr9:127819021 | T | G | 2 | a0001c0001t0001g0169 a0001c0002t0001g0038 |
2 | HG00741.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.1312-189A>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 10/14 | chr9 | 127819021 | |||||||
chr9:127819098 | C | T | 1 | a0001c0002t0001g0051 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1312-266G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 10/14 | chr9 | 127819098 | |||||||
chr9:127819099 | G | A | 4 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(1): Show |
4 | HG03017.hp2 HG03491.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.1312-267C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 10/14 | chr9 | 127819099 | |||||||
chr9:127819140 | T | C | 1 | a0001c0003t0002g0132 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1312-308A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 10/14 | chr9 | 127819140 | |||||||
chr9:127819172 | C | T | 1 | a0001c0001t0001g0305 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1312-340G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 10/14 | chr9 | 127819172 | |||||||
chr9:127819237 | CT | C | 6 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0162 others(3): Show |
6 | HG02572.hp1 NA18522.hp2 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.1311+384delA | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 10/14 | chr9 | 127819237 | |||||||
chr9:127819258 | A | G | 2 | a0001c0001t0001g0192 a0001c0001t0001g0287 |
2 | HG00408.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.1311+364T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 10/14 | chr9 | 127819258 | |||||||
chr9:127819444 | A | G | 280 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(277): Show |
286 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(283): Show |
intron_variant | MODIFIER | c.1311+178T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 10/14 | chr9 | 127819444 | |||||||
chr9:127819528 | T | C | 6 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0229 others(3): Show |
6 | HG01891.hp1 HG02145.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1311+94A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 10/14 | chr9 | 127819528 | |||||||
chr9:127819796 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1272+104G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 9/14 | chr9 | 127819796 | |||||||
chr9:127820045 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG02145.hp1 | splice_region_variant&intron_variant | LOW | c.1135-8C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127820045 | |||||||
chr9:127820293 | A | C | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG00673.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1135-256T>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127820293 | |||||||
chr9:127820324 | G | T | 2 | a0001c0001t0001g0114 a0001c0001t0001g0145 |
2 | HG01255.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.1135-287C>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127820324 | |||||||
chr9:127820506 | T | G | 92 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0077 others(89): Show |
93 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.1135-469A>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127820506 | |||||||
chr9:127820689 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1135-652G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127820689 | |||||||
chr9:127820690 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1135-653C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127820690 | |||||||
chr9:127820739 | A | G | 40 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0046 others(37): Show |
41 | HG00323.hp2 HG00544.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.1135-702T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127820739 | |||||||
chr9:127820746 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1135-709C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127820746 | |||||||
chr9:127820754 | G | A | 9 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(6): Show |
9 | HG02486.hp1 HG02572.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1135-717C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127820754 | |||||||
chr9:127820777 | C | T | 1 | a0001c0016t0001g0059 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1135-740G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127820777 | |||||||
chr9:127820791 | T | G | 1 | a0001c0016t0001g0059 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1135-754A>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127820791 | |||||||
chr9:127820828 | CA | C | 13 | a0001c0001t0001g0046 a0001c0001t0001g0050 a0001c0001t0001g0174 others(10): Show |
13 | HG00544.hp1 HG01891.hp1 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.1135-792delT | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127820828 | |||||||
chr9:127820837 | A | T | 2 | a0002c0004t0001g0092 a0012c0020t0001g0060 |
2 | HG00438.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1135-800T>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127820837 | |||||||
chr9:127820839 | A | AT | 31 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0069 others(28): Show |
33 | HG00597.hp1 HG00738.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.1135-803_1135-802i others(3): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127820839 | |||||||
chr9:127820839 | A | T | 68 | a0001c0001t0001g0013 a0001c0001t0001g0044 a0001c0001t0001g0045 others(65): Show |
70 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.1135-802T>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127820839 | |||||||
chr9:127820841 | T | A | 16 | a0001c0001t0001g0015 a0001c0001t0001g0160 a0001c0001t0001g0171 others(13): Show |
16 | HG00099.hp2 HG00423.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.1135-804A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127820841 | |||||||
chr9:127820843 | T | A | 1 | a0001c0016t0001g0059 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1135-806A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127820843 | |||||||
chr9:127820895 | A | G | 38 | a0001c0001t0001g0052 a0001c0001t0001g0112 a0001c0001t0001g0129 others(35): Show |
38 | HG00099.hp2 HG00738.hp2 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.1135-858T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127820895 | |||||||
chr9:127820948 | G | A | 1 | a0001c0002t0001g0055 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1135-911C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127820948 | |||||||
chr9:127820982 | C | G | 3 | a0002c0004t0001g0167 a0002c0004t0001g0190 a0002c0004t0001g0234 |
3 | HG00544.hp1 HG02040.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.1135-945G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127820982 | |||||||
chr9:127821009 | G | A | 1 | a0001c0016t0001g0059 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1135-972C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127821009 | |||||||
chr9:127821127 | C | T | 2 | a0001c0006t0010g0336 a0004c0015t0005g0032 |
2 | HG02647.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1135-1090G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127821127 | |||||||
chr9:127821146 | C | CA | 3 | a0003c0005t0001g0326 a0003c0005t0001g0330 a0003c0005t0001g0331 |
3 | HG01069.hp1 HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1135-1110dupT | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127821146 | |||||||
chr9:127821170 | G | T | 5 | a0001c0006t0001g0004 a0001c0006t0001g0057 a0001c0006t0001g0058 others(2): Show |
6 | HG01167.hp1 HG02723.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1135-1133C>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127821170 | |||||||
chr9:127821174 | G | A | 8 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0110 others(5): Show |
8 | HG01891.hp1 HG02145.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1135-1137C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127821174 | |||||||
chr9:127821242 | G | A | 5 | a0001c0001t0001g0072 a0001c0001t0001g0084 a0001c0001t0001g0086 others(2): Show |
5 | HG02027.hp2 NA18963.hp2 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1135-1205C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127821242 | |||||||
chr9:127821378 | C | A | 3 | a0004c0009t0001g0053 a0004c0009t0005g0054 a0004c0015t0005g0032 |
3 | HG02647.hp1 HG02818.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1135-1341G>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127821378 | |||||||
chr9:127821493 | G | T | 2 | a0001c0001t0001g0232 a0001c0001t0001g0236 |
2 | HG00408.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.1135-1456C>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127821493 | |||||||
chr9:127821525 | T | A | 1 | a0001c0001t0009g0201 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1135-1488A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127821525 | |||||||
chr9:127821713 | T | TA | 7 | a0001c0003t0002g0130 a0001c0006t0001g0004 a0001c0006t0001g0057 others(4): Show |
8 | HG01167.hp1 HG02723.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.1135-1677dupT | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127821713 | |||||||
chr9:127821713 | T | TAA | 129 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(126): Show |
132 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.1135-1678_1135-167 others(6): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127821713 | |||||||
chr9:127821723 | A | G | 3 | a0002c0004t0001g0167 a0002c0004t0001g0190 a0002c0004t0001g0234 |
3 | HG00544.hp1 HG02040.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.1135-1686T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127821723 | |||||||
chr9:127821751 | T | C | 6 | a0001c0008t0001g0017 a0001c0008t0001g0029 a0001c0016t0001g0059 others(3): Show |
6 | HG01099.hp1 HG02922.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1135-1714A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127821751 | |||||||
chr9:127821777 | G | C | 3 | a0002c0004t0001g0167 a0002c0004t0001g0190 a0002c0004t0001g0234 |
3 | HG00544.hp1 HG02040.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.1135-1740C>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127821777 | |||||||
chr9:127821832 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1135-1795C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127821832 | |||||||
chr9:127821880 | T | TA | 6 | a0001c0001t0001g0050 a0001c0001t0001g0202 a0001c0002t0001g0051 others(3): Show |
6 | HG02055.hp2 HG02647.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1135-1844dupT | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127821880 | |||||||
chr9:127821880 | TA | T | 275 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(272): Show |
280 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(277): Show |
intron_variant | MODIFIER | c.1135-1844delT | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127821880 | |||||||
chr9:127821880 | TAA | T | 12 | a0001c0001t0001g0084 a0001c0001t0001g0095 a0001c0001t0001g0114 others(9): Show |
12 | HG00642.hp1 HG01081.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.1135-1845_1135-184 others(6): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127821880 | |||||||
chr9:127821880 | TAAA | T | 19 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0137 others(16): Show |
20 | HG02280.hp1 HG02280.hp2 HG02615.hp1 others(17): Show |
intron_variant | MODIFIER | c.1135-1846_1135-184 others(7): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127821880 | |||||||
chr9:127821974 | C | T | 122 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(119): Show |
126 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.1135-1937G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127821974 | |||||||
chr9:127821975 | G | A | 2 | a0001c0001t0001g0050 a0001c0002t0001g0051 |
2 | HG02055.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1135-1938C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127821975 | |||||||
chr9:127822056 | A | G | 1 | a0001c0001t0003g0007 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1135-2019T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127822056 | |||||||
chr9:127822315 | G | T | 3 | a0001c0001t0001g0070 a0001c0001t0001g0079 a0001c0001t0001g0292 |
3 | HG02071.hp2 NA18966.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1134+1989C>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127822315 | |||||||
chr9:127822376 | CAGT | C | 14 | a0002c0004t0001g0066 a0002c0004t0001g0074 a0002c0004t0001g0075 others(11): Show |
14 | HG00438.hp1 HG02040.hp1 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.1134+1925_1134+192 others(7): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127822376 | |||||||
chr9:127822407 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1134+1897T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127822407 | |||||||
chr9:127822418 | A | G | 3 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0253 |
3 | HG01884.hp2 HG02572.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1134+1886T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127822418 | |||||||
chr9:127822488 | A | T | 1 | a0006c0028t0001g0148 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1134+1816T>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127822488 | |||||||
chr9:127822535 | T | G | 3 | a0004c0009t0001g0053 a0004c0009t0005g0054 a0004c0015t0005g0032 |
3 | HG02647.hp1 HG02818.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1134+1769A>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127822535 | |||||||
chr9:127822557 | A | G | 4 | a0001c0008t0001g0017 a0001c0008t0001g0029 a0001c0024t0001g0140 others(1): Show |
4 | HG01099.hp1 HG03130.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1134+1747T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127822557 | |||||||
chr9:127822640 | T | C | 6 | a0001c0001t0001g0052 a0001c0001t0001g0154 a0001c0001t0001g0195 others(3): Show |
6 | HG00323.hp2 HG00639.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.1134+1664A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127822640 | |||||||
chr9:127822713 | T | C | 2 | a0001c0001t0001g0050 a0001c0002t0001g0051 |
2 | HG02055.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1134+1591A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127822713 | |||||||
chr9:127822752 | T | C | 53 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0046 others(50): Show |
54 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.1134+1552A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127822752 | |||||||
chr9:127822954 | C | T | 4 | a0001c0001t0001g0146 a0001c0001t0001g0149 a0001c0001t0001g0158 others(1): Show |
4 | HG01123.hp2 HG01346.hp2 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.1134+1350G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127822954 | |||||||
chr9:127823001 | C | T | 1 | a0001c0002t0001g0034 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1134+1303G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127823001 | |||||||
chr9:127823014 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1134+1290G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127823014 | |||||||
chr9:127823122 | G | A | 1 | a0001c0002t0006g0056 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1134+1182C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127823122 | |||||||
chr9:127823170 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1134+1134C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127823170 | |||||||
chr9:127823224 | C | T | 1 | a0001c0016t0001g0059 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1134+1080G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127823224 | |||||||
chr9:127823238 | C | A | 1 | a0003c0029t0001g0334 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1134+1066G>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127823238 | |||||||
chr9:127823390 | C | CT | 18 | a0001c0001t0001g0050 a0001c0002t0001g0051 a0002c0004t0001g0066 others(15): Show |
18 | HG00438.hp1 HG00544.hp1 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.1134+913dupA | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127823390 | |||||||
chr9:127823390 | CT | C | 29 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0129 others(26): Show |
30 | HG01081.hp2 HG01433.hp1 HG01978.hp1 others(27): Show |
intron_variant | MODIFIER | c.1134+913delA | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127823390 | |||||||
chr9:127823505 | C | T | 1 | a0001c0003t0002g0258 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1134+799G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127823505 | |||||||
chr9:127823514 | G | A | 8 | a0002c0004t0001g0074 a0002c0004t0001g0075 a0002c0004t0001g0076 others(5): Show |
8 | HG02155.hp1 NA18947.hp1 NA18950.hp2 others(5): Show |
intron_variant | MODIFIER | c.1134+790C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127823514 | |||||||
chr9:127823673 | C | CT | 41 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0044 others(38): Show |
42 | HG00323.hp1 HG01071.hp2 HG01106.hp2 others(39): Show |
intron_variant | MODIFIER | c.1134+630dupA | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127823673 | |||||||
chr9:127823673 | C | CTT | 28 | a0001c0001t0001g0013 a0001c0001t0001g0050 a0001c0001t0001g0137 others(25): Show |
29 | HG02055.hp2 HG02280.hp1 HG02280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1134+629_1134+630d others(4): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127823673 | |||||||
chr9:127823673 | C | CTTTT | 11 | a0002c0004t0001g0066 a0002c0004t0001g0076 a0002c0004t0001g0083 others(8): Show |
11 | HG00544.hp1 HG02135.hp1 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.1134+627_1134+630d others(6): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127823673 | |||||||
chr9:127823673 | CT | C | 10 | a0001c0001t0001g0152 a0001c0001t0001g0178 a0001c0001t0001g0182 others(7): Show |
10 | HG00438.hp2 HG02132.hp1 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.1134+630delA | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127823673 | |||||||
chr9:127823712 | C | T | 1 | a0001c0001t0001g0115 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1134+592G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127823712 | |||||||
chr9:127823816 | G | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(115): Show |
121 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.1134+488C>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 8/14 | chr9 | 127823816 | |||||||
chr9:127824504 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.992-58C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 7/14 | chr9 | 127824504 | |||||||
chr9:127824512 | C | CT | 143 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0045 others(140): Show |
145 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.992-67dupA | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 7/14 | chr9 | 127824512 | |||||||
chr9:127824512 | C | CTT | 57 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0013 others(54): Show |
59 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.992-68_992-67dupAA | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 7/14 | chr9 | 127824512 | |||||||
chr9:127824512 | C | CTTT | 6 | a0001c0001t0001g0141 a0001c0001t0001g0256 a0001c0001t0001g0283 others(3): Show |
6 | HG00741.hp1 HG01081.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.992-69_992-67dupAA others(1): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 7/14 | chr9 | 127824512 | |||||||
chr9:127824512 | CT | C | 7 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(4): Show |
7 | HG02486.hp1 HG02572.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.992-67delA | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 7/14 | chr9 | 127824512 | |||||||
chr9:127824512 | CTTTTTTT | C | 7 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0110 others(4): Show |
7 | HG01891.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.992-73_992-67delAA others(5): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 7/14 | chr9 | 127824512 | |||||||
chr9:127824619 | A | G | 1 | a0001c0001t0001g0232 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.992-173T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 7/14 | chr9 | 127824619 | |||||||
chr9:127824742 | T | A | 7 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0110 others(4): Show |
7 | HG01891.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.991+58A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 7/14 | chr9 | 127824742 | |||||||
chr9:127824773 | A | AGGGAGG | 98 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0077 others(95): Show |
99 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.991+21_991+26dupCC others(4): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 7/14 | chr9 | 127824773 | |||||||
chr9:127824987 | A | G | 1 | a0001c0003t0002g0153 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.817-13T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 6/14 | chr9 | 127824987 | |||||||
chr9:127825219 | C | T | 1 | a0001c0016t0001g0059 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.816+12G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 6/14 | chr9 | 127825219 | |||||||
chr9:127825628 | C | CG | 181 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(178): Show |
185 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.689+66dupC | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 5/14 | chr9 | 127825628 | |||||||
chr9:127825628 | C | CGG | 131 | a0001c0001t0001g0011 a0001c0001t0001g0045 a0001c0001t0001g0047 others(128): Show |
132 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.689+65_689+66dupCC | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 5/14 | chr9 | 127825628 | |||||||
chr9:127825875 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0181 |
3 | HG01928.hp2 HG01993.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.524-15C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 4/14 | chr9 | 127825875 | |||||||
chr9:127825883 | G | T | 1 | a0001c0001t0001g0183 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.524-23C>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 4/14 | chr9 | 127825883 | |||||||
chr9:127825890 | C | T | 5 | a0001c0006t0001g0004 a0001c0006t0001g0057 a0001c0006t0001g0058 others(2): Show |
6 | HG01167.hp1 HG02723.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.524-30G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 4/14 | chr9 | 127825890 | |||||||
chr9:127826051 | C | T | 1 | a0006c0028t0001g0148 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.524-191G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 4/14 | chr9 | 127826051 | |||||||
chr9:127826124 | A | G | 1 | a0001c0016t0001g0059 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.524-264T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 4/14 | chr9 | 127826124 | |||||||
chr9:127826305 | C | A | 1 | a0001c0006t0001g0058 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.523+205G>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 4/14 | chr9 | 127826305 | |||||||
chr9:127826353 | C | T | 3 | a0001c0001t0001g0155 a0001c0010t0001g0194 a0001c0010t0007g0193 |
3 | NA18612.hp1 NA18994.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.523+157G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 4/14 | chr9 | 127826353 | |||||||
chr9:127826471 | C | T | 1 | a0001c0016t0001g0059 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.523+39G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 4/14 | chr9 | 127826471 | |||||||
chr9:127826832 | C | G | 1 | a0001c0002t0001g0042 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.361-160G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127826832 | |||||||
chr9:127826953 | C | T | 1 | a0001c0016t0001g0059 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.361-281G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127826953 | |||||||
chr9:127826962 | C | T | 1 | a0003c0005t0001g0327 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.361-290G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127826962 | |||||||
chr9:127826977 | G | GTC | 5 | a0001c0008t0001g0017 a0001c0008t0001g0029 a0001c0016t0001g0059 others(2): Show |
5 | HG01099.hp1 HG03130.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.361-307_361-306dup others(2): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127826977 | |||||||
chr9:127827031 | G | C | 3 | a0003c0005t0001g0326 a0003c0005t0001g0330 a0003c0005t0001g0331 |
3 | HG01069.hp1 HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.361-359C>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127827031 | |||||||
chr9:127827066 | C | T | 1 | a0001c0002t0001g0034 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.361-394G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127827066 | |||||||
chr9:127827149 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.361-477C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127827149 | |||||||
chr9:127827556 | G | C | 2 | a0001c0001t0001g0282 a0001c0001t0001g0283 |
2 | HG00741.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.361-884C>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127827556 | |||||||
chr9:127827574 | C | T | 121 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(118): Show |
125 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.361-902G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127827574 | |||||||
chr9:127827660 | A | G | 26 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0050 others(23): Show |
26 | HG00438.hp1 HG00544.hp1 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.361-988T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127827660 | |||||||
chr9:127827787 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.361-1115C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127827787 | |||||||
chr9:127827933 | T | A | 16 | a0002c0004t0001g0066 a0002c0004t0001g0074 a0002c0004t0001g0075 others(13): Show |
16 | HG00438.hp1 HG00544.hp1 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.361-1261A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127827933 | |||||||
chr9:127827961 | G | C | 1 | a0001c0003t0002g0088 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.361-1289C>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127827961 | |||||||
chr9:127827988 | C | T | 3 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0253 |
3 | HG01884.hp2 HG02572.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.361-1316G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127827988 | |||||||
chr9:127828019 | C | CA | 42 | a0001c0001t0001g0011 a0001c0001t0001g0046 a0001c0001t0001g0086 others(39): Show |
42 | HG00738.hp2 HG01074.hp1 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.361-1348dupT | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127828019 | |||||||
chr9:127828019 | C | CAA | 6 | a0001c0001t0001g0047 a0001c0001t0001g0170 a0001c0003t0002g0087 others(3): Show |
6 | HG00642.hp1 HG01106.hp1 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.361-1349_361-1348d others(4): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127828019 | |||||||
chr9:127828019 | C | CAAAAAA | 12 | a0001c0001t0001g0015 a0001c0001t0001g0052 a0001c0001t0001g0154 others(9): Show |
12 | HG00323.hp2 HG00639.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.361-1353_361-1348d others(8): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127828019 | |||||||
chr9:127828019 | C | CAAAAAAA | 11 | a0001c0001t0001g0013 a0001c0001t0001g0141 a0001c0001t0001g0256 others(8): Show |
12 | HG02280.hp1 HG02280.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.361-1354_361-1348d others(9): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127828019 | |||||||
chr9:127828019 | CA | C | 16 | a0001c0001t0001g0071 a0001c0001t0001g0082 a0001c0001t0001g0097 others(13): Show |
16 | HG01169.hp1 HG01496.hp1 HG02698.hp1 others(13): Show |
intron_variant | MODIFIER | c.361-1348delT | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127828019 | |||||||
chr9:127828064 | C | T | 1 | a0001c0025t0001g0257 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.361-1392G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127828064 | |||||||
chr9:127828065 | T | C | 10 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0050 others(7): Show |
10 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.361-1393A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127828065 | |||||||
chr9:127828157 | C | T | 3 | a0004c0009t0001g0053 a0004c0009t0005g0054 a0004c0015t0005g0032 |
3 | HG02647.hp1 HG02818.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.361-1485G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127828157 | |||||||
chr9:127828186 | A | G | 1 | a0001c0001t0001g0238 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.360+1501T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127828186 | |||||||
chr9:127828231 | T | C | 10 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0050 others(7): Show |
10 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.360+1456A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127828231 | |||||||
chr9:127828412 | T | C | 3 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0253 |
3 | HG01884.hp2 HG02572.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.360+1275A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127828412 | |||||||
chr9:127828553 | G | A | 6 | a0001c0001t0001g0052 a0001c0001t0001g0154 a0001c0001t0001g0195 others(3): Show |
6 | HG00323.hp2 HG00639.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.360+1134C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127828553 | |||||||
chr9:127828610 | C | T | 2 | a0001c0001t0001g0119 a0001c0001t0001g0124 |
2 | HG04199.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.360+1077G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127828610 | |||||||
chr9:127828667 | C | A | 1 | a0001c0001t0001g0070 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.360+1020G>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127828667 | |||||||
chr9:127828792 | C | T | 9 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(6): Show |
9 | HG01496.hp2 HG02615.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.360+895G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127828792 | |||||||
chr9:127828824 | G | C | 180 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(177): Show |
185 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.360+863C>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127828824 | |||||||
chr9:127828833 | A | C | 1 | a0001c0010t0007g0193 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.360+854T>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127828833 | |||||||
chr9:127828881 | G | A | 1 | a0001c0001t0001g0289 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.360+806C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127828881 | |||||||
chr9:127829082 | G | C | 4 | a0001c0008t0001g0017 a0001c0008t0001g0029 a0001c0024t0001g0140 others(1): Show |
4 | HG01099.hp1 HG03130.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+605C>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127829082 | |||||||
chr9:127829258 | C | T | 2 | a0001c0001t0001g0226 a0001c0002t0001g0031 |
2 | HG01517.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.360+429G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127829258 | |||||||
chr9:127829296 | C | G | 1 | a0001c0002t0006g0056 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.360+391G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127829296 | |||||||
chr9:127829333 | G | A | 1 | a0001c0001t0001g0298 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.360+354C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127829333 | |||||||
chr9:127829545 | C | T | 1 | a0001c0016t0001g0059 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.360+142G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127829545 | |||||||
chr9:127829666 | G | A | 7 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0110 others(4): Show |
7 | HG01891.hp1 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.360+21C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 3/14 | chr9 | 127829666 | |||||||
chr9:127830059 | A | C | 1 | a0001c0001t0001g0155 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.220-232T>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127830059 | |||||||
chr9:127830161 | G | A | 1 | a0001c0002t0001g0055 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.220-334C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127830161 | |||||||
chr9:127830340 | T | TA | 34 | a0001c0001t0001g0011 a0001c0001t0001g0050 a0001c0001t0001g0070 others(31): Show |
34 | HG00621.hp1 HG01106.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.220-514dupT | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127830340 | |||||||
chr9:127830340 | TA | T | 10 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0110 others(7): Show |
10 | HG01891.hp1 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.220-514delT | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127830340 | |||||||
chr9:127830437 | G | T | 5 | a0001c0001t0001g0154 a0001c0001t0001g0195 a0001c0001t0001g0294 others(2): Show |
5 | HG00323.hp2 HG00639.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.220-610C>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127830437 | |||||||
chr9:127830440 | C | G | 1 | a0001c0001t0012g0338 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.220-613G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127830440 | |||||||
chr9:127830446 | T | C | 1 | a0001c0001t0012g0338 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.220-619A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127830446 | |||||||
chr9:127830449 | T | C | 1 | a0001c0001t0012g0338 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.220-622A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127830449 | |||||||
chr9:127830453 | T | A | 1 | a0001c0001t0012g0338 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.220-626A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127830453 | |||||||
chr9:127830460 | T | C | 1 | a0001c0001t0001g0253 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.220-633A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127830460 | |||||||
chr9:127830603 | C | T | 1 | a0012c0020t0001g0060 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.220-776G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127830603 | |||||||
chr9:127830637 | C | T | 8 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0110 others(5): Show |
8 | HG01891.hp1 HG02040.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.220-810G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127830637 | |||||||
chr9:127830647 | CA | C | 9 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0110 others(6): Show |
9 | HG01891.hp1 HG02040.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.220-821delT | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127830647 | |||||||
chr9:127830713 | A | G | 4 | a0001c0006t0001g0004 a0001c0006t0001g0057 a0001c0006t0001g0058 others(1): Show |
5 | HG01167.hp1 HG02723.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.220-886T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127830713 | |||||||
chr9:127830889 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.220-1062C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127830889 | |||||||
chr9:127831068 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.220-1241C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127831068 | |||||||
chr9:127831074 | A | T | 1 | a0002c0004t0001g0083 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.220-1247T>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127831074 | |||||||
chr9:127831119 | A | G | 1 | a0001c0016t0001g0059 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.220-1292T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127831119 | |||||||
chr9:127831159 | A | AT | 22 | a0001c0001t0001g0052 a0001c0001t0001g0070 a0001c0001t0001g0077 others(19): Show |
22 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.220-1333dupA | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127831159 | |||||||
chr9:127831159 | A | ATT | 23 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0044 others(20): Show |
24 | HG02280.hp1 HG02280.hp2 HG02615.hp1 others(21): Show |
intron_variant | MODIFIER | c.220-1334_220-1333d others(4): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127831159 | |||||||
chr9:127831159 | AT | A | 5 | a0001c0001t0001g0006 a0001c0001t0001g0181 a0001c0001t0001g0249 others(2): Show |
6 | HG01928.hp2 HG01993.hp2 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.220-1333delA | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127831159 | |||||||
chr9:127831314 | C | T | 1 | a0001c0025t0001g0257 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.220-1487G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127831314 | |||||||
chr9:127831372 | G | T | 1 | a0001c0001t0012g0338 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.220-1545C>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127831372 | |||||||
chr9:127831432 | A | G | 30 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0052 others(27): Show |
30 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.220-1605T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127831432 | |||||||
chr9:127831489 | T | G | 30 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0052 others(27): Show |
30 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.220-1662A>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127831489 | |||||||
chr9:127831660 | C | T | 7 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(4): Show |
7 | HG02486.hp1 HG02572.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.220-1833G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127831660 | |||||||
chr9:127831684 | C | CT | 30 | a0001c0001t0001g0052 a0001c0001t0001g0098 a0001c0001t0001g0099 others(27): Show |
30 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.220-1858dupA | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127831684 | |||||||
chr9:127831697 | T | C | 2 | a0001c0001t0001g0095 a0001c0001t0001g0106 |
2 | HG03017.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.220-1870A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127831697 | |||||||
chr9:127831718 | G | T | 6 | a0001c0001t0001g0052 a0001c0001t0001g0154 a0001c0001t0001g0195 others(3): Show |
6 | HG00323.hp2 HG00639.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.220-1891C>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127831718 | |||||||
chr9:127831785 | G | A | 6 | a0001c0001t0001g0052 a0001c0001t0001g0154 a0001c0001t0001g0195 others(3): Show |
6 | HG00323.hp2 HG00639.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.220-1958C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127831785 | |||||||
chr9:127831893 | A | G | 1 | a0001c0001t0001g0183 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.220-2066T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127831893 | |||||||
chr9:127832003 | T | C | 1 | a0001c0006t0010g0336 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.220-2176A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127832003 | |||||||
chr9:127832028 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.220-2201C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127832028 | |||||||
chr9:127832040 | T | G | 14 | a0002c0004t0001g0066 a0002c0004t0001g0074 a0002c0004t0001g0075 others(11): Show |
14 | HG00438.hp1 HG02040.hp1 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.220-2213A>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127832040 | |||||||
chr9:127832069 | C | CT | 56 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0015 others(53): Show |
57 | HG00597.hp2 HG00741.hp2 HG01099.hp1 others(54): Show |
intron_variant | MODIFIER | c.220-2243dupA | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127832069 | |||||||
chr9:127832069 | C | CTTTTTT | 11 | a0001c0001t0001g0046 a0001c0001t0001g0052 a0001c0001t0001g0154 others(8): Show |
11 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.220-2248_220-2243d others(8): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127832069 | |||||||
chr9:127832069 | CT | C | 7 | a0001c0001t0001g0095 a0001c0001t0001g0102 a0001c0001t0001g0136 others(4): Show |
7 | HG00323.hp1 HG01496.hp2 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.220-2243delA | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127832069 | |||||||
chr9:127832069 | CTTTTTTT others(4): Show |
C | 14 | a0002c0004t0001g0066 a0002c0004t0001g0074 a0002c0004t0001g0075 others(11): Show |
14 | HG00438.hp1 HG02040.hp1 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.220-2253_220-2243d others(13): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127832069 | |||||||
chr9:127832202 | G | C | 1 | a0001c0001t0001g0139 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.220-2375C>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127832202 | |||||||
chr9:127832223 | T | G | 1 | a0012c0020t0001g0060 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.220-2396A>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127832223 | |||||||
chr9:127832473 | C | G | 2 | a0001c0001t0001g0220 a0001c0001t0001g0221 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.220-2646G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127832473 | |||||||
chr9:127832518 | CT | C | 122 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(119): Show |
125 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.220-2692delA | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127832518 | |||||||
chr9:127832530 | T | G | 1 | a0001c0016t0001g0059 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.220-2703A>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127832530 | |||||||
chr9:127832572 | G | A | 1 | a0001c0007t0001g0214 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.220-2745C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127832572 | |||||||
chr9:127832583 | C | G | 21 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0229 others(18): Show |
21 | HG00438.hp1 HG00642.hp1 HG02040.hp1 others(18): Show |
intron_variant | MODIFIER | c.220-2756G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127832583 | |||||||
chr9:127832607 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.220-2780C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127832607 | |||||||
chr9:127832610 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.220-2783G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127832610 | |||||||
chr9:127832837 | A | G | 24 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0110 others(21): Show |
24 | HG00438.hp1 HG00544.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.220-3010T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127832837 | |||||||
chr9:127832972 | G | T | 119 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(116): Show |
122 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.220-3145C>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127832972 | |||||||
chr9:127833248 | G | A | 14 | a0002c0004t0001g0066 a0002c0004t0001g0074 a0002c0004t0001g0075 others(11): Show |
14 | HG00438.hp1 HG02040.hp1 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.220-3421C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127833248 | |||||||
chr9:127833350 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.220-3523G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127833350 | |||||||
chr9:127833488 | C | G | 14 | a0002c0004t0001g0066 a0002c0004t0001g0074 a0002c0004t0001g0075 others(11): Show |
14 | HG00438.hp1 HG02040.hp1 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.220-3661G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127833488 | |||||||
chr9:127833522 | C | CA | 27 | a0001c0001t0001g0100 a0001c0001t0001g0112 a0001c0001t0001g0116 others(24): Show |
27 | HG00423.hp2 HG01071.hp1 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.220-3696dupT | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127833522 | |||||||
chr9:127833522 | CA | C | 29 | a0001c0001t0001g0048 a0001c0001t0001g0061 a0001c0001t0001g0062 others(26): Show |
30 | HG01081.hp2 HG01167.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.220-3696delT | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127833522 | |||||||
chr9:127833522 | CAA | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(133): Show |
140 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.220-3697_220-3696d others(4): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127833522 | |||||||
chr9:127833522 | CAAAA | C | 19 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0229 others(16): Show |
19 | HG00438.hp1 HG00642.hp1 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.220-3699_220-3696d others(6): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127833522 | |||||||
chr9:127833632 | C | G | 1 | a0010c0018t0001g0265 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.220-3805G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127833632 | |||||||
chr9:127833819 | C | T | 17 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0137 others(14): Show |
17 | HG02280.hp1 HG02280.hp2 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.220-3992G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127833819 | |||||||
chr9:127833865 | T | C | 1 | a0001c0024t0001g0140 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.220-4038A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127833865 | |||||||
chr9:127833907 | T | C | 1 | a0001c0001t0001g0272 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.220-4080A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127833907 | |||||||
chr9:127833909 | A | G | 334 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(331): Show |
340 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(337): Show |
intron_variant | MODIFIER | c.220-4082T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127833909 | |||||||
chr9:127834098 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.220-4271C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127834098 | |||||||
chr9:127834141 | C | T | 3 | a0001c0002t0001g0016 a0001c0008t0001g0017 a0003c0030t0001g0332 |
3 | HG01099.hp1 NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.220-4314G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127834141 | |||||||
chr9:127834173 | A | G | 5 | a0001c0001t0001g0154 a0001c0001t0001g0195 a0001c0001t0001g0294 others(2): Show |
5 | HG00323.hp2 HG00639.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.220-4346T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127834173 | |||||||
chr9:127834198 | A | G | 1 | a0001c0002t0006g0056 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.220-4371T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127834198 | |||||||
chr9:127834265 | T | C | 1 | a0001c0001t0001g0296 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.220-4438A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127834265 | |||||||
chr9:127834269 | G | C | 1 | a0001c0001t0001g0015 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.220-4442C>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127834269 | |||||||
chr9:127834301 | G | A | 1 | a0001c0006t0010g0336 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.220-4474C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127834301 | |||||||
chr9:127834387 | G | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | HG02145.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.220-4560C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127834387 | |||||||
chr9:127834395 | G | ACCCAACT others(160): Show |
1 | a0001c0001t0001g0093 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.220-4568_220-4567i others(169): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127834395 | |||||||
chr9:127834395 | G | ACCCAACT others(160): Show |
4 | a0001c0001t0001g0105 a0001c0001t0003g0008 a0001c0001t0003g0009 others(1): Show |
4 | HG00609.hp1 HG02129.hp1 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.220-4568_220-4567i others(169): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127834395 | |||||||
chr9:127834498 | G | A | 1 | a0001c0001t0001g0128 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.220-4671C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127834498 | |||||||
chr9:127834537 | T | G | 24 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(21): Show |
24 | HG00639.hp2 HG01069.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.220-4710A>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127834537 | |||||||
chr9:127834695 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.220-4868C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127834695 | |||||||
chr9:127834827 | C | T | 1 | a0001c0022t0001g0049 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.220-5000G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127834827 | |||||||
chr9:127834835 | T | TAGGTTGG others(291): Show |
1 | a0001c0001t0001g0261 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.220-5009_220-5008i others(300): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127834835 | |||||||
chr9:127834835 | T | TAGGTTGG others(289): Show |
1 | a0001c0001t0001g0264 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.220-5009_220-5008i others(298): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127834835 | |||||||
chr9:127834835 | T | TAGGTTGG others(291): Show |
9 | a0001c0001t0001g0137 a0001c0001t0001g0141 a0001c0001t0001g0215 others(6): Show |
9 | HG02602.hp2 HG02683.hp1 HG02683.hp2 others(6): Show |
intron_variant | MODIFIER | c.220-5009_220-5008i others(300): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127834835 | |||||||
chr9:127834835 | T | TAGGTTGG others(292): Show |
1 | a0001c0001t0001g0129 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.220-5009_220-5008i others(301): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127834835 | |||||||
chr9:127834835 | T | TAGGTTGG others(292): Show |
4 | a0001c0001t0001g0279 a0001c0001t0001g0317 a0001c0001t0001g0320 others(1): Show |
4 | HG03139.hp1 HG03239.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.220-5009_220-5008i others(301): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127834835 | |||||||
chr9:127834835 | T | TAGGTTGG others(293): Show |
8 | a0001c0001t0001g0015 a0001c0001t0001g0316 a0001c0001t0001g0318 others(5): Show |
8 | HG02280.hp1 HG02615.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.220-5009_220-5008i others(302): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127834835 | |||||||
chr9:127834835 | T | TAGGTTGG others(294): Show |
1 | a0001c0001t0001g0013 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.220-5009_220-5008i others(303): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127834835 | |||||||
chr9:127834895 | A | G | 1 | a0001c0002t0001g0055 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.220-5068T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127834895 | |||||||
chr9:127834944 | T | C | 53 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0115 others(50): Show |
54 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.220-5117A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127834944 | |||||||
chr9:127835325 | G | A | 1 | a0001c0001t0001g0250 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.220-5498C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127835325 | |||||||
chr9:127835680 | C | T | 3 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 |
3 | HG01496.hp2 HG02886.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.220-5853G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127835680 | |||||||
chr9:127835696 | C | T | 1 | a0001c0002t0001g0314 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.220-5869G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127835696 | |||||||
chr9:127835718 | T | G | 1 | a0001c0001t0001g0123 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.220-5891A>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127835718 | |||||||
chr9:127835774 | G | GA | 7 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 others(4): Show |
7 | HG02129.hp2 NA18960.hp2 NA18973.hp2 others(4): Show |
intron_variant | MODIFIER | c.220-5948dupT | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127835774 | |||||||
chr9:127835784 | G | A | 2 | a0001c0001t0001g0188 a0001c0001t0001g0303 |
2 | HG03834.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.220-5957C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127835784 | |||||||
chr9:127835846 | G | A | 33 | a0001c0001t0001g0118 a0001c0001t0001g0137 a0001c0001t0001g0142 others(30): Show |
33 | HG00099.hp2 HG00738.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.220-6019C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127835846 | |||||||
chr9:127835934 | T | A | 8 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(5): Show |
8 | HG02622.hp2 HG02922.hp1 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.220-6107A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127835934 | |||||||
chr9:127835982 | G | A | 8 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(5): Show |
8 | HG02622.hp2 HG02922.hp1 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.220-6155C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127835982 | |||||||
chr9:127836021 | A | G | 8 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(5): Show |
8 | HG02622.hp2 HG02922.hp1 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.220-6194T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127836021 | |||||||
chr9:127836109 | C | T | 1 | a0001c0001t0001g0255 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.220-6282G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127836109 | |||||||
chr9:127836155 | C | G | 1 | a0001c0001t0001g0145 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.220-6328G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127836155 | |||||||
chr9:127836177 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.220-6350T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127836177 | |||||||
chr9:127836267 | C | T | 11 | a0001c0001t0001g0293 a0001c0001t0001g0305 a0003c0005t0001g0326 others(8): Show |
11 | HG00639.hp2 HG01069.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.220-6440G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127836267 | |||||||
chr9:127836645 | G | A | 61 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0050 others(58): Show |
64 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(61): Show |
intron_variant | MODIFIER | c.219+6449C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127836645 | |||||||
chr9:127836880 | T | C | 1 | a0002c0004t0001g0092 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.219+6214A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127836880 | |||||||
chr9:127837216 | C | T | 1 | a0001c0003t0002g0087 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.219+5878G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127837216 | |||||||
chr9:127837384 | A | T | 1 | a0001c0001t0008g0138 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.219+5710T>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127837384 | |||||||
chr9:127837401 | T | G | 2 | a0001c0002t0001g0051 a0001c0002t0001g0055 |
2 | HG03041.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.219+5693A>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127837401 | |||||||
chr9:127837476 | C | A | 1 | a0001c0022t0001g0049 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.219+5618G>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127837476 | |||||||
chr9:127837679 | C | T | 6 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(3): Show |
6 | HG00099.hp2 HG00738.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.219+5415G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127837679 | |||||||
chr9:127837774 | G | GCATC | 36 | a0001c0001t0001g0048 a0001c0001t0001g0061 a0001c0001t0001g0062 others(33): Show |
36 | HG00408.hp1 HG00544.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.219+5316_219+5319d others(6): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127837774 | |||||||
chr9:127837774 | G | GCATCCAT others(1): Show |
3 | a0001c0001t0001g0196 a0001c0001t0001g0226 a0001c0001t0001g0261 |
3 | HG01169.hp1 HG04228.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.219+5312_219+5319d others(10): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127837774 | |||||||
chr9:127837774 | G | GCATCCAT others(5): Show |
1 | a0001c0001t0001g0169 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.219+5308_219+5319d others(14): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127837774 | |||||||
chr9:127837810 | C | CCACATCC others(7): Show |
1 | a0001c0001t0001g0294 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.219+5283_219+5284i others(16): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127837810 | |||||||
chr9:127837810 | C | CCATCCAT others(15): Show |
18 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(15): Show |
19 | HG00639.hp2 HG01069.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.219+5283_219+5284i others(24): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127837810 | |||||||
chr9:127837810 | C | CCATCCAT others(19): Show |
25 | a0001c0001t0001g0050 a0001c0001t0001g0064 a0001c0001t0001g0102 others(22): Show |
26 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.219+5283_219+5284i others(28): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127837810 | |||||||
chr9:127837810 | C | CCATCCAT others(23): Show |
19 | a0001c0001t0001g0044 a0001c0001t0001g0052 a0001c0001t0001g0154 others(16): Show |
20 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.219+5283_219+5284i others(32): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127837810 | |||||||
chr9:127837810 | C | CCATCCAT others(27): Show |
11 | a0001c0001t0001g0045 a0001c0001t0001g0173 a0001c0001t0001g0291 others(8): Show |
11 | HG00738.hp2 HG01106.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.219+5283_219+5284i others(36): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127837810 | |||||||
chr9:127837880 | G | A | 1 | a0001c0001t0001g0191 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.219+5214C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127837880 | |||||||
chr9:127838042 | G | A | 1 | a0001c0001t0001g0294 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.219+5052C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127838042 | |||||||
chr9:127838147 | C | T | 7 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(4): Show |
7 | HG02486.hp1 HG02572.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.219+4947G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127838147 | |||||||
chr9:127838150 | AC | A | 8 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0001c0001t0001g0227 others(5): Show |
8 | HG02056.hp1 HG02083.hp1 HG04184.hp2 others(5): Show |
intron_variant | MODIFIER | c.219+4943delG | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127838150 | |||||||
chr9:127838183 | A | G | 1 | a0001c0001t0001g0294 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.219+4911T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127838183 | |||||||
chr9:127838269 | G | A | 1 | a0001c0001t0001g0252 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.219+4825C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127838269 | |||||||
chr9:127838374 | A | G | 1 | a0001c0001t0012g0338 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.219+4720T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127838374 | |||||||
chr9:127838513 | C | T | 2 | a0001c0001t0001g0163 a0001c0001t0001g0206 |
2 | NA18960.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.219+4581G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127838513 | |||||||
chr9:127838800 | G | A | 1 | a0001c0001t0001g0293 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.219+4294C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127838800 | |||||||
chr9:127838890 | C | T | 3 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 |
3 | HG00408.hp1 HG00673.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.219+4204G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127838890 | |||||||
chr9:127838998 | C | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(131): Show |
137 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.219+4096G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127838998 | |||||||
chr9:127839020 | A | C | 1 | a0001c0001t0001g0268 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.219+4074T>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127839020 | |||||||
chr9:127839115 | C | T | 8 | a0001c0001t0001g0159 a0001c0001t0001g0161 a0001c0001t0001g0227 others(5): Show |
8 | HG02056.hp1 HG02083.hp1 HG04184.hp2 others(5): Show |
intron_variant | MODIFIER | c.219+3979G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127839115 | |||||||
chr9:127839178 | C | T | 8 | a0003c0005t0001g0326 a0003c0005t0001g0327 a0003c0005t0001g0328 others(5): Show |
8 | HG00639.hp2 HG01069.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.219+3916G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127839178 | |||||||
chr9:127839205 | C | T | 3 | a0001c0006t0001g0004 a0001c0006t0001g0057 a0001c0006t0001g0058 |
4 | HG01167.hp1 HG02723.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.219+3889G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127839205 | |||||||
chr9:127839297 | C | T | 64 | a0001c0001t0001g0044 a0001c0001t0001g0050 a0001c0001t0001g0064 others(61): Show |
67 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.219+3797G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127839297 | |||||||
chr9:127839317 | A | G | 6 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 others(3): Show |
6 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.219+3777T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127839317 | |||||||
chr9:127839326 | A | G | 333 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(330): Show |
339 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.219+3768T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127839326 | |||||||
chr9:127839462 | G | A | 6 | a0001c0001t0001g0013 a0001c0001t0001g0139 a0001c0001t0001g0141 others(3): Show |
6 | HG02145.hp2 HG02280.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.219+3632C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127839462 | |||||||
chr9:127839562 | T | C | 1 | a0012c0020t0001g0060 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.219+3532A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127839562 | |||||||
chr9:127839595 | G | A | 1 | a0001c0002t0001g0026 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.219+3499C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127839595 | |||||||
chr9:127839672 | CAGCCTCT others(5): Show |
C | 1 | a0001c0001t0001g0298 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.219+3410_219+3421d others(14): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127839672 | |||||||
chr9:127839746 | C | T | 12 | a0001c0001t0001g0070 a0001c0001t0001g0077 a0001c0001t0001g0079 others(9): Show |
12 | NA18941.hp1 NA18943.hp1 NA18947.hp1 others(9): Show |
intron_variant | MODIFIER | c.219+3348G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127839746 | |||||||
chr9:127839845 | T | C | 89 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0050 others(86): Show |
92 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.219+3249A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127839845 | |||||||
chr9:127839854 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.219+3240G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127839854 | |||||||
chr9:127839951 | G | A | 52 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0050 others(49): Show |
55 | HG00323.hp2 HG00639.hp1 HG01070.hp2 others(52): Show |
intron_variant | MODIFIER | c.219+3143C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127839951 | |||||||
chr9:127839971 | G | C | 1 | a0001c0001t0001g0050 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.219+3123C>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127839971 | |||||||
chr9:127840017 | G | A | 10 | a0001c0001t0001g0305 a0003c0005t0001g0326 a0003c0005t0001g0327 others(7): Show |
10 | HG00639.hp2 HG01069.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.219+3077C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127840017 | |||||||
chr9:127840129 | G | A | 220 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(217): Show |
223 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.219+2965C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127840129 | |||||||
chr9:127840147 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.219+2947C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127840147 | |||||||
chr9:127840281 | G | C | 1 | a0001c0001t0001g0099 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.219+2813C>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127840281 | |||||||
chr9:127840504 | A | C | 4 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 others(1): Show |
4 | HG01516.hp2 HG01517.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.219+2590T>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127840504 | |||||||
chr9:127840606 | T | C | 1 | a0002c0004t0001g0089 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.219+2488A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127840606 | |||||||
chr9:127840872 | A | C | 32 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0070 others(29): Show |
32 | HG00438.hp1 HG01099.hp2 HG01975.hp1 others(29): Show |
intron_variant | MODIFIER | c.219+2222T>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127840872 | |||||||
chr9:127841174 | C | T | 12 | a0001c0001t0001g0305 a0003c0005t0001g0324 a0003c0005t0001g0325 others(9): Show |
12 | HG00639.hp2 HG01069.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.219+1920G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127841174 | |||||||
chr9:127841215 | G | A | 1 | a0001c0002t0001g0036 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.219+1879C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127841215 | |||||||
chr9:127841367 | C | A | 3 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0016t0001g0059 |
3 | HG02572.hp1 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.219+1727G>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127841367 | |||||||
chr9:127841491 | G | GA | 12 | a0001c0001t0001g0305 a0003c0005t0001g0324 a0003c0005t0001g0325 others(9): Show |
12 | HG00639.hp2 HG01069.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.219+1602dupT | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127841491 | |||||||
chr9:127841655 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.219+1439C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127841655 | |||||||
chr9:127841717 | G | A | 1 | a0003c0005t0001g0323 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.219+1377C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127841717 | |||||||
chr9:127841861 | G | A | 3 | a0003c0005t0001g0326 a0003c0005t0001g0330 a0003c0005t0001g0331 |
3 | HG01069.hp1 HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.219+1233C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127841861 | |||||||
chr9:127841873 | G | A | 5 | a0001c0001t0001g0297 a0001c0001t0001g0298 a0001c0001t0001g0299 others(2): Show |
5 | HG02622.hp2 NA18522.hp1 NA20129.hp1 others(2): Show |
intron_variant | MODIFIER | c.219+1221C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127841873 | |||||||
chr9:127842025 | C | T | 3 | a0001c0001t0001g0048 a0001c0001t0001g0061 a0001c0001t0001g0062 |
3 | HG01884.hp1 HG02895.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.219+1069G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127842025 | |||||||
chr9:127842037 | G | T | 2 | a0001c0001t0001g0309 a0001c0001t0001g0310 |
2 | NA18941.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.219+1057C>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127842037 | |||||||
chr9:127842095 | GGTCTCCT others(10): Show |
G | 1 | a0003c0005t0001g0335 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.219+982_219+998del others(17): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127842095 | |||||||
chr9:127842220 | CTTTTCTT others(6): Show |
C | 1 | a0001c0002t0001g0311 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.219+861_219+873del others(13): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127842220 | |||||||
chr9:127842225 | CT | C | 48 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0064 others(45): Show |
50 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.219+868delA | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127842225 | |||||||
chr9:127842225 | CTT | C | 87 | a0001c0001t0001g0048 a0001c0001t0001g0061 a0001c0001t0001g0062 others(84): Show |
88 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.219+867_219+868del others(2): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127842225 | |||||||
chr9:127842225 | CTTT | C | 192 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(189): Show |
195 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.219+866_219+868del others(3): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127842225 | |||||||
chr9:127842231 | T | C | 8 | a0001c0001t0001g0064 a0001c0001t0001g0279 a0001c0001t0001g0316 others(5): Show |
8 | HG02280.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.219+863A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127842231 | |||||||
chr9:127842232 | T | C | 1 | a0001c0001t0012g0338 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.219+862A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127842232 | |||||||
chr9:127842285 | G | A | 3 | a0001c0002t0001g0051 a0001c0002t0001g0055 a0001c0002t0006g0056 |
3 | HG03041.hp1 HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.219+809C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127842285 | |||||||
chr9:127842371 | G | A | 3 | a0001c0001t0001g0048 a0001c0001t0001g0061 a0001c0001t0001g0062 |
3 | HG01884.hp1 HG02895.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.219+723C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127842371 | |||||||
chr9:127842427 | T | A | 7 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(4): Show |
7 | HG02486.hp1 HG02572.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.219+667A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127842427 | |||||||
chr9:127842492 | C | G | 1 | a0001c0001t0001g0048 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.219+602G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127842492 | |||||||
chr9:127842553 | T | G | 12 | a0001c0001t0001g0305 a0003c0005t0001g0324 a0003c0005t0001g0325 others(9): Show |
12 | HG00639.hp2 HG01069.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.219+541A>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127842553 | |||||||
chr9:127842587 | A | G | 332 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(329): Show |
338 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(335): Show |
intron_variant | MODIFIER | c.219+507T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127842587 | |||||||
chr9:127842600 | T | A | 1 | a0012c0020t0001g0060 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.219+494A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127842600 | |||||||
chr9:127842834 | C | CA | 40 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0016 others(37): Show |
42 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.219+259dupT | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127842834 | |||||||
chr9:127843069 | C | A | 20 | a0001c0001t0001g0118 a0001c0001t0001g0137 a0001c0001t0001g0260 others(17): Show |
20 | HG00741.hp1 HG01516.hp1 HG01993.hp1 others(17): Show |
intron_variant | MODIFIER | c.219+25G>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 2/14 | chr9 | 127843069 | |||||||
chr9:127843398 | C | G | 4 | a0001c0001t0001g0274 a0001c0002t0001g0021 a0001c0002t0001g0027 others(1): Show |
4 | HG01070.hp2 HG01071.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-153G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843398 | |||||||
chr9:127843460 | A | G | 13 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0064 others(10): Show |
13 | HG02280.hp1 HG02280.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.68-215T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843460 | |||||||
chr9:127843501 | T | C | 5 | a0001c0006t0001g0004 a0001c0006t0001g0057 a0001c0006t0001g0058 others(2): Show |
6 | HG01167.hp1 HG02723.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-256A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843501 | |||||||
chr9:127843623 | ATGTATAT others(9): Show |
A | 1 | a0001c0001t0001g0253 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.68-394_68-379delCA others(14): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843623 | |||||||
chr9:127843658 | C | T | 3 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0315 |
3 | HG04184.hp2 NA18941.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.68-413G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843658 | |||||||
chr9:127843688 | C | CAT | 289 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(286): Show |
293 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.68-445_68-444dupAT | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843688 | |||||||
chr9:127843699 | A | C | 1 | a0006c0028t0001g0148 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.68-454T>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843699 | |||||||
chr9:127843715 | A | C | 1 | a0006c0028t0001g0148 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.68-470T>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843715 | |||||||
chr9:127843732 | C | CACATATA others(5): Show |
1 | a0001c0001t0001g0317 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.68-488_68-487insAT others(10): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843732 | |||||||
chr9:127843732 | C | CACATATA others(7): Show |
2 | a0001c0001t0001g0279 a0001c0001t0001g0316 |
2 | HG02630.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.68-488_68-487insAT others(12): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843732 | |||||||
chr9:127843732 | C | CAT | 5 | a0001c0001t0001g0118 a0001c0001t0001g0142 a0001c0001t0001g0220 others(2): Show |
5 | HG00639.hp2 HG00642.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-489_68-488dupAT | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843732 | |||||||
chr9:127843732 | C | CATAT | 6 | a0001c0001t0001g0093 a0001c0001t0001g0219 a0001c0001t0001g0223 others(3): Show |
6 | HG00609.hp2 HG01192.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-488_68-487insAT others(2): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843732 | |||||||
chr9:127843732 | C | CATATAT | 12 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(9): Show |
12 | HG00438.hp1 HG01081.hp1 HG02155.hp2 others(9): Show |
intron_variant | MODIFIER | c.68-488_68-487insAT others(4): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843732 | |||||||
chr9:127843732 | C | CATATATA others(1): Show |
8 | a0001c0001t0001g0069 a0001c0001t0001g0309 a0001c0001t0001g0315 others(5): Show |
9 | HG01891.hp2 HG01975.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.68-488_68-487insAT others(6): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843732 | |||||||
chr9:127843732 | C | CATATATA others(3): Show |
2 | a0001c0013t0001g0040 a0004c0015t0005g0032 |
2 | HG01074.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.68-488_68-487insAT others(8): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843732 | |||||||
chr9:127843732 | C | CATATATA others(5): Show |
4 | a0001c0002t0001g0027 a0001c0002t0001g0028 a0001c0006t0001g0004 others(1): Show |
5 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-488_68-487insAT others(10): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843732 | |||||||
chr9:127843732 | C | CATATATA others(7): Show |
1 | a0001c0002t0001g0018 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.68-488_68-487insAT others(12): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843732 | |||||||
chr9:127843732 | C | CATATATA others(9): Show |
1 | a0004c0009t0001g0053 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.68-488_68-487insAT others(14): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843732 | |||||||
chr9:127843732 | C | T | 3 | a0001c0001t0001g0048 a0001c0001t0001g0061 a0001c0001t0001g0062 |
3 | HG01884.hp1 HG02895.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.68-487G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843732 | |||||||
chr9:127843732 | CATACATA others(3): Show |
C | 4 | a0001c0002t0001g0068 a0001c0002t0001g0312 a0001c0002t0001g0313 others(1): Show |
4 | NA18981.hp1 NA19002.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-497_68-488delAT others(8): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843732 | |||||||
chr9:127843734 | T | C | 11 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0064 others(8): Show |
11 | HG02280.hp1 HG02280.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.68-489A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843734 | |||||||
chr9:127843736 | C | T | 322 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(319): Show |
328 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(325): Show |
intron_variant | MODIFIER | c.68-491G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843736 | |||||||
chr9:127843745 | ATATATAT others(4): Show |
A | 1 | a0002c0012t0001g0308 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.68-511_68-501delAT others(9): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843745 | |||||||
chr9:127843747 | ATATATAT others(5): Show |
A | 1 | a0001c0002t0001g0026 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.68-514_68-503delAA others(10): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843747 | |||||||
chr9:127843749 | ATATATAT others(3): Show |
A | 2 | a0001c0002t0001g0051 a0001c0002t0001g0311 |
2 | HG03041.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.68-514_68-505delAA others(8): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843749 | |||||||
chr9:127843751 | ATATATTT others(3): Show |
A | 2 | a0001c0001t0001g0048 a0001c0001t0001g0062 |
2 | HG02895.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.68-516_68-507delAA others(8): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843751 | |||||||
chr9:127843753 | ATATTTTT others(3): Show |
A | 5 | a0001c0001t0001g0115 a0001c0001t0001g0228 a0001c0001t0001g0238 others(2): Show |
5 | NA18960.hp2 NA18998.hp1 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-518_68-509delAA others(8): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843753 | |||||||
chr9:127843753 | ATATTTTT others(9): Show |
A | 1 | a0001c0001t0001g0229 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.68-524_68-509delAA others(14): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843753 | |||||||
chr9:127843755 | A | ATATATAT others(22): Show |
1 | a0001c0001t0012g0338 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.68-511_68-510insAT others(27): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843755 | |||||||
chr9:127843755 | A | ATATATAT others(10): Show |
1 | a0001c0001t0001g0320 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.68-511_68-510insAA others(15): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843755 | |||||||
chr9:127843755 | A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0319 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.68-511_68-510insAA others(13): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843755 | |||||||
chr9:127843755 | A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0318 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.68-511_68-510insAA others(13): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843755 | |||||||
chr9:127843755 | A | T | 1 | a0001c0001t0001g0316 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.68-510T>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843755 | |||||||
chr9:127843755 | ATTTT | A | 6 | a0001c0001t0001g0110 a0001c0001t0001g0143 a0001c0001t0001g0144 others(3): Show |
6 | HG01255.hp2 HG02273.hp2 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.68-514_68-511delAA others(2): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843755 | |||||||
chr9:127843755 | ATTTTT | A | 7 | a0001c0001t0001g0146 a0001c0001t0001g0271 a0001c0001t0001g0294 others(4): Show |
7 | HG01123.hp2 HG02622.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.68-515_68-511delAA others(3): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843755 | |||||||
chr9:127843755 | ATTTTTT | A | 13 | a0001c0001t0001g0112 a0001c0001t0001g0131 a0001c0001t0001g0136 others(10): Show |
13 | HG01346.hp2 HG01952.hp1 HG01978.hp2 others(10): Show |
intron_variant | MODIFIER | c.68-516_68-511delAA others(4): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843755 | |||||||
chr9:127843755 | ATTTTTTT others(1): Show |
A | 34 | a0001c0001t0001g0001 a0001c0001t0001g0098 a0001c0001t0001g0106 others(31): Show |
35 | HG00597.hp2 HG01070.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.68-518_68-511delAA others(6): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843755 | |||||||
chr9:127843755 | ATTTTTTT others(3): Show |
A | 96 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0046 others(93): Show |
98 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.68-520_68-511delAA others(8): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843755 | |||||||
chr9:127843755 | ATTTTTTT others(4): Show |
A | 11 | a0001c0001t0001g0052 a0001c0001t0001g0100 a0001c0001t0001g0207 others(8): Show |
11 | HG00099.hp2 HG02135.hp2 HG02735.hp1 others(8): Show |
intron_variant | MODIFIER | c.68-521_68-511delAA others(9): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843755 | |||||||
chr9:127843755 | ATTTTTTT others(5): Show |
A | 14 | a0001c0001t0001g0113 a0001c0001t0001g0151 a0001c0001t0001g0152 others(11): Show |
14 | HG00438.hp2 HG00673.hp1 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.68-522_68-511delAA others(10): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843755 | |||||||
chr9:127843755 | ATTTTTTT others(6): Show |
A | 1 | a0001c0001t0001g0206 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.68-523_68-511delAA others(11): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843755 | |||||||
chr9:127843756 | T | TA | 4 | a0001c0001t0001g0221 a0001c0003t0002g0014 a0003c0005t0001g0328 others(1): Show |
4 | HG01516.hp2 HG02630.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-512_68-511insT | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843756 | |||||||
chr9:127843756 | T | TATA | 8 | a0001c0001t0001g0137 a0001c0001t0001g0260 a0001c0001t0001g0261 others(5): Show |
8 | HG01993.hp1 HG02683.hp1 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.68-512_68-511insTA others(1): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843756 | |||||||
chr9:127843756 | T | TATATA | 12 | a0001c0001t0001g0080 a0001c0001t0001g0084 a0001c0001t0001g0095 others(9): Show |
12 | HG01069.hp1 HG02055.hp1 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.68-512_68-511insTA others(3): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843756 | |||||||
chr9:127843756 | T | TATATATA | 9 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0253 others(6): Show |
9 | HG00738.hp1 HG01106.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.68-512_68-511insTA others(5): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843756 | |||||||
chr9:127843756 | T | TATATATA others(2): Show |
9 | a0001c0001t0001g0044 a0001c0001t0001g0064 a0001c0001t0001g0094 others(6): Show |
9 | HG01099.hp2 HG01192.hp1 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.68-512_68-511insTA others(7): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843756 | |||||||
chr9:127843756 | T | TATATATA others(4): Show |
1 | a0009c0026t0001g0262 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.68-512_68-511insTA others(9): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843756 | |||||||
chr9:127843756 | T | TATATATA others(6): Show |
2 | a0001c0002t0001g0036 a0001c0002t0001g0295 |
2 | HG01346.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.68-512_68-511insTA others(11): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843756 | |||||||
chr9:127843756 | T | TATATATA others(8): Show |
2 | a0001c0001t0001g0321 a0001c0008t0001g0017 |
2 | HG01099.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.68-512_68-511insTA others(13): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843756 | |||||||
chr9:127843756 | T | TATATATA others(10): Show |
3 | a0001c0002t0001g0002 a0001c0006t0001g0057 a0001c0006t0001g0058 |
3 | HG02723.hp1 HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.68-512_68-511insTA others(15): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843756 | |||||||
chr9:127843757 | T | A | 41 | a0001c0001t0001g0013 a0001c0001t0001g0050 a0001c0001t0001g0067 others(38): Show |
43 | HG00438.hp1 HG00609.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.68-512A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843757 | |||||||
chr9:127843758 | T | A | 38 | a0001c0001t0001g0064 a0001c0001t0001g0094 a0001c0001t0001g0095 others(35): Show |
39 | HG00738.hp1 HG00741.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.68-513A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843758 | |||||||
chr9:127843759 | T | A | 26 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0050 others(23): Show |
27 | HG00639.hp2 HG00642.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.68-514A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843759 | |||||||
chr9:127843760 | T | A | 19 | a0001c0001t0001g0218 a0001c0001t0001g0221 a0001c0001t0001g0224 others(16): Show |
19 | HG00738.hp1 HG01496.hp1 HG01516.hp2 others(16): Show |
intron_variant | MODIFIER | c.68-515A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843760 | |||||||
chr9:127843761 | T | A | 21 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0050 others(18): Show |
21 | HG00642.hp2 HG01074.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.68-516A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843761 | |||||||
chr9:127843762 | T | A | 15 | a0001c0001t0001g0146 a0001c0001t0001g0221 a0001c0001t0001g0224 others(12): Show |
15 | HG00738.hp1 HG01123.hp2 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.68-517A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843762 | |||||||
chr9:127843763 | T | A | 28 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0067 others(25): Show |
28 | HG00642.hp2 HG01255.hp2 HG01346.hp2 others(25): Show |
intron_variant | MODIFIER | c.68-518A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843763 | |||||||
chr9:127843764 | T | A | 15 | a0001c0001t0001g0011 a0001c0001t0001g0146 a0001c0001t0001g0160 others(12): Show |
15 | HG00738.hp1 HG01123.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.68-519A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843764 | |||||||
chr9:127843765 | T | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0015 others(52): Show |
56 | HG00597.hp2 HG01070.hp1 HG01081.hp2 others(53): Show |
intron_variant | MODIFIER | c.68-520A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843765 | |||||||
chr9:127843766 | T | A | 15 | a0001c0001t0001g0011 a0001c0001t0001g0108 a0001c0001t0001g0146 others(12): Show |
15 | HG00738.hp1 HG01123.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.68-521A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843766 | |||||||
chr9:127843767 | T | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(117): Show |
123 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.68-522A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843767 | |||||||
chr9:127843768 | T | A | 18 | a0001c0001t0001g0011 a0001c0001t0001g0052 a0001c0001t0001g0100 others(15): Show |
18 | HG00099.hp2 HG01243.hp1 HG02083.hp1 others(15): Show |
intron_variant | MODIFIER | c.68-523A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843768 | |||||||
chr9:127843769 | T | A | 122 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(119): Show |
125 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.68-524A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843769 | |||||||
chr9:127843770 | T | A | 15 | a0001c0001t0001g0052 a0001c0001t0001g0100 a0001c0001t0001g0108 others(12): Show |
15 | HG00099.hp2 HG01243.hp1 HG02083.hp1 others(12): Show |
intron_variant | MODIFIER | c.68-525A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843770 | |||||||
chr9:127843771 | T | A | 81 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0097 others(78): Show |
83 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.68-526A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843771 | |||||||
chr9:127843772 | T | A | 9 | a0001c0001t0001g0052 a0001c0001t0001g0100 a0001c0001t0001g0206 others(6): Show |
9 | HG00099.hp2 HG02135.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.68-527A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843772 | |||||||
chr9:127843773 | T | A | 13 | a0001c0001t0001g0006 a0001c0001t0001g0112 a0001c0001t0001g0211 others(10): Show |
14 | HG01081.hp2 HG01167.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.68-528A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843773 | |||||||
chr9:127843775 | T | A | 2 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.68-530A>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843775 | |||||||
chr9:127843998 | T | C | 335 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(332): Show |
341 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(338): Show |
intron_variant | MODIFIER | c.68-753A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127843998 | |||||||
chr9:127844409 | G | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0217 others(1): Show |
4 | HG02280.hp2 HG02615.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-1164C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127844409 | |||||||
chr9:127844469 | G | A | 4 | a0001c0001t0001g0048 a0001c0001t0001g0061 a0001c0001t0001g0062 others(1): Show |
4 | HG01884.hp1 HG02895.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-1224C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127844469 | |||||||
chr9:127844501 | G | GCAGCCT | 255 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(252): Show |
258 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.68-1262_68-1257dup others(6): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127844501 | |||||||
chr9:127844709 | A | G | 1 | a0012c0020t0001g0060 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.68-1464T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127844709 | |||||||
chr9:127844718 | C | T | 10 | a0001c0001t0001g0142 a0001c0001t0001g0218 a0001c0001t0001g0219 others(7): Show |
10 | HG00642.hp2 HG00738.hp1 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.68-1473G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127844718 | |||||||
chr9:127844727 | C | G | 1 | a0001c0001t0012g0338 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.68-1482G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127844727 | |||||||
chr9:127844927 | C | G | 1 | a0001c0001t0001g0013 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.68-1682G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127844927 | |||||||
chr9:127845031 | G | T | 3 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 |
3 | HG01255.hp2 HG02273.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.68-1786C>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127845031 | |||||||
chr9:127845080 | G | A | 115 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0102 others(112): Show |
115 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.68-1835C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127845080 | |||||||
chr9:127845176 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.68-1931G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127845176 | |||||||
chr9:127845209 | C | T | 3 | a0001c0001t0001g0302 a0001c0003t0002g0301 a0001c0016t0001g0059 |
3 | HG02970.hp1 HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.68-1964G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127845209 | |||||||
chr9:127845239 | T | G | 251 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(248): Show |
254 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.68-1994A>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127845239 | |||||||
chr9:127845359 | C | T | 6 | a0001c0001t0001g0139 a0001c0001t0001g0141 a0001c0001t0008g0138 others(3): Show |
6 | HG02145.hp2 HG02886.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-2114G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127845359 | |||||||
chr9:127845433 | T | C | 39 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0016 others(36): Show |
41 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.68-2188A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127845433 | |||||||
chr9:127845599 | T | C | 1 | a0001c0003t0002g0259 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.68-2354A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127845599 | |||||||
chr9:127845832 | A | G | 335 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(332): Show |
341 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(338): Show |
intron_variant | MODIFIER | c.68-2587T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127845832 | |||||||
chr9:127845853 | T | G | 258 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(255): Show |
261 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.68-2608A>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127845853 | |||||||
chr9:127845968 | A | T | 1 | a0001c0001t0001g0112 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.68-2723T>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127845968 | |||||||
chr9:127846017 | T | G | 45 | a0001c0001t0001g0064 a0001c0001t0001g0279 a0001c0001t0001g0316 others(42): Show |
47 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.68-2772A>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127846017 | |||||||
chr9:127846073 | T | G | 9 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0296 others(6): Show |
9 | HG02280.hp2 HG02615.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.68-2828A>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127846073 | |||||||
chr9:127846128 | G | A | 6 | a0001c0002t0001g0068 a0001c0002t0001g0311 a0001c0002t0001g0312 others(3): Show |
6 | NA18963.hp2 NA18981.hp1 NA19002.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-2883C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127846128 | |||||||
chr9:127846160 | C | A | 3 | a0001c0002t0001g0051 a0001c0002t0001g0055 a0001c0002t0006g0056 |
3 | HG03041.hp1 HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.68-2915G>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127846160 | |||||||
chr9:127846259 | G | A | 37 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0016 others(34): Show |
39 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.68-3014C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127846259 | |||||||
chr9:127846549 | G | T | 1 | a0001c0002t0001g0055 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.68-3304C>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127846549 | |||||||
chr9:127846620 | G | C | 2 | a0001c0001t0001g0302 a0001c0003t0002g0301 |
2 | HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.68-3375C>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127846620 | |||||||
chr9:127846667 | G | A | 19 | a0001c0001t0001g0137 a0001c0001t0001g0260 a0001c0001t0001g0261 others(16): Show |
19 | HG00741.hp1 HG01993.hp1 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.68-3422C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127846667 | |||||||
chr9:127846818 | G | A | 1 | a0001c0001t0012g0338 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.68-3573C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127846818 | |||||||
chr9:127847043 | CCTCT | C | 6 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 others(3): Show |
6 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.68-3802_68-3799del others(4): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127847043 | |||||||
chr9:127847050 | GAGCCTCA others(5): Show |
G | 1 | a0001c0002t0001g0051 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.68-3817_68-3806del others(12): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127847050 | |||||||
chr9:127847096 | G | T | 3 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0315 |
3 | HG04184.hp2 NA18941.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.68-3851C>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127847096 | |||||||
chr9:127847237 | T | C | 1 | a0001c0001t0012g0338 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.68-3992A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127847237 | |||||||
chr9:127847278 | C | T | 2 | a0001c0001t0001g0302 a0001c0003t0002g0301 |
2 | HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.68-4033G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127847278 | |||||||
chr9:127847450 | C | T | 3 | a0001c0002t0001g0051 a0001c0002t0001g0055 a0001c0002t0006g0056 |
3 | HG03041.hp1 HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.68-4205G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127847450 | |||||||
chr9:127847469 | C | T | 300 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(297): Show |
304 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(301): Show |
intron_variant | MODIFIER | c.68-4224G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127847469 | |||||||
chr9:127847560 | C | A | 1 | a0001c0003t0002g0135 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.68-4315G>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127847560 | |||||||
chr9:127847560 | C | T | 2 | a0001c0001t0001g0293 a0001c0001t0001g0294 |
2 | HG02647.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.68-4315G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127847560 | |||||||
chr9:127847638 | C | T | 2 | a0001c0001t0001g0302 a0001c0003t0002g0301 |
2 | HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.68-4393G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127847638 | |||||||
chr9:127847669 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.68-4424G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127847669 | |||||||
chr9:127847720 | C | G | 2 | a0001c0016t0001g0059 a0012c0020t0001g0060 |
2 | HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.68-4475G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127847720 | |||||||
chr9:127847736 | C | T | 268 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(265): Show |
273 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(270): Show |
intron_variant | MODIFIER | c.68-4491G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127847736 | |||||||
chr9:127847797 | C | A | 2 | a0001c0001t0001g0282 a0001c0001t0001g0283 |
2 | HG00741.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.68-4552G>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127847797 | |||||||
chr9:127847944 | T | C | 1 | a0001c0001t0001g0315 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.68-4699A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127847944 | |||||||
chr9:127847992 | T | C | 1 | a0002c0004t0001g0284 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.68-4747A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127847992 | |||||||
chr9:127848062 | C | A | 1 | a0001c0001t0001g0285 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.68-4817G>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127848062 | |||||||
chr9:127848083 | C | T | 3 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0002c0012t0001g0308 |
3 | HG02572.hp1 NA18522.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.68-4838G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127848083 | |||||||
chr9:127848084 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.68-4839C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127848084 | |||||||
chr9:127848116 | C | T | 3 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0003t0002g0014 |
3 | HG02280.hp2 HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.68-4871G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127848116 | |||||||
chr9:127848166 | T | C | 333 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(330): Show |
339 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.68-4921A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127848166 | |||||||
chr9:127848262 | A | G | 333 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(330): Show |
339 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.68-5017T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127848262 | |||||||
chr9:127848288 | C | CT | 32 | a0001c0001t0001g0097 a0001c0001t0001g0102 a0001c0001t0001g0103 others(29): Show |
32 | HG01070.hp1 HG01433.hp1 HG01496.hp2 others(29): Show |
intron_variant | MODIFIER | c.68-5044dupA | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127848288 | |||||||
chr9:127848329 | T | G | 333 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(330): Show |
339 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.68-5084A>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127848329 | |||||||
chr9:127848446 | C | G | 13 | a0001c0001t0001g0305 a0003c0005t0001g0324 a0003c0005t0001g0325 others(10): Show |
13 | HG00639.hp2 HG01069.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.68-5201G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127848446 | |||||||
chr9:127848471 | A | G | 2 | a0001c0016t0001g0059 a0012c0020t0001g0060 |
2 | HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.68-5226T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127848471 | |||||||
chr9:127848507 | T | C | 333 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(330): Show |
339 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.68-5262A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127848507 | |||||||
chr9:127848590 | A | G | 325 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(322): Show |
330 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(327): Show |
intron_variant | MODIFIER | c.68-5345T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127848590 | |||||||
chr9:127848817 | G | A | 3 | a0001c0006t0001g0004 a0001c0006t0001g0057 a0001c0006t0001g0058 |
4 | HG01167.hp1 HG02723.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+5472C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127848817 | |||||||
chr9:127848881 | C | G | 1 | a0001c0001t0001g0113 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.67+5408G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127848881 | |||||||
chr9:127849100 | G | T | 214 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(211): Show |
217 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.67+5189C>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127849100 | |||||||
chr9:127849125 | G | A | 2 | a0001c0001t0001g0050 a0001c0022t0001g0049 |
2 | HG02055.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.67+5164C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127849125 | |||||||
chr9:127849179 | C | A | 1 | a0001c0006t0001g0058 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.67+5110G>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127849179 | |||||||
chr9:127849244 | C | G | 43 | a0001c0001t0001g0305 a0001c0002t0001g0002 a0001c0002t0001g0003 others(40): Show |
45 | HG00323.hp2 HG00639.hp2 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.67+5045G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127849244 | |||||||
chr9:127849512 | G | A | 2 | a0001c0001t0001g0105 a0001c0001t0001g0287 |
2 | HG02056.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.67+4777C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127849512 | |||||||
chr9:127849523 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.67+4766G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127849523 | |||||||
chr9:127849614 | G | A | 3 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0010 |
3 | HG00609.hp1 HG02129.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.67+4675C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127849614 | |||||||
chr9:127849626 | G | A | 214 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(211): Show |
217 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.67+4663C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127849626 | |||||||
chr9:127849712 | C | T | 2 | a0003c0005t0001g0324 a0003c0005t0001g0325 |
2 | HG02615.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.67+4577G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127849712 | |||||||
chr9:127849732 | A | C | 1 | a0001c0001t0001g0111 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.67+4557T>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127849732 | |||||||
chr9:127849748 | T | C | 1 | a0001c0002t0001g0051 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.67+4541A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127849748 | |||||||
chr9:127849939 | A | C | 30 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0016 others(27): Show |
32 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.67+4350T>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127849939 | |||||||
chr9:127850104 | C | A | 247 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(244): Show |
250 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.67+4185G>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127850104 | |||||||
chr9:127850180 | A | G | 13 | a0001c0001t0001g0305 a0003c0005t0001g0324 a0003c0005t0001g0325 others(10): Show |
13 | HG00639.hp2 HG01069.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.67+4109T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127850180 | |||||||
chr9:127850344 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.67+3945G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127850344 | |||||||
chr9:127850386 | A | C | 30 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0016 others(27): Show |
32 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.67+3903T>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127850386 | |||||||
chr9:127850390 | T | G | 2 | a0001c0001t0001g0288 a0001c0001t0001g0289 |
2 | NA19006.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.67+3899A>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127850390 | |||||||
chr9:127850510 | G | C | 1 | a0001c0001t0001g0290 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.67+3779C>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127850510 | |||||||
chr9:127850748 | A | C | 1 | a0001c0016t0001g0059 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.67+3541T>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127850748 | |||||||
chr9:127850781 | C | T | 12 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0106 others(9): Show |
12 | HG02280.hp2 HG02615.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.67+3508G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127850781 | |||||||
chr9:127850840 | G | A | 1 | a0001c0001t0001g0300 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.67+3449C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127850840 | |||||||
chr9:127850977 | T | C | 1 | a0001c0006t0010g0336 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.67+3312A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127850977 | |||||||
chr9:127850987 | G | A | 1 | a0001c0001t0001g0291 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.67+3302C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127850987 | |||||||
chr9:127851003 | C | T | 2 | a0001c0002t0001g0018 a0001c0008t0001g0017 |
2 | HG01099.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.67+3286G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127851003 | |||||||
chr9:127851052 | A | T | 1 | a0001c0001t0001g0105 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.67+3237T>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127851052 | |||||||
chr9:127851105 | T | C | 38 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0296 others(35): Show |
40 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.67+3184A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127851105 | |||||||
chr9:127851312 | C | T | 1 | a0001c0016t0001g0059 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.67+2977G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127851312 | |||||||
chr9:127851364 | C | T | 3 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 |
3 | HG01496.hp2 HG02886.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.67+2925G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127851364 | |||||||
chr9:127851450 | C | A | 4 | a0001c0002t0001g0003 a0001c0002t0001g0041 a0001c0002t0001g0042 others(1): Show |
5 | HG01109.hp2 HG01891.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+2839G>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127851450 | |||||||
chr9:127851582 | G | T | 334 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(331): Show |
340 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(337): Show |
intron_variant | MODIFIER | c.67+2707C>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127851582 | |||||||
chr9:127851706 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.67+2583G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127851706 | |||||||
chr9:127851735 | C | T | 8 | a0001c0002t0001g0051 a0001c0002t0001g0055 a0001c0002t0006g0056 others(5): Show |
9 | HG01167.hp1 HG02723.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.67+2554G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127851735 | |||||||
chr9:127851747 | C | T | 2 | a0001c0001t0001g0099 a0001c0001t0001g0100 |
2 | HG00621.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.67+2542G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127851747 | |||||||
chr9:127852030 | T | C | 39 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0070 others(36): Show |
39 | HG00438.hp1 HG00609.hp2 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.67+2259A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127852030 | |||||||
chr9:127852077 | G | A | 3 | a0001c0001t0001g0293 a0001c0001t0001g0294 a0001c0002t0001g0295 |
3 | HG01346.hp1 HG02647.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.67+2212C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127852077 | |||||||
chr9:127852359 | G | T | 2 | a0001c0001t0001g0097 a0001c0001t0001g0098 |
2 | HG00597.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.67+1930C>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127852359 | |||||||
chr9:127852385 | G | A | 5 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(2): Show |
5 | HG02622.hp2 HG03486.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.67+1904C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127852385 | |||||||
chr9:127852457 | G | A | 2 | a0001c0001t0001g0302 a0001c0003t0002g0301 |
2 | HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.67+1832C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127852457 | |||||||
chr9:127852626 | T | C | 37 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(34): Show |
39 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.67+1663A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127852626 | |||||||
chr9:127852633 | G | A | 227 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(224): Show |
230 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.67+1656C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127852633 | |||||||
chr9:127852719 | G | A | 1 | a0001c0001t0001g0303 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.67+1570C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127852719 | |||||||
chr9:127852909 | C | T | 1 | a0001c0003t0002g0065 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.67+1380G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127852909 | |||||||
chr9:127852939 | G | A | 6 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(3): Show |
6 | HG02145.hp1 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.67+1350C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127852939 | |||||||
chr9:127852993 | A | C | 1 | a0001c0001t0001g0064 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.67+1296T>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127852993 | |||||||
chr9:127853303 | C | T | 1 | a0001c0002t0001g0016 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.67+986G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127853303 | |||||||
chr9:127853381 | G | A | 1 | a0001c0001t0001g0304 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.67+908C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127853381 | |||||||
chr9:127853472 | G | A | 265 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(262): Show |
268 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.67+817C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127853472 | |||||||
chr9:127853474 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.67+815G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127853474 | |||||||
chr9:127853543 | C | G | 1 | a0001c0002t0001g0051 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.67+746G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127853543 | |||||||
chr9:127853544 | C | A | 1 | a0001c0002t0001g0051 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.67+745G>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127853544 | |||||||
chr9:127853545 | C | A | 1 | a0001c0002t0001g0051 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.67+744G>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127853545 | |||||||
chr9:127853546 | C | A | 1 | a0001c0002t0001g0051 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.67+743G>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127853546 | |||||||
chr9:127853547 | A | AGACGAAA others(6): Show |
1 | a0001c0002t0001g0051 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.67+741_67+742insAA others(11): Show |
ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127853547 | |||||||
chr9:127853548 | C | G | 1 | a0001c0002t0001g0051 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.67+741G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127853548 | |||||||
chr9:127853551 | A | G | 1 | a0001c0002t0001g0051 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.67+738T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127853551 | |||||||
chr9:127853553 | C | T | 1 | a0001c0002t0001g0051 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.67+736G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127853553 | |||||||
chr9:127853554 | C | G | 1 | a0001c0002t0001g0051 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.67+735G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127853554 | |||||||
chr9:127853555 | C | G | 1 | a0001c0002t0001g0051 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.67+734G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127853555 | |||||||
chr9:127853556 | C | T | 1 | a0001c0002t0001g0051 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.67+733G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127853556 | |||||||
chr9:127853558 | A | G | 1 | a0001c0002t0001g0051 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.67+731T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127853558 | |||||||
chr9:127853583 | C | G | 1 | a0001c0002t0001g0051 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.67+706G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127853583 | |||||||
chr9:127853596 | T | G | 1 | a0001c0002t0001g0051 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.67+693A>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127853596 | |||||||
chr9:127853597 | C | G | 1 | a0001c0002t0001g0051 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.67+692G>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127853597 | |||||||
chr9:127853674 | C | T | 2 | a0001c0001t0001g0050 a0001c0022t0001g0049 |
2 | HG02055.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.67+615G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127853674 | |||||||
chr9:127853813 | C | T | 3 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0003t0002g0014 |
3 | HG02280.hp2 HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.67+476G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127853813 | |||||||
chr9:127853820 | G | A | 14 | a0001c0001t0001g0305 a0003c0005t0001g0323 a0003c0005t0001g0324 others(11): Show |
14 | HG00639.hp2 HG01069.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.67+469C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127853820 | |||||||
chr9:127853860 | A | G | 45 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0044 others(42): Show |
47 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.67+429T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127853860 | |||||||
chr9:127853984 | G | A | 10 | a0001c0001t0001g0306 a0001c0001t0001g0307 a0001c0001t0001g0309 others(7): Show |
10 | HG04184.hp2 NA18941.hp2 NA18963.hp2 others(7): Show |
intron_variant | MODIFIER | c.67+305C>T | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127853984 | |||||||
chr9:127854035 | T | C | 6 | a0001c0001t0001g0316 a0001c0001t0001g0317 a0001c0001t0001g0318 others(3): Show |
6 | HG02280.hp1 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.67+254A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127854035 | |||||||
chr9:127854091 | C | T | 1 | a0001c0003t0001g0012 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.67+198G>A | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127854091 | |||||||
chr9:127854114 | A | G | 2 | a0001c0001t0001g0001 a0001c0001t0001g0011 |
3 | NA18952.hp2 NA19000.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.67+175T>C | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127854114 | |||||||
chr9:127854259 | T | C | 1 | a0001c0001t0001g0322 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.67+30A>G | ENG | ENSG00000106991.14 | transcript | ENST00000373203.9 | protein_coding | 1/14 | chr9 | 127854259 |