Item | Value |
---|---|
geneid | 84717 |
ensemblid | ENSG00000167674.15 |
hgncid | 14680 |
symbol | HDGFL2 |
name | HDGF like 2 |
refseq_nuc | NM_001001520.3 |
refseq_prot | NP_001001520.1 |
ensembl_nuc | ENST00000616600.5 |
ensembl_prot | ENSP00000483345.1 |
mane_status | MANE Select |
chr | chr19 |
start | 4472297 |
end | 4502207 |
strand | + |
ver | v1.2 |
region | chr19:4472297-4502207 |
region5000 | chr19:4467297-4507207 |
regionname0 | HDGFL2_chr19_4472297_4502207 |
regionname5000 | HDGFL2_chr19_4467297_4507207 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 671 | 332 | 82 | 72 | 113 | 18 | 45 | 81 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | MPHAF others(666): Show |
chr19 | 4467297 | 4507207 |
a0002 | 0/0 | 671 | 7 | 0 | 0 | 7 | 0 | 0 | 2 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | MPHAF others(666): Show |
chr19 | 4467297 | 4507207 |
a0003 | 0/0 | 378 | 7 | 2 | 1 | 3 | 0 | 1 | 3 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | MPHAF others(373): Show |
chr19 | 4467297 | 4507207 |
a0004 | 0/0 | 671 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | MPHAF others(666): Show |
chr19 | 4467297 | 4507207 |
a0005 | 0/0 | 671 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | MPHAF others(666): Show |
chr19 | 4467297 | 4507207 |
a0006 | 0/0 | 671 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | MPHAF others(666): Show |
chr19 | 4467297 | 4507207 |
a0007 | 0/0 | 671 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | MPHAF others(666): Show |
chr19 | 4467297 | 4507207 |
a0008 | 0/0 | 671 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | MPHAF others(666): Show |
chr19 | 4467297 | 4507207 |
a0009 | 0/0 | 671 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | MPHAF others(666): Show |
chr19 | 4467297 | 4507207 |
a0010 | 0/0 | 671 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | MPHAF others(666): Show |
chr19 | 4467297 | 4507207 |
a0011 | 0/0 | 671 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | MPHAF others(666): Show |
chr19 | 4467297 | 4507207 |
a0012 | 0/0 | 671 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | MPHVF others(666): Show |
chr19 | 4467297 | 4507207 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2013 | 180 | 48 | 43 | 53 | 11 | 25 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | ATGCC others(2008): Show |
chr19 | 4467297 | 4507207 | ||
a0001c0002 | 1/1 | 2013 | 144 | 29 | 28 | 60 | 7 | 18 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | ATGCC others(2008): Show |
chr19 | 4467297 | 4507207 | ||
a0001c0008 | 0/0 | 2013 | 2 | 2 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | ATGCC others(2008): Show |
chr19 | 4467297 | 4507207 | ||
a0001c0011 | 0/0 | 2013 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | ATGCC others(2008): Show |
chr19 | 4467297 | 4507207 | ||
a0001c0014 | 0/0 | 2013 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | ATGCC others(2008): Show |
chr19 | 4467297 | 4507207 | ||
a0001c0015 | 0/0 | 2013 | 1 | 0 | 0 | 0 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | ATGCC others(2008): Show |
chr19 | 4467297 | 4507207 | ||
a0001c0016 | 0/0 | 2013 | 1 | 0 | 0 | 0 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | ATGCC others(2008): Show |
chr19 | 4467297 | 4507207 | ||
a0001c0017 | 0/0 | 2013 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | ATGCC others(2008): Show |
chr19 | 4467297 | 4507207 | ||
a0001c0019 | 0/0 | 2013 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | ATGCC others(2008): Show |
chr19 | 4467297 | 4507207 | ||
a0002c0003 | 0/0 | 2013 | 7 | 0 | 0 | 7 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | ATGCC others(2008): Show |
chr19 | 4467297 | 4507207 | ||
a0003c0004 | 0/0 | 2014 | 4 | 1 | 1 | 1 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | ATGCC others(2009): Show |
chr19 | 4467297 | 4507207 | ||
a0003c0006 | 0/0 | 2014 | 3 | 1 | 0 | 2 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | ATGCC others(2009): Show |
chr19 | 4467297 | 4507207 | ||
a0004c0005 | 0/0 | 2013 | 3 | 3 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | ATGCC others(2008): Show |
chr19 | 4467297 | 4507207 | ||
a0005c0007 | 0/0 | 2013 | 2 | 2 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | ATGCC others(2008): Show |
chr19 | 4467297 | 4507207 | ||
a0006c0009 | 0/0 | 2013 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | ATGCC others(2008): Show |
chr19 | 4467297 | 4507207 | ||
a0007c0010 | 0/0 | 2013 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | ATGCC others(2008): Show |
chr19 | 4467297 | 4507207 | ||
a0008c0020 | 0/0 | 2013 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | ATGCC others(2008): Show |
chr19 | 4467297 | 4507207 | ||
a0009c0013 | 0/0 | 2013 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | ATGCC others(2008): Show |
chr19 | 4467297 | 4507207 | ||
a0010c0018 | 0/0 | 2013 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | ATGCC others(2008): Show |
chr19 | 4467297 | 4507207 | ||
a0011c0012 | 0/0 | 2013 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | ATGCC others(2008): Show |
chr19 | 4467297 | 4507207 | ||
a0012c0021 | 0/0 | 2013 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | ATGCC others(2008): Show |
chr19 | 4467297 | 4507207 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2267 | 104 | 14 | 38 | 36 | 4 | 12 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | AGCCG others(2262): Show |
chr19 | 4467297 | 4507207 |
a0001c0001t0002 | 0/0 | 2267 | 8 | 5 | 1 | 2 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | AGCCG others(2262): Show |
chr19 | 4467297 | 4507207 |
a0001c0001t0003 | 0/0 | 2267 | 49 | 14 | 2 | 15 | 6 | 12 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | AGCCG others(2262): Show |
chr19 | 4467297 | 4507207 |
a0001c0001t0004 | 0/0 | 2267 | 6 | 4 | 1 | 0 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | AGCCG others(2262): Show |
chr19 | 4467297 | 4507207 |
a0001c0001t0006 | 0/0 | 2267 | 6 | 5 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | AGCCG others(2262): Show |
chr19 | 4467297 | 4507207 |
a0001c0001t0008 | 0/0 | 2267 | 4 | 4 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | AGCCG others(2262): Show |
chr19 | 4467297 | 4507207 |
a0001c0001t0012 | 0/0 | 2267 | 1 | 0 | 0 | 0 | 1 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | AGCCG others(2262): Show |
chr19 | 4467297 | 4507207 |
a0001c0001t0013 | 0/0 | 2267 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | AGCCG others(2262): Show |
chr19 | 4467297 | 4507207 |
a0001c0001t0014 | 0/0 | 2267 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | AGCCG others(2262): Show |
chr19 | 4467297 | 4507207 |
a0001c0002t0001 | 0/0 | 2267 | 13 | 6 | 1 | 4 | 1 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | AGCCG others(2262): Show |
chr19 | 4467297 | 4507207 |
a0001c0002t0002 | 1/1 | 2267 | 101 | 5 | 21 | 53 | 5 | 15 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | AGCCG others(2262): Show |
chr19 | 4467297 | 4507207 |
a0001c0002t0003 | 0/0 | 2267 | 3 | 2 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | AGCCG others(2262): Show |
chr19 | 4467297 | 4507207 |
a0001c0002t0004 | 0/0 | 2267 | 12 | 4 | 5 | 0 | 1 | 2 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | AGCCG others(2262): Show |
chr19 | 4467297 | 4507207 |
a0001c0002t0005 | 0/0 | 2267 | 9 | 9 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | AGCCG others(2262): Show |
chr19 | 4467297 | 4507207 |
a0001c0002t0007 | 0/0 | 2267 | 3 | 0 | 0 | 3 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | AGCCG others(2262): Show |
chr19 | 4467297 | 4507207 |
a0001c0002t0009 | 0/0 | 2267 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | AGCCG others(2262): Show |
chr19 | 4467297 | 4507207 |
a0001c0002t0010 | 0/0 | 2267 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | AGCCG others(2262): Show |
chr19 | 4467297 | 4507207 |
a0001c0002t0011 | 0/0 | 2267 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | AGCCG others(2262): Show |
chr19 | 4467297 | 4507207 |
a0001c0008t0003 | 0/0 | 2267 | 2 | 2 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | AGCCG others(2262): Show |
chr19 | 4467297 | 4507207 |
a0001c0011t0001 | 0/0 | 2267 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | AGCCG others(2262): Show |
chr19 | 4467297 | 4507207 |
a0001c0014t0009 | 0/0 | 2267 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | AGCCG others(2262): Show |
chr19 | 4467297 | 4507207 |
a0001c0015t0001 | 0/0 | 2267 | 1 | 0 | 0 | 0 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | AGCCG others(2262): Show |
chr19 | 4467297 | 4507207 |
a0001c0016t0002 | 0/0 | 2267 | 1 | 0 | 0 | 0 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | AGCCG others(2262): Show |
chr19 | 4467297 | 4507207 |
a0001c0017t0003 | 0/0 | 2267 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | AGCCG others(2262): Show |
chr19 | 4467297 | 4507207 |
a0001c0019t0001 | 0/0 | 2267 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | AGCCG others(2262): Show |
chr19 | 4467297 | 4507207 |
a0002c0003t0002 | 0/0 | 2267 | 5 | 0 | 0 | 5 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | AGCCG others(2262): Show |
chr19 | 4467297 | 4507207 |
a0002c0003t0007 | 0/0 | 2267 | 2 | 0 | 0 | 2 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | AGCCG others(2262): Show |
chr19 | 4467297 | 4507207 |
a0003c0004t0002 | 0/0 | 2268 | 3 | 0 | 1 | 1 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | AGCCG others(2263): Show |
chr19 | 4467297 | 4507207 |
a0003c0004t0005 | 0/0 | 2268 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | AGCCG others(2263): Show |
chr19 | 4467297 | 4507207 |
a0003c0006t0001 | 0/0 | 2268 | 2 | 1 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | AGCCG others(2263): Show |
chr19 | 4467297 | 4507207 |
a0003c0006t0003 | 0/0 | 2268 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | AGCCG others(2263): Show |
chr19 | 4467297 | 4507207 |
a0004c0005t0001 | 0/0 | 2267 | 3 | 3 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | AGCCG others(2262): Show |
chr19 | 4467297 | 4507207 |
a0005c0007t0003 | 0/0 | 2267 | 2 | 2 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | AGCCG others(2262): Show |
chr19 | 4467297 | 4507207 |
a0006c0009t0002 | 0/0 | 2267 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | AGCCG others(2262): Show |
chr19 | 4467297 | 4507207 |
a0007c0010t0002 | 0/0 | 2267 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | AGCCG others(2262): Show |
chr19 | 4467297 | 4507207 |
a0008c0020t0004 | 0/0 | 2267 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | AGCCG others(2262): Show |
chr19 | 4467297 | 4507207 |
a0009c0013t0002 | 0/0 | 2267 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | AGCCG others(2262): Show |
chr19 | 4467297 | 4507207 |
a0010c0018t0005 | 0/0 | 2267 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | AGCCG others(2262): Show |
chr19 | 4467297 | 4507207 |
a0011c0012t0002 | 0/0 | 2267 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | AGCCG others(2262): Show |
chr19 | 4467297 | 4507207 |
a0012c0021t0002 | 0/0 | 2267 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | AGCCG others(2262): Show |
chr19 | 4467297 | 4507207 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0003g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0004g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0004g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0004g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0006g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0006g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0006g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0006g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0006g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0008g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0008g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0008g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0008g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0012g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0013g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0001t0014g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0001g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0001 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0009 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0012 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0344 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0004g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0004g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0004g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0004g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0004g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0004g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0004g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0004g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0005g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0005g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0005g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0005g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0005g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0005g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0005g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0005g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0007g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0007g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0007g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0009g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0010g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0002t0011g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0008t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0008t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0011t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0014t0009g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0015t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0016t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0017t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0001c0019t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0002c0003t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0002c0003t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0002c0003t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0002c0003t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0002c0003t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0002c0003t0007g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0002c0003t0007g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0003c0004t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0003c0004t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0003c0004t0002g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0003c0004t0005g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0003c0006t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0003c0006t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0003c0006t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0004c0005t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0004c0005t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0004c0005t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0005c0007t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0005c0007t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0006c0009t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0007c0010t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0008c0020t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0009c0013t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0010c0018t0005g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0011c0012t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
a0012c0021t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0042 | EUR | GBR | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG00099 | hp2 | a0001 | c0002 | t0002 | g0312 | EUR | GBR | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0180 | EUR | GBR | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG00140 | hp2 | a0001 | c0001 | t0003 | g0056 | EUR | GBR | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0141 | EUR | FIN | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG00280 | hp2 | a0001 | c0001 | t0012 | g0294 | EUR | FIN | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG00323 | hp1 | a0001 | c0002 | t0001 | g0342 | EUR | FIN | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0197 | EUR | FIN | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG00438 | hp1 | a0002 | c0003 | t0002 | g0277 | EAS | CHS | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG00438 | hp2 | a0001 | c0002 | t0002 | g0276 | EAS | CHS | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG00544 | hp1 | a0001 | c0002 | t0002 | g0203 | EAS | CHS | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG00558 | hp1 | a0001 | c0002 | t0002 | g0222 | EAS | CHS | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG00558 | hp2 | a0001 | c0002 | t0002 | g0262 | EAS | CHS | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG00597 | hp1 | a0001 | c0002 | t0002 | g0227 | EAS | CHS | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG00597 | hp2 | a0002 | c0003 | t0002 | g0223 | EAS | CHS | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG00609 | hp1 | a0001 | c0002 | t0002 | g0244 | EAS | CHS | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | CHS | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG00642 | hp1 | a0001 | c0002 | t0002 | g0335 | AMR | PUR | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG00642 | hp2 | a0001 | c0002 | t0002 | g0238 | AMR | PUR | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG00673 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | CHS | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG00673 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | CHS | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG00735 | hp2 | a0001 | c0014 | t0009 | g0209 | AMR | PUR | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG00738 | hp2 | a0003 | c0004 | t0002 | g0270 | AMR | PUR | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0132 | AMR | PUR | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01069 | hp2 | a0001 | c0002 | t0002 | g0343 | AMR | PUR | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01070 | hp1 | a0001 | c0002 | t0002 | g0010 | AMR | PUR | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01070 | hp2 | a0001 | c0002 | t0004 | g0022 | AMR | PUR | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01071 | hp1 | a0001 | c0002 | t0004 | g0011 | AMR | PUR | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01074 | hp2 | a0001 | c0002 | t0004 | g0063 | AMR | PUR | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01081 | hp2 | a0001 | c0002 | t0002 | g0254 | AMR | PUR | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01099 | hp1 | a0001 | c0002 | t0004 | g0021 | AMR | PUR | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01099 | hp2 | a0001 | c0002 | t0002 | g0280 | AMR | PUR | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01106 | hp2 | a0001 | c0002 | t0002 | g0309 | AMR | PUR | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01109 | hp2 | a0001 | c0001 | t0006 | g0029 | AMR | PUR | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0139 | AMR | PUR | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01167 | hp2 | a0001 | c0002 | t0002 | g0337 | AMR | PUR | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01168 | hp1 | a0001 | c0002 | t0002 | g0331 | AMR | PUR | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01169 | hp1 | a0001 | c0002 | t0002 | g0338 | AMR | PUR | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01175 | hp2 | a0001 | c0002 | t0004 | g0025 | AMR | PUR | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01192 | hp1 | a0001 | c0002 | t0002 | g0260 | AMR | PUR | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01192 | hp2 | a0001 | c0002 | t0002 | g0265 | AMR | PUR | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01243 | hp1 | a0001 | c0002 | t0002 | g0315 | AMR | PUR | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01256 | hp1 | a0001 | c0002 | t0002 | g0322 | AMR | CLM | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01261 | hp1 | a0001 | c0002 | t0001 | g0250 | AMR | CLM | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01358 | hp2 | a0001 | c0002 | t0002 | g0310 | AMR | CLM | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01515 | hp1 | a0001 | c0001 | t0003 | g0140 | EUR | IBS | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0032 | EUR | IBS | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01516 | hp1 | a0001 | c0002 | t0002 | g0317 | EUR | IBS | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01516 | hp2 | a0001 | c0002 | t0002 | g0279 | EUR | IBS | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01517 | hp1 | a0001 | c0002 | t0002 | g0258 | EUR | IBS | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0043 | EUR | IBS | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01884 | hp1 | a0001 | c0002 | t0004 | g0070 | AFR | ACB | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01884 | hp2 | a0001 | c0001 | t0006 | g0160 | AFR | ACB | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01891 | hp1 | a0001 | c0008 | t0003 | g0037 | AFR | ACB | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01891 | hp2 | a0001 | c0001 | t0003 | g0076 | AFR | ACB | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01934 | hp2 | a0001 | c0002 | t0003 | g0064 | AMR | PEL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01952 | hp1 | a0001 | c0002 | t0002 | g0234 | AMR | PEL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01975 | hp2 | a0001 | c0002 | t0002 | g0320 | AMR | PEL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01978 | hp1 | a0001 | c0002 | t0002 | g0264 | AMR | PEL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02015 | hp1 | a0001 | c0002 | t0002 | g0291 | EAS | KHV | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02015 | hp2 | a0001 | c0002 | t0002 | g0259 | EAS | KHV | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02027 | hp1 | a0001 | c0002 | t0002 | g0205 | EAS | KHV | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02027 | hp2 | a0006 | c0009 | t0002 | g0228 | EAS | KHV | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02040 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02040 | hp2 | a0002 | c0003 | t0002 | g0247 | EAS | KHV | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02055 | hp1 | a0001 | c0002 | t0003 | g0024 | AFR | ACB | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02055 | hp2 | a0001 | c0002 | t0001 | g0248 | AFR | ACB | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02056 | hp1 | a0001 | c0002 | t0002 | g0268 | EAS | KHV | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02056 | hp2 | a0001 | c0002 | t0002 | g0204 | EAS | KHV | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02074 | hp2 | a0002 | c0003 | t0002 | g0257 | EAS | KHV | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02080 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | KHV | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02129 | hp1 | a0001 | c0002 | t0007 | g0334 | EAS | KHV | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02132 | hp1 | a0001 | c0002 | t0002 | g0275 | EAS | KHV | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0038 | EAS | KHV | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02148 | hp1 | a0001 | c0002 | t0002 | g0323 | AMR | PEL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02148 | hp2 | a0001 | c0001 | t0004 | g0044 | AMR | PEL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | CDX | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0324 | EAS | CDX | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02165 | hp1 | a0001 | c0002 | t0002 | g0297 | EAS | CDX | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02165 | hp2 | a0001 | c0002 | t0002 | g0307 | EAS | CDX | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02257 | hp1 | a0001 | c0002 | t0005 | g0068 | AFR | ACB | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02257 | hp2 | a0001 | c0001 | t0004 | g0162 | AFR | ACB | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0211 | AFR | ACB | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02258 | hp2 | a0001 | c0002 | t0010 | g0224 | AFR | ACB | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02273 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02280 | hp1 | a0001 | c0002 | t0005 | g0069 | AFR | ACB | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02280 | hp2 | a0001 | c0002 | t0011 | g0319 | AFR | ACB | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0054 | AMR | PEL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02300 | hp2 | a0007 | c0010 | t0002 | g0269 | AMR | PEL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02451 | hp1 | a0001 | c0002 | t0003 | g0147 | AFR | ACB | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0210 | AFR | ACB | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02523 | hp1 | a0001 | c0001 | t0003 | g0146 | EAS | KHV | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02523 | hp2 | a0001 | c0002 | t0002 | g0267 | EAS | KHV | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02572 | hp2 | a0003 | c0004 | t0005 | g0150 | AFR | GWD | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02602 | hp1 | a0001 | c0015 | t0001 | g0097 | SAS | PJL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02615 | hp1 | a0003 | c0006 | t0001 | g0199 | AFR | GWD | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02615 | hp2 | a0001 | c0002 | t0002 | g0237 | AFR | GWD | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02622 | hp1 | a0001 | c0001 | t0006 | g0003 | AFR | GWD | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02630 | hp1 | a0001 | c0001 | t0008 | g0082 | AFR | GWD | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02630 | hp2 | a0001 | c0008 | t0003 | g0137 | AFR | GWD | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02647 | hp1 | a0001 | c0001 | t0014 | g0135 | AFR | GWD | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02647 | hp2 | a0001 | c0002 | t0005 | g0067 | AFR | GWD | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0142 | SAS | PJL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02698 | hp1 | a0001 | c0002 | t0002 | g0240 | SAS | PJL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0055 | SAS | PJL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02717 | hp1 | a0001 | c0001 | t0008 | g0164 | AFR | GWD | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02717 | hp2 | a0001 | c0002 | t0001 | g0305 | AFR | GWD | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02735 | hp1 | a0001 | c0002 | t0002 | g0133 | SAS | PJL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02735 | hp2 | a0001 | c0002 | t0002 | g0299 | SAS | PJL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02738 | hp1 | a0001 | c0002 | t0004 | g0027 | SAS | PJL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02738 | hp2 | a0001 | c0002 | t0002 | g0282 | SAS | PJL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02809 | hp1 | a0001 | c0002 | t0001 | g0242 | AFR | GWD | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02809 | hp2 | a0001 | c0001 | t0006 | g0003 | AFR | GWD | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02818 | hp1 | a0001 | c0001 | t0004 | g0081 | AFR | GWD | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02818 | hp2 | a0001 | c0002 | t0002 | g0333 | AFR | GWD | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02886 | hp1 | a0008 | c0020 | t0004 | g0026 | AFR | GWD | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02895 | hp1 | a0001 | c0001 | t0008 | g0083 | AFR | GWD | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02895 | hp2 | a0001 | c0001 | t0006 | g0079 | AFR | GWD | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0074 | AFR | GWD | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02897 | hp1 | a0001 | c0001 | t0008 | g0084 | AFR | GWD | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | GWD | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02922 | hp1 | a0001 | c0002 | t0001 | g0318 | AFR | ESN | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0286 | AFR | ESN | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02965 | hp1 | a0001 | c0002 | t0005 | g0149 | AFR | ESN | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0221 | AFR | ESN | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02970 | hp1 | a0001 | c0002 | t0002 | g0290 | AFR | ESN | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02970 | hp2 | a0001 | c0001 | t0003 | g0158 | AFR | ESN | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02976 | hp2 | a0001 | c0002 | t0005 | g0002 | AFR | ESN | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG03017 | hp1 | a0001 | c0002 | t0004 | g0065 | SAS | PJL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG03041 | hp1 | a0001 | c0019 | t0001 | g0233 | AFR | GWD | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG03098 | hp1 | a0001 | c0001 | t0004 | g0078 | AFR | MSL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG03098 | hp2 | a0005 | c0007 | t0003 | g0072 | AFR | MSL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG03130 | hp1 | a0001 | c0001 | t0003 | g0048 | AFR | ESN | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | ESN | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ESN | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG03139 | hp2 | a0001 | c0001 | t0004 | g0155 | AFR | ESN | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG03195 | hp1 | a0001 | c0002 | t0001 | g0296 | AFR | ESN | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG03195 | hp2 | a0001 | c0001 | t0003 | g0077 | AFR | ESN | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG03209 | hp1 | a0005 | c0007 | t0003 | g0073 | AFR | MSL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG03209 | hp2 | a0004 | c0005 | t0001 | g0184 | AFR | MSL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG03225 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | MSL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG03225 | hp2 | a0009 | c0013 | t0002 | g0249 | AFR | MSL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG03453 | hp1 | a0001 | c0002 | t0004 | g0071 | AFR | MSL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0036 | AFR | MSL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG03486 | hp1 | a0004 | c0005 | t0001 | g0183 | AFR | MSL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG03486 | hp2 | a0001 | c0002 | t0004 | g0152 | AFR | MSL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG03490 | hp1 | a0001 | c0001 | t0003 | g0143 | SAS | PJL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG03491 | hp1 | a0001 | c0002 | t0002 | g0010 | SAS | PJL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG03491 | hp2 | a0001 | c0002 | t0002 | g0311 | SAS | PJL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG03492 | hp1 | a0001 | c0002 | t0002 | g0009 | SAS | PJL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0051 | SAS | PJL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG03540 | hp1 | a0010 | c0018 | t0005 | g0151 | AFR | GWD | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG03540 | hp2 | a0001 | c0002 | t0004 | g0154 | AFR | GWD | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | MSL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | MSL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG03654 | hp1 | a0001 | c0002 | t0002 | g0202 | SAS | PJL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0293 | SAS | PJL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG03669 | hp1 | a0001 | c0002 | t0001 | g0346 | SAS | PJL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0047 | SAS | PJL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG03688 | hp1 | a0001 | c0002 | t0002 | g0278 | SAS | STU | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | STU | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0052 | SAS | PJL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0041 | SAS | BEB | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG03831 | hp2 | a0001 | c0002 | t0002 | g0281 | SAS | BEB | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0295 | SAS | BEB | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG03927 | hp1 | a0001 | c0002 | t0002 | g0229 | SAS | BEB | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG03927 | hp2 | a0001 | c0016 | t0002 | g0206 | SAS | BEB | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0057 | SAS | BEB | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG03942 | hp2 | a0001 | c0002 | t0002 | g0266 | SAS | BEB | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0020 | SAS | STU | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | STU | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0053 | SAS | BEB | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG04184 | hp2 | a0003 | c0004 | t0002 | g0340 | SAS | BEB | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG04199 | hp1 | a0001 | c0001 | t0004 | g0058 | SAS | STU | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG04199 | hp2 | a0001 | c0002 | t0002 | g0263 | SAS | STU | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | STU | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG04204 | hp2 | a0001 | c0002 | t0002 | g0241 | SAS | STU | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG04228 | hp1 | a0001 | c0001 | t0003 | g0049 | SAS | STU | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG04228 | hp2 | a0001 | c0002 | t0002 | g0289 | SAS | STU | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18522 | hp1 | a0001 | c0002 | t0001 | g0330 | AFR | YRI | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | YRI | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18612 | hp1 | a0002 | c0003 | t0002 | g0326 | EAS | CHB | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18612 | hp2 | a0001 | c0002 | t0002 | g0292 | EAS | CHB | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18906 | hp1 | a0001 | c0002 | t0005 | g0002 | AFR | YRI | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0157 | AFR | YRI | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18939 | hp1 | a0001 | c0002 | t0002 | g0273 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18939 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18943 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18943 | hp2 | a0002 | c0003 | t0007 | g0327 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18944 | hp1 | a0001 | c0002 | t0002 | g0231 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18945 | hp1 | a0001 | c0002 | t0007 | g0306 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18952 | hp1 | a0001 | c0002 | t0002 | g0253 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18959 | hp1 | a0003 | c0006 | t0003 | g0039 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18959 | hp2 | a0001 | c0002 | t0001 | g0308 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18961 | hp2 | a0001 | c0002 | t0002 | g0301 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18966 | hp1 | a0001 | c0002 | t0002 | g0239 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18966 | hp2 | a0001 | c0002 | t0002 | g0235 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18971 | hp1 | a0002 | c0003 | t0007 | g0300 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18974 | hp2 | a0001 | c0002 | t0002 | g0303 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18975 | hp1 | a0001 | c0002 | t0002 | g0261 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18977 | hp1 | a0011 | c0012 | t0002 | g0283 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0274 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18979 | hp2 | a0001 | c0002 | t0002 | g0325 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18980 | hp1 | a0003 | c0006 | t0001 | g0005 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18980 | hp2 | a0001 | c0002 | t0002 | g0339 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18982 | hp2 | a0001 | c0002 | t0002 | g0243 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18983 | hp2 | a0001 | c0002 | t0002 | g0287 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18989 | hp1 | a0001 | c0002 | t0002 | g0332 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18990 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18990 | hp2 | a0001 | c0002 | t0002 | g0271 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18993 | hp1 | a0001 | c0002 | t0002 | g0232 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18995 | hp2 | a0001 | c0002 | t0002 | g0255 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18998 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18998 | hp2 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA19002 | hp1 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA19005 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA19005 | hp2 | a0001 | c0002 | t0002 | g0272 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA19006 | hp1 | a0001 | c0002 | t0002 | g0316 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA19007 | hp1 | a0001 | c0002 | t0002 | g0321 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA19009 | hp1 | a0001 | c0002 | t0002 | g0341 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA19011 | hp1 | a0001 | c0002 | t0007 | g0230 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0163 | AFR | LWK | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA19043 | hp2 | a0001 | c0002 | t0005 | g0153 | AFR | LWK | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA19054 | hp1 | a0001 | c0002 | t0002 | g0134 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA19057 | hp1 | a0001 | c0002 | t0002 | g0328 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA19060 | hp1 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA19062 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA19066 | hp1 | a0001 | c0002 | t0002 | g0251 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA19068 | hp2 | a0001 | c0002 | t0002 | g0298 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA19070 | hp2 | a0012 | c0021 | t0002 | g0256 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA19074 | hp1 | a0001 | c0002 | t0002 | g0236 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA19079 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA19079 | hp2 | a0001 | c0002 | t0002 | g0345 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA19081 | hp2 | a0001 | c0002 | t0002 | g0302 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA19084 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA19084 | hp2 | a0003 | c0004 | t0002 | g0252 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA19085 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA19085 | hp2 | a0001 | c0002 | t0002 | g0288 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA19090 | hp1 | a0001 | c0002 | t0002 | g0329 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA19090 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA19240 | hp1 | a0001 | c0002 | t0002 | g0314 | AFR | YRI | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA19240 | hp2 | a0001 | c0001 | t0003 | g0159 | AFR | YRI | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA20129 | hp1 | a0001 | c0002 | t0002 | g0336 | AFR | ASW | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA20129 | hp2 | a0001 | c0002 | t0005 | g0148 | AFR | ASW | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0040 | EUR | TSI | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA20752 | hp2 | a0001 | c0002 | t0004 | g0023 | EUR | TSI | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0104 | EUR | TSI | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA20805 | hp2 | a0001 | c0002 | t0002 | g0313 | EUR | TSI | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | GIH | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA20905 | hp2 | a0001 | c0001 | t0003 | g0144 | SAS | GIH | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG01123 | hp2 | a0001 | c0002 | t0002 | g0246 | AMR | CLM | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02109 | hp1 | a0004 | c0005 | t0001 | g0174 | AFR | ACB | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02109 | hp2 | a0001 | c0001 | t0013 | g0080 | AFR | ACB | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02486 | hp1 | a0001 | c0002 | t0005 | g0066 | AFR | ACB | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02486 | hp2 | a0001 | c0017 | t0003 | g0075 | AFR | ACB | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0208 | AFR | ACB | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG02559 | hp2 | a0001 | c0001 | t0006 | g0161 | AFR | ACB | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG03471 | hp1 | a0001 | c0011 | t0001 | g0245 | AFR | MSL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | MSL | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0187 | AFR | USA | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
HG06807 | hp2 | a0001 | c0002 | t0009 | g0015 | AFR | USA | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18955 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA18955 | hp2 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | USA | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | USA | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0156 | AFR | LWK | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | LWK | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
homoSapiens | chm13v2 | a0001 | c0002 | t0002 | g0344 | REF | REF | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0012 | REF | REF | HDGFL2_chr19_4467297_4507207 | HDGFL2 | chr19 | 4467297 | 4507207 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:4472361 | C | T | 1 | a0012 | 1 | NA19070.hp2 | missense_variant | MODERATE | c.11C>T | p.Ala4Val | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 1/16 | 65/2267 | 11/2016 | 4/671 | chr19 | 4472361 | |||
chr19:4488721 | G | A | 1 | a0005 | 2 | HG03098.hp2 HG03209.hp1 |
missense_variant | MODERATE | c.334G>A | p.Asp112Asn | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/16 | 388/2267 | 334/2016 | 112/671 | chr19 | 4488721 | |||
chr19:4488760 | G | A | 1 | a0004 | 3 | HG02109.hp1 HG03209.hp2 HG03486.hp1 |
missense_variant | MODERATE | c.373G>A | p.Val125Ile | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/16 | 427/2267 | 373/2016 | 125/671 | chr19 | 4488760 | |||
chr19:4488869 | C | T | 1 | a0010 | 1 | HG03540.hp1 | missense_variant | MODERATE | c.482C>T | p.Ala161Val | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/16 | 536/2267 | 482/2016 | 161/671 | chr19 | 4488869 | |||
chr19:4491645 | C | T | 1 | a0002 | 7 | HG00438.hp1 HG00597.hp2 HG02040.hp2 others(4): Show |
missense_variant | MODERATE | c.569C>T | p.Ser190Leu | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 5/16 | 623/2267 | 569/2016 | 190/671 | chr19 | 4491645 | |||
chr19:4491795 | G | A | 1 | a0006 | 1 | HG02027.hp2 | missense_variant | MODERATE | c.638G>A | p.Arg213Gln | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 6/16 | 692/2267 | 638/2016 | 213/671 | chr19 | 4491795 | |||
chr19:4493982 | C | T | 1 | a0009 | 1 | HG03225.hp2 | missense_variant&splice_region_variant | MODERATE | c.839C>T | p.Ala280Val | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 8/16 | 893/2267 | 839/2016 | 280/671 | chr19 | 4493982 | |||
chr19:4493996 | C | T | 1 | a0011 | 1 | NA18977.hp1 | missense_variant | MODERATE | c.853C>T | p.Pro285Ser | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 8/16 | 907/2267 | 853/2016 | 285/671 | chr19 | 4493996 | |||
chr19:4494341 | C | CG | 1 | a0003 | 7 | HG00738.hp2 HG02572.hp2 HG02615.hp1 others(4): Show |
frameshift_variant | HIGH | c.1094dupG | p.Ser366fs | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 9/16 | 1149/2267 | 1095/2016 | 365/671 | INFO_REALIGN_3_PRIME | chr19 | 4494341 | ||
chr19:4494358 | C | A | 1 | a0007 | 1 | HG02300.hp2 | missense_variant | MODERATE | c.1107C>A | p.Ser369Arg | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 9/16 | 1161/2267 | 1107/2016 | 369/671 | chr19 | 4494358 | |||
chr19:4494363 | G | A | 1 | a0008 | 1 | HG02886.hp1 | missense_variant | MODERATE | c.1112G>A | p.Gly371Glu | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 9/16 | 1166/2267 | 1112/2016 | 371/671 | chr19 | 4494363 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:4472371 | C | T | 1 | a0008c0020 | 1 | HG02886.hp1 | synonymous_variant | LOW | c.21C>T | p.Pro7Pro | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 1/16 | 75/2267 | 21/2016 | 7/671 | chr19 | 4472371 | |||
chr19:4475343 | A | T | 1 | a0001c0019 | 1 | HG03041.hp1 | synonymous_variant | LOW | c.141A>T | p.Thr47Thr | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 2/16 | 195/2267 | 141/2016 | 47/671 | chr19 | 4475343 | |||
chr19:4493711 | A | G | 9 | a0001c0001 a0001c0008 a0001c0014 others(6): Show |
194 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(191): Show |
synonymous_variant | LOW | c.687A>G | p.Pro229Pro | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 7/16 | 741/2267 | 687/2016 | 229/671 | chr19 | 4493711 | |||
chr19:4494217 | G | A | 1 | a0001c0014 | 1 | HG00735.hp2 | synonymous_variant | LOW | c.966G>A | p.Ala322Ala | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 9/16 | 1020/2267 | 966/2016 | 322/671 | chr19 | 4494217 | |||
chr19:4498003 | G | A | 1 | a0001c0015 | 1 | HG02602.hp1 | synonymous_variant | LOW | c.1374G>A | p.Ser458Ser | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 11/16 | 1428/2267 | 1374/2016 | 458/671 | chr19 | 4498003 | |||
chr19:4499601 | C | T | 1 | a0001c0017 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.1686C>T | p.Asn562Asn | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 14/16 | 1740/2267 | 1686/2016 | 562/671 | chr19 | 4499601 | |||
chr19:4499628 | C | T | 1 | a0001c0011 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.1713C>T | p.Ala571Ala | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 14/16 | 1767/2267 | 1713/2016 | 571/671 | chr19 | 4499628 | |||
chr19:4499643 | C | G | 1 | a0001c0016 | 1 | HG03927.hp2 | synonymous_variant | LOW | c.1728C>G | p.Ala576Ala | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 14/16 | 1782/2267 | 1728/2016 | 576/671 | chr19 | 4499643 | |||
chr19:4501213 | C | T | 1 | a0001c0008 | 2 | HG01891.hp1 HG02630.hp2 |
synonymous_variant | LOW | c.1812C>T | p.Gly604Gly | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 15/16 | 1866/2267 | 1812/2016 | 604/671 | chr19 | 4501213 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:4472312 | T | G | 1 | a0001c0002t0010 | 1 | HG02258.hp2 | 5_prime_UTR_variant | MODIFIER | c.-39T>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 1/16 | 39 | chr19 | 4472312 | ||||||
chr19:4472315 | A | C | 2 | a0001c0001t0006 a0001c0001t0014 |
7 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-36A>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 1/16 | 36 | chr19 | 4472315 | ||||||
chr19:4472325 | C | T | 16 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(13): Show |
100 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-26C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 1/16 | chr19 | 4472325 | |||||||
chr19:4502067 | C | T | 3 | a0001c0001t0012 a0001c0002t0007 a0002c0003t0007 |
6 | HG00280.hp2 HG02129.hp1 NA18943.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*57C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 16/16 | 57 | chr19 | 4502067 | ||||||
chr19:4502092 | A | G | 6 | a0001c0001t0013 a0001c0002t0005 a0001c0002t0009 others(3): Show |
14 | HG00735.hp2 HG02109.hp2 HG02257.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*82A>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 16/16 | 82 | chr19 | 4502092 | ||||||
chr19:4502105 | G | A | 1 | a0001c0002t0011 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*95G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 16/16 | 95 | chr19 | 4502105 | ||||||
chr19:4502164 | C | G | 1 | a0001c0001t0008 | 4 | HG02630.hp1 HG02717.hp1 HG02895.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*154C>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 16/16 | 154 | chr19 | 4502164 | ||||||
chr19:4502189 | T | C | 16 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0012 others(13): Show |
150 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(147): Show |
3_prime_UTR_variant | MODIFIER | c.*179T>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 16/16 | 179 | chr19 | 4502189 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:4472450 | TG | T | 65 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0293 others(62): Show |
69 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.72+45delG | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 4472450 | ||||||
chr19:4472460 | G | T | 1 | a0001c0002t0001g0346 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.72+38G>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 1/15 | chr19 | 4472460 | |||||||
chr19:4472463 | G | GGGT | 20 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(17): Show |
20 | HG00609.hp2 HG00735.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.72+43_72+44insTGG | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 4472463 | ||||||
chr19:4472463 | G | GGGTGGGG others(20): Show |
1 | a0001c0001t0003g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.72+43_72+44insTGGG others(23): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 4472463 | ||||||
chr19:4472463 | G | GGT | 105 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0085 others(102): Show |
108 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.72+42_72+43insTG | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 4472463 | ||||||
chr19:4472463 | G | GT | 72 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0168 others(69): Show |
73 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.72+41_72+42insT | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 1/15 | chr19 | 4472463 | |||||||
chr19:4472463 | G | T | 143 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(140): Show |
150 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.72+41G>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 1/15 | chr19 | 4472463 | |||||||
chr19:4472471 | C | CG | 7 | a0001c0001t0001g0136 a0001c0001t0001g0207 a0001c0001t0014g0135 others(4): Show |
7 | HG02647.hp1 HG02738.hp2 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.72+54dupG | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 4472471 | ||||||
chr19:4472487 | G | C | 2 | a0001c0008t0003g0037 a0001c0008t0003g0137 |
2 | HG01891.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.72+65G>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 1/15 | chr19 | 4472487 | |||||||
chr19:4472487 | G | GAGGC | 95 | a0001c0001t0003g0006 a0001c0001t0003g0016 a0001c0001t0003g0017 others(92): Show |
98 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.72+66_72+69dupAGGC | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 4472487 | ||||||
chr19:4472492 | G | C | 3 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 |
3 | HG01257.hp1 HG01258.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.72+70G>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 1/15 | chr19 | 4472492 | |||||||
chr19:4472506 | C | A | 94 | a0001c0001t0003g0006 a0001c0001t0003g0016 a0001c0001t0003g0017 others(91): Show |
97 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.72+84C>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 1/15 | chr19 | 4472506 | |||||||
chr19:4472652 | C | T | 28 | a0001c0001t0003g0006 a0001c0001t0003g0028 a0001c0001t0003g0036 others(25): Show |
30 | HG01109.hp2 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.72+230C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 1/15 | chr19 | 4472652 | |||||||
chr19:4472732 | GGGCTGCA others(93): Show |
G | 1 | a0011c0012t0002g0283 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.72+314_72+413delTG others(98): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr19 | 4472732 | ||||||
chr19:4472784 | A | C | 1 | a0001c0002t0002g0001 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.72+362A>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 1/15 | chr19 | 4472784 | |||||||
chr19:4472818 | G | A | 1 | a0001c0002t0002g0333 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.72+396G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 1/15 | chr19 | 4472818 | |||||||
chr19:4472837 | T | G | 1 | a0011c0012t0002g0283 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.72+415T>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 1/15 | chr19 | 4472837 | |||||||
chr19:4472852 | C | T | 1 | a0001c0002t0009g0015 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.72+430C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 1/15 | chr19 | 4472852 | |||||||
chr19:4472927 | C | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0014 |
2 | HG01496.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.72+505C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 1/15 | chr19 | 4472927 | |||||||
chr19:4472983 | A | G | 222 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0293 others(219): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.72+561A>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 1/15 | chr19 | 4472983 | |||||||
chr19:4473029 | C | T | 1 | a0001c0002t0002g0290 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.72+607C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 1/15 | chr19 | 4473029 | |||||||
chr19:4473056 | G | C | 43 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(40): Show |
43 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(40): Show |
intron_variant | MODIFIER | c.72+634G>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 1/15 | chr19 | 4473056 | |||||||
chr19:4473071 | T | A | 1 | a0001c0001t0004g0155 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.72+649T>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 1/15 | chr19 | 4473071 | |||||||
chr19:4473161 | C | T | 1 | a0001c0001t0001g0207 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.72+739C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 1/15 | chr19 | 4473161 | |||||||
chr19:4473251 | G | A | 5 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(2): Show |
5 | HG00609.hp2 HG02132.hp2 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.72+829G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 1/15 | chr19 | 4473251 | |||||||
chr19:4473305 | G | C | 1 | a0002c0003t0002g0223 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.72+883G>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 1/15 | chr19 | 4473305 | |||||||
chr19:4473458 | G | A | 1 | a0001c0014t0009g0209 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.72+1036G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 1/15 | chr19 | 4473458 | |||||||
chr19:4473639 | G | T | 39 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(36): Show |
39 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(36): Show |
intron_variant | MODIFIER | c.72+1217G>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 1/15 | chr19 | 4473639 | |||||||
chr19:4473710 | C | T | 4 | a0001c0001t0003g0061 a0001c0001t0003g0062 a0001c0001t0003g0145 others(1): Show |
4 | HG02523.hp1 NA19002.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.72+1288C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 1/15 | chr19 | 4473710 | |||||||
chr19:4473805 | C | T | 23 | a0001c0001t0003g0006 a0001c0001t0003g0028 a0001c0001t0003g0036 others(20): Show |
25 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.72+1383C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 1/15 | chr19 | 4473805 | |||||||
chr19:4474157 | T | G | 39 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(36): Show |
39 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(36): Show |
intron_variant | MODIFIER | c.73-1118T>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 1/15 | chr19 | 4474157 | |||||||
chr19:4474288 | G | A | 1 | a0001c0002t0010g0224 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.73-987G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 1/15 | chr19 | 4474288 | |||||||
chr19:4474309 | C | A | 1 | a0001c0001t0002g0088 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.73-966C>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 1/15 | chr19 | 4474309 | |||||||
chr19:4474388 | G | C | 3 | a0001c0001t0008g0082 a0001c0001t0008g0083 a0001c0001t0008g0084 |
3 | HG02630.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.73-887G>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 1/15 | chr19 | 4474388 | |||||||
chr19:4474424 | C | T | 1 | a0001c0002t0009g0015 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.73-851C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 1/15 | chr19 | 4474424 | |||||||
chr19:4474698 | C | G | 4 | a0001c0002t0001g0342 a0001c0002t0002g0279 a0001c0002t0002g0280 others(1): Show |
4 | HG00323.hp1 HG01069.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.73-577C>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 1/15 | chr19 | 4474698 | |||||||
chr19:4474699 | C | G | 1 | a0001c0001t0001g0035 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.73-576C>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 1/15 | chr19 | 4474699 | |||||||
chr19:4474728 | C | A | 1 | a0001c0001t0001g0089 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.73-547C>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 1/15 | chr19 | 4474728 | |||||||
chr19:4474845 | G | A | 1 | a0001c0001t0001g0090 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.73-430G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 1/15 | chr19 | 4474845 | |||||||
chr19:4474869 | C | A | 1 | a0001c0002t0002g0291 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.73-406C>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 1/15 | chr19 | 4474869 | |||||||
chr19:4474869 | C | G | 1 | a0001c0002t0004g0027 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.73-406C>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 1/15 | chr19 | 4474869 | |||||||
chr19:4475045 | C | G | 1 | a0001c0001t0003g0060 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.73-230C>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 1/15 | chr19 | 4475045 | |||||||
chr19:4475074 | G | A | 1 | a0001c0002t0009g0015 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.73-201G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 1/15 | chr19 | 4475074 | |||||||
chr19:4475078 | A | G | 1 | a0001c0001t0003g0163 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.73-197A>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 1/15 | chr19 | 4475078 | |||||||
chr19:4475098 | G | A | 1 | a0001c0002t0002g0292 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.73-177G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 1/15 | chr19 | 4475098 | |||||||
chr19:4475268 | A | C | 2 | a0001c0002t0004g0071 a0001c0002t0004g0154 |
2 | HG03453.hp1 HG03540.hp2 |
splice_region_variant&intron_variant | LOW | c.73-7A>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 1/15 | chr19 | 4475268 | |||||||
chr19:4475365 | T | G | 64 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(61): Show |
65 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.149+14T>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 2/15 | chr19 | 4475365 | |||||||
chr19:4475429 | C | T | 1 | a0001c0008t0003g0037 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.150-16C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 2/15 | chr19 | 4475429 | |||||||
chr19:4475609 | T | C | 177 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(174): Show |
181 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.288+26T>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4475609 | |||||||
chr19:4475833 | G | A | 1 | a0001c0002t0003g0147 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.288+250G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4475833 | |||||||
chr19:4475843 | T | C | 5 | a0001c0002t0002g0007 a0001c0002t0002g0227 a0001c0002t0002g0297 others(2): Show |
6 | HG00597.hp1 HG00673.hp1 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.288+260T>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4475843 | |||||||
chr19:4475891 | CT | C | 210 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(207): Show |
214 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.288+324delT | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4475891 | ||||||
chr19:4475920 | C | T | 1 | a0001c0001t0002g0286 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.288+337C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4475920 | |||||||
chr19:4476093 | TGTTA | T | 11 | a0001c0001t0003g0006 a0001c0001t0003g0028 a0001c0001t0003g0074 others(8): Show |
12 | HG01891.hp2 HG02486.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.288+512_288+515del others(4): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4476093 | ||||||
chr19:4476120 | G | C | 1 | a0001c0002t0005g0148 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.288+537G>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4476120 | |||||||
chr19:4476189 | C | CT | 39 | a0001c0001t0003g0018 a0001c0001t0003g0036 a0001c0001t0003g0054 others(36): Show |
39 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.288+628dupT | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4476189 | ||||||
chr19:4476189 | CT | C | 40 | a0001c0001t0001g0034 a0001c0001t0001g0128 a0001c0001t0001g0129 others(37): Show |
41 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.288+628delT | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4476189 | ||||||
chr19:4476189 | CTT | C | 108 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(105): Show |
109 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.288+627_288+628del others(2): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4476189 | ||||||
chr19:4476273 | A | G | 177 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(174): Show |
181 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.288+690A>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4476273 | |||||||
chr19:4476286 | G | A | 1 | a0001c0001t0003g0054 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.288+703G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4476286 | |||||||
chr19:4476313 | C | T | 2 | a0001c0001t0001g0197 a0001c0002t0002g0288 |
2 | HG00323.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.288+730C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4476313 | |||||||
chr19:4476340 | C | T | 3 | a0001c0001t0001g0130 a0001c0001t0001g0216 a0001c0001t0001g0217 |
3 | HG01168.hp2 HG01169.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.288+757C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4476340 | |||||||
chr19:4476485 | G | T | 1 | a0001c0001t0001g0285 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.288+902G>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4476485 | |||||||
chr19:4476577 | G | C | 216 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(213): Show |
220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.288+994G>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4476577 | |||||||
chr19:4476788 | G | A | 1 | a0001c0001t0003g0040 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.288+1205G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4476788 | |||||||
chr19:4477009 | C | T | 4 | a0001c0001t0003g0051 a0001c0001t0003g0052 a0001c0001t0003g0053 others(1): Show |
4 | HG03490.hp1 HG03492.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.288+1426C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4477009 | |||||||
chr19:4477203 | C | T | 25 | a0001c0001t0001g0005 a0001c0001t0001g0033 a0001c0001t0001g0034 others(22): Show |
25 | HG00741.hp1 HG01074.hp1 HG01257.hp1 others(22): Show |
intron_variant | MODIFIER | c.288+1620C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4477203 | |||||||
chr19:4477318 | G | A | 338 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(335): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.288+1735G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4477318 | |||||||
chr19:4477333 | G | A | 1 | a0001c0002t0002g0229 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.288+1750G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4477333 | |||||||
chr19:4477952 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.288+2369C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4477952 | |||||||
chr19:4478065 | A | G | 190 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(187): Show |
193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.288+2482A>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4478065 | |||||||
chr19:4478079 | C | CA | 22 | a0001c0001t0001g0034 a0001c0001t0001g0091 a0001c0001t0001g0092 others(19): Show |
22 | HG00544.hp1 HG00741.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.288+2514dupA | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4478079 | ||||||
chr19:4478079 | C | CAA | 37 | a0001c0001t0003g0016 a0001c0001t0003g0018 a0001c0001t0003g0019 others(34): Show |
37 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(34): Show |
intron_variant | MODIFIER | c.288+2513_288+2514d others(4): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4478079 | ||||||
chr19:4478079 | CA | C | 8 | a0001c0001t0001g0117 a0001c0001t0001g0131 a0001c0002t0002g0301 others(5): Show |
8 | HG01167.hp2 HG01169.hp1 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.288+2514delA | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4478079 | ||||||
chr19:4478133 | G | T | 1 | a0001c0002t0002g0341 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.288+2550G>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4478133 | |||||||
chr19:4478144 | G | A | 151 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(148): Show |
154 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.288+2561G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4478144 | |||||||
chr19:4478151 | G | A | 1 | a0001c0002t0002g0260 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.288+2568G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4478151 | |||||||
chr19:4478197 | G | GTT | 33 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(30): Show |
33 | HG00099.hp1 HG00280.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.288+2626_288+2627d others(4): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4478197 | ||||||
chr19:4478197 | GT | G | 146 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(143): Show |
149 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.288+2627delT | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4478197 | ||||||
chr19:4478204 | T | G | 1 | a0001c0002t0002g0203 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.288+2621T>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4478204 | |||||||
chr19:4478211 | G | T | 3 | a0001c0002t0002g0278 a0001c0002t0002g0335 a0001c0002t0002g0336 |
3 | HG00642.hp1 HG03688.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.288+2628G>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4478211 | |||||||
chr19:4478276 | A | C | 215 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(212): Show |
219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.288+2693A>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4478276 | |||||||
chr19:4478305 | C | T | 2 | a0001c0001t0001g0188 a0001c0001t0001g0201 |
2 | HG02572.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.288+2722C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4478305 | |||||||
chr19:4478347 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.288+2764C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4478347 | |||||||
chr19:4478494 | C | T | 6 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(3): Show |
6 | HG01261.hp2 HG01346.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.288+2911C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4478494 | |||||||
chr19:4478551 | C | G | 1 | a0001c0001t0002g0286 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.288+2968C>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4478551 | |||||||
chr19:4478688 | G | GT | 21 | a0001c0001t0001g0086 a0001c0001t0001g0185 a0001c0001t0001g0186 others(18): Show |
21 | HG01243.hp2 HG01978.hp1 HG02293.hp2 others(18): Show |
intron_variant | MODIFIER | c.288+3116dupT | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4478688 | ||||||
chr19:4478805 | C | T | 1 | a0001c0002t0002g0290 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.288+3222C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4478805 | |||||||
chr19:4478826 | A | G | 25 | a0001c0002t0003g0024 a0001c0002t0003g0064 a0001c0002t0003g0147 others(22): Show |
26 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.288+3243A>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4478826 | |||||||
chr19:4478841 | C | T | 39 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(36): Show |
39 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(36): Show |
intron_variant | MODIFIER | c.288+3258C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4478841 | |||||||
chr19:4478974 | C | T | 151 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(148): Show |
154 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.288+3391C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4478974 | |||||||
chr19:4479000 | C | A | 1 | a0001c0016t0002g0206 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.288+3417C>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4479000 | |||||||
chr19:4479174 | G | A | 338 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(335): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.288+3591G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4479174 | |||||||
chr19:4479290 | A | C | 1 | a0001c0001t0004g0155 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.288+3707A>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4479290 | |||||||
chr19:4479353 | G | T | 1 | a0001c0001t0001g0285 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.288+3770G>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4479353 | |||||||
chr19:4479419 | TA | T | 41 | a0001c0001t0001g0182 a0001c0001t0001g0189 a0001c0001t0003g0016 others(38): Show |
41 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(38): Show |
intron_variant | MODIFIER | c.288+3846delA | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4479419 | ||||||
chr19:4479450 | T | G | 6 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(3): Show |
6 | HG01261.hp2 HG01346.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.288+3867T>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4479450 | |||||||
chr19:4479545 | C | T | 2 | a0001c0001t0004g0162 a0001c0001t0013g0080 |
2 | HG02109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.288+3962C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4479545 | |||||||
chr19:4479579 | T | TA | 142 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(139): Show |
145 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.288+4011dupA | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4479579 | ||||||
chr19:4479619 | C | A | 3 | a0001c0002t0002g0231 a0001c0002t0002g0267 a0001c0002t0002g0303 |
3 | HG02523.hp2 NA18944.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.288+4036C>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4479619 | |||||||
chr19:4479813 | G | A | 1 | a0001c0002t0002g0268 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.288+4230G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4479813 | |||||||
chr19:4479904 | T | TA | 46 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 others(43): Show |
47 | HG00544.hp2 HG01070.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.288+4342dupA | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4479904 | ||||||
chr19:4479904 | TA | T | 93 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(90): Show |
93 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.288+4342delA | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4479904 | ||||||
chr19:4479951 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.288+4368A>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4479951 | |||||||
chr19:4479986 | G | T | 1 | a0001c0001t0003g0138 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.288+4403G>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4479986 | |||||||
chr19:4480022 | AG | A | 151 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(148): Show |
154 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.288+4440delG | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4480022 | |||||||
chr19:4480084 | G | A | 123 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(120): Show |
124 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.288+4501G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4480084 | |||||||
chr19:4480156 | C | G | 5 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(2): Show |
5 | HG00609.hp2 HG02132.hp2 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.288+4573C>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4480156 | |||||||
chr19:4480170 | T | A | 123 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(120): Show |
124 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.288+4587T>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4480170 | |||||||
chr19:4480371 | G | A | 1 | a0001c0002t0001g0305 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.288+4788G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4480371 | |||||||
chr19:4480444 | C | T | 1 | a0001c0002t0002g0263 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.288+4861C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4480444 | |||||||
chr19:4480456 | C | T | 1 | a0001c0002t0009g0015 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.288+4873C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4480456 | |||||||
chr19:4480517 | G | C | 1 | a0001c0001t0001g0295 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.288+4934G>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4480517 | |||||||
chr19:4480668 | G | A | 1 | a0001c0002t0007g0306 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.288+5085G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4480668 | |||||||
chr19:4480754 | G | T | 151 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(148): Show |
154 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.288+5171G>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4480754 | |||||||
chr19:4480799 | C | T | 1 | a0001c0002t0009g0015 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.288+5216C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4480799 | |||||||
chr19:4480921 | A | G | 1 | a0011c0012t0002g0283 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.288+5338A>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4480921 | |||||||
chr19:4480941 | C | G | 1 | a0001c0014t0009g0209 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.288+5358C>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4480941 | |||||||
chr19:4480959 | C | A | 1 | a0001c0002t0002g0235 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.288+5376C>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4480959 | |||||||
chr19:4480998 | G | A | 215 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(212): Show |
219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.288+5415G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4480998 | |||||||
chr19:4481023 | AT | A | 186 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(183): Show |
189 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.288+5455delT | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4481023 | ||||||
chr19:4481054 | C | T | 6 | a0001c0001t0006g0003 a0001c0001t0006g0029 a0001c0001t0006g0079 others(3): Show |
7 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.288+5471C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4481054 | |||||||
chr19:4481108 | G | A | 1 | a0007c0010t0002g0269 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.288+5525G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4481108 | |||||||
chr19:4481146 | C | T | 1 | a0001c0014t0009g0209 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.288+5563C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4481146 | |||||||
chr19:4481151 | A | T | 2 | a0005c0007t0003g0072 a0005c0007t0003g0073 |
2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.288+5568A>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4481151 | |||||||
chr19:4481188 | AT | A | 232 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(229): Show |
241 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.288+5625delT | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4481188 | ||||||
chr19:4481188 | ATT | A | 66 | a0001c0001t0003g0016 a0001c0001t0003g0018 a0001c0001t0003g0019 others(63): Show |
68 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.288+5624_288+5625d others(4): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4481188 | ||||||
chr19:4481271 | A | G | 1 | a0001c0001t0003g0062 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.288+5688A>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4481271 | |||||||
chr19:4481272 | C | A | 1 | a0001c0001t0003g0062 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.288+5689C>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4481272 | |||||||
chr19:4481516 | C | T | 25 | a0001c0002t0003g0024 a0001c0002t0003g0064 a0001c0002t0003g0147 others(22): Show |
26 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.288+5933C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4481516 | |||||||
chr19:4481615 | C | T | 5 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(2): Show |
5 | HG00609.hp2 HG02132.hp2 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.288+6032C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4481615 | |||||||
chr19:4481622 | G | A | 2 | a0005c0007t0003g0072 a0005c0007t0003g0073 |
2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.288+6039G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4481622 | |||||||
chr19:4481725 | G | T | 119 | a0001c0001t0001g0304 a0001c0002t0001g0242 a0001c0002t0001g0248 others(116): Show |
126 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.288+6142G>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4481725 | |||||||
chr19:4481826 | G | T | 1 | a0001c0001t0003g0062 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.288+6243G>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4481826 | |||||||
chr19:4481857 | G | A | 6 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0293 others(3): Show |
6 | HG00280.hp2 HG01433.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.288+6274G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4481857 | |||||||
chr19:4481939 | C | A | 1 | a0001c0001t0003g0062 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.288+6356C>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4481939 | |||||||
chr19:4481997 | G | C | 151 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(148): Show |
154 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.288+6414G>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4481997 | |||||||
chr19:4482007 | G | A | 25 | a0001c0002t0003g0024 a0001c0002t0003g0064 a0001c0002t0003g0147 others(22): Show |
26 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.288+6424G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4482007 | |||||||
chr19:4482026 | C | CT | 48 | a0001c0001t0003g0041 a0001c0001t0003g0049 a0001c0001t0003g0057 others(45): Show |
48 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.288+6467dupT | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4482026 | ||||||
chr19:4482026 | C | CTT | 24 | a0001c0001t0001g0089 a0001c0001t0001g0104 a0001c0001t0001g0176 others(21): Show |
25 | HG01169.hp2 HG01257.hp2 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.288+6466_288+6467d others(4): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4482026 | ||||||
chr19:4482026 | C | CTTT | 99 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(96): Show |
101 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.288+6465_288+6467d others(5): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4482026 | ||||||
chr19:4482026 | C | CTTTT | 34 | a0001c0001t0001g0033 a0001c0001t0001g0096 a0001c0001t0001g0102 others(31): Show |
34 | HG00544.hp2 HG00741.hp2 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.288+6464_288+6467d others(6): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4482026 | ||||||
chr19:4482026 | CT | C | 28 | a0001c0002t0001g0342 a0001c0002t0002g0279 a0001c0002t0002g0288 others(25): Show |
29 | HG00323.hp1 HG01069.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.288+6467delT | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4482026 | ||||||
chr19:4482131 | C | T | 1 | a0001c0002t0002g0298 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.289-6545C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4482131 | |||||||
chr19:4482189 | C | T | 1 | a0008c0020t0004g0026 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.289-6487C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4482189 | |||||||
chr19:4482215 | T | C | 25 | a0001c0002t0003g0024 a0001c0002t0003g0064 a0001c0002t0003g0147 others(22): Show |
26 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.289-6461T>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4482215 | |||||||
chr19:4482371 | A | T | 1 | a0001c0001t0003g0062 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.289-6305A>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4482371 | |||||||
chr19:4482372 | G | C | 39 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(36): Show |
39 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(36): Show |
intron_variant | MODIFIER | c.289-6304G>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4482372 | |||||||
chr19:4482430 | G | A | 2 | a0001c0001t0001g0098 a0001c0001t0001g0207 |
2 | NA19057.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.289-6246G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4482430 | |||||||
chr19:4482660 | G | A | 3 | a0001c0002t0002g0278 a0001c0002t0002g0335 a0001c0002t0002g0336 |
3 | HG00642.hp1 HG03688.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.289-6016G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4482660 | |||||||
chr19:4482666 | A | G | 338 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(335): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.289-6010A>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4482666 | |||||||
chr19:4482685 | C | A | 2 | a0001c0001t0003g0036 a0001c0001t0003g0077 |
2 | HG03195.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.289-5991C>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4482685 | |||||||
chr19:4482847 | C | T | 2 | a0001c0001t0001g0111 a0001c0001t0001g0129 |
2 | HG03017.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.289-5829C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4482847 | |||||||
chr19:4482908 | CAG | C | 3 | a0001c0001t0004g0155 a0001c0001t0004g0162 a0001c0001t0013g0080 |
3 | HG02109.hp2 HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.289-5767_289-5766d others(4): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4482908 | |||||||
chr19:4482950 | G | C | 1 | a0008c0020t0004g0026 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.289-5726G>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4482950 | |||||||
chr19:4483229 | G | C | 12 | a0001c0002t0003g0024 a0001c0002t0003g0064 a0001c0002t0004g0011 others(9): Show |
12 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.289-5447G>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4483229 | |||||||
chr19:4483250 | C | T | 2 | a0005c0007t0003g0072 a0005c0007t0003g0073 |
2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.289-5426C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4483250 | |||||||
chr19:4483303 | G | A | 11 | a0001c0001t0003g0006 a0001c0001t0003g0028 a0001c0001t0003g0074 others(8): Show |
12 | HG01891.hp2 HG02486.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.289-5373G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4483303 | |||||||
chr19:4483353 | G | C | 1 | a0001c0001t0002g0132 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.289-5323G>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4483353 | |||||||
chr19:4483488 | A | G | 48 | a0001c0001t0001g0004 a0001c0001t0001g0030 a0001c0001t0001g0031 others(45): Show |
49 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.289-5188A>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4483488 | |||||||
chr19:4483600 | G | A | 1 | a0008c0020t0004g0026 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.289-5076G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4483600 | |||||||
chr19:4483632 | C | T | 1 | a0010c0018t0005g0151 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.289-5044C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4483632 | |||||||
chr19:4483690 | A | G | 1 | a0001c0002t0002g0266 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.289-4986A>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4483690 | |||||||
chr19:4483787 | A | AT | 71 | a0001c0001t0003g0016 a0001c0001t0003g0018 a0001c0001t0003g0019 others(68): Show |
71 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.289-4867dupT | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4483787 | ||||||
chr19:4483787 | A | ATT | 9 | a0001c0001t0003g0017 a0001c0001t0003g0041 a0001c0001t0003g0048 others(6): Show |
9 | HG02738.hp1 HG03130.hp1 HG03831.hp1 others(6): Show |
intron_variant | MODIFIER | c.289-4868_289-4867d others(4): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4483787 | ||||||
chr19:4483787 | AT | A | 128 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(125): Show |
132 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.289-4867delT | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4483787 | ||||||
chr19:4483787 | ATT | A | 6 | a0001c0001t0001g0032 a0001c0001t0001g0131 a0001c0001t0001g0216 others(3): Show |
6 | HG01168.hp2 HG01515.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.289-4868_289-4867d others(4): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4483787 | ||||||
chr19:4483988 | A | C | 151 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(148): Show |
154 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.289-4688A>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4483988 | |||||||
chr19:4483991 | G | A | 25 | a0001c0002t0003g0024 a0001c0002t0003g0064 a0001c0002t0003g0147 others(22): Show |
26 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.289-4685G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4483991 | |||||||
chr19:4484019 | G | C | 1 | a0001c0002t0005g0068 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.289-4657G>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4484019 | |||||||
chr19:4484032 | G | A | 123 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(120): Show |
124 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.289-4644G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4484032 | |||||||
chr19:4484081 | A | G | 338 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(335): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.289-4595A>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4484081 | |||||||
chr19:4484088 | C | CT | 33 | a0001c0001t0001g0086 a0001c0001t0001g0096 a0001c0001t0001g0101 others(30): Show |
35 | HG00544.hp2 HG00558.hp1 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.289-4569dupT | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4484088 | ||||||
chr19:4484088 | CT | C | 12 | a0001c0001t0001g0182 a0001c0001t0001g0186 a0001c0001t0001g0216 others(9): Show |
12 | HG01070.hp2 HG01099.hp1 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.289-4569delT | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4484088 | ||||||
chr19:4484096 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.289-4580T>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4484096 | |||||||
chr19:4484189 | T | A | 25 | a0001c0002t0003g0024 a0001c0002t0003g0064 a0001c0002t0003g0147 others(22): Show |
26 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.289-4487T>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4484189 | |||||||
chr19:4484380 | G | A | 150 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(147): Show |
153 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.289-4296G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4484380 | |||||||
chr19:4484448 | C | T | 39 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(36): Show |
39 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(36): Show |
intron_variant | MODIFIER | c.289-4228C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4484448 | |||||||
chr19:4484450 | T | A | 1 | a0001c0002t0002g0133 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.289-4226T>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4484450 | |||||||
chr19:4484507 | CT | C | 338 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(335): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.289-4160delT | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4484507 | ||||||
chr19:4484656 | C | T | 25 | a0001c0002t0003g0024 a0001c0002t0003g0064 a0001c0002t0003g0147 others(22): Show |
26 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.289-4020C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4484656 | |||||||
chr19:4484666 | A | AT | 14 | a0001c0002t0001g0248 a0001c0002t0001g0274 a0001c0002t0002g0203 others(11): Show |
14 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(11): Show |
intron_variant | MODIFIER | c.289-3987dupT | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4484666 | ||||||
chr19:4484666 | A | ATTTTTTT | 76 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(73): Show |
77 | HG00280.hp2 HG00323.hp2 HG00738.hp1 others(74): Show |
intron_variant | MODIFIER | c.289-3993_289-3987d others(9): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4484666 | ||||||
chr19:4484666 | A | ATTTTTTT others(1): Show |
44 | a0001c0001t0001g0031 a0001c0001t0001g0091 a0001c0001t0001g0096 others(41): Show |
45 | HG00544.hp2 HG00735.hp1 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.289-3994_289-3987d others(10): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4484666 | ||||||
chr19:4484666 | A | ATTTTTTT others(2): Show |
38 | a0001c0001t0001g0034 a0001c0001t0001g0090 a0001c0001t0001g0207 others(35): Show |
39 | HG00099.hp1 HG00140.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.289-3995_289-3987d others(11): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4484666 | ||||||
chr19:4484666 | A | ATTTTTTT others(3): Show |
20 | a0001c0001t0001g0180 a0001c0001t0003g0017 a0001c0001t0003g0018 others(17): Show |
20 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.289-3996_289-3987d others(12): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4484666 | ||||||
chr19:4484666 | A | ATTTTTTT others(4): Show |
2 | a0001c0001t0003g0062 a0005c0007t0003g0072 |
2 | HG03098.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.289-3997_289-3987d others(13): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4484666 | ||||||
chr19:4484666 | A | ATTTTTTT others(10): Show |
1 | a0008c0020t0004g0026 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.289-4003_289-3987d others(19): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4484666 | ||||||
chr19:4484666 | ATTTTT | A | 13 | a0001c0002t0003g0024 a0001c0002t0003g0064 a0001c0002t0004g0011 others(10): Show |
13 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.289-3991_289-3987d others(7): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4484666 | ||||||
chr19:4484666 | ATTTTTT | A | 12 | a0001c0002t0003g0147 a0001c0002t0004g0071 a0001c0002t0005g0002 others(9): Show |
13 | HG02257.hp1 HG02280.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.289-3992_289-3987d others(8): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4484666 | ||||||
chr19:4484666 | ATTTTTTT others(3): Show |
A | 3 | a0001c0001t0002g0210 a0001c0001t0002g0211 a0001c0001t0002g0221 |
3 | HG02258.hp1 HG02451.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.289-3996_289-3987d others(12): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4484666 | ||||||
chr19:4484706 | C | CT | 151 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(148): Show |
154 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.289-3969dupT | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4484706 | ||||||
chr19:4484718 | C | T | 1 | a0001c0002t0001g0346 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.289-3958C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4484718 | |||||||
chr19:4484821 | G | A | 1 | a0001c0001t0003g0050 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.289-3855G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4484821 | |||||||
chr19:4484918 | G | A | 104 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(101): Show |
105 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.289-3758G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4484918 | |||||||
chr19:4484922 | C | T | 1 | a0001c0002t0001g0324 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.289-3754C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4484922 | |||||||
chr19:4484952 | T | C | 39 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(36): Show |
39 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(36): Show |
intron_variant | MODIFIER | c.289-3724T>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4484952 | |||||||
chr19:4485049 | A | G | 151 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(148): Show |
154 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.289-3627A>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4485049 | |||||||
chr19:4485119 | A | G | 1 | a0001c0002t0004g0063 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.289-3557A>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4485119 | |||||||
chr19:4485137 | C | A | 1 | a0001c0001t0003g0048 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.289-3539C>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4485137 | |||||||
chr19:4485250 | A | G | 1 | a0001c0001t0003g0141 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.289-3426A>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4485250 | |||||||
chr19:4485289 | G | A | 39 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(36): Show |
39 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(36): Show |
intron_variant | MODIFIER | c.289-3387G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4485289 | |||||||
chr19:4485296 | G | A | 1 | a0001c0002t0001g0324 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.289-3380G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4485296 | |||||||
chr19:4485378 | TGTTATAC others(3): Show |
T | 1 | a0001c0001t0001g0105 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.289-3294_289-3285d others(12): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4485378 | ||||||
chr19:4485388 | C | T | 3 | a0001c0001t0001g0108 a0001c0001t0001g0171 a0001c0001t0001g0220 |
3 | HG01069.hp1 HG01071.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.289-3288C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4485388 | |||||||
chr19:4485389 | G | A | 1 | a0011c0012t0002g0283 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.289-3287G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4485389 | |||||||
chr19:4485442 | A | T | 39 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(36): Show |
39 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(36): Show |
intron_variant | MODIFIER | c.289-3234A>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4485442 | |||||||
chr19:4485611 | G | A | 1 | a0001c0014t0009g0209 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.289-3065G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4485611 | |||||||
chr19:4485637 | G | A | 1 | a0001c0001t0003g0042 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.289-3039G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4485637 | |||||||
chr19:4485705 | G | C | 1 | a0001c0002t0004g0027 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.289-2971G>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4485705 | |||||||
chr19:4485741 | C | CA | 10 | a0001c0001t0001g0124 a0001c0001t0001g0127 a0001c0001t0001g0166 others(7): Show |
10 | HG01978.hp2 HG02559.hp1 HG03098.hp1 others(7): Show |
intron_variant | MODIFIER | c.289-2921dupA | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4485741 | ||||||
chr19:4485765 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.289-2911C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4485765 | |||||||
chr19:4485883 | C | CAAAA | 8 | a0001c0002t0003g0024 a0001c0002t0004g0011 a0001c0002t0004g0021 others(5): Show |
8 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.289-2786_289-2783d others(6): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4485883 | ||||||
chr19:4485883 | C | CAAAAAAA others(4): Show |
23 | a0001c0001t0004g0078 a0001c0002t0001g0242 a0001c0002t0001g0305 others(20): Show |
24 | HG00558.hp1 HG01192.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.289-2783_289-2782i others(13): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4485883 | ||||||
chr19:4485883 | C | CAAAAAAA others(5): Show |
185 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(182): Show |
193 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.289-2783_289-2782i others(14): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4485883 | ||||||
chr19:4485883 | C | CAAAAAAA others(6): Show |
104 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0093 others(101): Show |
106 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.289-2783_289-2782i others(15): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4485883 | ||||||
chr19:4485883 | C | CAAAAAAA others(7): Show |
17 | a0001c0001t0001g0105 a0001c0001t0003g0018 a0001c0001t0003g0019 others(14): Show |
17 | HG00609.hp2 HG01517.hp2 HG02080.hp1 others(14): Show |
intron_variant | MODIFIER | c.289-2783_289-2782i others(16): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4485883 | ||||||
chr19:4485891 | A | AAAAAAAA others(5): Show |
7 | a0002c0003t0002g0223 a0002c0003t0002g0247 a0002c0003t0002g0257 others(4): Show |
7 | HG00438.hp1 HG00597.hp2 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.289-2783_289-2782i others(14): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4485891 | ||||||
chr19:4485903 | G | A | 1 | a0001c0002t0002g0222 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.289-2773G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4485903 | |||||||
chr19:4485966 | T | C | 1 | a0001c0002t0002g0311 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.289-2710T>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4485966 | |||||||
chr19:4485981 | A | G | 1 | a0001c0002t0003g0064 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.289-2695A>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4485981 | |||||||
chr19:4486047 | C | T | 25 | a0001c0002t0003g0024 a0001c0002t0003g0064 a0001c0002t0003g0147 others(22): Show |
26 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.289-2629C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4486047 | |||||||
chr19:4486052 | C | CA | 61 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0019 others(58): Show |
61 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.289-2605dupA | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4486052 | ||||||
chr19:4486052 | C | CAA | 13 | a0001c0001t0003g0018 a0001c0001t0003g0020 a0001c0001t0003g0045 others(10): Show |
14 | HG00609.hp2 HG01109.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.289-2606_289-2605d others(4): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4486052 | ||||||
chr19:4486052 | CA | C | 13 | a0001c0001t0001g0105 a0001c0001t0003g0006 a0001c0001t0003g0028 others(10): Show |
14 | HG01891.hp2 HG02083.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.289-2605delA | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4486052 | ||||||
chr19:4486069 | A | AC | 7 | a0001c0001t0001g0031 a0001c0001t0001g0102 a0001c0001t0001g0114 others(4): Show |
7 | HG00735.hp1 HG00741.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.289-2607_289-2606i others(3): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4486069 | |||||||
chr19:4486069 | A | C | 116 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(113): Show |
117 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.289-2607A>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4486069 | |||||||
chr19:4486072 | C | A | 2 | a0001c0002t0001g0330 a0001c0002t0009g0015 |
2 | HG06807.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.289-2604C>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4486072 | |||||||
chr19:4486140 | C | T | 25 | a0001c0002t0003g0024 a0001c0002t0003g0064 a0001c0002t0003g0147 others(22): Show |
26 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.289-2536C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4486140 | |||||||
chr19:4486168 | G | A | 120 | a0001c0001t0001g0304 a0001c0002t0001g0121 a0001c0002t0001g0242 others(117): Show |
127 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.289-2508G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4486168 | |||||||
chr19:4486203 | G | T | 1 | a0001c0002t0003g0064 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.289-2473G>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4486203 | |||||||
chr19:4486266 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.289-2410C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4486266 | |||||||
chr19:4486352 | G | A | 12 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0212 others(9): Show |
12 | HG01243.hp2 HG02109.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.289-2324G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4486352 | |||||||
chr19:4486472 | C | G | 5 | a0001c0002t0002g0007 a0001c0002t0002g0227 a0001c0002t0002g0297 others(2): Show |
6 | HG00597.hp1 HG00673.hp1 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.289-2204C>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4486472 | |||||||
chr19:4486525 | C | CA | 63 | a0001c0001t0001g0033 a0001c0001t0001g0182 a0001c0001t0001g0195 others(60): Show |
64 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.289-2136dupA | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4486525 | ||||||
chr19:4486567 | C | T | 2 | a0001c0001t0001g0108 a0001c0001t0001g0171 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.289-2109C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4486567 | |||||||
chr19:4486692 | C | G | 1 | a0001c0001t0003g0018 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.289-1984C>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4486692 | |||||||
chr19:4486929 | G | A | 1 | a0001c0014t0009g0209 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.289-1747G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4486929 | |||||||
chr19:4486972 | C | CT | 26 | a0001c0001t0003g0144 a0001c0002t0003g0024 a0001c0002t0003g0064 others(23): Show |
27 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.289-1693dupT | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4486972 | ||||||
chr19:4486972 | CT | C | 6 | a0001c0001t0003g0074 a0001c0002t0002g0232 a0001c0002t0002g0243 others(3): Show |
6 | HG02896.hp2 NA18977.hp1 NA18982.hp2 others(3): Show |
intron_variant | MODIFIER | c.289-1693delT | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4486972 | ||||||
chr19:4486988 | C | T | 148 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(145): Show |
151 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.289-1688C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4486988 | |||||||
chr19:4487034 | C | T | 2 | a0001c0008t0003g0037 a0001c0008t0003g0137 |
2 | HG01891.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.289-1642C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4487034 | |||||||
chr19:4487121 | C | A | 1 | a0001c0002t0002g0335 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.289-1555C>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4487121 | |||||||
chr19:4487216 | G | A | 2 | a0001c0001t0003g0042 a0001c0001t0003g0139 |
2 | HG00099.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.289-1460G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4487216 | |||||||
chr19:4487300 | A | G | 149 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(146): Show |
152 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.289-1376A>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4487300 | |||||||
chr19:4487360 | G | A | 2 | a0001c0008t0003g0037 a0001c0008t0003g0137 |
2 | HG01891.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.289-1316G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4487360 | |||||||
chr19:4487413 | C | T | 25 | a0001c0002t0003g0024 a0001c0002t0003g0064 a0001c0002t0003g0147 others(22): Show |
26 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.289-1263C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4487413 | |||||||
chr19:4487437 | T | TGTAGAGA others(2): Show |
4 | a0001c0001t0008g0082 a0001c0001t0008g0083 a0001c0001t0008g0084 others(1): Show |
4 | HG02630.hp1 HG02717.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.289-1237_289-1229d others(11): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4487437 | ||||||
chr19:4487655 | G | A | 3 | a0001c0002t0002g0258 a0001c0002t0002g0312 a0001c0002t0002g0317 |
3 | HG00099.hp2 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.289-1021G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4487655 | |||||||
chr19:4487692 | C | T | 1 | a0008c0020t0004g0026 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.289-984C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4487692 | |||||||
chr19:4487809 | A | G | 39 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(36): Show |
39 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(36): Show |
intron_variant | MODIFIER | c.289-867A>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4487809 | |||||||
chr19:4487838 | G | A | 39 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(36): Show |
39 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(36): Show |
intron_variant | MODIFIER | c.289-838G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4487838 | |||||||
chr19:4487943 | TA | T | 116 | a0001c0001t0001g0293 a0001c0001t0001g0304 a0001c0001t0002g0088 others(113): Show |
123 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.289-719delA | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr19 | 4487943 | ||||||
chr19:4488044 | C | T | 1 | a0001c0008t0003g0037 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.289-632C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4488044 | |||||||
chr19:4488055 | C | G | 4 | a0001c0001t0008g0082 a0001c0001t0008g0083 a0001c0001t0008g0084 others(1): Show |
4 | HG02630.hp1 HG02717.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.289-621C>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4488055 | |||||||
chr19:4488061 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.289-615C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4488061 | |||||||
chr19:4488183 | T | C | 39 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(36): Show |
39 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(36): Show |
intron_variant | MODIFIER | c.289-493T>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4488183 | |||||||
chr19:4488212 | C | A | 1 | a0003c0006t0003g0039 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.289-464C>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4488212 | |||||||
chr19:4488356 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.289-320G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4488356 | |||||||
chr19:4488416 | G | GA | 25 | a0001c0002t0003g0024 a0001c0002t0003g0064 a0001c0002t0003g0147 others(22): Show |
26 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.289-260_289-259ins others(1): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4488416 | |||||||
chr19:4488419 | T | C | 25 | a0001c0002t0003g0024 a0001c0002t0003g0064 a0001c0002t0003g0147 others(22): Show |
26 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.289-257T>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4488419 | |||||||
chr19:4488473 | C | T | 149 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(146): Show |
152 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.289-203C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4488473 | |||||||
chr19:4488515 | C | T | 2 | a0001c0001t0004g0162 a0008c0020t0004g0026 |
2 | HG02257.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.289-161C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4488515 | |||||||
chr19:4488635 | C | T | 64 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(61): Show |
65 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.289-41C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4488635 | |||||||
chr19:4488648 | C | T | 2 | a0001c0008t0003g0037 a0001c0008t0003g0137 |
2 | HG01891.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.289-28C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 3/15 | chr19 | 4488648 | |||||||
chr19:4488899 | T | G | 1 | a0001c0002t0002g0203 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.489+23T>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4488899 | |||||||
chr19:4488929 | G | A | 212 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(209): Show |
216 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.489+53G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4488929 | |||||||
chr19:4488952 | C | CT | 6 | a0001c0001t0003g0017 a0001c0002t0001g0274 a0001c0002t0002g0133 others(3): Show |
6 | HG02148.hp1 HG02735.hp1 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.489+95dupT | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr19 | 4488952 | ||||||
chr19:4488952 | C | CTT | 24 | a0001c0001t0001g0136 a0001c0002t0003g0024 a0001c0002t0003g0064 others(21): Show |
25 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.489+94_489+95dupTT | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr19 | 4488952 | ||||||
chr19:4488952 | CT | C | 150 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(147): Show |
153 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(150): Show |
intron_variant | MODIFIER | c.489+95delT | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr19 | 4488952 | ||||||
chr19:4489111 | A | G | 213 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(210): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.489+235A>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4489111 | |||||||
chr19:4489124 | T | A | 1 | a0001c0001t0003g0158 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.489+248T>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4489124 | |||||||
chr19:4489134 | G | T | 25 | a0001c0001t0003g0006 a0001c0001t0003g0028 a0001c0001t0003g0036 others(22): Show |
27 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.489+258G>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4489134 | |||||||
chr19:4489156 | G | A | 25 | a0001c0002t0003g0024 a0001c0002t0003g0064 a0001c0002t0003g0147 others(22): Show |
26 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.489+280G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4489156 | |||||||
chr19:4489161 | C | T | 6 | a0001c0001t0006g0003 a0001c0001t0006g0029 a0001c0001t0006g0079 others(3): Show |
7 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.489+285C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4489161 | |||||||
chr19:4489163 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.489+287A>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4489163 | |||||||
chr19:4489245 | G | A | 39 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(36): Show |
39 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(36): Show |
intron_variant | MODIFIER | c.489+369G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4489245 | |||||||
chr19:4489259 | CT | C | 215 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(212): Show |
219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.489+396delT | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr19 | 4489259 | ||||||
chr19:4489301 | G | A | 3 | a0001c0002t0002g0262 a0001c0002t0007g0230 a0001c0002t0007g0334 |
3 | HG00558.hp2 HG02129.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.489+425G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4489301 | |||||||
chr19:4489367 | C | A | 1 | a0001c0001t0003g0017 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.489+491C>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4489367 | |||||||
chr19:4489409 | A | AT | 90 | a0001c0001t0003g0006 a0001c0001t0003g0016 a0001c0001t0003g0017 others(87): Show |
93 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.489+546dupT | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr19 | 4489409 | ||||||
chr19:4489452 | G | A | 1 | a0001c0001t0004g0155 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.489+576G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4489452 | |||||||
chr19:4489537 | G | A | 1 | a0001c0008t0003g0037 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.489+661G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4489537 | |||||||
chr19:4489561 | G | A | 2 | a0001c0001t0003g0042 a0001c0001t0003g0139 |
2 | HG00099.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.489+685G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4489561 | |||||||
chr19:4489621 | C | A | 6 | a0001c0001t0006g0003 a0001c0001t0006g0029 a0001c0001t0006g0079 others(3): Show |
7 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.489+745C>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4489621 | |||||||
chr19:4489632 | G | C | 1 | a0001c0014t0009g0209 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.489+756G>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4489632 | |||||||
chr19:4489786 | T | C | 148 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(145): Show |
151 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.489+910T>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4489786 | |||||||
chr19:4489844 | A | G | 1 | a0001c0014t0009g0209 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.489+968A>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4489844 | |||||||
chr19:4490051 | G | C | 1 | a0001c0001t0003g0047 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.489+1175G>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4490051 | |||||||
chr19:4490053 | A | T | 25 | a0001c0002t0003g0024 a0001c0002t0003g0064 a0001c0002t0003g0147 others(22): Show |
26 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.489+1177A>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4490053 | |||||||
chr19:4490060 | C | G | 1 | a0001c0001t0001g0034 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.489+1184C>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4490060 | |||||||
chr19:4490067 | C | T | 1 | a0008c0020t0004g0026 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.489+1191C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4490067 | |||||||
chr19:4490181 | G | A | 1 | a0001c0002t0005g0148 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.489+1305G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4490181 | |||||||
chr19:4490245 | G | A | 25 | a0001c0002t0003g0024 a0001c0002t0003g0064 a0001c0002t0003g0147 others(22): Show |
26 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.490-1321G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4490245 | |||||||
chr19:4490306 | C | T | 213 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(210): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.490-1260C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4490306 | |||||||
chr19:4490307 | G | A | 1 | a0009c0013t0002g0249 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.490-1259G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4490307 | |||||||
chr19:4490308 | A | G | 1 | a0009c0013t0002g0249 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.490-1258A>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4490308 | |||||||
chr19:4490336 | C | T | 148 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(145): Show |
151 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.490-1230C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4490336 | |||||||
chr19:4490419 | G | A | 147 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(144): Show |
150 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.490-1147G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4490419 | |||||||
chr19:4490513 | C | T | 39 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(36): Show |
39 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(36): Show |
intron_variant | MODIFIER | c.490-1053C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4490513 | |||||||
chr19:4490559 | G | A | 1 | a0001c0002t0002g0291 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.490-1007G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4490559 | |||||||
chr19:4490570 | C | G | 25 | a0001c0002t0003g0024 a0001c0002t0003g0064 a0001c0002t0003g0147 others(22): Show |
26 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.490-996C>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4490570 | |||||||
chr19:4490693 | G | A | 214 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(211): Show |
218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.490-873G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4490693 | |||||||
chr19:4490807 | CT | C | 212 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(209): Show |
216 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.490-747delT | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr19 | 4490807 | ||||||
chr19:4490877 | T | C | 212 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(209): Show |
216 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.490-689T>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4490877 | |||||||
chr19:4490878 | C | T | 2 | a0001c0008t0003g0037 a0001c0008t0003g0137 |
2 | HG01891.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.490-688C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4490878 | |||||||
chr19:4490881 | G | A | 1 | a0001c0001t0006g0003 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.490-685G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4490881 | |||||||
chr19:4490907 | G | C | 10 | a0001c0001t0003g0040 a0001c0001t0003g0042 a0001c0001t0003g0043 others(7): Show |
10 | HG00099.hp1 HG00280.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.490-659G>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4490907 | |||||||
chr19:4490917 | T | A | 1 | a0001c0001t0002g0132 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.490-649T>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4490917 | |||||||
chr19:4490919 | A | T | 1 | a0001c0001t0003g0139 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.490-647A>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4490919 | |||||||
chr19:4491042 | T | C | 1 | a0004c0005t0001g0183 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.490-524T>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4491042 | |||||||
chr19:4491121 | T | C | 11 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0096 others(8): Show |
11 | HG00544.hp2 HG03834.hp2 NA18950.hp1 others(8): Show |
intron_variant | MODIFIER | c.490-445T>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4491121 | |||||||
chr19:4491202 | C | T | 1 | a0001c0001t0004g0162 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.490-364C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4491202 | |||||||
chr19:4491249 | A | ACCCACCC others(1): Show |
7 | a0001c0001t0002g0210 a0001c0001t0002g0211 a0001c0001t0002g0221 others(4): Show |
7 | HG00738.hp2 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.490-289_490-282dup others(8): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr19 | 4491249 | ||||||
chr19:4491249 | A | C | 1 | a0001c0015t0001g0097 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.490-317A>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4491249 | |||||||
chr19:4491249 | ACCCACCC others(1): Show |
A | 3 | a0001c0001t0001g0092 a0001c0001t0014g0135 a0007c0010t0002g0269 |
3 | HG02300.hp2 HG02647.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.490-289_490-282del others(8): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr19 | 4491249 | ||||||
chr19:4491249 | ACCCACCC others(9): Show |
A | 31 | a0001c0001t0001g0089 a0001c0001t0001g0225 a0001c0001t0001g0226 others(28): Show |
32 | HG00280.hp2 HG01070.hp2 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.490-297_490-282del others(16): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr19 | 4491249 | ||||||
chr19:4491253 | A | C | 1 | a0001c0001t0003g0041 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.490-313A>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4491253 | |||||||
chr19:4491261 | A | AC | 40 | a0001c0001t0001g0004 a0001c0001t0001g0087 a0001c0001t0001g0105 others(37): Show |
40 | HG00140.hp2 HG00438.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.490-298dupC | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr19 | 4491261 | ||||||
chr19:4491261 | A | ACCCCCCC others(3): Show |
2 | a0001c0014t0009g0209 a0009c0013t0002g0249 |
2 | HG00735.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.490-298_490-297ins others(10): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr19 | 4491261 | ||||||
chr19:4491261 | A | C | 1 | a0001c0002t0002g0229 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.490-305A>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4491261 | |||||||
chr19:4491268 | C | CCA | 11 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0113 others(8): Show |
11 | HG01496.hp1 HG01496.hp2 HG02074.hp1 others(8): Show |
intron_variant | MODIFIER | c.490-298_490-297ins others(2): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4491268 | |||||||
chr19:4491268 | C | CCACCCCC others(3): Show |
1 | a0001c0002t0002g0315 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.490-298_490-297ins others(10): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4491268 | |||||||
chr19:4491269 | A | AC | 27 | a0001c0001t0001g0114 a0001c0001t0001g0189 a0001c0001t0001g0200 others(24): Show |
28 | HG00597.hp2 HG00741.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.490-290dupC | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr19 | 4491269 | ||||||
chr19:4491269 | A | C | 13 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0113 others(10): Show |
13 | HG01243.hp1 HG01496.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.490-297A>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4491269 | |||||||
chr19:4491277 | A | AC | 23 | a0001c0001t0001g0178 a0001c0001t0001g0219 a0001c0001t0001g0304 others(20): Show |
24 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(21): Show |
intron_variant | MODIFIER | c.490-281dupC | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr19 | 4491277 | ||||||
chr19:4491277 | A | ACCCCCCC others(3): Show |
1 | a0001c0014t0009g0209 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.490-281_490-280ins others(10): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr19 | 4491277 | ||||||
chr19:4491277 | A | C | 8 | a0001c0001t0001g0034 a0001c0001t0001g0118 a0001c0002t0002g0001 others(5): Show |
8 | HG01109.hp1 HG02056.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.490-289A>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4491277 | |||||||
chr19:4491288 | C | T | 1 | a0001c0002t0002g0240 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.490-278C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4491288 | |||||||
chr19:4491304 | C | G | 25 | a0001c0002t0003g0024 a0001c0002t0003g0064 a0001c0002t0003g0147 others(22): Show |
26 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.490-262C>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4491304 | |||||||
chr19:4491313 | C | T | 1 | a0008c0020t0004g0026 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.490-253C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4491313 | |||||||
chr19:4491479 | G | C | 214 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(211): Show |
218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.490-87G>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 4/15 | chr19 | 4491479 | |||||||
chr19:4491862 | A | G | 2 | a0005c0007t0003g0072 a0005c0007t0003g0073 |
2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.678+27A>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 6/15 | chr19 | 4491862 | |||||||
chr19:4491954 | T | A | 1 | a0001c0002t0002g0316 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.678+119T>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 6/15 | chr19 | 4491954 | |||||||
chr19:4491955 | A | G | 1 | a0001c0002t0002g0316 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.678+120A>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 6/15 | chr19 | 4491955 | |||||||
chr19:4491982 | C | T | 1 | a0001c0014t0009g0209 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.678+147C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 6/15 | chr19 | 4491982 | |||||||
chr19:4492120 | G | A | 1 | a0001c0001t0003g0017 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.678+285G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 6/15 | chr19 | 4492120 | |||||||
chr19:4492165 | G | A | 25 | a0001c0002t0003g0024 a0001c0002t0003g0064 a0001c0002t0003g0147 others(22): Show |
26 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.678+330G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 6/15 | chr19 | 4492165 | |||||||
chr19:4492340 | CTG | C | 119 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(116): Show |
120 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.678+515_678+516del others(2): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr19 | 4492340 | ||||||
chr19:4492441 | T | C | 25 | a0001c0002t0003g0024 a0001c0002t0003g0064 a0001c0002t0003g0147 others(22): Show |
26 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.678+606T>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 6/15 | chr19 | 4492441 | |||||||
chr19:4492461 | CTG | C | 25 | a0001c0002t0003g0024 a0001c0002t0003g0064 a0001c0002t0003g0147 others(22): Show |
26 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.678+635_678+636del others(2): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr19 | 4492461 | ||||||
chr19:4492541 | C | G | 20 | a0001c0001t0003g0006 a0001c0001t0003g0028 a0001c0001t0003g0036 others(17): Show |
22 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.678+706C>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 6/15 | chr19 | 4492541 | |||||||
chr19:4492743 | T | TGTC | 25 | a0001c0002t0003g0024 a0001c0002t0003g0064 a0001c0002t0003g0147 others(22): Show |
26 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.678+909_678+910ins others(3): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr19 | 4492743 | ||||||
chr19:4492795 | T | G | 25 | a0001c0002t0003g0024 a0001c0002t0003g0064 a0001c0002t0003g0147 others(22): Show |
26 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.679-908T>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 6/15 | chr19 | 4492795 | |||||||
chr19:4492802 | C | CTGTATGT others(6): Show |
25 | a0001c0002t0003g0024 a0001c0002t0003g0064 a0001c0002t0003g0147 others(22): Show |
26 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.679-898_679-897ins others(13): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr19 | 4492802 | ||||||
chr19:4492820 | C | CTGTGTGT others(1614): Show |
11 | a0001c0002t0004g0071 a0001c0002t0004g0154 a0001c0002t0005g0002 others(8): Show |
12 | HG02257.hp1 HG02280.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.679-854_679-853ins others(1621): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr19 | 4492820 | ||||||
chr19:4492820 | C | CTGTGTGT others(1614): Show |
13 | a0001c0002t0003g0024 a0001c0002t0003g0147 a0001c0002t0004g0011 others(10): Show |
13 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.679-854_679-853ins others(1621): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr19 | 4492820 | ||||||
chr19:4492820 | C | CTGTGTGT others(1607): Show |
1 | a0001c0002t0003g0064 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.679-854_679-853ins others(1614): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr19 | 4492820 | ||||||
chr19:4492891 | C | CTG | 92 | a0001c0001t0003g0006 a0001c0001t0003g0016 a0001c0001t0003g0017 others(89): Show |
95 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.679-809_679-808dup others(2): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr19 | 4492891 | ||||||
chr19:4492936 | GGT | G | 40 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(37): Show |
40 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(37): Show |
intron_variant | MODIFIER | c.679-755_679-754del others(2): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr19 | 4492936 | ||||||
chr19:4492936 | GGTGT | G | 3 | a0001c0001t0004g0155 a0001c0001t0004g0162 a0001c0001t0013g0080 |
3 | HG02109.hp2 HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.679-757_679-754del others(4): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr19 | 4492936 | ||||||
chr19:4492942 | T | A | 10 | a0001c0002t0002g0260 a0001c0002t0002g0299 a0001c0002t0002g0311 others(7): Show |
10 | HG00738.hp2 HG01167.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.679-761T>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 6/15 | chr19 | 4492942 | |||||||
chr19:4492959 | A | T | 25 | a0001c0002t0003g0024 a0001c0002t0003g0064 a0001c0002t0003g0147 others(22): Show |
26 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.679-744A>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 6/15 | chr19 | 4492959 | |||||||
chr19:4492961 | T | TTATC | 25 | a0001c0002t0003g0024 a0001c0002t0003g0064 a0001c0002t0003g0147 others(22): Show |
26 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.679-741_679-740ins others(4): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr19 | 4492961 | ||||||
chr19:4492963 | G | T | 1 | a0001c0001t0001g0122 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.679-740G>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 6/15 | chr19 | 4492963 | |||||||
chr19:4492965 | C | G | 25 | a0001c0002t0003g0024 a0001c0002t0003g0064 a0001c0002t0003g0147 others(22): Show |
26 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.679-738C>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 6/15 | chr19 | 4492965 | |||||||
chr19:4493004 | G | A | 12 | a0001c0002t0003g0024 a0001c0002t0003g0064 a0001c0002t0004g0011 others(9): Show |
12 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.679-699G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 6/15 | chr19 | 4493004 | |||||||
chr19:4493090 | C | CTGTG | 274 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(271): Show |
284 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.679-610_679-607dup others(4): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr19 | 4493090 | ||||||
chr19:4493093 | TGTG | T | 25 | a0001c0002t0003g0024 a0001c0002t0003g0064 a0001c0002t0003g0147 others(22): Show |
26 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.679-606_679-604del others(3): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr19 | 4493093 | ||||||
chr19:4493117 | C | CTG | 25 | a0001c0002t0003g0024 a0001c0002t0003g0064 a0001c0002t0003g0147 others(22): Show |
26 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.679-579_679-578dup others(2): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr19 | 4493117 | ||||||
chr19:4493134 | GTT | G | 39 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(36): Show |
39 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(36): Show |
intron_variant | MODIFIER | c.679-568_679-567del others(2): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 6/15 | chr19 | 4493134 | |||||||
chr19:4493198 | GTGTC | G | 39 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(36): Show |
39 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(36): Show |
intron_variant | MODIFIER | c.679-501_679-498del others(4): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr19 | 4493198 | ||||||
chr19:4493219 | TGTG | T | 3 | a0001c0002t0004g0011 a0001c0002t0004g0021 a0001c0002t0004g0022 |
3 | HG01070.hp2 HG01071.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.679-480_679-478del others(3): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr19 | 4493219 | ||||||
chr19:4493223 | G | T | 1 | a0001c0001t0003g0145 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.679-480G>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 6/15 | chr19 | 4493223 | |||||||
chr19:4493224 | T | G | 1 | a0001c0001t0003g0145 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.679-479T>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 6/15 | chr19 | 4493224 | |||||||
chr19:4493234 | C | G | 1 | a0008c0020t0004g0026 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.679-469C>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 6/15 | chr19 | 4493234 | |||||||
chr19:4493240 | G | T | 1 | a0008c0020t0004g0026 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.679-463G>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 6/15 | chr19 | 4493240 | |||||||
chr19:4493243 | A | C | 1 | a0008c0020t0004g0026 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.679-460A>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 6/15 | chr19 | 4493243 | |||||||
chr19:4493282 | CTGTGTGT others(4): Show |
C | 2 | a0001c0002t0001g0342 a0001c0002t0002g0280 |
2 | HG00323.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.679-397_679-387del others(11): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr19 | 4493282 | ||||||
chr19:4493392 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.679-311C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 6/15 | chr19 | 4493392 | |||||||
chr19:4493467 | G | A | 24 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(21): Show |
24 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(21): Show |
intron_variant | MODIFIER | c.679-236G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 6/15 | chr19 | 4493467 | |||||||
chr19:4493497 | C | T | 1 | a0001c0001t0003g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.679-206C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 6/15 | chr19 | 4493497 | |||||||
chr19:4493642 | G | A | 1 | a0001c0001t0004g0155 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.679-61G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 6/15 | chr19 | 4493642 | |||||||
chr19:4493936 | T | C | 1 | a0001c0002t0002g0231 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.839-46T>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 7/15 | chr19 | 4493936 | |||||||
chr19:4493967 | C | T | 1 | a0001c0002t0009g0015 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.839-15C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 7/15 | chr19 | 4493967 | |||||||
chr19:4494531 | T | C | 1 | a0001c0001t0006g0003 | 2 | HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1224+56T>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 9/15 | chr19 | 4494531 | |||||||
chr19:4494569 | C | T | 1 | a0008c0020t0004g0026 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1224+94C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 9/15 | chr19 | 4494569 | |||||||
chr19:4494641 | C | T | 1 | a0008c0020t0004g0026 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1224+166C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 9/15 | chr19 | 4494641 | |||||||
chr19:4494659 | C | T | 13 | a0001c0002t0003g0147 a0001c0002t0004g0071 a0001c0002t0004g0154 others(10): Show |
14 | HG02257.hp1 HG02280.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1224+184C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 9/15 | chr19 | 4494659 | |||||||
chr19:4494706 | G | A | 13 | a0001c0002t0003g0147 a0001c0002t0004g0071 a0001c0002t0004g0154 others(10): Show |
14 | HG02257.hp1 HG02280.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1224+231G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 9/15 | chr19 | 4494706 | |||||||
chr19:4494790 | C | T | 12 | a0001c0001t0004g0078 a0001c0001t0004g0155 a0001c0001t0006g0003 others(9): Show |
13 | HG01109.hp2 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.1224+315C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 9/15 | chr19 | 4494790 | |||||||
chr19:4494867 | C | G | 12 | a0001c0002t0003g0024 a0001c0002t0003g0064 a0001c0002t0004g0011 others(9): Show |
12 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.1224+392C>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 9/15 | chr19 | 4494867 | |||||||
chr19:4494988 | G | A | 1 | a0001c0008t0003g0137 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1224+513G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 9/15 | chr19 | 4494988 | |||||||
chr19:4495036 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1224+561A>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 9/15 | chr19 | 4495036 | |||||||
chr19:4495151 | G | T | 6 | a0001c0001t0001g0093 a0001c0001t0001g0131 a0001c0001t0001g0136 others(3): Show |
6 | NA18950.hp1 NA18951.hp2 NA19002.hp2 others(3): Show |
intron_variant | MODIFIER | c.1224+676G>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 9/15 | chr19 | 4495151 | |||||||
chr19:4495159 | G | A | 176 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(173): Show |
177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.1224+684G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 9/15 | chr19 | 4495159 | |||||||
chr19:4495162 | T | C | 210 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(207): Show |
214 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.1224+687T>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 9/15 | chr19 | 4495162 | |||||||
chr19:4495184 | A | G | 1 | a0001c0002t0003g0147 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1224+709A>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 9/15 | chr19 | 4495184 | |||||||
chr19:4495260 | T | C | 321 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(318): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1224+785T>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 9/15 | chr19 | 4495260 | |||||||
chr19:4495385 | C | CA | 57 | a0001c0001t0001g0293 a0001c0001t0003g0006 a0001c0001t0003g0028 others(54): Show |
60 | HG00140.hp2 HG00438.hp2 HG01081.hp2 others(57): Show |
intron_variant | MODIFIER | c.1225-893dupA | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr19 | 4495385 | ||||||
chr19:4495385 | C | CAA | 12 | a0001c0001t0003g0157 a0001c0001t0003g0158 a0001c0002t0001g0274 others(9): Show |
12 | HG01975.hp2 HG02027.hp1 HG02027.hp2 others(9): Show |
intron_variant | MODIFIER | c.1225-894_1225-893d others(4): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr19 | 4495385 | ||||||
chr19:4495385 | C | CAAA | 7 | a0001c0001t0001g0089 a0001c0001t0001g0092 a0001c0001t0001g0107 others(4): Show |
7 | HG00735.hp2 HG01257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1225-895_1225-893d others(5): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr19 | 4495385 | ||||||
chr19:4495385 | C | CAAAA | 111 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(108): Show |
111 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.1225-896_1225-893d others(6): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr19 | 4495385 | ||||||
chr19:4495385 | C | CAAAAA | 12 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0093 others(9): Show |
13 | HG00738.hp1 HG01081.hp1 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.1225-897_1225-893d others(7): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr19 | 4495385 | ||||||
chr19:4495385 | CA | C | 10 | a0001c0001t0003g0018 a0001c0001t0003g0141 a0001c0001t0004g0155 others(7): Show |
10 | HG00280.hp1 HG00609.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.1225-893delA | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr19 | 4495385 | ||||||
chr19:4495410 | T | A | 13 | a0001c0001t0003g0006 a0001c0001t0003g0028 a0001c0001t0003g0036 others(10): Show |
14 | HG01891.hp2 HG02486.hp2 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.1225-892T>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 9/15 | chr19 | 4495410 | |||||||
chr19:4495433 | A | T | 2 | a0001c0001t0001g0188 a0001c0001t0001g0201 |
2 | HG02572.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1225-869A>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 9/15 | chr19 | 4495433 | |||||||
chr19:4495505 | C | T | 10 | a0001c0001t0003g0006 a0001c0001t0003g0028 a0001c0001t0003g0074 others(7): Show |
11 | HG01891.hp2 HG02486.hp2 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.1225-797C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 9/15 | chr19 | 4495505 | |||||||
chr19:4495608 | C | T | 1 | a0008c0020t0004g0026 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1225-694C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 9/15 | chr19 | 4495608 | |||||||
chr19:4495611 | G | GT | 10 | a0001c0002t0001g0242 a0001c0002t0001g0248 a0001c0002t0001g0296 others(7): Show |
10 | HG02055.hp2 HG02258.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1225-690dupT | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr19 | 4495611 | ||||||
chr19:4495619 | A | C | 1 | a0001c0014t0009g0209 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1225-683A>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 9/15 | chr19 | 4495619 | |||||||
chr19:4495836 | T | A | 1 | a0001c0002t0002g0316 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1225-466T>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 9/15 | chr19 | 4495836 | |||||||
chr19:4495963 | C | T | 1 | a0001c0001t0002g0088 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1225-339C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 9/15 | chr19 | 4495963 | |||||||
chr19:4496035 | C | T | 13 | a0001c0002t0003g0147 a0001c0002t0004g0071 a0001c0002t0004g0154 others(10): Show |
14 | HG02257.hp1 HG02280.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1225-267C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 9/15 | chr19 | 4496035 | |||||||
chr19:4496049 | C | T | 64 | a0001c0001t0003g0006 a0001c0001t0003g0016 a0001c0001t0003g0017 others(61): Show |
66 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.1225-253C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 9/15 | chr19 | 4496049 | |||||||
chr19:4496201 | A | G | 213 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(210): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.1225-101A>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 9/15 | chr19 | 4496201 | |||||||
chr19:4496598 | A | G | 68 | a0001c0001t0003g0006 a0001c0001t0003g0016 a0001c0001t0003g0017 others(65): Show |
70 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.1328+193A>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 10/15 | chr19 | 4496598 | |||||||
chr19:4496615 | C | T | 210 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(207): Show |
214 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.1328+210C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 10/15 | chr19 | 4496615 | |||||||
chr19:4496636 | G | A | 13 | a0001c0002t0003g0147 a0001c0002t0004g0071 a0001c0002t0004g0154 others(10): Show |
14 | HG02257.hp1 HG02280.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1328+231G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 10/15 | chr19 | 4496636 | |||||||
chr19:4496711 | G | A | 42 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(39): Show |
42 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(39): Show |
intron_variant | MODIFIER | c.1328+306G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 10/15 | chr19 | 4496711 | |||||||
chr19:4496743 | C | G | 1 | a0001c0015t0001g0097 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1328+338C>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 10/15 | chr19 | 4496743 | |||||||
chr19:4496869 | C | CT | 194 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(191): Show |
197 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.1328+480dupT | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr19 | 4496869 | ||||||
chr19:4496869 | C | CTT | 7 | a0001c0001t0001g0178 a0001c0001t0001g0304 a0001c0001t0002g0211 others(4): Show |
7 | HG02258.hp1 HG02738.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1328+479_1328+480d others(4): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr19 | 4496869 | ||||||
chr19:4496890 | T | C | 1 | a0001c0001t0001g0201 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1328+485T>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 10/15 | chr19 | 4496890 | |||||||
chr19:4496891 | G | A | 1 | a0001c0001t0004g0044 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1328+486G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 10/15 | chr19 | 4496891 | |||||||
chr19:4496904 | T | C | 65 | a0001c0001t0003g0006 a0001c0001t0003g0016 a0001c0001t0003g0017 others(62): Show |
67 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.1328+499T>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 10/15 | chr19 | 4496904 | |||||||
chr19:4497031 | C | A | 1 | a0001c0001t0004g0162 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1328+626C>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 10/15 | chr19 | 4497031 | |||||||
chr19:4497094 | C | T | 2 | a0001c0008t0003g0037 a0001c0008t0003g0137 |
2 | HG01891.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1328+689C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 10/15 | chr19 | 4497094 | |||||||
chr19:4497181 | C | T | 3 | a0001c0002t0002g0309 a0001c0002t0002g0331 a0001c0002t0004g0065 |
3 | HG01106.hp2 HG01168.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1328+776C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 10/15 | chr19 | 4497181 | |||||||
chr19:4497200 | G | GT | 16 | a0001c0001t0001g0131 a0001c0001t0002g0132 a0001c0002t0003g0147 others(13): Show |
17 | HG00741.hp2 HG02257.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.1329-749dupT | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr19 | 4497200 | ||||||
chr19:4497200 | GT | G | 26 | a0001c0001t0003g0006 a0001c0001t0003g0028 a0001c0001t0003g0036 others(23): Show |
28 | HG01109.hp2 HG01884.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.1329-749delT | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr19 | 4497200 | ||||||
chr19:4497201 | T | TTTTTG | 42 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(39): Show |
42 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(39): Show |
intron_variant | MODIFIER | c.1329-753_1329-752i others(7): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr19 | 4497201 | ||||||
chr19:4497259 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1329-699G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 10/15 | chr19 | 4497259 | |||||||
chr19:4497394 | T | C | 1 | a0001c0002t0002g0278 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1329-564T>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 10/15 | chr19 | 4497394 | |||||||
chr19:4497412 | T | C | 1 | a0001c0001t0001g0178 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1329-546T>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 10/15 | chr19 | 4497412 | |||||||
chr19:4497420 | A | C | 3 | a0001c0002t0002g0237 a0001c0002t0002g0333 a0001c0002t0011g0319 |
3 | HG02280.hp2 HG02615.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1329-538A>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 10/15 | chr19 | 4497420 | |||||||
chr19:4497439 | C | T | 1 | a0001c0002t0004g0025 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1329-519C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 10/15 | chr19 | 4497439 | |||||||
chr19:4497517 | G | A | 13 | a0001c0002t0003g0147 a0001c0002t0004g0071 a0001c0002t0004g0154 others(10): Show |
14 | HG02257.hp1 HG02280.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1329-441G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 10/15 | chr19 | 4497517 | |||||||
chr19:4497529 | G | C | 64 | a0001c0001t0003g0006 a0001c0001t0003g0016 a0001c0001t0003g0017 others(61): Show |
66 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.1329-429G>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 10/15 | chr19 | 4497529 | |||||||
chr19:4497535 | C | G | 8 | a0001c0002t0003g0024 a0001c0002t0004g0011 a0001c0002t0004g0021 others(5): Show |
8 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1329-423C>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 10/15 | chr19 | 4497535 | |||||||
chr19:4497551 | G | A | 1 | a0001c0001t0003g0056 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1329-407G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 10/15 | chr19 | 4497551 | |||||||
chr19:4497734 | G | T | 1 | a0001c0002t0001g0121 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1329-224G>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 10/15 | chr19 | 4497734 | |||||||
chr19:4497772 | G | A | 1 | a0001c0002t0002g0204 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1329-186G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 10/15 | chr19 | 4497772 | |||||||
chr19:4497926 | G | A | 1 | a0001c0002t0002g0229 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1329-32G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 10/15 | chr19 | 4497926 | |||||||
chr19:4497932 | C | T | 2 | a0001c0001t0008g0083 a0001c0001t0008g0084 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1329-26C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 10/15 | chr19 | 4497932 | |||||||
chr19:4498097 | G | A | 26 | a0001c0001t0003g0006 a0001c0001t0003g0028 a0001c0001t0003g0036 others(23): Show |
28 | HG01109.hp2 HG01884.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.1402+66G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 11/15 | chr19 | 4498097 | |||||||
chr19:4498143 | C | T | 1 | a0008c0020t0004g0026 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1402+112C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 11/15 | chr19 | 4498143 | |||||||
chr19:4498151 | G | A | 1 | a0001c0001t0001g0172 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1402+120G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 11/15 | chr19 | 4498151 | |||||||
chr19:4498155 | T | A | 1 | a0001c0002t0002g0321 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1402+124T>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 11/15 | chr19 | 4498155 | |||||||
chr19:4498156 | G | T | 1 | a0001c0002t0002g0321 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1402+125G>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 11/15 | chr19 | 4498156 | |||||||
chr19:4498157 | G | A | 129 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(126): Show |
130 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.1402+126G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 11/15 | chr19 | 4498157 | |||||||
chr19:4498158 | C | A | 1 | a0001c0002t0002g0321 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1402+127C>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 11/15 | chr19 | 4498158 | |||||||
chr19:4498160 | G | A | 128 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(125): Show |
129 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.1402+129G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 11/15 | chr19 | 4498160 | |||||||
chr19:4498162 | C | A | 1 | a0001c0002t0002g0321 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1402+131C>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 11/15 | chr19 | 4498162 | |||||||
chr19:4498163 | G | C | 1 | a0001c0002t0002g0321 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1402+132G>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 11/15 | chr19 | 4498163 | |||||||
chr19:4498167 | C | T | 1 | a0001c0002t0002g0321 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1402+136C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 11/15 | chr19 | 4498167 | |||||||
chr19:4498168 | C | G | 1 | a0001c0002t0002g0321 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1402+137C>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 11/15 | chr19 | 4498168 | |||||||
chr19:4498170 | C | T | 1 | a0001c0002t0002g0321 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1403-136C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 11/15 | chr19 | 4498170 | |||||||
chr19:4498215 | A | C | 43 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(40): Show |
43 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(40): Show |
intron_variant | MODIFIER | c.1403-91A>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 11/15 | chr19 | 4498215 | |||||||
chr19:4498248 | A | G | 216 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(213): Show |
220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.1403-58A>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 11/15 | chr19 | 4498248 | |||||||
chr19:4498283 | C | T | 1 | a0001c0002t0002g0254 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1403-23C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 11/15 | chr19 | 4498283 | |||||||
chr19:4498399 | G | C | 1 | a0001c0001t0004g0081 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1473+23G>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 12/15 | chr19 | 4498399 | |||||||
chr19:4498443 | T | C | 187 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0185 others(184): Show |
195 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(192): Show |
intron_variant | MODIFIER | c.1473+67T>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 12/15 | chr19 | 4498443 | |||||||
chr19:4498703 | A | T | 283 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(280): Show |
292 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.1474-111A>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 12/15 | chr19 | 4498703 | |||||||
chr19:4498747 | C | T | 1 | a0001c0002t0002g0227 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1474-67C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 12/15 | chr19 | 4498747 | |||||||
chr19:4498923 | G | C | 3 | a0001c0001t0003g0046 a0001c0001t0003g0050 a0001c0001t0003g0060 |
3 | NA18955.hp2 NA18983.hp1 NA19005.hp1 |
splice_region_variant&intron_variant | LOW | c.1575+8G>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 13/15 | chr19 | 4498923 | |||||||
chr19:4498977 | C | T | 1 | a0001c0002t0001g0346 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1575+62C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 13/15 | chr19 | 4498977 | |||||||
chr19:4499007 | C | A | 1 | a0001c0002t0001g0330 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1575+92C>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 13/15 | chr19 | 4499007 | |||||||
chr19:4499026 | C | T | 139 | a0001c0001t0002g0088 a0001c0001t0002g0167 a0001c0001t0003g0038 others(136): Show |
147 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.1575+111C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 13/15 | chr19 | 4499026 | |||||||
chr19:4499083 | C | G | 1 | a0008c0020t0004g0026 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1575+168C>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 13/15 | chr19 | 4499083 | |||||||
chr19:4499088 | C | T | 1 | a0008c0020t0004g0026 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1575+173C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 13/15 | chr19 | 4499088 | |||||||
chr19:4499246 | T | C | 1 | a0001c0002t0002g0241 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1576-245T>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 13/15 | chr19 | 4499246 | |||||||
chr19:4499294 | C | T | 7 | a0001c0001t0003g0208 a0001c0001t0006g0003 a0001c0001t0006g0029 others(4): Show |
8 | HG01109.hp2 HG01884.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1576-197C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 13/15 | chr19 | 4499294 | |||||||
chr19:4499330 | G | A | 274 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(271): Show |
283 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.1576-161G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 13/15 | chr19 | 4499330 | |||||||
chr19:4499345 | C | CA | 135 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(132): Show |
136 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.1576-133dupA | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr19 | 4499345 | ||||||
chr19:4499417 | T | TGGGGCGA others(13): Show |
1 | a0001c0002t0002g0236 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1576-68_1576-49dup others(20): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr19 | 4499417 | ||||||
chr19:4499425 | G | T | 13 | a0001c0002t0003g0147 a0001c0002t0004g0071 a0001c0002t0004g0154 others(10): Show |
14 | HG02257.hp1 HG02280.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1576-66G>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 13/15 | chr19 | 4499425 | |||||||
chr19:4499718 | G | C | 1 | a0001c0002t0005g0153 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1789+14G>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 14/15 | chr19 | 4499718 | |||||||
chr19:4499838 | G | A | 127 | a0001c0001t0002g0088 a0001c0001t0002g0167 a0001c0001t0003g0038 others(124): Show |
134 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.1789+134G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 14/15 | chr19 | 4499838 | |||||||
chr19:4499845 | C | T | 1 | a0001c0001t0003g0144 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1789+141C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 14/15 | chr19 | 4499845 | |||||||
chr19:4499857 | G | A | 1 | a0001c0002t0005g0153 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1789+153G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 14/15 | chr19 | 4499857 | |||||||
chr19:4499927 | T | C | 274 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(271): Show |
283 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.1789+223T>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 14/15 | chr19 | 4499927 | |||||||
chr19:4499964 | T | C | 140 | a0001c0001t0002g0088 a0001c0001t0002g0167 a0001c0001t0003g0038 others(137): Show |
148 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.1789+260T>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 14/15 | chr19 | 4499964 | |||||||
chr19:4499997 | C | T | 2 | a0001c0001t0001g0188 a0001c0001t0001g0201 |
2 | HG02572.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1789+293C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 14/15 | chr19 | 4499997 | |||||||
chr19:4500046 | TG | T | 338 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(335): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.1789+347delG | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr19 | 4500046 | ||||||
chr19:4500150 | G | A | 3 | a0001c0001t0002g0210 a0001c0001t0002g0211 a0001c0001t0002g0221 |
3 | HG02258.hp1 HG02451.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1789+446G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 14/15 | chr19 | 4500150 | |||||||
chr19:4500193 | A | G | 274 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(271): Show |
283 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.1789+489A>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 14/15 | chr19 | 4500193 | |||||||
chr19:4500213 | T | A | 4 | a0001c0002t0001g0342 a0001c0002t0002g0279 a0001c0002t0002g0280 others(1): Show |
4 | HG00323.hp1 HG01069.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.1789+509T>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 14/15 | chr19 | 4500213 | |||||||
chr19:4500277 | T | C | 2 | a0005c0007t0003g0072 a0005c0007t0003g0073 |
2 | HG03098.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1789+573T>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 14/15 | chr19 | 4500277 | |||||||
chr19:4500337 | A | G | 1 | a0001c0002t0009g0015 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1789+633A>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 14/15 | chr19 | 4500337 | |||||||
chr19:4500452 | A | AT | 7 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0049 others(4): Show |
7 | HG00280.hp1 HG04184.hp1 HG04228.hp1 others(4): Show |
intron_variant | MODIFIER | c.1790-713dupT | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr19 | 4500452 | ||||||
chr19:4500452 | AT | A | 279 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(276): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.1790-713delT | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr19 | 4500452 | ||||||
chr19:4500452 | ATT | A | 7 | a0001c0001t0001g0127 a0001c0001t0001g0214 a0001c0001t0003g0028 others(4): Show |
7 | HG01256.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1790-714_1790-713d others(4): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr19 | 4500452 | ||||||
chr19:4500452 | ATTTTTTT others(3): Show |
A | 4 | a0001c0001t0008g0082 a0001c0001t0008g0083 a0001c0001t0008g0084 others(1): Show |
4 | HG02630.hp1 HG02717.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1790-722_1790-713d others(12): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr19 | 4500452 | ||||||
chr19:4500475 | T | G | 273 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(270): Show |
282 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.1790-716T>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 14/15 | chr19 | 4500475 | |||||||
chr19:4500521 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1790-670C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 14/15 | chr19 | 4500521 | |||||||
chr19:4500553 | T | C | 1 | a0001c0002t0002g0266 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1790-638T>C | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 14/15 | chr19 | 4500553 | |||||||
chr19:4500578 | A | AGCCTCCC others(5): Show |
35 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(32): Show |
35 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(32): Show |
intron_variant | MODIFIER | c.1790-606_1790-605i others(14): Show |
HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr19 | 4500578 | ||||||
chr19:4500812 | A | G | 338 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(335): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.1790-379A>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 14/15 | chr19 | 4500812 | |||||||
chr19:4500869 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1790-322G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 14/15 | chr19 | 4500869 | |||||||
chr19:4501105 | C | T | 6 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(3): Show |
6 | HG01261.hp2 HG01346.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.1790-86C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 14/15 | chr19 | 4501105 | |||||||
chr19:4501176 | C | G | 1 | a0001c0002t0002g0290 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1790-15C>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 14/15 | chr19 | 4501176 | |||||||
chr19:4501384 | G | A | 1 | a0001c0017t0003g0075 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1916+67G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 15/15 | chr19 | 4501384 | |||||||
chr19:4501585 | C | G | 1 | a0001c0002t0002g0290 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1916+268C>G | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 15/15 | chr19 | 4501585 | |||||||
chr19:4501602 | C | T | 1 | a0001c0001t0003g0077 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1916+285C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 15/15 | chr19 | 4501602 | |||||||
chr19:4501609 | G | A | 270 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(267): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.1916+292G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 15/15 | chr19 | 4501609 | |||||||
chr19:4501627 | C | T | 1 | a0001c0002t0002g0134 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1917-284C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 15/15 | chr19 | 4501627 | |||||||
chr19:4501691 | C | T | 1 | a0001c0001t0003g0055 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1917-220C>T | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 15/15 | chr19 | 4501691 | |||||||
chr19:4501789 | G | A | 3 | a0001c0002t0002g0258 a0001c0002t0002g0312 a0001c0002t0002g0317 |
3 | HG00099.hp2 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1917-122G>A | HDGFL2 | ENSG00000167674.15 | transcript | ENST00000616600.5 | protein_coding | 15/15 | chr19 | 4501789 |